{"title":"Nucleosides, Nucleotides, Oligonucleotides","description":"\u003cp\u003e\u003cstrong\u003eNucleosides, Nucleotides, Oligonucleotides\u003c\/strong\u003e — menghimpun basa nukleat, nukleosida, nukleotida beserta analognya, oligonukleotida, DNA, RNA, serta koenzim oksidoreduktase seperti NAD(P)(H) yang menjadi unit dasar asam nukleat dan metabolisme energi sel. Kelompok senyawa ini mencakup bentuk alami maupun termodifikasi yang lazim dipakai dalam biokimia molekuler.\u003c\/p\u003e\u003cp\u003eSenyawa dalam kategori ini digunakan peneliti biologi molekuler dan biokimia untuk sintesis asam nukleat, studi enzim polimerase dan kinase, serta reaksi enzimatik yang bergantung pada koenzim NAD(P)(H) sebagai kofaktor oksidoreduksi. Nukleosida dan nukleotida termodifikasi seperti analog terhalogenasi dipakai sebagai bahan uji in vitro dalam penelitian jalur metabolisme asam nukleat, sementara oligonukleotida sintetik mendukung teknik hibridisasi dan amplifikasi DNA\/RNA.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510i075936013\"\u003eTCI I0759 35109-88-7 2-Iodoadenosine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b679713713\"\u003eTCI B6797 4294-16-0 N6-Benzyladenosine\u003c\/a\u003e, \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\/tci2510a0158241\"\u003eTCI A0158 61-19-8 5'-Adenylic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c029314340\"\u003eTCI C0293 85-18-7 8-Chlorotheophylline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0157238\"\u003eTCI A0157 34369-07-8 Adenosine 5'-Triphosphate Disodium Salt Hydrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c037914465\"\u003eTCI C0379 1184-16-3 beta-Nicotinamide Adenine Dinucleotide Phosphate Sodium Salt Hydrate, oxidized form [for Biochemical Research]\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePemilihan senyawa perlu memperhatikan bentuk garam atau hidrat, kemurnian analitis, stereokimia gula ribosa atau deoksiribosa, serta kestabilan penyimpanan agar sesuai dengan protokol biokimia yang digunakan. 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 Biokimia \u0026amp; Reagen Hayati, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-pharmaceutical-research-reagents-for-experimental-use\"\u003ePharmaceutical Research Reagents (for Experimental Use)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-amino-acids\"\u003eAmino Acids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-carbohydrates\"\u003eCarbohydrates\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-lipids\"\u003eLipids\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-antibiotics\"\u003eAntibiotics\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-enzymes-enzyme-inhibitors-enzyme-substrates\"\u003eEnzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 8 kelompok yang lebih spesifik:\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-nucleobases-and-their-analogs\"\u003eNucleobases and their 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\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-oligonucleotides-dna-and-rna\"\u003eOligonucleotides, DNA, and RNA\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/biokimia-dan-reagen-hayati\"\u003eBiokimia \u0026amp; Reagen Hayati\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":"tci2510b679713713","title":"TCI B6797 4294-16-0 N6-Benzyladenosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6797 (CAS 4294-16-0) is N6-benzyladenosine, an adenosine analogue carrying a benzyl group on the exocyclic N6 nitrogen. It is widely studied as the riboside form within the N6-benzyladenine cytokinin family in plant science research. The compound also serves as an analytical standard for HPLC and mass spectrometry work and as a starting material for further nucleoside modification. AMI Scientific supplies this TCI reagent in 1 g and 5 g pack sizes for research laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMlejnek et al. (2000). Induction of apoptosis in HL-60 cells by N6-benzyladenosine. \u003cem\u003eJournal of Cellular Biochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/(sici)1097-4644(20000401)77:1\u0026lt;6::aid-jcb2\u0026gt;3.3.co;2-v\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/(sici)1097-4644(20000401)77:1\u0026lt;6::aid-jcb2\u0026gt;3.3.co;2-v\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eŠtarha et al. (2013). N6-Benzyladenosine Derivatives as Novel N-Donor Ligands of Platinum(II) Dichlorido Complexes. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules18066990\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules18066990\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCastiglioni et al. (2013). N6-Isopentenyladenosine and its Analogue N6-Benzyladenosine Induce Cell Cycle Arrest and Apoptosis in Bladder Carcinoma T24 Cells. \u003cem\u003eAnti-Cancer Agents in Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.2174\/1871520611313040016\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.2174\/1871520611313040016\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":"1g","offer_id":48085956559066,"sku":"TCI2510B679713713","price":2424000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085956591834,"sku":"TCI2510B679713714","price":8379000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6797.jpg?v=1769144609"},{"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":"tci2510c037914465","title":"TCI C0379 1184-16-3 beta-Nicotinamide Adenine Dinucleotide Phosphate Sodium Salt Hydrate, oxidized form [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0379 β-Nicotinamide Adenine Dinucleotide Phosphate Sodium Salt Hydrate, oxidized form (NADP⁺), CAS 1184-16-3, is a pyridine nucleotide coenzyme supplied for biochemical research. It serves as the hydride acceptor that is reduced to NADPH in dehydrogenase-catalysed reactions, making it a standard reagent for spectrophotometric enzyme assays. Typical uses include pentose phosphate pathway studies, cofactor regeneration systems, and microsomal drug metabolism experiments. Available in 100 mg and 1 g packs from AMI Scientific, it should be kept cool, dry, and protected from light in line with the manufacturer's instructions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085995028698,"sku":"TCI2510C037914465","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085995061466,"sku":"TCI2510C037914466","price":5023000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510c052214709","title":"TCI C0522 65-46-3 Cytidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0522 Cytidine (CAS 65-46-3) is a pyrimidine nucleoside composed of cytosine linked to a ribose sugar unit. It serves as a fundamental reference material in molecular biology, nucleoside synthesis, and pyrimidine metabolism research. The product is offered in 1 g, 5 g, and 25 g pack sizes to suit both pilot experiments and routine laboratory work. Please refer to the manufacturer's Certificate of Analysis and Safety Data Sheet for lot-specific specifications and handling guidance.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAriza et al. (2000). High-Yielding Preparation of [3-15N]Cytidine, [4-15NH2]Cytidine, and [3-15N,4-15NH2]Cytidine. \u003cem\u003eThe Journal of Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jo9918706\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jo9918706\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHASSAN (1991). ChemInform Abstract: Cytidine Nucleosides. Part 2. Photochemical Synthesis of 5‐ Alkylcytidine Nucleosides.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199146298\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199146298\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMorita et al. (2003). Forced Expression of Cytidine Deaminase Confers Sensitivity to Capecitabine. \u003cem\u003eOncology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1159\/000074480\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1159\/000074480\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":"1g","offer_id":48086007087322,"sku":"TCI2510C052214709","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086007120090,"sku":"TCI2510C052214710","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086007152858,"sku":"TCI2510C052214711","price":2197000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0522.jpg?v=1768816265"},{"product_id":"tci2510c052314712","title":"TCI C0523 34393-59-4 Cytidine 5'-Diphosphate Trisodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0523 Cytidine 5'-Diphosphate Trisodium Salt (CAS 34393-59-4) is the trisodium salt form of the pyrimidine nucleotide CDP. Its good aqueous solubility makes it convenient for enzyme assays, nucleotide metabolism studies, and in vitro biochemical systems. Available pack sizes of 10 mg, 100 mg, and 1 g allow researchers to match reagent volume to experimental scale. Store the sealed container under the manufacturer's recommended conditions and consult the Certificate of Analysis for lot-specific details.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZheng et al. (2019). Computation-aided rational design of a halophilic choline kinase for cytidine diphosphate choline production in high-salt condition. \u003cem\u003eJournal of Biotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jbiotec.2018.11.008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jbiotec.2018.11.008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGiménez et al. (1999). Cytidine diphosphate choline administration activates brain cytidine triphosphate: phosphocholine cytidylytransferase in aged rats. \u003cem\u003eNeuroscience Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0304-3940(99)00660-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0304-3940(99)00660-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNIGOU et al. (2002). Cytidine diphosphate-diacylglycerol synthesis in Mycobacterium smegmatis. \u003cem\u003eBiochemical Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1042\/bj20020370\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1042\/bj20020370\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":"10mg","offer_id":48086007185626,"sku":"TCI2510C052314712","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086007218394,"sku":"TCI2510C052314713","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086007251162,"sku":"TCI2510C052314714","price":5579000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0523.jpg?v=1768816264"},{"product_id":"tci2510c052414715","title":"TCI C0524 6757-06-8 Cytidine 5'-Monophosphate Disodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0524 Cytidine 5'-Monophosphate Disodium Salt (CAS 6757-06-8) is the disodium salt of the RNA building block CMP. The salt form offers convenient aqueous solubility for preparing working solutions in biochemical and detection-related assays. It is supplied in 1 g and 5 g pack sizes for flexible laboratory use. Keep the container tightly closed in a cool, dry place and follow the manufacturer's documentation for lot-specific specifications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086007283930,"sku":"TCI2510C052414715","price":607000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086007316698,"sku":"TCI2510C052414716","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0524.jpg?v=1767095435"},{"product_id":"tci2510c052514717","title":"TCI C0525 32747-18-5 Cytidine Sulfate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0525 Cytidine Sulfate (CAS 32747-18-5) is the sulfate salt form of the pyrimidine nucleoside cytidine, prepared for research use. It is commonly applied as a starting material for nucleoside analog synthesis and in pyrimidine metabolism studies. Pack sizes of 100 mg and 1 g support small to medium scale laboratory work. Store the sealed container in a cool, dry, light-protected place and refer to the manufacturer's Certificate of Analysis for specifications.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eLeng et al. (2023). Solubility, Crystallization, and Characterization of Cytidine Sulfate. \u003cem\u003eACS Omega\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/acsomega.3c02501\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/acsomega.3c02501\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":"100mg","offer_id":48086007382234,"sku":"TCI2510C052514717","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086007415002,"sku":"TCI2510C052514718","price":633000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0525.jpg?v=1768816265"},{"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":"tci2510c167516340","title":"TCI C1675 63-37-6 Cytidine 5'-Monophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytidine 5'-Monophosphate (CMP), with CAS number 63-37-6, is a nucleotide widely used in biochemical and molecular biology research. This compound serves as a key substrate in RNA synthesis and translation processes, making it essential for studies involving genetic expression and enzymatic reactions. Its high purity and stability ensure reliable and reproducible experimental results. In Indonesian laboratories, CMP is commonly utilized in drug development, genetic research, and biotechnology applications. The product is available in two packaging options, 1g and 5g, and is supplied in a solid powder form. Proper storage in airtight containers away from light and moisture is recommended to maintain its integrity.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2009). 597. Characterization of a Uridine\/Cytidine Monophosphate Kinase\/Deoxycytidine Kinase Fusion Enzyme for Suicide Gene Therapy. \u003cem\u003eMolecular Therapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s1525-0016(16)38955-9\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s1525-0016(16)38955-9\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":"1g","offer_id":48086084190426,"sku":"TCI2510C167516340","price":581000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086084223194,"sku":"TCI2510C167516341","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1675.jpg?v=1768816677"},{"product_id":"tci2510c203516667","title":"TCI C2035 147-94-4 Cytarabine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytarabine, with CAS number 147-94-4, is a widely used chemical compound in biomedical and pharmacological research. It is a nucleoside analog known for its strong antitumor activity, particularly effective against leukemia and lymphoma cells. In the laboratory, Cytarabine serves as a key reagent for cancer therapy research, drug efficacy testing, and the study of anti-cancer drug mechanisms. Its role is essential in understanding the biochemical pathways involved in tumor suppression and treatment development.