{"title":"Active Esters, Additives [Coupling Reagents]","description":"\u003cp\u003e\u003cstrong\u003eActive Esters, Additives [Coupling Reagents]\u003c\/strong\u003e — berisi ester aktif dan aditif seperti tosilimidazol, anhidrida asam trifluorometilbenzoat, 2,4,6-triklorobenzoil klorida, serta karbonat pentafluorofenil yang berfungsi mengaktifkan gugus karboksilat untuk pembentukan ikatan amida atau ester. Kategori ini juga mencakup garam piridinium terbrominasi yang bekerja sebagai aktivator alternatif dalam reaksi kondensasi.\u003c\/p\u003e\u003cp\u003eReagen ester aktif dan aditif ini banyak dipakai dalam sintesis peptida dan pembentukan ikatan amida, di mana gugus karboksilat diaktivasi terlebih dahulu sebelum bereaksi dengan amina agar hasil kopling lebih bersih dan efisien. Anhidrida aril terfluorinasi dan turunan benzoil klorida umum dipilih untuk esterifikasi Yamaguchi pada sintesis makrolida, sementara garam piridinium terbrominasi dipakai sebagai aktivator alternatif ketika reagen kopling konvensional kurang efektif.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t198553326\"\u003eTCI T1985 2232-08-8 1-(p-Toluenesulfonyl)imidazole\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c017814153\"\u003eTCI C0178 543-27-1 Isobutyl Chloroformate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t159352827\"\u003eTCI T1593 25753-16-6 4-Trifluoromethylbenzoic Anhydride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c090315224\"\u003eTCI C0903 14338-32-0 2-Chloro-1-methylpyridinium Iodide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t141352573\"\u003eTCI T1413 4136-95-2 2,4,6-Trichlorobenzoyl Chloride\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c090615228\"\u003eTCI C0906 7403-46-5 2-Chloro-1-methylpyridinium p-Toluenesulfonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b36049565\"\u003eTCI B3604 59483-84-0 Bis(pentafluorophenyl) Carbonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c107715483\"\u003eTCI C1077 4457-32-3 4-Nitrobenzyl Chloroformate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePilih berdasarkan tingkat reaktivitas dan selektivitas gugus pengaktif yang dibutuhkan, kepekaan senyawa terhadap kelembapan udara, serta kompatibilitas pelarut agar proses aktivasi karboksilat berjalan bersih tanpa efek samping. 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 Coupling [Synthetic Reagents], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-peptide-coupling-agents\"\u003ePeptide Coupling Agents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosphonium-salts-uronium-salts-formamidinium-salts-coupling-reagents\"\u003ePhosphonium Salts, Uronium Salts, Formamidinium Salts [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-coupling-reagents-other\"\u003eCoupling Reagents (Other)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-triflate-formation-coupling-reagents\"\u003eTriflate Formation [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbodiimides-coupling-reagents\"\u003eCarbodiimides [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosgene-derivatives-coupling-reagents\"\u003ePhosgene Derivatives [Coupling Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-coupling-synthetic-reagents\"\u003eCoupling [Synthetic Reagents]\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":"tci2510c017814153","title":"TCI C0178 543-27-1 Isobutyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0178 Isobutyl Chloroformate, CAS 543-27-1, is a versatile chloroformate reagent commonly used to activate carboxylic acids as mixed anhydrides. This classical approach supports amide and peptide bond formation at low temperature and is also applied to esters, carbamates, and analytical derivatization. AMI Scientific offers 25 g, 100 g, and 500 g packs so laboratories can match the quantity to their working scale. The reagent is corrosive, flammable, and moisture sensitive, so use a fume hood, dry glassware, and store it tightly closed in a cool, dry, well-ventilated place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNedev et al. (1993). A convenient method for synthesis of Fmoc-amino acid p-nitroanilides based on isobutyl chloroformate as condensation agent.. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(00)60527-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(00)60527-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAhmed Soomro (2014). Gas Chromatographic Determination of Amino Acids and Polyamines in Human Skin Samples using Trifluoroacetylacetone and Isobutyl Chloroformate as Derivatizing Reagents. \u003cem\u003eJournal of Chromatography \u0026amp; Separation Techniques\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4172\/2157-7064.1000248\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4172\/2157-7064.1000248\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eNEDEV et al. (1993). ChemInform Abstract: A Convenient Method for Synthesis of Fmoc‐Amino Acid p‐Nitroanilides, e.g. (S)‐(III), Based on Isobutyl Chloroformate as Condensation Agent.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199338293\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199338293\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":48085975400666,"sku":"TCI2510C017814153","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085975433434,"sku":"TCI2510C017814154","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085975466202,"sku":"TCI2510C017814155","price":1894000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0178.jpg?v=1767094828"},{"product_id":"tci2510c107715483","title":"TCI C1077 4457-32-3 4-Nitrobenzyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Nitrobenzyl Chloroformate (TCI C1077, CAS 4457-32-3) is a widely used reagent for installing the p-nitrobenzyloxycarbonyl (pNZ) protecting group on amines in peptide chemistry. Because the pNZ group is removed under reductive conditions, it provides valuable orthogonality against acid- and base-labile protecting groups. AMI Scientific supplies this TCI reagent in a 25 g pack size suited to research and development laboratories. As a moisture-sensitive and corrosive chloroformate, it should be handled in a fume hood following the official TCI Safety Data Sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086047588570,"sku":"TCI2510C107715483","price":3584000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1077.jpg?v=1768204581"},{"product_id":"tci2510c124215716","title":"TCI C1242 2942-58-7 Diethyl Cyanophosphonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1242 Diethyl Cyanophosphonate (DEPC) is a well-established coupling reagent for activating carboxylic acids toward amide and ester bond formation. It is frequently applied in peptide synthesis, where it offers effective coupling under comparatively mild conditions. The reagent is highly toxic and moisture-sensitive, and hydrolysis can release extremely hazardous gas, so it must be handled only by trained personnel in a fume hood. Available in 5 g and 25 g packs, it must be stored, used, and disposed of strictly in accordance with the official TCI safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGUZMAN et al. (1997). ChemInform Abstract: A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199747196\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199747196\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGuzmán et al. (1997). A Convenient Method for the Phosphorylation of Phenols with Diethyl Cyanophosphonate. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919708005008\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919708005008\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDemir et al. (2009). Cyanide Ion Promoted Addition of Acylphosphonates to Diethyl Cyanophosphonate: Synthesis of Phosphonocyanohydrin O-Phosphates. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1216634\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1216634\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":48086058598618,"sku":"TCI2510C124215716","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086058631386,"sku":"TCI2510C124215717","price":5300000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1242.jpg?v=1768204586"},{"product_id":"tci2510c140015931","title":"TCI C1400 7693-46-1 4-Nitrophenyl Chloroformate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1400 4-Nitrophenyl Chloroformate (CAS 7693-46-1) is a widely used activating reagent in peptide chemistry and bioconjugation. It converts alcohols and amines into activated 4-nitrophenyl carbonates or carbamates, in which 4-nitrophenolate serves as an excellent leaving group for subsequent nucleophilic attack. This two-step approach provides controlled access to unsymmetrical carbamates, prodrug linkers, activated PEG derivatives, and immobilised ligands without handling phosgene directly. AMI Scientific offers 25 g and 250 g packs; the reagent is moisture-sensitive and performs best when stored and handled under dry conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSammet (2009). 4-Nitrophenyl Chloroformate: A Versatile Coupling Reagent. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0029-1218291\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0029-1218291\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEl Seoud et al. (2006). Kinetics of the pH‐independent hydrolyses of 4‐nitrophenyl chloroformate and 4‐nitrophenyl heptafluorobutyrate in water‐acetonitrile mixtures: consequences of solvent composition and ester hydrophobicity. \u003cem\u003eJournal of Physical Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/poc.1081\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/poc.1081\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMikulec et al. (1996). Use ofp-nitrophenyl chloroformate chemistry to immobilize protein on orthopedic biomaterials. \u003cem\u003eJournal of Biomedical Materials Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/(sici)1097-4636(199610)32:2\u0026lt;203::aid-jbm8\u0026gt;3.0.co;2-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/(sici)1097-4636(199610)32:2\u0026lt;203::aid-jbm8\u0026gt;3.0.co;2-x\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":48086067675354,"sku":"TCI2510C140015931","price":2702000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086067708122,"sku":"TCI2510C140015932","price":16530000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1400.jpg?v=1768204595"},{"product_id":"tci2510c167616342","title":"TCI C1676 3140-73-6 2-Chloro-4,6-dimethoxy-1,3,5-triazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-4,6-dimethoxy-1,3,5-triazine is a heterocyclic compound widely used in organic chemistry for the synthesis of complex molecules. Its structure allows it to participate in various chemical reactions, making it a valuable building block for researchers. The presence of chlorine and methoxy groups enhances its reactivity, enabling targeted chemical modifications. This compound is commonly applied in pharmaceutical research, chemical synthesis, and academic studies. Its stability and versatility make it an essential material in Indonesian laboratories for scientific innovation and discovery.