{"title":"Controlled Radical Polymerization Reagents","description":"\u003cp\u003e\u003cstrong\u003eControlled Radical Polymerization Reagents\u003c\/strong\u003e — menghimpun reagen pengendali polimerisasi radikal, mencakup katalis dan inisiator untuk Atom Transfer Radical Polymerization (ATRP) serta agen transfer rantai golongan ditioester dan tritiokarbonat untuk Reversible Addition Fragmentation Chain Transfer (RAFT). Reagen ini mengatur kinetika pertumbuhan rantai polimer selama reaksi berlangsung.\u003c\/p\u003e\u003cp\u003eControlled Radical Polymerization Reagents dipakai peneliti polimer untuk mensintesis polimer dengan distribusi berat molekul sempit serta kopolimer blok berstruktur terkendali, termasuk pada riset biomaterial dan material biokompatibel. Agen RAFT seperti turunan tritiokarbonat dan ditiobenzoat dipilih sesuai kelas monomer target, sementara ligan dan inisiator ATRP digunakan bersama katalis logam transisi untuk polimerisasi terkendali.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510u012656343\"\u003eTCI U0126 925232-64-0 N-Succinimidyl 2-(Dodecylthiocarbonothioylthio)-2-methylpropionate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b606512871\"\u003eTCI B6065 870532-86-8 Bis(dodecylsulfanylthiocarbonyl) Disulfide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510u012556342\"\u003eTCI U0125 864066-74-0 N-Succinimidyl 4-Cyano-4-(phenylcarbonothioylthio)pentanoate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b606612873\"\u003eTCI B6066 27249-90-7 Benzyl Benzodithioate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t440556168\"\u003eTCI T4405 1239488-58-4 Tetrahydrofuran-2-yl Pyrrolidine-1-carbodithioate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b606712875\"\u003eTCI B6067 497931-76-7 3-[[(Benzylthio)carbonothioyl]thio]propionic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t424055987\"\u003eTCI T4240 355120-40-0 2,2'-[Thiocarbonylbis(sulfanediyl)]bis(2-methylpropanoic Acid)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b612912949\"\u003eTCI B6129 5873-93-8 Bis(thiobenzoyl) Disulfide\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003eSesuaikan struktur gugus R dan Z pada agen RAFT dengan kelas monomer yang dipolimerisasi, serta perhatikan kemurnian dan kestabilan reagen selama penyimpanan sebelum digunakan. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Polymerization Reagents (Initiators, Catalysts, Ligands) [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-l4-polymerization-initiators\"\u003ePolymerization Initiators\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-polymerization-catalysts\"\u003ePolymerization Catalysts\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-organocatalyzed-living-radical-polymerization-reagents\"\u003eOrganocatalyzed Living Radical Polymerization Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 2 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-atom-transfer-radical-polymerization-atrp-reagents\"\u003eAtom Transfer Radical Polymerization (ATRP) Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-reversible-addition-fragmentation-chain-transfer-raft-polymerization-reagents\"\u003eReversible Addition Fragmentation Chain Transfer (RAFT) Polymerization Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \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. 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":"tci2510b638113255","title":"TCI B6381 213453-02-2 2-[(2-Bromo-2-methylpropanoyl)oxy]ethyl Acrylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6381, 2-[(2-Bromo-2-methylpropanoyl)oxy]ethyl acrylate (CAS 213453-02-2), is a bifunctional acrylate monomer bearing an α-bromoisobutyrate group. This dual functionality allows it to act simultaneously as a polymerizable monomer and as an ATRP initiating site, making it a practical \"inimer\" for controlled radical polymerization. Researchers commonly apply it to hyperbranched polymers, star architectures, and bottlebrush copolymers where branch points must be introduced in a controlled manner. Supplied in 1 g and 5 g packs, it should be stored cool, tightly closed, and protected from light to prevent premature polymerization.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937029338,"sku":"TCI2510B638113255","price":4897000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937062106,"sku":"TCI2510B638113256","price":16631000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6381_84c9cd03-66a6-4e3c-ba51-095ce61de04b.jpg?v=1767865561"},{"product_id":"tci2510b638413261","title":"TCI B6384 213453-08-8 2-[(2-Bromo-2-methylpropanoyl)oxy]ethyl Methacrylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6384, 2-[(2-bromo-2-methylpropanoyl)oxy]ethyl methacrylate (CAS 213453-08-8), is a bifunctional methacrylate monomer carrying an ATRP-active α-bromoisobutyrate group. It serves as an inimer that lets researchers build hyperbranched polymers, star polymers, and bottlebrush copolymers without a separate functionalisation step. Compared with the acrylate analogue, the methacrylate backbone typically offers greater rigidity and ester stability, which suits demanding polymer architectures. Packaged in 1 g and 5 g sizes, it should be stored cool, dark, and tightly sealed, away from heat and radical sources.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937225946,"sku":"TCI2510B638413261","price":2576000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937258714,"sku":"TCI2510B638413262","price":9263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6384.jpg?v=1768193678"},{"product_id":"tci2510b706713894","title":"TCI B7067 248603-11-4 Ethylene Bis(2-bromoisobutyrate)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7067 Ethylene Bis(2-bromoisobutyrate) is a difunctional initiator designed for atom transfer radical polymerization (ATRP). Its two tertiary α-bromo ester groups initiate chain growth in both directions from a single ethylene glycol core. This makes it particularly suitable for symmetric ABA block copolymers and telechelic polymers bearing reactive bromo end groups. Supplied in 1 g and 5 g packs, it should be stored cool, dry, protected from light, and away from strong bases.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCai (2013). Influence of Ethylene bis-Stearamide on Crystallization Behaviour of Poly(L-lactide). \u003cem\u003eAsian Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14233\/ajchem.2013.14326\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14233\/ajchem.2013.14326\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBarbieri et al. (1999). Photochemistry of ansa-zirconocenes: ethylene-bis(1-indenyl)- and ethylene-bis(4,7-dimethyl-1-indenyl) zirconium dichlorides. \u003cem\u003eJournal of Photochemistry and Photobiology A: Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s1010-6030(99)00167-7\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s1010-6030(99)00167-7\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHavránek et al. (1991). 99mTc labeled ethylene-bis (valine) and ethylene-bis (α-alanine) and their preliminary biobistribution. \u003cem\u003eJournal of Radioanalytical and Nuclear Chemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/bf02168316\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/bf02168316\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085964751066,"sku":"TCI2510B706713894","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085964783834,"sku":"TCI2510B706713895","price":4669000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7067.jpg?v=1767094517"},{"product_id":"tci2510c079015052","title":"TCI C0790 535-13-7 Ethyl 2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0790 Ethyl 2-Chloropropionate (CAS 535-13-7) is an α-chloro ester that acts as a versatile alkylating reagent. The activated secondary halide readily undergoes substitution with oxygen, nitrogen, and sulfur nucleophiles, including phenols en route to aryloxypropionate derivatives. Its stereogenic C-2 centre also makes it a useful starting point for stereoselective studies, while α-haloesters of this type are widely used as controlled radical polymerisation initiators. TCI supplies it as a liquid in 25 mL and 100 mL packs for laboratory-scale reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086028583130,"sku":"TCI2510C079015052","price":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086028615898,"sku":"TCI2510C079015053","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0790.jpg?v=1767095758"},{"product_id":"tci2510c097015323","title":"TCI C0970 17639-93-9 Methyl 2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0970 Methyl 2-Chloropropionate (CAS 17639-93-9) is a compact aliphatic ester bearing a reactive chlorine atom alpha to the carbonyl group. The activated chloride is readily displaced by phenoxides, amines, thiols, and carbanions, making it a versatile alkylating intermediate in organic synthesis. Its chiral carbon centre also makes it a useful substrate for stereochemical and configuration-inversion studies. AMI Scientific offers 25 mL, 100 mL, and 500 mL sizes; dispense in a fume hood and follow the official TCI safety data sheet.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25mL","offer_id":48086040805594,"sku":"TCI2510C097015323","price":934000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086040838362,"sku":"TCI2510C097015324","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086040871130,"sku":"TCI2510C097015325","price":3584000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0970.jpg?v=1767096113"},{"product_id":"tci2510c163316283","title":"TCI C1633 77287-29-7 Methyl (R)-(+)-2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl (R)-(+)-2-Chloropropionate is a chiral compound widely used in asymmetric synthesis for the construction of optically active molecules. This compound plays a crucial role in organic chemistry research, particularly in the development of compounds with specific biological activities. Its chiral structure allows for the precise control of molecular configuration, making it an essential tool in asymmetric synthesis. The compound is commonly used in pharmaceutical and biotechnology research for the synthesis of complex molecules with targeted therapeutic applications. Its stability and availability in solid form make it a reliable choice for laboratory use. Due to its optical activity, it is ideal for applications requiring high specificity in chemical reactions, supporting the development of new compounds with potential medical uses.