\u003c\/p\u003e\n\u003cp\u003eCytarabine is chemically stable under certain conditions but is highly sensitive to UV light and oxidation. It exhibits good solubility in organic solvents such as ethanol and dimethyl sulfoxide (DMSO), making it easy to dissolve and use in various experimental protocols. Its consistent purity and quality make it a preferred choice for researchers who require reliable and reproducible results. These properties ensure that Cytarabine remains a critical component in many biochemical and pharmaceutical studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cytarabine is commonly used in cancer-related research, especially in the development of chemotherapy treatments and genetic therapy studies. It is also frequently utilized in toxicity testing and the evaluation of new potential anti-cancer compounds. Its versatility and effectiveness make it an essential tool for both academic and industrial research in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCancer Therapy Research: Cytarabine is used to study the mechanisms of action and effectiveness of anti-cancer drugs in leukemia and lymphoma treatments.\u003c\/li\u003e\n\u003cli\u003eDrug Efficacy Testing: It serves as a standard reagent for evaluating the potency and therapeutic potential of new chemotherapy agents.\u003c\/li\u003e\n\u003cli\u003eToxicity Assessment: Cytarabine is employed in toxicity studies to determine the safety profile of potential pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eGenetic Therapy Development: It plays a role in research focused on gene therapy and targeted treatment strategies for malignant diseases.\u003c\/li\u003e\n\u003cli\u003eAnti-Cancer Compound Evaluation: It is used to test the efficacy of novel compounds in inhibiting tumor cell growth and progression.\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: 147-94-4\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dark place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCytarabine should be stored in a cool, dark environment to prevent degradation due to UV exposure and oxidation. It is recommended to keep the compound in airtight containers to minimize moisture contact. Due to its sensitivity, it is best stored in a refrigerator at 2–8°C. When handling, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to avoid direct skin or eye contact. It is important to ensure that the compound is not exposed to heat or direct sunlight during storage or use. Proper labeling and secure storage are essential to maintain the integrity and safety of the reagent in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086097658074,"sku":"TCI2510C203516667","price":784000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086097690842,"sku":"TCI2510C203516668","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2035.jpg?v=1767097686"},{"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":"tci2510c219216864","title":"TCI C2192 146-77-0 2-Chloroadenosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloroadenosine is an adenosine analog belonging to the nucleoside group of compounds, consisting of a purine base attached to a ribose sugar. In the laboratory, it is used primarily as a stable adenosine receptor agonist, allowing researchers to investigate a wide range of cellular signaling pathways mediated by the A1, A2A, A2B, and A3 receptor subtypes. Because its structure closely resembles natural adenosine, it functions as a reliable experimental tool for probing physiological responses such as the inhibition of platelet aggregation, effects on the nervous system, and regulation of specific enzyme activities. This product is supplied by TCI in analytical packaging under CAS number 146-77-0.\u003c\/p\u003e\n\u003cp\u003eThe main property that leads researchers to select 2-Chloroadenosine is its substantially better stability compared with ordinary adenosine. The presence of a chlorine atom at position two of the purine ring shields the molecule from rapid deamination by the enzyme adenosine deaminase, so its biological effects persist much longer in test systems. This extended resistance to enzymatic breakdown makes the compound especially valuable in assays where prolonged receptor stimulation is required, and it reduces the variability that can arise from the rapid degradation of native adenosine. The compound is generally available as a white to off-white crystalline solid, which is convenient for accurate weighing, dissolution, and the preparation of reproducible stock solutions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in life science research focused on pharmacology, cell biology, and neuroscience. Academic institutions and research facilities working on receptor pharmacology commonly employ it to characterize adenosine receptor-mediated signaling in cultured cells and isolated tissues. It also appears in studies examining the regulation of enzyme activity and in experiments designed to evaluate the physiological role of adenosine signaling. In this way, it provides Indonesian researchers with a dependable and stable reference agonist for reproducible assays.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAdenosine receptor pharmacology studies: The compound acts as a stable agonist at the A1, A2A, A2B, and A3 receptors, enabling researchers to map signaling pathways with minimal interference from enzymatic degradation.\u003c\/li\u003e\n\u003cli\u003ePlatelet aggregation research: Because it inhibits platelet aggregation in a sustained manner, it is well suited for studying the role of adenosine signaling in hemostasis and thrombus formation in vitro.\u003c\/li\u003e\n\u003cli\u003eNeuroscience and nervous system studies: Its resistance to deamination allows prolonged receptor stimulation, making it useful for investigating adenosine-mediated effects on neuronal activity and neurotransmission.\u003c\/li\u003e\n\u003cli\u003eEnzyme activity regulation assays: The stable analog helps researchers examine how adenosine receptor activation modulates the activity of specific enzymes under controlled experimental conditions.\u003c\/li\u003e\n\u003cli\u003eSignal transduction and cell physiology experiments: Researchers can use this compound to trigger long-lasting, reproducible responses in cell-based assays, supporting consistent data across repeated experimental runs.\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: 146-77-0\u003c\/li\u003e\n\u003cli\u003eProduct code: C2192\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePhysical form: white to off-white crystalline solid\u003c\/li\u003e\n\u003cli\u003ePackaging: supplied in analytical packaging; refer to the product listing for available pack sizes\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the product in its original, tightly sealed container in a cool, dry place away from direct light and excessive moisture. Keep the container closed when not in use to protect the compound from humidity, which may affect its crystalline form. Always wear appropriate personal protective equipment, including laboratory gloves and safety glasses, when handling this material. Weigh out only the required amount for each experiment and avoid returning unused material to the original container to prevent contamination. Follow standard laboratory hygiene practices, label all working solutions clearly, and dispose of any waste in accordance with your institution's regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086109421786,"sku":"TCI2510C219216864","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086109454554,"sku":"TCI2510C219216865","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2192.jpg?v=1768816797"},{"product_id":"tci2510c220616888","title":"TCI C2206 5399-87-1 6-Chloropurine Riboside","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e6-Chloropurine Riboside (TCI C2206) is a purine nucleoside analogue consisting of a 6-chloropurine base linked to a ribose sugar moiety. In the laboratory, this compound serves as a highly valuable starting material in nucleoside chemistry, because the chlorine atom at the C-6 position of the purine ring acts as a leaving group that is reactive toward nucleophilic attack. Researchers use it to construct a wide range of substituted adenosine and inosine derivatives, making this product an important bridge between synthetic organic chemistry and biochemical research based on nucleosides and nucleotides.\u003c\/p\u003e\n\u003cp\u003eThe principal characteristic that makes this material a preferred choice is the combination of directed reactivity with an intact sugar framework. Aromatic nucleophilic substitution at the C-6 position proceeds with amines, thiols, or alkoxides to yield N6-, S6-, or O6- derivatives without the need to rebuild the complicated glycosidic bond. The hydroxyl groups on the ribose remain available for selective protection, phosphorylation, or further conversion into phosphoramidites. As a reagent-grade material from TCI, batch-to-batch quality consistency helps researchers obtain reproducible synthetic results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 6-Chloropurine Riboside is typically used in university synthetic chemistry groups, pharmaceutical research units, and biochemistry laboratories working on nucleoside and nucleotide chemistry. It is commonly employed on a small preparative scale for derivative synthesis, method development, and postgraduate research projects, where a reliable reagent-grade purine nucleoside starting material shortens the route to target compounds and reduces the number of preparation steps that must be carried out in-house.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside derivative synthesis: the reactive C-6 chlorine allows direct displacement by nucleophiles, giving researchers rapid access to substituted purine nucleosides without rebuilding the glycosidic bond.\u003c\/li\u003e\n\u003cli\u003eAdenosine analogue preparation: reaction with primary or secondary amines at the C-6 position produces N6-substituted adenosine derivatives, a widely used route in nucleoside-based research programmes.\u003c\/li\u003e\n\u003cli\u003eInosine and O6-derivative chemistry: treatment with alkoxides or related oxygen nucleophiles converts the C-6 chlorine into O6-substituted products used for further transformation into inosine-type structures.\u003c\/li\u003e\n\u003cli\u003eThionucleoside synthesis: thiols displace the C-6 chlorine to give S6-substituted derivatives, providing a straightforward entry point into sulfur-containing purine nucleoside chemistry.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide building block preparation: the free ribose hydroxyl groups support selective protection and phosphorylation, enabling downstream conversion into phosphoramidites for nucleotide and oligonucleotide 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: 5399-87-1\u003c\/li\u003e\n\u003cli\u003eProduct code: C2206\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eGrade: reagent grade\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this product code\u003c\/li\u003e\n\u003cli\u003eStorage: store as indicated on the manufacturer's label and product documentation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 6-Chloropurine Riboside in its original tightly closed container, following the storage temperature and conditions stated on the manufacturer's label and safety data sheet. Keep the container in a cool, dry, well-ventilated place, protected from moisture and direct sunlight, and reseal it promptly after each use to limit exposure to atmospheric humidity. Handle the compound in a fume hood or well-ventilated work area using standard laboratory personal protective equipment, including a laboratory coat, chemical-resistant gloves, and safety goggles. Avoid the generation and inhalation of dust, and avoid contact with skin and eyes. Weigh the material with clean, dry spatulas and glassware to prevent contamination between batches, and dispose of residues and contaminated materials in accordance with institutional chemical waste procedures. Consult the safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086111224026,"sku":"TCI2510C220616888","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086111256794,"sku":"TCI2510C220616889","price":3837000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2206.jpg?v=1769144412"},{"product_id":"tci2510c220716890","title":"TCI C2207 10212-25-6 Ancitabine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eAncitabine Hydrochloride (TCI C2207), also known as cyclocytidine hydrochloride, is a pyrimidine nucleoside derivative supplied as a hydrochloride salt, featuring an anhydro bridge that links the cytosine base to the arabinofuranose sugar moiety. This cyclic structure is what distinguishes it from ordinary nucleosides and makes it an interesting subject of study in medicinal chemistry laboratories. The compound is used as a research material and reference substance in studies of nucleoside antimetabolites, particularly those relating to the arabinonucleoside group, as well as a synthetic intermediate on the route toward other modified cytidine derivatives at laboratory scale.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a preferred choice are the combination of its hydrochloride salt form and its reactive anhydro framework. The salt form generally offers more practical handling of the solid and better solubility in aqueous media compared with the free base, which simplifies the preparation of stock solutions for in vitro assays. Meanwhile, the 2,2'-anhydro bridge can be opened by nucleophiles, thereby opening synthetic routes toward nucleosides with the arabino configuration or with particular 2'-substituents. The reagent quality supplied by TCI helps maintain consistency of results across repeated experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically encountered in university research groups, pharmaceutical chemistry departments, and institutional research centres working on nucleoside chemistry. It is generally ordered in small research quantities for synthetic route development, for use as a reference material in analytical comparison work, and for preliminary in vitro studies. Because it is a specialised biochemical rather than a routine bulk chemical, it is usually purchased per project according to the requirements of the experimental plan rather than kept as a standing stock item.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleoside antimetabolite research: the compound serves as a study material for investigating the behaviour of arabinonucleoside-type antimetabolites, allowing researchers to examine how the cyclic framework influences activity relative to conventional nucleosides.