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086084255962,"sku":"TCI2510C167616342","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086084288730,"sku":"TCI2510C167616343","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086084321498,"sku":"TCI2510C167616344","price":8329000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1676.jpg?v=1768816678"},{"product_id":"tci2510c344418484","title":"TCI C3444 153433-26-2 2-Chloro-1,3-dimethylimidazolinium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-1,3-dimethylimidazolinium Tetrafluoroborate is a chemical compound widely used as a catalyst in various chemical reactions within laboratory settings. This material belongs to the category of carbon-donor ligands and is known for its ability to facilitate both substitution and electrophilic reactions. Its ionic structure enhances its reactivity in reactive environments, making it a valuable tool for chemists working on complex organic synthesis. The compound is particularly effective in accelerating chemical processes without undergoing significant degradation, which is essential for maintaining the integrity of experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make this compound a preferred choice is its versatility in functioning as either a homogeneous or heterogeneous catalyst, depending on the reaction conditions. The presence of the tetrafluoroborate ion contributes to its stability and reactivity across a range of conditions. Additionally, its solubility in organic solvents simplifies handling and processing, making it a practical option for laboratory use. These characteristics ensure that it remains a reliable and efficient catalyst in diverse chemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in organic chemistry research, especially in the synthesis of heterocyclic compounds and substitution reactions. Its stability and reactivity make it highly relevant for a variety of chemical processes. Due to its effectiveness and ease of use, it is a popular choice among researchers and chemists in the region. Its role in advancing chemical synthesis and reaction mechanisms underscores its importance in modern laboratory practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound's ability to act as a versatile catalyst, enhancing reaction efficiency and yield in complex molecule formation.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound synthesis relies on its catalytic properties, enabling the formation of ring structures with high specificity and selectivity.\u003c\/li\u003e\n\u003cli\u003eElectrophilic substitution reactions are effectively catalyzed by this material, promoting the formation of desired products with minimal side reactions.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes utilize its stability and reactivity to improve reaction rates and reduce energy consumption in large-scale applications.\u003c\/li\u003e\n\u003cli\u003eResearch laboratories use it for studying catalytic mechanisms, providing insights into reaction pathways and improving synthetic methodologies.\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: 153433-26-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Carbon-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this material. Avoid contact with incompatible substances, and always follow standard laboratory safety protocols to minimize risks. Regular inspection of storage conditions is advised to ensure the material remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086247702746,"sku":"TCI2510C344418484","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086247735514,"sku":"TCI2510C344418485","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3444.jpg?v=1767099593"},{"product_id":"tci2510d166221508","title":"TCI D1662 74124-79-1 Di(N-succinimidyl) Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDi(N-succinimidyl) Carbonate (DSC) is a chemical reagent widely used in organic chemistry reactions, particularly in the synthesis of organic compounds and the modification of biological molecules. This compound is known for its ability to react with amino groups, making it a valuable tool in peptide and protein synthesis. Its role in activating amide bonds is critical in various biochemical processes, supporting research in chemical biology and molecular engineering. DSC is commonly employed in laboratories where efficient activation of amino groups is required, especially in the development of complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe reactivity and specificity of DSC make it a preferred choice for researchers working in chemical biology and peptide chemistry. Its high reactivity ensures effective activation of amino groups, which is essential for the formation of stable amide bonds. Additionally, DSC is known for its stability under controlled conditions, although it is sensitive to moisture and air exposure. These properties make it a reliable and efficient reagent for a wide range of laboratory applications. Its versatility and effectiveness in activating functional groups have made it a standard in many research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, DSC is frequently used in biological chemistry, pharmaceutical research, and biotechnology. It plays a key role in the modification of biological molecules and the synthesis of compounds with specific structural requirements. Its relevance in these fields is due to its ability to facilitate precise chemical reactions, supporting the development of new drugs and advanced biochemical techniques. DSC is an essential component in the toolkit of researchers working on molecular-level innovations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide and protein synthesis due to its ability to activate amino groups efficiently in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic compound modification where amide bond formation is required for structural stability.\u003c\/li\u003e\n\u003cli\u003eBiochemical research applications that rely on amide bond activation for molecular interactions.\u003c\/li\u003e\n\u003cli\u003eDrug development processes that involve the synthesis of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eBiotransformation studies requiring precise chemical activation of functional groups.\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: 74124-79-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\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 dry, cool place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDi(N-succinimidyl) Carbonate should be stored in a dry, cool environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which can degrade its reactivity. Due to its sensitivity, it is best stored in a desiccator or a container with a drying agent. Always handle the compound in a well-ventilated area and avoid direct contact with skin or eyes. Proper personal protective equipment, such as gloves and safety goggles, should be used when handling this reagent. It is important to ensure that the storage area is free from potential contaminants and that the compound is kept in a secure location to prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086454272218,"sku":"TCI2510D166221508","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086454304986,"sku":"TCI2510D166221509","price":5427000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1662.jpg?v=1767103435"},{"product_id":"tci2510d326223513","title":"TCI D3262 165534-43-0 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one is a synthetic reagent widely used in laboratory settings for its unique chemical properties. This compound plays a crucial role in coupling reactions, where it facilitates the formation of specific chemical bonds between molecules. Its complex structure allows for high reactivity and specificity, making it an essential component in organic synthesis. Due to its ability to interact with various molecular structures, it is highly valued in chemical research and development.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high reactivity and structural versatility make it a preferred choice for researchers seeking precision in their synthetic processes. Its stability under controlled conditions ensures reliable performance during experiments, reducing the risk of unwanted side reactions. Additionally, its compatibility with a range of solvents and reaction conditions enhances its utility across different laboratory applications. These characteristics contribute to its popularity among scientists working in both academic and industrial environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research and the development of new compounds. Its role in synthetic reactions is vital for advancing chemical studies and innovation. Due to its effectiveness and reliability, it is a sought-after material for researchers and practitioners in educational institutions and research facilities across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this reagent due to its ability to facilitate specific bond formations and its high reactivity in coupling processes.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for developing new chemical compounds as it enables controlled and efficient synthetic pathways in research settings.