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086082027738,"sku":"TCI2510C163316283","price":3105000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1633.jpg?v=1767097247"},{"product_id":"tci2510c163416284","title":"TCI C1634 73246-45-4 Methyl (S)-(-)-2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl (S)-(-)-2-Chloropropionate (TCI C1634, CAS 73246-45-4) is a chiral building block widely used in asymmetric synthesis. Its specific stereochemistry makes it essential for creating molecules with precise spatial configurations, particularly in pharmaceutical and organic chemistry research. This compound is valued for its stability and reactivity in controlled chemical environments, enabling the synthesis of complex and bioactive compounds. Its application in Indonesian laboratories supports advancements in drug development and chemical innovation, making it a crucial component in modern scientific research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086082093274,"sku":"TCI2510C163416284","price":2524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1634.jpg?v=1767097251"},{"product_id":"tci2510c216116825","title":"TCI C2161 7787-70-4 Copper(I) Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Copper(I) Bromide, catalog code C2161, is a monovalent copper salt that plays an important role as a catalyst and reagent in synthetic organic chemistry. In the laboratory, this compound is used as a source of active copper in a wide range of functional group transformation reactions, as a component of controlled radical polymerization catalyst systems, and as a reagent in the formation of carbon–carbon and carbon–heteroatom bonds. Its availability allows many coupling reactions to be carried out without requiring the more expensive noble metal catalysts that would otherwise be needed.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes copper(I) bromide a widely preferred choice is its +1 oxidation state, which moves readily to +2 and back again, making the compound highly suitable for catalytic cycles based on single-electron transfer. The bromide ion as a ligand provides solubility and reactivity that differ from those of chloride or iodide, so researchers can tune reaction rate and selectivity by choosing the appropriate halide. The compound also forms complexes readily with nitrogen ligands such as bipyridine or multidentate amines, and these complexes are central to atom transfer radical polymerization.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this material is typically found in university organic synthesis groups, polymer chemistry laboratories, and research institutions working on catalysis. It is generally used at bench scale for method development, reaction screening, and the preparation of intermediates, where a reliable copper(I) source is needed for routine coupling and polymerization work. Its role as an accessible alternative to noble metal catalysis makes it a practical staple for teaching laboratories and research groups operating under constrained reagent budgets.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAtom transfer radical polymerization — the copper(I)\/copper(II) redox couple, combined with nitrogen donor ligands such as bipyridine or multidentate amines, provides the reversible halogen transfer that controls chain growth.\u003c\/li\u003e\n\u003cli\u003eCarbon–heteroatom bond formation — the compound serves as an active copper source for coupling reactions that join carbon centers to nitrogen, oxygen, or sulfur nucleophiles in synthetic sequences.\u003c\/li\u003e\n\u003cli\u003eCarbon–carbon coupling reactions — copper(I) bromide functions as a reagent and catalyst for constructing carbon skeletons without recourse to more costly noble metal catalyst systems.\u003c\/li\u003e\n\u003cli\u003eFunctional group transformation — the salt acts as a source of active copper in substitution and interconversion reactions where bromide delivers reactivity distinct from chloride or iodide alternatives.\u003c\/li\u003e\n\u003cli\u003eCopper complex preparation — its ready complexation with nitrogen ligands makes it a convenient starting point for preparing defined copper catalyst species for single-electron transfer 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\u003eCatalog code: C2161\u003c\/li\u003e\n\u003cli\u003eCAS number: 7787-70-4\u003c\/li\u003e\n\u003cli\u003eChemical name: Copper(I) Bromide\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container in a cool, dry place away from moisture and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore copper(I) bromide in tightly closed original containers in a cool, dry, well-ventilated area, protected from moisture and prolonged exposure to air, since copper(I) compounds are susceptible to oxidation toward the copper(II) state. Where extended storage or particularly sensitive work is planned, keeping the material under inert atmosphere is advisable. Handle the solid in a fume hood using gloves, safety goggles, and a laboratory coat, and avoid generating dust during weighing and transfer. Use clean, dry spatulas and glassware to prevent contamination, reseal containers promptly after use, and consult the manufacturer's safety data sheet for full hazard information and disposal requirements before beginning work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086108012762,"sku":"TCI2510C216116825","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086108045530,"sku":"TCI2510C216116826","price":1213000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086108078298,"sku":"TCI2510C216116827","price":4190000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2161.jpg?v=1767097854"},{"product_id":"tci2510c216316831","title":"TCI C2163 7681-65-4 Copper(I) Iodide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Copper(I) Iodide, catalog code C2163, is a monovalent copper salt that ranks among the most frequently used catalysts in synthetic organic chemistry. In the laboratory it is best known as the co-catalyst in Sonogashira coupling reactions alongside a palladium catalyst, as a standalone catalyst in Ullmann–Goldberg type coupling reactions, and as a reagent for generating organocopper species. Beyond these roles, copper(I) iodide is also employed in azide–alkyne cycloaddition reactions, the transformation that forms the backbone of click chemistry.\u003c\/p\u003e\n\u003cp\u003eThe property that sets this compound apart is its relatively better stability compared with other copper(I) salts. The soft iodide ion stabilizes the equally soft monovalent copper center, giving a reagent that is more forgiving to handle than many alternatives. Copper(I) iodide is practically insoluble in water, yet it can be brought into solution with the help of donor ligands such as amines, phosphines, or an excess iodide solution, which makes it straightforward to introduce into a wide range of reaction systems. Its ability to form copper acetylides in situ is the key step behind many alkyne coupling reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is a routine fixture in synthetic organic chemistry research groups at universities and in research institutes, particularly where cross-coupling methodology and click chemistry are part of the workflow. It is used in medicinal chemistry and materials-oriented synthesis, in method development work, and in graduate research projects that build carbon–carbon and carbon–heteroatom bonds. Its versatility across several reaction classes means a single reagent supports many different lines of investigation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSonogashira coupling: serves as the classic co-catalyst with palladium, forming copper acetylide in situ so the terminal alkyne transfers efficiently to the palladium center.\u003c\/li\u003e\n\u003cli\u003eUllmann–Goldberg type coupling: acts as a standalone copper catalyst for carbon–heteroatom bond formation, avoiding the need for a separate palladium system in these transformations.\u003c\/li\u003e\n\u003cli\u003eAzide–alkyne cycloaddition (click chemistry): supplies the copper(I) source that drives the cycloaddition, the backbone reaction used to join molecular fragments reliably.\u003c\/li\u003e\n\u003cli\u003eOrganocopper reagent preparation: functions as the copper source for generating organocopper species used in a variety of synthetic transformations requiring copper-mediated reactivity.\u003c\/li\u003e\n\u003cli\u003eGeneral synthetic methodology development: its solubility control through amine, phosphine, or excess iodide donors lets researchers tune reaction systems during method optimization studies.\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\u003eCatalog code: C2163\u003c\/li\u003e\n\u003cli\u003eCAS number: 7681-65-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, white to brownish in color\u003c\/li\u003e\n\u003cli\u003eStorage note: protect from light, as the solid can change color on light exposure\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore copper(I) iodide in a tightly closed, light-protected container such as an amber glass bottle or the original supplier packaging kept inside a closed cabinet, since the solid can discolor when exposed to light. Keep it in a cool, dry chemical storage area away from moisture and strong oxidizing agents. Handle the powder in a fume hood or a well-ventilated area to limit dust inhalation, and wear standard laboratory personal protective equipment including safety glasses, gloves, and a lab coat. Use clean, dry spatulas when weighing to avoid contaminating the stock, and close the container promptly after use. Always consult the manufacturer's safety data sheet before first use and dispose of residues through the laboratory's chemical waste channel.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086108242138,"sku":"TCI2510C216316831","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086108274906,"sku":"TCI2510C216316832","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086108307674,"sku":"TCI2510C216316833","price":3382000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2163.jpg?v=1767097862"},{"product_id":"tci2510c220116879","title":"TCI C2201 32993-05-8 Cyclopentadienylbis(triphenylphosphine)ruthenium(II) Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCyclopentadienylbis(triphenylphosphine)ruthenium(II) Chloride is a ruthenium organometallic complex that binds one cyclopentadienyl ligand, two triphenylphosphine ligands, and one chloride ligand around a single metal center. Half-sandwich complexes of this type are important precatalysts in modern catalytic chemistry, particularly for C–H bond activation reactions that allow direct functionalization of carbon–hydrogen bonds without any need to prefunctionalize the substrate. In the laboratory, this material is used to construct carbon–carbon and carbon–heteroatom bonds through shorter synthetic routes, saving synthetic steps and reducing waste generation.