{"title":"Catalysis and Inorganic Chemistry","description":"\u003cp\u003e\u003cstrong\u003eCatalysis and Inorganic Chemistry\u003c\/strong\u003e — menghimpun katalis dan senyawa anorganik untuk sintesis organik, mencakup ligan (donor nitrogen, fosfor, karbon, diketon, olefin, dan lainnya), katalis organik, fotokatalis, katalis logam non-mulia, garam logam, serta senyawa unsur golongan utama, tanah jarang, dan logam transisi. Kategori ini menjadi tulang punggung reaksi pembentukan ikatan seperti kopling silang, hidrogenasi, oksidasi, dan aktivasi C–H.\u003c\/p\u003e\u003cp\u003eCatalysis and Inorganic Chemistry dipakai kimiawan sintesis untuk reaksi kopling silang (Suzuki, Negishi, Buchwald-Hartwig), hidrogenasi, metatesis olefin, kondensasi, serta aktivasi ikatan C–H dengan bantuan katalis logam transisi maupun organokatalis. Ligan dan katalis dalam kategori ini juga dipakai peneliti kimia anorganik dan material untuk merancang kompleks logam fungsional serta sistem fotokatalitik untuk transformasi molekul yang lebih efisien.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510y000756791\"\u003eTCI Y0007 1314-36-9 Yttrium(III) Oxide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552512177\"\u003eTCI B5525 2326-78-5 2,2'-Bipyridine-5,5'-diol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510p284948718\"\u003eTCI P2849 1310-58-3 Potassium Hydroxide (Pellets)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b556712226\"\u003eTCI B5567 40000-20-2 5-Bromo-1,10-phenanthroline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510o057544998\"\u003eTCI O0575 1310-73-2 Sodium Hydroxide (Granulated)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b559412267\"\u003eTCI B5594 904704-23-0 N,N-Bis[(diphenylphosphino)methyl]-3-(triethoxysilyl)propylamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510l023537159\"\u003eTCI L0235 1312-81-8 Lanthanum(III) Oxide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b560312281\"\u003eTCI B5603 917604-39-8 1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan tingkat oksidasi dan kemurnian logam, bentuk ligan (kiral atau akiral) untuk katalisis asimetris, serta stabilitas katalis terhadap udara dan kelembapan selama penyimpanan dan penanganan. 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 Chemistry, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/building-blocks-sintesis-organik\"\u003eBuilding Blocks untuk Sintesis Organik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-chemical-biology\"\u003eChemical Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-pharmaceutical-development-and-drug-discovery-research-reagents\"\u003ePharmaceutical Development and Drug Discovery Research Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/reagen-sintesis-organik\"\u003eReagen Sintesis Organik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/katalis-dan-kimia-anorganik\"\u003eKatalis \u0026amp; Kimia Anorganik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-organometallic-reagents\"\u003eOrganometallic Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l1-chemistry\"\u003eChemistry\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":"tci2510b560312281","title":"TCI B5603 917604-39-8 1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Bis(2,6-diisopropylphenyl)imidazolium-2-carboxylate (CAS 917604-39-8) is a masked N-Heterocyclic Carbene (NHC) precursor supplied by TCI, widely employed in organometallic catalyst synthesis. Upon thermal decarboxylation, it liberates the active NHC ligand in situ, offering a convenient and air-stable alternative to handling free carbenes. This compound is extensively applied in cross-coupling reactions, hydrogenation, and olefin metathesis catalyzed by transition metal complexes such as palladium, ruthenium, and iridium.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085890367706,"sku":"TCI2510B560312281","price":2784000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5603.jpg?v=1767092568"},{"product_id":"tci2510b560612285","title":"TCI B5606 74663-77-7 2,3-Bis(2,6-diisopropylphenylimino)butane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,3-Bis(2,6-diisopropylphenylimino)butane is an α-diimine nitrogen-donor ligand widely employed in homogeneous catalysis research. It readily coordinates with late transition metals such as nickel and palladium to form active catalysts for olefin polymerization and cross-coupling reactions. The bulky 2,6-diisopropylphenyl substituents provide effective steric shielding, enhancing catalyst stability and modulating reactivity in organometallic applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085890498778,"sku":"TCI2510B560612285","price":3121000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085890531546,"sku":"TCI2510B560612286","price":10765000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5606_1bed7fd5-5f28-4607-b569-f5cf5d094578.jpg?v=1767862597"},{"product_id":"tci2510b561312299","title":"TCI B5613 138124-32-0 (R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5613, commercially known as Jacobsen's catalyst, is a chiral manganese(III)-salen complex widely employed for highly enantioselective epoxidation of unfunctionalized alkenes. It is also utilized in asymmetric ring-opening reactions, enantioselective sulfide oxidation, and various other stereoselective transformations critical in medicinal chemistry and natural product synthesis. This compound is an essential tool for research laboratories focused on asymmetric catalysis and chiral building block preparation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48276771274970,"sku":"TCI2510B561312299","price":3317000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5613_9aff008e-8d59-44a2-b685-b6832842c906.jpg?v=1767862642"},{"product_id":"tci2510b573212458","title":"TCI B5732 176763-62-5 (R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) is a cobalt(II) salen complex commonly referred to as a Jacobsen-type catalyst, widely employed in C–H activation reactions and asymmetric catalysis. This chiral catalyst facilitates direct functionalization of unactivated carbon–hydrogen bonds and is also effective in enantioselective epoxidation and epoxide ring-opening reactions. It is a valuable reagent for synthetic organic chemistry laboratories working on pharmaceutical intermediates and fine chemical synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085899837658,"sku":"TCI2510B573212458","price":1771000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085899870426,"sku":"TCI2510B573212459","price":6606000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5732_33d79d36-3596-474e-aa43-15ed0e1fcec2.jpg?v=1767863128"},{"product_id":"tci2510b578712524","title":"TCI B5787 7787-64-6 Bismuth(III) Iodide Anhydrous","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5787 Bismuth(III) Iodide Anhydrous (CAS 7787-64-6) is a high-purity main-group inorganic compound widely utilized as a Lewis acid catalyst in organic synthesis and various chemical transformations. This anhydrous reagent is particularly valuable in cyclization, acylation, and carbon-heteroatom bond-forming reactions, making it a reliable choice for both research and analytical laboratories. Beyond catalysis, it serves as a bismuth precursor for synthesizing halide perovskites and thermoelectric materials in advanced materials research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085903278298,"sku":"TCI2510B578712524","price":1013000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085903311066,"sku":"TCI2510B578712525","price":3345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5787_0b282278-183d-4d93-b3cd-0ab306796290.jpg?v=1767863333"},{"product_id":"tci2510b591412687","title":"TCI B5914 1301706-47-7 (1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5914, (1R,2R)-1,2-Bis(2,4,6-trimethylphenyl)ethylenediamine Dihydrochloride (CAS 1301706-47-7), is a chiral nitrogen-donor ligand featuring a mesityl-substituted ethylenediamine backbone, supplied in its stable dihydrochloride salt form. This bidentate ligand is widely employed in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as enantioselective hydrogenation, C–C bond formation, and oxidation. It offers excellent chiral induction and is a reliable choice for researchers working in synthetic organic chemistry and coordination chemistry.