{"title":"Chemistry › Protection and Deprotection","description":"\u003cp\u003eReagen proteksi dan deproteksi gugus fungsi dari TCI untuk sintesis organik dan peptida: Boc, Fmoc, Cbz, TMS, TBDMS, nosyl. Distributor resmi TCI di Indonesia: AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510b558312247","title":"TCI B5583 76280-60-9 3,5-Bis(methoxymethyloxy)benzyl Alcohol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,5-Bis(methoxymethyloxy)benzyl Alcohol is a benzyl alcohol derivative featuring two methoxymethyl (MOM) protecting groups on the aromatic ring, making it a versatile building block for multi-step organic synthesis. This compound is widely utilized in medicinal chemistry, natural product synthesis, and pharmaceutical research where selective deprotection strategies are required. Its protected hydroxyl functionalities and free primary alcohol group provide orthogonal synthetic handles for constructing complex molecular architectures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085888205018,"sku":"TCI2510B558312247","price":1692000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085888237786,"sku":"TCI2510B558312248","price":1692000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5583.jpg?v=1769180198"},{"product_id":"tci2510b558812256","title":"TCI B5588 330793-01-6 N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile organoboron reagent featuring a Boc-protected aniline coupled with a pinacol boronate ester, primarily utilized as a key building block in Suzuki-Miyaura cross-coupling reactions. This compound enables the efficient synthesis of biaryl amine derivatives, which are essential structural motifs in medicinal chemistry and drug discovery programs. Its dual functionality — a protected amine and a reactive boronate — makes it an ideal intermediate for multi-step organic syntheses requiring orthogonal reactivity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085889351898,"sku":"TCI2510B558812256","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085889384666,"sku":"TCI2510B558812257","price":1086000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5588.jpg?v=1768204428"},{"product_id":"tci2510b564712345","title":"TCI B5647 146504-07-6 (1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine (TCI B5647) is a chiral building block widely used in asymmetric synthesis, featuring a Boc-protected primary amine that allows selective functionalization of the secondary amine position. This compound is particularly valuable for the preparation of chiral catalysts, enantioselective ligands, and pharmaceutical intermediates requiring high enantiomeric purity. With its well-defined (1R,2R) stereochemistry, it serves as a reliable scaffold in medicinal chemistry research, drug development, and total synthesis of natural products.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":67556232036570,"sku":"TCI2510B564712345","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5647_09289751-b5e4-4b03-a0f1-c82cd2c355e8.jpg?v=1767862785"},{"product_id":"tci2510b564812347","title":"TCI B5648 180683-64-1 (1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine (CAS 180683-64-1) is a chiral building block widely employed in asymmetric synthesis, featuring a free primary amine and a Boc-protected amine for selective functionalization. This compound serves as a key precursor for the construction of chiral ligands, organocatalysts, and enantiopure intermediates in medicinal chemistry and total synthesis. Manufactured by TCI, it is available in 1 g and 5 g pack sizes to accommodate both exploratory and scale-up laboratory needs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894103258,"sku":"TCI2510B564812347","price":2726000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894136026,"sku":"TCI2510B564812348","price":2726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5648_1444e967-cad8-493a-a142-cf8eb4fe863a.jpg?v=1767862792"},{"product_id":"tci2510b565812355","title":"TCI B5658 129378-52-5 2-(tert-Butyldimethylsilyl)-N,N-dimethyl-1H-imidazole-1-sulfonamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5658, 2-(*tert*-butyldimethylsilyl)-*N,N*-dimethyl-1*H*-imidazole-1-sulfonamide (CAS 129378-52-5), is a heterocyclic building block featuring a TBDMS-protected imidazole core with a dimethylsulfonamide substituent, supplied in 1 g and 5 g packaging. This compound serves as a versatile intermediate in medicinal chemistry and pharmaceutical research, where the TBDMS group enables selective protection during multi-step synthetic routes. Its sulfonamide-imidazole scaffold is particularly valuable for constructing enzyme inhibitors and other biologically active molecular frameworks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894398170,"sku":"TCI2510B565812355","price":2574000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894430938,"sku":"TCI2510B565812356","price":2574000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5658_88becc14-60c2-4481-b8f2-77d7f6b39f52.jpg?v=1767862815"},{"product_id":"tci2510b571512435","title":"TCI B5715 149198-47-0 tert-Butyl (3R,4S)-2-Oxo-4-phenyl-3-[(triethylsilyl)oxy]azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5715, tert-Butyl (3R,4S)-2-Oxo-4-phenyl-3-[(triethylsilyl)oxy]azetidine-1-carboxylate (CAS 149198-47-0), is a stereodefined chiral azetidinone building block supplied in a 1 g packaging, intended exclusively for research and experimental use in pharmaceutical development. This compound serves as a versatile intermediate for synthesizing β-lactam-based drug candidates, enzyme inhibitors, and other nitrogen-containing heterocycles of medicinal interest. Its well-defined (3R,4S) stereochemistry and triethylsilyl-protected hydroxyl group enable precise synthetic transformations, making it a valuable reagent for medicinal chemistry laboratories and drug discovery research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085898920154,"sku":"TCI2510B571512435","price":2020000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5715.jpg?v=1767092699"},{"product_id":"tci2510b573512462","title":"TCI B5735 20898-44-6 tele-Benzyl-Nalpha-(tert-butoxycarbonyl)-L-histidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003etele-Benzyl-Nalpha-(tert-butoxycarbonyl)-L-histidine (Boc-His(Bzl)-OH) is a doubly protected histidine derivative widely used in solid-phase peptide synthesis (SPPS). The Boc group protects the alpha-amino functionality while the benzyl group protects the imidazole side chain, ensuring regioselective coupling and minimizing undesired side reactions during peptide chain assembly. This building block is essential for synthesizing bioactive peptides, protein interaction probes, and peptide-based drug candidates in both academic and pharmaceutical research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085900001498,"sku":"TCI2510B573512462","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085900034266,"sku":"TCI2510B573512463","price":1515000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5735.jpg?v=1768204440"},{"product_id":"tci2510b584412603","title":"TCI B5844 885693-20-9 1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5844 is a Boc-protected tetrahydropyridine boronate ester (CAS 885693-20-9) that serves as a versatile organoboron building block for Suzuki-Miyaura cross-coupling reactions. This compound is widely employed in medicinal chemistry and pharmaceutical research for constructing substituted pyridine derivatives and complex heterocyclic scaffolds. Available in 200 mg and 1 g pack sizes, it is an essential reagent for C–C bond formation in drug discovery and advanced organic synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085906260186,"sku":"TCI2510B584412603","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085906292954,"sku":"TCI2510B584412604","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5844.jpg?v=1768204447"},{"product_id":"tci2510b585712620","title":"TCI B5857 114676-69-6 N-(tert-Butoxycarbonyl)-cis-4-hydroxy-D-proline Methyl Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(tert-Butoxycarbonyl)-cis-4-hydroxy-D-proline Methyl Ester is a chemical compound widely used in organic and biochemical research, particularly in peptide chemistry. This compound serves as a key building block in the synthesis of complex peptides and proteins, playing a crucial role in the development of bioactive molecules. Its structural complexity makes it an essential tool for scientists working on drug discovery and biotechnology applications. In laboratory settings, it is frequently employed to create modified amino acids that are integral to the design of therapeutic agents and functional biomolecules.\u003c\/p\u003e\n\u003cp\u003eThis compound is valued for its chemical stability under controlled conditions and its reactivity with various reagents during synthesis processes. Its ability to participate in specific chemical reactions makes it a preferred choice for researchers aiming to achieve precise modifications in peptide structures. The compound's high reactivity also allows for efficient and reproducible results in synthetic pathways, which is critical in both academic and industrial research environments. Its purity and consistent quality ensure reliable outcomes in experimental procedures, making it a trusted material in advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical research, biotechnology, and biochemical analysis. It is particularly relevant in studies related to protein structure and function, as well as in the development of new therapeutic agents. Its availability in pure form and suitable packaging makes it accessible for a wide range of experimental applications, supporting innovation in both academic and industrial research sectors.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing complex peptides due to its reactivity and structural versatility, enabling the creation of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery: It is used in the development of therapeutic agents, as it allows for the modification of amino acid sequences to enhance drug efficacy.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its role in protein structure studies makes it valuable for understanding molecular interactions and functional properties.\u003c\/li\u003e\n\u003cli\u003eBiotechnology Research: It supports the creation of modified amino acids, which are essential in the development of novel biotechnological applications.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its chemical stability and reactivity make it a key reagent in synthetic pathways for advanced organic chemistry 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: 114676-69-6\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, crystalline or powder depending on packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its high reactivity, it should be handled with care in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper disposal of any unused material in accordance with local safety regulations. Proper storage and handling are essential to ensure the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085906948314,"sku":"TCI2510B585712620","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085906981082,"sku":"TCI2510B585712621","price":733000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5857.jpg?v=1769180240"},{"product_id":"tci2510b588612656","title":"TCI B5886 135042-12-5 cis-N-(tert-Butoxycarbonyl)-4-hydroxy-D-proline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5886 135042-12-5 cis-N-(tert-Butoxycarbonyl)-4-hydroxy-D-proline is a chemical compound widely used in organic and biochemical research. It belongs to the category of peptide chemistry and plays a crucial role in the synthesis of complex peptide molecules. This compound is particularly valuable for its ability to protect hydroxyl groups during chemical reactions, making it essential in controlled peptide synthesis processes. Its presence in Indonesian laboratories highlights its importance in advancing research in biochemistry and pharmaceutical sciences.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique structure, featuring a tert-butoxycarbonyl group, makes it a preferred choice for protecting functional groups during synthesis. This protecting group ensures that the hydroxyl group at the fourth position of D-proline remains chemically inert until the desired reaction step. Its stability and reactivity under controlled conditions allow for precise manipulation in synthetic pathways. These properties make it a reliable reagent for researchers aiming to develop bioactive compounds and advanced pharmaceutical products.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in biochemical and pharmacological research. It is a key component in the synthesis of bioactive peptides, which are essential for drug development and biotechnology applications. Its application extends to both fundamental research and applied projects, supporting innovation in material science and life sciences. Researchers rely on its predictable behavior to achieve consistent results in complex chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for constructing complex peptide structures with specific biological activities, supporting drug development and bioactive material research.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: Its role in protecting hydroxyl groups makes it a valuable tool for studying molecular interactions and enzymatic reactions in biological systems.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: It is used to develop and test new pharmaceutical compounds, particularly those with high biological activity and therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Applications: The compound contributes to the creation of bioactive materials, enhancing the functionality of medical and industrial products.\u003c\/li\u003e\n\u003cli\u003eAcademic and Industrial Research: It supports both basic scientific inquiry and applied research in Indonesian laboratories, driving innovation in multiple scientific fields.