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this complex valuable are the stability of its coordination environment combined with the ability of the phosphine ligands to dissociate in a controlled manner, generating a vacant coordination site where the substrate binds. The cyclopentadienyl ligand locks the ruthenium center in place and stabilizes a range of oxidation states throughout the catalytic cycle, while the chloride can be replaced by other ligands to tune reactivity. The complex is also stable enough to be handled as a solid on the open bench for short periods, although proper storage remains important for preserving its performance over time.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this precatalyst is typically used by university research groups, graduate-level synthetic chemistry programmes, and industrial R\u0026amp;D units working on the preparation of fine chemicals and pharmaceutical intermediates. It suits work where step economy matters, where researchers want to reach a target scaffold with fewer transformations, and where reproducible catalytic behaviour is needed across repeated runs. It is normally handled together with standard inert-atmosphere equipment and stored alongside other air-sensitive organometallic reagents.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC–H bond activation reactions: the complex generates a vacant coordination site upon controlled phosphine loss, allowing the ruthenium center to engage carbon–hydrogen bonds directly for functionalization.\u003c\/li\u003e\n\u003cli\u003eCarbon–carbon bond formation: the stable coordination environment supports catalytic cycles that couple fragments without prefunctionalized partners, shortening synthetic routes toward complex target molecules.\u003c\/li\u003e\n\u003cli\u003eCarbon–heteroatom bond construction: the tunable ruthenium center accommodates substrates bearing nitrogen, oxygen, and other heteroatoms, enabling direct bond formation along a more economical pathway.\u003c\/li\u003e\n\u003cli\u003ePrecatalyst screening and reaction development: the chloride ligand can be exchanged for other ligands, so researchers may systematically tune reactivity while keeping the same ruthenium core.\u003c\/li\u003e\n\u003cli\u003eStep-economical synthesis of intermediates: by avoiding substrate prefunctionalization, the complex reduces the number of synthetic operations required and lowers the quantity of waste generated per target compound.\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: 32993-05-8\u003c\/li\u003e\n\u003cli\u003eProduct Code: TCI C2201\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, stable enough for short-term open-bench handling\u003c\/li\u003e\n\u003cli\u003eStorage: keep under appropriate storage conditions to preserve catalytic performance\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the complex in a tightly closed original container, kept cool, dry, and away from direct sunlight and heat sources. Although the solid is stable enough for brief handling on the open bench, prolonged exposure to air and moisture should be avoided, and storage under an inert atmosphere is recommended for long-term preservation of catalytic activity. Weigh and transfer the material using clean, dry spatulas and glassware, and return the container promptly after use. Handle the material in a well-ventilated area or fume hood, wearing gloves, safety goggles, and a laboratory coat. Keep the complex separate from strong oxidizing agents, and consult the manufacturer's safety data sheet before use and prior to any waste disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086110896346,"sku":"TCI2510C220116879","price":2752000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086110929114,"sku":"TCI2510C220116880","price":9514000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2201.jpg?v=1767097903"},{"product_id":"tci2510c238917149","title":"TCI C2389 7789-45-9 Copper(II) Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCopper(II) Bromide (CuBr) is a solid chemical compound widely used in laboratory settings for various chemical reactions. As a transition metal compound, it plays a crucial role in both organic and inorganic chemistry, particularly as a catalyst in synthetic processes. Its presence in laboratory experiments is essential for facilitating reactions that require redox mechanisms or catalytic activity. Due to its unique chemical properties, CuBr is a valuable reagent in the development of complex compounds and in electrochemical applications.\u003c\/p\u003e\n\u003cp\u003eThe chemical and physical properties of Copper(II) Bromide make it a preferred choice in laboratory environments. It exhibits a crystalline structure with a yellowish-white color, which is characteristic of its molecular arrangement. However, it is highly hygroscopic, meaning it readily absorbs moisture from the air, which can affect its stability. This property necessitates careful handling and storage. Despite its sensitivity to humidity and oxidation, CuBr remains a reliable reagent due to its consistent performance in controlled laboratory conditions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Copper(II) Bromide is commonly used in chemical research, especially in catalysis and organic synthesis. Its role in promoting chemical reactions and enabling the formation of new compounds makes it an essential material for researchers. The compound is frequently employed in the synthesis of complex organic molecules and in electroplating processes. Its reactivity and versatility make it a key component in various experimental setups across different scientific disciplines.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from CuBr’s catalytic properties, enabling the formation of complex organic compounds through efficient redox processes.\u003c\/li\u003e\n\u003cli\u003eIn inorganic chemistry, it is used to facilitate substitution reactions, aiding in the synthesis of new inorganic materials with specific properties.\u003c\/li\u003e\n\u003cli\u003eElectroplating processes rely on CuBr to deposit copper layers onto surfaces, enhancing conductivity and corrosion resistance.\u003c\/li\u003e\n\u003cli\u003eCatalytic oxidation reactions utilize CuBr to promote the conversion of reactants into desired products under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eResearch in transition metal chemistry often incorporates CuBr to study the behavior of copper compounds in various chemical 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: 7789-45-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Transition Elements\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Must be stored in airtight containers to prevent moisture absorption\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCopper(II) Bromide should be stored in a cool, dry place away from sources of moisture and oxidation. It is essential to use airtight containers to prevent hygroscopic absorption, which can degrade its chemical integrity. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to avoid direct contact. Due to its reactivity with water, it is recommended to keep it in a desiccated environment to maintain its stability. Proper labeling and storage conditions are crucial to ensure safe handling and effective use in experimental procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086124134618,"sku":"TCI2510C238917149","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086124167386,"sku":"TCI2510C238917150","price":2197000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2389.jpg?v=1767098260"},{"product_id":"tci2510c377118861","title":"TCI C3771 1617-17-0 2-Chloropropanenitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloropropanenitrile is a chemical compound widely used as a foundational building block in the synthesis of complex organic molecules. Its reactive nitrile group makes it a versatile reagent in various chemical reactions, including nucleophilic, substitution, and electrophilic processes. In laboratory settings, it plays a crucial role in the development of new compounds, particularly in organic synthesis and pharmaceutical research. Due to its high reactivity and ability to participate in controlled chemical transformations, it is a valuable tool for researchers aiming to create novel molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity stems from its nitrile functional group, which is highly susceptible to nucleophilic attack. This makes it an ideal candidate for a wide range of synthetic strategies. Additionally, its stability under certain conditions allows for safe storage and extended use. These properties make it a preferred choice for chemists and researchers who require reliable and effective reagents for their experiments. Its consistent performance in various reaction conditions further enhances its appeal in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Chloropropanenitrile is commonly used in research and educational settings. It supports chemical experiments, pharmaceutical development, and studies on organic reactivity. Its availability in the local market ensures that scientists and students can access this essential reagent for their work. Its role in advancing chemical research and education is significant, making it a staple in many laboratory environments across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from 2-Chloropropanenitrile due to its reactivity and ability to form diverse molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound as a key intermediate in the development of new drug compounds and therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eEducational laboratories use it to teach fundamental chemical reactions and synthetic techniques to students.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for the production of specialty chemicals and intermediates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications rely on its stability and reactivity for the study of organic compound behavior and reactivity.