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085909668058,"sku":"TCI2510B591412687","price":2334000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5914.jpg?v=1767092933"},{"product_id":"tci2510b598512764","title":"TCI B5985 129648-07-3 1,2-Bis[(2R,5R)-2,5-dimethylphospholano]ethane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Bis[(2R,5R)-2,5-dimethylphospholano]ethane is a chiral bidentate bisphospholane ligand widely used in asymmetric hydrogenation reactions with transition metal catalysts. It forms highly effective chiral complexes with rhodium and ruthenium, enabling the enantioselective reduction of prochiral olefins, ketones, and imines. This ligand is a reliable choice for pharmaceutical and fine chemical synthesis requiring high optical purity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085913075930,"sku":"TCI2510B598512764","price":3654000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085913108698,"sku":"TCI2510B598512765","price":11216000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5985_d672f8f2-2f0f-4676-bb0f-e77c5ee81da5.jpg?v=1767864076"},{"product_id":"tci2510b604512850","title":"TCI B6045 245679-18-9 1,3-Dimesityl-4,5-dihydro-1H-imidazol-3-ium Tetrafluoroborate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,3-Dimesityl-4,5-dihydro-1H-imidazol-3-ium Tetrafluoroborate is a widely used imidazolium salt serving as an N-Heterocyclic Carbene (NHC) ligand precursor for transition metal catalysis. It is commonly employed to generate active catalytic species for cross-coupling reactions, olefin metathesis, and asymmetric hydrogenation. The mesityl substituents provide optimal steric bulk and electronic properties, making this compound a standard building block in organometallic and synthetic chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916614874,"sku":"TCI2510B604512850","price":3936000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6045.jpg?v=1767093083"},{"product_id":"tci2510b612012935","title":"TCI B6120 2794-60-7 Barium(II) Trifluoromethanesulfonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBarium(II) Trifluoromethanesulfonate (CAS 2794-60-7) is a high-purity Lewis acid catalyst widely utilized in organic synthesis for activating carbonyl groups and facilitating carbon-carbon bond formation under mild conditions. This compound serves as a key reagent in Friedel-Crafts acylation, aldol condensations, and various fluorinated building block syntheses. Its stability and ease of handling make it a reliable choice for research laboratories working with fluorinated intermediates and catalytic transformations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085920776410,"sku":"TCI2510B612012935","price":2138000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085920809178,"sku":"TCI2510B612012936","price":6409000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6120.jpg?v=1768204486"},{"product_id":"tci2510b614612969","title":"TCI B6146 2102316-91-4 (-)-4-tert-Butyl-2,6-bis[(4S,5S)-4,5-tetramethylene-1-(2,4,6-trimethylbenzenesulfonyl)imidazolin-2-yl]phenol (contains 5% Dichloromethane at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-4-tert-Butyl-2,6-bis[(4S,5S)-4,5-tetramethylene-1-(2,4,6-trimethylbenzenesulfonyl)imidazolin-2-yl]phenol is a chiral bis(imidazoline) ligand designed for asymmetric synthesis applications. This compound features two (4S,5S)-configured imidazoline moieties attached to a tert-butyl-substituted phenol core, providing a well-defined chiral environment suitable for enantioselective catalytic reactions. It is commonly employed in asymmetric C-C and C-N bond-forming reactions and serves as a valuable tool in the development of new enantioselective synthetic methodologies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085922021594,"sku":"TCI2510B614612969","price":8826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6146.jpg?v=1767093225"},{"product_id":"tci2510b616112992","title":"TCI B6161 1092775-62-6 (2,2'-Bipyridine)bis[3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-kappaN][phenyl-kappaC]iridium(III) Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6161 (2,2'-Bipyridine)bis[3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN][phenyl-κC]iridium(III) Hexafluorophosphate is a cyclometalated iridium(III) complex widely employed as a photoredox catalyst in visible-light-driven organic synthesis. This compound exhibits strong photoluminescent properties, making it a valuable dopant in OLED (Organic Light-Emitting Diode) research and materials science. Its versatility extends to photocatalytic C-C and C-N bond-forming reactions, as well as mechanistic studies in electron transfer and biomimetic systems.\u003c\/p\u003e\n\u003cp\u003e--- *Asumsi: Catatan penyimpanan mengikuti rekomendasi umum penanganan kompleks iridium fotosensitif dari TCI.*\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085922873562,"sku":"TCI2510B616112992","price":4273000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085922906330,"sku":"TCI2510B616112993","price":14841000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6161_19dec429-90a9-45a3-a648-5726460c47b1.jpg?v=1767864767"},{"product_id":"tci2510b616913003","title":"TCI B6169 1352745-18-6 [1,3-Bis(ethoxycarbonyl)-2,4,5-trimethylcyclopentadien-1-yl]rhodium(III) Dichloride Dimer","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[1,3-Bis(ethoxycarbonyl)-2,4,5-trimethylcyclopentadien-1-yl]rhodium(III) Dichloride Dimer is a dimeric rhodium(III) catalyst specifically utilized in C–H bond activation reactions, enabling direct functionalization of inert carbon–hydrogen bonds without substrate pre-functionalization. This organometallic complex, featuring a substituted cyclopentadienyl ligand, is widely employed in oxidative annulation and directing-group-assisted cross-coupling methodologies. Its high reactivity and selectivity under mild conditions make it a preferred catalyst for the synthesis of fused heterocycles and the construction of C–C and C–heteroatom bonds in synthetic organic and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085923463386,"sku":"TCI2510B616913003","price":11496000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6169.jpg?v=1767093258"},{"product_id":"tci2510b618213009","title":"TCI B6182 13927-71-4 Copper(II) Dibutyldithiocarbamate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6182 Copper(II) Dibutyldithiocarbamate (CAS 13927-71-4) is a metal-dithiocarbamate complex widely utilized as a non-heterocyclic building block in chemical synthesis and coordination chemistry research. This compound serves as a catalyst precursor, analytical reagent for metal extraction, and a key component in studies involving transition metal-sulfur complexes. Its applications extend to functional materials development, lubricant additive research, and rubber vulcanization mechanism studies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085923725530,"sku":"TCI2510B618213009","price":901000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6182.jpg?v=1767093279"},{"product_id":"tci2510b619913024","title":"TCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6199 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride is a palladium(II) NHC catalyst specifically developed for C–H bond activation reactions. This catalyst enables direct functionalization of carbon–hydrogen bonds, streamlining synthetic pathways in organic chemistry. It is widely employed in C–H arylation, alkylation, and alkenylation reactions for the synthesis of pharmaceuticals, agrochemicals, and advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085924249818,"sku":"TCI2510B619913024","price":4105000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085924282586,"sku":"TCI2510B619913025","price":14053000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085924315354,"sku":"TCI2510B619913026","price":47778000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6199_8fb24a5d-0ce1-4fc9-b0bc-4be9be705d27.jpg?v=1767864859"},{"product_id":"tci2510b622113049","title":"TCI B6221 894086-00-1 5-(Di-tert-butylphosphino)-1',3',5'-triphenyl-1'H-1,4'-bipyrazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6221, 5-(Di-tert-butylphosphino)-1',3',5'-triphenyl-1'H-1,4'-bipyrazole (CAS 894086-00-1), is a bipyrazole-based phosphine ligand designed for transition metal-catalyzed cross-coupling reactions. This electron-rich ligand significantly enhances catalyst performance in challenging bond-forming processes, including Suzuki-Miyaura and Buchwald-Hartwig couplings. Supplied in a 200 mg packaging, it is suitable for both research-scale and method development applications requiring high ligand efficiency.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48276766884058,"sku":"TCI2510B622113049","price":1857000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6221_18556267-cf39-4841-9c7c-22c39c29b89e.jpg?v=1767864936"},{"product_id":"tci2510b624013072","title":"TCI B6240 1448897-87-7 (1R,2R)-1,2-Bis(4-methylphenyl)ethylenediamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1,2)-1,2-Bis(4-methylphenyl)ethylenediamine Dihydrochloride is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry. This material functions as a chiral reagent or catalyst, enabling precise control over the stereochemical outcome of chemical reactions. In laboratory settings, it plays a crucial role in the development of chiral compounds, particularly those with biological activity, such as pharmaceuticals and industrial chemicals. Its ability to influence reaction pathways makes it an essential tool for researchers aiming to achieve high enantiomeric purity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure, featuring two methylphenyl groups, provides high selectivity towards specific substrates, enhancing reaction efficiency and yield. Its chemical stability ensures consistent performance across multiple experimental runs. Additionally, its availability in dihydrochloride form simplifies handling and storage, making it a practical choice for laboratory use. The compound’s versatility and effectiveness in controlling stereochemistry make it a preferred option for advanced synthetic chemistry applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new chemical materials. It is a key component in experiments requiring precise stereoselective control, supporting research in pharmaceutical development and industrial chemical synthesis. Its application is widespread among research institutions and universities, contributing to the advancement of chiral compound synthesis in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with high enantiomeric purity, essential for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It supports the synthesis of bioactive compounds, aiding in drug discovery and formulation processes.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its role in controlling stereochemistry makes it a valuable tool for advanced synthetic pathways and structural modifications.