{"title":"Nucleobases and their Analogs","description":"\u003cp\u003e\u003cstrong\u003eNucleobases and their Analogs\u003c\/strong\u003e — mencakup basa nitrogen purin dan pirimidin beserta analog tersubstitusinya, seperti turunan terklorinasi, teraza, atau bentuk garamnya, yang menjadi unit dasar penyusun asam nukleat. Variasi substituen pada cincin heterosiklik memberi ragam sifat kelarutan dan reaktivitas untuk kebutuhan sintesis lanjutan.\u003c\/p\u003e\u003cp\u003eNucleobases and their Analogs dipakai dalam sintesis nukleosida dan nukleotida termodifikasi, riset biologi molekuler, serta pengembangan senyawa acuan untuk riset pada jalur metabolisme purin dan pirimidin. Analog seperti turunan azauracil atau klorpurin umum dipakai sebagai bahan awal reaksi substitusi heterosiklik untuk membangun struktur analog nukleosida yang lebih kompleks.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0558779\"\u003eTCI A0558 461-89-2 6-Azauracil\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c027814308\"\u003eTCI C0278 87-42-3 6-Chloropurine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0151233\"\u003eTCI A0151 6509-19-9 Adenine Sulfate Dihydrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c029314340\"\u003eTCI C0293 85-18-7 8-Chlorotheophylline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0150231\"\u003eTCI A0150 6055-72-7 Adenine Hydrochloride Hemihydrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c052814719\"\u003eTCI C0528 71-30-7 Cytosine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0149229\"\u003eTCI A0149 73-24-5 Adenine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c096915321\"\u003eTCI C0969 1820-81-1 5-Chlorouracil\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan bentuk garam atau hidrat, posisi substitusi pada cincin purin\/pirimidin, serta kemurnian yang sesuai untuk reaksi sintesis atau penggunaan sebagai bahan uji in vitro. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Nucleosides, Nucleotides, Oligonucleotides, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nucleoside-analogs\"\u003eNucleoside Analogs\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nucleosides\"\u003eNucleosides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nucleotides\"\u003eNucleotides\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nucleotide-analogs\"\u003eNucleotide Analogs\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nad-p-h-and-analogs\"\u003eNAD(P)(H) and Analogs\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-oxidoreductase-coenzymes-nucleosides-nucleotides-oligonucleotides\"\u003eOxidoreductase Coenzymes [Nucleosides, Nucleotides, Oligonucleotides]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-nucleosides-nucleotides-oligonucleotides\"\u003eNucleosides, Nucleotides, Oligonucleotides\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510c027814308","title":"TCI C0278 87-42-3 6-Chloropurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloropurine is a chemical compound classified under the heterocyclic category, featuring a purine core with a chlorine substituent at the 6-position. This compound plays a crucial role in laboratory settings as a building block for the synthesis of complex molecules, particularly in organic and pharmaceutical research. Its structural versatility makes it a valuable resource for chemists seeking to develop compounds with specific biological activities. In the context of modern scientific inquiry, 6-Chloropurine is often the starting point for the creation of novel drugs or specialized chemical entities.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stable molecular structure and controlled reactivity, which allows it to participate in various chemical reactions such as substitution, reduction, and nucleophilic reactions. These properties make it a preferred choice for researchers aiming to design efficient synthetic pathways. Its adaptability to different reaction conditions enhances its utility in laboratory workflows, enabling the production of a wide range of derivatives. This flexibility is essential for advancing both academic and industrial chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chloropurine is widely used across various research institutions and academic settings. Its availability in solid form and ease of processing make it a practical option for routine chemical synthesis. It is particularly favored in pharmaceutical and organic chemistry departments, where it supports the development of new compounds and the exploration of chemical reactivity. Its role in drug discovery and chemical innovation underscores its importance in the scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: 6-Chloropurine is widely used in organic synthesis due to its versatile structure and reactivity, enabling the creation of complex molecules with specific functionalities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: This compound is a key building block in the development of new drugs, as it can be modified to produce compounds with desired biological activities.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic chemistry: Its heterocyclic nature makes it ideal for studying the properties and reactivity of purine derivatives in various chemical contexts.\u003c\/li\u003e\n\u003cli\u003eDrug discovery: Researchers use 6-Chloropurine as a starting material for the synthesis of potential therapeutic agents, contributing to the advancement of medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eChemical education: It is commonly used in teaching laboratories to demonstrate the principles of chemical synthesis and molecular manipulation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 87-42-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Chloropurine should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. While it is generally stable under normal storage conditions, it is advisable to avoid prolonged exposure to extreme temperatures or reactive substances. Proper labeling and storage practices are essential to maintain the quality and usability of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085984608474,"sku":"TCI2510C027814308","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085984641242,"sku":"TCI2510C027814309","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0278.jpg?v=1767094944"},{"product_id":"tci2510c029314340","title":"TCI C0293 85-18-7 8-Chlorotheophylline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0293 8-Chlorotheophylline (CAS 85-18-7) is a chlorinated xanthine derivative listed under alkaloid biochemicals and reagents. It is closely related to theophylline and is frequently referenced in medicinal chemistry research, salt-form preparation, and analytical method development for purine compounds. Its acidic character makes it a practical partner for forming salts with amine bases in laboratory-scale formulation studies. AMI Scientific supplies this TCI reagent in 25 g and 250 g packs for research and laboratory use only.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGabhe et al. (2011). Isolation and characterization of impurities present in 8-chlorotheophylline. \u003cem\u003eIndian Journal of Pharmaceutical Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4103\/0250-474x.89762\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4103\/0250-474x.89762\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJIN et al. (1993). ChemInform Abstract: Reaction Between 8‐Chlorotheophylline and Epoxides. A Simple Preparation of Oxazolido(2,3‐f)purines.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199310270\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199310270\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eA. Abdul‐Reda et al. (2018). Synthesis, Identification and Biological Activity of Some New Chalcone derivatives from 8-Chlorotheophylline. \u003cem\u003eOriental Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.13005\/ojc\/340144\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.13005\/ojc\/340144\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085986115802,"sku":"TCI2510C029314340","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085986148570,"sku":"TCI2510C029314341","price":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0293.jpg?v=1769180306"},{"product_id":"tci2510c052814719","title":"TCI C0528 71-30-7 Cytosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0528 Cytosine (CAS 71-30-7) is one of the four nucleobases found in DNA and RNA, supplied as a heterocyclic building block for research. It is widely used in pyrimidine synthesis, medicinal chemistry exploration, and as a reference material for nucleobase analysis. Pack sizes of 5 g, 25 g, and 100 g cover both trial-scale and routine synthetic work. Keep the container tightly sealed in a cool, dry place and follow the manufacturer's Safety Data Sheet for handling requirements.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTucker (2001). Methylated Cytosine and the Brain. \u003cem\u003eNeuron\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0896-6273(01)00325-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0896-6273(01)00325-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMitchell (2007). Effects of Cytosine Methylation on Pyrimidine Dimer Formation in DNA. \u003cem\u003ePhotochemistry and Photobiology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1562\/0031-8655(2000)0710162eocmop2.0.co2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1562\/0031-8655(2000)0710162eocmop2.0.co2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTakanashi et al. (2014). Sequence-selective Modification of DNA Cytosine by Using Junction-forming DNA Probes and Its Application to the Detection of Single Cytosine Methylation. \u003cem\u003eAnalytical Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2116\/analsci.30.371\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2116\/analsci.30.371\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086007447770,"sku":"TCI2510C052814719","price":860000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086007480538,"sku":"TCI2510C052814720","price":2524000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086007513306,"sku":"TCI2510C052814721","price":7295000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0528.jpg?v=1768816268"},{"product_id":"tci2510c096915321","title":"TCI C0969 1820-81-1 5-Chlorouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0969 5-Chlorouracil (CAS 1820-81-1) is a halogenated pyrimidine base in which a chlorine atom occupies the 5-position of the uracil ring. It is widely used as a heterocyclic building block for modified nucleosides and nucleotides, and as a tool for studying halogenated bases in nucleic acid chemistry. The ring chlorine also enables further substitution and cross-coupling toward new pyrimidine derivatives. AMI Scientific supplies 5 g and 25 g packs; keep the solid dry and tightly closed, and follow the official TCI safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrtiz et al. (2014). FT-IR and FT-Raman spectra of 6-chlorouracil: Molecular structure, tautomerism and solid state simulation. A comparison between 5-chlorouracil and 6-chlorouracil. \u003cem\u003eSpectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.saa.2014.04.009\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.saa.2014.04.009\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSommerfeld (2001). Electron-induced Chemistry of 5-Chlorouracil. \u003cem\u003eChemPhysChem\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/1439-7641(20011119)2:11\u0026lt;677::aid-cphc677\u0026gt;3.0.co;2-c\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/1439-7641(20011119)2:11\u0026lt;677::aid-cphc677\u0026gt;3.0.co;2-c\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSommerfeld (2001). Electron-induced Chemistry of 5-Chlorouracil. \u003cem\u003eChemPhysChem\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/1439-7641(20011119)2:11\u0026lt;677::aid-cphc677\u0026gt;3.3.co;2-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/1439-7641(20011119)2:11\u0026lt;677::aid-cphc677\u0026gt;3.3.co;2-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086040740058,"sku":"TCI2510C096915321","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086040772826,"sku":"TCI2510C096915322","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0969.jpg?v=1769144531"},{"product_id":"tci2510c105715450","title":"TCI C1057 18592-13-7 6-Chloromethyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1057 6-Chloromethyluracil, CAS 18592-13-7, is a heterocyclic building block combining a uracil ring with a reactive chloromethyl side group. The chloromethyl handle readily undergoes nucleophilic substitution with amines, thiols, and other nucleophiles, enabling rapid access to modified nucleobase analogues. AMI Scientific offers this TCI reagent in a 5 g pack size suited to exploratory laboratory research. Handle it as a reactive alkylating solid, store it cool, dry, and protected from light, and follow the official TCI Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48276737425626,"sku":"TCI2510C105715450","price":960000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1057.jpg?v=1767096262"},{"product_id":"tci2510c209316748","title":"TCI C2093 4270-27-3 6-Chlorouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2093 6-Chlorouracil is a pyrimidine derivative formed by substituting a chlorine atom at the sixth position of the uracil skeleton. Uracil itself is one of the nitrogenous bases that make up ribonucleic acid, so its derivatives occupy an important position in biochemical research and nucleoside chemistry. Laboratories use this material as a starting material for constructing various pyrimidine base analogues, synthetic nucleosides, and compounds designed to interact with enzymes involved in nucleic acid metabolism. The presence of the chlorine group makes the normally less reactive uracil skeleton far easier to modify.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a material of choice is the reactivity of the chlorine atom on the electron-poor pyrimidine ring. The two carbonyl groups on the ring withdraw electron density, so the sixth position becomes susceptible to nucleophilic attack, and the chlorine atom can be displaced by amines, alkoxides, thiolates, or other nucleophiles under controlled reaction conditions. In addition, the nitrogen atoms at the first and third positions can be selectively alkylated to build more elaborate analogue structures. This solid material is also relatively stable, which supports predictable handling during multi-step synthetic work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chlorouracil is typically used in university and institutional research settings where nucleoside and pyrimidine chemistry is studied, as well as in synthetic organic chemistry groups preparing base analogues for further biochemical evaluation. Its role as a building block means it is generally weighed out in small portions for individual reactions rather than consumed in bulk, making it a stock-shelf item for laboratories that run ongoing programmes in biochemistry, medicinal chemistry, and nucleic acid related research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of pyrimidine base analogues: the reactive chlorine at position six allows direct nucleophilic displacement, giving researchers a straightforward route to structurally varied uracil derivatives.\u003c\/li\u003e\n\u003cli\u003ePreparation of synthetic nucleosides: the uracil skeleton provides the base component required for nucleoside construction, while the chlorine substituent permits modification before or after coupling steps.\u003c\/li\u003e\n\u003cli\u003eDevelopment of enzyme-directed compounds: it serves as a starting material for molecules designed to interact with enzymes involved in nucleic acid metabolism within biochemical studies.\u003c\/li\u003e\n\u003cli\u003eSelective N-alkylation studies: the nitrogen atoms at the first and third ring positions can be alkylated selectively, supporting the construction of more complex analogue frameworks.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution methodology work: the electron-poor ring created by the two carbonyl groups makes this compound a useful substrate for studying amine, alkoxide, and thiolate displacement reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 4270-27-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eProduct Code: C2093\u003c\/li\u003e\n\u003cli\u003ePhysical Form: solid\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container under the conditions indicated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 6-Chlorouracil in its original tightly closed container, kept in a cool, dry, and well ventilated area away from moisture and incompatible substances. Amber glass or the supplied manufacturer packaging is suitable for keeping the solid protected from light and humidity. Handle the material inside a fume hood using a laboratory coat, safety glasses, and chemical resistant gloves, and avoid generating dust when weighing. Use clean, dry spatulas to prevent contamination of the bulk stock, close the container immediately after use, and always consult the manufacturer's safety data sheet before handling, waste collection, or disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086102343898,"sku":"TCI2510C209316748","price":884000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086102376666,"sku":"TCI2510C209316749","price":2600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2093.jpg?v=1769144418"},{"product_id":"tci2510c222116910","title":"TCI C2221 1651-29-2 6-Chloro-2-fluoropurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-2-fluoropurine from TCI, catalogue code C2221, is a purine derivative carrying two different halogen atoms: chlorine at position six and fluorine at position two. The compound belongs to the family of fluorinated building blocks, a class of starting materials in high demand in modern medicinal chemistry. The purine scaffold itself is the structural core of the nucleobases adenine and guanine, which makes halogenated purine derivatives a principal entry point for constructing nucleoside analogues, kinase inhibitors, and a wide range of compounds directed at nucleotide-binding proteins inside the cell.\u003c\/p\u003e\n\u003cp\u003eIts synthetic value rests on the difference in reactivity between the two halogens. The chlorine atom at position six is displaced by nucleophiles such as amines, alkoxides, or thiolates far more readily than the fluorine atom at position two. This graded difference in reactivity allows chemists to carry out sequential functionalisation under control: the first substituent is installed at position six under mild conditions, and position two is then addressed under more forcing conditions. Fluorine is also frequently retained in the final product, since it can improve metabolic stability and alter the acidity of its surrounding environment.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is used in university and institutional research groups working on medicinal chemistry and heterocyclic synthesis, as well as in method development for nucleoside analogue routes. It is typically ordered in small research quantities for exploratory and multi-step synthesis rather than bulk production, and is handled alongside other catalogue reagents in organic synthesis laboratories where controlled, stepwise substitution chemistry is routine.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside analogue synthesis: the purine core mirrors adenine and guanine, so the halogenated positions give direct access to modified nucleoside frameworks used in research.\u003c\/li\u003e\n\u003cli\u003eKinase inhibitor development: purine derivatives target nucleotide-binding pockets, and the two displaceable halogens let researchers build diverse substitution patterns around that scaffold.\u003c\/li\u003e\n\u003cli\u003eSequential nucleophilic substitution studies: the reactivity gap between C6 chlorine and C2 fluorine supports controlled two-step functionalisation, first under mild then under more forcing conditions.\u003c\/li\u003e\n\u003cli\u003eFluorinated compound design: fluorine retained at position two can improve metabolic stability and modulate the acidity of neighbouring groups in candidate molecules.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic building block chemistry: as a fluorinated building block, it serves as a versatile starting material for assembling more elaborate purine-based target structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C2221\u003c\/li\u003e\n\u003cli\u003eCAS number: 1651-29-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research pack sizes; please confirm the currently listed options when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container in a cool, dry, well-ventilated place away from light and moisture.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry and well-ventilated area, protected from moisture, direct sunlight and sources of ignition. Keep the container sealed when not in use to limit exposure to atmospheric humidity, and return it promptly to designated chemical storage after weighing. Handle in a fume hood using appropriate personal protective equipment, including safety glasses, chemical-resistant gloves and a laboratory coat. Avoid inhaling dust and avoid contact with skin and eyes. Keep it separate from strong oxidising agents and strong bases, label all secondary containers clearly, and follow the manufacturer safety data sheet together with your institutional chemical waste procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086112141530,"sku":"TCI2510C222116910","price":1515000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2221.jpg?v=1767097935"},{"product_id":"tci2510c230017028","title":"TCI C2300 4318-56-3 6-Chloro-3-methyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-3-methyluracil is a chemical compound widely used in biochemical and biotechnological applications. As a nucleoside-related compound, it plays a crucial role in laboratory research focused on DNA and RNA studies. Its structural similarity to nucleotides allows scientists to modify its chemical structure for various experimental purposes. This compound is commonly used as a building block in the synthesis of organic compounds and in the development of pharmaceuticals. Its versatility makes it an essential tool for researchers in life sciences.