\u003c\/li\u003e\n\u003cli\u003eIn pharmaceutical research, it supports the creation of complex molecular structures necessary for drug development and testing.\u003c\/li\u003e\n\u003cli\u003eIt is used in analytical chemistry for its role in modifying and stabilizing compounds during various experimental procedures.\u003c\/li\u003e\n\u003cli\u003eIts stability under controlled conditions makes it suitable for long-term storage and use in multiple laboratory protocols.\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: 165534-43-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on formulation\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 reagent should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and goggles. It is advisable to store it away from incompatible substances to avoid any potential chemical interactions. Proper labeling of storage containers is essential for safety and easy identification. Regular inspection of storage conditions ensures that the reagent remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086605856986,"sku":"TCI2510D326223513","price":1995000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3262.jpg?v=1768204964"},{"product_id":"tci2510e036328108","title":"TCI E0363 16357-59-8 1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline is a chemical compound widely used in laboratory settings for its unique molecular structure and reactivity. This compound plays a crucial role in chemical and biochemical experiments, particularly in the synthesis of organic compounds and the development of peptide chemistry. Its complex structure allows it to participate in various chemical reactions, making it an essential reagent for researchers working in advanced synthetic pathways. Due to its versatility, it is frequently utilized in both academic and industrial research environments where precise chemical manipulation is required.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under controlled conditions and its solubility in organic solvents, which facilitates efficient chemical reactions and purification processes. Its reactivity and specificity make it a preferred choice for applications requiring high precision and controlled outcomes. The compound’s sensitivity to moisture and light necessitates careful handling and storage, but these properties also contribute to its effectiveness in targeted chemical synthesis. These characteristics ensure that it remains a reliable and consistent material for laboratory use.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in chemical and biochemical research, particularly in academic institutions and research centers. Its application spans various fields, including organic synthesis and molecular interaction studies. Researchers rely on its predictable behavior and chemical properties to achieve accurate and reproducible results in their experiments. Its presence in Indonesian laboratories underscores its importance in advancing scientific research and development in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic Synthesis: This compound is ideal for creating complex organic molecules due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry: It is used in the development of peptide-based compounds, offering a stable platform for molecular modifications.\u003c\/li\u003e\n\u003cli\u003eMolecular Interaction Studies: Its unique structure allows it to be used in studying molecular interactions and reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic Compound Research: It plays a key role in the synthesis of heterocyclic compounds, which are essential in pharmaceutical and biochemical applications.\u003c\/li\u003e\n\u003cli\u003eControlled Reaction Environments: Its stability under specific conditions makes it suitable for experiments requiring precise chemical control.\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: 16357-59-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent exposure to humidity and contaminants. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures in place. Always ensure that the storage area is well-ventilated and free from potential sources of contamination. Proper labeling and secure storage are essential to prevent accidental exposure and ensure safe usage in laboratory environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086840312026,"sku":"TCI2510E036328108","price":1868000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0363.jpg?v=1771058792"},{"product_id":"tci2510e084728644","title":"TCI E0847 3849-21-6 Ethyl Cyano(hydroxyimino)acetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyano(hydroxyimino)acetate is a chemical compound widely used in organic synthesis reactions within laboratory settings. It serves as a key building block for the creation of complex molecular structures, offering versatility in chemical reactions due to its unique functional groups. This compound is particularly valued for its ability to participate in specific chemical transformations, making it a preferred choice for researchers aiming to develop new compounds and materials. Its role in synthetic chemistry is crucial, especially in the design of pharmaceuticals and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits chemical stability under controlled conditions, yet it remains highly reactive to changes in pH, temperature, and catalysts. This reactivity allows for precise control in synthetic processes, ensuring the desired outcomes in laboratory experiments. Its ability to form various chemical bonds further enhances its utility in diverse applications. The compound’s reactivity and selectivity make it an essential tool in synthetic chemistry, enabling the development of new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl Cyano(hydroxyimino)acetate is commonly used by chemists in organic synthesis research and the development of new materials. It plays a vital role in academic and industrial research settings, supporting both educational and innovative projects. Its relevance in chemical education and research makes it a valuable resource for universities and research institutions focused on advancing chemical knowledge and applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research where precise chemical transformations are required due to its reactivity and selectivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds as a building block for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eChemical education in academic institutions for teaching synthetic chemistry techniques and molecular design.\u003c\/li\u003e\n\u003cli\u003eIndustrial research applications in the creation of specialty chemicals and advanced materials.\u003c\/li\u003e\n\u003cli\u003eCustom compound synthesis projects requiring versatile and adaptable chemical intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3849-21-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation\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\u003eEthyl Cyano(hydroxyimino)acetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. 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 potential chemical interactions. Regular monitoring of storage conditions ensures the compound remains suitable for use in research applications. Proper labeling and secure storage are essential to maintain safety and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086900506842,"sku":"TCI2510E084728644","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086900539610,"sku":"TCI2510E084728645","price":4871000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0847.jpg?v=1767111863"},{"product_id":"tci2510e090128722","title":"TCI E0901 137156-41-3 Ethyl 1-Hydroxy-1H-1,2,3-triazole-4-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-Hydroxy-1H-1,2,3-triazole-4-carboxylate is a synthetic chemical compound widely used in laboratory settings for its reactivity and versatility. As a coupling reagent, it plays a crucial role in the synthesis of heterocyclic compounds and triazole derivatives. This compound is particularly valuable in organic chemistry due to its ability to participate in a variety of chemical reactions, making it an essential tool for researchers. Its unique molecular structure, combining a triazole ring with an ethyl ester group, contributes to its effectiveness in forming complex molecular bonds.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and stability make it a preferred choice for synthetic chemists. Its molecular structure allows it to interact with various ligands and reagents, facilitating the formation of new chemical bonds. This property is especially important in applications requiring precise control over reaction conditions. Additionally, its chemical stability ensures that it remains effective even under a range of experimental conditions, making it reliable for use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of heterocyclic compounds and the development of new chemical materials. It is also found in pharmaceutical and food chemistry research, where its reactivity and stability make it a valuable component in the formulation of new compounds and the study of chemical interactions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and ability to form complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical materials in industrial and academic research settings.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the synthesis of triazole derivatives and related compounds.\u003c\/li\u003e\n\u003cli\u003eFood chemistry studies involving the creation of new compounds and chemical interactions.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions in synthetic chemistry where precise bond formation is required.