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Synthesis: It enables the production of specialized chemicals with specific stereochemical properties, enhancing product performance.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Studies: Its use in catalytic systems allows for the investigation of stereoselective reaction mechanisms and catalyst efficiency.\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: 1448897-87-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which could affect its performance. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to high temperatures or direct sunlight, as these conditions may compromise its effectiveness. Proper storage and handling are essential to preserve its chiral properties and ensure consistent results in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085926019290,"sku":"TCI2510B624013072","price":2306000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6240.jpg?v=1767093344"},{"product_id":"tci2510b625413088","title":"TCI B6254 1335047-34-1 (4,4'-Di-tert-butyl-2,2'-bipyridine-kappa~2~N~1~,N~1'~)[bis[3,5-difluoro-2-(5-methyl-2-pyridinyl-kappaN)phenyl-kappaC~1~]]iridium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis material is a metal-based complex compound used in catalytic reactions, particularly in organic synthesis. As a catalyst, it accelerates chemical reactions without being permanently consumed in the final product. The compound features a complex structure composed of bipyridine and iridium ligands, which contribute to its highly effective catalytic properties. Its unique molecular arrangement allows for specific interactions with substrates, enhancing reaction efficiency. This makes it a valuable tool for researchers aiming to optimize chemical processes in the laboratory.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its high chemical stability and ability to function under various reaction conditions. Its robust nature ensures it remains active even in harsh chemical environments, making it a reliable choice for demanding applications. The presence of difluoro and methyl groups in its structure further enhances its reactivity and selectivity. These characteristics make it particularly suitable for complex synthetic pathways where precision and control are essential. Its performance in multiple reaction types, such as coupling and oxidation, underscores its versatility in catalytic systems.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry and catalysis research. Many research institutions and universities rely on it for experiments requiring efficient and stable catalysts. Its unique properties make it an essential component in the development of new synthetic methods and the optimization of existing chemical processes. Its application in both academic and industrial settings highlights its importance in advancing chemical research in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions benefit from this compound's ability to facilitate selective and efficient transformations, making it ideal for complex molecule construction.\u003c\/li\u003e\n\u003cli\u003eCatalytic coupling reactions utilize its high reactivity and stability, enabling the formation of carbon-carbon bonds under controlled conditions.\u003c\/li\u003e\n\u003cli\u003eIsomerization processes leverage its structural specificity, allowing for precise control over reaction pathways and product formation.\u003c\/li\u003e\n\u003cli\u003eOxidation reactions take advantage of its robust catalytic properties, ensuring consistent performance in challenging chemical environments.\u003c\/li\u003e\n\u003cli\u003eIndustrial-scale chemical processes rely on its reliability and efficiency, making it a preferred choice for large-scale synthesis applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1335047-34-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Transition Elements\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its performance. Due to its chemical complexity, it should be handled with care to avoid any potential reactions with incompatible substances. Proper labeling and storage conditions are essential to ensure safety and maintain the integrity of the material. Laboratory personnel should follow standard safety protocols when handling this compound, including the use of appropriate personal protective equipment. Regular monitoring of storage conditions will help ensure the compound remains in optimal condition for use in catalytic applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085926641882,"sku":"TCI2604B625436","price":3598000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085926674650,"sku":"TCI2604B625437","price":12058000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6254_d6dc931a-826b-4975-abe2-3b3d296ce4a8.jpg?v=1767865045"},{"product_id":"tci2510b625513090","title":"TCI B6255 887919-35-9 Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II) is a palladium(II) pre-catalyst featuring a bulky electron-rich phosphine ligand, designed for high-performance cross-coupling reactions. This compound is widely employed in Suzuki-Miyaura, Buchwald-Hartwig amination, and Heck coupling reactions to construct carbon-carbon and carbon-heteroatom bonds. It is an essential reagent for synthetic chemistry laboratories working on pharmaceutical intermediates, agrochemicals, and advanced organic materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085926707418,"sku":"TCI2510B625513090","price":4891000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6255.jpg?v=1767093364"},{"product_id":"tci2510b625813094","title":"TCI B6258 808142-88-3 (4,4'-Di-tert-butyl-2,2'-bipyridine-kappa~2~N~1~,N~1'~)[bis[5-fluoro-2-(5-methyl-2-pyridinyl-kappaN)phenyl-kappaC~1~]]iridium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6258 (CAS 808142-88-3) is a cyclometalated iridium(III) complex featuring a 4,4'-di-tert-butyl-2,2'-bipyridine ligand and 5-fluoro-2-(5-methyl-2-pyridinyl)phenyl ligands, supplied as the hexafluorophosphate salt. This photoredox catalyst excels in visible-light-driven organic transformations including cross-coupling, radical cyclization, and C–H functionalization reactions. Its strong luminescence properties also make it suitable for optoelectronic research applications such as OLED development and photocatalytic energy conversion systems.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085926871258,"sku":"TCI2604B625838","price":3486000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085926904026,"sku":"TCI2604B625839","price":11721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6258_754d364a-f6fd-4663-bb30-44092cbc4e6a.jpg?v=1767865062"},{"product_id":"tci2510b628113116","title":"TCI B6281 1062158-66-0 3-[2,6-Bis(1-methylethyl)phenyl]-5,6,7,8-tetrahydro-4H-cycloheptathiazolium Perchlorate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6281 is a thiazolium perchlorate compound featuring a sterically demanding 2,6-diisopropylphenyl substituent, designed as a carbon-donor ligand precursor for catalytic applications. This compound serves as a valuable building block in the development of N-heterocyclic carbene (NHC)-based transition metal catalysts, widely utilized in cross-coupling reactions, olefin metathesis, and other catalytic transformations. Its well-defined structure and reliable purity make it suitable for both academic research and industrial chemistry laboratories focused on catalyst design and mechanistic studies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085928575194,"sku":"TCI2510B628113116","price":2980000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085928607962,"sku":"TCI2510B628113117","price":12058000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6281_78e9bf7a-9c62-4386-b1a1-effa392fbc3e.jpg?v=1767865123"},{"product_id":"tci2510b630913143","title":"TCI B6309 1304-76-3 Bismuth(III) Oxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Bismuth(III) Oxide (CAS 1304-76-3) is a high-purity inorganic reagent widely utilized in research laboratories as a precursor for bismuth-based compounds and as a catalyst in various organic and inorganic reactions. This yellow powder is commonly applied in the fabrication of technical ceramics, specialty optical glasses, and high-quality pigments, as well as serving as a key component in high-temperature superconductor materials. Available in 25g and 500g packaging, this product is also employed in solid oxide fuel cell development and next-generation solid-state battery research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085929591002,"sku":"TCI2510B630913143","price":592000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085929623770,"sku":"TCI2510B630913144","price":3205000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6309_e7a42440-2884-4676-8cc6-cfc503b8eeb3.jpg?v=1767865205"},{"product_id":"tci2510b631813159","title":"TCI B6318 14040-05-2 Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II) is a chemical compound widely used as a catalyst in various chemical reactions. It belongs to the category of transition metals and is particularly effective in oxidation and reduction reactions. In the laboratory, this compound functions as an efficient catalyst that accelerates chemical reactions without being consumed in the process. Its role is critical in enhancing reaction rates and improving the yield of desired products. This compound is commonly used in synthetic chemistry to facilitate complex transformations under controlled conditions.