\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: 135042-12-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\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. Since it is a chemical reagent, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Proper labeling of storage containers is essential for easy identification and safe handling. Regular monitoring of storage conditions is advised to ensure optimal stability and usability of the compound in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085908390106,"sku":"TCI2510B588612656","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085908422874,"sku":"TCI2510B588612657","price":783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5886.jpg?v=1768204455"},{"product_id":"tci2510b588712658","title":"TCI B5887 87691-27-8 cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5887 is cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline, a derivative of the amino acid proline in which the ring nitrogen has been protected with a tert-butoxycarbonyl (Boc) group and which carries a hydroxyl group at the 4-position in the cis orientation. The compound belongs to the family of peptide chemistry raw materials that are very frequently used as chiral building blocks in stepwise peptide synthesis, both on solid phase and in solution phase. The presence of two functional groups of differing reactivity, namely a free carboxylic acid and a secondary hydroxyl, makes this material a flexible starting point for chemists who wish to construct more elaborate molecular frameworks in a controlled and deliberate manner.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a preferred choice is its stereochemical purity. The compound is the cis isomer of 4-hydroxyproline, that is, the epimer of the naturally occurring trans-configured hydroxyproline, and it therefore gives researchers access to a different folding pattern of the pyrrolidine ring. That difference in hydroxyl orientation has been shown to influence the ring puckering preference and, ultimately, the conformation of the peptide chain built from it. The Boc protecting group adds a further practical advantage, since it masks the ring nitrogen during coupling steps and can be removed under acidic conditions without disturbing the stereocentres of the molecule, allowing the synthetic sequence to be planned with confidence.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a building block of this type is typically found in university research groups, pharmaceutical development units, and contract research facilities that work on peptide synthesis and medicinal chemistry programmes. It is generally ordered in modest quantities for exploratory and method-development work rather than for bulk production, and is handled within a standard synthetic organic chemistry setup equipped with a fume hood, an analytical balance, and facilities for chromatographic purification and structural confirmation of the products obtained.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eStepwise solid-phase peptide synthesis, where the Boc-protected ring nitrogen allows the residue to be introduced into a growing chain without side reactions at the amine, while the free carboxylic acid serves as the coupling handle.\u003c\/li\u003e\n\u003cli\u003eSolution-phase peptide assembly, in which the compound acts as a defined chiral building block that can be coupled, deprotected, and extended through a planned sequence of transformations under conventional organic synthesis conditions.\u003c\/li\u003e\n\u003cli\u003eConformational studies of peptide chains, because the cis orientation of the 4-hydroxyl group alters pyrrolidine ring puckering and therefore lets researchers probe how proline stereochemistry shapes the overall peptide fold.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold construction, where the secondary hydroxyl offers a selective attachment point for further derivatisation while the carboxylic acid remains available for amide bond formation elsewhere in the molecule.\u003c\/li\u003e\n\u003cli\u003ePreparation of non-natural proline analogues and peptidomimetics, since this epimer of natural trans-hydroxyproline gives access to structural variants that cannot be obtained directly from the naturally occurring amino acid.\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: 87691-27-8\u003c\/li\u003e\n\u003cli\u003eChemical name: cis-N-(tert-Butoxycarbonyl)-4-hydroxy-L-proline\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered by the manufacturer for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer's label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated place, away from heat sources, direct sunlight, and moisture, following the storage conditions indicated on the manufacturer's label. Keep the material in its original container or in a chemically compatible, clearly labelled vessel, and close it promptly after each use to limit exposure to atmospheric moisture. Handle the compound in a fume hood using standard laboratory personal protective equipment, including safety glasses, gloves, and a laboratory coat. Weigh and transfer the solid carefully to avoid generating dust, avoid contact with skin and eyes, and wash hands thoroughly after handling. Consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085908455642,"sku":"TCI2510B588712658","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085908488410,"sku":"TCI2510B588712659","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5887.jpg?v=1769180241"},{"product_id":"tci2510b596912751","title":"TCI B5969 161157-50-2 tert-Butyl 7-Oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 7-Oxa-3-azabicyclo[4.1.0]heptane-3-carboxylate is a chemical compound used as a foundational building block in the synthesis of complex molecules. This compound plays a crucial role in organic chemistry laboratories, where it serves as a versatile reagent for constructing intricate molecular structures. Its unique heterocyclic framework enables highly specific chemical reactions, making it an essential tool for researchers aiming to develop new compounds with precise functional properties.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions and its good solubility in organic solvents. These properties make it ideal for use in a wide range of synthetic processes, allowing for greater control and reproducibility in experimental outcomes. The ability to undergo substitution and other targeted reactions further enhances its utility, particularly in applications requiring high accuracy and precision.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely utilized by chemists and scientists for the development of new pharmaceuticals, materials, and organic compounds. Its availability in the local market supports research efforts without the need for imports, ensuring accessibility for academic and industrial research. Its role in advancing chemical innovation is significant, especially in fields where molecular complexity is key to achieving desired outcomes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research and development: This compound is used to synthesize complex drug molecules due to its ability to participate in specific chemical reactions.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry synthesis: Its heterocyclic structure allows for the creation of intricate molecular frameworks, supporting the development of new chemical entities.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications: The compound is employed in the synthesis of advanced materials, where precise molecular design is essential for desired properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry: It serves as a key reagent in teaching and experimental studies, providing students and researchers with a reliable building block.\u003c\/li\u003e\n\u003cli\u003eCompound modification and functionalization: Its reactivity enables the introduction of specific functional groups, facilitating the creation of tailored chemical structures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 161157-50-2\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 manufacturer specifications\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 to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical degradation. In laboratory settings, it is important to handle the compound with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during use. Proper labeling of storage containers is also essential for safe handling and to prevent accidental exposure. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085912420570,"sku":"TCI2510B596912751","price":2297000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085912453338,"sku":"TCI2510B596912752","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5969_3a0fcce5-8112-4d5f-8400-a98c2266c14d.jpg?v=1767864038"},{"product_id":"tci2510b599212776","title":"TCI B5992 864771-44-8 1-(tert-Butoxycarbonyl)-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)indazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)-5-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)indazole is a boronate ester building block featuring a Boc-protected indazole core, designed for Suzuki-Miyaura cross-coupling reactions. It is routinely employed in medicinal chemistry and pharmaceutical research to construct indazole-containing bioactive scaffolds with high efficiency and regioselectivity. This compound serves as a versatile intermediate for synthesizing drug candidates, functional materials, and agrochemicals.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085913567450,"sku":"TCI2510B599212776","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085913600218,"sku":"TCI2510B599212777","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5992.jpg?v=1769144660"},{"product_id":"tci2510b601312804","title":"TCI B6013 183062-96-6 2-[1-(tert-Butoxycarbonyl)azetidin-3-yl]acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6013 is 2-[1-(tert-Butoxycarbonyl)azetidin-3-yl]acetic Acid, a building block that combines a Boc-protected azetidine ring with an acetic acid side chain at the 3-position. This structural simplicity is precisely its strength, because it presents two clearly separated points of reactivity: a free carboxylic acid group ready for coupling, and a secondary amine nitrogen kept hidden behind a protecting group. In medicinal chemistry laboratories, compounds of this type are frequently used as linkers or core fragments when researchers want to introduce a small saturated framework into a molecule under development.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material sought after is how readily it fits into stepwise synthetic strategies. The carboxyl group can be activated with common peptide coupling reagents, such as the carbodiimide class or uronium salts, then reacted with an amine to form a stable amide bond. The Boc group is subsequently removed with acid, liberating a free azetidine that can be alkylated, acylated, or sulfonylated according to the design. Orthogonal sequences of this kind make it straightforward to prepare a series of related compounds in a short period of time, which is why the reagent earns a place on the shelf of groups running iterative analogue campaigns.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically encountered in university research groups, institutional synthetic chemistry facilities, and industrial R\u0026amp;D units engaged in preparing small-molecule intermediates. It is normally ordered in small quantities suited to exploratory work rather than bulk production, since the strained saturated ring contributes a compact three-dimensional element to candidate structures. Handling follows the same organic synthesis routines already established in those laboratories for moisture-sensitive protected intermediates.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAmide bond formation: the free carboxylic acid couples cleanly with amines using standard peptide coupling reagents, making this reagent a direct entry point into amide-linked analogue series.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry fragment work: the compact Boc-protected azetidine serves as a saturated core fragment when researchers need to introduce a small three-dimensional framework into a developing molecule.\u003c\/li\u003e\n\u003cli\u003eLinker construction: the two clearly separated reactive handles at opposite ends of the molecule let chemists join two larger structural segments through a short, rigid connecting unit.\u003c\/li\u003e\n\u003cli\u003eOrthogonal deprotection sequences: acid-mediated Boc removal liberates the secondary azetidine nitrogen for subsequent alkylation, acylation, or sulfonylation without disturbing amide bonds formed earlier in the route.\u003c\/li\u003e\n\u003cli\u003eParallel analogue synthesis: the predictable two-step coupling and deprotection sequence supports rapid preparation of compound series for structure-activity relationship studies within a short working period.\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: 183062-96-6\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-[1-(tert-Butoxycarbonyl)azetidin-3-yl]acetic Acid\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale packaging; please confirm the current catalogue options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area away from direct sunlight, moisture, and sources of ignition, following the conditions printed on the manufacturer label. Keep the material in its original supplier container or in a compatible sealed glass vessel, and avoid prolonged exposure to open air during weighing. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, and keep it separated from strong acids and strong bases, since acidic conditions will remove the Boc protecting group. Close the container promptly after use and label any aliquots clearly. Consult the manufacturer safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085914812634,"sku":"TCI2510B601312804","price":858000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085914845402,"sku":"TCI2510B601312805","price":858000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6013_c2386273-763e-48c3-9410-efd125264916.jpg?v=1767864198"},{"product_id":"tci2510b602612824","title":"TCI B6026 1073354-70-7 1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole is a complex organic compound widely used in laboratory settings for its unique reactivity and structural versatility. This reagent plays a crucial role in organic synthesis, particularly in the development of heterocyclic compounds and boron-containing molecules. Its application spans various synthetic pathways, making it an essential tool for researchers working in advanced chemical processes. Due to its functional groups, it is especially valuable in metal-catalyzed reactions, contributing to the efficiency and selectivity of synthetic protocols.