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 6-Chloro-3-methyluracil make it a preferred choice in laboratory settings. It exhibits stability under controlled conditions and can interact with different reagents, enabling a wide range of chemical reactions. The presence of both chloro and methyl groups influences its polarity and solubility, which are critical for applications requiring precise control over reactivity and stability. These characteristics make it suitable for use in complex synthetic processes and molecular modifications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chloro-3-methyluracil is frequently utilized in research related to the synthesis of organic compounds and drug development. Its role in biochemical studies, particularly in the context of nucleotide-based research, highlights its importance in both academic and industrial settings. Researchers rely on this compound for its reliability and adaptability in various experimental protocols.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA and RNA modification studies benefit from 6-Chloro-3-methyluracil due to its structural similarity to nucleotides, enabling precise molecular alterations.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis projects often use this compound as a key building block, allowing for the creation of complex chemical structures with controlled reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes 6-Chloro-3-methyluracil in the development of new drugs, leveraging its chemical properties for targeted molecular interactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays incorporate this compound to study molecular interactions and reactivity under controlled experimental conditions.\u003c\/li\u003e\n\u003cli\u003eBiomedical research employs 6-Chloro-3-methyluracil to investigate its potential in therapeutic applications and molecular targeting strategies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4318-56-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-3-methyluracil should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. The compound should be stored away from incompatible substances to avoid any potential chemical reactions. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086118170842,"sku":"TCI2510C230017028","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086118203610,"sku":"TCI2510C230017029","price":3332000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2300.jpg?v=1768816828"},{"product_id":"tci2510c230617039","title":"TCI C2306 3680-69-1 6-Chloro-7-deazapurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-7-deazapurine is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. Its structural similarity to purine, with modifications to nitrogen and chlorine atoms, makes it a valuable tool in organic chemistry research. In the laboratory, it serves as a flexible reagent that enables the development of compounds with specific biological activities. This compound plays a crucial role in the design and synthesis of complex molecules, supporting advancements in various scientific fields.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability under controlled conditions, though it is highly sensitive to moisture and UV light exposure. Its complex molecular structure allows for precise chemical reactions, making it ideal for applications requiring accuracy and reproducibility. These properties make it a preferred choice for researchers aiming to control reaction outcomes and achieve desired products with high efficiency.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chloro-7-deazapurine is extensively used in pharmacological, medicinal chemistry, and biochemical research. It is a key component in the development of new drugs, anticancer agents, and bioactive compounds. Its versatility and chemical properties make it a staple in academic and industrial research settings across the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes 6-Chloro-7-deazapurine for the synthesis of bioactive compounds due to its structural similarity to purine, enabling the design of molecules with targeted biological activities.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry applications benefit from its role as a heterocyclic building block, allowing the creation of compounds with therapeutic potential for various diseases.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies incorporate this compound to investigate its interactions with enzymes and proteins, aiding in the understanding of molecular mechanisms in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis projects rely on its chemical stability and reactivity to produce complex molecules with high purity and specificity.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesian universities uses it to explore new synthetic pathways and develop novel compounds for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3680-69-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Keep in a cool, dry place away from moisture and UV light exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Chloro-7-deazapurine should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption, which can degrade the compound. Exposure to UV light should be minimized to avoid decomposition. When handling, it is advisable to use appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety. Proper labeling of storage containers is essential for easy identification and safe handling. Regular monitoring of storage conditions is necessary to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086119088346,"sku":"TCI2510C230617039","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086119121114,"sku":"TCI2510C230617040","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2306.jpg?v=1767098108"},{"product_id":"tci2510c247017244","title":"TCI C2470 55052-28-3 4-Chloro-1H-pyrrolo[2,3-b]pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2470 4-Chloro-1H-pyrrolo[2,3-b]pyridine is a heterocyclic building block widely known as a 7-azaindole derivative, meaning an indole framework in which one of the carbon atoms of the benzene ring has been replaced by nitrogen. In this particular compound, a chlorine atom occupies the four position and serves as the principal site of reaction. The azaindole scaffold is highly valued in medicinal chemistry because it combines a pyrrole nitrogen that acts as a hydrogen bond donor with a pyridine nitrogen that acts as an acceptor, allowing it to mimic binding patterns frequently encountered in the nucleotide binding regions of target proteins.\u003c\/p\u003e\n\u003cp\u003eThe reason this material is so frequently selected lies in the directed reactivity of the four position. The chlorine atom sits on an electron poor pyridine ring, so it can be displaced through nucleophilic aromatic substitution or exploited in palladium catalysed cross coupling reactions such as Suzuki, Stille and Sonogashira couplings, as well as Buchwald-Hartwig amination. The pyrrole nitrogen can first be masked with a common protecting group so that the reaction proceeds cleanly, then deprotected at the final stage. The three position of the pyrrole ring remains available for halogenation or acylation, so the scaffold permits functionalisation at several distinct points.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this building block is typically encountered in synthetic organic and medicinal chemistry groups at universities and research institutes, as well as in contract research settings preparing kinase-directed compound libraries. It is normally used at small scale on the bench, weighed out for multi-step sequences in which the chlorinated position is elaborated first and the pyrrole nitrogen is unmasked afterwards. Groups working on heterocyclic methodology also use it as a reference substrate when developing coupling conditions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePalladium catalysed cross coupling research, because the chlorine at the four position participates directly in Suzuki, Stille and Sonogashira reactions to install aryl, vinyl or alkynyl groups.\u003c\/li\u003e\n\u003cli\u003eBuchwald-Hartwig amination studies, where the same four position chlorine is converted into a carbon-nitrogen bond, giving access to aminated azaindoles under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution work, since the electron poor pyridine ring activates the chlorine toward displacement by a range of nucleophiles without requiring a metal catalyst.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold construction, because the pyrrole nitrogen donor and pyridine nitrogen acceptor together mimic binding patterns found in nucleotide binding regions of target proteins.\u003c\/li\u003e\n\u003cli\u003eMulti-point functionalisation sequences, as the three position of the pyrrole ring stays open for halogenation or acylation after the four position has already been elaborated.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 55052-28-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 4-Chloro-1H-pyrrolo[2,3-b]pyridine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI research quantities; please refer to the current product listing for options\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer label and accompanying safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry and well ventilated place, away from direct sunlight, heat sources and incompatible materials, and follow any specific storage temperature stated on the manufacturer label. Keep the material in its original supplier container or in a clean, chemically compatible and clearly labelled alternative, and close it promptly after each weighing to limit exposure to moisture and air. Handle in a fume hood using a laboratory coat, chemical resistant gloves and safety glasses. Avoid generating dust, avoid contact with skin and eyes, and wash hands thoroughly after handling. Consult the safety data sheet before first use and dispose of residues and contaminated materials through the approved chemical waste route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086127870170,"sku":"TCI2510C247017244","price":633000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086127902938,"sku":"TCI2510C247017245","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2470.jpg?v=1767098381"},{"product_id":"tci2510c257517381","title":"TCI C2575 1839-18-5 2-Chloroadenine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloroadenine is a chemical compound classified under the heterocyclic category, playing a crucial role in the synthesis of complex molecules. It is widely used in laboratory settings as a foundational building block for creating compounds with specific structural and functional properties. This compound contains nitrogen and carbon atoms, making it essential for reactions that involve the formation of heterocyclic bonds. Its versatility allows it to be a key component in various chemical processes, supporting both research and development in multiple scientific fields.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions, which ensures consistent performance in experiments. However, it is sensitive to moisture and UV light, requiring careful handling to maintain its integrity. These properties make it a preferred choice for researchers who need reliable and reproducible results. Its solid form also simplifies storage and usage, reducing the risk of contamination and ensuring ease of application in laboratory workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Chloroadenine is commonly used in organic chemistry and pharmacology research. It is an essential material for developing new compounds with specific biological activities, such as pharmaceuticals and industrial chemicals. Due to its importance in heterocyclic synthesis, it is frequently sought after by researchers in chemistry and pharmacy fields. Its application extends to various experimental setups aimed at creating compounds with targeted properties and functions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from 2-Chloroadenine as it serves as a versatile building block for creating complex heterocyclic structures.\u003c\/li\u003e\n\u003cli\u003ePharmacological research utilizes this compound to develop new drugs with specific biological activities and molecular targets.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound development relies on 2-Chloroadenine for its structural contributions in forming stable and functional chemical frameworks.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis incorporates this material for producing compounds with unique chemical properties and applications.\u003c\/li\u003e\n\u003cli\u003eResearch into molecular interactions uses 2-Chloroadenine to study how heterocyclic structures influence chemical reactivity and binding behavior.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1839-18-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires protection from moisture and UV light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Chloroadenine should be stored in a cool, dry place away from direct sunlight and sources of moisture. It is recommended to use airtight containers to prevent exposure to humidity, which can degrade its chemical integrity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to minimize risk. Due to its sensitivity, it is important to maintain controlled storage conditions to ensure its stability and effectiveness in experimental applications. Regular monitoring of storage conditions is advised to maintain the compound's quality and usability in research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086133473498,"sku":"TCI2510C257517381","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086133506266,"sku":"TCI2510C257517382","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2575.jpg?v=1767098518"},{"product_id":"tci2510c292917828","title":"TCI C2929 34654-81-4 6-[(3-Chloropropyl)amino]-1,3-dimethyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-[(3-Chloropropyl)amino]-1,3-dimethyluracil is a chemical compound widely used in biochemical and molecular research applications. This nucleoside derivative plays a crucial role in laboratory settings, particularly in the synthesis of bioactive compounds and the development of pharmaceuticals. Its unique molecular structure enables it to participate in various chemical reactions, making it a valuable reagent for researchers working on drug discovery and molecular modification. As a key component in nucleoside-based studies, it supports advancements in biotechnology and genetic research.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity and stability under controlled conditions, which makes it a preferred choice for laboratory use. It dissolves well in organic solvents, allowing for easy handling and integration into complex synthetic protocols. These properties ensure consistent performance in experiments, contributing to reliable and reproducible results. Its chemical stability and solubility characteristics are essential for maintaining the integrity of research processes, especially in environments requiring precision and accuracy.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-[(3-Chloropropyl)amino]-1,3-dimethyluracil is commonly used in biomedical, pharmacological, and biotechnological research. It is a key reagent in molecular modification studies and drug development projects. Many research institutions and universities rely on this compound for experiments involving nucleic acid synthesis and therapeutic compound design. Its versatility and reliability make it a standard component in modern scientific laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in drug synthesis for developing new therapeutic agents due to its complex chemical structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eApplied in molecular modification studies to create novel compounds with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eUtilized in genetic research for DNA and RNA-related experiments requiring precise chemical reagents.\u003c\/li\u003e\n\u003cli\u003eEmployed in pharmaceutical research to support the development of targeted therapies and bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eIntegrated into biotechnology projects for the production of nucleoside-based compounds and bioengineered materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 34654-81-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity, which could affect its stability. Proper ventilation is necessary when handling the material to minimize inhalation risks. It is important to avoid contact with skin and eyes, and appropriate personal protective equipment should be worn during handling. The compound is best stored in a controlled laboratory setting to ensure its integrity and effectiveness for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086203465946,"sku":"TCI2510C292917828","price":1692000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2929.jpg?v=1768816965"},{"product_id":"tci2510c313018091","title":"TCI C3130 123148-78-7 6-Chloro-7-iodo-7-deazapurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C3130 6-Chloro-7-iodo-7-deazapurine is a doubly functionalized heterocyclic compound that serves as a core scaffold in the synthesis of nucleoside analogues and purine-based bioactive compounds. Structurally, it is a pyrrolo[2,3-d]pyrimidine core — a purine in which the nitrogen atom at position seven is replaced by carbon, which is why the class is widely known as 7-deazapurines. In medicinal chemistry and synthetic organic chemistry laboratories, this material is a highly valuable starting point because it provides two distinct reactive sites that can be modified sequentially and in a controlled manner, allowing researchers to build libraries of derivative compounds systematically from a single common starting material.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound such a frequent choice is the reactivity differentiation between the chloro group at position six and the iodo group at position seven. The chloro group on the pyrimidine ring is electrophilic and readily displaced through nucleophilic aromatic substitution by amines, alkoxides, or thiols, while the iodo group on the pyrrole ring is an ideal partner for palladium-catalysed cross-coupling reactions such as Suzuki, Sonogashira, and Stille couplings. Because the two positions respond to different reaction conditions, a chemist can address one site without disturbing the other, which makes reaction planning far more predictable and reduces the need for protecting-group strategies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university research groups, medicinal chemistry programmes, and institutional research centres working on nucleoside analogues and heterocyclic drug candidates. It is normally handled on a small preparative scale within a fume hood, using standard glassware and inert-atmosphere technique where the subsequent coupling step requires it. Because it is supplied as a defined catalogue item, it also suits teaching and method-development work where a reproducible, well-characterised starting material is needed.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside analogue synthesis — the 7-deazapurine core closely mimics the natural purine base, so the scaffold can be elaborated into modified nucleosides while retaining recognisable base geometry.\u003c\/li\u003e\n\u003cli\u003eSequential functionalisation and library building — the differing reactivity of the chloro and iodo positions lets researchers install two different substituents in a controlled, stepwise order from one starting material.\u003c\/li\u003e\n\u003cli\u003ePalladium-catalysed cross-coupling studies — the iodo substituent on the pyrrole ring is an excellent electrophilic partner for Suzuki, Sonogashira, and Stille coupling method development and optimisation.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution chemistry — the electrophilic chloro group at position six is readily displaced by amines, alkoxides, or thiols, making it useful for teaching and probing SNAr reactivity.