{"title":"Chemicals by Class › 4-Membered Cyclic Compounds","description":"\u003cp\u003eSenyawa siklik beranggota empat dari TCI: oxetane, azetidine, siklobutana, beta-laktam — penting dalam drug discovery sebagai bioisostere dan building block konformasional. Distributor resmi TCI di Indonesia: AMI Scientific.\u003c\/p\u003e","products":[{"product_id":"tci2510b564112333","title":"TCI B5641 2402-83-7 3,3-Bis(bromomethyl)oxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,3-Bis(bromomethyl)oxetane is a heterocyclic oxetane derivative that serves as a versatile building block in organic synthesis, featuring two reactive bromomethyl groups suitable for nucleophilic substitution reactions. This compound is widely used as a monomer in the synthesis of energetic polyoxetane polymers, such as poly(BAMO), which find applications in propellants and high-energy material research. It also functions as a crosslinking agent and synthetic intermediate in pharmaceutical research for developing drug candidates incorporating oxetane ring systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085893611738,"sku":"TCI2510B564112333","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085893644506,"sku":"TCI2510B564112334","price":1036000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5641_93385d61-f870-4f47-a28a-8ce6f19230fe.jpg?v=1767862747"},{"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":"tci2510b580112542","title":"TCI B5801 141699-58-3 tert-Butyl 3-[(Methylsulfonyl)oxy]azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-[(Methylsulfonyl)oxy]azetidine-1-carboxylate is a chemical compound widely used in organic synthesis reactions, particularly in the formation of heterocyclic compounds. This material serves as a key building block in the development of complex molecular structures, making it essential for researchers in both academic and industrial settings. Its role in laboratory environments is critical, as it enables the synthesis of compounds with potential applications in pharmaceuticals, materials science, and chemical engineering. Due to its structural versatility and functional groups, it is a fundamental reagent for chemists aiming to explore new synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique molecular structure, featuring both ester and sulfonate functional groups, makes it highly reactive and suitable for various chemical transformations. Its stability under controlled reaction conditions allows for precise manipulation in synthetic processes, ensuring reproducibility and reliability in experimental outcomes. The presence of the tert-butyl group further enhances its reactivity, enabling it to participate in ring-opening and substitution reactions. These properties make it a preferred choice for researchers requiring high chemical specificity and control in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists for the development of new drugs, organic compound modifications, and the study of advanced materials. Its relevance in heterocyclic synthesis and its adaptability to different reaction conditions make it a valuable tool for scientific innovation in the region. The compound’s versatility and reliability in laboratory applications continue to drive its use in diverse research fields.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its functional groups and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a building block for complex drug molecules.\u003c\/li\u003e\n\u003cli\u003eModification of organic compounds through ring-opening and substitution reactions.\u003c\/li\u003e\n\u003cli\u003eResearch in materials science for the creation of advanced chemical materials.\u003c\/li\u003e\n\u003cli\u003eInvestigation of biological activities in drug discovery and chemical biology studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 141699-58-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to heat and incompatible substances to prevent unwanted reactions. Proper storage and handling are essential to maintain the compound’s integrity and effectiveness in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085904031962,"sku":"TCI2510B580112542","price":1136000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085904064730,"sku":"TCI2510B580112543","price":1136000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5801_6db46852-483a-4c64-9e5c-d41e819d6f08.jpg?v=1767863386"},{"product_id":"tci2510b586712625","title":"TCI B5867 610791-05-4 1-tert-Butyl 3-Methyl Azetidine-1,3-dicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-tert-Butyl 3-Methyl Azetidine-1,3-dicarboxylate is a chemical compound widely used in laboratory settings, particularly in chemical biology and peptide chemistry. This compound plays a crucial role in the synthesis of complex organic molecules and biological molecules, making it an essential tool for researchers working on advanced chemical and biochemical projects. Its unique molecular structure enables precise chemical reactions, which are vital for the development of new compounds with specific biological activities. This compound is commonly found in research laboratories where high accuracy and controlled chemical processes are required.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under certain conditions, which simplifies handling, storage, and manipulation in the lab. Its specific molecular structure allows for controlled and precise chemical reactions, making it ideal for applications requiring high precision. This stability and reactivity make it a preferred choice for scientists aiming to achieve consistent results in their experiments. Additionally, its compatibility with various synthetic methods enhances its utility in diverse research contexts.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in chemical and biochemical research, especially in the development of new compounds or molecular modifications. Due to its limited availability in the local market, it is often imported or sourced from trusted international suppliers. Its application in peptide synthesis and drug development makes it a critical component in modern laboratory research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePeptide Synthesis: This compound is ideal for synthesizing peptides due to its structural compatibility with peptide bond formation, enabling the creation of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eDrug Development: Its use in the development of new pharmaceuticals is due to its ability to participate in controlled chemical reactions that mimic biological processes.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: The compound is widely used in organic chemistry for the synthesis of complex organic molecules with specific functional groups.\u003c\/li\u003e\n\u003cli\u003eMolecular Modification Studies: It is used to modify existing molecules, enhancing their biological activity or chemical properties for further research.\u003c\/li\u003e\n\u003cli\u003eBiochemical Analysis: Its stability and reactivity make it suitable for use in biochemical assays where precise chemical interactions are required.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 610791-05-4\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 or crystalline, depending on the batch\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 made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize exposure to any potential fumes. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085907112154,"sku":"TCI2510B586712625","price":1212000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085907144922,"sku":"TCI2510B586712626","price":1212000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5867.jpg?v=1771058058"},{"product_id":"tci2510b601112800","title":"TCI B6011 934664-41-2 tert-Butyl 3-Methyleneazetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6011 is tert-Butyl 3-Methyleneazetidine-1-carboxylate, a four-membered heterocyclic building block that carries an exocyclic double bond at the 3-position and a Boc protecting group on its nitrogen atom. The azetidine ring belongs to a class of scaffolds increasingly used in modern medicinal chemistry because of its compact size, rich sp3 character, and ability to present functional groups in a well-defined spatial orientation. In the laboratory, this material serves as a starting point for constructing a wide range of 3-substituted azetidines that were previously difficult to access through conventional synthetic routes.\u003c\/p\u003e\n\u003cp\u003eThe principal appeal of this compound lies in its highly versatile exocyclic methylene group. This double bond can undergo aza-Michael addition, hydroboration-oxidation, epoxidation, cyclopropanation, radical addition, photoredox-catalysed hydroamination, and metathesis reactions, so that a single starting material can branch into many different derivatives. The strain of the four-membered ring also confers a distinctive reactivity compared with larger rings. The Boc group, meanwhile, protects the amine nitrogen throughout these transformations and can be removed with acid at whatever stage the chemist chooses, giving flexible control over the synthetic sequence.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in synthetic organic chemistry groups at universities and research institutes, in pharmaceutical discovery programmes exploring new scaffolds, and in contract research work where sp3-rich fragments are required. It suits laboratories building compound libraries around saturated nitrogen heterocycles, as well as teaching and method-development settings where a reliable, well-characterised olefin handle is needed for exploring modern functionalisation chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMedicinal chemistry scaffold construction: the compact, sp3-rich azetidine ring offers a rigid three-dimensional framework that helps chemists move away from flat aromatic structures when designing new drug candidates.\u003c\/li\u003e\n\u003cli\u003eAza-Michael and conjugate addition chemistry: the exocyclic methylene accepts nucleophiles readily, giving straightforward access to 3-substituted azetidines bearing nitrogen, oxygen, or sulfur substituents from a single common precursor.\u003c\/li\u003e\n\u003cli\u003eHydroboration-oxidation and epoxidation routes: the olefin handle can be converted into hydroxymethyl or epoxide functionality, opening further pathways toward alcohols, ethers, and ring-opened derivatives for downstream elaboration.\u003c\/li\u003e\n\u003cli\u003eCyclopropanation and spirocycle synthesis: reaction across the exocyclic double bond builds strained spiro-fused systems that are valuable as conformationally restricted fragments in structure-activity relationship studies.\u003c\/li\u003e\n\u003cli\u003ePhotoredox and radical functionalisation studies: the methylene group participates in radical addition and catalysed hydroamination, making this material a practical substrate for developing and benchmarking modern photochemical methodologies.\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: 934664-41-2\u003c\/li\u003e\n\u003cli\u003eChemical name: tert-Butyl 3-Methyleneazetidine-1-carboxylate\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale catalogue pack sizes; please confirm the packing option required for your work\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original sealed 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, well-ventilated area away from direct sunlight, heat sources, strong acids, and strong oxidising agents, following the storage conditions given on the manufacturer's label and safety data sheet. Keep the material in its original supplier container or in a compatible, clearly labelled glass vessel with a secure closure; Boc-protected compounds are sensitive to acidic conditions, so avoid contact with acid residues during storage and transfer. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, and dispense with clean, dry equipment to limit moisture uptake. Reseal the container promptly after use, record each withdrawal, and dispose of residues and contaminated consumables as chemical waste in line with your institution's laboratory waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085914648794,"sku":"TCI2510B601112800","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085914681562,"sku":"TCI2510B601112801","price":1641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6011_0e99bfaa-dc6d-4a3a-825c-96851fc74be7.jpg?v=1767864185"},{"product_id":"tci2510b601212802","title":"TCI B6012 1002355-96-5 tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6012 is tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate, an azetidine building block that carries a conjugated α,β-unsaturated ester at the 3-position together with a Boc protecting group on the ring nitrogen. The structure combines two useful elements in a single molecule: a compact four-membered heterocyclic framework and a Michael acceptor group that is ready to react. In organic synthesis laboratories, a material of this kind serves as an efficient bridge for building side-chain substituted azetidine derivatives without having to go through ring-forming steps that normally demand special conditions and give low yields.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this compound a preferred choice is the directed reactivity of the conjugated double bond attached to the ethyl ester. The carbonyl group withdraws electron density, so the β-carbon becomes strongly electrophilic and is ready to accept nucleophiles in conjugate addition reactions, whether from amines, thiols, malonates, or suitable organometallic reagents. The ethyl ester itself can be hydrolysed to a carboxylic acid, reduced to an alcohol, or converted into an amide, so the range of accessible derivatives is very wide. The Boc group keeps the azetidine nitrogen protected throughout these transformations and can be removed under acidic conditions when the free amine is needed.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, building blocks of this type are used in university research groups, pharmaceutical development units, and contract synthesis facilities that prepare small-molecule libraries. The azetidine motif is valued in medicinal chemistry programmes for the rigidity and reduced conformational freedom it introduces into a candidate structure. Because the material is supplied ready to use, research teams can move directly to the derivatisation step, which shortens experimental timelines and reduces dependence on multi-step in-house ring construction.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugate addition chemistry: the electron-poor β-carbon of the unsaturated ester accepts amine, thiol, malonate, and organometallic nucleophiles cleanly, giving 3-substituted azetidine products in a single controlled step.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry library synthesis: the rigid four-membered azetidine core introduces conformational restriction into candidate molecules, a design element frequently sought when optimising small-molecule leads in drug discovery programmes.\u003c\/li\u003e\n\u003cli\u003eEster functional group interconversion: the ethyl ester can be hydrolysed to the carboxylic acid, reduced to the alcohol, or converted to amides, letting one starting material serve many downstream derivative targets.\u003c\/li\u003e\n\u003cli\u003eProtecting group strategy development: the Boc group on the ring nitrogen survives a wide range of transformations and is cleanly removed under acidic conditions to liberate the free azetidine amine when required.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic scaffold assembly: the compound avoids the demanding ring-closure steps normally needed to build azetidines, letting synthetic chemists access substituted derivatives without low-yielding cyclisation sequences.\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: 1002355-96-5\u003c\/li\u003e\n\u003cli\u003eChemical name: tert-Butyl 3-(2-Ethoxy-2-oxoethylidene)azetidine-1-carboxylate\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 catalogue pack sizes; please confirm the currently listed options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep under 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 container tightly closed in a cool, dry, well-ventilated area away from heat sources, direct sunlight, and incompatible materials, following the storage conditions printed on the manufacturer's label and safety data sheet. Keep the material in its original supplier container or in a clean, chemically compatible amber glass vessel with a secure closure, and label all secondary containers clearly. Handle the compound in a fume hood using safety goggles, nitrile gloves, and a laboratory coat. As an α,β-unsaturated ester, the material is an electrophilic Michael acceptor, so avoid skin and eye contact and avoid inhaling any vapour or dust. Review the manufacturer's safety data sheet before first use, minimise exposure to moisture when transferring, and dispose of residues and contaminated consumables through the laboratory's chemical waste stream.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085914747098,"sku":"TCI2510B601212802","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085914779866,"sku":"TCI2510B601212803","price":834000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6012_734e4b18-5669-44de-92d9-e6fffef3d53a.jpg?v=1767864192"},{"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":"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":"tci2510b642713311","title":"TCI B6427 18934-00-4 3,3'-[Oxybis(methylene)]bis(3-ethyloxetane)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6427 3,3'-[Oxybis(methylene)]bis(3-ethyloxetane) (CAS 18934-00-4) is a difunctional oxetane building block used mainly in cationic polymerisation research. Its two strained four-membered rings allow it to act as a crosslinking monomer that builds three-dimensional polymer networks. Researchers frequently study it within cationically initiated and light-activated curing formulations. Handle it in a fume hood with appropriate protective equipment, keep it away from strong acids, and consult the manufacturer's safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMali et al. (2025). Synthesis and Characterization of Ether-Dimer Impurity of Drug - Ranolazine Using 2, 2’- (oxybis (methylene)) Bis (Oxirane). \u003cem\u003eAmerican Journal of Applied Scientific Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.11648\/j.ajasr.20251102.12\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.11648\/j.ajasr.20251102.12\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAnnatelli et al. (2022). A Green Synthesis of 5,5′‐[Oxybis(methylene)]bis‐2‐Furfural: from By‐Product to Attractive Bio‐Based Platform Chemical. \u003cem\u003eAdvanced Sustainable Systems\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/adsu.202200297\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/adsu.202200297\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLo et al. (2020). Crystal structure of 4,4′-(oxybis(methylene))bis(bromobenzene), C14H12Br2O. \u003cem\u003eZeitschrift für Kristallographie - New Crystal Structures\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1515\/ncrs-2020-0280\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1515\/ncrs-2020-0280\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":48085939388634,"sku":"TCI2510B642713311","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085939421402,"sku":"TCI2510B642713312","price":1086000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6427.jpg?v=1768816050"},{"product_id":"tci2510b642913315","title":"TCI B6429 253176-93-1 tert-Butyl 3-(Bromomethyl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-(Bromomethyl)azetidine-1-carboxylate is a chemical compound widely used in organic synthesis, particularly in the formation of heterocyclic compounds. This building block plays a crucial role in laboratories where the development of new molecules, such as pharmaceuticals, industrial chemicals, or organic intermediates, is required. Its molecular structure enables it to participate in various chemical reactions, making it a versatile reagent for synthetic chemists. Due to its reactivity and specificity, it is often employed in substitution, nucleophilic, and catalytic reactions to produce compounds with precise structural features.