\u003c\/li\u003e\n\u003cli\u003eSynthetic intermediate work: the reactive 2,2'-anhydro bridge can be opened by nucleophiles, making this material a practical starting point for laboratory-scale preparation of modified cytidine derivatives and arabino-configured nucleosides.\u003c\/li\u003e\n\u003cli\u003eReference material in analytical comparison: the defined identity of this catalogue compound makes it suitable for use as a comparison standard when characterising related nucleoside structures by chromatographic or spectroscopic methods.\u003c\/li\u003e\n\u003cli\u003eIn vitro assay preparation: the hydrochloride salt form provides better solubility in aqueous media than the free base, which simplifies the preparation of stock solutions used in cell-based and biochemical assay work.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry teaching and methodology development: the distinctive anhydro-bridged structure makes it a useful example compound for advanced coursework and for developing and validating handling procedures for sensitive nucleoside derivatives.\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: 10212-25-6\u003c\/li\u003e\n\u003cli\u003eCatalogue Number: C2207\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eChemical Form: hydrochloride salt of a pyrimidine nucleoside derivative (solid)\u003c\/li\u003e\n\u003cli\u003ePack Sizes: available in laboratory research quantities; please refer to the current catalogue listing for the sizes offered\u003c\/li\u003e\n\u003cli\u003eStorage: refer to the manufacturer's label and safety data sheet for the recommended storage conditions\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in accordance with the conditions stated on the manufacturer's label and in the accompanying safety data sheet. As a general practice for nucleoside derivatives, keep the container tightly closed in a cool, dry place, protected from light and moisture, and use containers that are chemically compatible and well sealed to prevent moisture uptake by the solid. Handle the material in a well-ventilated area or fume hood, wearing gloves, safety glasses, and a laboratory coat, and avoid generating dust when weighing. Allow the container to reach room temperature before opening to reduce condensation. Label all prepared solutions clearly with the compound identity and preparation date, and dispose of residues and contaminated consumables through the laboratory's established chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086111322330,"sku":"TCI2510C220716890","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086111355098,"sku":"TCI2510C220716891","price":5224000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2207.jpg?v=1768204643"},{"product_id":"tci2510c220816892","title":"TCI C2208 3736-77-4 2,2'-O-Cyclouridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2'-O-Cyclouridine (TCI C2208), commonly known as 2,2'-anhydrouridine, is a heterocyclic building block derived from uridine in which a bridging bond links the oxygen atom at the 2' position of the ribose sugar to position 2 of the pyrimidine ring. This bridge is the very core of its usefulness in the laboratory, because the anhydro ring is strained and therefore opened very readily by nucleophiles. As a consequence, the compound serves as a classical synthetic gateway for converting inexpensive uridine into a wide range of 2'-modified nucleosides that are considerably more difficult to obtain by other routes.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes it the preferred choice is the selectivity of its reactions. Opening of the anhydro ring by fluoride sources, azides, halides, or other nucleophiles proceeds with inversion of configuration, thereby delivering products of arabino configuration or 2'-substituted derivatives with controlled stereochemistry. This approach spares researchers the repeated, time-consuming protection and deprotection steps that alternative routes demand. In addition, the compound is a solid that is relatively easy to handle and weigh out, and it is supplied at the consistent TCI reagent grade, making it well suited to multi-step syntheses that demand high reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on nucleoside and nucleotide chemistry, in medicinal chemistry programmes exploring antiviral and anticancer scaffolds, and in postgraduate research where modified nucleosides must be prepared on a laboratory scale. Because it is a stable, easily weighed solid of consistent reagent grade, it fits well into shared synthetic laboratories where several researchers run multi-step sequences and require results that can be repeated between batches and between operators.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of 2'-modified nucleosides: the strained anhydro bridge is opened directly by nucleophiles, converting inexpensive uridine into 2'-substituted analogues that are otherwise difficult to access.\u003c\/li\u003e\n\u003cli\u003ePreparation of arabino-configured nucleosides: ring opening proceeds with inversion of configuration at the 2' position, giving arabino products with predictable and controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003eIntroduction of 2'-fluoro substituents: fluoride sources open the anhydro ring cleanly, providing a classical and direct route to fluorinated nucleoside building blocks for further elaboration.\u003c\/li\u003e\n\u003cli\u003ePreparation of 2'-azido and 2'-halo derivatives: azide and halide nucleophiles attack the strained ring selectively, delivering functionalised intermediates suitable for subsequent transformation.\u003c\/li\u003e\n\u003cli\u003eMulti-step medicinal chemistry sequences: consistent TCI reagent grade and the avoidance of repeated protection–deprotection steps support reproducible results across extended synthetic routes.\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: 3736-77-4\u003c\/li\u003e\n\u003cli\u003eProduct code: C2208\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, relatively easy to handle and weigh\u003c\/li\u003e\n\u003cli\u003ePack sizes: please refer to the packaging options listed for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep the container tightly closed in a cool, dry place; follow 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 material in its original tightly closed container in a cool, dry, well-ventilated place away from moisture, direct sunlight, and incompatible chemicals, following the storage conditions stated on the manufacturer's label and safety data sheet. Suitable containers are the original amber or opaque chemical bottles with sealing caps; where material is transferred, use clean, dry glass vessels that can be closed securely and are clearly labelled. Handle the solid in a fume hood, wear a laboratory coat, safety glasses, and chemical-resistant gloves, and avoid generating or inhaling dust while weighing. Close the container promptly after use to limit moisture uptake, and dispose of residues and contaminated materials in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086111387866,"sku":"TCI2510C220816892","price":986000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086111420634,"sku":"TCI2510C220816893","price":2778000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2208.jpg?v=1769180378"},{"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":"tci2510c249917272","title":"TCI C2499 4291-63-8 Cladribine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCladribine is a chemical compound classified under the category of nucleosides and widely used in biochemical research. It is structurally similar to nucleotides, enabling it to participate in various biochemical reactions, including DNA and RNA synthesis. In laboratory settings, Cladribine serves as a key reagent for drug development, cancer research, and the study of drug mechanisms. Its role extends to understanding cellular processes and developing therapeutic strategies for various diseases. Due to its versatility, it is a valuable tool for researchers in multiple scientific disciplines.\u003c\/p\u003e\n\u003cp\u003eCladribine is preferred for its chemical stability under certain conditions and its solubility in organic solvents such as ethyl acetate. These properties make it easy to handle and integrate into a wide range of chemical and biochemical experiments. Its reactivity also allows for chemical modifications, enabling the synthesis of new compounds with specific functions. This adaptability makes Cladribine a reliable and efficient material for laboratory applications, especially in research requiring precise chemical manipulation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cladribine is commonly used by researchers in pharmacology, biochemistry, and medicine. It plays a crucial role in the development of therapies for autoimmune diseases and cancer research. Its application supports the understanding of disease mechanisms and the creation of innovative treatment approaches. As a result, Cladribine is an essential component in advancing scientific research and medical innovation in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDrug development for autoimmune disease treatment due to its ability to inhibit T-cell activity\u003c\/li\u003e\n\u003cli\u003eCancer research to understand tumor biology and develop targeted therapies\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to explore nucleotide synthesis and metabolic pathways\u003c\/li\u003e\n\u003cli\u003ePharmacological investigations to assess the effects of nucleoside analogs on cellular functions\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments involving DNA and RNA modification and 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: 4291-63-8\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\u003eCladribine should be stored in a cool, dry environment away from direct light to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its solubility in organic solvents, it should be handled in a well-ventilated area to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper labeling of containers is essential to ensure safe handling and prevent accidental misuse. Always follow standard laboratory safety protocols to ensure a secure working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48086129148122,"sku":"TCI2510C249917272","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2499.jpg?v=1769180397"},{"product_id":"tci2510c250017273","title":"TCI C2500 123318-82-1 Clofarabine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eClofarabine is a chemical compound classified under nucleosides, widely used in biochemical and pharmacological research. As an analog of adenine, it plays a crucial role in DNA and RNA synthesis experiments, as well as in studying the biological activity of anti-cancer agents. In the laboratory, it serves as a key reagent for evaluating drug efficacy and understanding the mechanisms of action of therapeutic compounds. Its application extends to cancer therapy research, where it helps in the development of targeted treatments and the assessment of cellular responses to chemotherapeutic agents.\u003c\/p\u003e\n\u003cp\u003eClofarabine is valued for its chemical stability and solubility in organic solvents such as DMSO and ethanol, making it highly versatile for various chemical and biochemical applications. Its specific molecular structure enables interactions with particular enzymes and proteins, which is essential for experiments requiring high precision. These properties ensure consistent performance and accuracy in laboratory settings, making it a reliable choice for researchers seeking reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Clofarabine is commonly used by researchers in academic institutions and research centers. It is integral to studies focused on drug development, cancer biology, and molecular mechanisms. Its role in both basic and applied research underscores its importance in advancing scientific understanding and innovation within the local scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical synthesis experiments due to its role as a nucleoside analog in DNA and RNA studies.\u003c\/li\u003e\n\u003cli\u003eAnti-cancer drug testing to evaluate biological activity against malignant cell lines.\u003c\/li\u003e\n\u003cli\u003eDrug mechanism research to understand how therapeutic agents interact with cellular components.\u003c\/li\u003e\n\u003cli\u003eCancer therapy development for the design of targeted treatments and therapeutic strategies.\u003c\/li\u003e\n\u003cli\u003eCellular response analysis to assess how cells react to chemotherapeutic agents in vitro.\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: 123318-82-1\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 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\u003eClofarabine should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. When handling, researchers should use appropriate personal protective equipment, such as gloves and safety goggles, to minimize contact with the compound. Due to its solubility in organic solvents, it is important to ensure proper ventilation in the laboratory workspace. The compound should be stored in a designated chemical storage area to prevent cross-contamination and ensure safe handling practices. Proper storage conditions are essential to preserve its integrity and effectiveness for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"20mg","offer_id":48086129180890,"sku":"TCI2510C250017273","price":3155000.0,"currency_code":"IDR","in_stock":true},{"title":"100mg","offer_id":48086129213658,"sku":"TCI2510C250017274","price":10019000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2500.jpg?v=1769180398"},{"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":"tci2510c268917533","title":"TCI C2689 73-03-0 Cordycepin from Cordyceps militaris","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCordycepin, a bioactive alkaloid derived from *Cordyceps militaris*, is a key compound widely used in life sciences research. This compound plays a crucial role in laboratories by serving as a reagent for biochemical and pharmacological studies. Its unique chemical structure and biological properties make it an essential tool for investigating the mechanisms of action of active compounds and the development of new therapeutic agents. Cordycepin is particularly valuable in research focused on immunomodulation, inflammation, and cancer treatment. Its presence in Indonesian laboratories supports advancements in health, pharmaceutical, and biotechnology research.