\u003c\/p\u003e\n\u003cp\u003eThe compound's structure includes both a boron-containing group and a tert-butoxycarbonyl moiety, which together provide stability and reactivity in a range of chemical environments. These properties make it a preferred choice for synthetic chemists seeking reliable and controllable reagents. The presence of the boron group allows it to participate in important coupling reactions, such as Suzuki-Miyaura and Kumada-Corriu, which are fundamental in the synthesis of complex organic molecules. Its chemical specificity ensures that it can be tailored for various synthetic applications without unwanted side reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and researchers in the fields of organic synthesis, pharmacology, and materials science. Its role in producing precise and controlled chemical outcomes makes it a valuable asset in both academic and industrial research settings. Its application is particularly relevant in projects requiring high levels of chemical accuracy and synthetic efficiency.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: This compound is ideal for creating complex heterocyclic structures due to its boron functionality and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: It is used in the development of new drug compounds, especially those involving boron-containing moieties.\u003c\/li\u003e\n\u003cli\u003eMaterials science: It contributes to the synthesis of advanced materials with specific chemical properties and structural features.\u003c\/li\u003e\n\u003cli\u003eMetal-catalyzed coupling reactions: Its ability to participate in Suzuki-Miyaura and Kumada-Corriu reactions makes it suitable for these specialized synthetic methods.\u003c\/li\u003e\n\u003cli\u003eCustom compound preparation: It is a key reagent in the synthesis of tailored organic compounds for specific research needs.\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: 1073354-70-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from 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 humidity, which could affect its stability. Due to its reactivity, it should be handled with appropriate laboratory safety measures, including the use of personal protective equipment. Proper ventilation is essential when working with this material to minimize inhalation risks. It is important to follow standard chemical handling protocols to ensure the safety of laboratory personnel and the integrity of the compound during storage and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085915631834,"sku":"TCI2510B602612824","price":1212000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085915664602,"sku":"TCI2510B602612825","price":1212000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6026.jpg?v=1769180251"},{"product_id":"tci2510b605712863","title":"TCI B6057 50654-94-9 (tert-Butoxycarbonyl)-D-histidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(tert-Butoxycarbonyl)-D-histidine (Boc-D-His-OH) is a protected D-histidine derivative with a Boc group attached to its amino terminus, serving as an essential building block for peptide synthesis. This high-purity reagent from TCI is commonly used in solid-phase and solution-phase peptide synthesis to introduce D-histidine residues into peptide chains, particularly for studies on stereochemical effects on biological activity. It finds broad application in peptide chemistry research, including the development of modified peptides, cyclic peptides, and peptide-based drug candidates with enhanced enzymatic stability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085917204698,"sku":"TCI2510B605712863","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085917237466,"sku":"TCI2510B605712864","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6057.jpg?v=1768204481"},{"product_id":"tci2510b607412881","title":"TCI B6074 51871-62-6 N-(tert-Butoxycarbonyl)-L-beta-homophenylalanine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6074 N-(tert-Butoxycarbonyl)-L-beta-homophenylalanine (CAS 51871-62-6) is a Boc-protected beta-homologated phenylalanine derivative widely used as a building block in peptide synthesis. Its beta-homo backbone confers enhanced proteolytic stability and distinct conformational properties to synthetic peptides, making it valuable in chemical biology research and peptide drug development. Available in 250mg and 1g packaging, this high-purity reagent is ideal for both solid-phase and solution-phase peptide chemistry applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085917827290,"sku":"TCI2510B607412881","price":2574000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085917860058,"sku":"TCI2510B607412882","price":2574000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6074.jpg?v=1771058403"},{"product_id":"tci2510b608612898","title":"TCI B6086 120728-10-1 N-tert-Butoxycarbonyl-1-aminocyclobutanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6086, N-tert-Butoxycarbonyl-1-aminocyclobutanecarboxylic Acid (CAS 120728-10-1), is a Boc-protected non-proteinogenic amino acid widely employed as a conformationally constrained building block in peptide synthesis. It is commonly utilized in medicinal chemistry research, particularly in the development of modified peptides, peptidomimetics, and cyclic peptide scaffolds for structure-activity relationship studies. This compound supports applications in chemical biology, including enzyme inhibitor design and protein-protein interaction research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085919203546,"sku":"TCI2510B608612898","price":858000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085919236314,"sku":"TCI2510B608612899","price":858000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6086.jpg?v=1768204484"},{"product_id":"tci2510b608812900","title":"TCI B6088 155976-13-9 N-(tert-Butoxycarbonyl)-L-cyclopropylglycine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI's N-(tert-Butoxycarbonyl)-L-cyclopropylglycine (Boc-L-Cpg) is a Boc-protected unnatural amino acid widely employed as a key building block in peptide synthesis. The tert-butoxycarbonyl group provides temporary N-terminal protection during solid-phase or solution-phase peptide coupling, while the cyclopropyl side chain introduces conformational rigidity into the peptide backbone. This compound is particularly valuable in chemical biology research for designing metabolically stable, constrained peptides used in enzyme inhibitor development, structure-activity relationship studies, and protein-protein interaction modulation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085919269082,"sku":"TCI2510B608812900","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085919301850,"sku":"TCI2510B608812901","price":1515000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6088.jpg?v=1768204483"},{"product_id":"tci2510b609112904","title":"TCI B6091 59379-02-1 (+\/-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-1-(tert-Butoxycarbonyl)pyrrolidine-3-carboxaldehyde is a heterocyclic building block built around a five-membered pyrrolidine ring in which the ring nitrogen is already protected by a tert-butoxycarbonyl (Boc) group, while an aldehyde group is attached at the third position. The combination of these two functional groups makes it a highly useful synthetic intermediate in organic chemistry and medicinal chemistry laboratories. Its primary role is to supply a saturated cyclic amine framework that is ready to be extended or modified through its carbonyl group, while the ring nitrogen remains \"locked\" so that it does not participate in reactions and interfere with the synthetic route the researcher is designing.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a frequent choice lies in the compatibility of its two functional groups. The aldehyde group is electrophilic and readily directed into a range of classical transformations such as reductive amination, Wittig and Horner-Wadsworth-Emmons reactions, addition of organometallic reagents, aldol condensation, and oxidation to the corresponding carboxylic acid. The Boc group, meanwhile, is orthogonal to many basic and nucleophilic conditions, yet can be removed cleanly under acidic conditions to liberate the free secondary amine when the synthetic sequence calls for it. This pairing allows chemists to plan multi-step routes with predictable protection and deprotection points.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in university research groups, pharmaceutical and medicinal chemistry laboratories, and contract research settings that build small-molecule libraries. It is generally handled on a small scale at the bench, weighed under controlled conditions, and carried directly into coupling or chain-extension steps. Because the saturated nitrogen heterocycle motif appears often in drug discovery scaffolds, this building block supports both academic method development and applied compound synthesis programmes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eReductive amination: the free aldehyde reacts with primary or secondary amines to form an imine that is reduced in situ, giving substituted aminomethyl pyrrolidines without disturbing the Boc-protected ring nitrogen.\u003c\/li\u003e\n\u003cli\u003eWittig and Horner-Wadsworth-Emmons olefination: the carbonyl group serves as the electrophilic partner for phosphorus ylides and phosphonate carbanions, allowing controlled carbon chain extension and introduction of alkene functionality.\u003c\/li\u003e\n\u003cli\u003eOrganometallic addition: Grignard and organolithium reagents add across the aldehyde to produce secondary alcohols, giving a straightforward route to branched substituents on the pyrrolidine three-position.\u003c\/li\u003e\n\u003cli\u003eAldol condensation and related carbonyl chemistry: the aldehyde participates in classical enolate chemistry, letting researchers assemble more complex carbon frameworks from a compact, readily available heterocyclic starting point.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry scaffold preparation: after acidic Boc removal the resulting secondary amine can be acylated, alkylated, or coupled further, which suits the iterative construction of small-molecule libraries for screening.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eProduct code: B6091\u003c\/li\u003e\n\u003cli\u003eCAS number: 59379-02-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep the container tightly closed and follow the storage conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, in a cool, dry, and well-ventilated place away from direct sunlight, heat sources, and incompatible chemicals, following the conditions stated on the manufacturer's label and safety data sheet. Amber glass or the supplied original packaging is suitable, and containers should be resealed promptly after each use to limit exposure to air and moisture, since aldehydes are susceptible to oxidation. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, avoid inhalation of vapours and contact with skin or eyes, and allow refrigerated material to reach room temperature before opening to prevent condensation. Dispose of residues and contaminated materials in accordance with institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085919531226,"sku":"TCI2510B609112904","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085919563994,"sku":"TCI2510B609112905","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6091_5d396dc4-9b94-4b3a-83e7-3a82f028514d.jpg?v=1767864510"},{"product_id":"tci2510b610712926","title":"TCI B6107 162558-25-0 (S)-3-(tert-Butoxycarbonylamino)-2-[(9H-fluoren-9-ylmethoxy)carbonylamino]propionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound is a doubly protected amino acid derivative featuring Fmoc and Boc orthogonal protecting groups, widely used as a versatile building block in solid-phase peptide synthesis (SPPS). It enables selective deprotection and stepwise modification of diaminopropionic acid residues in complex peptide chains. Common applications include the development of modified peptides, bioactive peptidomimetics, and molecular probes for biochemical and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085920383194,"sku":"TCI2510B610712926","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085920415962,"sku":"TCI2510B610712927","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6107.jpg?v=1768815983"},{"product_id":"tci2510b614412965","title":"TCI B6144 83673-98-7 2-[(tert-Butoxycarbonyl)amino]thiazole-4-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-[(tert-Butoxycarbonyl)amino]thiazole-4-carboxylic Acid is a Boc-protected thiazole amino acid derivative that serves as a versatile heterocyclic building block in organic synthesis. The Boc protecting group safeguards the amine functionality during synthetic transformations and can be readily removed under mild acidic conditions, enabling efficient incorporation of the thiazole scaffold into larger molecular frameworks. This compound is widely utilized in medicinal chemistry research for drug discovery programs, particularly in the development of bioactive thiazole-containing molecules with antimicrobial, anticancer, and anti-inflammatory properties.