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry lead exploration — purine-based bioactive compound programmes use this scaffold to generate structurally related analogues for structure–activity relationship investigations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 123148-78-7\u003c\/li\u003e\n\u003cli\u003eChemical name: 6-Chloro-7-iodo-7-deazapurine (6-chloro-7-iodo-pyrrolo[2,3-d]pyrimidine core)\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C3130\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard catalogue pack sizes offered for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the product label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its tightly closed original container, in a cool, dry, and well-ventilated area away from direct sunlight, moisture, and incompatible materials, following the storage conditions stated on the product label and safety data sheet. Amber glass or the supplied container is preferred to limit light exposure, and the container should be resealed promptly after each use. Handle the solid in a fume hood, wearing a laboratory coat, safety goggles, and chemical-resistant gloves, and avoid generating or inhaling dust. Weigh and transfer with clean, dry spatulas to prevent contamination and moisture uptake. Label all derived solutions clearly and dispose of residues and contaminated consumables through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086215229658,"sku":"TCI2510C313018091","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086215262426,"sku":"TCI2510C313018092","price":4065000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3130.jpg?v=1767099253"},{"product_id":"tci2510d113620852","title":"TCI D1136 26305-13-5 5,6-Dimethyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5,6-Dimethyluracil is a chemical compound classified under the heterocyclic category, commonly used as a foundational building block in the synthesis of complex compounds. This compound is derived from uracil, with two methyl groups added at positions 5 and 6, making it a versatile intermediate in organic chemistry. In laboratory settings, it plays a crucial role in the development of organic molecules, particularly in pharmacological and chemical research. Its structural simplicity and adaptability allow it to be modified into a wide range of biologically active compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound is chemically stable and exhibits reactivity with various reagents, making it a preferred choice for synthetic chemists. Its ability to form bonds with different functional groups enables its use in substitution and cyclic reactions. This flexibility is highly valued in the synthesis of complex organic molecules. Additionally, its non-toxic nature at standard usage levels ensures safe handling and broad applicability in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5,6-Dimethyluracil is widely used in research and development projects. It is a key component in the synthesis of pharmaceuticals and other organic compounds. Its availability and chemical properties make it a reliable material for academic and industrial applications. The compound is often used in both teaching and research settings to illustrate the principles of organic synthesis and heterocyclic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of pharmaceutical compounds due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex heterocyclic molecules as a foundational building block in chemical research.\u003c\/li\u003e\n\u003cli\u003eInvestigation of biological activity in drug discovery through modification of its functional groups.\u003c\/li\u003e\n\u003cli\u003eTeaching and demonstration of organic chemistry principles in academic and research institutions.\u003c\/li\u003e\n\u003cli\u003ePreparation of intermediates for cyclic and substitution reactions in synthetic chemistry applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 26305-13-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5,6-Dimethyluracil should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to moisture and air. The material is non-toxic at standard usage levels, but standard laboratory safety practices should still be followed. Avoid prolonged exposure to direct light, as it may affect its chemical integrity. Proper labeling and storage conditions ensure the compound remains suitable for use in research and educational settings. Always handle the material with appropriate personal protective equipment to ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086426157274,"sku":"TCI2510D113620852","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086426190042,"sku":"TCI2510D113620853","price":4292000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1136.jpg?v=1767102573"},{"product_id":"tci2510d162521445","title":"TCI D1625 402846-48-4 2,6-Diaminopurine Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Diaminopurine Monohydrate is a chemical compound widely used in laboratory experiments and biochemical research. As a heterocyclic building block, it shares structural similarities with adenine and guanin, two essential nucleotides found in DNA and RNA. This structural resemblance makes it a valuable starting material for the synthesis of complex molecules and for studying molecular structures. Its presence in biochemical processes allows researchers to explore nucleotide-related reactions and their implications in biological systems.\u003c\/p\u003e\n\u003cp\u003eThe compound is chemically stable under controlled conditions but is highly sensitive to moisture and air exposure. These properties necessitate careful handling and storage to maintain its integrity. Its monohydrate form contributes to specific melting points and solubility characteristics, which are advantageous in various chemical reactions. The stability of its molecular structure, combined with its reactivity, makes it a preferred choice for researchers requiring reliable and consistent results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Diaminopurine Monohydrate is commonly used in biochemical research, organic synthesis, and pharmaceutical development. Its availability and cost-effectiveness make it a go-to material for small to medium-scale experiments. Its versatility supports a wide range of applications, from basic research to advanced drug discovery projects. Its role in facilitating chemical reactions and molecular studies is crucial for scientific progress in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research – This compound is ideal for studying nucleotide-related reactions due to its structural similarity to adenine and guanin.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis – Its heterocyclic structure makes it a valuable building block for the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development – It is used in the design and synthesis of nucleotide-based drugs and therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eMolecular Structure Studies – Its stable molecular framework supports investigations into molecular interactions and bonding.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry – It serves as a reference standard for identifying and quantifying nucleotide-related compounds in samples.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 402846-48-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline monohydrate\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires airtight container and refrigeration to prevent degradation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in airtight containers to prevent moisture and air exposure, which can lead to degradation. It is recommended to keep it in a cool, dry place, preferably refrigerated, to maintain its chemical stability. Due to its sensitivity, it should be handled with care using appropriate personal protective equipment. Avoid prolonged exposure to light and ensure that storage conditions are consistent to preserve its integrity. Proper labeling and secure storage are essential to prevent contamination and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086451355866,"sku":"TCI2510D162521445","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086451388634,"sku":"TCI2510D162521446","price":3332000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1625.jpg?v=1767103360"},{"product_id":"tci2510d247022694","title":"TCI D2470 5451-40-1 2,6-Dichloropurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dichloropurine is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. It plays a crucial role in laboratory settings where the creation of complex molecular structures is required. This compound is particularly valuable in organic chemistry and biochemistry research due to its ability to participate in various chemical reactions that lead to the formation of purine-based structures. These structures are fundamental components of essential biological molecules such as DNA and RNA, making 2,6-Dichloropurine an indispensable tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stable chemical structure and high reactivity, which makes it suitable for substitution reactions and other synthetic processes. Its chemical properties allow it to be a versatile reagent in the development of pharmaceuticals, pesticides, and industrial chemicals. The reactivity and stability of 2,6-Dichloropurine make it a preferred choice for chemists seeking to create new compounds with specific biological or chemical functions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Dichloropurine is commonly used in pharmaceutical, organic chemistry, and biochemical research. Local researchers rely on this compound to develop new therapeutic agents and industrial materials. Its availability in various packaging formats supports both small-scale and mid-sized laboratory applications, ensuring accessibility for a wide range of research needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes 2,6-Dichloropurine for the synthesis of novel drug compounds due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments benefit from this compound as a key building block in the formation of heterocyclic structures.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ 2,6-Dichloropurine to investigate the synthesis of nucleotide-related molecules essential for genetic research.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development leverages its properties to create specialized compounds for agricultural and manufacturing applications.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesia frequently incorporates this compound to explore new synthetic pathways and molecular innovations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 5451-40-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes to suit different laboratory scales\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2,6-Dichloropurine should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. The material is typically stored in glass or plastic containers that are resistant to chemical reactions. Laboratory personnel should handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Proper ventilation is essential when working with this compound to minimize exposure. Due to its reactivity, it should be handled in a controlled laboratory setting to avoid unintended chemical interactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086543368410,"sku":"TCI2510D247022694","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086543401178,"sku":"TCI2510D247022695","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086543433946,"sku":"TCI2510D247022696","price":4013000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2470.jpg?v=1767104856"},{"product_id":"tci2510d360423937","title":"TCI D3604 3056-33-5 N2,9-Diacetylguanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN2,9-Diacetylguanine is a protected guanine derivative carrying acetyl groups on the exocyclic nitrogen at position two and on the nitrogen at position nine of the purine ring. This compound is classified as a heterocyclic building block and plays an important role in nucleoside and nucleotide chemistry. In laboratory settings, pure guanine is notoriously difficult to handle due to its extremely low solubility and reactive free amino groups. The installation of acetyl groups addresses both challenges simultaneously, making the purine framework far more practical for use in stepwise synthesis protocols.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound widely preferred stem from the dual role of the acetyl groups as both protecting and activating functionalities. Acetylation of the amino group prevents unwanted side reactions during alkylation or glycosylation procedures, while acetylation at the N9 position facilitates group exchange through Lewis acid-catalyzed transglycosylation reactions. Furthermore, the improved solubility in organic solvents such as acetonitrile and dimethylformamide enables reactions to proceed under homogeneous conditions, resulting in enhanced yields and greater reproducibility across multiple experimental runs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically employed in academic research groups and pharmaceutical development settings where nucleoside analogs are being synthesized for biological evaluation. Research institutions working on antiviral compounds, modified oligonucleotides, and purine-based drug candidates rely on this building block to construct complex molecular architectures. The compound's compatibility with standard laboratory solvents and its straightforward deprotection using ammonia in methanol or mild base make it particularly suitable for multi-step synthetic sequences commonly performed in these environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside synthesis: The protected amino group prevents side reactions during glycosylation, enabling clean formation of nucleoside bonds with high selectivity and yield.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide chemistry: Serves as a reliable building block for constructing modified DNA and RNA sequences where protected guanine residues are required for solid-phase synthesis.\u003c\/li\u003e\n\u003cli\u003ePurine derivative preparation: Facilitates the synthesis of various substituted purines through controlled alkylation reactions without interference from unprotected functional groups.\u003c\/li\u003e\n\u003cli\u003eAntiviral drug development: Provides a key intermediate for synthesizing nucleoside analogs that target viral polymerases in pharmaceutical research programs.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic library construction: Enables parallel synthesis of diverse purine-based compound libraries for structure-activity relationship studies in drug discovery projects.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 3056-33-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct Code: D3604\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage: Keep container tightly closed and store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this compound in its original container with the lid securely fastened to prevent moisture absorption and contamination. Maintain storage conditions in a cool, dry environment away from direct sunlight and heat sources. The material should be kept in a well-ventilated chemical storage area designated for organic compounds. When handling, use appropriate personal protective equipment including gloves, safety goggles, and laboratory coat. Avoid generating dust during weighing and transfer operations. Work in a fume hood when possible to minimize inhalation exposure. Ensure containers are properly labeled and segregated from incompatible materials such as strong oxidizing agents and strong acids.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086629155034,"sku":"TCI2510D360423937","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3604.jpg?v=1767106286"},{"product_id":"tci2510d389424314","title":"TCI D3894 938-55-6 6-(Dimethylamino)purine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-(Dimethylamino)purine is a chemical compound classified under the heterocyclic category, commonly used as a building block in the synthesis of complex molecules. It plays a crucial role in laboratory settings by enabling the formation of purine structures, which are fundamental components of biological molecules such as DNA and RNA. This compound is widely utilized in organic synthesis and pharmacological research due to its ability to participate in various chemical reactions. Its presence in laboratory workflows supports the development of new compounds and the exploration of molecular mechanisms in biological systems.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make 6-(Dimethylamino)purine a preferred choice is its stable chemical structure and high reactivity. These characteristics allow it to engage in a wide range of chemical transformations, making it versatile for different synthetic approaches. Additionally, its good solubility in organic solvents enhances its usability in diverse experimental conditions. The compound's reliability and flexibility in chemical behavior make it an essential tool for researchers aiming to design and synthesize bioactive molecules.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-(Dimethylamino)purine is frequently employed in chemical, pharmaceutical, and biochemical research. It is a key component in the development of bioactive compounds and is used by educational and research institutions to advance studies in molecular synthesis and drug development. Its availability and chemical properties make it a valuable resource for scientific investigations in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research benefits from this compound due to its ability to participate in various chemical reactions, enabling the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development utilizes 6-(Dimethylamino)purine as a building block for synthesizing bioactive compounds with potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies rely on this compound to investigate the formation and behavior of purine-based molecules, essential for understanding genetic and molecular processes.\u003c\/li\u003e\n\u003cli\u003eEducational institutions use it in teaching and research to demonstrate synthetic pathways and molecular construction techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial research applications leverage its chemical versatility for the development of new materials and chemical products.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 938-55-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-(Dimethylamino)purine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Researchers should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Proper labeling and storage conditions are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086643900634,"sku":"TCI2510D389424314","price":2449000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086643933402,"sku":"TCI2510D389424315","price":8177000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3894.jpg?v=1767106742"},{"product_id":"tci2510d428424836","title":"TCI D4284 90213-66-4 2,6-Dichloro-7-deazapurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,6-Dichloro-7-deazapurine is a chemical compound widely used in organic synthesis reactions, particularly in the formation of complex heterocyclic compounds. This material serves as a fundamental building block in laboratory settings, playing a crucial role in the development of pharmaceuticals and bioactive molecules. Its unique structure, derived from purine with two chlorine atoms at positions 2 and 6, enhances its reactivity and versatility in various chemical transformations. Due to its chemical stability and solubility properties, it is a valuable resource for researchers working on advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and ability to participate in substitution and ring-opening reactions make it a preferred choice for synthetic chemists. Its modified purine framework provides a platform for the creation of diverse molecular structures, which are essential in drug discovery and biochemical research. The high reactivity of 2,6-Dichloro-7-deazapurine allows it to interact effectively with various functional groups, making it suitable for a wide range of chemical applications. These properties contribute to its widespread use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,6-Dichloro-7-deazapurine is commonly utilized by researchers in universities and research institutions. It is employed in the synthesis of bioactive compounds and pharmaceutical intermediates, supporting scientific investigations and product development. Its availability and chemical characteristics make it an essential component in the toolkit of chemists working on complex molecular structures and functional group modifications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 2,6-Dichloro-7-deazapurine is used to create complex heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound as it serves as a building block for the development of new drugs and bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often incorporate this material to explore its role in molecular interactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry relies on 2,6-Dichloro-7-deazapurine for the synthesis of novel compounds with specific structural and functional properties.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications in chemical manufacturing utilize this compound for the production of specialized intermediates and specialty chemicals.