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability and controlled reactivity, making it a preferred choice for laboratory applications. Its complex structure, consisting of copper(II) ions coordinated with 2,2,6,6-tetramethyl-3,5-heptanedionato ligands, provides excellent catalytic properties. This structure allows the compound to maintain its activity across a range of reaction conditions, including varying temperatures and solvents. The compound’s resistance to oxidation further enhances its reliability in long-term experiments, ensuring consistent performance. These properties make it a reliable and versatile reagent in chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in chemical research, especially in catalysis and inorganic chemistry. It is a key component in the development of new synthetic methods and the study of reaction mechanisms. Many research institutions and universities in Indonesia rely on this compound for its effectiveness and reliability in experimental setups. Its widespread use underscores its importance in advancing chemical knowledge and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOxidation and Reduction Reactions: This compound is ideal for facilitating redox processes due to its ability to transfer electrons efficiently, making it suitable for a wide range of synthetic transformations.\u003c\/li\u003e\n\u003cli\u003eCatalytic Organic Synthesis: Its complex structure enables it to act as a versatile catalyst in organic reactions, enhancing reaction efficiency and selectivity in laboratory settings.\u003c\/li\u003e\n\u003cli\u003eInorganic Chemistry Experiments: The compound is frequently used in studies involving transition metals, where its coordination properties are essential for understanding reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eAnalytical Chemistry Applications: Its stability and controlled reactivity make it a valuable reagent for analytical procedures requiring precise chemical behavior under varied conditions.\u003c\/li\u003e\n\u003cli\u003eIndustrial Process Development: It is used in the development of industrial chemical processes, where its catalytic properties help improve reaction efficiency and product yield.\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: 14040-05-2\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 supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure. 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 substances to avoid any potential chemical interactions. In laboratory settings, it should be kept in a designated chemical storage area that is accessible only to authorized personnel. Proper labeling of containers is essential to ensure safe handling and prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085930246362,"sku":"TCI2510B631813159","price":4133000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085930279130,"sku":"TCI2510B631813160","price":13829000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6318.jpg?v=1768816030"},{"product_id":"tci2510b632713173","title":"TCI B6327 172418-32-5 trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6327, trans-Bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II), is a highly active palladacycle-based dimeric palladium(II) catalyst optimized for C-H activation and cross-coupling reactions. It exhibits excellent thermal stability and broad substrate compatibility in Heck, Suzuki, and Sonogashira coupling reactions, as well as direct C-H functionalization of aromatic systems. This catalyst is widely employed in academic and industrial laboratories for the synthesis of pharmaceutical intermediates, agrochemicals, and advanced functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085930770650,"sku":"TCI2510B632713173","price":1546000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085930803418,"sku":"TCI2510B632713174","price":5341000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085930836186,"sku":"TCI2510B632713175","price":18663000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6327.jpg?v=1768193647"},{"product_id":"tci2510b633313184","title":"TCI B6333 7787-32-8 Barium Fluoride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBarium Fluoride (TCI catalog number B6333, CAS 7787-32-8) is an inorganic alkaline earth metal halide supplied by AMI Scientific for research and analytical laboratory work. Classified under Main-group Elements within the Catalysis and Inorganic Chemistry range, it serves as a practical source of both barium and fluoride ions for inorganic synthesis and solid-state chemistry studies. The compound is frequently explored in optical material research, ionic conductivity investigations, and the preparation of main-group precursor systems. It is offered in 100 g and 500 g pack sizes, and should be handled with appropriate personal protective equipment and stored in a tightly closed container in a cool, dry, well-ventilated area, with the manufacturer's safety data sheet consulted prior to use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSato et al. (1993). Novel volatile barium .beta.-diketone chelates for chemical vapor deposition of barium fluoride thin films. \u003cem\u003eInorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ic00062a011\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ic00062a011\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eChaboy et al. (1993). Multiple Scattering Contributions at the L1 and L3 Barium EXAFS Spectra in Barium Fluoride. \u003cem\u003eJapanese Journal of Applied Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.7567\/jjaps.32s2.29\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.7567\/jjaps.32s2.29\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKolar et al. (1992). Kinetic study of the solution-mediated transformation of orthorhombic barium fluoride into cubic barium fluoride. \u003cem\u003eJournal of Crystal Growth\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0022-0248(92)90656-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0022-0248(92)90656-4\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":"100g","offer_id":48085931196634,"sku":"TCI2510B633313184","price":929000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085931229402,"sku":"TCI2510B633313185","price":3205000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6333_794d6966-2507-40a9-8afa-db338354f590.jpg?v=1767865333"},{"product_id":"tci2510b633813193","title":"TCI B6338 7787-61-3 Bismuth(III) Fluoride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBismuth(III) Fluoride (CAS 7787-61-3) is a main-group inorganic solid that serves as a convenient source of both bismuth(III) and fluoride in laboratory work. It is widely used as a precursor for bismuth-based ceramics and oxyfluoride phases, and it features in studies of fluoride-ion conducting materials and solid electrolytes. Its low water solubility makes gravimetric handling straightforward in solid-state preparations. TCI product B6338 is supplied in 25 g and 100 g packs; handle the powder in a fume hood, keep it tightly closed away from moisture and acids, and refer to the manufacturer's Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSawant et al. (1993). A study on the fluoride complexes of plutonium(III), samarium(III) and bismuth(III) using fluoride ion-selective potentiometry. \u003cem\u003eJournal of Radioanalytical and Nuclear Chemistry Articles\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/bf02134591\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/bf02134591\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKonishi et al. (2020). Effect of anion acceptor added to the electrolyte on the electrochemical performance of bismuth(III) fluoride in a fluoride shuttle battery. \u003cem\u003eChemical Physics Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.cplett.2020.137785\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.cplett.2020.137785\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKonishi et al. (2020). Reversible Electrochemical Reaction of a Fluoride Shuttle Battery with a Bismuth(III) Fluoride Electrode and Electrolyte Containing Triphenylboroxine as an Anion Acceptor. \u003cem\u003eChemistrySelect\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/slct.202001163\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/slct.202001163\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085931524314,"sku":"TCI2510B633813193","price":1687000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085931557082,"sku":"TCI2510B633813194","price":5032000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6338_299510c8-ec7d-43d0-bfa9-21dbeef8877c.jpg?v=1767865362"},{"product_id":"tci2510b633913195","title":"TCI B6339 7787-58-8 Bismuth(III) Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBismuth(III) Bromide (CAS 7787-58-8) is a moisture-sensitive main-group halide that is widely valued as a mild, relatively low-toxicity Lewis acid catalyst. It promotes carbonyl activation, acetal formation and deprotection, allylation and a range of multicomponent condensations, often at low catalyst loading. In materials chemistry it also serves as a bismuth and bromide source for BiOBr photocatalysts and lead-free bismuth-based semiconductors. TCI product B6339 comes in 5 g and 25 g packs; weigh it quickly under dry conditions, store it tightly sealed in a desiccator, and follow the manufacturer's Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSoltanzadeh et al. (2009). Syntheses and characterization of a new nano-structured bismuth(III) bromide coordination polymer; new precursor for preparation of bismuth(III) bromide and bismuth(III) oxide nanostructures. \u003cem\u003eJournal of Coordination Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00958970902951629\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00958970902951629\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSALVATORE et al. (1992). ChemInform Abstract: Bismuth(III) Bromide Complexes: On the Formation of Species Higher Than BiBr3‐ 6 in Concentrated Bromide Solutions.