{"title":"Divinyl Monomers and Diallyl Monomers [Biomaterials\/Biocompatible Materials Research Reagents]","description":"\u003cp\u003e\u003cstrong\u003eDivinyl Monomers and Diallyl Monomers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/strong\u003e — mencakup monomer dengan dua atau lebih gugus vinil maupun alil pada kerangka silikon, karbon, atau eter, termasuk turunan siklosiloksan tervinilasi dan alil eter bercabang. Gugus tak jenuh ganda pada struktur ini memungkinkan reaksi taut silang (crosslinking) untuk membentuk jaringan polimer tiga dimensi.\u003c\/p\u003e\u003cp\u003eDivinyl monomers and diallyl monomers dipakai peneliti material dalam reaksi hidrosilasi, polimerisasi radikal, atau tiol-ena untuk membangun jaringan silikon atau polieter yang digunakan sebagai basis hidrogel, elastomer, dan material biokompatibel. Turunan siklotrisiloksan dan siklotetrasiloksan tervinilasi umum dipakai sebagai unit taut silang pada sintesis polidimetilsiloksan (PDMS) termodifikasi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510a0235339\"\u003eTCI A0235 592-88-1 Allyl Sulfide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b605412857\"\u003eTCI B6054 4519-17-9 1,4-Bis(dimethylvinylsilyl)benzene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0229326\"\u003eTCI A0229 557-40-4 Allyl Ether\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c103815423\"\u003eTCI C1038 6299-73-6 Triallyl Citrate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t374555429\"\u003eTCI T3745 3901-77-7 2,4,6-Trimethyl-2,4,6-trivinylcyclotrisiloxane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d006919369\"\u003eTCI D0069 124-02-7 Diallylamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t351755165\"\u003eTCI T3517 60111-54-8 Tetrakis[dimethyl(vinyl)silyl] Orthosilicate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510d049819959\"\u003eTCI D0498 764-99-8 Diethylene Glycol Divinyl Ether\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan jumlah dan posisi gugus vinil atau alil per molekul serta kemungkinan campuran produk tersubstitusi (mono-, di-, atau tri-) yang memengaruhi densitas taut silang jaringan polimer akhir. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Biomaterials\/Biocompatible Materials Research Reagents, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-monomers-and-macromonomers-biomaterials-biocompatible-materials-resear\"\u003eMonomers and Macromonomers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polymerization-reagents-initiators-catalysts-ligands-biomaterials-bioc\"\u003ePolymerization Reagents (Initiators, Catalysts, Ligands) [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-polymers-biomaterials-biocompatible-materials-research-reagents\"\u003ePolymers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-acrylic-monomers-biomaterials-biocompatible-materials-research-reagents\"\u003eAcrylic Monomers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-diol-monomers-biomaterials-biocompatible-materials-research-reagents\"\u003eDiol Monomers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-diamine-monomers-biomaterials-biocompatible-materials-research-reagents\"\u003eDiamine Monomers [Biomaterials\/Biocompatible Materials Research Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-biomaterials-biocompatible-materials-research-reagents\"\u003eBiomaterials\/Biocompatible Materials Research Reagents\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510c103815423","title":"TCI C1038 6299-73-6 Triallyl Citrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTriallyl Citrate (TCI C1038, CAS 6299-73-6) is a trifunctional citric acid ester carrying three reactive allyl groups. Its multifunctional structure makes it an effective crosslinking monomer for free-radical polymerization and thiol-ene network formation. Researchers use it to increase network density, mechanical stability, and thermal performance in experimental resins, coatings, and gels. AMI Scientific supplies this monomer in a 5 mL pack, which should be stored cool, dark, and away from radical initiators to prevent premature polymerization.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":48086044737754,"sku":"TCI2510C103815423","price":2025000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1038.jpg?v=1767096224"},{"product_id":"tci2510d102720731","title":"TCI D1027 78-19-3 3,9-Divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,9-Divinyl-2,4,8,10-tetraoxaspiro[5.5]undecane is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. This compound belongs to the category of non-heterocyclic building blocks and is valued for its unique molecular structure, which features four oxygen atoms arranged symmetrically. Its role in organic chemistry is significant, as it serves as a versatile intermediate in various synthetic pathways. Due to its stability and controlled reactivity, it is a reliable choice for researchers aiming to develop new chemical structures.