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| Product | Description | |
|---|---|---|
| Silver carbonate | Mild oxidizing agent for conversion of alcohols to aldehydes and ketones. Biological stain. Group: Metal & ceramic materials. Alternative Names: Carbonicacid,disilver(1+)salt. CAS No. 534-16-7. Molecular formula: CAg2O3. Mole weight: 275.75. Appearance: Green-yellow to greenish granular powder. Purity: 99%+. IUPACName: Disilver;carbonate. Canonical SMILES: C(=O)([O-])[O-].[Ag+].[Ag+]. Density: 6.08 g/mL at 25 °C (lit.). ECNumber: 208-590-3. Catalog: ACM534167-2. |  |
| Silver carbonate | Silver carbonate. Group: Biochemicals. Grades: Highly Purified. CAS No. 534-16-7. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: Ag2CO3. US Biological Life Sciences. |  Worldwide |
| Silver carbonate | Silver carbonate. Uses: Mild oxidizing agent for conversion of alcohols to aldehydes and ketones. biological stain. Group: Salt electrolytes. Alternative Names: Carbonicacid,disilver(1+)salt. CAS No. 534-16-7. Pack Sizes: 1 kg. Product ID: Disilver; carbonate. Molecular formula: 275.75. Mole weight: CAg2O3. C(=O)([O-])[O-].[Ag+].[Ag+]. InChI=1S/CH2O3.2Ag/c2-1(3)4;/h(H2, 2, 3, 4);/q;2*+1/p-2. KQTXIZHBFFWWFW-UHFFFAOYSA-L. 99%+. |  |
| Silver Carbonate | SILVER CARBONATE, 99.5% pure, -100 mesh, Formula: Ag2CO3. CAS No. 534-16-7. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Silver carbonate, extent of labeling: ~50 wt. % loading | Silver carbonate is an odorless yellow to brown solid. Sinks in water. (USCG, 1999). Group: other glass and ceramic materials. CAS No. 534-16-7. Product ID: disilver; carbonate. Molecular formula: 275.745g/mol. Mole weight: Ag2CO3;CAg2O3. C(=O)([O-])[O-].[Ag+].[Ag+]. InChI=1S/CH2O3.2Ag/c2-1(3)4;;/h(H2, 2, 3, 4);;/q;2*+1/p-2. KQTXIZHBFFWWFW-UHFFFAOYSA-L. | |
| 1- [2- [4- [ [ [3- [ [ [ [2- (Heptylthio) ethyl] amino] carbonyl] amino] phenyl] sulfonyl] amino] phenyl] hydrazide] 2,2,3,3-Tetrafluoro-butanedioic Acid | 1- [2- [4- [ [ [3- [ [ [ [2- (Heptylthio) ethyl] amino] carbonyl] amino] phenyl] sulfonyl] amino] phenyl] hydrazide] 2,2,3,3-Tetrafluoro-butanedioic Acid can be used in technical or engineered material use of image-?forming method by developing silver halide photographic material containing thioxoimidazolone using ascorbic acid. Group: Biochemicals. Grades: Highly Purified. CAS No. 179098-76-1. Pack Sizes: 1mg, 2.5mg. Molecular Formula: C26H33F4N5O6S2, Molecular Weight: 651.69. US Biological Life Sciences. | Worldwide |
| 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl | Exceptional ligands for Pd-catalyzed amination and amidation of aryl sulfonates. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling reaction and carbonyl enolate coupling. Ligand used for the chemoselective amination of aryl chlorides. Ligand used for the Pd-catalyzed borylation of aryl chlorides, for the formation of trifluoroborates. Ligand used for the Pd-catalyzed amination of vinyl halides and triflates. Ligand used for the Pd-catalyzed three-component synthesis of indoles. Ligand used for the Pt-catalyzed regioselective hydrosilylation of functionalized terminal arylalkynes. Ligand used for the Pd-catalyzed synthesis of carbazoles. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling of aryl chloride and NHC-boranes. Ligand used for the direct arylation of picoline N-oxide. Ligand used for the Negishi coupling of 2-heterocyclic organozinc reagents. Catalyst for a phosphine-catalyzed Heine reaction. Ligand used for the palladium-catalyzed oxidative coupling of indoles and heteroarenes. Ligand used for the silver-catalyzed hydrogenation of aldehydes. Ligand used for the palladium-catalyzed cyanation of heterycyclic halides. Group: Organic phosphine compounds. Alternative Names: Dicyclohexyl(2', 4', 6'-Triisopropylbiphenyl-2-Yl)Phosphine. CAS No. 564483-18-7. Molecular formula: C33H49P. Mole weight: 476.72. Appearance: Solid. Purity: 0.98. IUPACName: dicyclohexyl-[2-[2,4, | |