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085921857754,"sku":"TCI2510B614412965","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085921890522,"sku":"TCI2510B614412966","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6144_30b774b8-53f0-43f4-a45f-a11d6bda12b0.jpg?v=1767864684"},{"product_id":"tci2510b614812972","title":"TCI B6148 54613-99-9 Boc-Lys(2-Cl-Z)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBoc-Lys(2-Cl-Z)-OH is a doubly protected lysine derivative widely employed as a building block in solid-phase peptide synthesis (SPPS). The Boc group protects the α-amino terminus while the 2-Cl-Z group safeguards the ε-amino side chain, enabling selective orthogonal deprotection during peptide chain elongation. This high-purity TCI reagent is suitable for the synthesis of branched peptides, cyclic peptides, and peptide conjugates in pharmaceutical and biochemical research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085922119898,"sku":"TCI2510B614812972","price":858000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085922152666,"sku":"TCI2510B614812973","price":858000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6148.jpg?v=1768204485"},{"product_id":"tci2510b617313004","title":"TCI B6173 89336-46-9 2-[2-[(tert-Butoxycarbonyl)amino]thiazol-4-yl]acetic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-[2-[(tert-Butoxycarbonyl)amino]thiazol-4-yl]acetic Acid is a complex organic compound widely used in laboratory settings for the synthesis of heterocyclic compounds. This chemical serves as a building block in the development of molecules with thiazole rings, which are known for their biological activity. Its role in chemical research is critical, especially in the design of pharmaceuticals and industrial chemicals. Due to its structural versatility, it is a valuable tool for chemists aiming to create functional molecules with specific properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structure, featuring a tert-butoxycarbonyl (Boc) group and a thiazole ring, makes it a preferred choice in synthetic chemistry. The Boc group provides stability and facilitates selective deprotection during synthesis, allowing for precise control over reaction pathways. The thiazole ring contributes to the molecule's reactivity, enabling substitution reactions and functional group modifications. These properties make it an essential reagent for researchers working on complex molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical research, organic chemistry, and industrial chemical development. It is particularly relevant in academic and research institutions where scientists are working on drug discovery and chemical innovation. Its application spans various fields, supporting both fundamental and applied research efforts in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound for the synthesis of bioactive molecules due to its thiazole ring structure, which is often found in drug molecules.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry laboratories use it as a versatile building block for creating complex heterocyclic compounds through functional group modifications.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development benefits from its reactivity and stability, allowing for the design of specialized chemical products with tailored properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions employ it in drug discovery projects to explore new therapeutic agents with potential biological activity.\u003c\/li\u003e\n\u003cli\u003eChemical synthesis laboratories rely on its Boc group for controlled deprotection steps, enabling precise synthetic strategies in multi-step reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 89336-46-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from 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 tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with incompatible substances such as strong acids or bases. Proper personal protective equipment, including gloves and safety goggles, should always be worn when handling this material. Regular inspection of storage conditions ensures the compound remains stable and suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085923496154,"sku":"TCI2510B617313004","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085923528922,"sku":"TCI2510B617313005","price":783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6173_3c32a927-9099-41fd-a930-c06aeda91824.jpg?v=1767864801"},{"product_id":"tci2510b622813057","title":"TCI B6228 112275-50-0 1-(tert-Butoxycarbonyl)homopiperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)homopiperazine is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. It plays a crucial role in organic chemistry laboratories, where it serves as a versatile intermediate for constructing complex molecular structures. This compound is particularly valuable in reactions that require controlled functional group modifications, making it an essential tool for researchers working with heterocyclic systems. Its stability and predictable reactivity make it a reliable choice for a variety of synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique chemical properties, including its ability to undergo substitution reactions and efficient Boc group cleavage, make it a preferred choice in synthetic chemistry. Its molecular structure allows for effective interactions with various reagents, enabling the synthesis of a wide range of heterocyclic derivatives. The compound’s controlled reactivity ensures that it can be used safely in laboratory settings without compromising the integrity of the reaction. These characteristics make it a go-to material for chemists seeking precision and reliability in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-(tert-Butoxycarbonyl)homopiperazine is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds. It is frequently found in experiments involving functional group modifications and ring formation. Its stability and compatibility with various reagents make it a valuable resource for both academic and industrial research settings in Indonesia. Its application is broad, supporting a wide array of chemical processes that require precise control over molecular structure.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its ability to undergo substitution and Boc group cleavage reactions.\u003c\/li\u003e\n\u003cli\u003eFunctional group modification in complex molecule construction, offering versatility in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eRing formation reactions where controlled reactivity and structural stability are essential for successful synthesis.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the development of pharmaceutical compounds requiring heterocyclic scaffolds.\u003c\/li\u003e\n\u003cli\u003eAcademic and industrial research applications in Indonesia, supporting advanced chemical investigations and innovation.\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: 112275-50-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline or powder form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated laboratory setting to ensure safety. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment such as gloves and safety goggles. The compound is generally stable under standard laboratory conditions but should be kept away from incompatible substances. Proper labeling and storage are essential to ensure safe handling and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085925462234,"sku":"TCI2510B622813057","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085925495002,"sku":"TCI2510B622813058","price":808000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6228_7c77eed6-dd9e-487f-b722-d98d2b0deae2.jpg?v=1767864959"},{"product_id":"tci2510b634313200","title":"TCI B6343 51077-14-6 (S)-1-(tert-Butoxycarbonyl)azetidine-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6343, also known as (S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic Acid, is a chiral building block essential in asymmetric synthesis. This compound is widely used in laboratories to create complex molecules with specific stereochemistry. Its azetidine ring structure, modified with a tert-butoxycarbonyl group, makes it a versatile tool for chemists aiming to control the spatial arrangement of atoms in organic molecules. This material plays a crucial role in the development of pharmaceuticals and bioactive compounds, where precise stereochemistry is required for biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability under controlled conditions and its solubility in various organic solvents. These properties make it an ideal candidate for use in a wide range of synthetic reactions. Its ability to act as a precursor in asymmetric reactions allows for the selective formation of stereoisomers, which is essential in drug development and fine chemical synthesis. The compound's reliability and reproducibility in laboratory settings make it a preferred choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to pharmacology, organic chemistry, and biochemistry. It is particularly valuable in the development of new drugs and in the study of molecular mechanisms. Many research institutions and universities in Indonesia rely on this material to advance their scientific work and contribute to the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound enables the selective formation of stereoisomers, crucial for drug development and bioactive compound creation.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its role as a chiral building block, allowing for the synthesis of complex molecules with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drugs, as its stereochemistry can influence biological activity and pharmacological properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often incorporate this material to investigate molecular interactions and structural requirements for biological function.\u003c\/li\u003e\n\u003cli\u003eIt is also used in the synthesis of fine chemicals, where precise stereochemical control is essential for industrial and research 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: 51077-14-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral 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 stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organic nature, it is best stored in airtight glass or plastic containers that are resistant to chemical degradation. Proper labeling and storage conditions are essential to ensure the integrity of the material. In laboratory settings, it should be handled with care, using appropriate personal protective equipment. Regular monitoring of storage conditions is advised to maintain the quality and effectiveness of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085931851994,"sku":"TCI2510B634313200","price":2676000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6343.jpg?v=1767093516"},{"product_id":"tci2510b636213230","title":"TCI B6362 13726-76-6 Boc-Arg-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6362, Boc-Arg-OH (CAS 13726-76-6), is an Nα-Boc-protected arginine derivative intended for peptide chemistry applications. The tert-butoxycarbonyl group masks the α-amino function so that coupling reactions proceed selectively, and it can subsequently be removed under acidic conditions within a Boc-based synthetic strategy. Arginine residues contribute the guanidine side chain that underpins molecular recognition, charge-driven interactions, and the design of cell-penetrating peptides. AMI Scientific offers this TCI reagent in 1 g and 5 g pack sizes for solid-phase and solution-phase peptide synthesis in research laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eImaizumi et al. (2000). Anterograde axonal transport of Boc-Arg-Val-Arg-Arg-MCA hydrolyzing enzyme in rat sciatic nerves: cleavage occurs between basic residues. \u003cem\u003eBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0167-4838(99)00239-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0167-4838(99)00239-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085932933338,"sku":"TCI2510B636213230","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085932966106,"sku":"TCI2510B636213231","price":910000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6362.jpg?v=1769180264"},{"product_id":"tci2510b641513300","title":"TCI B6415 1000931-72-5 4-[(tert-Butoxycarbonyl)amino]-1-cubanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6415 4-[(tert-Butoxycarbonyl)amino]-1-cubanecarboxylic Acid (CAS 1000931-72-5) is a non-heterocyclic building block built on the rigid cubane framework, carrying a free carboxylic acid and a Boc-protected amine on opposite positions. This bifunctional design lets researchers introduce the cubane motif into peptides and small molecules through familiar amide coupling chemistry without an extra protection step. Cubane derivatives are widely studied as benzene bioisosteres, offering a rigid three-dimensional alternative that preserves substituent vectors. AMI Scientific offers this TCI product in a 100 mg pack suited to exploratory synthesis, with full quality details available in the manufacturer's Certificate of Analysis and Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eIHLE et al. (1996). ChemInform Abstract: Preparation of 4‐Alkyl‐2‐(N‐(tert‐butoxycarbonyl)amino)pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2‐(N‐(tert‐ Butoxycarbonyl)amino)‐4‐picoline.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199646162\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199646162\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085938929882,"sku":"TCI2510B641513300","price":7395000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6415.jpg?v=1767093637"},{"product_id":"tci2510b643713325","title":"TCI B6437 115951-16-1 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6437 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid (CAS 115951-16-1) is a Boc-protected cyclic amino acid in which the amino and carboxyl groups share a quaternary carbon. Its rigid cyclohexane framework makes it valuable for designing conformationally constrained peptides and peptide analogues. The pre-installed Boc group saves a protection step and can be removed under well-established acidic conditions. Store the solid tightly sealed in a cool, dry place away from strong acids, and refer to the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBadland et al. (2010). An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2010.04.049\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2010.04.049\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939912922,"sku":"TCI2510B643713325","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939945690,"sku":"TCI2510B643713326","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6437_d1e882c4-5446-4e40-b77f-bf0c8053c12b.jpg?v=1767865775"},{"product_id":"tci2510b648613389","title":"TCI B6486 4530-18-1 Boc-DL-Phe-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6486, Boc-DL-Phe-OH (CAS 4530-18-1), is racemic phenylalanine protected at the amino group with a tert-butoxycarbonyl group. The Boc group is stable to basic and nucleophilic conditions yet readily removed under acidic treatment, making this a dependable building block for solution- and solid-phase peptide synthesis. Its racemic nature makes it particularly cost-effective for coupling method development, chiral analysis reference work, and advanced teaching laboratories. AMI Scientific offers this TCI product in 25 g and 100 g pack sizes, to be stored cool, dry, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRodriguez et al. (1990). A general route to “carba” peptide bond replacements: Unequivocal synthesis of Boc--Phe-ψ(CH2-CH2)--Ala-OH and Boc--Phe-ψ(CH2-CH2)--Ala-OH.. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(00)97829-8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(00)97829-8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHayashi et al. (2014). Development of potent antagonists for formyl peptide receptor 1 based on Boc-Phe-d-Leu-Phe-d-Leu-Phe-OH. \u003cem\u003eBioorganic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bmc.2014.06.048\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bmc.2014.06.048\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKarle et al. (2002). Infinite pleated β-sheet formed by the β-hairpin Boc-β-Phe-β-Phe- d -Pro-Gly-β-Phe-β-Phe-OMe. \u003cem\u003eProceedings of the National Academy of Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1073\/pnas.022616499\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1073\/pnas.022616499\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":48085942960346,"sku":"TCI2510B648613389","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085942993114,"sku":"TCI2510B648613390","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6486.jpg?v=1769144627"},{"product_id":"tci2510b649413397","title":"TCI B6494 3601-66-9 Boc-DL-Phg-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6494, Boc-DL-Phg-OH (CAS 3601-66-9), is racemic phenylglycine protected with a tert-butoxycarbonyl group at the amino position. With the aryl ring attached directly to the alpha carbon, phenylglycine offers greater conformational rigidity than phenylalanine and a well-documented tendency toward racemisation during coupling. This makes the DL form especially useful as a reference standard for chiral chromatography method development, coupling condition evaluation, and kinetic resolution studies, in addition to routine peptide synthesis. AMI Scientific supplies this TCI product in a 25 g pack, to be kept cool, dry, tightly closed, and away from strong acid vapours.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085943255258,"sku":"TCI2510B649413397","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6494.jpg?v=1768204508"},{"product_id":"tci2510b660513559","title":"TCI B6605 62129-44-6 Boc-Phe(4-I)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6605 Boc-Phe(4-I)-OH is a Boc-protected 4-iodophenylalanine derivative widely used as a building block in peptide chemistry. The acid-labile Boc group allows controlled deprotection during chain assembly, while the para-iodo substituent serves as a versatile handle for palladium-catalysed cross-coupling. Researchers commonly employ it to incorporate unnatural amino acid residues and to enable late-stage diversification of peptide scaffolds. AMI Scientific supplies this TCI reagent in 1 g and 5 g pack sizes for peptide synthesis, medicinal chemistry, and chemical biology laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRodriguez et al. (1990). A general route to “carba” peptide bond replacements: Unequivocal synthesis of Boc--Phe-ψ(CH2-CH2)--Ala-OH and Boc--Phe-ψ(CH2-CH2)--Ala-OH.. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(00)97829-8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(00)97829-8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHayashi et al. (2014). Development of potent antagonists for formyl peptide receptor 1 based on Boc-Phe-d-Leu-Phe-d-Leu-Phe-OH. \u003cem\u003eBioorganic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.bmc.2014.06.048\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.bmc.2014.06.048\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKarle et al. (2002). Infinite pleated β-sheet formed by the β-hairpin Boc-β-Phe-β-Phe- d -Pro-Gly-β-Phe-β-Phe-OMe. \u003cem\u003eProceedings of the National Academy of Sciences\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1073\/pnas.022616499\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1073\/pnas.022616499\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085949907162,"sku":"TCI2510B660513559","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085949939930,"sku":"TCI2510B660513560","price":808000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6605.jpg?v=1768204515"},{"product_id":"tci2510b660713563","title":"TCI B6607 1035325-28-0 5-[(tert-Butoxycarbonyl)amino]bicyclo[3.1.1]heptane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6607 is 5-[(tert-butoxycarbonyl)amino]bicyclo[3.1.1]heptane-1-carboxylic acid, a rigid saturated building block with orthogonal carboxylic acid and Boc-protected amine handles. The bicyclo[3.1.1]heptane core is widely investigated as a three-dimensional bioisostere for meta-substituted benzene rings. Replacing flat aromatic rings with such saturated cages can improve solubility and reduce metabolic liability in lead optimisation programmes. AMI Scientific supplies this TCI building block in a 100 mg pack size for synthetic and medicinal chemistry laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaenziger et al. (2015). ChemInform Abstract: Development Approaches Towards a 4‐Spiro Cyclopropane Proline Scaffold (S)‐5‐(tert‐Butoxycarbonyl)‐5‐azaspiro[2.4]heptane‐6‐carboxylic Acid. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.201536288\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.201536288\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMatković (2024). 4-(2-(5-(2-(tert-Butoxycarbonyl)hydrazinecarbonyl)-2-methylthiophen-3-yl)cyclopent-1-enyl)-5-methylthiophene-2-carboxylic Acid. \u003cem\u003eMolbank\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m1760\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m1760\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085950071002,"sku":"TCI2510B660713563","price":6587000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6607.jpg?v=1767094012"},{"product_id":"tci2510b660913565","title":"TCI B6609 1050886-56-0 4-[(tert-Butoxycarbonyl)amino]bicyclo[2.1.1]hexane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6609 is 4-[(tert-butoxycarbonyl)amino]bicyclo[2.1.1]hexane-1-carboxylic acid, a compact and rigid saturated building block. It carries orthogonal carboxylic acid and Boc-protected amine handles on opposite bridgehead positions, allowing stepwise elaboration. The bicyclo[2.1.1]hexane core is actively studied as a three-dimensional bioisostere for ortho- and meta-substituted benzene rings in drug discovery. AMI Scientific supplies this TCI building block in a 100 mg pack size for medicinal chemistry and advanced synthesis laboratories.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWang et al. (2013). A scalable synthesis of (1R,3S,5R)-2-(tert-butoxycarbonyl)-2-azabicyclo[3.1.0]hexane-3-carboxylic acid. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2013.09.114\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2013.09.114\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBakonyi et al. (2013). Synthesis of All Four Stereoisomers of 3-(tert-Butoxycarbonyl)-3-azabicyclo[3.1.0]hexane-2-carboxylic Acid. \u003cem\u003eThe Journal of Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jo4013282\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jo4013282\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085950136538,"sku":"TCI2510B660913565","price":4821000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6609.jpg?v=1767094020"},{"product_id":"tci2510b661113567","title":"TCI B6611 848821-61-4 (2S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl]pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6611, with the CAS number 848821-61-4, is a complex chiral compound that plays a vital role in asymmetric synthesis. This material is specifically designed for use in chemical laboratories where precise control over stereochemistry is essential. Its unique molecular structure allows it to act as a chiral reagent, facilitating the synthesis of enantiomerically pure compounds. In the context of modern organic chemistry, this compound is indispensable for achieving high enantioselectivity in various reactions.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes of TCI B6611 is its highly complex chiral architecture, which enables it to interact selectively with specific substrates. This property makes it an ideal choice for researchers aiming to develop efficient and targeted synthetic pathways. The compound’s stability under certain conditions further enhances its utility, allowing for consistent performance in laboratory settings. Its ability to direct chemical reactions with high specificity is a major factor in its popularity among chemists working in the field of asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI B6611 is widely used in organic chemistry research, particularly in the development of bioactive compounds and pharmaceuticals. It is a preferred tool for academic and industrial researchers who require precise control over stereochemical outcomes. Its application extends to various areas of chemical synthesis, making it a valuable asset in both academic and applied research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in organic chemistry laboratories for the production of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules and pharmaceuticals requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eResearch in chiral catalysis and ligand design for advanced synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eInvestigation of reaction mechanisms involving chiral reagents and substrates.\u003c\/li\u003e\n\u003cli\u003eSupport for academic and industrial research in drug discovery and chemical innovation.\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: 848821-61-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, 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. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its complex molecular structure, it is important to handle it with care to avoid contamination or degradation. Laboratory personnel should ensure proper ventilation when working with this material. Always follow standard safety protocols for handling chiral compounds, including the use of personal protective equipment. The compound is not known to be hazardous under normal storage conditions, but it is advisable to follow general chemical safety guidelines to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085950202074,"sku":"TCI2510B661113567","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6611.jpg?v=1767094028"},{"product_id":"tci2510b695913839","title":"TCI B6959 111331-82-9 3-[(tert-Butoxycarbonyl)amino]benzoic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6959 is 3-[(tert-butoxycarbonyl)amino]benzoic acid, a Boc-protected aminobenzoic acid building block widely used in peptide and medicinal chemistry. Its free carboxylic acid is ready for standard amide coupling, while the Boc group keeps the aromatic amine masked until acidic deprotection. This orthogonality makes it convenient for stepwise assembly of linkers, scaffolds, and analogue libraries. AMI Scientific offers 5 g and 25 g pack sizes; keep the material dry, cool, and away from strong acids and heat.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eIHLE et al. (1996). ChemInform Abstract: Preparation of 4‐Alkyl‐2‐(N‐(tert‐butoxycarbonyl)amino)pyridines by Alkylation, Nucleophilic Addition, and Acylation of 2‐(N‐(tert‐ Butoxycarbonyl)amino)‐4‐picoline.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199646162\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199646162\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":48085962424538,"sku":"TCI2510B695913839","price":984000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085962457306,"sku":"TCI2510B695913840","price":984000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6959.jpg?v=1767094429"},{"product_id":"tci2510c157316204","title":"TCI C1573 15263-20-4 N-(tert-Butoxycarbonyloxy)phthalimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1573 N-(tert-Butoxycarbonyloxy)phthalimide is a mild reagent for introducing the tert-butoxycarbonyl protecting group onto amines. It releases N-hydroxyphthalimide as a readily separated by-product, which makes work-up straightforward on sensitive substrates. The reagent is widely used in peptide synthesis and medicinal chemistry where orthogonal protection and low racemisation risk are essential. AMI Scientific supplies this TCI reagent in 1 g and 5 g packs, with dry storage recommended to preserve activity.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2009). Gold(I)-catalyzed Tandem Cyclization of 3-(tert-Butoxycarbonyloxy)-1,6-enynes. \u003cem\u003eBulletin of the Korean Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.5012\/bkcs.2009.30.6.1239\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.5012\/bkcs.2009.30.6.1239\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eIto et al. (2000). 4-(tert-Butoxycarbonyloxy)benzylp-toluenesulfonates as acid amplifiers applicable to chemically amplified photoresists. \u003cem\u003eMacromolecular Chemistry and Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/(sici)1521-3935(20000101)201:1\u0026lt;132::aid-macp132\u0026gt;3.0.co;2-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/(sici)1521-3935(20000101)201:1\u0026lt;132::aid-macp132\u0026gt;3.0.co;2-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGRAPSAS et al. (1994). ChemInform Abstract: N‐(tert‐Butoxycarbonyloxy)‐5‐norbornene‐endo‐2,3‐dicarboximide, a Reagent for the Regioselective Introduction of the tert‐Butoxycarbonyl (BOC) Protective Group at Unhindered Amines: Application to Aminoglycoside Chemistry.