\u003c\/p\u003e\n\u003cp\u003eCordycepin is favored for its high chemical stability and purity, which ensure reliable and reproducible experimental results. The compound’s resistance to degradation under certain conditions enhances its usability in repeated experiments and long-term storage. Its alkaloid nature also allows for a wide range of applications in both analytical and biological testing. The compound’s ability to modulate immune responses and exhibit anti-inflammatory and antitumor properties further solidifies its position as a preferred reagent in scientific research. These characteristics make Cordycepin a trusted choice for researchers seeking precision and consistency in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cordycepin is commonly used in studies related to health, pharmacology, and biotechnology. It supports research into chronic diseases and the development of new drugs. Its availability and reliability make it a valuable resource for scientists working on innovative projects. Cordycepin’s role in these contexts highlights its importance in advancing scientific knowledge and practical applications in the field of life sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCordycepin is used in pharmacological research to study its antitumor and anti-inflammatory properties, aiding in the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eIt is applied in biochemical assays to analyze the effects of alkaloids on cellular processes and signaling pathways.\u003c\/li\u003e\n\u003cli\u003eCordycepin supports immunological studies by modulating immune responses and investigating immune-related diseases.\u003c\/li\u003e\n\u003cli\u003eThe compound is utilized in analytical chemistry for its stability and purity, ensuring accurate and reproducible results in experimental settings.\u003c\/li\u003e\n\u003cli\u003eIt plays a role in biotechnology research, particularly in the exploration of natural compounds for drug discovery and health-related 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: 73-03-0\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Alkaloids\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: 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\u003eCordycepin 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 minimize exposure to moisture and air. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling Cordycepin to ensure safety. The compound should be stored away from incompatible substances to prevent chemical interactions. Regular inspection of storage conditions ensures that Cordycepin remains in optimal condition for experimental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mg","offer_id":48086191767770,"sku":"TCI2510C268917533","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2689.jpg?v=1767098656"},{"product_id":"tci2510c287817762","title":"TCI C2878 154361-50-9 Capecitabine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCapecitabine is a chemical compound widely utilized in biochemical and pharmacological research. As an analog of nucleosides, it plays a crucial role in the study of nucleotide metabolism and the activation of specific enzymes. In the laboratory, it serves as a key reagent for the synthesis of complex compounds, biological activity testing, and cancer therapy research. Its stability and controlled reactivity make it a reliable choice for experiments requiring precision and reproducibility.\u003c\/p\u003e\n\u003cp\u003eCapecitabine is valued for its high purity and consistent quality, ensuring accurate and dependable results in laboratory settings. Its simple yet specific chemical structure allows for easy identification and processing under various reaction conditions. Additionally, its solubility in organic solvents such as ethyl acetate and acetone facilitates separation and application in diverse analytical methods. These properties make it a preferred material for researchers seeking reliable and reproducible outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Capecitabine is commonly used in chemical, pharmaceutical, and biomedical research. It supports a wide range of studies, including drug development, enzyme activity investigations, and cancer-related research. Its availability and reliability make it an essential component for scientific inquiry in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: Capecitabine is ideal for studying nucleotide metabolism and enzyme activation due to its nucleoside analog properties.\u003c\/li\u003e\n\u003cli\u003eCancer Therapy Development: It is used in the synthesis of compounds and testing of biological activities relevant to anti-cancer drug development.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Analysis: Its solubility in organic solvents makes it suitable for analytical methods in drug formulation and quality control.\u003c\/li\u003e\n\u003cli\u003eEnzyme Kinetics Studies: The compound is useful for investigating enzyme interactions and catalytic mechanisms in biochemical processes.\u003c\/li\u003e\n\u003cli\u003eSynthetic Chemistry Applications: Capecitabine serves as a building block for the synthesis of more complex organic molecules in laboratory settings.\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: 154361-50-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003ePack sizes: 50g\u003c\/li\u003e\n\u003cli\u003ePhysical form: 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\u003eCapecitabine should be stored in a cool, dry place away from direct light to maintain its chemical stability and purity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is essential when working with this compound to minimize exposure. In laboratory settings, it should be stored separately from incompatible substances to ensure safety. Regular monitoring of storage conditions helps maintain the integrity of the material for reliable experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086201041114,"sku":"TCI2510C287817762","price":2778000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086201073882,"sku":"TCI2510C287817763","price":9616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2878.jpg?v=1768204709"},{"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":"tci2510c343818476","title":"TCI C3438 987-78-0 Cytidine 5'-Diphosphocholine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytidine 5'-Diphosphocholine (CDP-choline) is a chemical compound widely used in biochemical and neuroscience research. It serves as a key precursor in the synthesis of molecules involved in cellular metabolism, particularly in the formation of cell membranes and intercellular communication. In the laboratory, CDP-choline functions as a reagent for studying neuronal function, drug development, and lipid metabolism. Its molecular structure combines nucleotide and phosphate components, enabling it to participate in various biochemical pathways.\u003c\/p\u003e\n\u003cp\u003eCDP-choline is valued for its chemical stability and ability to engage in specific reactions with diverse substrates. Its high purity ensures reliable results in sensitive experiments, making it a preferred choice for researchers requiring precision. The compound’s molecular complexity allows it to be a versatile tool in both basic and applied research. Its consistent performance across different experimental conditions further enhances its reliability in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, CDP-choline is commonly used in health sciences, pharmaceutical development, and biotechnology research. It supports studies on neurodegenerative diseases, vaccine development, and the effects of drugs on the nervous system. Its availability facilitates advanced research in these fields, contributing to scientific innovation and medical advancements in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNeurodegenerative disease research benefits from CDP-choline’s role in studying membrane formation and neuronal communication, aiding in the development of therapeutic strategies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes CDP-choline to investigate lipid metabolism and its impact on drug efficacy and cellular function.\u003c\/li\u003e\n\u003cli\u003eVaccine development incorporates CDP-choline to explore its involvement in immune response mechanisms and cellular signaling pathways.\u003c\/li\u003e\n\u003cli\u003eBiotransformation studies rely on CDP-choline to analyze metabolic pathways and the breakdown of complex molecules in biological systems.\u003c\/li\u003e\n\u003cli\u003eToxicology research employs CDP-choline to assess its effects on cell membranes and neurotransmitter activity under various experimental 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: 987-78-0\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 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\u003eCDP-choline should be stored in a cool, dry place, away from light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent exposure to humidity and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage conditions should avoid extreme temperatures to prevent degradation. Proper labeling of containers is essential for safe handling and to ensure correct identification in a laboratory setting. Regular monitoring of storage conditions helps maintain the integrity of the compound for reliable experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086246949082,"sku":"TCI2510C343818476","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086246981850,"sku":"TCI2510C343818477","price":3332000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3438.jpg?v=1769144285"},{"product_id":"tci2510c344518486","title":"TCI C3445 33818-15-4 Cytidine 5'-Diphosphocholine Sodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytidine 5'-Diphosphocholine Sodium Salt (CDP-Choline) is a vital biochemical compound widely used in life science research, particularly in biochemistry and biomedicine. This reagent plays a crucial role in the synthesis of biomolecules, including nucleotides and components of DNA and RNA. As a key building block in molecular research, it is essential for experiments involving nucleotide modification and metabolic pathway studies. Its presence in laboratory workflows supports the development of new therapeutic agents and the understanding of cellular processes.\u003c\/p\u003e\n\u003cp\u003eCDP-Choline is valued for its chemical stability and solubility in organic solvents such as acetone and ethyl acetate, making it versatile for a wide range of chemical reactions. The sodium ion in its structure enhances its reactivity and allows for precise control in various experimental conditions. These properties make it a reliable and consistent choice for researchers requiring accuracy in complex synthesis processes. Its compatibility with different reaction environments further contributes to its popularity in advanced biochemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, CDP-Choline is commonly used in applied research across disciplines such as neurobiology, pharmacology, and biotechnology. Its role in studying cellular metabolism and developing new drug formulations makes it an indispensable tool for scientists working on innovative projects. The compound's reliability and effectiveness support high-quality research outcomes in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNeurobiology research utilizes CDP-Choline to study the role of phosphocholine in neuronal function and membrane dynamics.\u003c\/li\u003e\n\u003cli\u003ePharmacological studies benefit from CDP-Choline as it aids in the synthesis of choline derivatives used in drug development.\u003c\/li\u003e\n\u003cli\u003eBiotechnological applications rely on CDP-Choline for the production of nucleotide-based compounds in genetic engineering projects.\u003c\/li\u003e\n\u003cli\u003eMetabolic pathway investigations use CDP-Choline to explore the biochemical mechanisms of nucleotide synthesis and degradation.\u003c\/li\u003e\n\u003cli\u003eCellular signaling research incorporates CDP-Choline to analyze the impact of phosphocholine on signal transduction processes.\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: 33818-15-4\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 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCDP-Choline 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 exposure to moisture and contaminants. Due to its solubility in organic solvents, proper labeling of containers is essential to prevent cross-contamination. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Regular monitoring of storage conditions ensures the integrity of the reagent for use in research applications. Proper storage practices help maintain the quality and effectiveness of CDP-Choline in laboratory experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086247801050,"sku":"TCI2510C344518486","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086247833818,"sku":"TCI2510C344518487","price":4266000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3445.jpg?v=1769144285"},{"product_id":"tci2510c360118697","title":"TCI C3601 163042-96-4 Chloro-IB-MECA","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eChloro-IB-MECA (1-(2-Chloro-4-iodophenyl)-3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)urea) is a chemical compound widely used in life science research. It serves as a key reagent in biochemical and pharmaceutical studies, playing a crucial role in the synthesis of bioactive compounds. This compound is commonly found in laboratories where researchers are working on the development of new drugs and the study of biological activities. Its presence in such environments highlights its importance in advancing scientific understanding and innovation.\u003c\/p\u003e\n\u003cp\u003eThe compound's complex chemical structure contributes to its high reactivity, making it a preferred choice for various laboratory applications. Its ability to participate in chemical reactions under different conditions allows for precise control over synthetic processes. Additionally, its stability under certain conditions ensures consistent results, which is essential in scientific research. These properties make Chloro-IB-MECA a reliable and versatile material for researchers aiming for accuracy and reproducibility in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Chloro-IB-MECA is frequently used in pharmacological and biochemical research. It is particularly valuable in the study of synthetic compounds and their biological activities. Researchers in Indonesia rely on this compound for its reliability and effectiveness in experimental settings, contributing to advancements in drug development and biological studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Chloro-IB-MECA to investigate the biological activity of synthetic compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies employ this compound as a reagent in the synthesis of bioactive molecules, enabling the exploration of molecular mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects benefit from Chloro-IB-MECA's reactivity, allowing for the creation of compounds with targeted biological effects.