\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: 137156-41-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific product variant\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\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Proper ventilation is essential when working with this material to ensure safe laboratory conditions. Avoid exposure to incompatible substances to maintain its stability and effectiveness in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086906339546,"sku":"TCI2510E090128722","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086906372314,"sku":"TCI2510E090128723","price":5553000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0901.jpg?v=1768205246"},{"product_id":"tci2510f118431289","title":"TCI F1184 2118332-08-2 2-Fluoro-6-(trifluoromethyl)benzoic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Fluoro-6-(trifluoromethyl)benzoic Anhydride is a fluorinated organic compound widely used in chemical laboratories for the synthesis of complex organic molecules. This compound serves as a key building block in various chemical reactions, particularly those involving electrophilic substitution and functional group transformations. Its unique molecular structure, featuring both fluorine and trifluoromethyl groups, makes it an essential reagent in the development of new pharmaceuticals and bioactive compounds. Due to its chemical stability and reactivity, it is a valuable tool for researchers aiming to explore novel synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s fluorinated structure contributes to its high reactivity and selectivity in chemical reactions. The presence of fluorine atoms enhances the molecule’s stability while also influencing its reactivity in different reaction conditions. This combination of properties makes it a preferred choice for chemists working on advanced synthetic strategies. Its ability to participate in a wide range of reactions, including acylation and esterification, further solidifies its role in modern chemical research. The compound is especially useful in applications requiring precise control over molecular functionality.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Fluoro-6-(trifluoromethyl)benzoic Anhydride is commonly used in pharmaceutical and industrial chemistry research. It plays a crucial role in the development of new drugs and chemical materials. Researchers in Indonesia rely on this compound for its versatility and effectiveness in complex synthetic processes. Its application is widespread in both academic and industrial settings, supporting innovation in chemical synthesis and drug discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical synthesis for the development of bioactive compounds due to its fluorinated structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for electrophilic substitution reactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for the creation of specialized materials and intermediates.\u003c\/li\u003e\n\u003cli\u003eDrug discovery projects requiring precise molecular modifications and synthetic flexibility.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical analysis in laboratories focusing on fluorinated compound behavior and reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2118332-08-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent moisture exposure, which can affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong bases or reducing agents. Keep the material away from heat sources and ensure proper labeling for safe handling and disposal. Regular monitoring of storage conditions is essential to ensure optimal performance and safety in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087065329882,"sku":"TCI2510F118431289","price":1920000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1184.jpg?v=1768360372"},{"product_id":"tci2510h039532937","title":"TCI H0395 524-38-9 N-Hydroxyphthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxyphthalimide (NHP) is a chemical compound widely used in various laboratory applications, particularly in peptide chemistry and chemical biology. It serves as a key reagent in the synthesis of peptides and their derivatives, playing a crucial role in molecular conjugation and modification processes. Its reactivity allows it to participate in reactions with amines, amino acids, and other substrates, making it indispensable in biochemical research. Due to its stability and controlled reactivity, NHP is a preferred choice for experiments requiring precise chemical interactions.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons NHP is favored in laboratories is its ability to undergo nucleophilic reactions while maintaining structural integrity. This property ensures consistent results in complex synthetic procedures. Additionally, NHP exhibits good solubility in organic solvents, which simplifies mixing and separation during experiments. These characteristics make it highly suitable for use in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NHP is commonly utilized in peptide synthesis, biomedical compound development, and pharmaceutical research. Its reliability and effectiveness in chemical reactions make it a valuable tool for scientists working in the fields of chemistry and biology. The compound's versatility supports a wide range of experimental needs, contributing to the advancement of scientific research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: NHP is used to facilitate peptide bond formation through nucleophilic reactions, enhancing the efficiency of peptide synthesis processes.\u003c\/li\u003e\n\u003cli\u003eBiomedical Compound Development: Its reactivity and solubility make it ideal for synthesizing complex biologically active compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: NHP supports the development of pharmaceuticals by enabling controlled chemical modifications of molecular structures.\u003c\/li\u003e\n\u003cli\u003eMolecular Conjugation Studies: The compound's ability to react with various substrates aids in the study of molecular interactions and conjugation mechanisms.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Experiments: NHP is a preferred reagent in reactions requiring stable and reactive intermediates, supporting a broad range of chemical 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: 524-38-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxyphthalimide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Due to its solid form, it is best stored in a sealed container made of inert material such as glass or polyethylene to avoid chemical interactions. Laboratory personnel should handle NHP with care, using appropriate personal protective equipment when necessary. Proper storage ensures the compound remains effective for use in various biochemical and chemical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087200891098,"sku":"TCI2510H039532937","price":633000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087200923866,"sku":"TCI2510H039532938","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087200956634,"sku":"TCI2510H039532939","price":4771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0395.jpg?v=1768205514"},{"product_id":"tci2510h046833022","title":"TCI H0468 80029-43-2 1-Hydroxybenzotriazole Monohydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Hydroxybenzotriazole Monohydrate is a chemical compound widely utilized in various chemical reactions and biosynthetic processes. It plays a crucial role in laboratory settings as a reagent for the formation of ester and amide bonds. This compound is particularly valued for its ability to activate carboxyl groups in organic compounds, thereby accelerating chemical reactions. Its unique molecular structure makes it an essential component in many synthetic pathways, especially in the field of glycoscience. Due to its stability and reactivity, it is frequently employed in biochemical and pharmacological research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability under normal conditions, combined with its high reactivity in specific environments, makes it a preferred choice for researchers. The presence of a water molecule in its monohydrate form enhances its reactivity, allowing for more efficient reactions. This property is particularly beneficial in applications requiring precise functional group activation. Additionally, its solubility in organic solvents simplifies its use in a wide range of experimental procedures. These characteristics contribute to its popularity among scientists working in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Hydroxybenzotriazole Monohydrate is commonly used in chemical and biological research. It is a key reagent in the synthesis of glycosides and other complex organic molecules. Many research institutions in Indonesia rely on this compound for its reliability and effectiveness in various experimental setups. Its consistent performance and availability make it a go-to material for researchers in the field of chemical biology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGlycoside Synthesis: This compound is ideal for activating carboxyl groups in sugar derivatives, enabling efficient glycosidic bond formation.\u003c\/li\u003e\n\u003cli\u003ePeptide Coupling Reactions: Its ability to activate carboxylic acid groups makes it suitable for peptide synthesis and modification processes.\u003c\/li\u003e\n\u003cli\u003eBioconjugation Studies: The compound facilitates the coupling of biomolecules, making it useful in bioconjugation and molecular labeling techniques.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It is widely used in the preparation of esters and amides, supporting a variety of organic reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eEnzymatic Reaction Optimization: Its reactivity and stability help in studying enzyme mechanisms and substrate interactions in biochemical experiments.