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199436241\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199436241\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086078619866,"sku":"TCI2510C157316204","price":1060000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086078652634,"sku":"TCI2510C157316205","price":1060000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1573.jpg?v=1767097169"},{"product_id":"tci2510c175716420","title":"TCI C1757 245365-64-4 N-Benzyloxycarbonyl-2-nitrobenzenesulfonamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-Benzyloxycarbonyl-2-nitrobenzenesulfonamide is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound is known for its ability to participate in substitution reactions and molecular coupling processes, making it essential in the synthesis of complex organic compounds. Its stable structure allows it to react selectively with various reagents such as amines, acids, and bases. In laboratory applications, it is commonly used in research related to the development of bioactive compounds and pharmaceuticals. Due to its reactivity and specificity, this compound is a preferred choice for experiments requiring precision and controlled chemical reactions. Its versatility makes it a valuable tool for both academic and industrial research in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086087106778,"sku":"TCI2510C175716420","price":2600000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086087139546,"sku":"TCI2510C175716421","price":2600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1757.jpg?v=1769144442"},{"product_id":"tci2510c253517325","title":"TCI C2535 73821-95-1 4-Cyclohexyl N-(tert-Butoxycarbonyl)-L-aspartate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Cyclohexyl N-(tert-Butoxycarbonyl)-L-aspartate is a specialized chemical compound used in laboratory settings for advanced chemical and biochemical experiments, particularly in peptide chemistry. This compound plays a crucial role in the synthesis of peptides and other complex molecules, offering researchers a versatile tool for molecular modification and structural analysis. Its unique molecular structure enables it to participate in targeted chemical reactions, making it an essential component in various synthetic processes.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions, which facilitates efficient synthesis and reaction processes. Its solid form and reactivity under specific conditions make it a preferred choice for laboratories requiring precise and controllable chemical interactions. Additionally, its ability to undergo specific chemical transformations enhances its utility in both organic and biological research applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in biochemical, pharmacological, and organic chemistry research. It is a common reagent in experiments that require compounds with specific structural characteristics. Many research institutions and universities rely on this material for experiments involving molecular synthesis and modification. Its availability and reliability make it a go-to choice for researchers seeking high-quality chemical reagents.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for peptide synthesis due to its ability to participate in controlled chemical reactions, enabling the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its reactivity and stability make it suitable for organic chemistry experiments requiring precise molecular modifications and reactions.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: It is used in biochemical studies to investigate molecular interactions and structural changes in biological systems.\u003c\/li\u003e\n\u003cli\u003eDrug Development: The compound's structural versatility supports its use in drug development, where specific molecular configurations are essential.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: Its capacity for targeted chemical transformations makes it valuable in studies focused on molecular modification 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: 73821-95-1\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 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 light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Proper labeling of storage containers is essential for safety and traceability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation in the workspace. Regular monitoring of storage conditions helps maintain the compound's integrity and effectiveness for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086131179738,"sku":"TCI2510C253517325","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086131212506,"sku":"TCI2510C253517326","price":783000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2535.jpg?v=1769144381"},{"product_id":"tci2510d151621280","title":"TCI D1516 62365-34-8 1-(Dimethylethylsilyl)imidazole [Dimethylethylsilylating Agent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(Dimethylethylsilyl)imidazole is a chemical compound widely used as a silylating agent in various organic chemical reactions. It plays a crucial role in the synthesis of heterocyclic compounds, particularly in the formation of silicon bonds within complex molecular structures. In laboratory settings, this compound functions as a reagent that facilitates molecular structure modification, especially in substitution and silylation reactions. Its reactivity makes it an essential tool in organic chemistry research and the synthesis of pharmacological compounds.\u003c\/p\u003e\n\u003cp\u003eThis compound is valued for its high efficiency in forming silicon bonds and its ability to produce high-purity products. Its chemical stability under specific conditions, combined with its reactivity towards water and oxidizers, makes it a versatile reagent. The compound's effectiveness in silylation reactions, where it acts as a key intermediate, ensures its reliability in both academic and industrial research. Its chemical properties make it a preferred choice for applications requiring precision and accuracy.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-(Dimethylethylsilyl)imidazole is commonly used in organic chemistry research, particularly in pharmaceutical and material science fields. Its role in the synthesis of heterocyclic compounds makes it relevant for studies involving drug development and advanced material synthesis. The compound is essential for researchers aiming to achieve high-quality results in complex chemical processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its efficient silylating properties and ability to form stable silicon bonds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drugs, as it aids in the modification of molecular structures with high precision.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications where silicon-based bonds are required for the creation of advanced polymers and composites.\u003c\/li\u003e\n\u003cli\u003eChemical modification of complex molecules through substitution reactions, leveraging its reactivity and selectivity.\u003c\/li\u003e\n\u003cli\u003eResearch in synthetic chemistry requiring high-purity products, as it consistently delivers reliable and reproducible results.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 62365-34-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and oxidizing agents\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 oxidizing agents to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent exposure to air and humidity. Due to its reactivity towards water and oxidizers, it should be handled with care in a well-ventilated laboratory setting. Protective gloves and safety goggles should be worn during handling to ensure personal safety. Avoid contact with skin and eyes, and ensure proper disposal of any unused material in accordance with local regulations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086444671194,"sku":"TCI2510D151621280","price":1716000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086444703962,"sku":"TCI2510D151621281","price":1716000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1516.jpg?v=1767103171"},{"product_id":"tci2510d159621403","title":"TCI D1596 81452-04-2 1-(Dimethylisopropylsilyl)imidazole [Dimethylisopropylsilylating Agent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(Dimethylisopropylsilyl)imidazole is a chemical compound widely used as a silylating agent in various organic reactions. It plays a crucial role in laboratories, particularly in the synthesis of heterocyclic compounds. This reagent is essential for introducing silyl groups into molecules, enabling the formation of silicon-oxygen bonds and facilitating substitution reactions. Its presence in chemical laboratories is vital for the development of complex molecular structures with high precision. The compound is commonly utilized in both academic and industrial research settings where controlled chemical modifications are required.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make 1-(Dimethylisopropylsilyl)imidazole a preferred choice is its stability under specific conditions and its ability to act as an electron donor. These characteristics allow it to participate effectively in a wide range of chemical reactions without undergoing unwanted side reactions. Additionally, its complex chemical structure enables it to interact with various substrates, making it a versatile tool in modern synthetic chemistry. The reactivity and compatibility with different reaction conditions further enhance its utility in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1-(Dimethylisopropylsilyl)imidazole is frequently used in organic chemistry research, especially in the synthesis of heterocyclic compounds and molecular modifications. It is a common choice for researchers in pharmacology, food chemistry, and material science due to its reliability and effectiveness. Its availability and consistent performance make it an essential component in many chemical processes conducted in Indonesian research institutions.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds where silyl groups are needed for structural modification.\u003c\/li\u003e\n\u003cli\u003ePreparation of silicon-oxygen bonds in complex molecule construction for pharmaceutical and material applications.\u003c\/li\u003e\n\u003cli\u003eSubstitution reactions requiring a stable and reactive silylating agent for controlled chemical transformations.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmacology for drug development involving molecular modifications and functional group introduction.\u003c\/li\u003e\n\u003cli\u003eDevelopment of advanced materials where precise chemical modifications and cross-linking are essential.\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: 81452-04-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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 stability and reactivity. It is recommended to use airtight containers made of glass or inert materials to prevent contamination and degradation. Laboratory personnel should handle the material with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its chemical nature, it should be kept away from incompatible substances like strong acids or bases. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications. Proper labeling and storage practices are essential to ensure safety and compliance with laboratory protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086449619162,"sku":"TCI2510D159621403","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086449651930,"sku":"TCI2510D159621404","price":2020000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1596.jpg?v=1767103310"},{"product_id":"tci2510d370124060","title":"TCI D3701 347838-12-4 3,4-Difluoro-2,5-bis(trimethylsilyl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3701 (CAS 347838-12-4), 3,4-Difluoro-2,5-bis(trimethylsilyl)thiophene, is a fluorinated thiophene compound carrying two fluorine atoms at the 3- and 4-positions of the ring and two trimethylsilyl groups at the 2- and 5-positions. In the laboratory, this compound serves as a specialised fluorinated building block for the synthesis of functional organic materials, particularly organic semiconductors, conjugated polymers, and small molecules intended for electronic devices. The presence of silyl groups at both ends of the ring makes it a protected, activation-ready precursor, allowing researchers to direct subsequent reactions precisely at the alpha positions of the thiophene ring.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that lead researchers to select this material lie in the combination of the electronic effect of fluorine and the dual function of the trimethylsilyl groups. The fluorine atoms lower the orbital energy levels of the ring, thereby increasing electron-accepting character and improving the oxidative stability of the resulting material — an important consideration in the design of both n-type materials and donor–acceptor copolymers. The trimethylsilyl groups act simultaneously as protecting groups and as directing groups: they keep the alpha positions free from unwanted reactions and can be replaced selectively through desilylation reactions, giving synthetic chemists controlled access to those positions when the sequence calls for it.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used within university and institutional research groups working on organic electronics and polymer materials, as well as in synthetic chemistry laboratories developing fluorinated heterocyclic intermediates. It is generally handled at the bench scale in multi-step synthesis routes, where a well-defined and regiochemically protected thiophene core shortens the path to a target monomer or small molecule. Because it is a specialised research chemical rather than a routine reagent, it is normally ordered per project and stored under controlled conditions between synthesis campaigns.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic semiconductor synthesis — the fluorinated, silyl-capped thiophene core provides a low-lying orbital building block suited to charge-transport materials for electronic device research.\u003c\/li\u003e\n\u003cli\u003eConjugated polymer preparation — the protected alpha positions allow controlled activation and coupling, giving researchers regiochemical certainty when building thiophene-containing polymer backbones.\u003c\/li\u003e\n\u003cli\u003eDonor–acceptor copolymer design — fluorine substitution at the 3- and 4-positions strengthens electron-accepting character, making the compound useful for tuning donor–acceptor electronic structures.\u003c\/li\u003e\n\u003cli\u003en-Type material development — the reduced orbital energy levels imparted by the two fluorine atoms support the design of electron-transporting organic materials in device-oriented studies.\u003c\/li\u003e\n\u003cli\u003eSmall-molecule electronic material synthesis — as a bifunctional protected precursor, it enables stepwise construction of well-defined small molecules for organic electronic device fabrication.