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications use the compound to test the efficacy and stability of synthesized materials under various experimental conditions.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments incorporate Chloro-IB-MECA to study interactions between chemical structures and biological systems, enhancing understanding of molecular 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: 163042-96-4\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, as per standard chemical product description\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\u003eChloro-IB-MECA should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to minimize exposure to air and moisture. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental contamination. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Regular inspection of storage conditions is advised to ensure compliance with safety standards. The compound should not be stored near incompatible materials to avoid potential chemical reactions. Maintaining a controlled environment is crucial for preserving the integrity of the material during long-term storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mg","offer_id":48086269264090,"sku":"TCI2510C360118697","price":2903000.0,"currency_code":"IDR","in_stock":true},{"title":"50mg","offer_id":48086269296858,"sku":"TCI2510C360118698","price":10071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3601.jpg?v=1769180457"},{"product_id":"tci2510c377318864","title":"TCI C3773 892-48-8 5'-Chloro-5'-deoxyadenosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5'-Chloro-5'-deoxyadenosine is a chemical compound widely used in biochemical and molecular biology research. As an analog of adenine, one of the fundamental components of DNA and RNA, it plays a crucial role in laboratory settings where the synthesis of bioactive compounds is required. This compound is frequently utilized as a building block for the development of molecules with specific biological activities. Its structural similarity to adenine allows it to interact with key enzymes such as DNA polymerase, making it an essential tool in the study of biochemical reaction mechanisms.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make 5'-Chloro-5'-deoxyadenosine a preferred choice is its ability to bind specifically to DNA. This characteristic makes it highly relevant in molecular interaction studies. Additionally, its chemical stability under laboratory conditions ensures reliable performance and ease of storage. The compound’s specificity in reactivity also makes it suitable for experiments requiring high target molecule interaction. These features contribute to its widespread use in various research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 5'-Chloro-5'-deoxyadenosine is commonly employed in biomedical, pharmacological, and molecular biology research. It supports studies on DNA interactions, enzyme activity, and the development of new therapeutic agents. Its reliability and chemical properties make it a valuable resource for researchers aiming to explore molecular mechanisms and develop innovative solutions in the life sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolecular biology research benefits from this compound due to its ability to interact with DNA polymerase and other enzymatic systems, aiding in the study of DNA replication and repair mechanisms.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies utilize this compound to investigate the structural and functional roles of nucleosides in biological systems, particularly in the context of nucleic acid synthesis.\u003c\/li\u003e\n\u003cli\u003ePharmacological research employs this compound as a model for developing new drugs targeting DNA-related pathways, offering insights into potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eGenetic engineering applications leverage its structural similarity to adenine to design modified nucleic acids for use in gene editing and expression studies.\u003c\/li\u003e\n\u003cli\u003eBiomedical research incorporates this compound in the development of targeted therapies, particularly in the study of DNA-targeting agents for cancer and genetic 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: 892-48-8\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 suitable for laboratory use\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\u003eThis compound should be stored in a cool, dry environment, away from direct light to maintain its chemical stability. It is recommended to use airtight containers 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 and ensure proper ventilation in the workspace. Regular monitoring of storage conditions is advised to maintain the integrity of the compound for extended use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086287122650,"sku":"TCI2510C377318864","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086287155418,"sku":"TCI2510C377318865","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3773.jpg?v=1768817147"},{"product_id":"tci2510c383818938","title":"TCI C3838 69-74-9 Cytarabine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCytarabine Hydrochloride TCI C3838 is a chemical compound widely utilized in laboratory settings, particularly in biochemical and pharmacological research. It plays a crucial role in the development and testing of antitumor drugs, especially in the treatment of leukemia. Its chemical properties make it an essential reagent for studying the mechanisms of drug action and evaluating therapeutic efficacy. This compound is commonly used in both academic and industrial research to advance understanding of cancer treatments and improve pharmaceutical formulations.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make Cytarabine Hydrochloride a preferred choice is its stability under controlled conditions. It is a solid substance that dissolves easily in water, making it convenient for various experimental applications. However, it is sensitive to moisture and light, which requires careful handling and storage. These properties ensure its reliability in laboratory experiments while also highlighting the need for proper preservation to maintain its effectiveness.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cytarabine Hydrochloride is extensively used in scientific research and pharmaceutical product development. It is a common component in studies related to cancer treatment and the testing of new compounds. Many research institutions and universities rely on this compound for experiments that aim to improve therapeutic outcomes and develop innovative medical solutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntitumor Drug Efficacy Testing: Cytarabine Hydrochloride is ideal for assessing the effectiveness of chemotherapy agents in cancer research.\u003c\/li\u003e\n\u003cli\u003eCancer Treatment Research: Its antitumor activity makes it a key reagent in experiments focused on leukemia and other malignancies.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Formulation Development: It is used to create solutions for testing the bioavailability and stability of new drug compounds.\u003c\/li\u003e\n\u003cli\u003eMechanism of Action Studies: Its chemical properties allow researchers to investigate how it interacts with cellular processes in targeted therapies.\u003c\/li\u003e\n\u003cli\u003eDrug Screening Protocols: It supports high-throughput screening methods to identify potential therapeutic agents for various diseases.\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: 69-74-9\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\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: Requires protection from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCytarabine Hydrochloride 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 quality. Due to its sensitivity, it should be kept in a controlled environment to maintain its chemical integrity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Proper storage conditions are essential to ensure its effectiveness in experimental applications and to comply with safety standards in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086294593754,"sku":"TCI2510C383818938","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086294626522,"sku":"TCI2510C383818939","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3838.jpg?v=1767100156"},{"product_id":"tci2510c384518949","title":"TCI C3845 163252-36-6 Clevudine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eClevudine, with CAS number 163252-36-6, is a chemical compound widely used in life science research and pharmacological studies. It plays a crucial role in laboratories focused on biochemical and pharmaceutical applications, particularly in the development of antiviral agents. This compound is essential for investigating the mechanisms of viral infections and exploring potential therapeutic interventions. Its presence in research settings highlights its importance in advancing scientific understanding of disease and treatment options.\u003c\/p\u003e\n\u003cp\u003eClevudine is valued for its chemical stability under controlled conditions, which makes it suitable for various biochemical reactions and analytical processes. Its complex molecular structure allows researchers to study molecular interactions and biological effects with precision. Additionally, its potential as an anti-HIV agent makes it a key component in the development of new therapeutic strategies. These properties make it a preferred choice for scientists seeking reliable and versatile research materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Clevudine is commonly used in pharmacological, virological, and biochemical research. It supports efforts to develop new drugs and understand disease mechanisms. Its role in biological activity testing and synthesis of new compounds underscores its significance in scientific research. As a fundamental reagent, it contributes to the advancement of medical and scientific knowledge in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmacological research utilizes Clevudine to study its potential as an anti-HIV agent and its effects on viral replication.\u003c\/li\u003e\n\u003cli\u003eVirological studies benefit from Clevudine's role in analyzing viral mechanisms and developing targeted therapies.\u003c\/li\u003e\n\u003cli\u003eBiochemical experiments rely on Clevudine for its stability and ability to participate in complex molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDrug development projects use Clevudine to test the efficacy and safety of new antiviral compounds.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications leverage Clevudine for its utility in biological activity assays and molecular structure 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: 163252-36-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\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 light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eClevudine 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 moisture absorption and maintain chemical integrity. 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 minimize exposure. Storage conditions should be consistent to preserve its stability and effectiveness for research purposes. Regular monitoring of storage conditions ensures the material remains suitable for use in scientific experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086294986970,"sku":"TCI2510C384518949","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3845.jpg?v=1767100177"},{"product_id":"tci2510d004619344","title":"TCI D0046 16373-93-6 2'-Deoxyadenosine Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2'-Deoxyadenosine Monohydrate is a chemical compound classified under the category of nucleosides, commonly used in biochemical and molecular laboratory experiments. It plays a vital role in DNA and RNA research, serving as a foundational building block for nucleotide synthesis. This compound is essential for various experimental procedures, including the production of nucleotides and oligonucleotides, which are critical in genetic studies and molecular biology. Its chemical structure closely resembles adenine, one of the primary components of nucleotides, making it a valuable reagent for researchers working on DNA-related applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its high purity and solubility in organic solvents, which ensures consistent and reliable results in laboratory settings. Its chemical stability allows it to be used across a range of experimental conditions, making it a versatile reagent. The ability to dissolve in common organic solvents simplifies its handling and integration into various biochemical protocols. Additionally, its purity level supports precise and reproducible outcomes, which are crucial for advanced research techniques such as PCR, hybridization, and genetic analysis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2'-Deoxyadenosine Monohydrate is widely utilized in biomedical, pharmacological, and biotechnological research. It is frequently found in labs focused on drug development, genetic analysis, and the study of genetic disorders. Its availability and reliability make it a preferred choice for researchers aiming to achieve accurate and high-quality experimental results.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA synthesis and oligonucleotide production due to its structural similarity to adenine and role in nucleotide formation.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments such as PCR and hybridization where high purity and solubility are essential for accurate results.\u003c\/li\u003e\n\u003cli\u003eGenetic research and analysis for studying DNA structure and function in various biological systems.\u003c\/li\u003e\n\u003cli\u003eBiomedical and pharmaceutical studies for drug development and understanding genetic disorders.\u003c\/li\u003e\n\u003cli\u003eBiotecnological applications in the creation of genetic engineering tools and molecular diagnostic techniques.