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique chemical properties, including the presence of a bromomethyl group and an azetidine ring, make it a preferred choice for high reactivity and molecular specificity. These features allow it to be used in reactions that require controlled and targeted chemical transformations. Its stability under certain conditions also contributes to its reliability in laboratory settings, although it remains sensitive to moisture and air exposure. These characteristics ensure that it remains a valuable tool for researchers working on complex synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers in educational institutions and research organizations for experimental purposes. It is frequently found in projects related to organic synthesis, drug development, and material science. Its availability through AMI Scientific ensures that Indonesian scientists have access to this essential building block for their research needs.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the development of pharmaceutical compounds due to its reactivity and specificity in forming complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound synthesis as a key building block for creating nitrogen-containing ring systems in medicinal chemistry.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions in the production of functionalized organic molecules where controlled chemical transformations are required.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions to introduce functional groups into organic molecules with high selectivity.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the synthesis of advanced polymers and specialty chemicals with tailored 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: 253176-93-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\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 dry, cool place away from moisture and air exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to prevent degradation due to moisture and air exposure. It is recommended to use airtight containers made of materials such as glass or high-density polyethylene to maintain its chemical integrity. Due to its sensitivity, it should be handled in a controlled laboratory setting with appropriate safety measures, including the use of gloves and a fume hood. Proper labeling and storage conditions are essential to ensure its effectiveness and safety during use. Laboratories should avoid prolonged exposure to humidity and ensure that the compound is kept in a secure location to prevent contamination or accidental use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":67556219289818,"sku":"TCI2510B642913315","price":3205000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6429_5835253d-f662-4a7b-8705-68fb2508e0d2.jpg?v=1767865746"},{"product_id":"tci2510b654913476","title":"TCI B6549 1374014-30-8 3-(Bromomethyl)oxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(Bromomethyl)oxetane (CAS 1374014-30-8) combines a strained four-membered oxetane ring with a reactive bromomethyl handle, making it a versatile heterocyclic building block. It is used to alkylate amines, alkoxides, thiolates, and carbanions, introducing an oxetane motif that medicinal chemists often employ as a bioisostere for gem-dimethyl or carbonyl groups to tune solubility and metabolic stability. As a reactive alkylating agent it should be handled in a fume hood with gloves and eye protection, kept away from strong acids that can open the oxetane ring, and stored cool, dry, and tightly closed. AMI Scientific offers a 200 mg pack size for synthetic and drug discovery laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085946663130,"sku":"TCI2510B654913476","price":4619000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6549.jpg?v=1767093882"},{"product_id":"tci2510c076915019","title":"TCI C0769 5445-51-2 1,1-Cyclobutanedicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0769 1,1-Cyclobutanedicarboxylic Acid (CAS 5445-51-2) features two carboxyl groups on the same carbon of a strained cyclobutane ring. This gem-dicarboxylate arrangement forms stable bidentate chelates and is well known in platinum coordination chemistry. The compound also serves as a precursor to cyclobutanecarboxylic acid derivatives and to rigid, three-dimensional building blocks. AMI Scientific supplies this TCI product in 5 g and 25 g pack sizes for flexible laboratory use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSANTARSIERO (1990). ChemInform Abstract: The Crystal Structure of 1,1‐Cyclobutanedicarboxylic Acid at 20 K. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199028037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199028037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRao (1993). A Convenient Preparation of 1-Mercapto-3-azidocyclo-butane from 1,1-Cyclobutanedicarboxylic Acid. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397919308012613\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397919308012613\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRAO (1994). ChemInform Abstract: A Convenient Preparation of 1‐Mercapto‐3‐azidocyclobutane from 1,1‐ Cyclobutanedicarboxylic Acid.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199417106\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199417106\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":48086027174106,"sku":"TCI2510C076915019","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086027206874,"sku":"TCI2510C076915020","price":733000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0769.jpg?v=1767095729"},{"product_id":"tci2510c088815198","title":"TCI C0888 3721-95-7 Cyclobutanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0888 Cyclobutanecarboxylic Acid (CAS 3721-95-7) is a strained four-membered cyclic carboxylic acid widely used as a non-heterocyclic building block in organic synthesis. Its carboxyl group is readily converted into amides, esters, and other acyl derivatives, making it a practical entry point for multi-step synthetic routes. The cyclobutyl motif is frequently explored in medicinal chemistry to introduce conformational rigidity and modulate the three-dimensional profile of target molecules. Available through AMI Scientific in 10 g and 25 g packs, it should be stored in a tightly closed container in a cool, dry, well-ventilated area in line with the official TCI documentation.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDEHMLOW et al. (1990). ChemInform Abstract: Synthesis of Stereoisomeric 3‐Substituted Cyclobutanecarboxylic Acid Derivatives.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199036116\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199036116\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGrigor’ev et al. (2018). Complexes of An(VI) with Cyclobutanecarboxylic Acid Anions and Outer-Sphere Alkali Metal Cations. \u003cem\u003eRadiochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1134\/s1066362218050065\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1134\/s1066362218050065\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKabalka et al. (2005). Synthesis of a boronated amino acid as a potential neutron therapy agent: 1-amino-3-[(dihydroxyboryl)ethyl]cyclobutanecarboxylic acid. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2005.04.130\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetlet.2005.04.130\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":"10g","offer_id":48086035792090,"sku":"TCI2510C088815198","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086035824858,"sku":"TCI2510C088815199","price":1616000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0888.jpg?v=1767095945"},{"product_id":"tci2510c094215279","title":"TCI C0942 3779-29-1 Diethyl 1,1-Cyclobutanedicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethyl 1,1-cyclobutanedicarboxylate is a malonate-type diester in which both ester groups sit on a single quaternary carbon of a strained four-membered ring. Hydrolysis followed by decarboxylation provides a classical route to cyclobutanecarboxylic acid derivatives, an increasingly popular motif for adding three-dimensional character to drug candidates. The ester groups can equally be reduced to diols or converted to amides, making the compound a flexible entry point into substituted and spirocyclic cyclobutanes. TCI supplies this liquid in 5 mL and 25 mL packs; handle it in a fume hood and store it tightly closed in a cool, dry, well-ventilated area.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086039068890,"sku":"TCI2510C094215279","price":557000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086039101658,"sku":"TCI2510C094215280","price":557000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0942.jpg?v=1767096043"},{"product_id":"tci2510c122915697","title":"TCI C1229 822-48-0 3-(Chloromethyl)-3-methyloxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1229 3-(Chloromethyl)-3-methyloxetane is a strained four-membered oxetane building block bearing a reactive chloromethyl handle. The chloride is readily displaced by oxygen, nitrogen, or sulfur nucleophiles, giving rapid access to a wide range of functionalised oxetane derivatives. Oxetane motifs are widely studied in medicinal chemistry and in ring-opening polymerisation research. Supplied in 5 g and 25 g packs, the reagent should be handled in a fume hood following the official TCI safety data sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086057713882,"sku":"TCI2510C122915697","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086057746650,"sku":"TCI2510C122915698","price":1792000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1229.jpg?v=1767096570"},{"product_id":"tci2510c203816672","title":"TCI C2038 5006-22-4 Cyclobutanecarbonyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclobutanecarbonyl Chloride (CAS No. 5006-22-4) is an organic compound widely used in synthetic chemical reactions within laboratory settings. It serves as a versatile reagent, particularly in the formation of heterocyclic compounds and cyclic structures due to its unique molecular structure. The compound features a carbonyl group attached to a cyclobutane ring, which enables it to participate in complex substitution and other chemical reactions. Its reactivity makes it a valuable tool in various synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity stems from its ability to form covalent bonds with a variety of substrates, including amines, hydroxyl groups, and sulfides. This characteristic makes it ideal for nucleophilic substitution reactions and bond formation processes. Additionally, Cyclobutanecarbonyl Chloride exhibits stability under specific conditions, which enhances its usability and storage convenience. These properties make it a preferred choice for chemists working on synthetic and analytical projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyclobutanecarbonyl Chloride is commonly used in organic chemistry research, especially in the development of pharmaceutical compounds and industrial chemicals. Its application extends to studies involving cyclic structures and high reactivity, making it a key component in various research initiatives. The compound’s reliability and effectiveness contribute to its widespread use in both academic and industrial research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its unique cyclobutane structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where it acts as an electrophilic reagent for bond formation.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds through its ability to form covalent bonds with functional groups.\u003c\/li\u003e\n\u003cli\u003eResearch on cyclic structures requiring stability and reactivity in controlled environments.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical applications where precise chemical reactions and compound formation 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: 5006-22-4\u003c\/li\u003e\n\u003cli\u003eCategory: TCI\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per standard supplier packaging\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 direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyclobutanecarbonyl Chloride should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers made of materials resistant to chemical reactions, such as glass or high-density polyethylene. The compound should be kept away from moisture and direct sunlight to avoid unwanted reactions. In laboratory settings, proper ventilation is essential to minimize exposure. Always handle the compound with appropriate personal protective equipment, including gloves and safety goggles, to ensure safe usage and prevent accidental contact. Regular monitoring of storage conditions is advised to maintain the integrity of the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086097887450,"sku":"TCI2510C203816672","price":2221000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086097920218,"sku":"TCI2510C203816673","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2038.jpg?v=1771058136"},{"product_id":"tci2510c206116707","title":"TCI C2061 4415-82-1 Cyclobutanemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclobutanemethanol is a chemical compound widely used as a building block in the synthesis of complex molecules. It plays a crucial role in organic chemistry by enabling the construction of molecular structures with specific stereochemistry and functionality. This compound is particularly valuable in the development of new chemical entities, as its cyclic structure provides a stable yet reactive platform for further modifications. In laboratory settings, Cyclobutanemethanol is essential for researchers working on the synthesis of both heterocyclic and non-heterocyclic compounds, offering versatility in reaction pathways and functional group introduction.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes that make Cyclobutanemethanol a preferred choice is its unique cyclic structure, which allows for controlled reactivity and compatibility with a wide range of synthetic strategies. Its chemical stability ensures that it remains intact under various reaction conditions, while its reactivity can be modulated by appropriate catalysts or reaction conditions. Additionally, Cyclobutanemethanol is typically available in liquid form, making it convenient for handling and incorporation into reaction mixtures. Its distinct aroma also aids in identification during laboratory work.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyclobutanemethanol is extensively used in scientific research, particularly in academic institutions and research centers. It is a common reagent in projects focused on organic synthesis, drug development, and material science. Its broad applicability and reliable performance make it a staple in the chemical laboratories of Indonesia, supporting both educational and industrial research initiatives.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules due to its cyclic structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds as a building block in drug synthesis.\u003c\/li\u003e\n\u003cli\u003eCreation of new materials in polymer chemistry for advanced applications.\u003c\/li\u003e\n\u003cli\u003eResearch in heterocyclic chemistry for the design of functional molecules.\u003c\/li\u003e\n\u003cli\u003eEducational use in teaching organic chemistry and synthetic methodologies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 4415-82-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyclobutanemethanol should be stored in a cool, dry, and well-ventilated area away from direct sunlight. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent evaporation and contamination. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid accidental exposure. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper labeling of containers is essential to ensure safe handling and prevent misuse. Regular inspection of storage conditions is advised to maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086100508890,"sku":"TCI2510C206116707","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086100541658,"sku":"TCI2510C206116708","price":1641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2061.jpg?v=1768816753"},{"product_id":"tci2510c226216973","title":"TCI C2262 4415-87-6 1,2,3,4-Cyclobutanetetracarboxylic Dianhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2,3,4-Cyclobutanetetracarboxylic Dianhydride is a chemical compound widely used in organic synthesis as a key building block. Its anhydride structure enables participation in various chemical reactions, such as esterification and amidation, making it a versatile reagent in laboratory settings. This compound is particularly valuable for creating functionalized molecules with specific chemical properties. Due to its stability and controlled reactivity, it is often selected for reactions requiring precision and consistency.\u003c\/p\u003e\n\u003cp\u003eThe compound’s non-polar nature facilitates solubility and reactivity under diverse laboratory conditions, enhancing its utility in both research and industrial applications. Its ability to undergo chemical transformations makes it a preferred choice for chemists working on complex molecular structures. The compound’s predictable behavior and compatibility with various solvents further contribute to its reliability in synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2,3,4-Cyclobutanetetracarboxylic Dianhydride is extensively used in both fundamental and applied chemical research. It plays a crucial role in the development of new technologies, pharmaceutical compounds, and advanced materials. Its application spans across academic institutions and research centers, supporting innovation in chemical synthesis and material science. The compound’s widespread use highlights its importance in the Indonesian scientific community.