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 347838-12-4\u003c\/li\u003e\n\u003cli\u003eChemical name: 3,4-Difluoro-2,5-bis(trimethylsilyl)thiophene\u003c\/li\u003e\n\u003cli\u003eCatalogue reference: D3701\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the pack size options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the manufacturer's original container under the conditions stated on the product label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original, tightly closed manufacturer container, kept in a cool, dry, and well-ventilated chemical store away from heat sources, ignition sources, and direct sunlight. As an organosilicon building block, it is best kept sealed and protected from moisture and air to preserve the integrity of the trimethylsilyl groups; inert-atmosphere storage and handling are advisable where the intended synthesis demands it. Handle inside a fume hood using safety glasses, chemical-resistant gloves, and a laboratory coat, and avoid inhalation of vapours or contact with skin and eyes. Keep the container clearly labelled, transfer with clean and dry glassware, and dispose of residues and contaminated materials as chemical waste in accordance with institutional procedures. Always consult the manufacturer's Safety Data Sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086633906394,"sku":"TCI2510D370124060","price":7597000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3701.jpg?v=1767106418"},{"product_id":"tci2510d384324231","title":"TCI D3843 848821-58-9 (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI D3843, with CAS number 848821-58-9, is a chiral reagent known as (S)-(-)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether. This compound plays a crucial role in asymmetric synthesis, where it acts as a chiral catalyst or ligand to facilitate the formation of chiral molecules. In laboratory settings, it is widely used to produce enantiomerically pure compounds, which are essential in pharmaceutical and biochemical research. Its ability to control stereochemistry makes it a valuable tool for researchers aiming to develop new drugs and bioactive compounds.\u003c\/p\u003e\n\u003cp\u003eThis reagent is preferred due to its high chiral purity and structural complexity, which enhance its reactivity in various synthetic conditions. The presence of the trimethylsilyl group contributes to its stability and solubility, making it suitable for a wide range of reaction environments. Additionally, its well-defined stereochemistry ensures consistent results in asymmetric reactions, which is vital for reproducibility in scientific research. These properties make it an ideal choice for applications requiring precise control over the stereochemical outcome of chemical reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists, pharmacologists, and biochemists working in academic and research institutions. It supports the development of new pharmaceuticals and bioactive compounds by enabling the synthesis of molecules with specific stereochemical configurations. Its application is particularly relevant in drug discovery and the creation of compounds with targeted biological activities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for producing enantiomerically pure compounds due to its chiral structure and catalytic properties.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research to develop drugs with specific stereochemistry for enhanced biological activity and reduced side effects.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies to synthesize chiral molecules with potential therapeutic applications in medicine and biotechnology.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over reaction stereochemistry for academic and industrial research.\u003c\/li\u003e\n\u003cli\u003eLigand development in asymmetric catalysis to improve reaction efficiency and selectivity in complex chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 848821-58-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply practices\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on formulation and supplier specifications\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\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 contamination and degradation. In laboratory settings, proper personal protective equipment, such as gloves and safety goggles, should be worn when handling this material. Due to its chiral nature and potential reactivity, it should be kept in a secure location to prevent accidental exposure. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications in chemical synthesis and research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086640754906,"sku":"TCI2510D384324231","price":3811000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086640787674,"sku":"TCI2510D384324232","price":3811000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3843.jpg?v=1767106652"},{"product_id":"tci2510d386724272","title":"TCI D3867 943757-71-9 (R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-alpha,alpha-Diphenyl-2-pyrrolidinemethanol Trimethylsilyl Ether is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific optical configurations. This compound plays a crucial role in chemical reactions where stereochemical control is essential. It functions as a chiral catalyst or ligand, enabling the selective formation of enantiomers. Its unique molecular structure allows for precise interactions with other reactants, making it a valuable tool in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound’s optically active nature and molecular complexity make it a preferred choice for researchers aiming at high stereocontrol. Its ability to influence reaction pathways and yield desired stereoisomers is critical in the development of pharmaceuticals and organic compounds. The trimethylsilyl ether group enhances its solubility and reactivity, contributing to its effectiveness in various synthetic protocols. These properties ensure its reliability in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new chemical materials. Researchers in educational and research institutions rely on it for experiments requiring precise molecular structure control. Its availability in small packaging makes it accessible for laboratory-scale applications, supporting innovation in chemical synthesis and drug discovery.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis for producing chiral compounds with specific optical activity, due to its ability to control stereochemistry in reaction pathways.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research where precise molecular structure control is required, as it enables selective formation of enantiomers.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and bioactive compounds, as its chiral nature is essential for creating molecules with desired biological activity.\u003c\/li\u003e\n\u003cli\u003eLigand-based catalytic reactions, where its chiral properties enhance reaction selectivity and efficiency in complex chemical transformations.\u003c\/li\u003e\n\u003cli\u003eSynthetic chemistry experiments requiring high stereocontrol, as it provides a reliable and consistent reagent for achieving desired stereochemical outcomes.\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: 943757-71-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in small laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chiral nature, it is important to maintain the integrity of the compound during handling to avoid contamination or degradation. Proper labeling and safe storage practices are essential to ensure its effectiveness in laboratory applications. Always use appropriate personal protective equipment when handling this material to ensure safety in the laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086642360538,"sku":"TCI2510D386724272","price":3307000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086642393306,"sku":"TCI2510D386724273","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3867.jpg?v=1767106701"},{"product_id":"tci2510d394124377","title":"TCI D3941 207742-50-5 3,3'-Dibromo-5,5'-bis(trimethylsilyl)-2,2'-bithiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3941 3,3'-Dibromo-5,5'-bis(trimethylsilyl)-2,2'-bithiophene is a bithiophene building block developed specifically for materials chemistry, and in particular for the preparation of polymer semiconductors and conjugated macromolecules. The molecule is built around a core of two thiophene rings joined at the 2 and 2' positions, carrying bromine atoms at the 3 and 3' positions and trimethylsilyl groups at the 5 and 5' positions. This carefully arranged substitution pattern makes it a highly valuable starting material for researchers who need to construct fused aromatic frameworks with genuinely controlled reaction sites.\u003c\/p\u003e\n\u003cp\u003eThe property that leads researchers to select this compound is the presence of two distinct classes of functional group, each playing a different role. The bromine atoms at the 3 and 3' positions act as reactive handles for metal-catalysed cross-coupling reactions and for halogen–metal exchange, the key step in forming bridges between the rings. The trimethylsilyl groups at the 5 and 5' positions, meanwhile, work simultaneously as protecting groups and as blocking groups on the most reactive alpha positions, preventing reactions from occurring at unwanted sites. These silyl groups can then be removed or replaced at a later stage, giving a level of regiochemical control that is otherwise difficult to achieve.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic electronics and functional polymer materials. It suits synthetic work where a conjugated backbone must be assembled step by step, with the position of each new bond defined in advance. Because the reactive and protected sites are already differentiated within the molecule, research teams can plan multi-step routes with fewer separation problems and a more predictable outcome at each stage.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer semiconductor synthesis: the differentiated bromine and trimethylsilyl positions allow a conjugated backbone to be extended in a defined direction rather than randomly.\u003c\/li\u003e\n\u003cli\u003eMetal-catalysed cross-coupling reactions: the 3,3'-bromine atoms serve as ready reactive handles for coupling chemistry, giving controlled bridge formation between thiophene rings.\u003c\/li\u003e\n\u003cli\u003eHalogen–metal exchange chemistry: the bromine substituents can be converted into organometallic intermediates, opening access to further functionalisation at precisely those two positions.\u003c\/li\u003e\n\u003cli\u003eFused aromatic framework construction: the fixed substitution pattern lets researchers build fused ring systems where every new bond is formed at a predetermined site.\u003c\/li\u003e\n\u003cli\u003eConjugated macromolecule research: the removable silyl groups protect the reactive alpha positions during assembly, then free them again for later modification of the macromolecule.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 207742-50-5\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Polymer\/Macromolecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: TCI D3941\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes offered by TCI for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer's label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container, in a cool, dry and well-ventilated area away from heat, direct sunlight, moisture and incompatible chemicals, following the conditions stated on the manufacturer's label and safety data sheet. Organosilicon and organohalogen building blocks of this type are best kept sealed to limit exposure to air and humidity. Handle in a fume hood using gloves, safety glasses and a laboratory coat, avoid inhalation of dust or vapour, and keep containers clearly labelled. Consult the safety data sheet before use and dispose of residues and contaminated materials through approved chemical waste channels.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086646718682,"sku":"TCI2510D394124377","price":3307000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086646751450,"sku":"TCI2510D394124378","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3941.jpg?v=1768817978"},{"product_id":"tci2510d435724932","title":"TCI D4357 185990-03-8 2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound plays a crucial role in laboratory settings where complex molecular structures need to be synthesized with high precision. Its unique chemical structure enables it to participate in various reaction mechanisms, making it an essential tool for chemists working on advanced synthetic pathways. It is particularly valuable in applications that require controlled reactivity and compatibility with a wide range of substrates.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under specific conditions, combined with its reactivity in targeted chemical environments, makes it a preferred choice in modern synthetic chemistry. Its molecular framework, containing both boron and silicon atoms, provides versatility in reaction types such as coupling and substitution. These properties allow it to be used in a variety of synthetic strategies, including those involving boron-based reagents. Its ability to maintain structural integrity during synthesis processes ensures consistent results, which is vital for research and development in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in academic and research institutions. It supports the development of new synthetic techniques and contributes to the advancement of chemical knowledge. Its application in molecular modification and complex compound synthesis makes it a key component in the toolkit of chemists working on innovative projects. The compound's relevance in both educational and industrial research contexts underscores its importance in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent's ability to form stable C-X bonds, enabling the creation of complex molecular structures with high efficiency.\u003c\/li\u003e\n\u003cli\u003eBoron-based reaction systems often require reagents with specific reactivity profiles, and this compound provides the necessary chemical versatility for such processes.