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1617-17-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Chloropropanenitrile should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its chemical nature, it should be stored away from incompatible substances such as strong bases or oxidizing agents. Laboratory personnel should handle the compound with appropriate personal protective equipment, including gloves and safety goggles. Proper ventilation is essential when working with this material to ensure safe handling and minimize exposure risks. Regular inspection of storage conditions is advised to maintain optimal safety and performance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086286500058,"sku":"TCI2510C377118861","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3771.jpg?v=1767100043"},{"product_id":"tci2510d112220846","title":"TCI D1122 2648-61-5 2,2-Dichloroacetophenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2-Dichloroacetophenone is a chemical compound with an aromatic structure featuring chlorine substituents at the 2 and 2 positions of the acetophenone group. This compound plays a crucial role in laboratory settings, particularly in organic chemistry research. It is widely used as a building block in the synthesis of complex organic compounds, especially in substitution and electrophilic reactions. Its versatility makes it an essential reagent for chemists working on a variety of synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of 2,2-Dichloroacetophenone make it a preferred choice for many applications. It exhibits reactivity towards various reagents such as bases, acids, and alkali metals, which allows it to participate in a wide range of chemical transformations. Despite its reactivity, it maintains stability under specific conditions, enabling controlled reactions in laboratory environments. Its solid form and ease of handling further enhance its usability across different experimental scales.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,2-Dichloroacetophenone is commonly used in research related to organic synthesis, pharmaceutical development, and industrial chemistry. Its ability to engage in multiple reaction types makes it a valuable resource for scientists and researchers. The compound's availability and chemical characteristics support its frequent use in both academic and applied research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: This compound is ideal for synthesizing complex organic molecules due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: It is used in the development of new drugs, particularly in the synthesis of heterocyclic compounds and medicinal agents.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemistry: Its application in industrial processes is due to its role in creating a variety of chemical intermediates.\u003c\/li\u003e\n\u003cli\u003eMechanism studies: The compound is valuable for studying reaction mechanisms and molecular structures in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry: It serves as a reference material for analytical procedures and quality control in chemical 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: 2648-61-5\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\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\u003e2,2-Dichloroacetophenone should be stored in a cool, dry place, away from moisture and direct sunlight. It is recommended to use airtight containers to prevent exposure to air and potential moisture absorption. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential hazards. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure. Always follow standard laboratory safety protocols when working with reactive chemicals.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086425895130,"sku":"TCI2510D112220846","price":2474000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1122.jpg?v=1767102561"},{"product_id":"tci2510d199722009","title":"TCI D1997 15529-49-4 Tris(triphenylphosphine)ruthenium(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTris(triphenylphosphine)ruthenium(II) Dichloride (TCI D1997, CAS 15529-49-4) is a chemical compound widely used in catalytic reactions, particularly in C-H activation processes. This compound is a metal complex of ruthenium, playing a crucial role in both organic and inorganic chemical reactions. Its unique structure and reactivity make it an essential reagent in modern synthetic chemistry. In laboratory settings, it is employed as a catalyst for various transformations, including substitution, oxidation, and reduction reactions. Its ability to activate carbon-hydrogen bonds makes it particularly valuable in the development of new catalytic methodologies.\u003c\/p\u003e\n\u003cp\u003eThe compound’s high reactivity and structural stability under controlled conditions make it a preferred choice for researchers. Its complex structure, featuring three tripheylphosphine ligands and two chloride ions, contributes to its catalytic efficiency. This composition allows it to participate effectively in a wide range of chemical transformations. The compound is also known for its stability in certain environments, which simplifies its handling and storage. These properties make it a reliable and versatile material for advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Tris(triphenylphosphine)ruthenium(II) Dichloride is commonly used in organic chemistry, catalysis, and the synthesis of complex compounds. Its availability in the local market and growing demand for research in these fields have made it a popular choice among scientists. It is frequently used in academic and industrial research settings to support the development of new chemical processes and materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic chemistry research benefits from this compound due to its role in C-H activation, enabling the synthesis of complex organic molecules with high selectivity.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions in the laboratory rely on this material for its ability to facilitate substitution and oxidation processes efficiently.\u003c\/li\u003e\n\u003cli\u003eIn inorganic chemistry, it is used to study the behavior of ruthenium complexes and their reactivity in various chemical environments.\u003c\/li\u003e\n\u003cli\u003eThe compound supports the development of new catalytic methods, making it valuable for innovation in chemical synthesis.\u003c\/li\u003e\n\u003cli\u003eIndonesian laboratories use it extensively for the synthesis of complex compounds, where its catalytic properties are essential for achieving desired chemical outcomes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 15529-49-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; C-H Activation [Catalysis]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. It is important to store it away from incompatible substances to avoid any potential chemical reactions. Proper labeling and storage conditions are essential to ensure its safe use and long-term availability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086487695578,"sku":"TCI2510D199722009","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086487728346,"sku":"TCI2510D199722010","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1997.jpg?v=1767104009"},{"product_id":"tci2510d436824947","title":"TCI D4368 29263-94-3 Diethyl 2-Bromo-2-methylmalonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDiethyl 2-Bromo-2-methylmalonate is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and complex molecules. This reagent plays a crucial role in laboratory settings where the creation of carbon-based structures with bromo and carbonyl groups is required. Its versatility makes it an essential component in various synthetic pathways, supporting the development of advanced chemical structures. Due to its chemical stability and reactivity, it is a reliable choice for researchers aiming to achieve specific chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's bromo group at the 2-position makes it highly reactive towards nucleophiles such as alkoxides and amines, enabling targeted substitutions in organic synthesis. This reactivity, combined with its structural simplicity, allows for precise control over reaction outcomes. Its ability to participate in nucleophilic substitution and carbon-carbon bond formation reactions further enhances its utility in synthetic chemistry. These properties make it a preferred choice for chemists working on complex molecule synthesis and functional group manipulation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Diethyl 2-Bromo-2-methylmalonate is extensively used in organic chemistry research, especially in academic institutions and research centers. It is a key reagent in the development of new compounds and the study of complex chemical structures. Its role in drug development and chemical synthesis makes it a valuable asset for both educational and industrial research applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of Heterocyclic Compounds: This compound is ideal for creating complex ring structures, commonly used in pharmaceutical research due to its ability to form stable intermediates.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Reactions: Its reactivity with nucleophiles makes it suitable for substitution reactions, allowing for the creation of diverse functional groups in organic molecules.\u003c\/li\u003e\n\u003cli\u003eCarbon-Carbon Bond Formation: The compound is used in reactions that build carbon frameworks, essential for developing new chemical entities with specific properties.\u003c\/li\u003e\n\u003cli\u003eFunctional Group Manipulation: Its bromo group facilitates targeted modifications, making it useful in the synthesis of compounds with specific chemical functionalities.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research: It is frequently employed in the synthesis of potential pharmaceutical compounds, supporting the creation of novel therapeutic agents.\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: 29263-94-3\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 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 materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDiethyl 2-Bromo-2-methylmalonate 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 polyethylene to prevent contamination and evaporation. Due to its reactivity, it should be kept separate from strong bases, oxidizing agents, and other incompatible substances. Always ensure proper ventilation when handling the compound, and wear appropriate personal protective equipment such as gloves and safety goggles. The compound is not classified as hazardous under standard conditions, but standard laboratory safety protocols should still be followed to ensure safe handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086689054938,"sku":"TCI2510D436824947","price":1920000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4368.jpg?v=1767107463"},{"product_id":"tci2510d665427620","title":"TCI D6654 728034-24-0 2-Bromoisobutanoic Acid N-Hydroxysuccinimide Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromoisobutanoic Acid N-Hydroxysuccinimide Ester is a chemical compound widely used in laboratory settings for its reactivity and versatility in organic synthesis. It plays a crucial role in polymerization reactions and molecular modification processes, where it serves as a key reagent for forming covalent bonds with various functional groups. This compound is particularly valuable in the development of polymers and the functionalization of biomolecules, making it an essential tool for researchers in materials science and chemical engineering. Its ability to react with amines, carboxylates, and hydroxyl groups allows it to be used in a wide range of chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and functional group compatibility make it a preferred choice in synthetic chemistry. It is known for its stability under controlled laboratory conditions, which ensures consistent performance during experiments. Its ability to participate in nucleophilic reactions and its solubility in common organic solvents further enhance its utility. These properties make it suitable for use in both academic and industrial research environments where precision and reliability are critical.