\u003c\/p\u003e\n\u003cp\u003eThe compound’s chemical properties make it a preferred choice in laboratory environments. It exhibits good reactivity towards substitution and addition reactions, allowing it to participate in a wide range of chemical transformations. Its molecular complexity enables it to be a key component in the synthesis of more intricate compounds, including heterocyclic structures and polymers. The predictable behavior of this compound under different reaction conditions enhances its utility in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of complex molecules. It is widely utilized by research institutions and universities for experimental purposes and the development of new chemical products. Its availability in various packaging options makes it convenient for use in both small-scale and larger laboratory operations. Its role in advancing chemical synthesis is well-recognized among Indonesian scientific communities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of complex organic compounds due to its unique molecular structure and reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of heterocyclic compounds as a versatile building block in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePolymer research as a component in the creation of advanced polymeric materials.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring stable and reactive intermediates for chemical transformations.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical synthesis to explore new molecular structures and reaction mechanisms.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 78-19-3\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 suitable for laboratory use\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, 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 maintain stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. Avoid exposure to incompatible substances such as strong oxidizing agents. Ensure proper ventilation in the workspace to minimize inhalation risks. Regular monitoring of storage conditions is advised to maintain the integrity of the compound during long-term use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086419144922,"sku":"TCI2510D102720731","price":2840000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086419177690,"sku":"TCI2510D102720732","price":7983000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086419210458,"sku":"TCI2510D102720733","price":24424000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1027.jpg?v=1767102437"},{"product_id":"tci2510d118320902","title":"TCI D1183 3195-24-2 Diethyl Diallylmalonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethyl Diallylmalonate is a chemical compound widely used as a foundational building block in organic synthesis. It plays a crucial role in laboratories by enabling the formation of carbon-carbon bonds through various chemical reactions, such as condensation or substitution. This compound is particularly valuable for researchers aiming to develop new organic molecules, including pharmaceuticals and advanced materials. Its versatility makes it an essential tool in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure is stable, and it exhibits good reactivity, allowing for efficient chemical transformations. These properties make it a preferred choice for chemists working on complex synthesis pathways. Its non-heterocyclic nature also simplifies its handling and processing under different reaction conditions, enhancing its applicability across multiple experimental setups. This stability and reactivity contribute to its reliability in both small-scale and large-scale chemical processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diethyl Diallylmalonate is a highly sought-after material for organic chemistry research. It is commonly used in the synthesis of new compounds and in studies related to drug development. Its availability and chemical properties make it a staple in academic institutions and research facilities, supporting both teaching and innovation in the field of chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis experiments benefit from Diethyl Diallylmalonate due to its ability to form carbon-carbon bonds efficiently, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound for the development of new drug compounds, as it enables the synthesis of various functional groups.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications rely on its stability and reactivity to create advanced chemical materials with specific properties.\u003c\/li\u003e\n\u003cli\u003eTeaching laboratories use it as a key reagent for demonstrating fundamental chemical reactions and synthesis techniques.\u003c\/li\u003e\n\u003cli\u003eIndustrial research settings employ it for large-scale production of organic compounds, ensuring consistency and efficiency in chemical manufacturing.\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: 3195-24-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard chemical packaging sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on supplier packaging\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\u003eDiethyl Diallylmalonate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed containers to prevent exposure to moisture and air, which may affect its chemical stability. Proper labeling of storage containers is essential to ensure safe handling. In laboratory settings, it should be kept away from incompatible materials such as strong oxidizers or acids. Always use appropriate personal protective equipment when handling this compound to minimize exposure risks. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in chemical experiments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086428745946,"sku":"TCI2510D118320902","price":4723000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086428778714,"sku":"TCI2510D118320903","price":15487000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1183.jpg?v=1767102627"},{"product_id":"tci2510d200322016","title":"TCI D2003 7398-69-8 Diallyldimethylammonium Chloride (60% in Water)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiallyldimethylammonium Chloride (60% in Water), also known as TCI D2003, is a chemical compound widely used as a phase transfer catalyst in laboratory settings. It plays a crucial role in facilitating reactions between polar and non-polar phases, which is essential for many synthetic processes. This compound is particularly valuable in chemical synthesis where reactions require interaction between two distinct phases, such as aqueous and organic solvents. Its ability to transfer ions or molecules across phases makes it indispensable in complex chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound is chemically stable and retains its catalytic activity under various reaction conditions. It is highly soluble in water, making it suitable for use in a wide range of experimental scales. Its effectiveness lies in its ability to enhance reaction efficiency without being consumed or degraded during the process. This characteristic ensures consistent performance and reliability in laboratory applications. Additionally, its non-toxic nature and ease of handling make it a preferred choice for researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diallyldimethylammonium Chloride is commonly used in chemical research, product development, and analytical testing. Its versatility and efficiency make it a go-to reagent for scientists working on diverse chemical processes. It is especially favored in applications that require precise control over phase interactions, ensuring accurate and reproducible results. Its widespread use reflects its importance in supporting scientific innovation and experimentation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChemical synthesis applications benefit from its ability to enhance reaction efficiency between polar and non-polar phases.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for organic reactions that require phase transfer catalysis, improving reaction rates and yield.\u003c\/li\u003e\n\u003cli\u003eIn analytical chemistry, it facilitates the separation and detection of compounds in complex mixtures.\u003c\/li\u003e\n\u003cli\u003eIt supports the development of new pharmaceuticals by enabling efficient synthetic pathways in drug research.\u003c\/li\u003e\n\u003cli\u003eEnvironmental testing laboratories use it to analyze pollutants in water and soil samples through phase transfer 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: 7398-69-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; Phase Transfer Catalysts\u003c\/li\u003e\n\u003cli\u003ePack sizes: 500 mL, 1 L\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid solution\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 keep it in a tightly sealed container to prevent evaporation and contamination. Due to its aqueous nature, it should be stored in glass or polyethylene containers to avoid chemical reactions with the container material. Proper labeling is essential for safe handling and identification. Always use appropriate personal protective equipment, such as gloves and safety goggles, when handling this reagent. It should not be exposed to incompatible substances, and it is important to ensure good ventilation in the workspace to minimize inhalation risks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086487957722,"sku":"TCI2510D200322016","price":592000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086487990490,"sku":"TCI2510D200322017","price":1125000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2003.jpg?v=1767104025"},{"product_id":"tci2510d214622215","title":"TCI D2146 17018-07-4 Glycerol alpha,alpha'-Diallyl Ether","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D2146, CAS number 17018-07-4, is Glycerol alpha,alpha'-Diallyl Ether, a glycerol-derived compound in which the two terminal hydroxyl groups have been etherified with allyl groups while the hydroxyl group at the central position remains free. In the laboratory it is classified as a monomer within the polymer and macromolecule reagent group. Its role is to supply a small molecule carrying two terminal double bonds that are ready to participate in polymerization and cross-linking reactions, while at the same time bringing along a single hydroxyl group available for further functionalization.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this monomer a frequent choice is the combination of allyl difunctionality and a free hydroxyl group within one relatively small molecule built on a glycerol backbone. The two allyl groups allow the formation of three-dimensional networks through thiol-ene reactions, hydrosilylation, or radical polymerization, producing materials whose cross-link density can be adjusted as required. The central hydroxyl group raises polarity, improves adhesion to polar surfaces, and provides an entry point for esterification or reaction with isocyanates. Its liquid form means it can be mixed directly into formulations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this monomer is typically handled in polymer and materials science work, where researchers prepare cross-linked networks, coating formulations, and modified resin systems on a bench scale. Because it is supplied as a liquid, it is measured and blended directly with other components without a separate dissolution step. It is generally used in university research groups, materials characterization laboratories, and industrial development units that build and evaluate polymer networks with adjustable cross-link density.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eThiol-ene network formation: the two terminal allyl double bonds react with polythiol partners, giving cross-linked networks whose density can be tuned by adjusting the monomer proportion in the mixture.