\u003c\/li\u003e\n\u003cli\u003eMolecular modification projects rely on its capacity to undergo substitution and coupling reactions, making it ideal for functional group transformations.\u003c\/li\u003e\n\u003cli\u003eResearch in synthetic chemistry frequently involves the use of non-halogen bond-forming agents, and this compound is a reliable choice for such investigations.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis in Indonesian laboratories utilizes this reagent to develop new methodologies and improve existing synthetic routes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 185990-03-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid 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 chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure, which can affect its reactivity. In laboratory settings, it should be handled with appropriate personal protective equipment to ensure safety. Due to its chemical nature, it should be stored separately from incompatible substances to avoid potential reactions. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory applications. Proper labeling and storage practices are essential to maintain the integrity of the compound and ensure safe handling in research environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086688465114,"sku":"TCI2510D435724932","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086688497882,"sku":"TCI2510D435724933","price":1868000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4357.jpg?v=1769141984"},{"product_id":"tci2510d599727005","title":"TCI D5997 40733-27-5 3'-O-[tert-Butyl(dimethyl)silyl]thymidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3'-O-[tert-Butyl(dimethyl)silyl]thymidine is a chemical compound widely used in chemical biology, particularly in the study of nucleic acids. It belongs to the class of nucleotide analogs, which are structurally similar to DNA and RNA but with specific chemical modifications. This compound is commonly employed in laboratory settings as a building block for the synthesis of more complex molecules, including nucleotide analogs and enzyme inhibitors. Its unique structure allows it to be a versatile tool in various biochemical and pharmaceutical research applications.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and resistance to unwanted reactions make it a preferred choice for synthetic processes. The tert-Butyl(dimethyl)silyl group at the 3' position acts as a protective group, preventing premature chemical reactions and ensuring the compound remains intact during synthesis. This property enhances its utility in controlled laboratory environments where precision and reliability are essential. Additionally, its solubility in organic solvents facilitates its use in purification and reaction processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in biochemistry, pharmacology, and genetics research. Researchers in educational institutions and research centers rely on it to study enzyme mechanisms, synthesize complex molecules, and explore potential therapeutic applications. Its role in advancing scientific understanding in these fields is significant and well-established.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiochemical synthesis of nucleotide analogs due to its stable structure and reactivity control.\u003c\/li\u003e\n\u003cli\u003eEnzyme inhibition studies as a model compound for understanding nucleotide interactions.\u003c\/li\u003e\n\u003cli\u003eGenetic research for designing modified nucleic acids and DNA\/RNA analogs.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development to create novel therapeutic agents targeting nucleic acid pathways.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry for use in nucleic acid hybridization and molecular probe 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: 40733-27-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Nucleic Acid 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 powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its organic nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid exposure to incompatible substances and ensure proper disposal according to local regulations. Regular monitoring of storage conditions is advised to ensure the compound remains suitable for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086787096794,"sku":"TCI2510D599727005","price":2271000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086787129562,"sku":"TCI2510D599727006","price":2271000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5997.jpg?v=1769142156"},{"product_id":"tci2510d601027020","title":"TCI D6010 147081-29-6 (S)-1-Boc-3-methylpiperazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-1-Boc-3-methylpiperazine is a chiral building block widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in the development of pharmaceuticals and organic chemicals, enabling the creation of enantiomerically pure substances. Its importance lies in its ability to influence the stereochemistry of target molecules, which is essential for achieving desired pharmacological effects. As a key component in synthetic pathways, it supports the design of compounds with high specificity and efficacy in various therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability and controlled reactivity, making it a reliable choice for complex synthetic processes. Its Boc (tert-butoxycarbonyl) group provides additional functionality, allowing for versatile chemical modifications. The chiral nature of (S)-1-Boc-3-methylpiperazine ensures that it can be used to generate enantiomerically pure products, which are critical in drug development. This property makes it a preferred material for researchers aiming to produce molecules with specific stereochemical configurations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, (S)-1-Boc-3-methylpiperazine is commonly used in pharmacology, organic chemistry, and biochemistry research. It supports the development of new drugs and the modification of existing chemical compounds for medical and industrial applications. Its availability from reliable suppliers ensures that researchers can access this essential material for their experimental needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating enantiomerically pure compounds, which are essential for drug development and therapeutic applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It supports the synthesis of active pharmaceutical ingredients with specific stereochemical configurations, enhancing drug efficacy and selectivity.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its reactivity and stability make it a valuable tool for exploring new synthetic pathways and chemical transformations.\u003c\/li\u003e\n\u003cli\u003eBiochemical Investigations: It is used in the development of bioactive molecules that interact with specific biological targets, aiding in the study of molecular mechanisms.\u003c\/li\u003e\n\u003cli\u003eDrug Modification Projects: Its Boc group allows for controlled chemical modifications, facilitating the design of new therapeutic agents with improved 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: 147081-29-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its reactivity. Proper labeling of storage containers is essential to ensure safe handling and prevent cross-contamination. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize exposure. Regular monitoring of storage conditions is advised to ensure the material remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086787588314,"sku":"TCI2510D601027020","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086787621082,"sku":"TCI2510D601027021","price":1263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6010.jpg?v=1767109571"},{"product_id":"tci2510d617327217","title":"TCI D6173 81379-52-4 Fmoc-His(Boc)-OH","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6173 81379-52-4 Fmoc-His(Boc)-OH is a chemical compound widely utilized in peptide chemistry within laboratory settings. It serves as a key building block in the synthesis of peptides, particularly in the sequential coupling of amino acids. This compound plays a vital role in the formation of complex peptide chains, making it essential for biochemical and pharmacological research. Its application extends to the development of bioactive molecules, contributing to advancements in drug discovery and molecular biology. Due to its controlled reactivity and stability, it is a reliable choice for researchers working on intricate synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stable chemical structure and controlled reactivity, which are critical for precise peptide synthesis. The Fmoc group can be selectively removed using specific reagents, allowing for the sequential attachment of amino acids. This feature ensures accuracy and efficiency in the synthesis process, making it a preferred option for laboratories requiring high precision. Its reliability in maintaining structural integrity during chemical reactions enhances its utility in various synthetic applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI D6173 81379-52-4 Fmoc-His(Boc)-OH is extensively used in chemical and molecular biology research. It is commonly found in academic institutions and research centers that focus on peptide structure and function. Its availability in the local market supports ongoing scientific investigations, enabling researchers to conduct experiments with confidence and consistency.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for solid-phase peptide synthesis due to its controlled reactivity and stability, allowing for precise amino acid coupling.\u003c\/li\u003e\n\u003cli\u003eBiochemical Research: It is frequently used in studies involving protein structure and function, supporting investigations into enzyme mechanisms and receptor interactions.\u003c\/li\u003e\n\u003cli\u003ePharmacological Studies: The compound aids in the development of bioactive peptides, contributing to drug discovery and therapeutic research.\u003c\/li\u003e\n\u003cli\u003eMolecular Biology Experiments: It is essential for constructing custom peptides used in gene expression studies and molecular interaction analysis.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: Widely utilized in Indonesian universities and research institutes for teaching and experimental work in peptide chemistry.\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: 81379-52-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Peptide Chemistry\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, 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. Proper labeling of storage containers is essential to ensure safe handling and prevent accidental exposure. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize risk. Regular monitoring of storage conditions ensures the compound remains chemically stable and suitable for use in research applications. Maintaining a clean and organized workspace further supports safe and efficient handling of this material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086794436826,"sku":"TCI2510D617327217","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086794469594,"sku":"TCI2510D617327218","price":960000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6173.jpg?v=1768205170"},{"product_id":"tci2510d618427235","title":"TCI D6184 303752-38-7 3-[(tert-Butoxycarbonyl)amino]bicyclo[1.1.1]pentane-1-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-[(tert-Butoxycarbonyl)amino]bicyclo[1.1.1]pentane-1-carboxylic Acid is a complex organic compound widely used in synthetic chemistry applications. This compound serves as a building block in the synthesis of various organic molecules, particularly those requiring controlled chemical transformations. Its unique molecular structure, featuring a bicyclo framework and a protected amino group, makes it a versatile reagent in laboratory settings. It is especially valuable in the development of new compounds with complex structures, supporting research in pharmaceutical and organic chemistry fields.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity make it a preferred choice for synthetic chemists. The tert-butoxycarbonyl (Boc) group provides chemical stability, allowing for controlled reactions under various conditions. This feature is crucial for maintaining the integrity of the molecule during synthesis. Additionally, its reactivity enables participation in substitution, hydrolysis, and organic solvent reactions, making it suitable for a wide range of synthetic processes. These properties ensure its reliability 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 development of new compounds with complex structures. Its role in pharmaceutical research is significant, as it supports the synthesis of compounds with potential therapeutic applications. The compound's ability to participate in multiple chemical reactions makes it an essential tool for researchers aiming to achieve high precision and control in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its bicyclo framework and protected amino group.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds where controlled chemical transformations are required.\u003c\/li\u003e\n\u003cli\u003eResearch in synthetic chemistry requiring reactivity and stability in various reaction conditions.\u003c\/li\u003e\n\u003cli\u003ePreparation of complex molecules in academic and industrial research settings.\u003c\/li\u003e\n\u003cli\u003eUse in chemical processes involving substitution, hydrolysis, and organic solvent reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 303752-38-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated laboratory setting. Avoid contact with strong acids or bases to prevent unwanted chemical reactions. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. The compound is best stored in airtight containers made of materials that are chemically inert to ensure long-term stability and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086795026650,"sku":"TCI2510D618427235","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086795059418,"sku":"TCI2510D618427236","price":2121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6184.jpg?v=1767109862"}],"url":"https:\/\/amiscientific.com\/en\/collections\/chemistry-protection-and-deprotection.oembed?page=19","provider":"AMI Scientific","version":"1.0","type":"link"}