\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: 16373-93-6\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 sizes as per standard laboratory requirements\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\u003e2'-Deoxyadenosine Monohydrate should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to air and humidity. When handling, ensure that the substance is used in a well-ventilated area to minimize inhalation risks. Avoid contact with skin and eyes, and use appropriate personal protective equipment such as gloves and safety goggles. The compound is non-hazardous under normal conditions but should be treated with care to maintain its integrity and effectiveness in experimental applications. Always follow standard laboratory safety protocols to ensure safe handling and storage practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086336045274,"sku":"TCI2510D004619344","price":2702000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086336078042,"sku":"TCI2510D004619345","price":9161000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0046.jpg?v=1768817197"},{"product_id":"tci2510d004819347","title":"TCI D0048 3992-42-5 2'-Deoxycytidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2'-Deoxycytidine Hydrochloride is a chemical compound widely used in biochemical and molecular biology experiments. It belongs to the class of nucleosides and plays a crucial role in DNA and RNA studies. This compound is essential for various laboratory applications, including the synthesis of oligonucleotides and enzymatic reactions related to nucleotide metabolism. Its importance lies in its ability to serve as a building block for genetic research and biomedicine. Due to its stability and controlled reactivity, it is a reliable choice for researchers working in diverse scientific fields.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high purity and consistent quality, making it a preferred material for laboratory use. It is water-soluble and exhibits good stability under specific conditions, which ensures reliable results in experiments. Its chemical structure, featuring a hydroxyl group attached to the 2' position of the purine ring, contributes to its functional versatility. These properties make it suitable for precise and reproducible research, especially in high-precision laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2'-Deoxycytidine Hydrochloride is extensively used in DNA and RNA-related research. It supports studies on transcription, replication, and genetic modifications. Its availability and reliability make it a popular choice among researchers working on molecular biology and biotechnology projects. The compound is integral to many experimental protocols, ensuring accurate and consistent outcomes in scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA sequencing and synthesis applications benefit from its role as a nucleoside building block, enabling accurate oligonucleotide construction.\u003c\/li\u003e\n\u003cli\u003eEnzymatic reactions involving nucleotide metabolism utilize its stability and reactivity for controlled biochemical processes.\u003c\/li\u003e\n\u003cli\u003eMolecular biology research relies on its use in DNA and RNA studies, supporting genetic and biotechnological investigations.\u003c\/li\u003e\n\u003cli\u003eGenetic modification experiments leverage its structural properties for precise nucleotide incorporation and manipulation.\u003c\/li\u003e\n\u003cli\u003eBiomedical research applications require its consistent quality for reliable results in nucleotide-related studies.\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: 3992-42-5\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 various quantities as per standard laboratory requirements\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 moisture and 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 place, away from moisture and direct light to maintain its stability and integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its water solubility, it should be handled in a well-ventilated area to avoid inhalation of fine particles. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. It is important to ensure that the storage area is secure and inaccessible to unauthorized personnel. Regular monitoring of storage conditions is advised to ensure optimal preservation of the compound's quality and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086336176346,"sku":"TCI2510D004819347","price":3079000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086336209114,"sku":"TCI2510D004819348","price":10727000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0048.jpg?v=1769180475"},{"product_id":"tci2510d005219356","title":"TCI D0052 961-07-9 2'-Deoxyguanosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2'-Deoxyguanosine is a chemical compound classified under nucleosides, widely used in biochemical and biomedical experiments. It plays a crucial role in DNA and RNA synthesis, serving as a fundamental building block for nucleic acids. Its presence is essential in enzymatic reactions involving DNA polymerases, making it a key component in molecular biology research. In the laboratory, it is used to study DNA replication mechanisms, enzymatic activity, and the development of therapeutic agents related to cellular processes.\u003c\/p\u003e\n\u003cp\u003eThe stability of 2'-Deoxyguanosine and its ability to bind with other nucleotides make it a preferred choice for high-precision experiments. Its non-toxic nature in appropriate dosages ensures a safe working environment for researchers. Additionally, its availability in various packaging options allows for easy customization to meet the needs of different experimental setups. This versatility enhances its utility across a wide range of scientific applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2'-Deoxyguanosine is commonly used in genetic research, biotechnology, and pharmacology. It is particularly relevant for vaccine development, genetic analysis, and the study of genetic disorders. Its application supports both basic and applied research, contributing to advancements in life sciences and medical science.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDNA replication studies benefit from 2'-Deoxyguanosine as it is a core component in DNA synthesis and enzymatic reactions.\u003c\/li\u003e\n\u003cli\u003eEnzymatic activity assays use this compound to evaluate DNA polymerase performance in biochemical processes.\u003c\/li\u003e\n\u003cli\u003eGenetic research relies on 2'-Deoxyguanosine for constructing DNA sequences and analyzing genetic material.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development incorporates this nucleoside in the design of therapeutic agents targeting cellular mechanisms.\u003c\/li\u003e\n\u003cli\u003eMolecular biology experiments utilize 2'-Deoxyguanosine for nucleic acid synthesis and structural 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: 961-07-9\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 to suit different research needs\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\u003e2'-Deoxyguanosine should be stored in a cool, dry environment away from direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its non-toxic nature, it is generally safe to handle, but standard laboratory precautions should still be followed, such as wearing gloves and safety goggles. The compound should be kept in a well-ventilated area to ensure safe handling. Proper labeling of containers is essential to avoid cross-contamination and ensure safe usage in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086336962778,"sku":"TCI2510D005219356","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086336995546,"sku":"TCI2510D005219357","price":2650000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086337028314,"sku":"TCI2510D005219358","price":9642000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0052.jpg?v=1768817198"},{"product_id":"tci2510d006019362","title":"TCI D0060 951-78-0 2'-Deoxyuridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2'-Deoxyuridine is a chemical compound classified under nucleosides, widely used in biochemical and molecular biology experiments. It serves as an analog of nucleotides and plays a crucial role in DNA and RNA synthesis. In the laboratory, it is commonly utilized as a building block for the synthesis of oligonucleotides and as a substrate in enzymatic reactions involving DNA polymerase. Its chemical structure is highly specific, making it ideal for applications requiring precision and consistency.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its high purity and stability under controlled conditions, which ensures reliable results in experimental settings. Its non-toxic nature at low concentrations makes it a safe choice for use in various laboratory applications. These properties contribute to its popularity among researchers working in molecular biology and biochemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2'-Deoxyuridine is particularly relevant in genetic research, biotechnology, and pharmacology. It is frequently used in experiments related to DNA modification, vaccine development, and the study of disease mechanisms. Its versatility and reliability make it an essential component in many research projects conducted by academic institutions and research centers.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzymatic Reaction Studies - 2'-Deoxyuridine is ideal for testing DNA polymerase activity due to its role as a substrate in enzymatic processes.\u003c\/li\u003e\n\u003cli\u003eOligonucleotide Synthesis - Its chemical structure allows it to be used as a building block in the creation of synthetic oligonucleotides for various molecular biology applications.\u003c\/li\u003e\n\u003cli\u003eGenetic Modification Research - It supports experiments involving DNA modification, helping scientists understand genetic mechanisms and mutations.\u003c\/li\u003e\n\u003cli\u003eVaccine Development - It is used in studies aimed at developing vaccines by analyzing DNA-based immunological responses.\u003c\/li\u003e\n\u003cli\u003eDisease Mechanism Studies - Researchers use it to investigate the molecular basis of diseases, aiding in the discovery of potential therapeutic targets.\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: 951-78-0\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 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\u003e2'-Deoxyuridine should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the compound in a sealed container to prevent moisture absorption and contamination. When handling, it is important to use appropriate personal protective equipment such as gloves and safety goggles to ensure laboratory safety. The compound is non-toxic in small quantities, but standard laboratory safety protocols should still be followed. Proper storage and handling help maintain its chemical integrity and ensure consistent performance in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086337585370,"sku":"TCI2510D006019362","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086337618138,"sku":"TCI2510D006019363","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086337650906,"sku":"TCI2510D006019364","price":7698000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0060.jpg?v=1768817198"},{"product_id":"tci2510d091920578","title":"TCI D0919 53-84-9 beta-Nicotinamide Adenine Dinucleotide oxidized form [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBeta-Nicotinamide Adenine Dinucleotide (NAD+) is a critical molecule in biochemical reactions that play a fundamental role in cellular metabolism. As an oxidized form of NAD, it serves as a coenzyme in redox reactions, facilitating energy transfer processes in key metabolic pathways such as glycolysis and the citric acid cycle. This compound is essential for maintaining cellular function and is widely used in biochemical research to study enzyme activity and reaction mechanisms under controlled laboratory conditions. Its presence in oxidized form allows researchers to observe and analyze biochemical transformations with high precision.\u003c\/p\u003e\n\u003cp\u003eNAD+ is chemically stable under specific conditions, making it a reliable reagent for laboratory use. Its ability to bind with enzymes makes it an active participant in biochemical reactions, enabling the study of enzyme kinetics and substrate interactions. The compound is also sensitive to moisture and light, which necessitates careful handling and storage to preserve its integrity. These properties make NAD+ a preferred choice for researchers seeking accurate and reproducible results in biochemical experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NAD+ is commonly used in biochemical and pharmacological studies to investigate enzyme mechanisms and their impact on cellular metabolism. Its role in energy transfer and redox reactions makes it an essential component for research focused on metabolic pathways and enzyme function. Researchers in Indonesia rely on NAD+ to conduct experiments that contribute to advancements in biotechnology and life sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research – NAD+ is used to study redox reactions and enzyme activity in metabolic pathways, providing insights into cellular energy transfer mechanisms.\u003c\/li\u003e\n\u003cli\u003eEnzyme Kinetics Studies – The compound serves as a substrate or coenzyme in experiments that measure enzyme efficiency and reaction rates under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis – NAD+ is essential in analyzing glycolysis and the citric acid cycle, helping researchers understand cellular energy production.\u003c\/li\u003e\n\u003cli\u003eDrug Development – It is used in pharmacological studies to assess the impact of compounds on enzyme activity and metabolic processes.\u003c\/li\u003e\n\u003cli\u003eCellular Stress Studies – NAD+ plays a role in understanding how cells respond to oxidative stress and metabolic imbalances in experimental models.