{"title":"Copper Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]","description":"\u003cp\u003e\u003cstrong\u003eCopper Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/strong\u003e — menghimpun kompleks tembaga(I) dan tembaga(II) dengan berbagai ligan dan counter-ion seperti triflat, tetrafluoroborat, atau heksafluorofosfat yang berperan sebagai katalis logam transisi. Kompleks ini menyediakan pusat tembaga aktif untuk mempercepat pembentukan ikatan karbon-karbon maupun karbon-heteroatom.\u003c\/p\u003e\u003cp\u003eKatalis tembaga dipakai kimiawan sintesis organik pada reaksi kopling silang, reaksi klik azida-alkuna (CuAAC), serta reaksi tipe Ullmann untuk membentuk ikatan C-N, C-O, atau C-C. Kompleks tetrakis(asetonitril)tembaga(I) umum dipilih sebagai sumber Cu(I) yang larut dalam pelarut organik pada berbagai protokol katalisis homogen.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510t390555619\"\u003eTCI T3905 58452-28-1 Tetrakis(acetonitrile)copper(I) Trifluoromethanesulfonate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c038414469\"\u003eTCI C0384 13395-16-9 Bis(2,4-pentanedionato)copper(II)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t266654072\"\u003eTCI T2666 15418-29-8 Tetrakis(acetonitrile)copper(I) Tetrafluoroborate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c195216562\"\u003eTCI C1952 544-92-3 Copper(I) Cyanide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t266554071\"\u003eTCI T2665 64443-05-6 Tetrakis(acetonitrile)copper(I) Hexafluorophosphate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c216116825\"\u003eTCI C2161 7787-70-4 Copper(I) Bromide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t144252612\"\u003eTCI T1442 42152-46-5 Copper(I) Trifluoromethanesulfonate Benzene Complex\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c216216828\"\u003eTCI C2162 7758-89-6 Copper(I) Chloride\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan bilangan oksidasi tembaga (Cu(I) atau Cu(II)), jenis counter-ion yang memengaruhi kelarutan dan stabilitas kompleks, serta tingkat kemurnian yang disyaratkan untuk katalisis sensitif. 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 Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation], sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phosphine-ligands-cross-coupling-reaction-using-transition-metal-catalysts\"\u003ePhosphine Ligands [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-palladium-catalysts-cross-coupling-reaction-using-transition-metal-catalysts\"\u003ePalladium Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-n-heterocyclic-carbene-nhc-ligands-cross-coupling-reaction-using-transition-metal-catalysts\"\u003eN-Heterocyclic Carbene (NHC) Ligands [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nickel-catalysis-and-inorganic-chemistry\"\u003eNickel [Catalysis and Inorganic Chemistry]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-nickel-catalysts-cross-coupling-reaction-using-transition-metal-catalysts\"\u003eNickel Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-bases-and-additives-cross-coupling-reaction-using-transition-metal-catalysts\"\u003eBases and Additives [Cross-coupling Reaction using Transition Metal Catalysts]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-cross-coupling-reaction-using-transition-metal-catalysts-c-c-bond-form\"\u003eCross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]\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":"tci2510c038414469","title":"TCI C0384 13395-16-9 Bis(2,4-pentanedionato)copper(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0384 Bis(2,4-pentanedionato)copper(II), CAS 13395-16-9, is the well-known copper(II) acetylacetonate chelate used as a versatile copper source in synthesis and materials science. Its stable β-diketonate framework makes the complex convenient to weigh and dissolve, while the ligands are readily displaced once the active catalytic species forms. It is commonly applied as a catalyst precursor in copper-mediated coupling and C–H functionalisation studies, and as a precursor for copper-based thin films and nanoparticles. AMI Scientific supplies it in 25 g and 250 g packs; store in a tightly closed container in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085995159770,"sku":"TCI2510C038414469","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085995192538,"sku":"TCI2510C038414470","price":2784000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0384.jpg?v=1767095147"},{"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":507000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086108045530,"sku":"TCI2510C216116826","price":1350000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086108078298,"sku":"TCI2510C216116827","price":4667000.0,"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":564000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086108274906,"sku":"TCI2510C216316832","price":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086108307674,"sku":"TCI2510C216316833","price":3768000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2163.jpg?v=1767097862"},{"product_id":"tci2510c231217049","title":"TCI C2312 68986-76-5 Copper(I) 2-Thiophenecarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCopper(I) 