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199207011\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199207011\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSoltanzadeh et al. (2009). Metal–organic supramolecular assemblies generated from bismuth(III) bromide and polyimine ligands. \u003cem\u003ePolyhedron\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.poly.2008.12.048\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.poly.2008.12.048\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085931622618,"sku":"TCI2510B633913195","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085931655386,"sku":"TCI2510B633913196","price":2840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6339_998498b1-6e13-4d0b-8419-e8c7340834c0.jpg?v=1767865368"},{"product_id":"tci2510b637113242","title":"TCI B6371 21319-43-7 Bis(2,2,6,6-tetramethyl-3,5-heptanedionato)lead(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6371, bis(2,2,6,6-tetramethyl-3,5-heptanedionato)lead(II) (CAS 21319-43-7), commonly abbreviated Pb(TMHD)₂, is a sterically shielded β-diketonate complex used as a volatile, organic-soluble lead source. The bulky tert-butyl substituents improve thermal stability and volatility relative to simpler β-diketonates, which is precisely what vapour-phase deposition demands. It is applied primarily as a precursor in MOCVD\/CVD and ALD processes for lead-containing thin films, including ferroelectric and piezoelectric oxide materials, as well as in solution-based precursor preparation. AMI Scientific supplies this TCI product in 1 g and 5 g pack sizes for research use by trained personnel, noting that lead compounds are toxic and require strict handling controls.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085936537818,"sku":"TCI2510B637113242","price":2362000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085936570586,"sku":"TCI2510B637113243","price":8180000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6371.jpg?v=1768816045"},{"product_id":"tci2510b639013269","title":"TCI B6390 (1S,2S)-N~1~,N~2~-Dibenzylcyclohexane-1,2-diamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6390 is (1S,2S)-N1,N2-dibenzylcyclohexane-1,2-diamine dihydrochloride (CAS 3070821-54-1), a chiral building block based on the widely used trans-1,2-diaminocyclohexane scaffold. Its C2-symmetric, enantiodefined framework underpins many chiral ligands and bifunctional organocatalysts, including salen-type ligands and thiourea or squaramide catalysts. The dihydrochloride salt form improves handling and shelf stability relative to the free base, which can be liberated immediately before use. Available in 1 g and 5 g packs, it should be kept tightly closed in a cool, dry place because amine salts readily take up moisture.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937586394,"sku":"TCI2604B639040","price":3824000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937619162,"sku":"TCI2604B639041","price":14841000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6390_733bda7c-e15c-4504-b30f-33f31b557564.jpg?v=1767865604"},{"product_id":"tci2510b639313272","title":"TCI B6393 212611-88-6 (1R,2R)-N1,N2-Dibenzylcyclohexane-1,2-diamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6393 is (1R,2R)-N1,N2-dibenzylcyclohexane-1,2-diamine dihydrochloride (CAS 212611-88-6), the enantiomeric counterpart within this chiral building block series. Built on the rigid, C2-symmetric trans-1,2-diaminocyclohexane scaffold, it is a versatile precursor to chiral diamine ligands and bifunctional thiourea or squaramide organocatalysts. Having both enantiomers available lets researchers switch the sense of asymmetric induction simply by changing the chirality source. Supplied in 1 g and 5 g packs, the hygroscopic salt should be stored cool, dry, and tightly sealed, with the free base generated shortly before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937717466,"sku":"TCI2510B639313272","price":3824000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937750234,"sku":"TCI2510B639313273","price":15038000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6393_d3d375f2-12ec-42f0-9f22-168ec7a061e2.jpg?v=1767865612"},{"product_id":"tci2510b642613309","title":"TCI B6426 513-77-9 Barium Carbonate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6426 Barium Carbonate (CAS 513-77-9) is an inorganic main-group compound widely used as a convenient solid source of barium. It serves as a classic precursor in solid-state routes toward barium-containing oxides and electroceramic materials. The product is also applied in catalyst preparation and in general inorganic chemistry work. Barium compounds are toxic if ingested or inhaled, so avoid dust formation, keep the material away from acids, and follow the manufacturer's safety data sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBittarello et al. (2007). Self-assembled nanocrystals of barium carbonate in biomineral-like structures. \u003cem\u003eEuropean Journal of Mineralogy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1127\/0935-1221\/2007\/0019-1730\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1127\/0935-1221\/2007\/0019-1730\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBlanco López et al. (1997). Identification of Barium Carbonate in Barium Titanate powders. \u003cem\u003eKey Engineering Materials\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4028\/www.scientific.net\/kem.132-136.252\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4028\/www.scientific.net\/kem.132-136.252\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMasukume (2013). Processing of Barium Sulphide to Barium Carbonate and Sulphur. \u003cem\u003eJournal of Chemical Engineering \u0026amp; Process Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4172\/2157-7048.1000157\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4172\/2157-7048.1000157\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085939290330,"sku":"TCI2510B642613309","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085939323098,"sku":"TCI2510B642613310","price":1069000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6426.jpg?v=1768193714"},{"product_id":"tci2510b643813327","title":"TCI B6438 10553-31-8 Barium Bromide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6438 Barium Bromide (CAS 10553-31-8) is an inorganic alkaline earth metal salt supplied for research and laboratory use. It serves as a convenient source of barium and bromide ions in salt metathesis, precipitation work, and the preparation of other barium compounds. The material is available in 25 g and 100 g pack sizes suitable for routine synthetic and analytical workflows. Handle it in a fume hood with appropriate personal protective equipment and store it tightly sealed in a cool, dry place away from moisture.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePatil et al. (1991). Thermodynamic properties of aqueous electrolyte solutions. 2. Vapor pressure of aqueous solutions of sodium bromide, sodium iodide, potassium chloride, potassium bromide, potassium iodide, rubidium chloride, cesium chloride, cesium bromide, cesium iodide, magnesium chloride, calcium chloride, calcium bromide, calcium iodide, strontium chloride, strontium bromide, strontium iodide, barium chloride, and barium bromide. \u003cem\u003eJournal of Chemical \u0026amp; Engineering Data\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/je00002a021\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/je00002a021\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLocke et al. (2025). Binary salt mixture barium bromide-barium chloride for sorption applications. \u003cem\u003eApplied Thermal Engineering\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.applthermaleng.2025.126730\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.applthermaleng.2025.126730\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZaitseva et al. (2013). Interaction between lead bromide and barium bromide. \u003cem\u003eRussian Journal of Inorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1134\/s003602361308024x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1134\/s003602361308024x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085939978458,"sku":"TCI2510B643813327","price":2503000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085940011226,"sku":"TCI2510B643813328","price":7534000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6438_f9ca9199-68af-4b5c-b138-88155c3de65a.jpg?v=1767865781"},{"product_id":"tci2510b643913329","title":"TCI B6439 13718-50-8 Barium Iodide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6439 Barium Iodide (CAS 13718-50-8) is an inorganic alkaline earth metal halide intended for research and experimental use. It provides both barium and iodide ions, making it useful for salt metathesis, iodide transfer, and the preparation of halide-based inorganic materials. Pack sizes of 25 g and 100 g support both small-scale trials and repeated synthetic work. Handle the material in a fume hood with full personal protective equipment and keep it tightly closed in a cool, dry, light-protected location.