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring anhydride reactivity for functional group introduction\u003c\/li\u003e\n\u003cli\u003eProduction of polymers with tailored structural properties through controlled chemical reactions\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds by enabling precise chemical modifications\u003c\/li\u003e\n\u003cli\u003eResearch in material science for creating advanced polymers and composite materials\u003c\/li\u003e\n\u003cli\u003eSupport for academic studies in chemical reaction mechanisms and molecular design\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: 4415-87-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\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 airtight containers to prevent exposure to moisture and air. Due to its chemical nature, it should be handled in a well-ventilated area to minimize inhalation risks. Avoid contact with skin and eyes, and use appropriate personal protective equipment when handling. Proper storage ensures the compound remains stable and effective for use in laboratory applications. Always follow standard safety protocols when working with chemical reagents to ensure a safe laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086115942618,"sku":"TCI2510C226216973","price":1718000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086115975386,"sku":"TCI2510C226216974","price":1718000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2262.jpg?v=1767098027"},{"product_id":"tci2510c250217277","title":"TCI C2502 53159-92-5 1,2,3,4-Cyclobutanetetracarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2,3,4-Cyclobutanetetracarboxylic Acid is a chemical compound widely used as a fundamental building block in the synthesis of complex molecules. Its unique cyclic structure with four carboxylate groups makes it highly versatile in organic chemistry applications. In the laboratory, this compound plays a critical role in the development of new compounds, including pharmaceuticals, industrial chemicals, and organic materials. Its ability to participate in various chemical reactions and form stable intermediates makes it an essential tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity and compatibility with a wide range of functional groups, which allows for the creation of diverse molecular structures. Its stability under controlled conditions further enhances its utility in precise chemical synthesis. These properties make it a preferred choice for chemists aiming to modify complex molecular frameworks. The compound’s predictable behavior and consistent performance contribute to its reliability in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2,3,4-Cyclobutanetetracarboxylic Acid is commonly used in organic chemistry, pharmaceutical research, and material science. It is a key component in experiments involving the synthesis of new compounds and the development of advanced chemical techniques. Its availability and reliability make it a staple in research institutions and universities across Indonesia, supporting a wide range of scientific investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its cyclic structure and multiple carboxylate groups, enabling the creation of complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drug molecules through structural modifications and functional group manipulations.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments rely on its reactivity and stability to create advanced polymers and chemical intermediates.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions use it as a standard building block for teaching and experimental purposes in organic chemistry courses.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production incorporates it to synthesize specialty chemicals and functional materials with specific 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: 53159-92-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\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 stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity. Since it is a solid powder, it should be kept in a sealed container to avoid exposure to air and contaminants. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to ensure safety. Regular monitoring of storage conditions is advised to maintain the compound’s integrity and usability in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086129344730,"sku":"TCI2510C250217277","price":2071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2502.jpg?v=1767098414"},{"product_id":"tci2510c267917524","title":"TCI C2679 4415-88-7 1,2,3,4-Cyclobutanetetracarboxdiimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2,3,4-Cyclobutanetetracarboxdiimide is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. This compound features a cyclic structure with four carboxyl groups attached to carbon atoms and two nitrogen atoms forming a diimide structure. Its unique molecular architecture makes it a valuable building block in organic chemistry. It is commonly used in molecular modification reactions and the formation of heterocyclic compounds. Due to its reactivity and stability, it is a preferred choice for researchers working on advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity is primarily attributed to its carboxyl groups and diimide nitrogen atoms, which participate in various chemical reactions. Its cyclic structure provides a degree of stability, allowing it to be used under a range of reaction conditions. These properties make it highly sought after in organic synthesis, especially in reactions such as Diels-Alder and substitution reactions. Additionally, its chemical characteristics make it useful in the study of bioactive compounds, supporting research in pharmaceutical and medicinal chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,2,3,4-Cyclobutanetetracarboxdiimide is utilized in a variety of chemical research projects. It is frequently employed in the synthesis of new compounds, the development of pharmaceutical intermediates, and the investigation of bioactive molecules. Its availability and chemical versatility make it a popular choice among researchers in both academic and industrial settings. The compound plays a key role in advancing chemical innovation and scientific discovery in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this compound serves as a versatile building block for creating complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic compound formation benefits from its cyclic structure and diimide functionality, enabling the synthesis of nitrogen-containing rings.\u003c\/li\u003e\n\u003cli\u003eMolecular modification reactions often use this compound due to its reactivity at carboxyl and nitrogen sites, allowing for functional group transformations.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research leverages its chemical properties to develop new drug candidates and intermediates with potential therapeutic applications.\u003c\/li\u003e\n\u003cli\u003eBioactive compound studies utilize its reactivity and structural features to explore compounds with biological activity and pharmacological relevance.\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: 4415-88-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per 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 sealed container to prevent moisture absorption, which could affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize exposure to airborne particles. Avoid storing near incompatible substances to prevent unwanted reactions. Proper labeling of storage containers is essential for safe handling and easy identification.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086191341786,"sku":"TCI2510C267917524","price":4544000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086191374554,"sku":"TCI2510C267917525","price":4544000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2679.jpg?v=1767098643"},{"product_id":"tci2510c284217723","title":"TCI C2842 4415-87-6 1,2,3,4-Cyclobutanetetracarboxylic Dianhydride (purified by sublimation)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2842 4415-87-6 1,2,3,4-Cyclobutanetetracarboxylic Dianhydride (purified by sublimation) is a chemical compound widely used in organic synthesis as a building block. This compound is essential in the development of complex organic molecules due to its anhydride functionality. Its ability to undergo esterification and reaction with amines makes it a versatile reagent in synthetic chemistry. In laboratory settings, it plays a crucial role in the synthesis of heterocyclic compounds and polymers, contributing to advancements in pharmaceutical and materials science.\u003c\/p\u003e\n\u003cp\u003eThe compound is purified through sublimation, which enhances its purity and consistency, making it a preferred choice for high-precision experiments. Its stability under controlled conditions ensures reliable results, while its reactivity with water and heat requires careful handling. This purification process minimizes contamination, improving the accuracy of chemical reactions. The compound's purity and reactivity are key factors in its selection for specialized laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, drug development, and studies on anhydride reactivity. Its availability in the local market makes it a go-to choice for researchers and chemists. The compound's role in creating complex molecular structures supports various scientific investigations, particularly in the fields of pharmaceutical and polymer chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its anhydride functionality and reactivity with amines.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a key intermediate in the synthesis of complex drug molecules.\u003c\/li\u003e\n\u003cli\u003ePolymer science research for the creation of advanced materials with tailored chemical properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications for studying the reactivity and behavior of anhydride compounds.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical reactivity and molecular structure building in Indonesian universities and research institutions.\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: 4415-87-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry and cool conditions to maintain stability and prevent degradation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its sensitivity to heat and water, it should be kept away from sources of heat and humidity. Proper labeling and storage in a designated chemical storage area are essential for safety. Laboratory personnel should wear appropriate personal protective equipment when handling the compound to ensure safe working conditions. Regular monitoring of storage conditions is advised to maintain the compound's integrity and effectiveness in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086199501018,"sku":"TCI2510C284217723","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086199533786,"sku":"TCI2510C284217724","price":1818000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2842.jpg?v=1767098883"},{"product_id":"tci2510c316118129","title":"TCI C3161 28049-61-8 1-(4-Chlorophenyl)cyclobutanecarbonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(4-Chlorophenyl)cyclobutanecarbonitrile is a nitrile compound that combines a strained cyclobutane ring with both a 4-chlorophenyl group and a cyano group attached to the same quaternary carbon atom. This structural arrangement makes it a valuable starting material in organic synthesis, particularly when researchers require a pre-built substituted cyclobutane framework. Constructing four-membered rings from scratch typically demands specialized conditions and considerable effort, so having this compound available as a building block delivers meaningful time savings and allows attention to focus on subsequent functional group transformations.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound widely selected is the versatility of the nitrile group as a synthetic branching point. The cyano group can be reduced to primary amines, hydrolyzed to carboxylic acids or amides, or subjected to organometallic reagent addition to produce ketones. Because this functional group is attached to the quaternary carbon of the cyclobutane ring, the resulting derivative products inherit a rigid framework that restricts conformational flexibility—a characteristic highly valued in modern drug molecule design where precise three-dimensional geometry matters.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratory settings, this TCI building block serves medicinal chemistry research groups, academic organic synthesis laboratories, and pharmaceutical development teams working on novel molecular entities. Researchers typically employ it when designing synthetic routes that require cyclobutane-containing intermediates or when exploring structure-activity relationships in drug discovery projects. The compound's availability through established chemical suppliers supports ongoing research programs across university chemistry departments and industrial research facilities throughout Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMedicinal chemistry synthesis: provides pre-built cyclobutane scaffolds for drug candidate development, eliminating the need to construct strained four-membered rings from simpler precursors\u003c\/li\u003e\n\u003cli\u003eFunctional group transformation studies: the nitrile moiety enables multiple downstream reactions including reduction, hydrolysis, and organometallic addition for diverse derivative generation\u003c\/li\u003e\n\u003cli\u003eStructure-activity relationship research: the rigid cyclobutane framework restricts molecular conformation, allowing systematic investigation of three-dimensional geometry effects on biological activity\u003c\/li\u003e\n\u003cli\u003eOrganic methodology development: serves as a model substrate for testing new synthetic procedures involving nitrile chemistry or cyclobutane ring functionalization strategies\u003c\/li\u003e\n\u003cli\u003eAcademic teaching and demonstration: illustrates principles of strained ring chemistry, quaternary carbon center reactivity, and nitrile group versatility in advanced organic chemistry courses\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: 28049-61-8\u003c\/li\u003e\n\u003cli\u003eProduct Code: C3161\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical Name: 1-(4-Chlorophenyl)cyclobutanecarbonitrile\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid (typical for this compound class)\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore in a cool, dry location away from direct sunlight and heat sources. Keep the container tightly sealed when not in use to prevent moisture absorption and contamination. Standard laboratory glass bottles or original manufacturer packaging are suitable storage vessels. Handle with appropriate personal protective equipment including gloves and safety glasses. Work in a well-ventilated area or fume hood when handling the material. Follow standard laboratory safety protocols for nitrile compounds and aromatic halides. Dispose of waste according to institutional chemical waste management procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086216605914,"sku":"TCI2510C316118129","price":2676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086216638682,"sku":"TCI2510C316118130","price":2676000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3161.jpg?v=1768817034"},{"product_id":"tci2510c372118803","title":"TCI C3721 2507954-86-9 tert-Butyl 3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate is a complex organic compound used as a building block in chemical synthesis. This heterocyclic compound contains both an azetidine ring and a boronic acid group, making it a versatile reagent for various synthetic pathways. It is commonly employed in reactions that require specific chemical transformations, such as nucleophilic substitution and coupling reactions. Its structural complexity allows it to participate in advanced organic chemistry processes, supporting the development of new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and reactivity make it a preferred choice for synthetic chemists. The presence of the boronic acid group enables it to undergo efficient coupling reactions, particularly in cross-coupling methodologies. Its compatibility with a range of solvents and reaction conditions enhances its utility in laboratory settings. Additionally, its ability to form stable intermediates under controlled conditions ensures reliable results in synthetic processes, making it a valuable tool in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, especially in the synthesis of heterocyclic compounds and drug development. Its unique structure and reactivity make it an essential component in studies focused on creating new pharmaceuticals and functional materials. Researchers rely on its predictable behavior and high reactivity to achieve precise chemical outcomes 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 azetidine and boronic acid groups enabling efficient coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDrug development research as it supports the creation of complex molecular structures with pharmaceutical potential.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where its stability and reactivity contribute to the formation of desired products.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reactions benefiting from its compatibility with various reagents and reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical research in Indonesian laboratories focusing on new material synthesis and functional 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: 2507954-86-9\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 or liquid depending on 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. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Due to its potential chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid contact with incompatible substances to ensure safe storage and use. In laboratory settings, it should be kept in a designated chemical storage area with proper labeling and access control. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086279848154,"sku":"TCI2510C372118803","price":3861000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086279880922,"sku":"TCI2510C372118804","price":3861000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3721.jpg?v=1767099967"},{"product_id":"tci2510c375718844","title":"TCI C3757 2987-17-9 Cyclobutanecarbaldehyde","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclobutanecarbaldehyde (TCI C3757) is a chemical compound widely utilized in organic synthesis as a foundational building block. It serves as a key reagent in the development of complex organic molecules, offering versatility in chemical reactions. This compound is particularly valued for its cyclic structure and the presence of an aldehyde group, which allows it to participate in various chemical transformations. In laboratory settings, it is essential for researchers aiming to create new molecular structures through substitution reactions and bond formation. Its role extends across multiple scientific disciplines, making it a critical component in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for synthetic chemists. Its aldehyde group is highly reactive, enabling it to interact with a wide range of reagents such as bases, acids, and organic reagents. This reactivity is crucial for initiating and facilitating chemical reactions, especially in oxidation and reduction processes. Additionally, its stability under controlled conditions ensures that it remains effective during synthesis without premature degradation. These characteristics make it a reliable and efficient reagent for laboratory applications, particularly in the development of pharmaceuticals and polymers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyclobutanecarbaldehyde is commonly used in organic chemistry research, especially in academic institutions and research centers. It is frequently employed in the synthesis of pharmacological compounds, polymers, and other cyclic chemical structures. Its availability and chemical properties make it a go-to material for scientists working on complex molecular designs. Its role in advancing chemical research is significant, supporting both fundamental and applied studies in the field.