\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 – 53-84-9\u003c\/li\u003e\n\u003cli\u003eCategory – Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack Sizes – As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form – Powder\u003c\/li\u003e\n\u003cli\u003eStorage Note – Store in a cool, dark place, away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eNAD+ should be stored in a cool, dark environment to prevent degradation due to light exposure. It is recommended to keep the compound in airtight containers to minimize moisture contact, which can affect its stability. Laboratory personnel should handle NAD+ with care, using appropriate personal protective equipment to avoid direct contact. The compound is sensitive to environmental conditions, so maintaining consistent storage conditions is crucial for preserving its chemical integrity. Proper labeling of containers and adherence to standard safety protocols are essential to ensure safe handling and usage in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086413213914,"sku":"TCI2510D091920578","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086413246682,"sku":"TCI2510D091920579","price":5755000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510d092020580","title":"TCI D0920 606-68-8 beta-Nicotinamide Adenine Dinucleotide Disodium Salt, reduced form [for Biochemical Research]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBeta-Nicotinamide Adenine Dinucleotide Disodium Salt (NADH) is a critical biochemical compound widely used in laboratory research. As a reduced form of NAD, it plays a vital role in enzymatic reactions, particularly in redox processes essential for cellular metabolism. NADH functions as a coenzyme and substrate in various biochemical pathways, supporting the activity of enzymes such as alcohol dehydrogenase and lactate dehydrogenase. Its presence is crucial for energy metabolism and metabolic regulation in biological systems. This compound is indispensable for researchers studying metabolic processes and enzymatic mechanisms.\u003c\/p\u003e\n\u003cp\u003eNADH is valued for its chemical stability under controlled conditions and its high solubility in water, which facilitates its use in a wide range of biochemical applications. The disodium salt form enhances its bioavailability, making it easier to incorporate into experimental setups. Its sensitivity to oxidation and light necessitates careful handling and storage to preserve its functional integrity. These properties make NADH a preferred choice for laboratories requiring reliable and consistent performance in biochemical assays.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NADH is extensively used in biomedical, pharmacological, and biotechnological research. It supports studies on cellular metabolism, enzyme activity, and biochemical reaction mechanisms. Researchers in universities and research institutions rely on NADH for experiments that require precise control over redox reactions and metabolic pathways. Its versatility and reliability make it a fundamental component in many experimental protocols.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical Research: NADH is essential for studying redox reactions and metabolic pathways, providing a stable and reliable substrate for enzyme assays.\u003c\/li\u003e\n\u003cli\u003eEnzyme Activity Studies: It serves as a coenzyme in experiments involving alcohol dehydrogenase and lactate dehydrogenase, enabling accurate measurement of enzymatic activity.\u003c\/li\u003e\n\u003cli\u003eMetabolic Pathway Analysis: NADH supports investigations into cellular energy metabolism and the role of NAD in metabolic regulation.\u003c\/li\u003e\n\u003cli\u003eBiomedical Research: It is used in studies related to cellular respiration, oxidative stress, and the effects of metabolic disorders on biological systems.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: NADH aids in evaluating drug interactions and the impact of compounds on metabolic processes and enzyme function.\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: 606-68-8\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Enzymes, Enzyme Inhibitors, Enzyme Substrates\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Sodium salt of NADH, typically in powder form\u003c\/li\u003e\n\u003cli\u003eStorage note: Should be stored in a cool, dark place to prevent oxidation and maintain stability\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eNADH should be stored in a cool, dark environment to prevent oxidation and maintain its chemical integrity. It is recommended to keep the compound in airtight containers to minimize exposure to moisture and light. Due to its sensitivity, it is advisable to use it promptly after preparation to ensure optimal performance in experiments. Proper labeling and storage conditions are essential to prevent degradation and contamination. Laboratories should handle NADH with care, using appropriate safety measures when handling and preparing solutions. Maintaining a controlled storage environment ensures the reliability and consistency of experimental results.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086413279450,"sku":"TCI2510D092020580","price":633000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086413312218,"sku":"TCI2510D092020581","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086413344986,"sku":"TCI2510D092020582","price":10071000.0,"currency_code":"IDR","in_stock":true}]},{"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":"tci2510d223522348","title":"TCI D2235 50-91-9 2'-Deoxy-5-fluorouridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2'-Deoxy-5-fluorouridine is a chemical compound widely used in pharmaceutical research and drug development. It serves as a key reagent in the synthesis of antiviral and antitumor drugs, playing a crucial role in laboratory experiments aimed at understanding molecular interactions and therapeutic mechanisms. This compound is essential for researchers exploring new drug delivery systems and optimizing the efficacy of targeted therapies. Its chemical structure closely resembles nucleotides, enabling it to participate in complex biochemical reactions that are vital for drug design and formulation.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its high purity and consistent quality, making it a reliable choice for scientific research. It exhibits stability under controlled conditions, which ensures accurate and reproducible results in experimental settings. Its chemical versatility allows it to be used in a variety of applications, from basic research to advanced drug development projects. The compound’s ability to interact with specific cellular targets enhances its utility in studying biological effects and drug mechanisms.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2'-Deoxy-5-fluorouridine is commonly used in pharmacological studies, drug discovery, and biological effect investigations. It is a preferred material for academic and research institutions aiming to advance their understanding of molecular interactions and therapeutic applications. Many universities and research centers in Indonesia rely on this compound to support their scientific endeavors and contribute to the development of new pharmaceutical solutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical Development: Used for synthesizing antiviral and antitumor compounds due to its nucleotide-like structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eDrug Delivery Systems Research: Ideal for studying targeted drug release mechanisms and optimizing delivery efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: Applied in experiments to investigate drug interactions and biological effects on target cells.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: Utilized in experiments involving nucleotide-based reactions and genetic material analysis.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Employed in studies to explore enzyme activity and metabolic pathways in cellular environments.\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: 50-91-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Pharmaceutical Development and Drug Discovery Research Reagents \u0026gt; Drug Delivery Systems (DDS)\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 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 to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air, which can affect its chemical integrity. Due to its potential reactivity, it should be handled in a well-ventilated laboratory setting, with appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances and ensure proper disposal procedures are followed to maintain a safe laboratory environment. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086505980122,"sku":"TCI2510D223522348","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48086506012890,"sku":"TCI2510D223522349","price":4316000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086506045658,"sku":"TCI2510D223522350","price":7648000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2235.jpg?v=1768204919"},{"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":"tci2510d306523383","title":"TCI D3065 4097-22-7 2',3'-Dideoxyadenosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2',3'-Dideoxyadenosine is a chemical compound widely used in biochemical and pharmacological experiments conducted in laboratories. It serves as a key reagent in various research applications, particularly in enzyme kinetics and molecular biology studies. This compound is essential for investigating enzyme mechanisms, especially those involving reverse transcriptase, which plays a critical role in viral replication. Its unique molecular structure makes it an important tool for understanding biological processes at the molecular level.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure closely resembles adenine, but with the absence of two oxygen atoms at the 2' and 3' positions. This structural difference allows it to act as a specific inhibitor or substrate in enzymatic reactions, making it highly selective in its interactions. Its specificity is crucial for studies requiring precise control over biochemical pathways. Additionally, its role in antibacterial and pharmacological research highlights its versatility in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2',3'-Dideoxyadenosine is a valuable resource for researchers working on infectious diseases, drug development, and biochemical studies. Its application in diagnostic and therapeutic research underscores its importance in advancing scientific understanding and innovation. Scientists rely on this compound to explore biological mechanisms and develop new methodologies for medical and scientific applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMonitoring enzyme activity in reverse transcriptase assays due to its specific binding properties.\u003c\/li\u003e\n\u003cli\u003eStudying the mechanism of action of antiretroviral drugs in virology research.\u003c\/li\u003e\n\u003cli\u003eInvestigating the effects of nucleoside analogs on DNA synthesis in molecular biology experiments.\u003c\/li\u003e\n\u003cli\u003eSupporting research on the development of new therapeutic agents for infectious diseases.\u003c\/li\u003e\n\u003cli\u003eEnhancing the accuracy of biochemical assays requiring precise substrate inhibition studies.\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: 4097-22-7\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\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\u003e2',3'-Dideoxyadenosine should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. 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 direct sunlight or high humidity conditions. Proper labeling of containers is essential for safe handling and to prevent accidental misuse. Always follow standard laboratory safety protocols when working with this compound to ensure a secure and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086600745178,"sku":"TCI2510D306523383","price":11887000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3065.jpg?v=1767105692"},{"product_id":"tci2510d306623384","title":"TCI D3066 69655-05-6 2',3'-Dideoxyinosine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2',3'-Dideoxyinosine is a chemical compound widely used in biochemical and pharmacological research. It is a nucleoside analog with a modified deoxyribose sugar structure at the 2' and 3' positions, making it structurally similar to nucleotides but with distinct functional properties. In the laboratory, it plays a crucial role in the synthesis of various compounds and in the study of drug mechanisms and antiviral therapies. Its unique molecular structure allows it to interact with specific enzymes, making it a valuable tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits chemical stability under controlled conditions but is highly sensitive to moisture and light exposure. This sensitivity necessitates careful handling and storage to maintain its integrity. Its high affinity for enzymes such as reverse transcriptase makes it particularly useful in HIV-related research. This specificity is essential for applications requiring precise molecular interactions and reaction outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2',3'-Dideoxyinosine is commonly used in research related to infectious diseases, especially in the study of viruses and immune response mechanisms. It is also frequently found in studies aimed at understanding the molecular basis of pathogenesis and developing new therapeutic strategies. Its versatility and relevance in biomedical research make it a sought-after reagent in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAntiviral Research: This compound is ideal for studying HIV and other viral infections due to its interaction with reverse transcriptase, aiding in the development of antiviral therapies.\u003c\/li\u003e\n\u003cli\u003eDrug Mechanism Studies: Its structural similarity to nucleotides allows it to be used in investigating how drugs interact with cellular processes and enzyme activity.\u003c\/li\u003e\n\u003cli\u003eBiochemical Synthesis: It serves as a key reagent in the synthesis of other nucleoside analogs and related compounds for pharmaceutical and biotechnological applications.\u003c\/li\u003e\n\u003cli\u003eImmunological Studies: It is used in research on immune responses to viral infections, helping to understand how the body combats pathogens.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Research: Its unique properties make it a valuable tool in molecular biology experiments, particularly those involving nucleic acid interactions and enzyme kinetics.