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eRowe et al. (2013). Double Salts Iodide Scintillators: Cesium Barium Iodide, Cesium Calcium Iodide, and Barium Bromine Iodide. \u003cem\u003eCrystal Research and Technology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/crat.201300010\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/crat.201300010\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWei et al. (2022). High-Pressure Structures and Superconductivity of Barium Iodide. \u003cem\u003eMaterials\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/ma15020522\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/ma15020522\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWengert et al. (2000). Ba3SiI2, a Double Salt of Barium Iodide and the Zintl Phase Ba2Si. \u003cem\u003eJournal of Solid State Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/jssc.2000.8713\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/jssc.2000.8713\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085940043994,"sku":"TCI2510B643913329","price":2784000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085940076762,"sku":"TCI2510B643913330","price":8292000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6439_454dcb70-130a-4ed9-b7f6-997221d0c057.jpg?v=1767865788"},{"product_id":"tci2510b645113341","title":"TCI B6451 1973375-72-2 [5,5'-Bis(trifluoromethyl)-2,2'-bipyridine-kappa~2~N~1~,N~1'~][bis[3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-kappaN]phenyl-kappaC~1~]]iridium Hexafluorophosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6451 (CAS 1973375-72-2) is a cationic cyclometalated iridium complex supplied as its hexafluorophosphate salt for use as a visible-light photocatalyst. The fluorinated and trifluoromethylated ligands tune the excited-state redox properties, supporting demanding single-electron transfer and energy transfer processes. It is widely applied in photoredox and metallaphotoredox methodologies, including nickel-catalyzed cross-coupling under mild conditions. Store the catalyst tightly closed in a cool, dry place protected from light, and weigh it in a fume hood using standard personal protective equipment.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHeuer et al. (1990). Preparation of bis[2,4-bis(trifluoromethyl)phenyl]fluorophosphine and 2,4-bis[trifluoromethyl) phenyl-[2,6-bis(trifluoromethyl)phenyl]-fluorophosphine - two distillable monofluorophosphines. Structure of cis-dichloro-bis[2,4-bis(trifluoromethyl)phenyl)fluorophosphino]platinum(II). \u003cem\u003eJournal of Fluorine Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-1139(00)80993-8\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-1139(00)80993-8\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHEUER et al. (1990). ChemInform Abstract: Preparation of Bis(2,4‐bis(trifluoromethyl)phenyl)fluorophosphine (III) and 2,4‐Bis(trifluoromethyl)phenyl(2,6‐bis(trifluoromethyl)phenyl)fluorophosphine (IV) ‐ Two Distillable Monofluorophosphines. Structure of cis‐Dichlorobis(bis(2,4‐bis‐(trifluoromethyl)phenyl)fluorophosphino)platinum(II) (VI).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199027261\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199027261\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHan et al. (2018). Efficient electroluminescence of bluish green iridium complexes with 2-(3,5-bis(trifluoromethyl)phenyl)pyrimidine and 2-(3,5-bis(trifluoromethyl)phenyl)-5-fluoropyrimidine as the main ligands. \u003cem\u003eInorganic Chemistry Frontiers\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c8qi00294k\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c8qi00294k\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085940764890,"sku":"TCI2604B645144","price":4779000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085940797658,"sku":"TCI2604B645145","price":16724000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6451_a44c0f49-9dfa-42bb-83a6-0aceba622015.jpg?v=1767865822"},{"product_id":"tci2510b647413370","title":"TCI B6474 10361-43-0 Bismuth(III) Hydroxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBismuth(III) Hydroxide is an inorganic main-group compound valued for the comparatively low toxicity profile of bismuth relative to other heavy metals. It commonly serves as a convenient precursor to bismuth oxide and other bismuth salts through calcination or acid treatment. Researchers apply it in catalysis development, ceramic and photocatalytic material preparation, and adsorbent studies. TCI provides the material in 50 g and 250 g pack sizes for laboratory research.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKobayashi et al. (2010). Copper(II) and Bismuth(III) Hydroxide Catalyzed Addition Reactions of Hydrazonoester with Allenylboronate in Aqueous Media. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0030-1258485\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0030-1258485\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eUeda et al. (1990). Graphite Furnace Atomic Absorption Spectrometric Determination of Bismuth(III) after Coprecipitation with Hafnium Hydroxide. \u003cem\u003eBulletin of the Chemical Society of Japan\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/bcsj.63.544\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/bcsj.63.544\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHanifehpour et al. (2015). Synthesis and structural characterization of new bismuth (III) nano coordination polymer: A precursor to produce pure phase nano-sized bismuth (III) oxide. \u003cem\u003eJournal of Molecular Structure\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molstruc.2015.02.074\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molstruc.2015.02.074\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":"50g","offer_id":48085942173914,"sku":"TCI2510B647413370","price":2671000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085942206682,"sku":"TCI2510B647413371","price":9305000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6474_8770fc89-74db-4ed6-8f29-5158a1fd4370.jpg?v=1767865913"},{"product_id":"tci2510b650113404","title":"TCI B6501 103595-81-9 6,6'-[[Ethane-1,2-diylbis(azaneylylidene)]bis(methaneylylidene)]bis(2,4-di-tert-butylphenol)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6501 (CAS 103595-81-9) is a salen-type ligand, N,N'-bis(3,5-di-tert-butylsalicylidene)ethylenediamine, offering a tetradentate N₂O₂ donor set for transition metal coordination. The bulky tert-butyl groups provide steric protection around the metal centre and improve solubility in organic solvents. Salen complexes of manganese, cobalt, chromium, nickel, and copper are widely studied in homogeneous catalysis, coordination chemistry, bioinorganic model systems, and functional materials research. AMI Scientific supplies this TCI product in a 1 g pack; store it cool, dry, and tightly closed, since the imine linkages are sensitive to moisture.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085943517402,"sku":"TCI2510B650113404","price":3486000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6501.jpg?v=1767093755"},{"product_id":"tci2510b651413424","title":"TCI B6514 10049-01-1 Bismuth(III) Phosphate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6514 Bismuth(III) Phosphate (CAS 10049-01-1) is an inorganic main-group compound supplied as a solid powder for research use. It is studied in catalysis, photocatalysis, and functional materials work, where bismuth-based systems are of ongoing interest. The material also serves as a precursor and reference solid in inorganic characterisation studies such as diffraction and thermal analysis. Available in 50 g and 250 g packs, it should be weighed with dust control measures and stored dry in a tightly closed container.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBiswal et al. (2013). Bismuth(III) dialkyldithiophosphates: Facile single source precursors for the preparation of bismuth sulfide nanorods and bismuth phosphate thin films. \u003cem\u003eJournal of Solid State Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.jssc.2013.06.011\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.jssc.2013.06.011\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBarve et al. (1993). Extraction and Separation Studies of Bismuth(III) and Antimony(III) with Tris(2-ethylhexyl)phosphate. \u003cem\u003eBulletin of the Chemical Society of Japan\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/bcsj.66.1079\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/bcsj.66.1079\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eCheek et al. (2024). Electrochemical and Spectroscopic Investigations of Bismuth(III) Pharmaceuticals with L-Glutathione. \u003cem\u003eECS Meeting Abstracts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1149\/ma2024-01422379mtgabs\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1149\/ma2024-01422379mtgabs\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":"50g","offer_id":48085944238298,"sku":"TCI2510B651413424","price":2812000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085944271066,"sku":"TCI2510B651413425","price":9894000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6514_8d6b4910-c60a-4931-80a1-31aa0919ee37.jpg?v=1767866109"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552.jpg?v=1767093890"},{"product_id":"tci2510b656813499","title":"TCI B6568 10294-40-3 Barium Chromate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6568 is barium chromate (BaCrO₄), a bright yellow inorganic solid that is notably poorly soluble in water. This low solubility makes it a classic subject for precipitation and solubility-equilibrium work, while its hexavalent chromium content gives it oxidising character useful in certain solid-state and inorganic syntheses. It must be treated with serious caution: it combines toxic barium with carcinogenic hexavalent chromium, so all handling belongs in a fume hood with full personal protective equipment and dust control. AMI Scientific supplies this TCI product in a 25 g pack; read the official safety data sheet in full before opening the container.