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules due to its reactive aldehyde group and cyclic structure.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds as a building block for drug molecule design.\u003c\/li\u003e\n\u003cli\u003ePolymer synthesis where cyclic structures are required for specific material properties.\u003c\/li\u003e\n\u003cli\u003eResearch in heterocyclic chemistry for the creation of new chemical frameworks.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications for testing reactivity and chemical behavior in controlled environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2987-17-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dark place away from moisture and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCyclobutanecarbaldehyde should be stored in a cool, dark location to prevent degradation and maintain its chemical integrity. It is recommended to use airtight containers made of glass or inert materials to avoid contamination and reaction with air. Due to its reactivity, it should be kept away from strong oxidizing agents and reducing substances. Proper ventilation is essential when handling the compound to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular monitoring of storage conditions is necessary to maintain the compound's effectiveness and safety in research environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086284763354,"sku":"TCI2510C375718844","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086284796122,"sku":"TCI2510C375718845","price":1491000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3757.jpg?v=1768817143"},{"product_id":"tci2510c391119027","title":"TCI C3911 4426-11-3 Cyclobutanecarbonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclobutanecarbonitrile (C3H4N2) is a chemical compound widely used as a foundational building block in organic synthesis. Its cyclic structure enables highly specific chemical reactions, making it a valuable tool in organic chemistry research. In the laboratory, it serves as a key component in the development of complex molecules, including heterocyclic compounds and other intricate chemical structures. This compound is particularly useful for chemists aiming to create new materials or pharmaceuticals through precise synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits stable chemical properties under controlled conditions, yet it remains highly reactive in specific chemical environments. Its high boiling point and relatively high density facilitate efficient separation and purification processes, which are essential in laboratory settings. These characteristics make it a preferred choice for applications requiring precision and control. Additionally, its predictable behavior in various reaction conditions enhances its utility in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Cyclobutanecarbonitrile is commonly used in organic chemistry research, especially in academic institutions and research centers. It plays a crucial role in the development of new chemical compounds with potential industrial or medical applications. Its availability through suppliers like AMI Scientific ensures that researchers have access to this essential reagent for their experiments and innovations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules due to its cyclic structure enabling specific chemical reactions\u003c\/li\u003e\n\u003cli\u003eDevelopment of heterocyclic compounds as a fundamental building block in synthetic pathways\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical chemistry for the creation of new drug candidates and therapeutic agents\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical applications in the production of advanced materials and specialty chemicals\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical education and innovation for students and scientists\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: 4426-11-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\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\u003eCyclobutanecarbonitrile should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Always wear appropriate personal protective equipment, including gloves, safety goggles, and a lab coat. Avoid contact with skin and eyes, and ensure proper disposal according to local regulations. Regular monitoring of storage conditions is essential to maintain the compound's integrity and safety in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086302392538,"sku":"TCI2510C391119027","price":1439000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086302425306,"sku":"TCI2510C391119028","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3911.jpg?v=1768817163"},{"product_id":"tci2510d025819619","title":"TCI D0258 933-52-8 Tetramethyl-1,3-cyclobutanedione [Precursor to Dimethyl Ketene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTetramethyl-1,3-cyclobutanedione is a chemical compound widely used in organic synthesis as a building block for creating complex organic molecules. This compound features a cyclic structure with two carbonyl groups positioned at the 1 and 3 positions, making it a versatile intermediate in various chemical reactions. In laboratory settings, it serves as a precursor to dimethyl ketene, a reactive compound essential in multiple synthetic pathways. Its unique structural properties make it a valuable resource for chemists working on the development of new compounds and materials.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high reactivity, particularly in oxygen-rich environments, which makes it an important tool in organic chemistry research. Despite its reactivity, it maintains chemical stability under controlled conditions, allowing for efficient use in synthetic processes. Its high density and tendency to degrade if not stored properly require careful handling. These characteristics make it a preferred choice for laboratories seeking a reliable and efficient starting material for complex chemical transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Tetramethyl-1,3-cyclobutanedione is commonly used in organic chemistry research, especially in academic institutions and research centers. Its role as a precursor to dimethyl ketene makes it essential for studies involving cyclic and heterocyclic compound synthesis. The compound's availability and chemical properties support its widespread application in both teaching and research environments, contributing to the advancement of chemical sciences in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its cyclic structure and reactivity, enabling the creation of complex organic molecules with high efficiency.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for the synthesis of dimethyl ketene, which is a key intermediate in various chemical reactions requiring high reactivity.\u003c\/li\u003e\n\u003cli\u003eThe compound supports research into cyclic and heterocyclic compound development, making it a valuable tool for advanced chemical studies.\u003c\/li\u003e\n\u003cli\u003eIt is frequently used in academic research settings to provide students and researchers with a reliable starting material for synthetic experiments.\u003c\/li\u003e\n\u003cli\u003eIts stability under controlled conditions makes it suitable for use in both teaching and industrial laboratory environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 933-52-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires storage in a cool, dry place away from oxygen and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eTetramethyl-1,3-cyclobutanedione should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to minimize exposure to oxygen, which can increase its reactivity. Due to its high reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Storage in a well-ventilated area is essential to prevent the accumulation of volatile compounds. Regular monitoring of storage conditions ensures the compound remains suitable for use in laboratory applications. Proper handling and storage practices are crucial to maintaining the integrity and effectiveness of this valuable chemical building block.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086362783962,"sku":"TCI2510D025819619","price":631000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086362816730,"sku":"TCI2510D025819620","price":631000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D0258.jpg?v=1767101066"},{"product_id":"tci2510d390724330","title":"TCI D3907 18621-17-5 1-(Diphenylmethyl)-3-hydroxyazetidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(Diphenylmethyl)-3-hydroxyazetidine is a chemical compound that plays a crucial role in laboratory settings, particularly in the field of organic chemistry. As a heterocyclic building block, it serves as a foundational material for synthesizing complex molecular structures, especially those containing azetidine rings. Its unique chemical structure, featuring a nitrogen atom within a three-membered ring, makes it highly versatile for various chemical reactions. This compound is widely used in research to develop new compounds with specific biological activities, supporting advancements in both pharmaceutical and chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound's ability to react with a wide range of functional groups makes it a preferred choice in synthetic chemistry. Its heterocyclic nature allows for the formation of diverse derivatives, enhancing its utility in drug discovery and molecular design. The stability of the compound under controlled laboratory conditions further supports its reliability in experimental settings. These properties contribute to its popularity among researchers who require a flexible and effective building block for complex molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry and pharmaceutical research. It is a key component in the development of new drugs and chemical compounds, supporting academic and industrial research initiatives. Its availability through trusted suppliers like AMI Scientific ensures that researchers have access to high-quality materials necessary for their work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: This compound is ideal for constructing complex molecules due to its reactive heterocyclic structure, enabling the formation of various functional groups.\u003c\/li\u003e\n\u003cli\u003eDrug discovery: Its ability to form derivatives with biological activity makes it valuable in the development of pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eChemical research: The compound’s versatility supports a wide range of chemical reactions, making it a key tool in synthetic chemistry.\u003c\/li\u003e\n\u003cli\u003eAcademic research: Used in university and research institutions for teaching and experimental studies in organic chemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development: Its role in creating compounds with specific biological properties is crucial in drug formulation and testing.\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: 18621-17-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard chemical properties)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Storage conditions should be controlled to maintain its stability and effectiveness. Proper labeling and storage practices are essential to prevent accidental exposure and ensure safe handling in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086644654298,"sku":"TCI2510D390724330","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086644687066,"sku":"TCI2510D390724331","price":505000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3907.jpg?v=1767106758"},{"product_id":"tci2510d522526083","title":"TCI D5225 107496-54-8 3,3-Difluorocyclobutanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,3-Difluorocyclobutanecarboxylic Acid is a chemical compound widely used in organic synthesis as a building block for complex molecule development. This compound is essential in laboratories where fluorinated compounds are required, due to its unique molecular structure. It features two fluorine atoms at the 3-position of a cyclobutane ring, which contributes to its distinct reactivity and stability. Its presence in chemical reactions allows for the creation of a variety of functional groups, making it a versatile tool in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound's fluorinated structure provides specific polarity and solubility characteristics, which are different from non-fluorinated analogs. These properties make it ideal for substitution reactions and other chemical processes that require precise control. Additionally, its chemical stability ensures that it remains effective under various reaction conditions without degrading easily. This reliability is crucial for maintaining the integrity of experimental outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,3-Difluorocyclobutanecarboxylic Acid is commonly used in organic chemistry research, particularly in the development of new compounds with pharmaceutical or industrial applications. Research institutions and universities in Indonesia utilize this compound to expand knowledge about fluorinated molecules, which are a key area of modern chemical research. Its application is widespread in both academic and industrial settings, supporting innovation in chemical synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research as a building block for fluorinated compound development due to its unique molecular structure.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the creation of new drug molecules requiring precise fluorination patterns.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical development where controlled fluorination is essential for product functionality.\u003c\/li\u003e\n\u003cli\u003eAcademic studies focused on fluorinated molecule behavior and reactivity in different reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical reaction testing where stability and reactivity under varied conditions are critical.\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: 107496-54-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light to maintain its stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which could affect its chemical integrity. Due to its fluorinated nature, it is important to handle it with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. The compound is generally non-hazardous under normal storage conditions but should be kept out of reach of children and not mixed with incompatible substances. Proper labeling and storage practices help ensure safe handling and long-term usability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086750036186,"sku":"TCI2510D522526083","price":631000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086750068954,"sku":"TCI2510D522526084","price":631000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5225.jpg?v=1768818336"},{"product_id":"tci2510d597526977","title":"TCI D5975 288315-03-7 3,3-Difluoroazetidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5975 3,3-Difluoroazetidine Hydrochloride is a fluorinated building block based on the azetidine ring, a saturated four-membered heterocycle containing a single nitrogen atom. In this compound, two fluorine atoms are bonded to the carbon at the three position, and the cyclic amine is supplied as its hydrochloride salt. In organic synthesis and medicinal chemistry laboratories, the material serves as a ready-to-use secondary amine unit that is attached to a target molecular framework through amidation, reductive alkylation, nucleophilic aromatic substitution, or transition-metal-catalysed coupling reactions to form carbon–nitrogen bonds.\u003c\/p\u003e\n\u003cp\u003eSeveral properties make this material highly sought after. The azetidine ring provides a compact and rigid three-dimensional framework, raising the proportion of sp3 carbon in the final molecule without adding excessive molecular weight, which makes it an attractive alternative to the larger piperidine or pyrrolidine rings. The two fluorine atoms at the three position withdraw electron density strongly and markedly lower the basicity of the azetidine nitrogen, an adjustment frequently used to tune the physicochemical properties of a designed molecule. Fluorination at this position is a well-established strategy in modern building-block chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic synthesis, medicinal chemistry, and the preparation of compound libraries. It is handled at bench scale in fume hoods during multi-step synthetic routes, where the hydrochloride salt form makes it convenient to weigh out and store between reaction campaigns. Research teams commonly order it alongside coupling reagents and bases required to liberate the free amine in situ before the bond-forming step.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAmide bond formation: the secondary amine is coupled with carboxylic acids or acid chlorides to install a compact difluorinated azetidine cap on a target scaffold.\u003c\/li\u003e\n\u003cli\u003eReductive alkylation: the free amine released from the hydrochloride salt condenses with aldehydes or ketones, giving N-alkylated azetidines that increase the sp3 character of the product.\u003c\/li\u003e\n\u003cli\u003eNucleophilic aromatic substitution: the amine displaces suitable leaving groups on electron-poor aromatic and heteroaromatic rings, building carbon–nitrogen bonds without metal catalysis.\u003c\/li\u003e\n\u003cli\u003eTransition-metal-catalysed coupling: the azetidine nitrogen serves as the amine partner in catalysed carbon–nitrogen bond-forming couplings onto aryl and heteroaryl halides.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry library synthesis: the ring lowers nitrogen basicity through the two fluorine atoms, letting chemists tune physicochemical properties across a series of analogues.