\u003c\/li\u003e\n\u003cli\u003eRadical polymerization and cross-linking: the difunctional allyl structure lets this monomer act as a cross-linking agent that converts linear chains into three-dimensional networks during radical-initiated reactions.\u003c\/li\u003e\n\u003cli\u003eHydrosilylation chemistry: the terminal double bonds serve as reaction sites for silicon-hydride addition, making the compound useful for building organosilicon-modified networks and hybrid materials in the laboratory.\u003c\/li\u003e\n\u003cli\u003ePolar surface coating formulations: the free central hydroxyl group raises overall polarity and improves adhesion to polar substrates, which suits the material to coating and adhesive development work.\u003c\/li\u003e\n\u003cli\u003ePost-polymerization functionalization: the untouched central hydroxyl group provides an entry point for esterification or reaction with isocyanates, allowing further chemical modification after the network has formed.\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: 17018-07-4\u003c\/li\u003e\n\u003cli\u003eChemical name: Glycerol alpha,alpha'-Diallyl Ether\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, suitable for direct mixing into formulations\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue packaging options for this product code\u003c\/li\u003e\n\u003cli\u003eStorage: store in a closed container under the conditions stated on the manufacturer label\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore this monomer in its original tightly closed container, kept upright in a cool, dry, and well-ventilated area away from heat sources, open flames, and direct sunlight. As an allyl-functional liquid monomer, it should be kept away from radical initiators, peroxides, and strong oxidizing agents to avoid unintended polymerization. Use chemically compatible glass or manufacturer-supplied containers, and reseal immediately after dispensing to limit exposure to air and moisture. Handle inside a fume hood while wearing safety goggles, chemically resistant gloves, and a laboratory coat. Transfer using clean, dry glassware, keep labels intact, and always consult the manufacturer safety data sheet before use, storage, or disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086498377946,"sku":"TCI2510D214622215","price":2784000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086498410714,"sku":"TCI2510D214622216","price":20574000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2146.jpg?v=1767104285"},{"product_id":"tci2510d376824136","title":"TCI D3768 20306-22-3 Diallyl 1,4-Cyclohexanedicarboxylate (cis- and trans- mixture)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3768 Diallyl 1,4-Cyclohexanedicarboxylate (cis- and trans- mixture), CAS 20306-22-3, is the diallyl ester of 1,4-cyclohexanedicarboxylic acid, positioned as a monomer for polymer chemistry work. The molecule carries two polymerizable allyl groups at either end of the cyclohexane skeleton, which allows it to act both as a bifunctional monomer and as a crosslinking agent. In materials synthesis laboratories, a compound of this type serves as a starting point for building thermoset polymer networks, allyl resins, and copolymer systems that require crosslink junctions distributed evenly throughout the matrix.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this monomer a preferred choice lie in the combination of two allyl double bonds reactive toward radical polymerization and a cyclohexane skeleton that is aliphatic in nature. Unlike aromatic analogues such as phthalate diesters, the cyclohexane ring does not absorb ultraviolet light strongly, so the networks formed are generally valued in applications that demand optical clarity and resistance to light-induced ageing. The cis- and trans- mixture also introduces geometric diversity that influences how densely the chains pack within the cured network.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this monomer is typically handled in academic and industrial research settings working on polymer and coating formulation. It is used at small to moderate scale for network formulation trials, crosslink density studies, and the preparation of specimens for characterization. Because the material functions as a reactive crosslinker rather than a routine analytical reagent, it is usually ordered per project requirement and consumed within a defined series of synthesis experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eThermoset network synthesis: the two allyl end groups let a single molecule bridge growing chains, producing crosslinked networks whose density can be tuned by adjusting monomer loading.\u003c\/li\u003e\n\u003cli\u003eAllyl resin preparation: as a diallyl ester it belongs to the same chemical family as established allyl resin monomers, making it a direct candidate for casting and curing studies.\u003c\/li\u003e\n\u003cli\u003eCrosslinking agent in copolymer systems: added in small proportions to a comonomer mixture, it distributes crosslink junctions evenly through the matrix rather than concentrating them locally.\u003c\/li\u003e\n\u003cli\u003eOptically clear coating and cured-film research: the aliphatic cyclohexane skeleton avoids strong ultraviolet absorption, so it suits formulations where clarity and light-ageing resistance are evaluated.\u003c\/li\u003e\n\u003cli\u003eStructure–property investigations: the cis- and trans- mixture supplies geometric variation useful for studying how ring configuration affects chain packing and cured network behaviour.