| Acetyl Bromide | Acetyl Bromide is a useful and commonly used intermediate. Acetyl Bromide has been used in the synthetic preparation of carbonyl N-heterocyclic carbene silver and selenium compounds, which exhibit antibacterial and DNA cleavage activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 506-96-7. Pack Sizes: 5g, 10g. Molecular Formula: C2H3BrO, Molecular Weight: 122.95. US Biological Life Sciences. | Worldwide |
| Carbon Nanotubes Silver Nanoparticles | Carbon Nanotubes Silver Nanoparticles. Group: Multi wall cnt. CAS No. 308068-56-6. >99wt% (MWNT). | |
| [NH2Me2][(RuCl((R)-binap))2(μ -Cl)3] | (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand | |
| [NH2Me2][(RuCl((S)-binap))2(μ -Cl)3] | (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. 3. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. 4. Ligand employed in rhodium-catalyzed 1,4-additions to enones. 5. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. 6. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. 7. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. 8. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. 9. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. 10. Ligand employed in palladium-catalyzed synthesis of chiral allenes. 11. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. 12. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. 13. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organy | |
| Platinum | Platinum on carbon, often referred to as Pt/C, is a form of platinum used as a catalyst. The metal is supported on activated carbon in order to maximize its surface area and activity. Uses: Platinum is a white noble metal that looks very much like metallic silver found in copper ore. the name platinum comes from the spanish word plata, meaning silver. platinum compounds were used in the platinum printing process and for toning silver images. nanoscale platinum powders possess improved reaction rates compared to bulk powders owing to their high surface area. platinum nanopowders have found use in applications including in fuel cells and oxidation catalysts. Group: Metal nano dispersion. Alternative Names: Platinul; Platinum; Platin; PLATINIUM; Platinum3. CAS No. 7440-6-4. Product ID: platinum. Molecular formula: 195.08. Mole weight: Pt. [Pt]. 99.99%. | |
| Platinum | Platinum on carbon, often referred to as Pt/C, is a form of platinum used as a catalyst. The metal is supported on activated carbon in order to maximize its surface area and activity. Uses: Platinum is a white noble metal that looks very much like metallic silver found in copper ore. the name platinum comes from the spanish word plata, meaning silver. platinum compounds were used in the platinum printing process and for toning silver images. nanoscale platinum powders possess improved reaction rates compared to bulk powders owing to their high surface area. platinum nanopowders have found use in applications including in fuel cells and oxidation catalysts. Group: Organic & printed electronics. Alternative Names: Platinul; Platinum; Platin; PLATINIUM; Platinum3. CAS No. 7440-6-4. Molecular formula: Pt. Mole weight: 195.08. Appearance: Silvery-grey metal. Purity: 0.9999. IUPACName: platinum. Canonical SMILES: [Pt]. Density: 21.45. ECNumber: 231-116-1. Catalog: ACM7440064-32. | |