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 90213-66-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Due to its reactivity, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. In laboratory settings, it is important to ensure proper ventilation when working with this material to minimize inhalation risks. Always follow standard chemical safety protocols to ensure safe handling and storage practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086682697946,"sku":"TCI2510D428424836","price":4065000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086682730714,"sku":"TCI2510D428424837","price":14183000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4284.jpg?v=1767107368"},{"product_id":"tci2510d429524854","title":"TCI D4295 1087737-96-9 5,6-Dichlorobenzimidazole Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5,6-Dichlorobenzimidazole Hydrochloride is a chemical compound widely used in laboratory settings for its versatility in organic synthesis and chemical reactions. As a heterocyclic building block, it plays a crucial role in the development of new compounds with specific biological activities. Its complex structure, featuring a benzimidazole ring substituted with two chlorine atoms at positions 5 and 6, makes it a valuable tool in pharmaceutical and industrial research. This compound is often utilized as a starting material for the synthesis of various pharmacological agents and functional chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability and controlled reactivity, which makes it suitable for substitution and cyclic reactions. Its ability to dissolve in organic solvents and exist in crystalline form enhances its usability in diverse experimental conditions. The flexibility of its molecular structure allows for modifications tailored to specific research applications. These properties make it a preferred choice for chemists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5,6-Dichlorobenzimidazole Hydrochloride is commonly used in organic chemistry, pharmacology, and biochemistry research. It is frequently employed in the development of new drugs and chemical compounds, supporting both fundamental and applied scientific investigations. Its availability and chemical properties make it a reliable reagent for researchers aiming to explore complex molecular interactions and biological activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its heterocyclic structure, allowing for the creation of complex molecules with tailored biological properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes it as a building block for developing new drug candidates with specific therapeutic effects.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production relies on its stability and reactivity for the synthesis of functional compounds used in various sectors.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies use it to investigate molecular interactions and biological activities in cellular systems.\u003c\/li\u003e\n\u003cli\u003eAcademic research employs it in teaching and experimental protocols to demonstrate synthetic methodologies and chemical reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1087737-96-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper ventilation is essential when working with this compound to avoid inhalation of vapors. It is advisable to store it away from incompatible substances to prevent unwanted reactions. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086683353306,"sku":"TCI2510D429524854","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086683386074,"sku":"TCI2510D429524855","price":5023000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4295.jpg?v=1767107385"},{"product_id":"tci2510d432424889","title":"TCI D4324 3680-71-5 7-Deazahypoxanthine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4324 7-Deazahypoxanthine is an analogue of hypoxanthine in which the nitrogen atom at position 7 of the purine ring has been replaced by a carbon atom, giving a pyrrolo[2,3-d]pyrimidinone framework. This compound is an important heterocyclic building block in nucleoside and nucleotide chemistry, because it preserves the overall shape of the natural purine base while removing one hydrogen-bond acceptor point. In the laboratory, the material serves as a starting material for the synthesis of 7-deazapurine nucleosides, modified oligonucleotide probes, and test compounds in enzyme research involving purine bases.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it so widely chosen is its very close structural resemblance to hypoxanthine, combined with a meaningful electronic change. Replacing N7 with CH strengthens the aromatic character of the five-membered ring, alters basicity and tautomeric patterns, and opens position 7 to functionalisation through halogenation or cross-coupling reactions — something that is not possible with the natural purine. Nucleosides built from it are also generally more resistant to glycosidic bond hydrolysis, making them suitable for probes and analogues that require higher stability in aqueous media.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on synthetic organic chemistry, nucleoside chemistry, and molecular biology reagent development. It is normally handled on a small synthetic scale as a starting material for multi-step routes toward modified bases and probes. Researchers preparing enzyme assay substrates or oligonucleotide modifications rely on it where a purine-shaped scaffold with an addressable position 7 is required.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of 7-deazapurine nucleosides, where the carbon at position 7 provides a stable, functionalisable site that natural purine bases cannot offer to the synthetic chemist.\u003c\/li\u003e\n\u003cli\u003ePreparation of modified oligonucleotide probes, since nucleosides derived from this base resist glycosidic bond hydrolysis and remain more stable in aqueous working media.\u003c\/li\u003e\n\u003cli\u003eEnzyme research using purine bases, where the removal of one hydrogen-bond acceptor point allows recognition and binding requirements to be probed systematically.\u003c\/li\u003e\n\u003cli\u003eHalogenation and cross-coupling chemistry at position 7, giving access to substituted analogues through routes that are simply unavailable on the natural purine scaffold.\u003c\/li\u003e\n\u003cli\u003eStructure–activity studies in nucleoside chemistry, because the compound keeps the overall shape of hypoxanthine while introducing a defined and meaningful electronic change.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3680-71-5\u003c\/li\u003e\n\u003cli\u003eChemical name: 7-Deazahypoxanthine (pyrrolo[2,3-d]pyrimidinone framework)\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: D4324\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale packaging; please refer to the current catalogue listing for available sizes\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's label and the accompanying safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, in a cool, dry and well-ventilated area away from direct sunlight, moisture and incompatible materials, following the storage conditions stated on the manufacturer's label and safety data sheet. Keep the container sealed when not in use to limit exposure to atmospheric moisture. Handle in a fume hood using standard laboratory personal protective equipment, including safety glasses, gloves and a laboratory coat. Weigh and transfer using clean, dry spatulas and glassware to avoid cross-contamination, and allow the container to reach room temperature before opening if it has been kept refrigerated. Dispose of residues and contaminated materials in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086687023322,"sku":"TCI2510D432424889","price":1062000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4324.jpg?v=1767107418"},{"product_id":"tci2510d514625997","title":"TCI D5146 6478-73-5 5,6-Dichlorobenzimidazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5,6-Dichlorobenzimidazole is a chemical compound widely used in scientific experiments, particularly in the fields of biochemistry and biotechnology. This compound plays a critical role in laboratory settings where DNA, RNA, and genetic transcription processes are studied. As a key component in the category of nucleosides and nucleotides, it supports research into molecular structures and biological interactions. Its presence in laboratory reagents makes it indispensable for various analytical and synthetic procedures.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and ability to interact with a wide range of biological molecules. These properties make it a preferred choice for researchers seeking reliable and consistent results in their experiments. Its complex chemical structure enables it to participate in diverse chemical reactions and biological processes, enhancing its versatility in laboratory applications. Additionally, its resistance to degradation ensures that it remains effective under prolonged storage and use conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5,6-Dichlorobenzimidazole is commonly utilized by researchers in universities, research centers, and pharmaceutical industries. It is a fundamental component in experiments related to genetics and biochemistry, supporting both academic and industrial research. Its availability in the local market facilitates its use in various scientific projects, contributing to the advancement of scientific knowledge in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGenetic research and molecular biology experiments benefit from its role in DNA and RNA analysis, providing a stable reagent for genetic sequencing and modification.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays require its chemical stability and reactivity to ensure accurate and reproducible results in enzyme activity and protein interaction studies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development utilizes its properties in the synthesis of nucleoside-based compounds, supporting drug discovery and formulation processes.\u003c\/li\u003e\n\u003cli\u003eMolecular docking and structural analysis applications rely on its complex chemical structure to model interactions with biological targets.\u003c\/li\u003e\n\u003cli\u003eBiotechnology research employs it in the development of diagnostic tools and therapeutic agents, enhancing the precision of molecular-level investigations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6478-73-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5,6-Dichlorobenzimidazole should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances to prevent unwanted reactions. Proper labeling of containers is essential for safe handling and storage. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in scientific research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086746857690,"sku":"TCI2510D514625997","price":2929000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086746890458,"sku":"TCI2510D514625998","price":9995000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5146.jpg?v=1769142086"},{"product_id":"tci2510d633627379","title":"TCI D6336 523-87-5 Dimenhydrinate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDimenhydrinate (523-87-5) is a chemical compound widely used in laboratory experiments, particularly in the fields of bio-pharmaceuticals and organic chemistry. As an alkaloid derived from specific plant sources, it exhibits antihistaminic properties, making it a valuable reagent for various scientific applications. Its chemical stability and solubility in organic solvents such as ethyl acetate and ethanol further enhance its utility in laboratory settings. This compound is commonly used as a starting material for the synthesis of other compounds or in biological activity assays.\u003c\/p\u003e\n\u003cp\u003eDimenhydrinate is preferred due to its stable chemical properties and ease of availability. It dissolves well in organic solvents, which simplifies its use in analytical procedures. Its molecular structure is well-defined, allowing for accurate identification through techniques like UV-Vis spectroscopy and chromatography. These characteristics make it a reliable and versatile reagent for researchers working in biochemistry and pharmacology. The compound's consistent performance and compatibility with various analytical methods contribute to its popularity in scientific research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dimenhydrinate is frequently used in pharmacological, pharmaceutical, and organic chemistry research. It plays a key role in drug development and clinical testing, supporting studies aimed at understanding its biological effects and therapeutic potential. Its presence in research institutions highlights its importance in advancing scientific knowledge and innovation in the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Dimenhydrinate to study antihistaminic effects and drug interactions in biological systems.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments often employ it as a starting material for the synthesis of complex molecules and derivatives.\u003c\/li\u003e\n\u003cli\u003eBiochemical assays use Dimenhydrinate to evaluate its biological activity and potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development incorporates it in the formulation of drugs and the testing of new compounds for efficacy.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry relies on Dimenhydrinate for its solubility and stability, making it suitable for spectroscopic and chromatographic analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 523-87-5\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDimenhydrinate should be stored in a cool, dry place, away from direct sunlight and moisture. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. Suitable storage containers include glass or plastic vessels with tight-fitting lids. Due to its chemical stability, it does not require refrigeration under normal conditions. In laboratory settings, it is important to handle Dimenhydrinate with care, using appropriate personal protective equipment when necessary. Proper labeling and storage practices ensure the compound remains safe and effective for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086802792666,"sku":"TCI2510D633627379","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086802825434,"sku":"TCI2510D633627380","price":6082000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6336.jpg?v=1768205182"},{"product_id":"tci2510e080728598","title":"TCI E0807 4212-49-1 5-Ethyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Ethyluracil is a pyrimidine base analogue derived from uracil, carrying an ethyl group substituted at the fifth position of the ring. Uracil itself is one of the constituent bases of RNA, so modification at position five yields a compound that remains recognizable to biological systems while carrying distinctly different steric and electronic character. In the laboratory, this compound serves as a starting material for the synthesis of modified nucleosides, as a comparison compound in studies of pyrimidine metabolism, and as a test substrate in research on enzymes that act on pyrimidine bases.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material important is the strategic position of its substituent. Position five of the pyrimidine ring is the most widely explored point of modification in nucleoside chemistry, because substituents placed there are relatively well tolerated by many enzymes while still being able to alter base-pairing behaviour, solubility, and metabolic stability. The ethyl group contributes a moderate increase in hydrophobicity — greater than the methyl group of thymine, yet still compact. The pyrimidine ring also presents NH and carbonyl groups that are readily available for glycosylation, directed alkylation, and the formation of characteristic hydrogen bonds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Ethyluracil is typically used in university and institutional research settings working on nucleoside chemistry, biochemistry, and pyrimidine metabolism. It is normally handled at small scale on the synthetic bench or in enzyme assay work, where it functions either as a building block toward modified nucleoside targets or as a reference compound alongside natural bases such as uracil and thymine. Its role suits organic synthesis groups and life science research units rather than routine analytical service work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eModified nucleoside synthesis — the free NH and carbonyl positions on the pyrimidine ring make this base a direct substrate for glycosylation reactions that build nucleoside analogues with a five-position ethyl group.\u003c\/li\u003e\n\u003cli\u003ePyrimidine metabolism studies — serves as a comparison compound against uracil and thymine, allowing researchers to trace how an enlarged five-position substituent affects metabolic recognition and processing.\u003c\/li\u003e\n\u003cli\u003eEnzyme substrate specificity research — used as a test compound for enzymes acting on pyrimidine bases, since position-five substituents are often tolerated while still probing the limits of the active site.\u003c\/li\u003e\n\u003cli\u003eDirected alkylation chemistry — the ring nitrogen and carbonyl functionalities provide defined reactive handles for selective alkylation work aimed at building more elaborate pyrimidine derivatives.\u003c\/li\u003e\n\u003cli\u003eBase-pairing and hydrogen bonding investigations — the retained NH and carbonyl groups permit characteristic hydrogen bond formation, making the compound useful for studying how five-position bulk influences pairing behaviour.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalogue number: E0807\u003c\/li\u003e\n\u003cli\u003eCAS number: 4212-49-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale packaging as supplied by TCI; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: store in a cool, dry place in the tightly closed original container\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 5-Ethyluracil in its original tightly closed container in a cool, dry, and well-ventilated place, protected from moisture and away from strong oxidising agents and incompatible chemicals. Amber glass or the manufacturer's supplied container is suitable for keeping the material sealed and dry; transfer any working portions into clean, clearly labelled vessels. Handle the compound in a fume hood or well-ventilated area, wearing safety glasses, gloves, and a laboratory coat, and avoid generating or inhaling dust when weighing out solid material. Wash hands thoroughly after handling, keep the container closed when not in use, and consult the manufacturer's safety data sheet before first use for full hazard and disposal guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086897885402,"sku":"TCI2510E080728598","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086897918170,"sku":"TCI2510E080728599","price":986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0807.jpg?v=1768818738"},{"product_id":"tci2510e109628983","title":"TCI E1096 59989-18-3 5-Ethynyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Ethynyluracil is a chemical compound widely used in research applications within the fields of chemical biology and click chemistry. It serves as a key reagent in the development of bioconjugates, enabling the specific chemical reaction with various molecules such as amines or alcohols. Its unique molecular structure allows for precise and controlled chemical modifications, making it an essential tool in synthetic and analytical laboratory settings. This compound is particularly valuable in experiments requiring high specificity and reproducibility.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 5-Ethynyluracil, including its stability and controlled reactivity, make it a preferred choice for researchers. It exhibits good solubility in organic solvents, which simplifies its use in a variety of chemical reactions. These characteristics allow for efficient synthesis and modification of molecular structures, supporting advanced research in biomedicine and pharmacology. Its predictable behavior under different reaction conditions enhances its reliability in laboratory experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Ethynyluracil is commonly used in scientific research, especially in the fields of chemical biology and pharmaceutical sciences. It is frequently found in experiments related to drug development, molecular modification, and the study of molecular interactions. Its availability in the local market ensures that researchers can access this compound for their studies, supporting ongoing scientific advancements in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBioconjugate synthesis where specific molecular linkages are required for labeling and functionalization of biomolecules.\u003c\/li\u003e\n\u003cli\u003eClick chemistry experiments that rely on the efficient and selective reaction of azide and alkyne groups for rapid bond formation.\u003c\/li\u003e\n\u003cli\u003eDrug development research involving the modification of molecular structures to enhance therapeutic properties and bioavailability.\u003c\/li\u003e\n\u003cli\u003eMolecular interaction studies that require precise chemical modifications to investigate binding affinities and biological activity.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications where controlled reactivity and solubility are essential for accurate and reproducible results.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 59989-18-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Conjugation Chemistry\/Click Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Ethynyluracil should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its reactivity. In laboratory settings, proper personal protective equipment such as gloves and safety goggles should be worn when handling the compound to ensure safety. It is important to store the material in a well-ventilated area to minimize any potential risks associated with its chemical properties. Regular monitoring of storage conditions will help maintain the integrity and effectiveness of the compound during its use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086923509978,"sku":"TCI2510E109628983","price":4266000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086923542746,"sku":"TCI2510E109628984","price":14991000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1096.jpg?v=1767112332"},{"product_id":"tci2510f015129860","title":"TCI F0151 51-21-8 5-Fluorouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Fluorouracil (5-FU) is a chemical compound widely used in organic chemistry and pharmaceutical research. As a building block, it plays a crucial role in the synthesis of complex molecules, especially those containing fluorine atoms. Its versatility makes it a valuable tool in laboratories where the development of new compounds and drug formulations is essential. 