\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: 288315-03-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003eChemical form: cyclic secondary amine supplied as the hydrochloride salt\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered by TCI for this item\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the manufacturer label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, and well-ventilated place, away from moisture, heat sources, and incompatible materials, following the conditions specified on the manufacturer label and safety data sheet. Amine hydrochloride salts are generally hygroscopic, so keep the original container sealed and allow it to reach room temperature before opening to reduce condensation. Weigh and transfer the solid inside a fume hood using clean, dry spatulas and tightly closing glass or suitable plastic containers. Wear a laboratory coat, chemical-resistant gloves, and safety goggles during handling, avoid inhaling dust, and dispose of residues and contaminated materials through the institution's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086786113754,"sku":"TCI2510D597526977","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086786146522,"sku":"TCI2510D597526978","price":1313000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5975.jpg?v=1767109513"},{"product_id":"tci2510d639127424","title":"TCI D6391 1408075-52-4 tert-Butyl 3-(Bromomethyl)-3-methylazetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6391 is tert-Butyl 3-(Bromomethyl)-3-methylazetidine-1-carboxylate, a heterocyclic synthesis building block consisting of a Boc-protected azetidine derivative that carries a bromomethyl group on a quaternary carbon. In the organic chemistry laboratory, this compound serves as a ready-to-use alkylating reagent: its bromine atom is a good leaving group and is therefore readily displaced by a wide range of nucleophiles. In a single reaction step, researchers can attach the entire methylated azetidine framework to a target molecule, then remove the Boc protecting group whenever a free amine is required at a later stage.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this reagent a preferred choice lie in the four-membered azetidine ring, which is both rigid and compact, together with the quaternary carbon bearing a methyl group. A framework of this kind contributes high sp3 character to drug candidate molecules, helping to improve solubility and reduce structural flatness without adding excessive molecular weight. The methyl group on the same carbon also blocks certain metabolic pathways and locks the conformation of the bromomethyl group. Boc protection on the nitrogen keeps the cyclic amine unreactive while the substitution reaction proceeds, so that reaction selectivity is maintained.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in medicinal chemistry and organic synthesis research groups at universities, national research institutes, and pharmaceutical development units. It is normally handled at small scale on the bench during analogue preparation and structure-activity relationship studies, where a single well-defined fragment must be introduced reproducibly. Users generally combine it with standard base and polar aprotic solvent systems already available in a routine synthesis laboratory.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleophilic substitution chemistry: the bromomethyl group is displaced cleanly by amines, alcohols, thiols, and stabilised carbanions, installing the azetidine fragment in one step.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry fragment installation: the compact azetidine ring raises sp3 content in candidate molecules, improving solubility and reducing structural flatness without a large molecular weight penalty.\u003c\/li\u003e\n\u003cli\u003eProtecting group strategies: the Boc group on the ring nitrogen keeps the cyclic amine masked during coupling, then is removed to reveal the free secondary amine.\u003c\/li\u003e\n\u003cli\u003eAnalogue and structure-activity relationship studies: the quaternary carbon with its methyl substituent blocks certain metabolic pathways, making it useful for systematic metabolic stability comparisons.\u003c\/li\u003e\n\u003cli\u003eConformationally constrained scaffold synthesis: the rigid four-membered ring and locked bromomethyl orientation give predictable three-dimensional presentation of substituents in designed target molecules.\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: 1408075-52-4\u003c\/li\u003e\n\u003cli\u003eChemical name: tert-Butyl 3-(Bromomethyl)-3-methylazetidine-1-carboxylate\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 currently offered size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the original tightly closed container, protected from light and moisture\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, protected from light and away from moisture, since the bromomethyl group is sensitive to hydrolysis and nucleophilic contaminants. Retain the material in its original supplier container or transfer it to a clean, dry amber glass vessel with a chemically resistant closure. Handle the compound in a fume hood using safety glasses, gloves, and a laboratory coat, and avoid contact with skin, eyes, and inhalation of dust or vapour. As an alkylating agent, it should be kept separate from strong bases, strong oxidising agents, and incompatible nucleophiles. Allow sealed containers to reach room temperature before opening to prevent moisture condensation, and dispose of residues and contaminated consumables through the laboratory's chemical waste procedures. Always consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086804758746,"sku":"TCI2510D639127424","price":3811000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6391.jpg?v=1767110131"},{"product_id":"tci2510d648727527","title":"TCI D6487 454703-20-9 tert-Butyl 3-(Methylamino)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-(Methylamino)azetidine-1-carboxylate is a chemical compound widely used in laboratory settings for the synthesis of heterocyclic compounds. As a building block in organic chemistry, it plays a crucial role in the development of complex molecular structures. This compound is particularly valuable for its ability to undergo various chemical reactions, including substitution and cyclization, which are essential in the creation of pharmaceutical and industrial chemicals. Its versatility makes it a go-to material for researchers working on advanced chemical synthesis projects.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structure, featuring an azetidine ring and functional groups such as tert-butyl and methylamine, contributes to its reactivity and stability under controlled conditions. These properties make it an ideal candidate for use in both academic and industrial research environments. Its ability to participate in multiple reaction pathways allows chemists to tailor its behavior to suit specific synthetic needs. This adaptability is a key factor in its popularity among laboratory professionals.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Tert-Butyl 3-(Methylamino)azetidine-1-carboxylate is commonly used in scientific research and product development. It is frequently found in experiments involving heterocyclic synthesis, particularly in pharmaceutical and chemical industries. Its availability in the local market supports ongoing research efforts, enabling scientists to access high-quality materials for their experiments without the need for international sourcing.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical research and development, as it is used in the synthesis of drug molecules due to its ability to form complex heterocyclic structures.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments, where its reactivity and structural versatility make it suitable for a wide range of synthetic reactions.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production, as it serves as a building block for the creation of various chemical compounds with specific functional properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research in universities and research institutions, where it is employed in studies focused on heterocyclic chemistry and molecular design.\u003c\/li\u003e\n\u003cli\u003eDrug discovery programs, where its structural features are utilized to develop new therapeutic agents with targeted biological activities.\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: 454703-20-9\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 (as per standard chemical 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 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 with appropriate personal protective equipment, including gloves and safety goggles. It is advisable to store it away from incompatible substances such as strong oxidizers. Proper ventilation is essential when working with this material to ensure a safe laboratory environment. Regular monitoring of storage conditions will help preserve the compound's stability and effectiveness for use in chemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086808723674,"sku":"TCI2510D648727527","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086808756442,"sku":"TCI2510D648727528","price":1162000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6487.jpg?v=1767110281"},{"product_id":"tci2510d649227534","title":"TCI D6492 1008526-71-3 tert-Butyl 3-(Aminomethyl)-3-hydroxyazetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6492 tert-Butyl 3-(Aminomethyl)-3-hydroxyazetidine-1-carboxylate is a building block that presents three useful functional groups at once within a remarkably compact azetidine framework: a primary amine on the aminomethyl group, a tertiary hydroxyl on the third carbon of the ring, and a ring nitrogen protected as a Boc carbamate. In the synthesis laboratory, this compound serves as a source of a rigid amino alcohol motif that is ready to be installed onto a target molecule, giving researchers a polar attachment point together with an element of structural rigidity without having to work through a long, multi-step sequence prone to loss of yield.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this material sought after is its balance between polarity and rigidity. The tertiary hydroxyl group adds hydrophilic character that helps improve aqueous solubility, while its position on a quaternary ring carbon leaves it relatively sterically hindered and therefore less likely to interfere with reactions at the primary amine. The primary amine itself is a highly reactive nucleophile, ready to form amides, sulfonamides, ureas, and thioureas, or to create new bonds through reductive amination. The Boc group on the ring nitrogen ensures that these reactions proceed at the intended position, and it can be removed later when the ring nitrogen is needed for further elaboration.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic synthesis and medicinal chemistry, as well as in industrial research units developing new molecules. It is usually ordered in small quantities for exploratory routes and analogue series, then handled on a milligram to gram scale in standard synthetic glassware. Because it arrives with the ring nitrogen already protected, teams can begin building their target structures immediately rather than preparing the protected intermediate in house.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMedicinal chemistry analogue synthesis: the compact azetidine core introduces three-dimensional character and a polar hydroxyl group that can improve aqueous solubility in candidate molecules under investigation.\u003c\/li\u003e\n\u003cli\u003eAmide and sulfonamide coupling: the reactive primary amine readily forms amide, sulfonamide, urea, and thiourea linkages, allowing rapid assembly of diverse compound sets from a single common intermediate.\u003c\/li\u003e\n\u003cli\u003eReductive amination routes: the primary amine couples cleanly with aldehydes and ketones to generate secondary amines, providing a straightforward way to extend molecular frameworks from this starting point.\u003c\/li\u003e\n\u003cli\u003eRigid amino alcohol scaffold installation: the fixed geometry of the four-membered ring constrains conformational freedom, which is valuable when a defined spatial arrangement of donor groups is required.\u003c\/li\u003e\n\u003cli\u003eOrthogonal protection strategies: the Boc-protected ring nitrogen allows chemistry to be performed selectively at the primary amine first, with the ring nitrogen deprotected and functionalised in a later, separate step.\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: 1008526-71-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003eProduct code: TCI D6492\u003c\/li\u003e\n\u003cli\u003ePack sizes: supplied in standard research-scale packs; please confirm the available size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the tightly closed original container under 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 tightly closed original container, kept in a cool, dry, and well-ventilated place away from direct sunlight, moisture, and ignition sources, and follow the specific storage conditions printed on the manufacturer's label and safety data sheet. Boc-protected amino compounds are best protected from humidity and acidic vapours, so reseal the container promptly after each use. Handle the material in a fume hood while wearing a laboratory coat, chemical-resistant gloves, and safety goggles. Weigh out quantities using clean, dry spatulas and glassware to avoid contaminating the bulk stock. Consult the safety data sheet before first use and dispose of residues and contaminated consumables through your institution's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086809084122,"sku":"TCI2510D649227534","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086809116890,"sku":"TCI2510D649227535","price":1818000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6492.jpg?v=1767110293"},{"product_id":"tci2510d650827556","title":"TCI D6508 2098131-64-5 tert-Butyl 3,3-Bis(bromomethyl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6508 tert-Butyl 3,3-Bis(bromomethyl)azetidine-1-carboxylate is a heterocyclic building block that carries two bromomethyl groups on the third carbon of an azetidine ring, with the ring nitrogen protected as a Boc carbamate. In the organic synthesis laboratory, this compound functions as a bis-electrophile, that is, a reagent capable of performing two sequential alkylations on a bifunctional nucleophile. Its role is highly distinctive: it builds spirocyclic ring systems in a single synthetic operation, so that complex three-dimensional frameworks can be assembled without the long sequence of steps that would normally be required.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent a preferred choice is the placement of its two leaving groups, which are symmetric and spaced exactly right for ring closure. When reacted with primary amines, malonates, sulfonamides, or other bidentate nucleophiles, the two bromides are substituted one after the other and generate a new ring connected in spiro fashion to the azetidine. The bromine atoms are good leaving groups in nucleophilic substitution reactions, while the Boc group keeps the azetidine nitrogen unreactive so that destructive internal alkylation does not occur.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used in university and institutional research groups working on medicinal chemistry and methodology development, where saturated spirocyclic scaffolds are of interest. It is handled on small synthetic scales in fume-hooded organic synthesis benches, usually as part of multi-step route development. It should be noted that the same strong electrophilic character that makes the reagent useful also demands careful handling by trained personnel.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSpirocyclic scaffold construction: the two symmetric bromomethyl arms close a new ring onto the azetidine in one operation, giving three-dimensional frameworks without long step sequences.\u003c\/li\u003e\n\u003cli\u003eDouble alkylation of primary amines: the amine nitrogen attacks both bromides in turn, producing a spiro-fused azetidine–azacycle system directly from a simple bifunctional nucleophile.\u003c\/li\u003e\n\u003cli\u003eMalonate-based ring annulation: stabilized malonate carbanions displace each bromide sequentially, delivering a carbocyclic spiro ring joined at the third carbon of the azetidine core.\u003c\/li\u003e\n\u003cli\u003eSulfonamide cyclization chemistry: deprotonated sulfonamides serve as bidentate nucleophiles, undergoing two consecutive substitutions to build nitrogen-containing spiro rings on the protected azetidine.\u003c\/li\u003e\n\u003cli\u003eProtected-intermediate route development: the Boc carbamate holds the ring nitrogen unreactive during alkylation, allowing chemists to plan multi-step sequences that unmask the amine at a later stage.\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: 2098131-64-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: supplied as a Boc-protected azetidine derivative; consult the manufacturer's data sheet for the form of the lot supplied\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 material in its original tightly closed container, kept in a cool, dry, well-ventilated chemical store away from direct sunlight, heat, and moisture, and observe the storage conditions printed on the manufacturer's label. Keep it separated from strong bases, strong oxidizing agents, and nucleophilic reagents, since the compound is a reactive bis-electrophile. All weighing and transfer operations should be carried out in a functioning fume hood by trained personnel wearing safety glasses, a laboratory coat, and chemically resistant gloves. Alkylating agents of this type should be treated as potentially harmful on skin contact, inhalation, or eye contact. Use clean, dry glassware or compatible plastic containers for handling, close the container promptly after use to limit moisture uptake, and collect residues and contaminated consumables as halogenated organic chemical waste for disposal according to institutional procedures. Consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500mg","offer_id":48086810132698,"sku":"TCI2510D650827556","price":6032000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6508.jpg?v=1767110337"},{"product_id":"tci2510d651727563","title":"TCI D6517 1158758-85-0 tert-Butyl 3-(Aminomethyl)-3-methylazetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D6517 tert-Butyl 3-(Aminomethyl)-3-methylazetidine-1-carboxylate is a heterocyclic building block built around an azetidine ring that carries both an aminomethyl group and a methyl group on the same quaternary carbon, with the ring nitrogen protected as a Boc carbamate. In synthetic laboratory work, this compound supplies a reactive primary amine on a small, rigid, sp3-rich framework. That arrangement makes it straightforward for researchers to attach a branched amine fragment to a target molecule without adding excessive molecular weight, while providing a defined geometry that open aliphatic chains cannot easily deliver.