| Platinum on carbon | Silvery, whitish-gray, malleable, ductile metal. Mp: 1772°C; bp: 2187°C. Density: 21.45 g cm-3 at room conditions (very dense). Also shipped as a finely divided powder (platinum black), as a sponge, and as particles deposited on a supporting material such as alumina. Has strong catalytic activity in these forms; finely divided platinum can be dangerous to handle in the vicinity of other chemicals on this account. Used platinum catalysts are particularly dangerous and can be explosive.;OtherSolid;Solid;BLACK POWDER.;Silvery, whitish-gray, malleable, ductile metal.;Silvery, whitish-gray, malleable, ductile metal. Uses: Platinum is a white noble metal that looks very much like metallic silver found in copper ore. the name platinum comes from the spanish word plata, meaning silver. platinum compounds were used in the platinum printing process and for toning silver images. Group: Fuel cell catalysts. Product ID: platinum. Molecular formula: 195.08g/mol. Mole weight: Pt. [Pt]. InChI=1S/Pt. BASFCYQUMIYNBI-UHFFFAOYSA-N. | |
| Platinum on graphitized carbon | Platinum on graphitized carbon. Uses: Platinum is a white noble metal that looks very much like metallic silver found in copper ore. the name platinum comes from the spanish word plata, meaning silver. platinum compounds were used in the platinum printing process and for toning silver images. Group: Fuel cell catalysts. Molecular formula: 195.08. | |
| Polyaniline (emeraldine salt) | Inherently conductive polymer. Stable at 100 °C and at 200 °C for short periods. Dispersed particles tend to reaggregrate in molded articles forming conductive pathways. Acidic salt of an organic acid, incompatible with most bases. Form of polyaniline complexed (doped) with proprietary organic sulfonic acid Form of polyaniline complexed (doped) with proprietary organic sulfonic acid. Polyaniline is environmentally stable and with tunable conductivity. Synthesis of polyaniline (PANI) emeraldine salt by chemical oxidation has been reported. It was observed that sulfonated dyes chemically interact with the charged backbone of PANI. PANI selectively adsorbs the sulfonated dye. Spectral, diffraction and conductivity measurements of the polymer has been reported in the same study. Uses: A variety of nanomaterials like silver nanoparticles (agnps), graphene oxide(go), aluminum oxide(α-al2o3), carbon fiber and graphite can be potentially used in conjunction with pani for the development of translational medicine, supercapacitors, triboelectric nanogenerators, and other energy storage applications. additive in polymer blends and liquid dispersions for electromagnetic shielding. Group: 3d printing materials bioelectronic materials organic light-emitting diode (oled) materials. Alternative Names: PANI. Pack Sizes: 10 g in poly bottle. Molecular formula: average Mw >15,000. | |
| (R)-(+)-BINAP | (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Ligand for palladium-catalyzed enantioselective hetero Michael addition to form b-amino acid derivatives. Ligand employed in rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols. Ligand employed in rhodium-catalyzed 1,2-addition of aluminium organyl compounds to cyclic enones. Ligand employed in iridium-cataly | |