5-FU is commonly used as a starting material for the production of pharmaceuticals, diagnostic reagents, and other bioactive chemicals. Its stability and controlled reactivity make it a reliable choice for various chemical experiments.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure consists of a carbon chain with fluorine atoms, giving it unique chemical properties. It is typically colorless and solid, with a high melting point, which facilitates storage and handling. Its high purity and consistent chemical properties make it ideal for scientific research requiring precision and accuracy. In Indonesian laboratories, 5-FU is a key component in studies related to pharmacology, organic chemistry, and biochemical research. It is frequently found in chemical, pharmaceutical, and public health research settings.\u003c\/p\u003e\n\u003cp\u003eIn the context of Indonesian laboratories, 5-FU is used in a variety of research applications. Its role in drug development and diagnostic reagents is particularly significant. Researchers rely on its predictable behavior and chemical stability to conduct experiments that require precise control over reaction conditions. Its presence in both academic and industrial research environments underscores its importance in advancing scientific knowledge and practical applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes 5-FU as a foundational compound in the development of anti-cancer and anti-inflammatory drugs due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 5-FU’s ability to participate in various chemical reactions, enabling the creation of complex fluorinated compounds.\u003c\/li\u003e\n\u003cli\u003eDiagnostic reagent preparation leverages 5-FU’s stability and controlled reactivity for the production of bioactive compounds used in medical testing.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies use 5-FU to investigate its interactions with biological systems, aiding in the understanding of cellular processes and drug mechanisms.\u003c\/li\u003e\n\u003cli\u003ePublic health research incorporates 5-FU in the development of therapeutic agents, contributing to advancements in disease treatment and prevention.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 51-21-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Fluorouracil should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. Due to its solid form, it is best stored in airtight glass or plastic containers that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated and free from incompatible substances. Proper labeling and storage conditions help maintain the integrity of the compound and ensure safe handling in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086982164698,"sku":"TCI2510F015129860","price":860000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086982197466,"sku":"TCI2510F015129861","price":2524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0151.jpg?v=1767113413"},{"product_id":"tci2510f032130103","title":"TCI F0321 2022-85-7 5-Fluorocytosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Fluorocytosine is a chemical compound widely used in laboratory experiments, particularly in the synthesis of fluorinated compounds. As a fluorinated building block, it plays a crucial role in organic chemistry by enabling the construction of complex molecules that require the presence of fluorine atoms. Its versatility makes it a valuable tool for researchers aiming to develop new compounds with specific functional properties. This compound is commonly found in chemical laboratories where fluorination is a key part of the research process.\u003c\/p\u003e\n\u003cp\u003eThe stability and controlled reactivity of 5-Fluorocytosine make it a preferred choice for synthetic applications. Its unique chemical structure, with fluorine atoms positioned at specific sites, allows it to participate in substitution reactions and other chemical transformations effectively. The compound’s predictable behavior under controlled laboratory conditions ensures reliable results, reducing the risk of unexpected side reactions. These properties make it an essential component in the toolkit of chemists working on fluorinated molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Fluorocytosine is commonly used in organic chemistry research, especially in academic institutions and research centers. It is frequently employed in projects focused on the synthesis of new compounds or the modification of existing ones. Its role in advancing chemical research in Indonesia highlights its importance in both educational and industrial applications within the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis projects benefit from 5-Fluorocytosine due to its ability to introduce fluorine atoms into complex molecular structures, enhancing the compound's functional properties.\u003c\/li\u003e\n\u003cli\u003eFluorination studies often use this compound as a building block because of its stable and predictable reactivity, allowing for precise control over the synthesis process.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry may incorporate 5-Fluorocytosine to develop new pharmaceutical compounds with improved therapeutic properties.\u003c\/li\u003e\n\u003cli\u003eEducational institutions use it as a teaching tool to demonstrate fluorinated compound synthesis and reaction mechanisms in undergraduate and graduate courses.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories may employ it as a standard reference material for testing and calibrating analytical instruments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2022-85-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Fluorocytosine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and potential degradation. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid contamination. In a laboratory setting, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is advised to maintain the compound’s effectiveness and safety in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086994747610,"sku":"TCI2510F032130103","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086994780378,"sku":"TCI2510F032130104","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086994813146,"sku":"TCI2510F032130105","price":2399000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0321.jpg?v=1767113534"},{"product_id":"tci2510f038230192","title":"TCI F0382 220141-70-8 5-Fluoroorotic Acid Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Fluoroorotic Acid Monohydrate is a chemical compound widely used in laboratory experiments and scientific research. It belongs to the category of fluorinated building blocks, playing a crucial role in the synthesis of complex molecules. This compound is particularly valued for its ability to participate in chemical reactions that require fluorine substitution, making it essential for the development of fluorinated compounds. Its unique chemical properties make it a versatile reagent in various scientific applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is chemically stable and soluble in organic solvents such as ethylamine, which enhances its usability in different experimental setups. Its fluorinated structure provides distinct advantages in specific chemical reactions, enabling precise control over molecular synthesis. This stability and reactivity make it a preferred choice for researchers aiming for accuracy and reproducibility in their experiments. Additionally, its compatibility with a range of solvents allows for flexibility in experimental design.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Fluoroorotic Acid Monohydrate is commonly used in organic and biochemical research. It is a key component in the synthesis of bioactive compounds and is frequently employed in academic and research institutions. Its availability supports a wide range of scientific investigations, contributing to advancements in both chemical and biological sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its fluorinated structure, enabling the creation of complex fluorinated compounds with high specificity.\u003c\/li\u003e\n\u003cli\u003eBiochemical research utilizes it for the synthesis of bioactive molecules, supporting studies in pharmacology and molecular biology.\u003c\/li\u003e\n\u003cli\u003eFluorination studies rely on its reactivity, allowing for controlled substitution of hydrogen atoms with fluorine in various organic frameworks.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry experiments use it as a standard for fluorine-containing compound identification and quantification.\u003c\/li\u003e\n\u003cli\u003eDrug development projects incorporate it in the design of fluorinated pharmaceuticals, enhancing compound stability and biological activity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 220141-70-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, monohydrate form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Fluoroorotic Acid Monohydrate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to moisture, which could affect its integrity. Storage away from direct sunlight and in a well-ventilated area is essential to avoid any potential degradation. The compound is generally handled in standard laboratory conditions, with appropriate personal protective equipment worn when handling. Due to its chemical nature, it should be stored separately from incompatible substances to ensure safety. Proper labeling and storage practices help maintain the compound’s quality and usability for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086999171290,"sku":"TCI2510F038230192","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086999204058,"sku":"TCI2510F038230193","price":2903000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0382.jpg?v=1769056018"},{"product_id":"tci2510f064730566","title":"TCI F0647 700-49-2 2-Fluoroadenine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Fluoroadenine, supplied under TCI catalogue code F0647, is a purine analogue derived from adenine in which a fluorine atom is bonded to the two position of the purine ring. The compound occupies an important place in nucleoside chemistry and medicinal chemistry, since adenine itself is one of the nitrogenous bases that make up nucleic acids. By replacing a single hydrogen atom on the purine ring with fluorine, researchers obtain a modified base that can be used to construct analogue nucleosides and nucleotides. The material is widely employed as a starting building block in the synthesis of purine-based active compounds and in biochemical studies of nucleic acids in research laboratories.\u003c\/p\u003e\n\u003cp\u003eThe property that gives this compound its high value is the influence the fluorine atom exerts on the behaviour of the purine ring. Fluorine at the two position provides an electron-withdrawing effect that alters the basicity of the ring and the hydrogen bonding pattern of the base, while at the same time conferring resistance to the enzymatic degradation pathways that normally attack adenine. Because the size of a fluorine atom is very close to that of hydrogen, the change in molecular shape is extremely small, so the resulting analogue is still recognised by biological systems even though its chemical behaviour has already changed. This combination of minimal steric disturbance and substantial electronic modification is the principle that makes fluorinated purines so useful to synthetic chemists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Fluoroadenine is typically handled as a fine research-scale building block rather than a bulk reagent. It is most often found in university and institutional research groups working on nucleoside chemistry, in medicinal chemistry programmes exploring purine scaffolds, and in biochemistry laboratories investigating nucleic acid behaviour. Quantities are usually modest, reactions are run on a small scale, and the material is stored alongside other sensitive organic building blocks in a controlled chemical store.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of analogue nucleosides, where the fluorinated purine serves as the base component that is coupled to a sugar unit to produce modified nucleosides for further chemical study.\u003c\/li\u003e\n\u003cli\u003ePreparation of nucleotide analogues for nucleic acid research, taking advantage of the altered hydrogen bonding pattern that fluorine substitution introduces into the purine base.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry exploration of purine scaffolds, where researchers use this building block to construct libraries of purine-based active compounds for structure and activity investigations.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies of enzymatic stability, since the fluorine substituent confers resistance to the degradation pathways that normally act upon unmodified adenine in biological systems.\u003c\/li\u003e\n\u003cli\u003eFluorinated building block work in general synthetic chemistry, where the near-identical size of fluorine and hydrogen allows the electronic character of a purine ring to be tuned without significant steric change.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalogue code: F0647\u003c\/li\u003e\n\u003cli\u003eCAS number: 700-49-2\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-Fluoroadenine\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003eStorage: store as indicated on the manufacturer label and product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 2-Fluoroadenine in its original tightly closed container, following the storage conditions stated on the manufacturer label and the accompanying product documentation. Keep the container in a cool, dry and well ventilated chemical store, away from direct sunlight, moisture and incompatible materials. As with all fine organic building blocks, handle the material in a fume hood using appropriate personal protective equipment, including gloves, safety glasses and a laboratory coat. Weigh out only the quantity required, close the container promptly afterwards to limit exposure to atmospheric moisture, and consult the safety data sheet supplied with the product before first use and before disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087021453530,"sku":"TCI2510F064730566","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087021486298,"sku":"TCI2510F064730567","price":3155000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0647.jpg?v=1767113763"},{"product_id":"tci2510f132231467","title":"TCI F1322 1195-08-0 5-Formyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Formyluracil is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. As a building block in organic chemistry, it plays a crucial role in creating complex molecular structures. This compound is commonly found in chemical laboratories as a raw material for the production of various heterocyclic substances. Its versatility makes it an essential component in many synthetic pathways, enabling the development of new compounds with diverse chemical properties.\u003c\/p\u003e\n\u003cp\u003eThe stability of 5-Formyluracil’s chemical structure, combined with its moderate reactivity, allows for controlled chemical reactions. It is soluble in organic solvents such as ethyl acetate and acetone, which facilitates its handling and application in laboratory processes. These properties make it a reliable and user-friendly material for both research and educational purposes. Its solubility and reactivity contribute to its effectiveness in various chemical transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Formyluracil is frequently used in organic chemistry research, particularly in the synthesis of heterocyclic compounds. It is also relevant in higher-level chemistry education, where students study molecular structures and chemical reactions. Its availability in the local market ensures easy access for researchers and academic institutions, supporting both practical and theoretical studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eEducational use in advanced chemistry courses to demonstrate molecular structure and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eResearch applications in pharmaceutical and material science for compound development.\u003c\/li\u003e\n\u003cli\u003eChemical process development where controlled reactivity and solubility are required.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry for use as a standard in qualitative and quantitative analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1195-08-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: 50g, 250g, 1kg\u003c\/li\u003e\n\u003cli\u003ePhysical form: White crystalline powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Formyluracil should be stored in a cool, dry place, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. As a solid compound, it is generally stable under normal laboratory conditions but should be handled with care to avoid contamination. Proper labeling and storage are essential to ensure safe handling and prevent accidental exposure. Always follow standard laboratory safety protocols when working with chemical compounds to maintain a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087076667610,"sku":"TCI2510F132231467","price":2071000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087076700378,"sku":"TCI2510F132231468","price":7219000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1322.jpg?v=1768360406"},{"product_id":"tci2510g016831776","title":"TCI G0168 10333-92-3 Guanine Sulfate Dihydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGuanine Sulfate Dihydrate is a chemical compound classified under nucleotides and plays a crucial role in laboratory research, particularly in biochemical and molecular studies. It is a fundamental component of DNA and RNA structures, making it essential for understanding genetic material and its associated functions. This compound is widely used in experiments related to nucleotide metabolism, DNA synthesis, and enzyme activity testing. Its presence in various biological processes makes it a valuable tool for researchers aiming to explore molecular mechanisms and biochemical pathways.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make Guanine Sulfate Dihydrate a preferred choice is its chemical stability under controlled conditions. This stability ensures consistent performance during experiments and simplifies storage and handling over extended periods. Additionally, its high solubility in water allows for easy dissolution in aqueous solutions, facilitating its use in a wide range of chemical reactions and analytical procedures. These characteristics contribute to its reliability and versatility in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Guanine Sulfate Dihydrate is extensively utilized in biochemistry, pharmacology, and genetics research. Its role in studying metabolic processes and genetic material makes it a critical reagent for both academic and industrial research. Its availability and consistent quality make it a go-to choice for scientists and researchers in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical research for studying nucleotide metabolism and DNA synthesis due to its structural similarity to nucleic acids.\u003c\/li\u003e\n\u003cli\u003eEnzyme activity assays where it serves as a substrate or cofactor in biochemical reactions.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments involving DNA and RNA analysis, including sequencing and hybridization techniques.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies to investigate the effects of nucleotide-based compounds on cellular functions.\u003c\/li\u003e\n\u003cli\u003eGenetic research for understanding the role of nucleotides in gene expression and mutation analysis.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 10333-92-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eGuanine Sulfate Dihydrate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in airtight containers to avoid moisture absorption, which could affect its solubility and purity. Since it is highly soluble in water, it should be handled in a well-ventilated area to prevent airborne exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. Proper labeling of containers is essential to ensure safe handling and prevent accidental contamination. Regular inspection of storage conditions is advised to maintain optimal quality and usability of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087095312602,"sku":"TCI2510G016831776","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0168.jpg?v=1771057922"},{"product_id":"tci2510g016931777","title":"TCI G0169 73-40-5 Guanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGuanine (73-40-5) is a chemical compound classified under the heterocyclic category and is one of the four nitrogenous bases found in DNA and RNA. As a fundamental building block, Guanine plays a crucial role in various chemical reactions aimed at synthesizing complex compounds, including pharmaceuticals, pesticides, and industrial chemicals. In the laboratory, it is widely used as a key reagent in organic synthesis reactions, particularly in the production of heterocyclic compounds with intricate molecular structures. Its presence in nucleic acids makes it essential for biochemical research and molecular studies.