\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: 80029-43-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities, including 5g, 25g, and 100g\u003c\/li\u003e\n\u003cli\u003ePhysical form: White crystalline powder\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 direct sunlight and moisture. It is recommended to keep it in a sealed container to prevent exposure to air and humidity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is not flammable but may react with strong acids or bases. Proper ventilation is advised during handling to ensure a safe laboratory environment. Always follow standard chemical safety protocols to minimize any potential risks associated with its use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087212294362,"sku":"TCI2510H046833022","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48087212327130,"sku":"TCI2510H046833023","price":5527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0468.jpg?v=1767116459"},{"product_id":"tci2510h052833110","title":"TCI H0528 21715-90-2 N-Hydroxy-5-norbornene-2,3-dicarboximide [for Peptide Synthesis]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxy-5-norbornene-2,3-dicarboximide, frequently abbreviated in the literature as HONB, is a coupling additive reagent prepared specifically for peptide synthesis work. Structurally it is a cyclic imide fused to a norbornene framework, with the N-hydroxy group serving as its reactive centre. In a laboratory workflow, this reagent is used together with a carbodiimide or another activating reagent to convert a carboxylic acid into an active ester, which then reacts with an amine group to form the amide bond. Its role is to make the coupling reaction proceed more cleanly and under better control.\u003c\/p\u003e\n\u003cp\u003eThe principal reason chemists select this reagent is its ability to suppress racemisation at the alpha carbon of an amino acid during activation — a classic problem that can compromise the chiral purity of a peptide product. The active esters it forms are reactive enough to complete the coupling at a reasonable rate, yet stable enough to be isolated and stored when a workflow calls for it. The hydrophobic norbornene framework offers a practical advantage during purification, because reagent by-products are generally easier to separate than those of comparable additives.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories the reagent is typically found in university research groups, pharmaceutical and biotechnology development units, and contract synthesis facilities engaged in peptide chemistry. It is normally handled at the bench scale alongside standard carbodiimide activators, and is ordered as a supporting reagent within a wider peptide synthesis programme rather than as a bulk consumable. Its packaging and grade designation for peptide synthesis make it suitable for work where chiral integrity of the product must be preserved.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSolution-phase peptide coupling — added with a carbodiimide to generate the active ester in situ, giving cleaner amide bond formation and reduced side reactions.\u003c\/li\u003e\n\u003cli\u003eRacemisation-sensitive fragment condensation — chosen where two peptide fragments are joined and the alpha carbon of the C-terminal residue is most vulnerable to epimerisation.\u003c\/li\u003e\n\u003cli\u003ePreparation of isolable active esters — the esters formed are stable enough to be purified and stored, allowing coupling steps to be staged across separate working sessions.\u003c\/li\u003e\n\u003cli\u003eAmide bond formation in general organic synthesis — applicable wherever a carboxylic acid must be activated toward an amine under mild and controllable conditions.\u003c\/li\u003e\n\u003cli\u003eMethod development and reagent comparison studies — used as a reference additive when evaluating coupling efficiency, chiral purity, and by-product removal against alternative additives.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI, catalogue number H0528\u003c\/li\u003e\n\u003cli\u003eCAS number: 21715-90-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Coupling [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003eGrade designation: for Peptide Synthesis\u003c\/li\u003e\n\u003cli\u003ePack sizes: supplied in the manufacturer's standard catalogue pack sizes; please refer to the current product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form and storage class: refer to the manufacturer's specification sheet and safety data sheet supplied with the product\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry place, away from direct sunlight, heat sources, moisture, and incompatible materials such as strong bases and strong oxidising agents. Keep the container sealed when not in use to limit moisture uptake, and allow refrigerated stock to reach room temperature before opening so that condensation does not enter the bottle. Handle in a well-ventilated area or fume hood using a laboratory coat, chemical-resistant gloves, and eye protection. Use clean, dry spatulas and glassware when weighing to avoid contaminating the bulk material. Follow the manufacturer's safety data sheet for detailed exposure controls, spill response, and waste disposal, and observe institutional procedures for chemical waste handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087219372250,"sku":"TCI2510H052833110","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48087219405018,"sku":"TCI2510H052833111","price":6587000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0528.jpg?v=1771058577"},{"product_id":"tci2510h062333251","title":"TCI H0623 6066-82-6 N-Hydroxysuccinimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0623 N-Hydroxysuccinimide, commonly abbreviated as NHS, is a carboxyl-activating reagent that forms the backbone of modern peptide chemistry and bioconjugation. When paired with a carbodiimide such as EDC or DCC, NHS converts carboxylic acids into NHS esters that are considerably more reactive toward primary amines. These active esters then form amide bonds efficiently with the amino groups of lysine residues on proteins, with amine groups on linkers, or with the next amino acid in a peptide synthesis sequence, which is why this reagent is almost always kept on hand in biochemistry laboratories.\u003c\/p\u003e\n\u003cp\u003eThe property that makes NHS so dependable is its ability to suppress side reactions while simultaneously improving coupling yields. Without NHS, the O-acylisourea intermediate generated from a carbodiimide readily rearranges into unreactive N-acylurea or is wastefully hydrolysed; the presence of NHS traps that intermediate as an active ester that is far more stable and remains selective toward amines. NHS also helps suppress racemisation during peptide synthesis, an important advantage whenever stereochemical purity is a requirement. It takes the form of a white crystalline solid that dissolves in water and in polar organic solvents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, NHS is a routine item in university biochemistry groups, research institutes, and industrial R\u0026amp;D units engaged in peptide synthesis, protein labelling, and the preparation of conjugated reagents. Because it is used in small portions across many separate couplings, a single container typically supports an extended series of experiments. Its stability as a crystalline solid also makes it practical for facilities where reagents are ordered periodically rather than continuously, provided humidity is properly controlled.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide bond formation in solution-phase and solid-phase synthesis, where NHS esters couple amino acid building blocks efficiently while suppressing the racemisation that would compromise stereochemical purity of the final peptide.\u003c\/li\u003e\n\u003cli\u003eProtein bioconjugation via lysine residues, where NHS activation of carboxyl-bearing labels allows stable amide linkage to primary amine groups on the protein surface under mild aqueous conditions.\u003c\/li\u003e\n\u003cli\u003eCarbodiimide-mediated coupling with EDC or DCC, in which NHS intercepts the unstable O-acylisourea intermediate and converts it into a longer-lived active ester, markedly raising coupling efficiency.\u003c\/li\u003e\n\u003cli\u003ePreparation of crosslinkers and linker reagents, where NHS-activated termini are introduced onto spacer molecules so that the resulting reagent reacts selectively with amine functionalities during later assembly steps.\u003c\/li\u003e\n\u003cli\u003eSurface functionalisation of amine-bearing supports and resins, where NHS ester chemistry immobilises carboxyl-containing molecules through covalent amide bonds that resist hydrolysis better than physically adsorbed alternatives.\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: 6066-82-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePhysical form: white crystalline solid\u003c\/li\u003e\n\u003cli\u003eSolubility: soluble in water and polar organic solvents\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the pack sizes listed on this product page\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore N-Hydroxysuccinimide in a tightly closed original container in a cool, dry place away from moisture, since the solid is hygroscopic in practice and water uptake degrades activation performance. Keep the container closed when not in use and allow it to reach room temperature before opening if it has been stored cold, so that condensation does not form on the crystals. Handle the material in a fume hood or a well-ventilated area, wearing gloves, safety glasses, and a laboratory coat, and avoid generating or inhaling dust during weighing. Prepare activated ester solutions fresh where the protocol calls for it, as NHS esters hydrolyse in aqueous media over time. Consult the manufacturer's safety data sheet before first use and follow local institutional rules for chemical waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087224975578,"sku":"TCI2510H062333251","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087225008346,"sku":"TCI2510H062333252","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087225041114,"sku":"TCI2510H062333253","price":9137000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0623.jpg?v=1767116767"},{"product_id":"tci2510h130434102","title":"TCI H1304 106627-54-7 N-Hydroxysulfosuccinimide Sodium Salt","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H1304 N-Hydroxysulfosuccinimide Sodium Salt, commonly abbreviated as Sulfo-NHS, is a carboxyl-activating reagent of central importance in bioconjugation chemistry. It is used together with a water-soluble carbodiimide such as EDC to convert carboxylate groups into a far more stable active ester intermediate, so that the subsequent reaction with primary amine groups on proteins, peptides, or material surfaces proceeds with higher and more reproducible yields. Its role in the laboratory is that of a supporting reagent that transforms an otherwise inefficient aqueous amidation reaction into a reliable routine procedure.