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 20306-22-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003eChemical class: diallyl ester of 1,4-cyclohexanedicarboxylic acid; cis- and trans- isomer mixture\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 note: keep in the closed original container, cool and away from light and heat 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, away from direct sunlight, heat, and sources of ignition, and separated from oxidizing agents. Because the material carries polymerizable allyl double bonds, avoid prolonged exposure to elevated temperature or light that could initiate unintended reaction. Keep it in the original supplier container or in a compatible, clearly labelled glass or chemically resistant vessel with a secure closure. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, avoid skin and eye contact and inhalation of vapour, and close the container promptly after dispensing. 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":"25g","offer_id":48086636855514,"sku":"TCI2510D376824136","price":3121000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48086636888282,"sku":"TCI2510D376824137","price":14109000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3768.jpg?v=1767106542"},{"product_id":"tci2510d550826421","title":"TCI D5508 999-21-3 Diallyl Maleate (stabilized with HQ)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiallyl Maleate (stabilized with HQ), with CAS number 999-21-3, is a versatile chemical compound widely used in laboratory settings for polymer synthesis and chemical reactions. As a monomer, it plays a crucial role in the development of complex chemical structures, particularly in materials science. Its ability to undergo polymerization makes it an essential component in the production of composite materials, resins, and other polymer-based products. This compound is commonly utilized in research and development activities where stable and consistent chemical reactions are required.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of Diallyl Maleate, including its stability and reactivity, make it a preferred choice for various laboratory applications. Stabilization with hydroquinone (HQ) enhances its resistance to oxidation and degradation, ensuring longer shelf life and consistent performance. Its appropriate melting point and solubility characteristics further contribute to its usability in different synthetic methods and chemical reactions. These properties make it a reliable material for both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diallyl Maleate is extensively used in polymer research and development. It supports studies in the chemical industry, material science, and technology sectors, where the creation of advanced materials is essential. Its role in producing high-performance polymers and composites aligns with the growing demand for innovative materials in Indonesia’s scientific and industrial communities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer synthesis for creating advanced composite materials and resins due to its ability to undergo polymerization.\u003c\/li\u003e\n\u003cli\u003eChemical reaction experiments requiring stable and consistent reagents for reliable results in material science research.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new polymer-based products in the chemical industry for industrial applications and innovation.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the production of high-performance polymers and structural materials.\u003c\/li\u003e\n\u003cli\u003eTesting and formulation of synthetic materials in technology and engineering sectors for improved product development.\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: 999-21-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes 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 light and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiallyl Maleate should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep the material in a sealed container to prevent exposure to air and moisture. Due to its chemical reactivity, it should be stored separately from strong oxidizing agents and incompatible substances. Proper ventilation is essential when handling this compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this material. Regular monitoring of storage conditions ensures the stability and safety of the compound during its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086762881242,"sku":"TCI2510D550826421","price":592000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086762914010,"sku":"TCI2510D550826422","price":2924000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5508.jpg?v=1767108826"},{"product_id":"tci2510h008432436","title":"TCI H0084 592-42-7 1,5-Hexadiene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI H0084 1,5-Hexadiene is an unsaturated six-carbon hydrocarbon carrying two terminal double bonds, one at each end of the chain and separated by two saturated carbons in the middle. This symmetrical arrangement, with two free vinyl groups, makes it a highly useful building block in synthetic laboratories and in polymer chemistry. The two reactive ends allow the molecule to act as a linker joining two fragments at once, or as a monomer that generates chains and networks when reacted through polymerization, metathesis, or controlled hydrosilylation.