\u003c\/p\u003e\n\u003cp\u003eGuanine is known for its stable molecular structure and aromatic properties, which contribute to its reactivity under diverse chemical conditions. It exhibits good solubility in organic solvents such as ethylamine and acetone, making it a preferred choice for precise and stable chemical reactions. These characteristics ensure its reliability in laboratory settings where accuracy and consistency are paramount. Its chemical stability and solubility properties make it a versatile reagent for a wide range of applications in both organic and biochemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Guanine is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and the development of pharmaceutical materials. It is also utilized in biochemical studies to investigate the structure and function of biological molecules. Its presence in DNA and RNA makes it a valuable tool for molecular biology research, contributing to advancements in both academic and industrial scientific fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its stable molecular structure and aromatic nature.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development for the synthesis of nucleoside derivatives and other bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eBiochemical research to study the structural and functional properties of nucleic acids.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for the creation of pesticides and specialty chemicals.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments involving DNA and RNA analysis and modification.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 73-40-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Crystalline solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eGuanine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and air, which could affect its solubility and reactivity. In laboratory settings, proper ventilation is essential to avoid inhalation of any vapors, although Guanine is generally considered to have low volatility. Handling should be done with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during preparation and use. The compound is non-toxic in small quantities but should be treated with care to prevent any unnecessary exposure. Its stable nature makes it safe for routine laboratory use when stored and handled correctly.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087095378138,"sku":"TCI2510G016931777","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087095410906,"sku":"TCI2510G016931778","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48087095443674,"sku":"TCI2510G016931779","price":6008000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0169.jpg?v=1767114754"},{"product_id":"tci2510g017031780","title":"TCI G0170 635-39-2 Guanine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eGuanine Hydrochloride TCI G0170, with CAS number 635-39-2, is a chemical compound widely used in laboratory experiments, particularly in the synthesis of heterocyclic compounds. As a fundamental building block in organic chemistry, it plays a crucial role in the development of pharmaceuticals, industrial chemicals, and various biological compounds. Its structural versatility makes it an essential component in chemical reactions that require heterocyclic frameworks, such as the synthesis of nucleotides and related DNA and RNA compounds. This compound is valued for its chemical stability and reactivity under controlled conditions, which facilitates its use in a variety of synthetic processes.\u003c\/p\u003e\n\u003cp\u003eOne of the key reasons for its popularity is its solubility in water, which simplifies mixing and application in chemical reactions. Additionally, its non-toxic nature and availability make it a preferred choice for researchers seeking reliable and safe materials. Its ability to dissolve easily in aqueous solutions enhances its utility in both basic and advanced laboratory settings. These properties contribute to its widespread use in various scientific fields, ensuring consistent results and efficient experimentation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Guanine Hydrochloride is extensively used in chemical, pharmaceutical, and biotechnology research. It is a common reagent in academic and industrial settings, supporting experiments that require high-quality chemical building blocks. Many research institutions and universities rely on this compound for its reliability and effectiveness in synthetic processes, making it an essential part of the laboratory toolkit in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in the synthesis of heterocyclic compounds due to its structural versatility and reactivity in organic reactions.\u003c\/li\u003e\n\u003cli\u003eApplied in pharmaceutical research for the development of nucleotide-based drugs and related biological compounds.\u003c\/li\u003e\n\u003cli\u003eUtilized in DNA and RNA-related studies for the synthesis of nucleotides and other nucleic acid derivatives.\u003c\/li\u003e\n\u003cli\u003eEmployed in biotechnology applications for the production of bioactive molecules and enzyme substrates.\u003c\/li\u003e\n\u003cli\u003eIntegrated into chemical synthesis workflows for the preparation of complex organic molecules with heterocyclic frameworks.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 635-39-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eGuanine Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption, which could affect its solubility and purity. Since it is non-toxic, general laboratory safety protocols should be followed when handling, including the use of gloves and appropriate ventilation. It is important to keep the compound away from incompatible materials to avoid any potential chemical reactions. Regular inspection of storage conditions ensures that the material remains suitable for use in laboratory experiments. Proper labeling of containers is also essential for safe handling and easy identification.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087095541978,"sku":"TCI2510G017031780","price":1289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510G0170.jpg?v=1767114758"},{"product_id":"tci2510h031132829","title":"TCI H0311 68-94-0 Hypoxanthine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eHypoxanthine is a chemical compound classified under nucleotides and plays a crucial role in nucleotide metabolism. It is a key component in biochemical and genetic research, particularly in the study of purine metabolism and RNA synthesis. This compound is widely used in laboratory settings for its versatility and reliability in various experimental applications. Hypoxanthine serves as a substrate in enzymatic reactions and is also used as a building block for the synthesis of more complex compounds. Its presence in laboratory research supports the investigation of fundamental biological processes and the development of new biochemical methodologies.\u003c\/p\u003e\n\u003cp\u003eHypoxanthine is chemically stable under specific conditions and is highly soluble in water, making it easy to handle and incorporate into chemical reactions. Its high purity and consistent quality ensure accurate and reproducible results in experiments. The compound's ability to participate in complex reactions without interfering with the main reaction makes it a preferred choice for researchers. Additionally, its stability and solubility properties enhance its usability in a wide range of biochemical and genetic studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Hypoxanthine is commonly used in biochemistry and genetic research, particularly in academic institutions and research centers. It supports studies related to enzyme activity, metabolic pathways, and molecular biology. Its reliability and availability make it an essential reagent for scientists working in these fields. The compound's role in advancing scientific understanding and innovation is well recognized in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Hypoxanthine is used to study purine metabolism and enzyme activity, particularly in the investigation of xanthine oxidase.\u003c\/li\u003e\n\u003cli\u003eGenetic Studies: It supports RNA synthesis and is essential in experiments related to nucleotide-based molecular biology.\u003c\/li\u003e\n\u003cli\u003eEnzymatic Reactions: Hypoxanthine serves as a substrate in enzymatic processes, aiding in the analysis of metabolic pathways and biochemical transformations.\u003c\/li\u003e\n\u003cli\u003eCompound Synthesis: It is a key building block for the creation of more complex chemical structures, facilitating drug development and molecular design.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis: Hypoxanthine is integral to understanding the biochemical processes involved in purine metabolism and related metabolic disorders.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 68-94-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Powder or crystalline solid, depending on the packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eHypoxanthine should be stored in a cool, dry location, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent contamination and degradation. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is essential when working with this substance to avoid inhalation of airborne particles. Due to its chemical properties, it should be stored separately from incompatible materials. Regular inspection of storage conditions ensures the integrity of the compound and supports safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087187652826,"sku":"TCI2510H031132829","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087187685594,"sku":"TCI2510H031132830","price":1995000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0311.jpg?v=1769056287"},{"product_id":"tci2510h129034088","title":"TCI H1290 707-99-3 9-(2-Hydroxyethyl)adenine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-(2-Hydroxyethyl)adenine is a chemical compound widely used in laboratory experiments related to biochemistry and molecular biology. It belongs to the category of nucleosides and plays a crucial role in research involving DNA, RNA, and the processes of transcription and translation. This compound is commonly utilized as a building block for the synthesis of other chemical substances or as a reagent in specific chemical reactions requiring nucleoside structures. Its molecular structure is complex, enabling it to interact with various biological molecules, making it a versatile tool in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under certain conditions makes it an ideal choice for laboratory applications. Its high purity ensures accurate and precise experimental results, which are essential in scientific research. The stability and purity of 9-(2-Hydroxyethyl)adenine contribute to its reliability in both routine and advanced laboratory procedures. These characteristics make it a preferred material for researchers aiming to maintain the integrity of their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-(2-Hydroxyethyl)adenine is frequently used in genetic, pharmacological, and biotechnological research. Local researchers employ this compound in drug development, disease mechanism studies, and DNA modification experiments. Its availability and reliability make it a key component in various scientific investigations conducted in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGenetic research utilizes 9-(2-Hydroxyethyl)adenine for studying DNA structure and function due to its nucleoside properties.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies benefit from this compound as it aids in the synthesis of drug-related molecules and biochemical pathways.\u003c\/li\u003e\n\u003cli\u003eBiotechnological applications rely on this compound for DNA modification and molecular biology experiments.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments use it as a reagent in nucleic acid synthesis and hybridization processes.\u003c\/li\u003e\n\u003cli\u003eBiochemical research employs it to investigate enzyme interactions and metabolic pathways in biological systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 707-99-3\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Laboratory personnel should wear appropriate personal protective equipment when handling this material. Avoid direct contact with skin and eyes, and ensure adequate ventilation in the workspace. Regular monitoring of storage conditions helps maintain the integrity and usability of the compound for scientific research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087269179610,"sku":"TCI2510H129034088","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087269212378,"sku":"TCI2510H129034089","price":4795000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1290.jpg?v=1769180904"},{"product_id":"tci2510i021935248","title":"TCI I0219 696-07-1 5-Iodouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Iodouracil is a chemical compound widely used in chemical and biochemical experiments, particularly in the synthesis of heterocyclic compounds. As a building block in organic chemistry, it plays a crucial role in the development of new molecules with potential biological activity. This compound belongs to the uracil family, which has a pyrimidine ring structure, with the unique feature of an iodine atom substituting at the fifth position. Its presence in the molecular structure allows for versatile chemical reactivity and makes it an essential reagent in synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe properties of 5-Iodouracil make it a preferred choice for laboratory applications. Its chemical stability and controlled reactivity enable it to participate effectively in substitution and electrophilic reactions. The iodine at position five enhances its solubility in organic solvents, facilitating efficient reactions and purification processes. Additionally, its thermal stability allows it to be used in a variety of reaction conditions, ensuring consistent results. These characteristics make it a reliable and versatile compound for synthetic chemists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Iodouracil is commonly used in research and development settings. It is a key component in the synthesis of bioactive compounds and is frequently utilized in academic and industrial research. Its availability and chemical properties make it a standard reagent in many chemical laboratories across Indonesia, supporting both teaching and advanced research activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBioorganic Synthesis: 5-Iodouracil is used in the synthesis of bioactive compounds due to its ability to participate in substitution reactions and its halogen substituent.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic Compound Development: The compound is ideal for creating new heterocyclic structures because of its pyrimidine backbone and iodine substitution.\u003c\/li\u003e\n\u003cli\u003eMedicinal Chemistry Research: It serves as a building block for developing pharmaceuticals, as its structure can be modified to create compounds with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used as a standard in analytical procedures due to its stability and predictable chemical behavior.\u003c\/li\u003e\n\u003cli\u003eTeaching and Training: It is commonly used in educational settings to demonstrate organic synthesis techniques and reaction mechanisms.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 696-07-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Iodouracil should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. The compound is generally stable under normal laboratory conditions but should be handled with care to avoid contamination. As a halogenated compound, it may react with certain substances, so it is important to use appropriate personal protective equipment when handling. Proper labeling and storage in a designated chemical storage area are essential to ensure safety and maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087362076890,"sku":"TCI2510I021935248","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087362109658,"sku":"TCI2510I021935249","price":2878000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0219.jpg?v=1767119256"},{"product_id":"tci2510i037035470","title":"TCI I0370 3373-53-3 Isoguanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIsoguanine is a chemical compound classified under heterocyclic building blocks, with a structure similar to guanine, a nitrogenous base found in DNA and RNA. This compound plays a crucial role in laboratory settings, particularly in the synthesis of complex molecules that require heterocyclic frameworks as structural components. It is widely used in organic chemistry, pharmacology, and biochemistry research, serving as a key precursor for the development of pharmaceutical compounds and other specialized chemical substances. Its versatility makes it an essential material for researchers aiming to create novel compounds with specific functional properties.\u003c\/p\u003e\n\u003cp\u003eIsoguanine is valued for its chemical stability under certain conditions and its high reactivity towards various chemical reactions, including substitution, condensation, and catalytic processes. These properties make it an ideal choice for the synthesis of complex molecules that demand both reactivity and structural integrity. Additionally, it is relatively easy to isolate and can be stored under specific conditions without significant degradation, ensuring its reliability in long-term research applications. Its chemical behavior and physical characteristics contribute to its widespread use in scientific investigations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Isoguanine is commonly utilized in scientific research, particularly in the fields of organic chemistry, pharmacology, and biochemistry. Researchers and educational institutions frequently employ this compound to develop new substances with potential medical applications. Its availability and performance make it a preferred material for advancing scientific knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis where heterocyclic structures are required for complex molecule development.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research to create new compounds with potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies involving nitrogenous bases and their structural analogs.\u003c\/li\u003e\n\u003cli\u003eChemical research focusing on reactivity and stability of heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eEducational purposes in academic institutions for teaching and experimental work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3373-53-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eIsoguanine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its reactivity and purity. Due to its high reactivity, it should be handled with care in a well-ventilated laboratory setting. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment when working with this compound. Proper storage and handling ensure its effectiveness and safety in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087370924250,"sku":"TCI2510I037035470","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0370.jpg?v=1767119515"},{"product_id":"tci2510i053135715","title":"TCI I0531 52522-99-3 5-Iodo-2,4-dimethoxypyrimidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI I0531 5-Iodo-2,4-dimethoxypyrimidine is a heterocyclic building block based on a pyrimidine ring that carries two methoxy groups at the two and four positions together with an iodine atom at the five position. Pyrimidine is the nucleobase core that forms the underlying skeleton of cytosine, thymine, and uracil, which is why its derivatives are in such high demand in nucleoside research, antiviral work, and anticancer compound development. This material supplies that core in an already functionalised, ready-to-couple state, saving a considerable number of synthetic steps that would otherwise demand harsh reaction conditions and repeated, time-consuming purification if prepared in house.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this compound a frequent first choice lies in the combination of two complementary types of reactive site. The iodine atom at the five position is an ideal entry point for palladium-catalysed cross-coupling reactions, because the C–I bond undergoes oxidative addition readily. The two methoxy groups, meanwhile, play a dual role: they act as protected latent carbonyl functions and as electron-donating substituents that stabilise the ring. Those methoxy groups can be hydrolysed at a late stage to reveal a pyrimidinedione structure closely resembling the natural nucleobase, and the clear difference in reactivity between the sites allows transformations to be carried out in a controlled, sequential manner.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used by university and institutional research groups pursuing medicinal chemistry and nucleoside analogue programmes, as well as by process development teams preparing heterocyclic intermediates. Because locally synthesising a functionalised pyrimidine of this kind requires equipment and reaction control that are not always available, obtaining the core ready-made allows a research group to focus its effort on the coupling and derivatisation steps that actually generate novel structures.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePalladium-catalysed cross-coupling chemistry: the carbon–iodine bond at position five undergoes oxidative addition readily, making it a dependable handle for Suzuki, Sonogashira, Stille, and Heck type bond formation.