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2015). Use of Barium Chromate in Photocatalytic Degradation of Eosin Yellow. \u003cem\u003eChemical Science Transactions\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.7598\/cst2015.1069\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.7598\/cst2015.1069\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2013). The Study of Solubility of Barium Nitrate Prepared from Barium Chromate and Nitric Acid. \u003cem\u003eAdvanced Materials Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4028\/www.scientific.net\/amr.803.173\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4028\/www.scientific.net\/amr.803.173\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSingh et al. (2026). Relative kinetics of precipitation of barium chromate and barite in groundwater. \u003cem\u003eApplied Geochemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.apgeochem.2026.107022\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.apgeochem.2026.107022\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48276761739482,"sku":"TCI2510B656813499","price":901000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6568.jpg?v=1767093914"},{"product_id":"tci2510b657813518","title":"TCI B6578 5892-10-4 Bismuth Carbonate Oxide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6578 Bismuth Carbonate Oxide (bismuth subcarbonate, CAS 5892-10-4) is a stable white inorganic powder that serves as a convenient bismuth source. It is frequently used as a precursor for bismuth oxide and other bismuth-based materials prepared through thermal treatment. Applications include photocatalyst preparation, main-group Lewis acid catalysis research, and general inorganic materials synthesis. Supplied in 25 g and 500 g pack sizes, it should be stored in a cool, dry place, kept away from strong acids, and handled to minimize dust inhalation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085948301530,"sku":"TCI2510B657813518","price":985000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085948334298,"sku":"TCI2510B657813519","price":3626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6578.jpg?v=1767093945"},{"product_id":"tci2510b658213525","title":"TCI B6582 60884-92-6 Barium(II) Trifluoroacetate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6582 Barium(II) Trifluoroacetate (CAS 60884-92-6) is a main-group inorganic reagent whose trifluoroacetate anion provides useful solubility in polar organic solvents. This makes it a practical barium source for precursor solutions used in chemical solution deposition and thin-film preparation. It is also studied in the synthesis of fluorine-containing and complex oxide materials, where the organic component decomposes during thermal treatment. Supplied in 1 g and 5 g pack sizes, it must be handled with care as soluble barium salts are toxic, and stored in a tightly closed container in a cool, dry place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eFarjas et al. (2012). The thermal decomposition of barium trifluoroacetate. \u003cem\u003eThermochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tca.2012.06.020\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tca.2012.06.020\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEloussifi et al. (2013). Thermal decomposition of barium trifluoroacetate thin films. \u003cem\u003eThermochimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tca.2013.01.022\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tca.2013.01.022\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWojtczak et al. (1998). Synthesis, Characterization, and Thermal Behavior of Polydentate Ligand Adducts of Barium Trifluoroacetate. \u003cem\u003eInorganic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ic9613220\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ic9613220\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":48085948727514,"sku":"TCI2510B658213525","price":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085948760282,"sku":"TCI2510B658213526","price":7590000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6582.jpg?v=1767093957"},{"product_id":"tci2510b660613561","title":"TCI B6606 2897656-97-0 N1-([1,1'-Biphenyl]-2-yl)-N2-(2-phenylnaphthalen-1-yl)benzene-1,2-diamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6606 is a sterically demanding N,N'-diaryl benzene-1,2-diamine bearing biphenyl-2-yl and 2-phenylnaphthalen-1-yl substituents. Such o-phenylenediamine frameworks are commonly used as precursors to benzimidazolium salts and N-heterocyclic carbene ligands for organometallic catalysis. The bulky aryl groups create a well-defined steric pocket that can influence catalytic selectivity, and the scaffold is also of interest in functional organic materials. AMI Scientific offers this TCI building block in 250 mg and 1 g pack sizes for catalysis and materials research laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085950005466,"sku":"TCI2510B660613561","price":2166000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085950038234,"sku":"TCI2510B660613562","price":6409000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6606.jpg?v=1767094008"},{"product_id":"tci2510b663913600","title":"TCI B6639 133463-88-4 2,2'-Bis[(4S)-4-benzyl-2-oxazoline]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6639 2,2'-Bis[(4S)-4-benzyl-2-oxazoline] (CAS 133463-88-4) is a C2-symmetric chiral bis(oxazoline) — or BOX — ligand available from AMI Scientific. Complexed with transition metals such as copper, zinc, magnesium, or palladium, it creates a well-defined chiral pocket that delivers high enantioselectivity. Typical uses include asymmetric cyclopropanation, aldol and Michael additions, and chiral Lewis acid Diels-Alder reactions. Supplied in 200 mg and 1 g research packs, it should be kept tightly sealed in a cool, dry, moisture-free environment for reliable catalytic performance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085951578330,"sku":"TCI2510B663913600","price":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085951611098,"sku":"TCI2510B663913601","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6639.jpg?v=1767094079"},{"product_id":"tci2510b664913613","title":"TCI B6649 1345-07-9 Bismuth(III) Sulfide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6649 Bismuth(III) Sulfide (CAS 1345-07-9) is a narrow-band-gap semiconducting main-group chalcogenide available from AMI Scientific. Its visible-light absorption makes it a widely studied material for photocatalytic pollutant degradation, photovoltaic absorber layers, and thermoelectric research. It is also explored in optoelectronic sensing and as an inorganic phase in nanocomposite synthesis. Supplied in 50 g and 250 g packs, the powder should be stored sealed in a cool, dry place and kept away from strong acids, which can liberate toxic hydrogen sulfide.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSalavati‐Niasari et al. (2013). Synthesis of bismuth sulfide nanostructures by using bismuth(III) monosalicylate precursor and fabrication of bismuth sulfide based p–n junction solar cells. \u003cem\u003eAsia-Pacific Journal of Chemical Engineering\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/apj.1741\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/apj.1741\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBenattou et al. (2017). Thin film bismuth(III) sulfide\/zinc sulfide composites deposited by spray pyrolysis. \u003cem\u003eResults in Physics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.rinp.2017.09.038\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.rinp.2017.09.038\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eVidal (2001). Bismuth(III) Derivatives: New Catalysts. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2001-15163\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2001-15163\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":"50g","offer_id":48085952168154,"sku":"TCI2510B664913613","price":2475000.0,"currency_code":"IDR","in_stock":true},{"title":"250g","offer_id":48085952200922,"sku":"TCI2510B664913614","price":8601000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6649.jpg?v=1767094090"},{"product_id":"tci2510b667313632","title":"TCI B6673 12230-71-6 Barium Hydroxide Octahydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6673 is Barium Hydroxide Octahydrate (CAS 12230-71-6), a strong inorganic base supplied as the familiar white crystalline octahydrate. Its ability to precipitate carbonate as insoluble barium carbonate makes it valuable for preparing carbonate-free basic solutions and for qualitative carbon dioxide testing. It also serves as a strong base in acid–base titrations and in hydrolysis reactions at laboratory scale. AMI Scientific offers this TCI product in a 500 g pack size; because soluble barium compounds are toxic and the material is corrosive, careful personal protection and waste handling are essential.