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent the preferred choice is the sulfonate group in its structure, which confers excellent solubility in water and in buffer solutions. Because of this, activation can be carried out directly in aqueous systems without the addition of organic solvents such as dimethylformamide, which can potentially damage protein structure or reduce biological activity. The negative charge of the sulfonate group also prevents the reagent and its active ester from crossing cell membranes, making it well suited to the selective labelling of cell-surface proteins. The Sulfo-NHS active ester also remains sufficiently long-lived at near-neutral pH for practical handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, biotechnology laboratories, and diagnostic development units that prepare protein conjugates in-house. It is commonly ordered alongside EDC as a working pair for coupling antibodies, enzymes, or peptides to carriers, particles, or plate surfaces. Because the entire procedure can be performed in aqueous buffer, it fits laboratories that work with biological samples and prefer to avoid organic solvent handling at the bench.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProtein and peptide conjugation, where the stabilised active ester allows amide bond formation with primary amines in aqueous buffer at higher and more reproducible yields.\u003c\/li\u003e\n\u003cli\u003eAntibody labelling and immunoassay development, since the reagent supports controlled coupling of antibodies to enzymes, reporters, or carrier proteins without organic solvent exposure.\u003c\/li\u003e\n\u003cli\u003eCell-surface protein labelling, because the negatively charged sulfonate group prevents membrane penetration so only proteins exposed on the outer surface are modified.\u003c\/li\u003e\n\u003cli\u003eSurface functionalisation of particles and materials, where carboxyl-bearing surfaces are activated in water and then coupled to amine-containing ligands or biomolecules.\u003c\/li\u003e\n\u003cli\u003eImmobilisation of biomolecules onto plates, resins, or sensor supports, providing a stable activated intermediate that makes routine aqueous amidation procedures more predictable.\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: 106627-54-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Bioconjugation\u003c\/li\u003e\n\u003cli\u003eProduct code: H1304\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research pack sizes; please confirm the current options when ordering.\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's recommendation stated on the product label.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this reagent in its original tightly closed container, kept dry and protected from moisture, since activating reagents of this type are sensitive to water uptake during storage. Keep the container in a cool place away from heat, direct sunlight, and incompatible chemicals, and allow it to reach room temperature before opening to reduce condensation inside the bottle. Handle in a well-ventilated area or fume hood, wearing a laboratory coat, safety goggles, and suitable gloves. Prepare working solutions fresh immediately before use, and follow the manufacturer's safety data sheet and your institutional chemical waste procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087270359258,"sku":"TCI2510H130434102","price":1566000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087270392026,"sku":"TCI2510H130434103","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1304.jpg?v=1767117758"},{"product_id":"tci2510h145434311","title":"TCI H1454 26198-21-0 1-Hydroxy-6-(trifluoromethyl)benzotriazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Hydroxy-6-(trifluoromethyl)benzotriazole is a chemical compound widely used in organic synthesis as a building block for the development of complex molecular structures. This compound plays a crucial role in laboratory settings, particularly in the creation of pharmaceuticals and specialty chemicals. Its unique molecular structure, which includes a trifluoromethyl group, makes it a versatile reagent for various chemical transformations. Due to its stability and reactivity, it is frequently employed in synthetic pathways that require controlled chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's fluorinated structure provides it with distinctive electronic properties, making it highly desirable in both organic and pharmaceutical research. The presence of fluorine atoms enhances the molecule's stability and reactivity, allowing it to participate effectively in substitution and condensation reactions. These properties make it a preferred choice for chemists aiming to design molecules with specific functional groups and desired biological activities. Its compatibility with a wide range of reaction conditions further contributes to its popularity in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-Hydroxy-6-(trifluoromethyl)benzotriazole is commonly used in scientific research and drug development projects. Its ability to facilitate the synthesis of active pharmaceutical ingredients makes it a valuable tool for researchers working on new drug formulations. The compound's role in creating stable molecular structures also supports its application in the development of advanced chemical products. Its reliability and effectiveness in laboratory settings have made it a standard component in many research programs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring fluorine substitution due to its stable and reactive fluorinated structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds where controlled reactivity and molecular stability are essential for drug design.\u003c\/li\u003e\n\u003cli\u003eCondensation reactions in the creation of functionalized aromatic compounds for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry to produce active pharmaceutical ingredients with enhanced bioavailability and stability.\u003c\/li\u003e\n\u003cli\u003eSynthesis of specialty chemicals that require precise molecular modifications and controlled chemical reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 26198-21-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its fluorinated nature, it is important to handle it with care, using appropriate personal protective equipment. The compound is generally stable under normal laboratory conditions but should be stored away from incompatible substances. Proper ventilation should be maintained in the laboratory to ensure safe handling. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087291855066,"sku":"TCI2510H145434311","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087291887834,"sku":"TCI2510H145434312","price":3534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1454.jpg?v=1768819076"},{"product_id":"tci2510h176534694","title":"TCI H1765 85342-65-0 N-Hydroxytetrachlorophthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxytetrachlorophthalimide is a chemical compound widely used in laboratory settings for its versatile reactivity in organic and catalytic reactions. As a key reagent in synthetic chemistry, it plays a crucial role in the development of complex organic molecules and catalytic processes. Its unique chemical structure allows it to participate in various reaction mechanisms, making it a valuable tool for chemists seeking to manipulate molecular structures with precision. This compound is particularly useful in applications where high reactivity and specificity are required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, including its ability to undergo substitution, redox, and bond-forming reactions, make it a preferred choice for researchers. Its stability under controlled conditions enhances its reliability in laboratory experiments, while its reactivity ensures that it can be effectively utilized in a wide range of chemical transformations. These characteristics make it an essential component in both organic and inorganic chemistry research. Its compatibility with various reaction conditions further broadens its applicability in synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, N-Hydroxytetrachlorophthalimide is commonly used in academic and research institutions. It is particularly favored in organic chemistry departments for its role in catalytic and synthetic processes. Its presence in laboratory workflows supports the advancement of chemical research, contributing to the development of new compounds and methodologies. Its use is widespread in both teaching and experimental settings, making it a standard reagent in many chemical laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from its reactivity in forming new chemical bonds and modifying molecular structures.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes utilize its ability to act as a catalyst in various reaction mechanisms, enhancing reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eRedox reactions take advantage of its electron transfer properties, making it suitable for oxidation and reduction pathways.\u003c\/li\u003e\n\u003cli\u003eSubstitution reactions rely on its capacity to replace functional groups in organic molecules with high specificity.\u003c\/li\u003e\n\u003cli\u003eResearch in inorganic chemistry uses its unique chemical properties to explore new reaction pathways and molecular interactions.