\u003c\/li\u003e\n\u003cli\u003eNucleoside and nucleobase analogue synthesis: the pyrimidine ring is the same core found in cytosine, thymine, and uracil, so derivatives built from it map directly onto biologically relevant scaffolds.\u003c\/li\u003e\n\u003cli\u003eAntiviral compound research: modified pyrimidine cores are a long-standing structural motif in antiviral discovery, and this pre-functionalised building block shortens the route to new candidate structures.\u003c\/li\u003e\n\u003cli\u003eAnticancer agent discovery programmes: the ability to introduce diverse substituents at the five position lets medicinal chemists rapidly explore structure–activity relationships around a pharmaceutically proven heterocyclic core.\u003c\/li\u003e\n\u003cli\u003eLate-stage pyrimidinedione preparation: the two methoxy groups serve as protected latent carbonyls that can be hydrolysed at the end of a sequence to unmask a natural nucleobase-like structure.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 52522-99-3\u003c\/li\u003e\n\u003cli\u003eProduct code: I0531\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes offered by TCI for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: refer to the storage condition stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated place away from direct sunlight, heat sources, and strong oxidising agents, following the storage condition printed on the manufacturer's label. Iodinated organic compounds are generally best protected from prolonged light exposure, so keep the material in its original amber or opaque container whenever possible and avoid unnecessary transfer between vessels. Handle the solid inside a fume hood while wearing safety goggles, chemical-resistant gloves, and a laboratory coat, and avoid generating or inhaling dust. Allow a chilled container to warm to room temperature before opening to prevent moisture condensation, and consult the safety data sheet before use and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087392256218,"sku":"TCI2510I053135715","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087392288986,"sku":"TCI2510I053135716","price":6866000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0531.jpg?v=1767119855"},{"product_id":"tci2510i081436085","title":"TCI I0814 108-53-2 Isocytosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eIsocytosine is a pyrimidine compound known as an isomer of cytosine, one of the nucleobases that make up nucleic acids. In the laboratory, this material serves as a model molecule and building block for studying the behaviour of nitrogenous bases outside the context of natural DNA and RNA. Its framework presents a combination of amino and carbonyl groups on the pyrimidine ring, allowing researchers to trace how rearranging the positions of functional groups alters patterns of molecular recognition. The product is commonly encountered in fundamental biochemistry research, medicinal chemistry, and the development of nucleoside analogues.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes isocytosine a frequent choice is its ability to form hydrogen bonds with donor and acceptor patterns that differ from those of the canonical bases. This property makes it a favoured material in supramolecular chemistry, molecular self-assembly, and the design of non-natural base pairs. Its physical form is a solid that is relatively easy to weigh and handle on the milligram to gram scale, making it well suited to small-scale reactions. The stability of the pyrimidine framework also simplifies medium-term storage without complicated special handling, provided it is protected from moisture and excessive light.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, isocytosine is typically used in university and institutional research settings where synthetic organic chemistry, biochemistry, and materials chemistry work is carried out. It suits groups preparing nucleoside analogues, investigating hydrogen-bonding motifs, or assembling supramolecular systems on a bench scale. Because it is handled in small quantities and requires no elaborate storage infrastructure, it fits readily into the workflow of teaching laboratories and research groups alike.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside analogue development — the pyrimidine scaffold serves as a starting base for constructing modified nucleosides, letting chemists explore structural variations away from the canonical nucleic acid bases.\u003c\/li\u003e\n\u003cli\u003eNon-natural base pair design — its donor and acceptor arrangement differs from canonical bases, making it a direct tool for building and evaluating artificial base-pairing schemes in the laboratory.\u003c\/li\u003e\n\u003cli\u003eSupramolecular chemistry studies — the compound's hydrogen bonding capability supports the construction of ordered assemblies, allowing researchers to probe how complementary functional groups organise molecules together.\u003c\/li\u003e\n\u003cli\u003eMolecular self-assembly experiments — the combination of amino and carbonyl groups on the ring drives predictable association, giving a reliable model system for investigating spontaneous ordering of small molecules.\u003c\/li\u003e\n\u003cli\u003eFundamental biochemistry and medicinal chemistry research — as a cytosine isomer it acts as a model compound for tracing how functional group position governs molecular recognition in biologically relevant systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: I0814\u003c\/li\u003e\n\u003cli\u003eCAS number: 108-53-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, suitable for weighing on the milligram to gram scale\u003c\/li\u003e\n\u003cli\u003eStorage: store protected from moisture and excessive light; no complicated special handling required for medium-term storage\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore isocytosine in its original tightly closed container, kept protected from moisture and excessive light. The stability of the pyrimidine framework means medium-term storage does not demand complicated special handling, but containers should be resealed promptly after each use to limit exposure to humid air. Transfer the solid using clean, dry spatulas and weigh it into appropriate glass or chemically resistant vessels. As with any laboratory chemical, handle it in a well-ventilated area, wear standard personal protective equipment including gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust during weighing and transfer operations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087418601690,"sku":"TCI2510I081436085","price":6361000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0814.jpg?v=1768361035"},{"product_id":"tci2510i094136237","title":"TCI I0941 151266-23-8 3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine is a chemical compound widely used as a building block in the synthesis of complex heterocyclic compounds. This material plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate for various synthetic pathways. Its unique chemical structure, combining pyrazole and pyrimidine rings, makes it an essential component for the development of new compounds in pharmaceutical and industrial research. Due to its functional group versatility, it is frequently employed in reactions that require high reactivity and specificity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high reactivity, driven by the iodine atom attached to the nitrogen, makes it a preferred choice for nucleophilic substitution and coupling reactions. Its stability under a range of reaction conditions ensures reliable performance in synthetic processes. Additionally, its ability to participate in multiple reaction types without significant degradation enhances its utility in laboratory settings. These properties make it a valuable tool for chemists seeking to design and synthesize complex molecules with controlled structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic and industrial settings. It is a key reagent in the development of new drugs and materials, supporting both fundamental research and applied projects. Its availability and performance make it a go-to choice for researchers working on heterocyclic synthesis and related applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its unique pyrazole and pyrimidine structure, enabling the construction of complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where the iodine atom serves as a good leaving group, facilitating efficient reaction pathways.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions in the development of pharmaceuticals and agrochemicals, as it provides a stable and reactive platform for functional group introduction.\u003c\/li\u003e\n\u003cli\u003eStructural modification of molecules in drug discovery, allowing for the fine-tuning of biological activity and pharmacological properties.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the synthesis of bioactive compounds, leveraging its reactivity and compatibility with various reaction conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 151266-23-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline or powder form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which may affect its stability. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored separately from incompatible substances to avoid any potential chemical interactions. Proper ventilation is essential when working with this material to ensure a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087428759770,"sku":"TCI2510I094136237","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087428792538,"sku":"TCI2510I094136238","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0941.jpg?v=1767120554"},{"product_id":"tci2510i116136540","title":"TCI I1161 163622-50-2 5-Iodo-7H-pyrrolo[2,3-d]pyrimidin-4-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Iodo-7H-pyrrolo[2,3-d]pyrimidin-4-amine is a chemical compound widely used as a building block in the synthesis of complex heterocyclic structures. This compound plays a crucial role in laboratory settings, particularly in organic chemistry research, where it serves as a versatile intermediate for constructing diverse molecular frameworks. Its unique chemical structure, featuring an iodine atom and a pyrrolopyrimidine ring system, makes it a valuable tool for chemists aiming to develop new compounds with specific functional properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and ability to participate in various chemical reactions, such as substitution and condensation, make it a preferred choice in synthetic chemistry. The presence of the iodine atom enhances its reactivity, allowing it to interact effectively with a range of reagents under controlled conditions. This reactivity, combined with its structural versatility, makes it an essential component in the development of pharmaceuticals, agrochemicals, and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmacological research, the synthesis of novel compounds, and the development of chemicals with broad applications. Its ability to undergo precise and specific chemical reactions makes it a key material for researchers working on drug discovery, pesticide formulation, and other advanced chemical applications. The compound's role in creating complex molecular structures is vital for advancing scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDrug discovery and development: This compound is used to synthesize potential pharmaceutical agents due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003ePesticide formulation: Its chemical properties make it suitable for the development of agrochemicals with targeted biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis: It serves as a key intermediate in the creation of complex heterocyclic compounds, enabling the design of new molecular structures.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production: Its unique reactivity allows it to be incorporated into the synthesis of various industrial chemicals with specific functional groups.\u003c\/li\u003e\n\u003cli\u003eResearch and development in chemical engineering: It is utilized in the exploration of new chemical processes and materials with enhanced properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 163622-50-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored separately from incompatible substances to avoid unintended chemical reactions. Proper labeling and storage conditions are essential to ensure the safety of laboratory personnel and the stability of the compound over time.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087447306458,"sku":"TCI2510I116136540","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087447339226,"sku":"TCI2510I116136541","price":6158000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I1161.jpg?v=1767120854"},{"product_id":"tci2510k000936767","title":"TCI K0009 525-79-1 Kinetin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eKinetin is a chemical compound classified under nucleosides, playing a crucial role in the synthesis of DNA and RNA. As a key biochemical reagent, it is widely used in laboratory experiments, particularly in studies related to cell growth, differentiation, and enzymatic activity. Its complex chemical structure requires precise processing to ensure accurate experimental results. Kinetin is a valuable tool for researchers in life sciences, offering a reliable source for molecular analysis and biological compound synthesis.\u003c\/p\u003e\n\u003cp\u003eKinetin is chemically stable under specific conditions but is sensitive to UV light and high temperatures. These properties make it a preferred choice for high-precision research, such as molecular analysis and the synthesis of bioactive compounds. Its purity and controlled form allow researchers to maintain accurate concentrations, enhancing the reliability of experimental data. The stability and sensitivity of kinetin make it suitable for applications where precision and reproducibility are essential.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, kinetin is extensively used across various scientific disciplines, including biotechnology, pharmacology, and molecular biology. It is particularly relevant in research related to plant growth, drug development, and cellular mechanisms. Its presence in pure form enables precise control over experimental parameters, supporting high-quality scientific outcomes. Kinetin is a fundamental component in many biochemical and molecular studies conducted in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular biology research utilizes kinetin for DNA and RNA synthesis due to its role as a nucleoside building block.\u003c\/li\u003e\n\u003cli\u003eEnzymatic activity studies benefit from kinetin as it supports biochemical reactions essential for metabolic pathways.\u003c\/li\u003e\n\u003cli\u003eCell growth and differentiation experiments rely on kinetin to investigate cellular processes in controlled environments.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research incorporates kinetin in the development of bioactive compounds for therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePlant growth studies use kinetin to explore its effects on cellular development and tissue regeneration in botanical research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 525-79-1\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from UV light and high temperatures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKinetin should be stored in a cool, dark environment to prevent degradation caused by UV exposure and high temperatures. It is recommended to use airtight containers to minimize moisture and contamination risks. Proper labeling and secure storage are essential to maintain product integrity. Laboratory personnel should handle kinetin with care, using appropriate protective equipment when necessary. Avoid exposure to direct sunlight and ensure storage conditions remain consistent to preserve its chemical stability. Regular monitoring of storage conditions ensures the compound remains suitable for use in scientific experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087461200090,"sku":"TCI2510K000936767","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087461232858,"sku":"TCI2510K000936768","price":2600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510K0009.jpg?v=1769056596"},{"product_id":"tci2510l008636982","title":"TCI L0086 487-21-8 Lumazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eLumazine is a chemical compound widely used in laboratory settings as a building block for various chemical reactions, particularly in the synthesis of heterocyclic compounds. Its simple yet essential molecular structure plays a crucial role in the formation of complex molecules such as vitamin B2 (riboflavin) and other bioactive substances. In research and development, Lumazine serves as a key intermediate, enabling the creation of compounds with specific functional groups and desired chemical properties. Its versatility makes it an important tool for chemists working on synthetic pathways and molecular design.\u003c\/p\u003e\n\u003cp\u003eLumazine is valued for its chemical stability under controlled conditions, which allows for consistent performance in laboratory processes. However, it is sensitive to oxidation and light, requiring careful handling and storage to maintain its integrity. These properties make it a preferred choice for applications where precision and reliability are critical. Its ability to act as a precursor in multiple reactions also enhances its utility in organic chemistry research, where reproducibility and accuracy are paramount.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Lumazine is commonly used in organic chemistry research, particularly in academic institutions and research centers. It plays a vital role in the development of new compounds with potential applications in medicine and industry. Its availability in the local market supports ongoing scientific studies and innovation, making it an essential component in the chemical research landscape of Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its structural versatility and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules such as riboflavin and related derivatives for pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eSupport in the creation of complex chemical structures requiring precise functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eUse in research involving light-sensitive compounds that require controlled environmental conditions.\u003c\/li\u003e\n\u003cli\u003eContribution to the synthesis of industrial chemicals with specific molecular properties and applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 487-21-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from light and oxidizing agents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eLumazine should be stored in a cool, dark environment to prevent degradation due to light exposure. It is recommended to use airtight containers to minimize contact with air and moisture, which can lead to oxidation. Laboratory personnel should handle Lumazine with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid prolonged exposure to heat and direct sunlight to maintain its chemical stability. Proper labeling and storage conditions are essential to ensure the compound remains effective for its intended applications. Always follow standard safety protocols when working with light-sensitive and potentially reactive materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087471030490,"sku":"TCI2510L008636982","price":2147000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087471063258,"sku":"TCI2510L008636983","price":5781000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510L0086.jpg?v=1767121384"},{"product_id":"tci2510m006337568","title":"TCI M0063 6112-76-1 6-Mercaptopurine Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Mercaptopurine Monohydrate is a chemical compound widely used in laboratory settings for its role in various chemical reactions, particularly in the synthesis of heterocyclic compounds. As a member of the purine group, it plays a crucial role in biochemical processes and is often employed as a building block for the development of pharmaceutical and organic chemical compounds. Its structural complexity makes it a valuable reagent in the creation of molecules with specific pharmacological or biochemical properties. This compound is essential in research aimed at understanding molecular interactions and designing new therapeutic agents.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and controlled reactivity make it a preferred choice for use in substitution reactions and other chemical transformations. Its ability to form complexes with various ligands enhances its versatility in synthetic applications. The monohydrate form simplifies handling and storage, making it a practical option for laboratory use. Its chemical properties allow it to participate in a range of reactions, contributing to the development of new compounds with potential applications in medicine and industry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Mercaptopurine Monohydrate is commonly used in scientific research, particularly in the fields of pharmacy, organic chemistry, and biochemistry. Researchers and scientists rely on this compound to develop new substances with therapeutic potential or industrial applications. Its availability and chemical properties make it a key reagent in the pursuit of scientific innovation and discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes 6-Mercaptopurine Monohydrate for the synthesis of nucleotide derivatives and drug development due to its structural similarity to purine bases.