\u003c\/p\u003e\n\u003cp\u003eThe most notable characteristic of this material is the combination of a quaternary carbon and a free primary amine. Because the quaternary carbon bears the methyl group, there is no acidic proton at that position, so the framework becomes more resistant to elimination and to epimerisation over the course of a synthetic sequence. The methyl group also contributes a mild lipophilic character that is frequently useful for balancing the solubility of the final molecule. The primary amine, meanwhile, is a highly versatile nucleophile, ready to form amides, sulfonamides, ureas, thioureas, or secondary amines through reductive amination.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university and institutional research groups working on medicinal chemistry and organic synthesis, as well as in contract and industrial research settings that prepare intermediates on a small scale. It is generally ordered as part of a fragment collection used for analogue preparation, where the Boc-protected ring nitrogen allows a coupling step to be performed first and the ring nitrogen to be released and functionalised later in the sequence.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAmide bond formation: the free primary amine couples readily with carboxylic acids or activated esters, letting researchers install a compact azetidine fragment into a larger target scaffold.\u003c\/li\u003e\n\u003cli\u003eReductive amination: the primary amine reacts with aldehydes and ketones to give secondary amines, providing a direct route to branched amine analogues on a rigid sp3 framework.\u003c\/li\u003e\n\u003cli\u003eSulfonamide and urea synthesis: the amine handle is well suited to reaction with sulfonyl chlorides or isocyanates, generating sulfonamide, urea, and thiourea derivatives for structure-activity studies.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry analogue preparation: the small, sp3-rich azetidine core adds three-dimensional character to a molecule without the excessive molecular weight that larger fragments contribute.\u003c\/li\u003e\n\u003cli\u003eOrthogonal two-stage functionalisation: the Boc-protected ring nitrogen lets chemists react the primary amine first, then deprotect and functionalise the ring nitrogen in a separate, controlled step.\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: 1158758-85-0\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D6517\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard research-scale pack sizes; please confirm the currently available options when ordering\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 this building block in its original tightly closed container, following the storage temperature and conditions given on the manufacturer's label and safety data sheet. Keep the container in a cool, dry, well-ventilated area away from moisture, direct sunlight, heat sources, and incompatible materials, and reseal it promptly after each use. Because the material carries a free primary amine and a Boc carbamate, exposure to acidic vapours and prolonged exposure to air or humidity should be avoided. Handle the compound in a fume hood using appropriate personal protective equipment, including safety glasses, a laboratory coat, and chemically resistant gloves. Weigh and transfer with clean, dry spatulas and glassware to prevent contamination, and dispose of any residues and contaminated materials in accordance with applicable laboratory waste procedures. Consult the full safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086810394842,"sku":"TCI2510D651727563","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086810427610,"sku":"TCI2510D651727564","price":2121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6517.jpg?v=1767110349"},{"product_id":"tci2510e054628348","title":"TCI E0546 3047-32-3 3-Ethyl-3-oxetanemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Ethyl-3-oxetanemethanol is a chemical compound widely used as a foundational building block in the synthesis of complex molecules. In laboratory settings, it plays a crucial role in organic chemistry by enabling the construction of more intricate molecular structures. Its versatility makes it an essential component for researchers aiming to develop new compounds with specific functional groups or properties. This compound is particularly valuable in synthetic pathways where controlled reactivity and structural flexibility are required.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and predictable chemical behavior make it a preferred choice for laboratory use. Its simple yet adaptable molecular structure allows it to react efficiently with a variety of reagents, facilitating the creation of diverse chemical products. Additionally, its availability in multiple packaging formats supports its use in both small-scale and large-scale experiments. These properties ensure that it remains a reliable and consistent material for chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Ethyl-3-oxetanemethanol is commonly utilized in research related to organic chemistry, pharmaceutical development, and material science. Its relevance spans across academic institutions and research centers, where it supports the advancement of scientific knowledge. The compound’s reliability and adaptability make it an indispensable tool for chemical experimentation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where 3-Ethyl-3-oxetanemethanol serves as a versatile building block for constructing complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research benefits from its reactivity and stability, allowing the development of new drug compounds with specific functional groups.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments utilize this compound to create polymers and other advanced materials with tailored properties.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry laboratories use it as a standard reference material for testing and calibrating chemical processes.\u003c\/li\u003e\n\u003cli\u003eEducational institutions incorporate it into curriculum-based experiments to teach students about molecular structure and chemical reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3047-32-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes to suit different experimental needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\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 stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its chemical integrity. Proper labeling of containers is essential for safety and identification. In laboratory settings, it should be handled with appropriate personal protective equipment to ensure safe usage. Regular monitoring of storage conditions is advised to maintain optimal performance and safety standards.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086879011034,"sku":"TCI2510E054628348","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086879043802,"sku":"TCI2510E054628349","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086879076570,"sku":"TCI2510E054628350","price":1641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0546.jpg?v=1769180749"},{"product_id":"tci2510e093128768","title":"TCI E0931 14924-53-9 Ethyl Cyclobutanecarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyclobutanecarboxylate is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It serves as a fundamental reagent in laboratory settings, enabling the construction of more intricate molecular structures through carbon-carbon bond formation. Its role is critical in organic synthesis and chemical research, where it provides a stable and predictable starting point for various chemical transformations. This compound is particularly valued for its versatility and reliability in experimental processes.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its chemical stability under controlled conditions, which minimizes unwanted side reactions and degradation. It dissolves well in common organic solvents such as ethyl acetate and ethanol, making it easy to handle and incorporate into reaction mixtures. Its non-reactive nature also makes it suitable for applications requiring precise environmental control. These properties contribute to its popularity among researchers and chemists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl Cyclobutanecarboxylate is commonly used in both pure and applied chemical research. Its availability and stable properties make it a preferred choice for academic and industrial studies. It is frequently employed in the development of new chemical compounds and in educational settings to teach fundamental organic chemistry principles.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Ethyl Cyclobutanecarboxylate due to its role in forming carbon-carbon bonds and its stability during reactions.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for research projects involving complex molecule construction as it provides a reliable and predictable starting material.\u003c\/li\u003e\n\u003cli\u003eIn chemical education, this compound is used to demonstrate fundamental reaction mechanisms and synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eIt supports the development of new pharmaceutical compounds by serving as a key intermediate in various synthetic routes.\u003c\/li\u003e\n\u003cli\u003eIts solubility in organic solvents makes it suitable for use in solution-based reactions and purification 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: 14924-53-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl Cyclobutanecarboxylate 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 evaporation and contamination. The compound should be stored away from strong oxidizing agents and reactive materials to avoid unintended chemical interactions. Due to its solubility in organic solvents, it is important to ensure that storage containers are made of appropriate materials that do not react with the compound. Proper labeling and safe handling procedures should be followed to ensure laboratory safety and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086909485274,"sku":"TCI2510E093128768","price":707000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086909518042,"sku":"TCI2510E093128769","price":707000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0931.jpg?v=1767112008"},{"product_id":"tci2510e124529205","title":"TCI E1245 35120-18-4 Ethyl 1-Bromocyclobutanecarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-Bromocyclobutanecarboxylate is a chemical compound widely used in organic laboratory reactions. It serves as a key building block in the synthesis of complex organic molecules, offering versatility in chemical transformations. This compound is particularly valuable for its ability to participate in substitution and ring-opening reactions, making it a fundamental tool in synthetic chemistry. Its structural features enable it to be a starting point for the development of various functional compounds, including heterocyclic and specialized organic structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for researchers. It exhibits stability under certain conditions but remains reactive towards bases and high temperatures, which is advantageous for controlled chemical reactions. The presence of the bromo group enhances its reactivity, allowing for highly specific substitution reactions. This reactivity is crucial in the synthesis of targeted molecules, offering chemists a reliable and efficient tool for their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 1-Bromocyclobutanecarboxylate is commonly used in academic and research settings. It is a staple in universities and research institutions where organic chemistry is a focus. Its role in building complex molecular structures supports both educational and applied research, contributing to the advancement of chemical knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its reactivity and structural versatility, enabling the creation of complex molecules.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for substitution reactions due to its bromo group, allowing for precise chemical modifications in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eRing-opening reactions are effectively facilitated by its cyclic structure, making it suitable for polymer and functional group synthesis.\u003c\/li\u003e\n\u003cli\u003eIt supports the development of heterocyclic compounds, which are essential in pharmaceutical and materials science research.\u003c\/li\u003e\n\u003cli\u003eIts use in educational settings helps students understand reaction mechanisms and synthetic strategies in organic 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: 35120-18-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on the specific product variant\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-Bromocyclobutanecarboxylate 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 reactivity, it should be stored away from strong bases and high-temperature sources. Appropriate personal protective equipment, such as gloves and safety goggles, should be used when handling the compound. In laboratory settings, it is essential to follow standard safety protocols to ensure safe handling and minimize potential hazards. Proper ventilation should be maintained when working with this compound to avoid inhalation of vapors.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086940287194,"sku":"TCI2510E124529205","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086940319962,"sku":"TCI2510E124529206","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1245.jpg?v=1767112584"},{"product_id":"tci2510e139029397","title":"TCI E1390 158602-35-8 Ethyl 1-(tert-Butoxycarbonyl)-3-azetidineacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 1-(tert-Butoxycarbonyl)-3-azetidineacetate is a complex chemical compound widely used in the synthesis of heterocyclic compounds. This material plays a crucial role in laboratory settings where the formation of azetidine structures is required. Its chemical structure enables it to act as a building block in the development of more complex molecules, making it a valuable resource for researchers in various scientific disciplines. Due to its stability and reactivity, it is frequently employed in organic chemistry and pharmaceutical research to create compounds with specific functional groups and molecular frameworks.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure is highly stable, allowing it to serve as a reliable precursor in substitution and coupling reactions. Its ability to form new bonds with high precision makes it a preferred choice for synthetic chemists aiming to design and synthesize complex molecules. The compound is available in solid form, which simplifies handling and storage, making it a practical option for laboratories that require consistent and reliable chemical reagents. Its versatility and chemical properties contribute to its widespread use in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in scientific research and the development of new compounds, particularly in the fields of pharmacy and organic chemistry. Many research institutions and universities rely on it to expand their understanding of heterocyclic synthesis. Its availability and performance make it an essential tool for researchers working on drug discovery, material science, and other advanced chemical applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic Compound Synthesis: This compound is ideal for synthesizing complex heterocyclic structures due to its stable molecular framework and reactivity in forming azetidine rings.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development to create molecules with specific functional groups and molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its role as a building block makes it suitable for exploring new synthetic pathways and molecular transformations.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Investigations: The compound's chemical properties are valuable in the development of new materials with unique structural characteristics.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is frequently used in university laboratories to teach and conduct experiments on advanced chemical synthesis techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 158602-35-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is essential when working with this material to minimize exposure. It should not be stored near incompatible substances or in areas with high humidity. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086956638426,"sku":"TCI2510E139029397","price":2852000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1390.jpg?v=1767112769"},{"product_id":"tci2510e156629619","title":"TCI E1566 298695-60-0 3-Ethyl-3-[[(2-ethylhexyl)oxy]methyl]oxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Ethyl-3-[[(2-ethylhexyl)oxy]methyl]oxetane, supplied by TCI under catalogue code E1566, is an oxetane monomer carrying a 2-ethylhexyl ether side chain. The oxetane unit is a four-membered cyclic ether that holds a considerable degree of ring strain, which makes it open readily under cationic polymerisation conditions. Because of this behaviour, oxetane compounds are widely used as monomers or reactive diluents in cationic curing systems initiated by ultraviolet light. Within the heterocyclic building block group, this material also serves as a starting framework for the synthesis of oxetane-containing molecules, a class that has attracted growing interest in organic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this monomer a preferred choice is its balance between reactivity and viscosity. The oxetane ring reacts in a more controlled manner than epoxides in several systems, while the long, branched 2-ethylhexyl chain lowers the viscosity of the formulation and at the same time improves the flexibility and hydrophobic character of the film that is formed. The branched structure also helps prevent crystallisation, so the material remains a liquid that is easy to blend into a formulation. In UV-curing formulations, oxetane monomers are frequently combined with cycloaliphatic epoxide resins.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically handled in research and development work on coatings, inks and adhesives, as well as in synthetic organic chemistry groups building oxetane-containing structures. It is usually drawn in small volumes for formulation trials, cure studies and comparative screening against epoxide-based systems. University and industrial laboratories alike use it where a reactive diluent is needed that keeps a mixture workable without compromising the properties of the cured layer.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCationic UV-curing formulation development: the strained oxetane ring opens readily under photoinitiated cationic conditions, making the monomer a direct participant in the curing network rather than an inert additive.\u003c\/li\u003e\n\u003cli\u003eReactive diluent in coating systems: the branched 2-ethylhexyl chain lowers formulation viscosity so that mixtures remain workable, while the oxetane group still reacts into the final cured film.\u003c\/li\u003e\n\u003cli\u003eCo-monomer with cycloaliphatic epoxide resins: oxetane monomers are commonly paired with these resins, allowing formulators to tune the overall reactivity and handling of a cationic system.