\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: 85342-65-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Organocatalysts [Catalysis]\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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eN-Hydroxytetrachlorophthalimide should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the workspace to minimize inhalation risks. Avoid contact with incompatible materials to prevent potential chemical reactions. Proper storage and handling practices help maintain the integrity and effectiveness of the compound in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087320723674,"sku":"TCI2510H176534694","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087320756442,"sku":"TCI2510H176534695","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1765.jpg?v=1767118468"},{"product_id":"tci2510m118639166","title":"TCI M1186 68985-08-0 2,4-Mesitylenedisulfonyl Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,4-Mesitylenedisulfonyl Dichloride is a chemical compound widely used as a building block in the synthesis of complex organic compounds. Its unique molecular structure features two disulfonyl groups attached to carbon atoms at positions 2 and 4 of mesitylene, making it a valuable reagent in organic chemistry. In laboratory settings, this compound plays a crucial role in various synthetic reactions, particularly those involving substitution and coupling mechanisms. Its versatility allows chemists to create molecules with specific functional groups, enhancing its importance in research and development.\u003c\/p\u003e\n\u003cp\u003eThe compound's highly reactive nature makes it suitable for a range of chemical reactions, including nucleophilic, electrophilic, and redox processes. Its reactivity is complemented by its stability under certain conditions, which facilitates long-term storage and use. This combination of reactivity and stability ensures that it remains a reliable choice for researchers working on complex organic syntheses. Additionally, its chemical properties make it an essential tool for those exploring new synthetic pathways and molecular designs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,4-Mesitylenedisulfonyl Dichloride is commonly used in organic chemistry research, especially in the study of heterocyclic compound synthesis and the development of complex molecular structures. Many research institutions and universities rely on this compound as a key component in advanced chemical experiments. Its presence in these laboratories underscores its significance in both academic and industrial chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for the development of new pharmaceuticals due to its ability to form complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions in organic synthesis where it acts as a versatile reagent for bond formation between different molecular entities.\u003c\/li\u003e\n\u003cli\u003eRedox reactions where its reactive nature facilitates electron transfer processes in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions due to its electrophilic characteristics that allow for efficient reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eStructural modification of organic molecules to create compounds with desired functional groups and properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 68985-08-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and potential degradation. Due to its reactivity, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087591190746,"sku":"TCI2510M118639166","price":3155000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087591223514,"sku":"TCI2510M118639167","price":9817000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1186.jpg?v=1767124493"},{"product_id":"tci2510m143939522","title":"TCI M1439 434935-69-0 2-Methyl-6-nitrobenzoic Anhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Methyl-6-nitrobenzoic Anhydride is a chemical compound widely used in organic reactions for the synthesis of complex molecules. As an anhydride of benzoic acid, it possesses high reactivity, making it a valuable reagent in various synthetic pathways. This compound is commonly employed in laboratory settings to facilitate reactions such as nucleophilic substitution and carbon-carbon bond formation. Its versatility allows it to be a key component in the development of heterocyclic compounds, pharmaceuticals, and industrial chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity stems from its anhydride functionality, which readily reacts with amines, alcohols, and other functional groups. This makes it a preferred choice for chemists seeking efficient and reliable synthetic routes. Its stability under controlled conditions also contributes to its practicality in laboratory applications. The compound’s ability to participate in a wide range of reactions, combined with its predictable behavior, ensures its reliability in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Methyl-6-nitrobenzoic Anhydride is frequently used in organic chemistry research. It is a staple in academic institutions and research centers, where it supports the synthesis of complex molecules. Its availability and effectiveness make it a go-to reagent for researchers working on drug development, material science, and chemical synthesis. Its role in advancing chemical research is well-recognized in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds due to its reactivity in forming carbon-carbon bonds and its compatibility with various functional groups.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a key intermediate in the synthesis of drugs and medicinal compounds.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research for its versatility in facilitating nucleophilic substitution reactions and other synthetic transformations.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production as a reliable building block for the creation of specialty chemicals and materials.\u003c\/li\u003e\n\u003cli\u003eAcademic teaching and experimentation in chemistry laboratories for its use in demonstrating reaction mechanisms and synthetic 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: 434935-69-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which may affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential risks associated with its chemical nature. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. Always follow standard laboratory safety protocols when working with reactive chemicals.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087610294490,"sku":"TCI2510M143939522","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087610327258,"sku":"TCI2510M143939523","price":5629000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087610360026,"sku":"TCI2510M143939524","price":16935000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1439.jpg?v=1767124996"},{"product_id":"tci2510m357142185","title":"TCI M3571 173962-59-9 2-Hydroxy-5-methylisoindoline-1,3-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxy-5-methylisoindoline-1,3-dione is a chemical compound widely used in research applications within organic and biochemical laboratories. It serves as a key intermediate in the synthesis of complex molecules, particularly in the development of bioactive compounds and peptides. This compound is essential for researchers aiming to create molecules with specific biological activities, such as pharmaceuticals or therapeutic agents. Its presence in laboratory workflows supports the advancement of chemical biology and medicinal chemistry by enabling the construction of complex molecular frameworks.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique chemical structure, featuring two carbonyl groups and one hydroxyl group, contributes to its reactivity and polarity. These properties make it highly suitable for chemical reactions involving substitution and condensation processes. Its ability to participate in a variety of synthetic pathways enhances its utility in laboratory settings, where versatility and reactivity are critical. The compound’s chemical profile allows it to be a valuable tool for researchers working on the development of new bioactive substances.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Hydroxy-5-methylisoindoline-1,3-dione is commonly used in biochemical and pharmacological research. It is a staple in academic and research institutions, where it is employed to study the mechanisms of biological activity in various compounds. Its role in the synthesis of bioactive molecules makes it an important component in the pursuit of scientific discovery and innovation within the local scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBioactive Compound Synthesis: This compound is ideal for synthesizing bioactive molecules due to its reactive functional groups and structural versatility, making it a key reagent in pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry Research: Its ability to participate in condensation reactions makes it suitable for peptide synthesis, supporting studies in protein structure and function.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Applications: The compound’s polar nature and reactivity make it a valuable intermediate in the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is frequently used in drug development to explore the chemical pathways of bioactive substances and their biological effects.\u003c\/li\u003e\n\u003cli\u003eChemical Biology Investigations: Its structural complexity supports research into molecular interactions and biochemical mechanisms in living systems.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 173962-59-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: As available from supplier\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactive nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound to minimize exposure. Avoid contact with incompatible materials, and follow standard laboratory safety protocols to ensure safe handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087760863450,"sku":"TCI2510M357142185","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087760896218,"sku":"TCI2510M357142186","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M3571.jpg?v=1771058142"},{"product_id":"tci2510m357242187","title":"TCI M3572 214754-50-4 2-Hydroxy-5-methoxyisoindoline-1,3-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxy-5-methoxyisoindoline-1,3-dione is a chemical compound widely used in research applications within organic and biochemical laboratories. This compound plays a crucial role in the synthesis of complex molecules with specific biological activities, such as enzyme inhibitors and signal transduction modulators. Its unique molecular structure, featuring two hydroxyl groups and one methoxy group, contributes to its versatility in chemical reactions and molecular modifications. Due to its structural complexity, it is often utilized as a building block in the development of new compounds with potential pharmaceutical applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties, including its polarity and solubility in organic solvents, make it a preferred choice for various synthetic processes. Its ability to participate in intricate chemical reactions with high precision is a key factor in its popularity among researchers. Additionally, its stability under controlled conditions allows for reliable use in laboratory settings, provided proper storage and handling protocols are followed. These characteristics make it an essential reagent for advanced chemical synthesis and molecular design.