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eYoung (2006). Barium Hydroxide Octahydrate. \u003cem\u003eJournal of Chemical Education\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ed083p539\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ed083p539\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2019). Experimental study on powdered expansion of barium hydroxide octahydrate crystal. \u003cem\u003eJournal of Molecular Liquids\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molliq.2019.111907\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molliq.2019.111907\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eWang et al. (2019). Experimental investigation of barium hydroxide octahydrate as latent heat storage materials. \u003cem\u003eSolar Energy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.solener.2018.11.013\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.solener.2018.11.013\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":"500g","offer_id":48085953085658,"sku":"TCI2510B667313632","price":732000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6673.jpg?v=1768204519"},{"product_id":"tci2510b680113716","title":"TCI B6801 3035177-77-3 N,N'-Bis(2-phenyl-1-naphthyl)-1,2-benzenediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6801 (CAS 3035177-77-3) is N,N'-bis(2-phenyl-1-naphthyl)-1,2-benzenediamine, an aromatic diamine bearing two highly bulky naphthyl substituents. Its ortho-phenylenediamine core is well suited to cyclisation toward benzimidazolium salts and, in turn, N-heterocyclic carbene ligands. The bulky aryl walls allow chemists to tune the steric environment around a metal centre in organometallic catalyst design. AMI Scientific offers this TCI reagent in 250 mg and 1 g pack sizes; store it cool, dark, and tightly closed, as aromatic diamines may darken on air exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085956690138,"sku":"TCI2510B680113716","price":2812000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085956722906,"sku":"TCI2510B680113717","price":8741000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6801.jpg?v=1767094245"},{"product_id":"tci2510b697013849","title":"TCI B6970 175136-66-0 Bis[3,5-bis(trifluoromethyl)phenyl]methanone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6970 is bis[3,5-bis(trifluoromethyl)phenyl]methanone, a strongly electron-poor diaryl ketone carrying four trifluoromethyl groups. The 3,5-bis(trifluoromethyl)phenyl motif is widely used to tune acidity, lipophilicity, and oxidative stability in ligands, catalysts, and drug candidates. Its carbonyl group serves as a versatile entry point for reduction or addition with organometallic reagents. AMI Scientific offers this TCI fluorinated building block in a 1 g pack; keep it tightly sealed in a cool, dry, light-protected place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHEUER et al. (1990). ChemInform Abstract: Preparation of Bis(2,4‐bis(trifluoromethyl)phenyl)fluorophosphine (III) and 2,4‐Bis(trifluoromethyl)phenyl(2,6‐bis(trifluoromethyl)phenyl)fluorophosphine (IV) ‐ Two Distillable Monofluorophosphines. Structure of cis‐Dichlorobis(bis(2,4‐bis‐(trifluoromethyl)phenyl)fluorophosphino)platinum(II) (VI).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199027261\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199027261\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSülü dkk. (2001). Acetalization and Transacetalization Reactions Catalyzed by Ruthenium, Rhodium, and Iridium Complexes with {2-{{Bis[3-(trifluoromethyl)phenyl]phosphino}methyl}-2-methylpropane- 1,3-diyl}bis[bis[3-(trifluoromethyl)phenyl]phosphine] (MeC[CH2P(m-CF3C6H4)2]3). \u003cem\u003eHelvetica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/1522-2675(20010418)84:4\u0026lt;898::aid-hlca898\u0026gt;3.0.co;2-v\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/1522-2675(20010418)84:4\u0026lt;898::aid-hlca898\u0026gt;3.0.co;2-v\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":48276756988122,"sku":"TCI2510B697013849","price":2053000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6970.jpg?v=1767094447"},{"product_id":"tci2510b706413892","title":"TCI B7064 10035-06-0 Bismuth(III) Nitrate Pentahydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7064 Bismuth(III) Nitrate Pentahydrate is a widely used inorganic source of Bi³⁺ for both synthesis and materials research. It serves as a mild Lewis acid catalyst in organic transformations and as a convenient precursor for bismuth oxides and mixed-oxide photocatalysts. The crystalline hydrate dissolves readily in dilute acidic media, simplifying precursor solution preparation. Being a nitrate salt, it acts as an oxidizer and must be stored cool, dry, and away from combustible materials.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMohan et al. (2004). Deprotection of Ketoximes Using Bismuth(III) Nitrate Pentahydrate. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2001-14568\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2001-14568\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMulamoottil (2005). Bismuth(III) Nitrate Pentahydrate - A Versatile Reagent in Organic Synthesis. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-2005-917080\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-2005-917080\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRogers et al. (1992). Alcoholysis of bismuth(III) nitrate pentahydrate by polyethylene glycols. Comparison with bismuth(III) nitrate crown ether complexation. \u003cem\u003eJournal of the American Chemical Society\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/ja00034a031\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/ja00034a031\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085964685530,"sku":"TCI2510B706413892","price":536000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085964718298,"sku":"TCI2510B706413893","price":2503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7064.jpg?v=1767094513"},{"product_id":"tci2510b708113899","title":"TCI B7081 1071965-73-5 Bromo[4-(trifluoromethyl)phenyl][tris(1,1-dimethylethyl)phosphine]palladium","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B7081 is a well-defined palladium oxidative addition complex bearing a 4-(trifluoromethyl)phenyl group, a bromide, and a tri-tert-butylphosphine ligand. It functions as a ready-to-use precatalyst that delivers the highly active Pd\/P(t-Bu)₃ system without in-situ ligand mixing. The bulky, electron-rich phosphine promotes oxidative addition to challenging substrates, including aryl chlorides and sterically hindered partners. Supplied in a 250 mg research pack, it is best handled under inert atmosphere and stored cool and dry.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085964947674,"sku":"TCI2510B708113899","price":6662000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B7081.jpg?v=1767094525"},{"product_id":"tci2510c001513929","title":"TCI C0015 3144-16-9 (+)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, CAS 3144-16-9, is a strong, optically active sulfonic acid built on the camphor framework. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallisation. The compound also serves as a convenient solid Brønsted acid catalyst for protection and deprotection steps, and as an ion-pairing additive in chromatography. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g pack sizes; because it is hygroscopic, keep the container tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan et al. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085966127322,"sku":"TCI2510C001513929","price":844000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1969000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4975000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015.jpg?v=1767094558"},{"product_id":"tci2510c007914012","title":"TCI C0079 32607-23-1 Chloranilic Acid Lanthanum(III) Salt Decahydrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI Chloranilic Acid Lanthanum(III) Salt Decahydrate (catalog C0079, CAS 32607-23-1) is a rare-earth based analytical reagent used chiefly for the spectrophotometric determination of fluoride. In the presence of fluoride, the lanthanum centre is captured and coloured chloranilate ligand is released into solution, producing a measurable signal proportional to the fluoride content. It is therefore valuable for drinking water testing, environmental monitoring, and analytical method development, as well as for coordination studies of lanthanide complexes. AMI Scientific supplies this TCI product in 5g and 25g pack sizes; keep it cool, dry, tightly closed, and protected from light and moisture.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMolčanov et al. (2010). Salts and co-crystals of chloranilic acid with organic bases: is it possible to predict a salt formation?. \u003cem\u003eCrystEngComm\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/b908492d\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/b908492d\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDeng et al. (1993). Synthesis and Magnetism of Binuclear Nd(III), Gd(III) and Dy(III) Complexes Using the Dianions of Chloranilic Acid as Bridging Ligands. \u003cem\u003eSynthesis and Reactivity in Inorganic and Metal-Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/15533179308016634\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/15533179308016634\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHussein (2000). SPECTROPHOTOMETRIC DETERMINATION OF SOME LOCAL-ANAESTHETICS BY USING PICRYL-CHLORIDE AND CHLORANILIC ACID. \u003cem\u003eBulletin of Pharmaceutical Sciences. Assiut\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.21608\/bfsa.2000.66125\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.21608\/bfsa.2000.66125\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085969633498,"sku":"TCI2510C007914012","price":676000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085969666266,"sku":"TCI2510C007914013","price":2222000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0079.jpg?v=1767094634"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l2-catalysis-and-inorganic-chemistry.oembed?page=3","provider":"AMI Scientific","version":"1.0","type":"link"}