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in chemical, pharmaceutical, and materials research. It is a key component in the synthesis of complex organic molecules and in the modification of polymer structures. Due to its reliability and effectiveness, it is a popular choice among researchers and students working on polymerization and molecular modification projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymer synthesis and modification where covalent bonding with functional groups is required.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis reactions involving nucleophilic substitution and cross-linking processes.\u003c\/li\u003e\n\u003cli\u003eDevelopment of biocompatible materials and functionalized polymers for biomedical applications.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical chemistry for the creation of drug delivery systems and molecular conjugates.\u003c\/li\u003e\n\u003cli\u003eAnalytical chemistry applications requiring the use of reactive reagents for molecular labeling and detection.\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: 728034-24-0\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to humidity and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize inhalation risks. Avoid contact with incompatible materials such as strong acids or bases. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086812393690,"sku":"TCI2510D665427620","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086812426458,"sku":"TCI2510D665427621","price":5881000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D6654.jpg?v=1767110436"},{"product_id":"tci2510e119829132","title":"TCI E1198 31253-08-4 Ethyl 2-Iodopropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Iodopropionate is a chemical compound widely used in laboratory settings, particularly in organic synthesis reactions. It serves as a versatile reagent due to its functional groups, which include an iodide and an ester group. These groups contribute to its reactivity and make it suitable for various chemical transformations. In the laboratory, it is commonly employed in nucleophilic substitution reactions and polymerization processes, depending on the desired outcome of the experiment. Its ability to participate in multiple reaction types makes it a valuable tool for chemists working in both research and educational environments.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for laboratory applications. Its iodide group provides electrophilic characteristics, enabling efficient substitution reactions under appropriate conditions. The ester functionality further enhances its reactivity, making it suitable for a range of synthetic pathways. Ethyl 2-Iodopropionate is stable under certain conditions but reacts vigorously with strong bases or organic solvents. These properties make it a reliable reagent for controlled chemical processes. Its versatility and reactivity are key factors in its widespread use across different laboratory disciplines.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 2-Iodopropionate is frequently used in organic chemistry research, especially in polymerization and the synthesis of complex compounds. It is also commonly utilized in higher education institutions for teaching purposes, where students gain hands-on experience with reactive organic compounds. The compound's role in both research and education underscores its importance in the chemical sciences within Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where nucleophilic substitution and electrophilic reactivity are required.\u003c\/li\u003e\n\u003cli\u003ePolymerization processes that benefit from the reactivity of iodide and ester functional groups.\u003c\/li\u003e\n\u003cli\u003eResearch in polymer science and macromolecular chemistry due to its compatibility with various reaction conditions.\u003c\/li\u003e\n\u003cli\u003eEducational experiments focused on understanding the behavior of reactive organic compounds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new chemical compounds through controlled synthetic pathways involving iodinated esters.\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: 31253-08-4\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory 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 and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Iodopropionate 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. Due to its reactivity, it should be stored away from strong bases and organic solvents to avoid unwanted chemical interactions. Suitable containers for storage include glass or high-density polyethylene vessels that are resistant to chemical degradation. In laboratory settings, proper ventilation and personal protective equipment should be used when handling this compound to ensure safety. Regular monitoring of storage conditions is essential to maintain the integrity and effectiveness of the reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086934225114,"sku":"TCI2510E119829132","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086934257882,"sku":"TCI2510E119829133","price":5452000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1198.jpg?v=1767112510"},{"product_id":"tci2510e119929134","title":"TCI E1199 7425-55-0 Ethyl 2-Iodo-2-methylpropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Iodo-2-methylpropionate is a chemical compound widely used in laboratory settings for its versatile reactivity in organic synthesis. As a reagent with an iodide group, it plays a crucial role in various chemical reactions, including nucleophilic substitution and radical processes. This compound is commonly found in chemical and materials science laboratories, particularly in polymerization and functional group modification reactions. Its presence in these environments makes it a valuable tool for researchers working on complex organic molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound’s iodide group contributes to its high reactivity and polarity, making it suitable for reactions involving polar solvents such as ethanol or water. Its ability to participate in SN1, SN2, and radical mechanisms enhances its utility in synthetic pathways. Additionally, Ethyl 2-Iodo-2-methylpropionate exhibits reasonable stability under controlled conditions, which facilitates its use in a wide range of experimental applications. These properties make it a preferred choice for chemists seeking reliable and effective reagents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 2-Iodo-2-methylpropionate is frequently used in material science, organic chemistry, and pharmaceutical research. It is commonly applied in the synthesis of new compounds, polymer development, and studies on organic reactivity. Its availability and effectiveness make it a standard component in many research projects, supporting both academic and industrial applications in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from Ethyl 2-Iodo-2-methylpropionate due to its reactivity in nucleophilic substitution reactions, enabling the formation of complex organic structures.\u003c\/li\u003e\n\u003cli\u003ePolymerization processes utilize this compound as a functional group modifier, enhancing the properties of polymers through controlled chain reactions.\u003c\/li\u003e\n\u003cli\u003eRadical reaction studies rely on its ability to participate in free radical mechanisms, making it useful for exploring reaction pathways and mechanisms.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research leverages its reactivity for the synthesis of novel drug compounds, supporting the development of new therapeutic agents.\u003c\/li\u003e\n\u003cli\u003eMaterials science experiments use this reagent to investigate the behavior of functional groups in various chemical environments, aiding in the design of advanced materials.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 7425-55-0\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\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 light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Iodo-2-methylpropionate should be stored in a cool, dry place away from direct light to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its chemical integrity. 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 unintended chemical interactions. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086934487258,"sku":"TCI2510E119929134","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086934520026,"sku":"TCI2510E119929135","price":5452000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1199.jpg?v=1767112514"},{"product_id":"tci2510e120029136","title":"TCI E1200 78489-65-3 Ethyl alpha-Iodophenylacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl alpha-Iodophenylacetate is a chemical compound widely used in laboratory settings, particularly in organic synthesis reactions. As a key reagent in materials science, it plays a vital role in facilitating carbon-carbon bond formation and polymerization processes. Its unique molecular structure, featuring an iodine atom at the alpha position, makes it highly reactive and suitable for a variety of chemical transformations. This reagent is essential for researchers and students engaged in synthetic chemistry, offering versatility in experimental design and application.