\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: 69655-05-6\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Antibiotics\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\u003eThis compound 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 contaminants. Due to its sensitivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. In laboratory settings, it should be stored in a designated chemical storage area that is well-ventilated and accessible only to authorized personnel. Regular monitoring of storage conditions is essential to ensure the compound remains stable and suitable for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086600810714,"sku":"TCI2510D306623384","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48086600843482,"sku":"TCI2510D306623385","price":3131000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3066.jpg?v=1767105696"},{"product_id":"tci2510d354523844","title":"TCI D3545 9007-49-2 Deoxyribonucleic Acid Sodium Salt from Salmon Milt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDeoxyribonucleic Acid Sodium Salt from Salmon Milt is a naturally derived, high-molecular-weight DNA isolated from salmon milt (the seminal fluid of salmon) and supplied as its sodium salt, a form that dissolves readily in water and remains stable during storage as a dry solid. In life science and materials science laboratories, this material serves as a bulk source of genomic DNA for work that does not require any specific nucleotide sequence. Researchers use it as a substrate for nuclease enzyme assays, as carrier or blocking DNA in hybridization experiments, as a test substrate for studying drug–DNA interactions, and as a biopolymer for fabricating DNA-based films, gels, and composite materials.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this product a preferred choice is its availability as long, naturally occurring double-stranded DNA at a handling cost far lighter than that of synthetic oligonucleotides. Salmon milt is an exceptionally rich natural source of DNA, and the sodium salt form dissolves into a viscous solution that is straightforward to handle in aqueous buffers. The phosphate backbone of DNA carries a strong negative charge, so the material can be paired with cationic surfactants, metal ions, or positively charged polymers to form functional complexes. Its double-helical structure also provides binding sites that make it useful wherever a genuine nucleic acid scaffold is needed rather than a synthetic mimic.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research settings where biochemistry, molecular biology, and materials chemistry groups need a dependable, non-sequence-specific DNA supply. It fits routine enzyme characterisation work, method development for hybridization protocols, and exploratory studies on DNA-binding compounds. Because it is supplied as a stable solid rather than a frozen solution, it suits facilities that prepare working solutions in-house as needed and store the bulk material long-term.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNuclease enzyme assays — the material provides abundant natural double-stranded DNA as a cleavage substrate, allowing activity measurement without the expense of preparing sequence-defined synthetic templates.\u003c\/li\u003e\n\u003cli\u003eHybridization blocking and carrier DNA — its non-specific, high-molecular-weight character lets it saturate non-target binding sites or carry trace nucleic acids through precipitation steps without interfering with the sequence of interest.\u003c\/li\u003e\n\u003cli\u003eDrug–DNA interaction studies — the intact double helix offers authentic intercalation and groove-binding sites, making it a realistic test substrate for screening how candidate compounds associate with nucleic acids.\u003c\/li\u003e\n\u003cli\u003eDNA-based films and gels — as a long-chain biopolymer it can be cast or crosslinked into self-supporting films and hydrogels, giving materials researchers a renewable natural polymer with defined charge behaviour.\u003c\/li\u003e\n\u003cli\u003ePolyelectrolyte complex formation — the strongly anionic phosphate backbone pairs readily with cationic surfactants, metal ions, or polycations, supporting the preparation of functional composite and optical 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: 9007-49-2\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eProduct Code: TCI D3545\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid, supplied as the sodium salt\u003c\/li\u003e\n\u003cli\u003eStorage: Store as a dry solid under the conditions stated on the manufacturer's label; pack sizes available on request\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the product in its original tightly closed container, stored as a dry solid and protected from moisture, since the sodium salt is hygroscopic in character and readily takes up water from humid air. Follow the storage temperature indicated on the manufacturer's label. Use clean, dry glass or inert plastic containers for weighing and for preparing aqueous stock solutions, and allow closed containers to reach room temperature before opening to limit condensation. Prepare solutions in aqueous buffer with gentle mixing, as concentrated solutions become viscous. Handle with standard laboratory practice: wear a lab coat, safety glasses, and gloves, work in a well-ventilated area, avoid generating dust when weighing the solid, and consult the manufacturer's safety data sheet before use. Aqueous solutions are susceptible to nuclease contamination, so prepare them with clean technique and store or divide them according to your laboratory's established protocol.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086623027418,"sku":"TCI2510D354523844","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086623060186,"sku":"TCI2510D354523845","price":2500000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510d356623879","title":"TCI D3566 40615-39-2 5'-O-(4,4'-Dimethoxytrityl)thymidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3566 5'-O-(4,4'-Dimethoxytrityl)thymidine is a protected nucleoside that serves as an essential starting material in oligonucleotide synthesis. The molecule is thymidine in which the hydroxyl group at the 5' position has been protected by a dimethoxytrityl group, while the 3' hydroxyl group is left free. This selective protection is precisely what makes directed assembly of DNA chains possible, because each coupling step can only occur at one planned position. In the laboratory, this material is the point of departure for preparing phosphoramidites and for attaching nucleosides to solid supports.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound especially valuable is the character of the dimethoxytrityl group, which is labile toward weak acid yet stable under basic and neutral conditions. The group can be removed rapidly and cleanly with dilute acid solution, and the trityl cation that is formed has a characteristic color, so the efficiency of every coupling cycle can be monitored quantitatively through absorbance measurement. This capacity for direct monitoring is what has established the dimethoxytrityl strategy as the standard in automated oligonucleotide synthesis. The large size of the protecting group additionally blocks side reactions at the 5' position.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used by research groups and service facilities engaged in nucleic acid chemistry, molecular biology support work, and the in-house preparation of synthetic DNA building blocks. It is handled as a bench-scale synthetic intermediate, weighed out for phosphoramidite preparation or solid-support loading, and its color-based coupling readout makes it well suited to teaching and method-development settings where each synthetic cycle needs to be verified rather than assumed.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePhosphoramidite preparation: the free 3' hydroxyl group is available for phosphitylation while the 5' position stays protected, giving a clean single-site reaction for building synthesis-ready monomers.\u003c\/li\u003e\n\u003cli\u003eSolid-support loading: the compound serves as the starting nucleoside attached to a solid support, establishing the defined 3' anchor point from which the oligonucleotide chain is extended.\u003c\/li\u003e\n\u003cli\u003eAutomated oligonucleotide synthesis: acid-labile yet base-stable protection fits standard synthesis cycles, allowing repeated deprotection and coupling steps without disturbing other functional groups.\u003c\/li\u003e\n\u003cli\u003eCoupling efficiency monitoring: removal of the dimethoxytrityl group releases a characteristically colored trityl cation, so absorbance measurement gives a quantitative stepwise yield for each cycle.\u003c\/li\u003e\n\u003cli\u003eDirected DNA chain assembly: selective protection of only the 5' hydroxyl ensures each elongation step proceeds at a single planned position, preventing uncontrolled branching or side reaction.\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: 40615-39-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical name: 5'-O-(4,4'-Dimethoxytrityl)thymidine\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required quantity when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the container tightly closed and store it in a cool, dry place away from moisture, direct sunlight, and sources of acid, since the dimethoxytrityl protecting group is sensitive to acidic conditions. Original manufacturer packaging or a tightly sealed amber glass container is suitable, and transfers are best carried out in a dry environment to limit exposure to atmospheric humidity. Handle the material in a fume hood using gloves, safety glasses, and a laboratory coat, and weigh it with clean, dry spatulas to avoid cross-contamination. Always consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated consumables through the laboratory's chemical waste procedure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48275706183898,"sku":"TCI2510D356623879","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3566.jpg?v=1768204987"},{"product_id":"tci2510d357923895","title":"TCI D3579 3094-09-5 5'-Deoxy-5-fluorouridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3579 5'-Deoxy-5-fluorouridine, widely known as doxifluridine or 5'-DFUR, is a synthetic fluoropyrimidine nucleoside that holds an important position as a reference material in biochemistry and pharmacology laboratories. The compound is a uridine derivative that lacks the hydroxyl group at the 5' position and carries a fluorine atom at position 5 of the pyrimidine ring. This distinctive structure makes it a classic prodrug studied intensively in antimetabolite metabolism research, because its conversion into the active form depends on thymidine phosphorylase activity within tissues. In the laboratory, this material serves as a test compound, an analytical standard, and a starting material for mechanistic studies of fluoropyrimidine-based drugs.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that lead many researchers to select 5'-Deoxy-5-fluorouridine are the combination of reasonable storage stability in solid form and highly specific biological reactivity once it is enzymatically activated. The presence of the fluorine atom at position 5 gives the molecule electronic properties different from those of natural uracil, allowing the compound to interfere with the thymidylate synthesis pathway after conversion. Its well-defined structure and consistent behaviour as a nucleoside derivative make it suitable for use as a comparison compound, so that experimental results obtained in different laboratories remain interpretable against a common reference point.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically used in university research groups, pharmacology and biochemistry teaching laboratories, and pharmaceutical research units that study antimetabolite mechanisms. It is commonly employed in enzyme activity assays, cell-based studies, and analytical method development where a defined fluoropyrimidine nucleoside is required. Because it is supplied by TCI as a catalogue chemical, it fits routine research workflows in which reproducibility and traceable identity of the compound matter as much as the experiment itself.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProdrug activation studies — the compound depends on thymidine phosphorylase for conversion, making it a direct model for investigating tissue-dependent enzymatic activation of nucleoside prodrugs in controlled experiments.\u003c\/li\u003e\n\u003cli\u003eAntimetabolite mechanism research — because the activated form interferes with the thymidylate synthesis pathway, it allows researchers to trace how fluoropyrimidines disrupt nucleotide biosynthesis at the biochemical level.\u003c\/li\u003e\n\u003cli\u003eAnalytical standard preparation — its defined identity as a fluoropyrimidine nucleoside makes it suitable as a reference substance for chromatographic and spectroscopic method development and system suitability checks.\u003c\/li\u003e\n\u003cli\u003eEnzyme activity assays — thymidine phosphorylase studies can use this substrate to compare conversion rates between sample types, since the enzymatic dependency of the molecule is well characterised.\u003c\/li\u003e\n\u003cli\u003eStructure–activity relationship studies — the 5'-deoxy modification and 5-fluoro substitution provide a defined structural template for comparing uridine derivatives and evaluating how each modification changes biological behaviour.\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: 3094-09-5\u003c\/li\u003e\n\u003cli\u003eCatalogue Number: D3579\u003c\/li\u003e\n\u003cli\u003eCategory: Life Science \u0026gt; Biochemicals and Reagents \u0026gt; Nucleosides, Nucleotides, Oligonucleotides\u003c\/li\u003e\n\u003cli\u003eChemical Class: Synthetic fluoropyrimidine nucleoside, uridine derivative (doxifluridine \/ 5'-DFUR)\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in standard TCI research-scale packaging; please confirm the size required when ordering\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 and protected from light and moisture, following the storage conditions stated on the manufacturer's label and safety data sheet. Amber glass or the supplied original packaging is appropriate, and containers should be resealed promptly after each use to limit exposure to humid air. Handle the solid in a well-ventilated area or fume hood, wearing a laboratory coat, nitrile gloves, and eye protection, and avoid generating dust during weighing or transfer. As a biologically active fluoropyrimidine compound intended for research use only, it should be handled by trained personnel, kept away from food and drink, and disposed of as chemical waste in accordance with institutional and local regulations. Consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086627516634,"sku":"TCI2510D357923895","price":1995000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086627549402,"sku":"TCI2510D357923896","price":5956000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3579.jpg?v=1769180615"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-nucleosides-nucleotides-oligonucleotides.oembed?page=19","provider":"AMI Scientific","version":"1.0","type":"link"}