| (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (R,R)-QuinoxP* | Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction. Cu-catalyzed enantioconvergent allyllic borylation. Cu-catalyzed enantioselective cyclopropylation. Group: Heterocyclic organic compound. Alternative Names: AK173366; 866081-62-1; (R,R)-(-)-2,3-Bis(tert-butylmethylphosphino)quinoxaline; (R,R)-QuinoxP; (R,R)-(-)-2,3-Bis(t-butylmethylphosphino)quinoxaline. CAS No. 866081-62-1. Molecular formula: C18H28N2P2. Mole weight: 334.384g/mol. IUPACName: (R)-tert-butyl-[3-[tert-butyl(methyl)phosphanyl]quinoxalin-2-yl]-methylphosphane. Canonical SMILES: CC (C) (C)P (C)C1=NC2=CC=CC=C2N=C1P (C)C (C) (C)C. Catalog: ACM866081621. | |
| (S)-(-)-BINAP | (R)-BINAP or (R)-Tol-BINAP can be combined with dichloro(1,5-cyclooctadiene)ruthenium to form precursors to NOYORI CATALYST SYSTEMS. These systems exhibit very high catalytic activity and enantioselectivity in the hydrogenation of a wide range of substrates. NOYORI CATALYST SYSTEMS have been shown to effect highly enantioselective hydrogenation of functionalized ketones where the substituents are dialkylamino, hydroxy, siloxy, carbonyl, ester, amide or thioester. Useful ligand in asymmetric Heck processes. Ligand employed in palladium-catalyzed asymmetric arylation of ketones. Ligand employed in rhodium-catalyzed 1,4-additions to enones. Ligand employed in palladium-catalyzed hydroamination of styrene derivatives. Ligand employed in silver-catalyzed asymmetric Sakuri-Hosomi allylation and Mukaiyama aldol reaction. Ligand employed in rhodium-catalyzed kinetic resolution of enynes. Ligand employed in asymmetric rhodium-catalyzed hydroboration of cyclopropenes. Ligand employed in silver-catalyzed a-hydroxylation of stannyl enol ethers. Ligand employed in palladium-catalyzed synthesis of chiral allenes. Group: Organic phosphine compounds. Alternative Names: (+)-2,2'-bis(diphenylphosphino)-1,1'binaphthyl; (R)-(+)-2,2 bis(diphenylphosphino)-1,1-binaphthyl; 13648-EP2311831A1; (R)-(+)-(1,1'-Binaphthalene-2,2'-diyl)bis(diphenylphosphine); FT-0604001; [2'-(diphenylphosphanyl)-[1, 1'-binaphthalene]-2-yl]diphenylphosphane; 1, 1'-[(1R)- | |
| Silver acetate | Silver acetate is an inorganic compound with the empirical formula CH3CO2Ag (or AgC2H3O2). It is a photosensitive, white, crystalline solid. It is a useful reagent in the laboratory as a source of silver ions lacking an oxidizing anion. It has been used in some antismoking drugs. Uses: 3 - 1 - carbonylation silver acetate, when combined with carbon monoxide (co), can induce the carbonylation of primary and secondary amines. other silver salts can be used but the acetate gives the best yield. 2 r2nh + 2 agoac + co → [r2n]2co + 2 hoac + 2 ag 3 - 2 - hydrogenation silver acetate in a solution of pyridine absorbs hydrogen and is reduced to metallic silver. 3 - 3 - direct ortho - arylation silver acetate is a useful reagent for direct ortho-arylation (to install two adjacent substituents on an aromatic ring) for of benzylamines and n-methylbenzylamines. the reaction is palladiumcatalized and requires a slight excess of silver acetate.this reaction is shorter than previous ortho-arylation methods. Group: Solution deposition precursors. Alternative Names: Acetic acid silver(I) salt. CAS No. 563-63-3. Product ID: Silver; acetate. Molecular formula: 166.91. Mole weight: C2H3AgO2. CC(=O)[O-].[Ag+]. InChI=1S/C2H4O2.Ag/c1-2(3)4;/h1H3, (H, 3, 4);/q;+1/p-1. CQLFBEKRDQMJLZ-UHFFFAOYSA-M. 95%+. | |
| Silver Carbon Core Shell Nanoparticles | Silver Carbon Core Shell Nanoparticles. Group: Core shell nanoparticles. 99.9%. | |
| Silver coated Carbon Nanotubes | Silver coated Carbon Nanotubes. Group: Metal and metal oxide nanoparticles coated cnt. | |