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it a popular choice is the presence of terminal double bonds, which are more readily approached by catalysts than internal double bonds. The terminal vinyl groups react rapidly in acyclic diene metathesis, hydroboration, epoxidation, and a variety of radical and catalytic addition reactions. The two-carbon spacer between the two double bonds also provides enough conformational flexibility for ring formation in ring-closing metathesis reactions. Its physical form is a colourless, readily volatile liquid, so transfer and volume measurement are practical, although this same volatility demands care during handling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 1,5-hexadiene is typically used in organic synthesis groups at universities and research institutes, as well as in polymer and materials development work. It serves as a starting material or linker in route development, as a diene substrate in metathesis studies, and as a comonomer in the preparation of crosslinked networks. Because it is supplied as a volatile liquid, it is generally dispensed in a fume hood with syringe or cannula techniques familiar to synthetic chemistry workflows.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRing-closing metathesis substrate studies: the two-carbon spacer between the terminal double bonds gives sufficient conformational flexibility for the chain to fold and close into a ring under catalysis.\u003c\/li\u003e\n\u003cli\u003eAcyclic diene metathesis polymerization: both ends carry unhindered terminal vinyl groups that engage metathesis catalysts rapidly, building polymer chains from a symmetrical difunctional monomer.\u003c\/li\u003e\n\u003cli\u003eBifunctional linker in multistep synthesis: the two equivalent reactive ends let the molecule join two separate fragments in one connecting unit during synthetic route development.\u003c\/li\u003e\n\u003cli\u003eHydroboration and hydrosilylation work: terminal double bonds are far more accessible to boron and silicon reagents than internal alkenes, giving cleaner and faster addition at both chain ends.\u003c\/li\u003e\n\u003cli\u003eEpoxidation and radical addition chemistry: the exposed terminal alkenes react readily in epoxidation as well as radical and catalytic addition reactions, allowing controlled functionalization of one or both ends.\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: 592-42-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the current size options when ordering.\u003c\/li\u003e\n\u003cli\u003ePhysical form: colourless, readily volatile liquid\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed original container in a cool, well-ventilated place away from heat and ignition sources.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 1,5-Hexadiene in its tightly closed original container in a cool, well-ventilated area, away from heat, sparks, open flames, and other ignition sources, and separated from strong oxidizing agents. Because the material is a volatile liquid, containers should be resealed immediately after use and kept upright to limit evaporation losses. All dispensing, transfer, and volume measurement should be carried out in a working fume hood, using syringe or cannula transfer where an inert atmosphere is preferred. Laboratory workers should wear safety glasses, chemically resistant gloves, and a laboratory coat, and should keep the work area free of ignition sources. Consult the manufacturer's safety data sheet before first use and follow institutional procedures for waste collection and disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087148789978,"sku":"TCI2510H008432436","price":901000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48087148822746,"sku":"TCI2510H008432437","price":2390000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48087148855514,"sku":"TCI2510H008432438","price":7730000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0084.jpg?v=1767115618"},{"product_id":"tci2510h080733488","title":"TCI H0807 1069-23-4 1,5-Hexadiene-3,4-diol (stabilized with HQ)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,5-Hexadiene-3,4-diol (CAS 1069-23-4) from TCI is an unsaturated diol that carries two adjacent hydroxyl groups at the 3 and 4 positions together with two vinyl groups at either end of the carbon chain. The product is supplied in a form stabilized with hydroquinone (HQ) to prevent spontaneous polymerization during storage. Within the polymer reagent category, this compound serves as both a monomer and a versatile intermediate: its diene backbone opens routes to polymerization and addition reactions, while its diol pair provides attachment points for further modification. The 10 mL pack suits laboratory-scale synthesis and formulation work.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this material a preferred choice is the presence of four reactive centers within a single small molecule: two terminal double bonds and two vicinal hydroxyl groups. The terminal double bonds are readily engaged in metathesis, hydroformylation, epoxidation, and radical polymerization, while the vicinal diol can be protected as an acetonide, converted into esters or ethers, or used as a stereochemistry-directing group. The compound also possesses multiple stereogenic centers, which makes it of interest for asymmetric synthesis studies. The presence of the hydroquinone stabilizer keeps the material usable across a normal working period without premature crosslinking.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically encountered in university and institutional research groups working on polymer chemistry, organic synthesis methodology, and materials development. The 10 mL format matches the scale at which such groups run exploratory reactions, screen conditions, and prepare small batches of modified monomers. It is generally ordered as a specialty item for a defined project rather than held as a bulk consumable, and is handled alongside other air- and heat-sensitive reagents in the same fume hood workflow.