2-Thiophenecarboxylate (TCI C2312) is a chemical compound widely used in laboratory settings, particularly in catalysis and inorganic chemistry. This material plays a crucial role in facilitating complex chemical reactions, especially those involving C-H activation. Its unique chemical structure, featuring a thiophenecarboxylate group, enables it to act as an effective catalyst in various synthetic processes. In modern chemical research, it is a key component in the development of new materials and pharmaceutical compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its reactivity and specificity, making it a preferred choice for researchers aiming to achieve controlled and selective chemical transformations. Its ability to interact with both organic and inorganic molecules enhances its versatility in different experimental setups. Additionally, Copper(I) 2-Thiophenecarboxylate exhibits stability under controlled conditions, ensuring consistent performance in laboratory applications. This stability, combined with its reactivity, makes it a reliable reagent for advanced chemical studies.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Copper(I) 2-Thiophenecarboxylate is commonly used in research focused on catalytic processes and material synthesis. Its role in C-H activation has made it a valuable tool for scientists working on innovative chemical reactions. Due to its chemical properties, it is also utilized in studies related to coordination chemistry and organometallic reactions. Its presence in Indonesian research facilities highlights its importance in advancing chemical science in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eC-H Activation Reactions: This compound is ideal for C-H activation due to its ability to facilitate selective bond cleavage in organic molecules, making it a key reagent in synthetic chemistry.\u003c\/li\u003e\n\u003cli\u003eCoordination Chemistry Studies: Its interaction with metal ions enables it to be used in investigations of coordination complexes and metal-ligand bonding mechanisms.\u003c\/li\u003e\n\u003cli\u003eOrganometallic Reaction Development: The compound’s reactivity with organic substrates makes it suitable for the synthesis of organometallic compounds and functional materials.\u003c\/li\u003e\n\u003cli\u003eCatalytic Conversion Processes: It is used in catalytic systems where efficient and selective transformation of substrates is required, especially in green chemistry applications.\u003c\/li\u003e\n\u003cli\u003eMaterial Synthesis Research: Its unique chemical structure allows it to participate in the creation of new materials, including polymers and nanomaterials, with tailored properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 68986-76-5\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 standard laboratory supply options\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCopper(I) 2-Thiophenecarboxylate 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 moisture and air, which may affect its reactivity. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper ventilation in the laboratory. Regular monitoring of storage conditions is advised to ensure the material remains suitable for use in chemical experiments. Always follow standard laboratory safety protocols when working with this compound to minimize risks and ensure safe handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086119547098,"sku":"TCI2510C231217049","price":1013000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086119579866,"sku":"TCI2510C231217050","price":3514000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2312.jpg?v=1767098120"},{"product_id":"tci2510c241017177","title":"TCI C2410 38465-60-0 Copper(II) Tetrafluoroborate (ca. 45% in Water)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCopper(II) Tetrafluoroborate (ca. 45% in Water), with CAS number 38465-60-0, is a chemical compound widely used in various chemical reactions and catalytic processes. This compound is a salt of copper(II) and tetrafluoroboric acid, known for its reactive and stable chemical properties under specific conditions. In laboratory settings, it plays a crucial role as a catalyst in oxidation and reduction reactions, as well as in the synthesis of both organic and inorganic compounds. Its ability to facilitate chemical transformations makes it a valuable reagent for researchers and chemists.\u003c\/p\u003e\n\u003cp\u003eThe reactive nature and catalytic properties of Copper(II) Tetrafluoroborate make it a preferred choice in chemical synthesis. It exhibits good solubility in water, which simplifies its use in a variety of laboratory applications. Its stability under controlled conditions ensures consistent performance in experiments, making it reliable for use in both academic and industrial research. The compound’s versatility allows it to be integrated into a wide range of chemical processes, enhancing efficiency and effectiveness in laboratory workflows.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Copper(II) Tetrafluoroborate is commonly used in chemical research and applied studies. It is frequently employed in catalytic experiments, complex compound synthesis, and other chemical processes that require precise control over reaction conditions. Its availability and performance make it a standard reagent in both academic and research institutions across Indonesia, supporting advancements in chemical science and technology.