\u003c\/p\u003e\n\u003cp\u003eThe reactivity of Ethyl alpha-Iodophenylacetate is primarily due to the presence of the iodine atom, which acts as a good leaving group in nucleophilic and electrophilic reactions. This characteristic allows it to participate effectively in substitution reactions and other complex chemical mechanisms. Its ability to undergo various reaction pathways makes it a preferred choice for those seeking reagents with specific functional properties. The compound’s chemical stability under controlled conditions further enhances its reliability in laboratory experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl alpha-Iodophenylacetate is commonly used in organic chemistry research and educational settings. It is particularly relevant for institutions focused on pure and applied chemistry, where its role in polymerization and molecular modification is highly valued. Its application supports both academic and industrial research, contributing to the advancement of chemical sciences in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions where carbon-carbon bond formation is required, due to its reactivity and ability to participate in nucleophilic substitution.\u003c\/li\u003e\n\u003cli\u003ePolymerization processes that need a versatile reagent for chain growth and cross-linking, leveraging its iodine-containing structure.\u003c\/li\u003e\n\u003cli\u003eModification of organic compounds through functional group transformations, benefiting from its electrophilic nature in reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eTeaching demonstrations in undergraduate chemistry courses, providing hands-on experience with a key synthetic reagent.\u003c\/li\u003e\n\u003cli\u003eResearch in materials science for developing new polymers and macromolecules, utilizing its role in macromolecular synthesis.\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: 78489-65-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier guidelines\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 direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eEthyl alpha-Iodophenylacetate should be stored in a cool, dark place, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of materials compatible with organic solvents to prevent contamination and evaporation. Due to its reactivity, it should be handled in a well-ventilated area, ideally under a fume hood, to minimize exposure. Avoid contact with incompatible substances such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this reagent. Proper storage and handling ensure the safety of laboratory personnel and the effectiveness of the reagent in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086934585562,"sku":"TCI2510E120029136","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086934618330,"sku":"TCI2510E120029137","price":5452000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1200.jpg?v=1767112518"},{"product_id":"tci2510e144529469","title":"TCI E1445 4773-33-5 Ethyl 2-Chloro-2-phenylacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Chloro-2-phenylacetate is a chemical compound widely used in organic laboratory reactions. It serves as a key building block in the synthesis of aromatic and heterocyclic compounds, making it essential for researchers engaged in chemical synthesis. Its role as a precursor allows it to react with various reagents to form more complex molecules, supporting a wide range of experimental applications. This compound is particularly valued for its stability and reliability in laboratory settings, ensuring consistent results across multiple experiments.\u003c\/p\u003e\n\u003cp\u003eOne of the primary reasons for its popularity is its chemical stability and non-reactive nature under normal conditions. This makes it easy to store and handle, reducing the risk of unintended chemical reactions. Additionally, its solubility in organic solvents simplifies purification and reaction processes, enhancing its utility in synthetic chemistry. These properties make it a preferred choice for laboratories requiring high-quality, dependable reagents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Ethyl 2-Chloro-2-phenylacetate is commonly used in chemical research, especially in the synthesis of aromatic compounds and the development of new chemical products. Its availability and reliability make it a go-to material for both academic and industrial research settings, supporting innovation and scientific advancement in the field of organic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of aromatic and heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePreparation of intermediates for pharmaceutical and agrochemical research as a reliable starting material.\u003c\/li\u003e\n\u003cli\u003eUse in analytical chemistry for calibration and as a standard in chromatographic analysis.\u003c\/li\u003e\n\u003cli\u003eSupport in the development of new materials through controlled chemical reactions and functional group modifications.\u003c\/li\u003e\n\u003cli\u003eApplication in academic research for teaching and experimental studies in organic chemistry courses.\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: 4773-33-5\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 sizes 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, 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 2-Chloro-2-phenylacetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and evaporation. Due to its solubility in organic solvents, it should be kept away from incompatible substances such as strong bases or oxidizing agents. Proper labeling and storage conditions ensure safety and prolong the shelf life of the compound. Always follow standard laboratory safety protocols when handling this material to minimize risks and ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086961029338,"sku":"TCI2510E144529469","price":884000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086961062106,"sku":"TCI2510E144529470","price":2650000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1445.jpg?v=1767112870"},{"product_id":"tci2510e152529573","title":"TCI E1525 2882-19-1 Ethyl 2-Bromo-2-phenylacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl 2-Bromo-2-phenylacetate is an α-bromo ester that carries a phenyl group on the same carbon as its bromine atom. The combination of the electron-withdrawing ester function and the adjacent aromatic ring leaves the alpha position strongly activated, which makes this compound a versatile electrophile in the organic synthesis laboratory. Its role is to supply a ready-to-couple phenylacetate unit that can be joined to a wide range of nucleophiles, while also serving as a precursor to reactive intermediates such as carbanions, carbenes and radicals that are widely used in the construction of new molecular frameworks.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that leads chemists to select this reagent is its high but still controllable substitution reactivity, allowing reactions to be run at moderate temperatures with bases that are not excessively harsh. The bromine atom is both a good leaving group and readily abstracted homolytically, which opens up radical chemistry routes including its use as an initiator in controlled radical polymerisation. Its liquid form makes it easy to dispense with a micropipette or syringe in air-free reactions, and its good solubility in common organic solvents simplifies both reaction system design and the product purification stage.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this material is typically used in academic and industrial research settings where organic synthesis, building-block chemistry and polymer work are carried out. University chemistry departments, government research institutes and private R\u0026amp;D laboratories draw on reagents of this type for method development, the preparation of intermediates and postgraduate research projects. Because it is a liquid reagent handled in relatively small volumes, it fits well into the standard bench-scale synthetic workflows found in local facilities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleophilic substitution chemistry: the activated alpha carbon reacts readily with a broad range of nucleophiles, allowing the phenylacetate unit to be transferred under mild conditions with straightforward reaction control.\u003c\/li\u003e\n\u003cli\u003eCarbanion generation: treatment with suitable bases converts the compound into stabilised carbanion intermediates, giving chemists a reliable entry point for carbon–carbon bond forming sequences in multi-step synthesis.\u003c\/li\u003e\n\u003cli\u003eCarbene precursor chemistry: the bromine and ester substituents on a single carbon centre make this reagent a practical starting material for generating carbene intermediates used in framework construction.\u003c\/li\u003e\n\u003cli\u003eControlled radical polymerisation: the easily abstracted bromine atom allows the compound to serve as an initiator, providing defined chain starting points for polymer chemists working on controlled architectures.\u003c\/li\u003e\n\u003cli\u003eBuilding block synthesis: as a non-heterocyclic building block it introduces a phenyl-bearing ester fragment into larger target molecules, supporting intermediate preparation in research-scale synthetic programmes.\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: 2882-19-1\u003c\/li\u003e\n\u003cli\u003eCatalogue code: E1525\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid, soluble in common organic solvents\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed container 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\u003eStore the reagent in its original tightly sealed container in a cool, dry and well-ventilated area, protected from light, moisture and sources of ignition. Amber glass bottles or the manufacturer's supplied packaging are suitable containers, and bottles should be resealed promptly after each withdrawal to limit exposure to atmospheric moisture. As an alkylating-type organobromine compound it should be handled in a fume hood using gloves, safety goggles and a laboratory coat, avoiding skin and eye contact as well as inhalation of vapour. Dispense with a clean, dry syringe or micropipette, keep it away from strong bases and oxidising agents, and dispose of residues through the laboratory's designated chemical waste stream.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086966993114,"sku":"TCI2510E152529573","price":1616000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086967025882,"sku":"TCI2510E152529574","price":5755000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E1525.jpg?v=1767112998"},{"product_id":"tci2510h137134207","title":"TCI H1371 3083-10-1 1,1,4,7,10,10-Hexamethyltriethylenetetramine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,1,4,7,10,10-Hexamethyltriethylenetetramine, known among polymer researchers by the abbreviation HMTETA, is a linear polyamine ligand carrying four donor nitrogen atoms along a single chain, with six methyl groups distributed across terminal and internal positions. Its principal role in the laboratory is to act as the ligand that binds copper ions in atom transfer radical polymerization systems. Without an appropriate ligand, copper salts neither dissolve in organic media nor possess a suitable redox potential, and controlled polymerization reactions therefore fail to proceed as intended.