\u003c\/li\u003e\n\u003cli\u003eSynthesis of oxetane-containing molecules: as a heterocyclic building block, it provides a ready oxetane framework for organic chemists working on this increasingly studied structural class.\u003c\/li\u003e\n\u003cli\u003eFlexibility and hydrophobicity studies in cured films: the long branched side chain contributes both flexibility and hydrophobic character, making the monomer useful for comparative film property work.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI, catalogue number E1566\u003c\/li\u003e\n\u003cli\u003eCAS number: 298695-60-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research packaging; please confirm the pack size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, the branched structure helping to prevent crystallisation\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool place, closed tightly, and away from light and ignition sources\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, well-ventilated area, protected from direct light and away from heat, sparks and open flames. Keep the material in its original supplier packaging or in a compatible, clearly labelled closed container, and avoid contact with acids or strong Lewis acid species, since these can initiate cationic ring opening of the oxetane. Handle in a fume hood using gloves, safety glasses and a laboratory coat, transfer with clean dry glassware or syringes, and close the container promptly after use to limit exposure to air and moisture. Consult the manufacturer's safety data sheet before first use and follow institutional chemical waste procedures for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086970106074,"sku":"TCI2510E156629619","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086970138842,"sku":"TCI2510E156629620","price":2020000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1566.jpg?v=1768818850"},{"product_id":"tci2510f109931184","title":"TCI F1099 193693-64-0 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]azetidine-3-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI F1099, 1-[(9H-Fluoren-9-ylmethoxy)carbonyl]azetidine-3-carboxylic Acid, is a specialized chemical compound used in the synthesis of complex heterocyclic structures. This compound plays a critical role in organic chemistry laboratories, particularly in the development of pharmaceuticals and industrial chemicals. Its unique molecular structure enables it to participate in a variety of chemical reactions, making it an essential building block for researchers aiming to create new compounds with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical stability under controlled conditions ensures that it remains effective throughout the synthesis process without undergoing excessive degradation. This stability, combined with its ability to form specific and precise chemical reactions, makes it a preferred choice for chemists working on intricate molecular designs. Its non-reactive nature in uncontrolled environments further enhances its reliability as a reagent in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, especially in the synthesis of pharmaceutical compounds and specialty chemicals. It is a key component in the development of new drugs and materials, supporting both academic and industrial research. Many research institutions and universities in Indonesia rely on this compound to advance their understanding of molecular structures and reactivity in heterocyclic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of pharmaceutical compounds due to its ability to form stable and specific chemical bonds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of industrial chemicals through its role in building complex molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eResearch in heterocyclic chemistry for studying molecular reactivity and structural modifications.\u003c\/li\u003e\n\u003cli\u003eCreation of novel drug candidates by facilitating the formation of functional groups in target molecules.\u003c\/li\u003e\n\u003cli\u003eSupport for academic research in chemical engineering and medicinal chemistry laboratories.\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: 193693-64-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and maintain its chemical integrity. Due to its stability, it does not require refrigeration but should be kept in a secure location to avoid contamination. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment to ensure safety. Regular monitoring of storage conditions is advised to maintain its effectiveness for research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087058022618,"sku":"TCI2510F109931184","price":2197000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1099.jpg?v=1767114146"},{"product_id":"tci2510f118631292","title":"TCI F1186 617718-46-4 3-Fluoroazetidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Fluoroazetidine Hydrochloride is a chemical compound widely used as a building block in the synthesis of complex molecules, particularly in the fields of organic chemistry and pharmacology. This compound features a fluorinated azetidine ring, making it a key component in the development of compounds with specific biological activities. Its structural uniqueness allows it to serve as a versatile intermediate in various synthetic pathways, supporting the creation of new compounds with therapeutic or industrial potential. In laboratory settings, it plays a crucial role in molecular synthesis and modification processes, contributing to the advancement of research in multiple scientific disciplines.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high polarity due to the fluorine atom, which enhances its solubility in organic solvents such as ethyl acetate and acetone. This property makes it suitable for reactions requiring high reactivity and structural stability. Additionally, it exhibits chemical stability under certain conditions, although it remains reactive to various chemical environments. These characteristics make it a preferred choice for researchers aiming to achieve precise and efficient synthetic outcomes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Fluoroazetidine Hydrochloride is commonly utilized in organic chemistry research, especially within academic institutions and research organizations. It is an essential part of the process for developing new compounds, supporting both educational and applied research initiatives. Its availability through suppliers like AMI Scientific ensures that it remains a valuable resource for scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis research utilizes 3-Fluoroazetidine Hydrochloride for constructing complex molecular frameworks due to its fluorinated azetidine ring.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from this compound as it contributes to the creation of bioactive molecules with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eAcademic laboratories employ it in teaching and research to demonstrate fluorinated building blocks in synthetic chemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for the production of specialty chemicals requiring precise molecular structures.\u003c\/li\u003e\n\u003cli\u003eDrug discovery initiatives use it as a starting material to explore new compounds with potential pharmaceutical applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 617718-46-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Fluorinated Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid 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\u003e3-Fluoroazetidine Hydrochloride 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, which could affect its reactivity. Suitable storage conditions include a controlled temperature range between 15°C and 25°C. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Due to its reactivity, it should be stored separately from incompatible substances to avoid any chemical interactions. Proper labeling and storage practices ensure safe handling and long-term usability in research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48087065493722,"sku":"TCI2510F118631292","price":984000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087065526490,"sku":"TCI2510F118631293","price":984000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1186.jpg?v=1767114224"},{"product_id":"tci2510h077333445","title":"TCI H0773 61266-70-4 2-Hydroxymethyloxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxymethyloxetane is a chemical compound widely used in organic reactions to construct complex heterocyclic structures. As a building block, it plays a crucial role in the synthesis of cyclic compounds with functional group substitutions. Its versatility makes it a valuable tool for researchers aiming to develop new organic molecules. This compound is particularly useful in laboratories where precise chemical reactions and structural modifications are required.\u003c\/p\u003e\n\u003cp\u003eThe compound's cyclic structure is stable and allows it to participate in a variety of chemical reactions, including nucleophilic, electrophilic, and substitution reactions. Its high polarity enables it to dissolve easily in polar solvents such as ethylamine or acetone, making it ideal for reactions that require strong molecular interactions. These properties make it a preferred choice for synthetic chemists working on intricate molecular designs.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Hydroxymethyloxetane is commonly used by chemists and scientists for the synthesis of new organic compounds, especially in the fields of pharmacology and material science. Its reliability and chemical stability make it an essential component in experiments that demand accuracy and consistency. It is frequently utilized in research projects that require the development of heterocyclic compounds for various applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic Compound Synthesis: This compound is ideal for creating complex ring structures, essential in pharmaceutical and material science research.\u003c\/li\u003e\n\u003cli\u003eOrganic Reaction Building Blocks: Its ability to participate in multiple reaction types makes it a go-to choice for synthetic pathways requiring functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Substitution Studies: The compound's reactivity allows for precise substitution reactions, useful in modifying molecular structures for targeted applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: Its role in synthesizing bioactive molecules supports drug development and medicinal chemistry studies.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Development: It contributes to the creation of advanced materials with specific chemical properties and structural integrity.\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: 61266-70-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Liquid\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 location, away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and evaporation. Due to its high polarity, it is important to handle it with care to avoid exposure to incompatible materials. Always ensure proper ventilation when working with this compound to minimize inhalation risks. In laboratory settings, it should be kept in a secure area that is accessible only to authorized personnel. Regular monitoring of storage conditions is advised to maintain its chemical stability and ensure safe handling practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087235363034,"sku":"TCI2510H077333445","price":14107000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0773.jpg?v=1769142559"},{"product_id":"tci2510h126434043","title":"TCI H1264 18621-18-6 3-Hydroxyazetidine Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Hydroxyazetidine Hydrochloride is a chemical compound widely used in organic synthesis reactions, particularly in the formation of heterocyclic compounds. As a key building block in chemical research, it serves as a versatile intermediate in the development of complex molecular structures. Its role in laboratory settings is critical, especially in the synthesis of compounds with biological activity, such as pharmaceuticals and industrial chemicals. Due to its chemical stability and reactivity, it is a preferred choice for chemists working on advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThis compound exhibits solubility in organic solvents and has a relatively high melting point, which facilitates purification and thermal processing in laboratory procedures. These physical properties make it ideal for use in both preparative and analytical chemistry applications. Its ability to participate in various chemical reactions, such as nucleophilic substitutions and cyclizations, further enhances its utility in synthetic chemistry. The compound's reliability and consistency in performance make it a trusted material in research laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Hydroxyazetidine Hydrochloride is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and bioactive molecules. It is also utilized in scientific studies that require specific chemical building blocks for the development of new materials and pharmaceuticals. Its presence in laboratory workflows supports innovation and discovery in both academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and bioactive molecules as a precursor in complex synthesis pathways.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the creation of compounds with therapeutic potential.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production requiring stable and reactive building blocks for compound development.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications where precise chemical intermediates are essential for reaction control.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 18621-18-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e3-Hydroxyazetidine Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and air, which could affect its integrity. Due to its chemical nature, it should be handled in a well-ventilated laboratory setting to minimize inhalation risks. Avoid contact with skin and eyes, and use appropriate personal protective equipment when handling. Proper storage conditions ensure the compound remains effective for use in chemical synthesis and research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087264723162,"sku":"TCI2510H126434043","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087264755930,"sku":"TCI2510H126434044","price":1363000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1264.jpg?v=1767117696"},{"product_id":"tci2510i087236163","title":"TCI I0872 26272-85-5 3-Iodooxetane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Iodooxetane is a chemical compound widely used as a building block in the synthesis of heterocyclic compounds. Its simple molecular structure plays a crucial role in the formation of more complex chemical structures. In laboratory settings, it serves as a key reagent for functional group transformations and the creation of new chemical bonds. This compound is particularly valuable in organic chemistry due to its reactivity and versatility.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of 3-Iodooxetane is primarily attributed to the presence of the iodine atom, which readily participates in various chemical reactions. Its solubility in organic solvents further enhances its usability in laboratory processes. These properties make it a preferred choice for chemists working on synthetic routes that require high reactivity and compatibility with a range of reagents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Iodooxetane is extensively used in scientific research, particularly in the fields of organic chemistry and heterocyclic synthesis. It is highly relevant for academic institutions and research organizations focused on the development of new compounds. Its application supports both educational and industrial research activities, making it an essential material for laboratory work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeterocyclic Compound Synthesis: 3-Iodooxetane is ideal for creating complex ring structures due to its reactivity and compatibility with various functional groups.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Transformation: Its iodine atom facilitates substitution reactions, making it suitable for modifying existing chemical structures in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: The compound is widely used in academic and industrial research for developing new chemical compounds and materials.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Production: Its versatility supports large-scale synthesis processes in chemical manufacturing.\u003c\/li\u003e\n\u003cli\u003eEducational Laboratory Work: It is commonly used in teaching laboratories to demonstrate chemical reactivity and synthetic techniques.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 26272-85-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e3-Iodooxetane should be stored in a cool, dry place, away from direct light and incompatible substances. It is recommended to use airtight containers made of materials that do not react with the compound, such as glass or stainless steel. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Proper personal protective equipment, including gloves and safety goggles, should be worn when handling the compound. It is important to avoid contact with moisture and to keep it away from heat sources to ensure safe storage and use in the laboratory.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087422206170,"sku":"TCI2510I087236163","price":2271000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0872.jpg?v=1769142752"},{"product_id":"tci2510m113639095","title":"TCI M1136 3143-02-0 3-Methyl-3-oxetanemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI M1136 3-Methyl-3-oxetanemethanol is an alcohol that carries a four-membered oxetane ring within its structure. The oxetane ring is a small cyclic ether that holds a considerable amount of ring strain, and it is precisely that strain which makes the compound interesting both as a reactive group and as a structural motif. The molecule also bears a free primary hydroxyl group that is ready to react without disturbing the ring itself, so researchers can attach the oxetane ring to other molecules through esterification, etherification, or reaction with isocyanates, and then exploit the ring in a subsequent step.\u003c\/p\u003e\n\u003cp\u003eThe usefulness of this building block rests on two properties at once. First, the oxetane ring can be opened through cationic polymerization, which makes the compound an important raw material in the preparation of polymers and resins that cure under ultraviolet light. Second, in medicinal chemistry the oxetane ring is valued as a replacement for gem-dimethyl and carbonyl groups, because it occupies a similar spatial volume while improving solubility in water and altering the metabolic profile of a molecule. Its primary hydroxyl group is reactive yet not excessively hindered on steric grounds, so coupling reactions proceed smoothly.