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Hydroxy-5-methoxyisoindoline-1,3-dione is commonly used in pharmaceutical and chemical biology research. Its role in the development of bioactive compounds aligns with the growing focus on drug discovery and molecular innovation in the region. Researchers in Indonesia rely on this compound for its chemical versatility and potential applications in creating new therapeutic agents and biochemical tools.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eEnzyme Inhibition Studies – This compound is ideal for investigating enzyme inhibition due to its structural similarity to natural substrates and its ability to modulate enzymatic activity.\u003c\/li\u003e\n\u003cli\u003eSignal Transduction Modulation – Its molecular structure allows it to interact with cellular signaling pathways, making it useful in studying receptor-ligand interactions and pathway regulation.\u003c\/li\u003e\n\u003cli\u003ePeptide Chemistry Research – The compound’s functional groups enable it to be incorporated into peptide synthesis, supporting the development of bioactive peptides with specific biological functions.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis – Its reactivity and solubility in organic solvents make it a valuable reagent in the synthesis of complex organic molecules and heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Programs – It serves as a starting material for the design and synthesis of novel compounds with potential pharmaceutical 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: 214754-50-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: 50 g\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\u003eThis compound should be stored in a cool, dark place to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from exposure to moisture and air. Due to its sensitivity to light and environmental factors, it should be kept in a controlled environment with minimal temperature fluctuations. Proper ventilation is necessary when handling the compound to ensure safe laboratory practices. Always use appropriate personal protective equipment, such as gloves and safety goggles, to minimize direct contact. Regular monitoring of storage conditions ensures the compound remains viable for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087760928986,"sku":"TCI2510M357242187","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087760961754,"sku":"TCI2510M357242188","price":4342000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M3572.jpg?v=1769143056"},{"product_id":"tci2510n022042881","title":"TCI N0220 100-02-7 4-Nitrophenol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Nitrophenol is a versatile chemical compound widely used in various chemical reactions and the synthesis of complex molecules. As a fundamental building block in chemistry, it plays a crucial role in the development of aromatic and heterocyclic compounds. This compound is commonly found in chemical laboratories, particularly in research involving substitution reactions, structural coupling, and organic compound modification. Its reactivity makes it an essential reagent for the production of more complex chemical products, including pharmaceuticals, industrial chemicals, and synthetic precursors.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 4-Nitrophenol make it a preferred choice for laboratory applications. It exhibits a stable molecular structure and is highly reactive under various chemical conditions. It is soluble in organic solvents such as ethyl acetate and ethanol, but it is not soluble in water. This solubility profile allows it to be easily used in reactions requiring non-aqueous solvents. Additionally, its well-defined melting and boiling points facilitate precise heating and cooling processes in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 4-Nitrophenol is frequently used in chemical research and educational settings. It is a common reagent in academic and industrial research institutions, supporting both teaching and experimental work. Its availability and chemical properties make it an essential component in the chemical supply chain within the country, contributing to the advancement of scientific studies and technological development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis for the preparation of substituted aromatic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eApplied in pharmaceutical research for the development of drug molecules requiring nitro group functionality.\u003c\/li\u003e\n\u003cli\u003eUtilized in analytical chemistry for the detection and quantification of aromatic compounds through spectroscopic methods.\u003c\/li\u003e\n\u003cli\u003eEmployed in environmental studies to analyze the presence of nitrophenolic compounds in water and soil samples.\u003c\/li\u003e\n\u003cli\u003eIncorporated in teaching laboratories for demonstrating substitution reactions and functional group transformations.\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: 100-02-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e4-Nitrophenol should be stored in a cool, dry place away from direct sunlight and incompatible materials. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and maintain chemical integrity. Due to its reactivity, it should be kept away from strong oxidizing agents and strong acids. Proper labeling and safe handling procedures are essential to ensure laboratory safety. Always use appropriate personal protective equipment when handling this compound to minimize exposure risks. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087798022362,"sku":"TCI2510N022042881","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087798055130,"sku":"TCI2510N022042882","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48087798087898,"sku":"TCI2510N022042883","price":3913000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0220.jpg?v=1767129439"},{"product_id":"tci2510n047743224","title":"TCI N0477 24807-55-4 3-Nitro-1,2,4-triazole [Coupling Agent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Nitro-1,2,4-triazole is a chemical compound widely used as a coupling agent in various organic chemical reactions. This versatile reagent plays a crucial role in facilitating the interaction between molecules that would otherwise not react under normal conditions. Its ability to bridge two reactive species makes it an essential tool in synthetic chemistry, particularly in the development of complex molecular structures. This compound is commonly employed in laboratory settings where precise control over chemical reactions is required.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique heterocyclic structure and high reactivity make it a preferred choice for chemists. It exhibits stability under specific reaction conditions and can form bonds with a variety of functional groups, enhancing its utility in different synthetic pathways. Its reactivity allows it to participate in coupling, substitution, and redox reactions, making it a valuable reagent in both academic and industrial research. Due to its versatility, it is often selected for applications requiring high precision and control.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Nitro-1,2,4-triazole is extensively used in organic chemistry, pharmaceutical research, and materials science. It supports the development of new compounds, molecular modifications, and the synthesis of complex chemical structures. Its relevance in these fields underscores its importance as a key reagent in modern chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic chemistry research benefits from this compound's ability to facilitate coupling reactions, enabling the synthesis of complex molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development relies on its reactivity and stability, allowing for the creation of novel drug compounds through targeted chemical modifications.\u003c\/li\u003e\n\u003cli\u003eMaterials science applications utilize its functional group compatibility to design new polymers and advanced chemical materials with tailored properties.\u003c\/li\u003e\n\u003cli\u003eSynthetic pathway optimization leverages its versatility in redox and substitution reactions, enhancing reaction yields and selectivity in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eCompound modification studies benefit from its ability to interact with multiple functional groups, supporting the design of new molecular architectures.\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: 24807-55-4\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\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 and sources of heat. 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. It is important to ensure proper ventilation in the laboratory when working with this material. Avoid contact with incompatible substances, and follow standard laboratory safety protocols to minimize risk. Always store it in a designated chemical storage area to maintain safety and compliance with laboratory regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087817879770,"sku":"TCI2510N047743224","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087817912538,"sku":"TCI2510N047743225","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510N0477.jpg?v=1767129907"},{"product_id":"tci2510p091946421","title":"TCI P0919 771-61-9 Pentafluorophenol","description":"\u003cp\u003e\u003cstrong\u003ePentafluorophenol\u003c\/strong\u003e (CAS 771-61-9) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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