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound so useful is its ability to supply four nitrogen donor sites simultaneously from a single molecule, producing a highly stable chelate complex with copper. The methyl groups on every nitrogen render the ligand fully tertiary, so it carries no amine hydrogens that could interfere with the reaction, while at the same time improving the solubility of the resulting complex in both nonpolar and polar organic solvents. Being liquid at room temperature, it is straightforward to measure volumetrically and to add directly into a reaction flask. The flexibility of its backbone allows the coordination geometry to adjust as the oxidation state of the metal centre changes during the catalytic cycle.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, HMTETA is typically encountered in university and institutional research groups working on controlled radical polymerization, functional polymer synthesis, and coordination chemistry. It is usually ordered in small quantities alongside a copper halide source and purified monomer, since catalyst loadings in these systems are low relative to the monomer charge. Groups preparing block copolymers, polymer brushes, or well-defined macromolecular architectures generally keep a single bottle on hand for repeated small-scale reactions rather than for bulk consumption.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAtom transfer radical polymerization catalysis — the four nitrogen donors chelate copper halide tightly, solubilising the metal in organic media and tuning its redox potential so that chain growth stays controlled.\u003c\/li\u003e\n\u003cli\u003eControlled synthesis of block copolymers — stable ligand–copper coordination maintains reversible activation and deactivation across sequential monomer additions, allowing defined block lengths and narrow molecular weight distributions to be obtained.\u003c\/li\u003e\n\u003cli\u003eSurface-initiated polymerization and polymer brush growth — the liquid form and good organic solubility let researchers prepare homogeneous catalyst solutions that reach initiator sites anchored on substrate surfaces.\u003c\/li\u003e\n\u003cli\u003eCoordination chemistry and complex preparation — the flexible tetradentate backbone accommodates different coordination geometries, making it a convenient starting ligand for preparing and studying transition metal complexes.\u003c\/li\u003e\n\u003cli\u003eMechanistic and kinetic studies of polymerization — the fully tertiary structure removes interfering amine protons, giving reproducible catalyst behaviour suitable for comparing rate constants and equilibrium measurements.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code H1371)\u003c\/li\u003e\n\u003cli\u003eCAS number: 3083-10-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Nitrogen-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003eChemical name: 1,1,4,7,10,10-Hexamethyltriethylenetetramine (HMTETA)\u003c\/li\u003e\n\u003cli\u003ePhysical form: liquid at room temperature\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale pack sizes; please confirm the current options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry place away from light and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the bottle tightly closed in a cool, dry, well-ventilated area, protected from light and kept away from oxidising agents and acids. As an amine liquid, it is best kept in its original supplier container with the cap firmly sealed; for frequent use, transfer under inert gas into a septum-capped vial so that the bulk stock is not repeatedly exposed to air and moisture. Handle inside a fume hood, wearing safety goggles, nitrile gloves, and a laboratory coat, and use a dry syringe or pipette for volumetric transfer. Wipe up any spillage promptly and consult the supplier safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5mL","offer_id":50506755506394,"sku":"TCI2510H137134207","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1371.jpg?v=1767117916"},{"product_id":"tci2510h175134679","title":"TCI H1751 189324-13-8 2-Hydroxyethyl 2-Bromo-2-methylpropanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxyethyl 2-Bromo-2-methylpropanoate is a chemical compound widely used in laboratory settings for various chemical reactions and the synthesis of complex molecules. As a polymerization reagent, it plays a crucial role in the formation of polymers and macromolecules. This compound is particularly valuable in synthetic chemistry due to its reactivity and versatility in participating in substitution reactions. Its unique chemical structure, featuring both a bromo group and a hydroxyl group, allows it to interact with a wide range of other molecules, making it an essential tool for organic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity and functional groups make it a preferred choice for researchers seeking to create complex organic structures. Its ability to participate in multiple chemical reactions, especially those requiring high reactivity, sets it apart from other reagents. The presence of the hydroxyl group also contributes to its solubility properties, which are beneficial in various synthetic protocols. These characteristics ensure that it remains a reliable and effective reagent in modern laboratory practices.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in chemical, material, and pharmaceutical research. Its availability in a solid form and high purity make it an ideal choice for laboratory applications. Researchers in Indonesia rely on this compound for its consistent performance and reliability in complex synthesis processes. Its importance is further underscored by its limited availability, making it a critical resource for many research facilities.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis is a key application where this compound is used due to its reactivity and ability to participate in substitution reactions.\u003c\/li\u003e\n\u003cli\u003ePolymer science research benefits from this reagent as it contributes to the formation of macromolecules and polymers.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development often incorporates this compound in the synthesis of complex organic compounds.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments utilize this reagent for creating new materials with specific chemical properties.\u003c\/li\u003e\n\u003cli\u003eChemical research in Indonesian laboratories frequently employs this compound for its versatility in various synthetic pathways.\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: 189324-13-8\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or high-density polyethylene, to prevent any unwanted reactions. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment like gloves and safety goggles. Avoid exposure to heat or incompatible substances to ensure safe storage and usage. Proper labeling of containers is essential for safe handling and to prevent accidental contamination. Laboratories should follow standard safety protocols when working with this compound to ensure a safe and efficient research environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087319871706,"sku":"TCI2510H175134679","price":5048000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510H1751.jpg?v=1767118448"},{"product_id":"tci2510i095436253","title":"TCI I0954 19481-79-9 2-Iodo-2-methylpropionitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Iodo-2-methylpropionitrile is a chemical compound widely used as a foundational building block in organic synthesis. Its unique structure, featuring an iodine atom and a nitrile group, makes it a versatile reagent in the laboratory. This compound plays a critical role in the development of complex organic molecules, serving as a key intermediate in various synthetic pathways. Due to its reactivity, it is frequently employed in nucleophilic and electrophilic substitution reactions, contributing to the creation of functionalized compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity stems from its nitrile group, which is highly reactive under appropriate conditions. This makes it an ideal choice for chemists seeking to introduce functional groups into organic molecules. Additionally, its stability in certain environments allows for controlled use in laboratory settings. The availability of this compound in both solid and liquid forms enhances its usability, as it can be easily handled and incorporated into different experimental protocols.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Iodo-2-methylpropionitrile is commonly used in organic chemistry research, particularly in the synthesis of complex compounds. It is also integrated into educational programs to help students understand the reactivity and applications of such compounds. Its role in both research and teaching underscores its importance in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the preparation of functionalized compounds due to its reactive nitrile group and iodine substituent.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where the iodine atom serves as a good leaving group for substitution processes.\u003c\/li\u003e\n\u003cli\u003eElectrophilic addition reactions as a versatile intermediate in the formation of more complex organic structures.\u003c\/li\u003e\n\u003cli\u003eTeaching demonstrations in chemistry courses to illustrate the reactivity of nitrile and halogenated compounds.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production for the development of pharmaceuticals and specialty chemicals requiring specific functional groups.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 19481-79-9\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 supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on the batch\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Personal protective equipment such as gloves, goggles, and a lab coat should be worn when handling this material. Avoid contact with skin and eyes, and ensure proper disposal according to local regulations. Always follow standard laboratory safety protocols when working with reactive chemicals.