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments benefit from its role in heterocyclic compound synthesis, offering a reliable building block for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ this compound to investigate molecular interactions and enzyme mechanisms, leveraging its presence in biological systems.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use it as a standard reference material for spectroscopic and chromatographic analyses.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it in the production of intermediates for pharmaceutical and agrochemical formulations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 6112-76-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid in monohydrate form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Mercaptopurine Monohydrate should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep the compound in a sealed container to prevent moisture absorption, as it is a monohydrate. Avoid exposure to direct sunlight and high humidity to ensure stability. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to prevent skin contact or inhalation. Proper ventilation is essential when working with this compound to minimize any potential health risks. Its chemical nature requires careful handling to ensure safe and effective use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087508910298,"sku":"TCI2510M006337568","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087508943066,"sku":"TCI2510M006337569","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0063.jpg?v=1767122141"},{"product_id":"tci2510m020437804","title":"TCI M0204 58366-64-6 5-Methylcytosine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Methylcytosine Hydrochloride is a chemical compound widely used in biochemical and molecular biology experiments. As a derivative of cytosine, one of the essential nucleotides in DNA and RNA, it plays a crucial role in various laboratory applications. This compound is commonly utilized as a building block for the synthesis of complex molecules, enabling researchers to explore chemical reactivity and molecular interactions. Its presence in DNA modification studies makes it an indispensable tool for understanding epigenetic mechanisms and nucleotide modifications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, including its stability and reactivity, make it a preferred choice for laboratory use. It exhibits high specificity in interacting with enzymes and proteins, which is vital for precise experimental outcomes. Its solubility in organic solvents further enhances its utility in separation and analytical procedures. These characteristics ensure that it is suitable for high-precision chemical reactions and molecular studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-Methylcytosine Hydrochloride is extensively used in molecular biology research, particularly in DNA modification studies and gene expression analysis. Many research institutions and universities rely on this compound for advancing their studies in epigenetics and nucleotide chemistry. Its reliability and performance make it a standard component in biochemical and molecular biology laboratories across the country.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA modification studies benefit from 5-Methylcytosine Hydrochloride as it is essential for investigating epigenetic mechanisms and methylation patterns in genetic material.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments often use this compound for synthesizing complex nucleotide derivatives and studying their interactions with biological systems.\u003c\/li\u003e\n\u003cli\u003eGene expression analysis relies on this reagent to understand how DNA modifications affect transcriptional activity and regulatory processes.\u003c\/li\u003e\n\u003cli\u003eChemical reactivity testing utilizes its stable yet reactive nature to explore molecular interactions and reaction pathways in controlled environments.\u003c\/li\u003e\n\u003cli\u003eNucleotide synthesis projects incorporate this compound as a key building block for creating modified nucleotides with specific functional properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 58366-64-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e5-Methylcytosine Hydrochloride should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. Due to its chemical reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to avoid any potential hazards. The compound should not be stored near incompatible materials, and all laboratory safety protocols should be followed to maintain a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48087520084186,"sku":"TCI2510M020437804","price":557000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087520116954,"sku":"TCI2510M020437805","price":3508000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087520149722,"sku":"TCI2510M020437806","price":11887000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0204.jpg?v=1768361289"},{"product_id":"tci2510m044338135","title":"TCI M0443 56-04-2 6-Methyl-2-thiouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Methyl-2-thiouracil is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. As a building block in organic chemistry, it plays a crucial role in the development of complex molecular structures. Its unique chemical properties make it a valuable reagent for researchers working on advanced chemical reactions. This compound is particularly useful in the creation of new materials and pharmaceutical compounds due to its reactivity and structural versatility.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity stems from its sulfur atom and methyl group, which enable a variety of chemical transformations such as substitution and ring-opening reactions. These properties make it a preferred choice for chemists seeking to modify heterocyclic frameworks. Additionally, its stability under certain conditions allows for reliable storage and consistent performance during experiments. The presence of sulfur also contributes to its ability to participate in multiple synthetic pathways, enhancing its utility in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Methyl-2-thiouracil is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds. It serves as a key reagent in the development of pharmaceuticals and other specialized chemical products. Its availability and chemical properties make it a standard component in many research projects, supporting innovation and scientific discovery in the field of chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its sulfur-containing structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds as a building block for drug molecule design.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the creation of advanced chemical materials.\u003c\/li\u003e\n\u003cli\u003eChemical modification of ring structures through substitution and ring-opening reactions.\u003c\/li\u003e\n\u003cli\u003eInvestigation of sulfur-based compounds for their unique chemical and biological properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 56-04-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Methyl-2-thiouracil should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture, which could affect its stability. The compound should be stored away from direct sunlight and sources of heat to avoid degradation. In laboratory settings, it is important to handle the material with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safe usage. Proper ventilation should be maintained when handling the compound to minimize inhalation risks. Regular inspection of storage conditions is advised to ensure the material remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087539089626,"sku":"TCI2510M044338135","price":708000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087539122394,"sku":"TCI2510M044338136","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0443.jpg?v=1769056677"},{"product_id":"tci2510m045438155","title":"TCI M0454 626-48-2 6-Methyluracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Methyluracil is a chemical compound classified under heterocyclic building blocks, featuring a modified uracil structure with a methyl group attached to the sixth carbon atom. This compound plays a vital role in laboratory settings, particularly in the synthesis of complex organic molecules. Its unique chemical structure makes it a valuable tool for researchers working in pharmacology and organic chemistry. In the lab, it serves as a foundational component for developing compounds with biological activity, including pharmaceuticals and anticancer agents.\u003c\/p\u003e\n\u003cp\u003eThe stability and predictable reactivity of 6-Methyluracil make it a preferred choice for chemical synthesis. It can participate in various reactions such as substitution and addition, allowing for the formation of diverse functional groups. Its ability to interact with other chemical entities enhances its utility in creating new compounds with specific applications. The compound’s controlled stability under laboratory conditions ensures reliable results in experimental processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Methyluracil is widely used in organic chemistry research, particularly in academic and industrial settings. It is a common reagent in the development of bioactive compounds and is integral to studies focused on drug discovery and chemical innovation. Its consistent performance and compatibility with various synthetic methods make it a staple in chemical laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 6-Methyluracil is used to build complex molecules with specific biological activities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from this compound due to its role in creating drug candidates with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eAnticancer drug development often incorporates 6-Methyluracil as a building block for novel compounds targeting cancer cells.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry utilizes it for teaching and experimental purposes in heterocyclic compound studies.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes rely on its stability and reactivity for the production of specialized organic materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 626-48-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Methyluracil should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent moisture absorption. Suitable storage containers include glass or high-density polyethylene vessels. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to strong oxidizing agents to ensure safe laboratory practices. Regular monitoring of storage conditions helps maintain the integrity of the compound during extended use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087539843290,"sku":"TCI2510M045438155","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0454.jpg?v=1767122973"},{"product_id":"tci2510m099438909","title":"TCI M0994 636-26-0 5-Methyl-2-thiouracil","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M0994 5-Methyl-2-thiouracil is a pyrimidine nucleobase analogue in which the oxygen atom at position 2 has been replaced by a sulfur atom, while a methyl group is carried at position 5 in the same manner found in thymine. This sulfur substitution is not a minor modification, because it alters the electronic character, the hydrogen-bonding capability, and the light-absorption behaviour of the pyrimidine framework. In biochemistry and medicinal chemistry laboratories, the compound serves as a base analogue for studying molecular recognition in nucleic acids, and equally as a building block for the synthesis of more complex heterocyclic derivatives.\u003c\/p\u003e\n\u003cp\u003eThe most prominent property of this compound is the presence of a thiocarbonyl group that is considerably more nucleophilic and far more readily polarised than the carbonyl group of ordinary uracil. As a consequence, the sulfur atom becomes the preferred reaction site for selective alkylation, and at the same time acts as a capable donor in the formation of complexes with metal ions. The shift in ultraviolet absorption brought about by the sulfur substitution also makes this compound useful as a photoreactive marker in nucleic acid structural studies. Its form as a stable solid simplifies weighing and storage.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5-methyl-2-thiouracil is typically encountered in university biochemistry and medicinal chemistry groups, in research institute settings, and in synthetic laboratories preparing heterocyclic derivatives. Because it is supplied as a stable solid, it is well suited to routine analytical-balance weighing and to preparation of stock solutions as required by the experimental protocol, and it can be kept alongside other reagents in a standard chemical store without special infrastructure.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleic acid base analogue studies, where the sulfur-for-oxygen replacement at position 2 changes hydrogen-bonding capability and allows researchers to probe how bases are recognised within nucleic acid structures.\u003c\/li\u003e\n\u003cli\u003ePhotoreactive labelling in nucleic acid structural work, taking advantage of the ultraviolet absorption shift produced by the thiocarbonyl group to mark and follow structural features under light.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic synthesis, where the molecule serves as a building block for preparing more complex heterocyclic derivatives in medicinal chemistry and general synthetic organic programmes.\u003c\/li\u003e\n\u003cli\u003eSelective alkylation chemistry, since the thiocarbonyl sulfur is markedly more nucleophilic than a carbonyl oxygen and therefore acts as the preferred and predictable site of reaction.\u003c\/li\u003e\n\u003cli\u003eMetal complexation experiments, in which the polarisable sulfur atom behaves as a good donor for forming coordination complexes with metal ions under laboratory conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 636-26-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: stable solid\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container under normal laboratory reagent conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, kept in a cool, dry place away from direct sunlight, moisture, and incompatible chemicals. Amber glass or the supplier's own container is suitable, and the cap should be replaced immediately after each weighing to limit exposure to atmospheric moisture. Handle the solid in a well-ventilated area or fume hood, using gloves, safety glasses, and a laboratory coat, and avoid raising dust during transfer or weighing. Use a clean, dry spatula for each withdrawal to prevent cross-contamination of the bulk material, label all prepared solutions clearly, and consult the manufacturer's safety data sheet before first use and before disposal of any residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48087579099354,"sku":"TCI2510M099438909","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087579132122,"sku":"TCI2510M099438910","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M0994.jpg?v=1769142878"},{"product_id":"tci2510m192540003","title":"TCI M1925 1074-89-1 6-Methoxypurine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Methoxypurine is a chemical compound classified under the heterocyclic category and is commonly used as a building block in the synthesis of complex compounds. This compound is derived from the purine structure with an additional methoxy group, which imparts unique reactivity. In the laboratory, it serves as a versatile intermediate for the development of pharmaceuticals, biochemicals, and organic materials. Its structural characteristics make it a valuable tool in synthetic chemistry, especially in reactions requiring heterocyclic substrates.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability and reactivity, make it a preferred choice for various synthetic applications. It is capable of participating in substitution, condensation, and electrophilic reactions, which are essential in the creation of complex molecular structures. The heterocyclic nature of 6-Methoxypurine allows it to interact effectively with a wide range of reagents and catalysts, enhancing its utility in organic synthesis. These properties make it a sought-after material in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Methoxypurine is widely used in scientific research and education, particularly in the fields of organic chemistry and biochemistry. It is frequently applied in the development of new compounds and in teaching practical laboratory techniques. Its availability and reliability make it a staple in both research and educational institutions across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical synthesis as a key intermediate for drug development due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for the creation of complex heterocyclic compounds through substitution and condensation reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to explore the compound’s potential in molecular interactions and biological activity.\u003c\/li\u003e\n\u003cli\u003eEducational use in teaching synthetic methods and heterocyclic chemistry to undergraduate and graduate students.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications in the synthesis of organic materials with specific functional properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1074-89-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (exact form may vary based on supplier specifications)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e6-Methoxypurine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances to prevent unwanted chemical reactions. Proper ventilation is essential when working with this compound to ensure a safe laboratory environment. Always follow standard safety protocols when handling and storing chemical substances.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506729291994,"sku":"TCI2510M192540003","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1925.jpg?v=1767125768"},{"product_id":"tci2510m207340202","title":"TCI M2073 1076-22-8 3-Methylxanthine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Methylxanthine is a chemical compound classified under heterocyclic building blocks, commonly used in various chemical reactions for the synthesis of complex compounds. This material plays a crucial role in laboratory settings by serving as a foundational component in the development of bioactive substances. Its structural similarity to caffeine and theobromine makes it a valuable tool in pharmacological and organic chemistry research. In the lab, it is often used as a precursor for creating compounds with specific biological activities, contributing to drug discovery and development.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 3-Methylxanthine make it a preferred choice for researchers. It exhibits stability under certain conditions, which simplifies storage and handling. Additionally, its ability to act as an electron donor in specific chemical reactions enhances its utility in synthetic pathways. These characteristics allow it to be integrated into a wide range of experimental designs, making it a versatile reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Methylxanthine is widely utilized in pharmaceutical, organic chemistry, and biochemical studies. Its availability, quality, and compatibility with various experimental requirements make it a top choice for researchers. The compound’s reliability and consistent performance support its application in diverse scientific investigations, contributing to the advancement of chemical research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes 3-Methylxanthine for synthesizing compounds with therapeutic potential due to its structural similarity to caffeine and theobromine.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments benefit from its stability and reactivity, allowing for the creation of complex molecular structures through controlled chemical reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ this compound to investigate its biological activity and potential applications in drug development and metabolic pathways.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications leverage its chemical properties for the development of standardized reagents and calibration standards.\u003c\/li\u003e\n\u003cli\u003eIndustrial research and development use 3-Methylxanthine as a building block for the production of specialty chemicals and pharmaceutical intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1076-22-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: As available from supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e3-Methylxanthine should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is generally stable under normal storage conditions, it should be kept in a secure location to prevent accidental spills or contamination. Proper labeling of storage containers is essential to ensure safe handling and easy identification. These precautions help maintain the integrity of the compound and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087646273754,"sku":"TCI2510M207340202","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087646306522,"sku":"TCI2510M207340203","price":2979000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2073.jpg?v=1767125999"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-nucleobases-and-their-analogs.oembed?page=7","provider":"AMI Scientific","version":"1.0","type":"link"}