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMonomer for polymerization studies: the two terminal vinyl groups allow the molecule to be incorporated as a difunctional monomer or crosslinker in radical polymerization experiments where network formation is being investigated.\u003c\/li\u003e\n\u003cli\u003eOlefin metathesis substrate: the pair of terminal double bonds makes this diol a convenient starting point for ring-closing or cross-metathesis routes toward cyclic and functionalized unsaturated frameworks in methodology work.\u003c\/li\u003e\n\u003cli\u003eBuilding block for diol-functionalized intermediates: the vicinal hydroxyl pair can be esterified, etherified, or protected as an acetonide, giving synthetic chemists a flexible handle for multi-step sequences.\u003c\/li\u003e\n\u003cli\u003eAsymmetric synthesis investigations: because the molecule contains multiple stereogenic centers alongside its reactive alkenes, it is useful for studying stereocontrol and chiral induction in laboratory-scale transformations.\u003c\/li\u003e\n\u003cli\u003eEpoxidation and hydroformylation chemistry: the unhindered terminal alkenes respond well to oxidation and carbonylation conditions, making this compound a practical test substrate when developing or benchmarking such reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1069-23-4\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Monomers\u003c\/li\u003e\n\u003cli\u003eProduct code: H0807\u003c\/li\u003e\n\u003cli\u003ePack size: 10 mL\u003c\/li\u003e\n\u003cli\u003eStorage note: supplied stabilized with hydroquinone (HQ) to inhibit spontaneous polymerization during storage\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eKeep the container tightly closed in its original packaging and store it in a cool, dark place away from heat sources, direct sunlight, and ignition sources, since polymerizable monomers are sensitive to warmth and light. Do not remove or dilute the hydroquinone stabilizer, and avoid prolonged storage of decanted portions. Handle the material in a fume hood using nitrile gloves, safety glasses, and a laboratory coat, and transfer it with clean glass or otherwise compatible equipment. Keep it separated from strong oxidizing agents, acids, and radical initiators, and follow your institution's waste procedures for organic residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48087236870362,"sku":"TCI2510H080733488","price":5200000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H0807.jpg?v=1767117036"},{"product_id":"tci2510o049144896","title":"TCI O0491 69655-76-1 Octavinyloctasilasesquioxane","description":"\u003cp\u003e\u003cstrong\u003eOctavinyloctasilasesquioxane\u003c\/strong\u003e (CAS 69655-76-1) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087913464026,"sku":"TCI2510O049144896","price":1969000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087913496794,"sku":"TCI2510O049144897","price":6887000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510O0491.jpg?v=1767131980"},{"product_id":"tci2510p026445561","title":"TCI P0264 1623-19-4 Triallyl Phosphate","description":"\u003cp\u003e\u003cstrong\u003eTriallyl Phosphate\u003c\/strong\u003e (CAS 1623-19-4) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48087952556250,"sku":"TCI2510P026445561","price":5172000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48087952589018,"sku":"TCI2510P026445562","price":14025000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510P0264.jpg?v=1767132881"},{"product_id":"tci2510a08241077","title":"TCI A0824 2998-04-1 Diallyl Adipate","description":"\u003cp\u003e\u003cstrong\u003eDiallyl Adipate\u003c\/strong\u003e (CAS 2998-04-1) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085343469786,"sku":"TCI2510A11881606","price":2896000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085343502554,"sku":"TCI2510A11881607","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510A1188.jpg?v=1767080904"},{"product_id":"tci2510b30038718","title":"TCI B3003 682-09-7 2,2-Bis(allyloxymethyl)-1-butanol (contains Mono- and Tri-substituted Product)","description":"\u003cp\u003e\u003cstrong\u003e2,2-Bis(allyloxymethyl)-1-butanol (contains Mono- and Tri-substituted Product)\u003c\/strong\u003e (CAS 682-09-7) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085696184538,"sku":"TCI2510B30038718","price":732000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085696217306,"sku":"TCI2510B30038719","price":2475000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B3003.jpg?v=1768193496"},{"product_id":"tci2510t374555429","title":"TCI T3745 3901-77-7 2,4,6-Trimethyl-2,4,6-trivinylcyclotrisiloxane","description":"\u003cp\u003e\u003cstrong\u003e2,4,6-Trimethyl-2,4,6-trivinylcyclotrisiloxane\u003c\/strong\u003e (CAS 3901-77-7) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Synthesis reagent for a wide range of organic chemistry transformations in laboratory and industrial 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48088570560730,"sku":"TCI2510T374555429","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48088570593498,"sku":"TCI2510T374555430","price":1857000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510T3745.jpg?v=1767144314"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-divinyl-monomers-and-diallyl-monomers-biomaterials-biocompatible-materials-research-reagents.oembed","provider":"AMI Scientific","version":"1.0","type":"link"}