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this compound is typically encountered in synthetic organic chemistry groups, polymer and coating research units, and pharmaceutical discovery programmes that build candidate molecules from defined fragments. It is handled on the bench as a starting material for multi-step routes, where the free hydroxyl group is coupled first and the strained ring is carried forward intact. Its role is that of a versatile intermediate rather than a finished formulation, supplied for research and development work.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCationic photopolymerization and UV-curable resin development, where the strained oxetane ring opens under acid initiation to build polymer networks that harden on exposure to ultraviolet light.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry fragment design, where the oxetane ring substitutes for a gem-dimethyl or carbonyl group to occupy similar space while improving aqueous solubility of the candidate molecule.\u003c\/li\u003e\n\u003cli\u003eEsterification chemistry, in which the free primary hydroxyl group is acylated cleanly without disturbing the four-membered ring, delivering oxetane-bearing esters for later transformation.\u003c\/li\u003e\n\u003cli\u003eEtherification and alkylation routes, where the relatively unhindered primary alcohol allows oxetane motifs to be grafted onto larger scaffolds through straightforward coupling steps.\u003c\/li\u003e\n\u003cli\u003eReaction with isocyanates to form carbamate linkages, letting researchers install the oxetane ring into urethane-type structures and then exploit ring strain in a subsequent stage.\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: 3143-02-0\u003c\/li\u003e\n\u003cli\u003eCatalogue number: M1136\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 TCI research-scale packaging; please confirm the currently listed sizes when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in a tightly closed original container, away from heat and ignition sources\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 area, away from heat, open flames, and sources of ignition, and keep it in the original supplier packaging or another compatible tightly sealed vessel that protects the contents from moisture. Handle the material inside a fume hood while wearing safety goggles, chemical-resistant gloves, and a laboratory coat, and avoid contact with skin, eyes, and clothing as well as inhalation of vapour. Because the strained oxetane ring is susceptible to acid-catalysed ring opening, keep the compound away from strong acids and strong oxidising agents. Always consult the manufacturer safety data sheet before use, and dispose of residues and contaminated materials according to institutional chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087587815642,"sku":"TCI2510M113639095","price":884000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087587848410,"sku":"TCI2510M113639096","price":884000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M1136.jpg?v=1768361431"},{"product_id":"tci2510m252140799","title":"TCI M2521 100202-39-9 Methyl Azetidine-3-carboxylate Hydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl Azetidine-3-carboxylate Hydrochloride is a chemical compound widely used in organic synthesis reactions, particularly in the development of heterocyclic compounds. This material serves as a key building block in laboratories, enabling the construction of complex molecular structures through various chemical transformations. Its role is essential in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals, where precise molecular design is required. Due to its versatility and reactivity, it is a fundamental reagent in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stable chemical structure and favorable reactivity, which allow for efficient and selective chemical reactions. Its solubility in organic solvents enhances its usability in purification and reaction processes, making it a preferred choice for chemists. The compound’s ability to participate in multiple synthetic pathways further solidifies its importance in the field of organic chemistry. These properties make it a reliable and effective reagent for a wide range of applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Methyl Azetidine-3-carboxylate Hydrochloride is commonly used in organic chemistry research, especially in the development of new compounds with pharmaceutical or industrial applications. It is also utilized in educational settings to teach students about organic synthesis and the behavior of heterocyclic compounds. Its presence in both research and teaching environments highlights its significance in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and agrochemicals through targeted molecular modifications.\u003c\/li\u003e\n\u003cli\u003eEducational use in teaching organic chemistry and heterocyclic compound reactivity.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the design of bioactive molecules.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications in the production of specialty chemicals requiring precise molecular 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: 100202-39-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\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\u003eMethyl Azetidine-3-carboxylate Hydrochloride should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent exposure to moisture and contaminants. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid direct contact with skin and eyes, and ensure proper ventilation when working with the compound. It is important to store it away from incompatible substances to prevent any potential chemical reactions. Proper storage conditions help preserve the integrity and effectiveness of the compound for laboratory use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087694082266,"sku":"TCI2510M252140799","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087694115034,"sku":"TCI2510M252140800","price":1641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2521.jpg?v=1767126745"},{"product_id":"tci2510m288441313","title":"TCI M2884 765-85-5 Methyl Cyclobutanecarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl Cyclobutanecarboxylate (MCBC), with CAS number 765-85-5, is a chemical compound widely used as a building block in organic synthesis. It plays a crucial role in laboratories where the development of complex organic molecules is required. This compound is particularly valuable for its ability to participate in various chemical reactions, making it a versatile tool for synthetic chemists. Its presence in both academic and industrial research settings highlights its importance in the field of chemical innovation.\u003c\/p\u003e\n\u003cp\u003eMCBC is favored for its chemical stability and moderate reactivity, which allow it to undergo a range of reactions such as substitution, coupling, and cyclization. Its simple molecular structure provides a flexible foundation for the synthesis of more complex compounds. These properties make it a preferred choice for researchers aiming to modify existing molecules or create new ones with specific functional groups. Its reliability and adaptability contribute to its widespread use in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, MCBC is commonly used in organic chemistry research, particularly in universities and research institutions. It is essential for projects involving the synthesis of new compounds, structural modifications, and the development of chemically useful products. Its relevance extends to industrial applications, supporting the creation of materials and pharmaceuticals with practical uses.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for drug development due to its ability to form stable ring structures.\u003c\/li\u003e\n\u003cli\u003eProduction of aromatic compounds through functional group modifications and coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical entities in pharmaceutical research for improved therapeutic properties.\u003c\/li\u003e\n\u003cli\u003eStructural modification of existing molecules to enhance chemical and biological activity.\u003c\/li\u003e\n\u003cli\u003eCreation of industrial chemical products requiring precise molecular design and synthetic flexibility.\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: 765-85-5\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: Liquid\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\u003eMethyl Cyclobutanecarboxylate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Suitable storage containers include glass or high-density polyethylene bottles. Due to its chemical nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and goggles should be worn. Avoid contact with incompatible substances and ensure proper disposal according to local regulations. Regular monitoring of storage conditions is advised to ensure the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087721279706,"sku":"TCI2510M288441313","price":1413000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087721312474,"sku":"TCI2510M288441314","price":1413000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2884.jpg?v=1767127395"},{"product_id":"tci2510m296241410","title":"TCI M2962 28562-68-7 3-Methyl-3-oxetanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Methyl-3-oxetanecarboxylic Acid is a versatile chemical compound widely used in laboratory settings for the synthesis of complex molecules. As a heterocyclic building block, it plays a crucial role in organic chemistry by enabling the formation of diverse molecular structures. This compound is particularly valuable in pharmaceutical research, where it contributes to the development of bioactive compounds and synthetic intermediates. Its unique chemical properties make it a preferred choice for researchers seeking to explore new synthetic pathways and molecular designs.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity are key factors that make it a preferred choice in chemical synthesis. Its oxetane ring structure provides a stable yet reactive framework, allowing it to participate in various chemical reactions such as substitution and cyclization. The compound exhibits good solubility in organic solvents, which facilitates its use in a wide range of experimental procedures. These characteristics make it an essential component in the synthesis of pharmaceuticals, agrochemicals, and other complex organic compounds.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3-Methyl-3-oxetanecarboxylic Acid is commonly used in organic chemistry research, especially in pharmaceutical and synthetic chemistry applications. It is a key reagent in the development of new compounds and is frequently utilized in academic and research institutions. Its role in advancing chemical synthesis and drug discovery makes it an important material for scientific innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound due to its stable oxetane ring and reactivity in substitution reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes it for the development of bioactive compounds and synthetic intermediates.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for cyclization reactions due to its ability to form stable ring structures under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eAgrochemical synthesis often incorporates this compound for the creation of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eIt supports the development of new chemical entities in academic and industrial research settings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 28562-68-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or crystalline, depending on the batch\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 stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Proper labeling of containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment when handling the material. Due to its chemical nature, it should be stored separately from incompatible substances. Regular inspection 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":48087725932762,"sku":"TCI2510M296241410","price":2979000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2962.jpg?v=1767127534"},{"product_id":"tci2510m336941926","title":"TCI M3369 2507954-88-1 tert-Butyl 3-(4-Methoxybenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-(4-Methoxybenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate is a complex organic compound widely used in the synthesis of heterocyclic compounds. This building block is essential for chemists and pharmacologists working on the development of new bioactive molecules. Its unique structure combines an azetidine ring with a boronic acid derivative, making it a versatile reagent in various chemical reactions. The compound is particularly valuable in synthetic pathways that require precise control over molecular structure and reactivity.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and controlled reactivity make it a preferred choice for high-precision chemical reactions. Its tert-butyl group enhances solubility and reduces unwanted side reactions, ensuring reliable results in laboratory settings. The presence of the boronic acid group allows for efficient coupling reactions, especially in S-N coupling processes. These properties make it an ideal reagent for applications that demand both stability and reactivity. Its molecular complexity also supports the synthesis of a wide range of target molecules with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical and chemical research projects. It plays a crucial role in the development of new drugs and organic compounds with potential therapeutic applications. Researchers rely on its predictable behavior and compatibility with various synthetic methods to achieve consistent and reproducible results. Its availability and performance make it a go-to reagent for advanced chemical synthesis in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis for creating complex heterocyclic structures due to its azetidine and boronic acid functionalities.\u003c\/li\u003e\n\u003cli\u003eApplied in drug development projects to build molecules with potential therapeutic properties through precise chemical modifications.\u003c\/li\u003e\n\u003cli\u003eEmployed in S-N coupling reactions to form new carbon-nitrogen bonds, enhancing the efficiency of synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eUtilized in pharmaceutical research for the synthesis of bioactive compounds with targeted molecular features.\u003c\/li\u003e\n\u003cli\u003eIntegrated into medicinal chemistry workflows to design and develop novel compounds with improved pharmacological profiles.\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: 2507954-88-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, crystalline 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 sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area with appropriate personal protective equipment. Avoid contact with incompatible substances such as strong oxidizers. The compound is best stored in airtight containers made of glass or high-density polyethylene to ensure long-term preservation. Proper labeling and storage conditions are essential to maintain its integrity and ensure safe usage in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48087748608218,"sku":"TCI2510M336941926","price":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087748640986,"sku":"TCI2510M336941927","price":2171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M3369.jpg?v=1767128119"},{"product_id":"tci2510m337041928","title":"TCI M3370 2507954-87-0 tert-Butyl 3-(4-Methylbenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThe TCI M3370, tert-Butyl 3-(4-Methylbenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate, is a complex heterocyclic building block used extensively in organic chemistry laboratories. This compound plays a crucial role in the synthesis of various organic molecules, particularly those requiring high reactivity and functional group versatility. Its unique molecular structure enables it to participate in a wide range of chemical transformations, making it an essential component in modern synthetic strategies. In Indonesia, this compound is widely used in academic and industrial research settings to develop new compounds with specific biological activities.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure features a boronic acid group and an azetidine ring, which contribute to its reactivity and selectivity in chemical reactions. These properties make it a preferred choice for chemists working on complex syntheses, especially in the context of cross-coupling reactions such as the Suzuki-Miyaura reaction. The presence of the boron atom allows for efficient coupling with a variety of aromatic and aliphatic compounds, enhancing the versatility of this building block. Its stability under controlled conditions further supports its use in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical and chemical research to develop new drugs and functional materials. It is a key reagent in the synthesis of bioactive compounds, particularly those with potential therapeutic applications. Researchers rely on its predictable reactivity and compatibility with various reaction conditions to achieve desired chemical outcomes in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthetic Organic Chemistry: This compound is ideal for synthesizing complex organic molecules due to its reactivity and compatibility with various reaction conditions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development for creating bioactive compounds with specific therapeutic properties.\u003c\/li\u003e\n\u003cli\u003eCross-Coupling Reactions: Its boronic acid group makes it suitable for Suzuki-Miyaura reactions, enabling the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eFunctional Material Development: It is employed in the creation of advanced materials with tailored chemical and physical properties.\u003c\/li\u003e\n\u003cli\u003eAcademic and Industrial Research: Its versatility and reliability make it a preferred choice for both academic studies and industrial 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: 2507954-87-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Not specified in the provided data\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 with care in a well-ventilated laboratory setting. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment such as gloves and safety goggles. Ensure that storage conditions are consistent to prevent degradation. Proper labeling and storage away from incompatible materials are essential for safe handling and long-term stability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48087748673754,"sku":"TCI2510M337041928","price":1894000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48087748706522,"sku":"TCI2510M337041929","price":1894000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M3370.jpg?v=1767128123"}],"url":"https:\/\/amiscientific.com\/en\/collections\/chemicals-by-class-4-membered-cyclic-compounds.oembed?page=6","provider":"AMI Scientific","version":"1.0","type":"link"}