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087429382362,"sku":"TCI2510I095436253","price":2752000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48087429415130,"sku":"TCI2510I095436254","price":10171000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0954.jpg?v=1767120566"},{"product_id":"tci2510m203840155","title":"TCI M2038 3042-81-7 Methyl alpha-Bromophenylacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl alpha-Bromophenylacetate is a chemical compound widely used in organic laboratory reactions. It serves as a key building block in the synthesis of complex molecules, particularly in the field of organic chemistry. This compound is valued for its versatility and reactivity, making it an essential tool in various synthetic pathways. Its presence in laboratory settings enables chemists to construct intricate molecular structures with precision and control. Due to its stability and predictable chemical behavior, it is a reliable choice for a wide range of experimental applications.\u003c\/p\u003e\n\u003cp\u003eThe compound’s alpha-bromo group makes it highly suitable for nucleophilic substitution reactions and alkylation processes. This functional group enhances the reactivity of the carbon atom, allowing for efficient chemical transformations. Its chemical properties are well-documented, which ensures consistent results in laboratory experiments. The compound’s ability to react with various reagents further expands its utility in synthetic chemistry. These characteristics make it a preferred choice for researchers aiming to develop new compounds and materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Methyl alpha-Bromophenylacetate is commonly used in academic and research settings. It plays a crucial role in the study of aromatic and heterocyclic compounds. Its stability and reactivity make it a popular choice among chemists working on organic synthesis projects. The compound’s widespread application in both educational and research institutions highlights its importance in advancing chemical knowledge and innovation in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of aromatic and heterocyclic compounds due to its reactive alpha-bromo group and ability to participate in nucleophilic substitution reactions.\u003c\/li\u003e\n\u003cli\u003eAlkylation reactions where the compound serves as a versatile alkylating agent for the introduction of functional groups into complex molecules.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the development of pharmaceutical compounds requiring specific substitution patterns on aromatic rings.\u003c\/li\u003e\n\u003cli\u003eEducational laboratory experiments to teach students about nucleophilic substitution and functional group reactivity in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes that require the synthesis of intermediate compounds for the production of fine chemicals and specialty products.\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: 3042-81-7\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: 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\u003eMethyl alpha-Bromophenylacetate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a sealed container to prevent exposure to air and moisture. Suitable storage containers should be made of materials that are chemically inert to the compound, such as glass or high-density polyethylene. The substance should be kept away from strong oxidizing agents and incompatible chemicals to avoid potential reactions. In laboratory settings, proper ventilation is essential to minimize inhalation risks. Always follow standard safety protocols when handling this compound to ensure a safe working environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":50506728734938,"sku":"TCI2510M203840155","price":1289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2038.jpg?v=1767125926"},{"product_id":"tci2510m220840394","title":"TCI M2208 23426-63-3 Methyl 2-Bromo-2-methylpropanoate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl 2-Bromo-2-methylpropanoate is a chemical compound widely used in organic laboratory reactions. As a key building block in synthetic chemistry, it serves as a versatile intermediate for the creation of more complex molecular structures. Its reactivity and functional group make it an essential tool for chemists engaged in research and development. This compound is commonly employed in nucleophilic substitution reactions, where its bromo group acts as a good leaving group, facilitating the formation of new chemical bonds.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity make it a preferred choice for various synthetic pathways. Its molecular structure allows it to interact effectively with a range of reagents, enabling the synthesis of diverse organic compounds. The presence of the bromo group at a specific position enhances its utility in substitution reactions, particularly in electrophilic and nucleophilic processes. Its consistent chemical properties and ease of handling contribute to its popularity among researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Methyl 2-Bromo-2-methylpropanoate is extensively used in organic chemistry research. It is a common reagent in both academic and industrial settings, supporting the development of new compounds and structural modifications. Many universities and research institutions rely on this compound for educational purposes and experimental studies. Its availability and reliability make it a staple in the chemical supply chain for Indonesian laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNucleophilic Substitution Reactions: This compound is ideal for nucleophilic substitution due to its bromo group, which facilitates the formation of new bonds in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: It serves as a building block for creating complex molecules, making it essential in research and development of new chemical compounds.\u003c\/li\u003e\n\u003cli\u003eStructural Modification Studies: Its reactivity allows for the modification of molecular structures, supporting studies in chemical engineering and pharmaceutical research.\u003c\/li\u003e\n\u003cli\u003eTeaching and Learning in Chemistry: It is frequently used in educational settings to demonstrate key reaction mechanisms and synthetic strategies.\u003c\/li\u003e\n\u003cli\u003eResearch in Pharmaceutical Chemistry: Its versatility makes it a valuable tool in the development of new drug compounds and therapeutic agents.\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: 23426-63-3\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: Solid\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible materials such as strong bases or reducing agents. Proper personal protective equipment, including gloves and safety goggles, should be worn during handling to ensure safety. The compound is stable under standard laboratory conditions but should be kept sealed when not in use to maintain its integrity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48087660560602,"sku":"TCI2510M220840394","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48087660593370,"sku":"TCI2510M220840395","price":2424000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510M2208.jpg?v=1767126268"},{"product_id":"tci2510p088146372","title":"TCI P0881 3030-47-5 N,N,N',N'',N''-Pentamethyldiethylenetriamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN,N,N',N'',N''-Pentamethyldiethylenetriamine (PMDETA), with CAS number 3030-47-5, is a versatile chemical compound widely used in laboratory settings. As a substituted amine, it plays a crucial role in polymerization reactions, particularly in the synthesis of thermoplastic and elastomeric polymers. Its complex molecular structure, featuring five methyl groups attached to nitrogen atoms, makes it a valuable reagent for crosslinking and functional group modification. PMDETA is commonly found in materials science research, where it contributes to the development of advanced polymer systems and organic compounds.\u003c\/p\u003e\n\u003cp\u003eThe chemical properties of PMDETA make it a preferred choice for various applications. It exhibits good solubility in organic solvents, facilitating easy handling and integration into reaction mixtures. Its reactivity towards acids, bases, and oxidizing agents allows it to participate in a wide range of chemical transformations. Despite its reactivity, PMDETA maintains a degree of stability under controlled conditions, which is essential for maintaining the integrity of synthesized compounds. This balance of reactivity and stability makes it ideal for use in complex synthetic processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, PMDETA is frequently utilized in polymerization research, especially in the development of new materials and composite structures. Its role in crosslinking and chain extension is critical for creating polymers with specific mechanical and thermal properties. Researchers in materials science and chemical engineering often rely on PMDETA to achieve desired molecular architectures and functional properties in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePolymerization reactions benefit from PMDETA due to its ability to act as a multifunctional crosslinking agent, enhancing the structural integrity of thermoplastic and elastomeric materials.\u003c\/li\u003e\n\u003cli\u003eIn the synthesis of complex organic compounds, PMDETA serves as a versatile reagent for introducing multiple nitrogen functionalities into molecular frameworks.\u003c\/li\u003e\n\u003cli\u003ePMDETA is commonly used in the modification of polymer chains to improve properties such as thermal stability and mechanical strength in advanced material development.\u003c\/li\u003e\n\u003cli\u003eIts solubility in organic solvents makes it suitable for use in solution-based polymerization techniques, enabling precise control over reaction conditions.\u003c\/li\u003e\n\u003cli\u003eThe reactivity of PMDETA allows it to participate in catalytic systems, supporting the development of more efficient and selective chemical transformations.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 3030-47-5\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Polymer\/Macromolecule Reagents \u0026gt; Polymerization Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes 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 and incompatible materials\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003ePMDETA should be stored in a cool, dry environment to prevent degradation and maintain its chemical integrity. It is recommended to use sealed, airtight containers made of materials compatible with its chemical nature, such as glass or high-density polyethylene. Due to its reactivity, it should be kept away from strong acids, bases, and oxidizing agents to avoid unwanted side reactions. Proper ventilation is essential when handling PMDETA to minimize exposure. In laboratory settings, personal protective equipment such as gloves, goggles, and lab coats should be worn at all times. 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