| (S,S)-(+)-2,3-Bis(t-butylmethylphosphino)quinoxaline, min. 98% (S,S)-QuinoxP* | Ligand for the rhodium-catalyzed, asymmetric hydrogenation of dehydroamino acid esters and α-enamides. Ligand for the rhodium-catalyzed, asymmetric 1,4-addition of arylboronic acids to α,β-unsaturated carbonyl compounds. Ligand for the rhodium-catalyzed, asymmetric alkylative ring opening reaction Ligand for the palladium-catalyzed asymmetric allylic alkylation and amination of racemic substrates. Ligand for the ruthenium-catalyzed asymmetric hydrogenation of ketones. Ligand for the rhodium-catalyzed, asymmetric hydroacylation of 1,1-disubstituted alkenes with aldehydes. Ligand for the silver-catalyzed asymmetric nitroso aldol reaction. Group: Polydentate phosphine ligandsphosphorus catalysts. Alternative Names: (S, S)-(+)-2, 3-Bis(t-butylmethylphosphino)quinoxaline; 1107608-80-9; (S, S)-2, 3-Bis(tert-butylmethylphosphino)quinoxaline; (S, S)-QuinoxP*; SCHEMBL2559367; 2, 3-Bis[(S)-tert-butylmethylphosphino]quinoxaline; J-002473; (S, S)-(+)-2, 3-Bis(tert-butylmethylphosphino)quinoxaline. CAS No. 1107608-80-9. Molecular formula: C18H28N2P2. Mole weight: 334.384g/mol. IUPACName: (S)-tert-butyl-[3-[tert-butyl(methyl)phosphanyl]quinoxalin-2-yl]-methylphosphane. Canonical SMILES: CC (C) (C)P (C)C1=NC2=CC=CC=C2N=C1P (C)C (C) (C)C. Catalog: ACM1107608809. | |
| Trihexyl(tetradecyl)phosphonium chloride | Trihexyltetradecylphosphonium chloride is a hydrophobic ionic liquid, which is soluble in carbon dioxide. It can be used as binder to develop a silver particle-modified carbon paste electrode, which can determine nitrite ions at low concentration. Uses: Synthesis and catalysis. Group: Battery materials. Alternative Names: Tetradecyltrihexylphosphonium chloride. CAS No. 258864-54-9. Product ID: trihexyl(tetradecyl)phosphanium; chloride. Molecular formula: 519.31. Mole weight: C32H68ClP. CCCCCCCCCCCCCC[P+] (CCCCCC) (CCCCCC)CCCCCC. [Cl-]. JCQGIZYNVAZYOH-UHFFFAOYSA-M. InChI= 1S / C32H68P. ClH / c1-5-9-13-17-18-19-20-21-22-23-24-28- 32-33 (29-25-14-10-6-2, 30-26-15-11-7-3) 31-27-16-12-8-4; / h5-32H2, 1-4H3; 1H / q + 1; / p-1. 98%. | |
| Trihexyl(tetradecyl)phosphonium chloride | Trihexyltetradecylphosphonium chloride is a hydrophobic ionic liquid, which is soluble in carbon dioxide. It can be used as binder to develop a silver particle-modified carbon paste electrode, which can determine nitrite ions at low concentration. Uses: Synthesis and catalysis. Group: Phosphonium salts. Alternative Names: Tetradecyltrihexylphosphonium chloride. CAS No. 258864-54-9. Molecular formula: C32H68ClP. Mole weight: 519.31. Appearance: Liquid. Purity: 0.98. IUPACName: trihexyl(tetradecyl)phosphanium; chloride. Canonical SMILES: CCCCCCCCCCCCCC[P+] (CCCCCC) (CCCCCC)CCCCCC. [Cl-]. Density: 0.895 g/mL at 20 °C(lit.). Catalog: ACM258864549-2. | |
| Urease, Recombinant | Ureases, functionally, belong to the superfamily of amidohydrolases and phosphotriesterases. It is an enzyme that catalyzes the hydrolysis of urea into carbon dioxide and ammonia. The reaction occurs as follows: (NH2)2CO + H2O ? CO2 + 2NH3. Group: Enzymes. Synonyms: Urease. CAS No. 9002-13-5. Purity: Greater than 95.0% as determined by: (a) Analysis by RP-HPLC. (b) Anion-exchange FPLC. (c) Analysis by reducing and non-reducing SDS-PAGE Silver Stained gel. Urease. Activity: 219IU/mg. Stability: Lyophilized Urease although stable at room temperature for 3 weeks, should be stored desiccated below -18° C. Upon reconstitution Urease should be stored at 4° C between 2-7 days and for future use below -18°C. For long-term storage it is recommended to add a carrier protein (0.1% HSA or BSA). Please avoid freeze-thaw cycles. Appearance: Sterile Filtered White lyophilized (freeze-dried) powder. Source: E. coli. Urease. Cat No: NATE-0923. |  |
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