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| Product | Description | |
|---|---|---|
| Nickel Carbonate | Nickel plating, as catalyst for hardening of fats, in ceramic colors & glazes. Group: Nickel plating chemicals. CAS No. 3333-67-3. ECNumber: 222-068-2. Catalog: ACEP3333673. |  |
| Nickel carbonate, basic hydrate | Nickel carbonate, basic hydrate. Group: Electrolytes. CAS No. 958638-02-3. Product ID: nickel; carbonate; hydroxide; hydrate. Molecular formula: 153.72g/mol. Mole weight: CH3NiO5-3. C(=O)([O-])[O-].O.[OH-].[Ni]. InChI=1S/CH2O3.Ni.2H2O/c2-1(3)4; ; ; /h(H2, 2, 3, 4); ; 2*1H2/p-3. VLVVKKSBFDPDOX-UHFFFAOYSA-K. |  |
| Nickel carbonate hydroxide | High Purity Salts. Alternative Names: Nickel(II) carbonate tetrahydroxide. CAS No. 12607-70-4. Mole weight: 376.18. Appearance: Green powder. Purity: 99%+. Catalog: ACM12607704. | |
| Nickel (II) Carbonate | NICKEL (II) CARBONATE, 99.9% pure, -100 mesh, (Synonym: Nickelous Carbonate), Formula: NiCO3. CAS No. 3333-67-3. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). | Nickel(II) carbonate basic tetrahydrate 98+% (48-50% ex Ni). Group: Biochemicals. Grades: Highly Purified. CAS No. 12607-70-4. Pack Sizes: 100g, 250g, 25g, 1Kg, 2.5Kg. US Biological Life Sciences. |  Worldwide |
| 1, 1'-Bis (dicyclohexylphosphino)ferrocene | Ligand for palladium-catalyzed synthesis of oxindoles by amide ?-arylation. Ligand for palladium-catalyzed alkoxycarbonylation of aryl chlorides. Ligand for ruthenium-catalyzed alcohol-allene C-C coupling reaction via hydrohydroxyalkylation of 1,1-disubstituted allenes employing alcohols. Ligand for nickel-catalyzed cross-coupling reaction of arylboronic acids with aryl carbonates. Ligand for palladium-catalyzed regiodivergent hydroesterification of aryl olefins with phenyl formate to form linear structured phenyl arylpropanoates. Ligand for palladium-catalyzed direct borylation of benzyl alcohol and its analogues in the absence of bases. Group: Organic phosphine compounds. Alternative Names: 1,1-Bis(dicyclohexylphosphino)ferrocene; 1,1-Bis(Dicyclohexylphosphino)Ferrocene; 1,1-BIS(DICYCLOHEXYLPHOSPHINO)FERROCENE. CAS No. 146960-90-9. Molecular formula: C34H52FeP2. Mole weight: 578.57. Appearance: Orange-red powder. Purity: 0.98. IUPACName: dicyclohexyl(cyclopentyl)phosphane; iron. Canonical SMILES: C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. C1CCC (CC1)P (C2CCCCC2)[C]3[CH][CH][CH][CH]3. [Fe]. Catalog: ACM146960909. | |
| 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl | Phosphine Ligand Kit component. Useful ligand for palladium-catalyzed carbon-nitrogen bond formation. Useful ligand for rhodium-catalyzed C-C bond formation. Useful ligand for palladium-catalyzed intramolecular acylation of aryl bromides via C-H activation. Used in the preparation of Buchwald third generation precatalyst. Used in methoxy directed Rhodium migration. Used in Nickel catalyzed C-N cross-coupling reactions. Group: Organic phosphine compounds. Alternative Names: F0001-2326; DB-009478; AC1LCPMX; (S)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL; AN-10356; SC-19338; (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene, puriss.; PubChem8136; TL8005203; (S)-(-)-2,2 inverted exclamation mark -Bis(diphenylphosphino)-1,1 inverted exclamation mark -binaphthalene. CAS No. 98327-87-8. Molecular formula: C44H32P2. Mole weight: 622.688g/mol. IUPACName: [1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. ECNumber: 616-304-7. Catalog: ACM98327878. | |
| 4,4'-Di-tert-butyl-2,2'-bipyridine | Ligand for the iridium-catalyzed borylation of arenes Ligand for the iridium-catalyzed synthesis of arylboronic acids and aryl trifluoroborates Ligand for the nickel-catalyzed hydroxycarboxylation of 1,2-dienes by reaction carbon dioxide and oxygen Ligand for the iridium-catalyzed meta borylation followed by halogenation of 1,3-disubstituted arenes Ligand for the iridium-catalyzed silyl-directed ortho-borylation of arenes Ligand for the iridium-catalyzed silane borylation followed by aryl borylation Ligand for the iridium-catalyzed microwave-accelerated borylation of aromatic C-H bonds Ligand for the iridium-catalyzed silyl-directed borylation of indoles Ligand for the nickel-catalyzed synthesis of functionalized dialkyl ketones from carboxylic acids and alkyl halides Ligand for the iron-catalyzed arylation of heterocycles. Group: Polymer/macromolecule. Alternative Names: BBBPY; 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. CAS No. 72914-19-3. Molecular formula: C18H24N2. Mole weight: 268.4. Appearance: White solid. Purity: 0.98. IUPACName: 4-tert-butyl-2-(4-tert-butylpyridin-2-yl)pyridine. Canonical SMILES: CC (C) (C)C1=CC (=NC=C1)C2=NC=CC (=C2)C (C) (C)C. Catalog: ACM72914193-2. | |