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eCatalytic Oxidation Reactions: Copper(II) Tetrafluoroborate is ideal for oxidation processes due to its ability to facilitate electron transfer and stabilize reactive intermediates.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: This compound is widely used in the synthesis of complex organic molecules, where its catalytic properties enhance reaction efficiency and yield.\u003c\/li\u003e\n\u003cli\u003eInorganic Compound Formation: It plays a key role in the synthesis of various inorganic compounds, offering stability and reactivity in aqueous environments.\u003c\/li\u003e\n\u003cli\u003eRedox Reactions: Its redox properties make it suitable for reduction and oxidation reactions, supporting diverse chemical transformations in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry: It is used in analytical procedures to modify reaction conditions and improve the accuracy of chemical analyses.\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: 38465-60-0\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 sizes as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Aqueous solution with ca. 45% concentration\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eCopper(II) Tetrafluoroborate should be stored in a cool, dry place, away from direct sunlight and moisture to maintain its chemical stability. It is recommended to use containers made of inert materials such as glass or polyethylene to prevent any chemical interactions. In laboratory settings, proper personal protective equipment, including gloves and safety goggles, should be worn when handling this compound. Due to its reactive nature, it should be handled in a well-ventilated area to minimize exposure. Regular monitoring of storage conditions ensures the compound remains effective for its intended applications. Always follow standard laboratory safety protocols to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"500g","offer_id":48086125215962,"sku":"TCI2510C241017177","price":1659000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2410.jpg?v=1767098307"},{"product_id":"tci2510d254222798","title":"TCI D2542 30698-64-7 Di-mu-hydroxo-bis[(N,N,N',N'-tetramethylethylenediamine)copper(II)] Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound, TCI D2542 30698-64-7 Di-mu-hydroxo-bis[(N,N,N',N'-tetramethylethylenediamine)copper(II)] Chloride, is a complex copper(II) compound with a unique structure featuring tetramethylethylenediamine (TME) ligands. It plays a crucial role in catalytic reactions, particularly in C-H activation processes within inorganic chemistry and catalysis. As a key reagent in advanced chemical research, it supports the development of new synthetic methods and reaction pathways. Its stability and reactivity make it an essential tool for researchers aiming to explore complex molecular transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's preferred status stems from its stable complex structure and strong coordination ability with copper. These properties allow it to act as an efficient catalyst in various chemical reactions without undergoing rapid degradation. Its chemical stability under controlled laboratory conditions ensures consistent performance, making it suitable for a wide range of experimental setups. Additionally, its ability to facilitate C-H activation makes it particularly valuable in organic and inorganic synthesis, where precise control over reaction mechanisms is essential.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in advanced chemical research, especially in higher education institutions and research centers. It supports studies in catalysis, inorganic chemistry, and synthetic organic chemistry. Its role in accelerating reactions without compromising stability makes it a reliable choice for both academic and industrial research applications. 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It is recommended to keep the solution in a sealed container to avoid exposure to moisture and air, which can affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it away from incompatible materials, such as strong oxidizers or acids, to prevent unwanted reactions. 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Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085365915866,"sku":"TCI2510A15402113","price":1659000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085365948634,"sku":"TCI2510A15402114","price":5397000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510A1540.jpg?v=1767081629"},{"product_id":"tci2510b15136806","title":"TCI B1513 32270-93-2 Bis(1,3-propanediamine) Copper(II) Dichloride","description":"\u003cp\u003e\u003cstrong\u003eBis(1,3-propanediamine) Copper(II) Dichloride\u003c\/strong\u003e (CAS 32270-93-2) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eReagent Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Used as a monomer in the synthesis of polyimides, polyurethanes, and 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