| anaerobic carbon-monoxide dehydrogenase | This prokaryotic enzyme catalyses the reversible reduction of CO2 to CO. The electrons are transferred to redox proteins such as ferredoxin. In purple sulfur bacteria and methanogenic archaea it catalyses the oxidation of CO to CO2, which is incorporated by the Calvin-Benson-Basham cycle or released, respectively. In acetogenic and sulfate-reducing microbes it catalyses the reduction of CO2 to CO, which is incorporated into acetyl CoA by EC 2.3.1.169, CO-methylating acetyl CoA synthase, with which the enzyme forms a tight complex in those organisms. The enzyme contains five metal clusters per homodimeric enzyme: two nickel-iron-sulfur clusters called the C-Clusters, one [...-4S] clusters exist, presumably as part of the electron transfer chain. In purple sulfur bacteria the enzyme forms complexes with the Ni-Fe-S protein EC 1.12.7.2, ferredoxin hydrogenase, which catalyse the overall reaction: CO + H2O = CO2 + H2. cf. EC 1.2.5.3, aerobic carbon monoxide dehydrogenase. Group: Enzymes. Synonyms: Ni-CODH; carbon-monoxide dehydrogenase (ferredoxin). Enzyme Commission Number: EC 1.2.7.4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1227; anaerobic carbon-monoxide dehydrogenase; EC 1.2.7.4; Ni-CODH; carbon-monoxide dehydrogenase (ferredoxin). Cat No: EXWM-1227. |  |
| Bis(triphenylphosphine)nickel dicarbonyl | Nickel Complexes. Alternative Names: Carbon monoxide;nickel;triphenylphosphane. CAS No. 13007-90-4. Molecular formula: C38H30NiO2P2. Mole weight: 639.29. Appearance: Crystal. Purity: 0.98. Canonical SMILES: [C-]#[O+]. [C-]#[O+]. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Ni]. Catalog: ACM13007904. | |
| Carbon Nanotube Nickel | Carbon Nanotube Nickel. Group: Single wall cnt. CAS No. 308068-56-6. >99% (SWCNT). | |
| Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core) | Carbonyl Nickel Coated Aluminum Powder (Ni Shell, Al Core). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. | |
| Carbonyl Nickel Iron Alloy Powder | Carbonyl Nickel Iron Alloy Powder. Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Alloys nanopowders. | |
| Carbonyl Nickel Powder (2-3 μm) | Carbonyl Nickel Powder (2-3 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| Carbonyl Nickel Powder (2-3 μm) | Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. Catalog: ACM8049318. | |
| Carbonyl Nickel Powder (4-7 μm) | Carbonyl Nickel Powder (4-7 μm). Uses: Combustion catalyst, additive, electronics, purification of uranium. Group: Elements nanoparticles. CAS No. 8049-31-8. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (bis (4-fluorophenyl) phosphinoferrocenyl]ethyl (di-t-butylphosphine) }nickel (II) is used for: 1.Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. 4.Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-37-3. Mole weight: 774.69. Catalog: ACM2049086373. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II) | Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-35-1. Mole weight: 802.88. Catalog: ACM2049086351. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (dicyclohexylphosphino) ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is useful in these fields: Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-36-2. Mole weight: 790.79. Catalog: ACM2049086362. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) has the following various uses:1.Versatile, air-stable, low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-34-0. Mole weight: 738.71. Catalog: ACM2049086340. | |
| CO-methylating acetyl-CoA synthase | Contains nickel, copper and iron-sulfur clusters. Involved, together with EC 1.2.7.4, carbon-monoxide dehydrogenase (ferredoxin), in the synthesis of acetyl-CoA from CO2 and H2. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.169. CAS No. 176591-19-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2109; CO-methylating acetyl-CoA synthase; EC 2.3.1.169; 176591-19-8. Cat No: EXWM-2109. | |
| Fluopsin N | Fluopsin N is an antibiotic containing metallic nickel produced by Pseudomonas fluorescent KY 4032 cultured with n-alkane as a carbon source. It has strong anti-Gram-positive and negative bacteria activity and anti-tumor activity. CAS No. 31541-90-9. Molecular formula: C4H8O2N2S2Ni. Mole weight: 238.94. |  |
| MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated | MWCNT-Ni Type 1 Carbon Nanotubes Multi Walled, Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 2 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 3 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated | MWCNT-Ni Type 4 Carbon Nanotubes Multi Walled , Nickel coated. Group: Nanotubes. CAS No. 308068-56-6. | |
| N6-Carbobenzyloxy-N2,N2-bis(carboxymethyl)-L-lysine | It is used in the synthesis of nickel-chelating fluorinated lipids for protein monolayer crystallizations. Group: Biochemicals. Alternative Names: N2, N2-Bis (carboxymethyl) -N6-[ (phenylmethoxy) carbonyl]-. Grades: Highly Purified. CAS No. 113231-04-2. Pack Sizes: 1g. US Biological Life Sciences. | Worldwide |
| Nickel Carbon-Coated nanoparticles | Nickel Carbon-Coated nanoparticles. Group: Compounds nanoparticles. | |
| Nickel Carbon Core Shell Nanoparticles | Nickel Carbon Core Shell Nanoparticles. Group: Core shell nanoparticles. 99.9%. | |
| Nickel Carbon Nanotubes | Nickel Carbon Nanotubes. Group: Nanotubes. Mole weight: SiC. | |
| Nickel Nanoparticles, Carbon Coated | Nickel Nanoparticles, Carbon Coated. Group: Elements nanoparticles. 99.9 %. | |
| oxalate oxidoreductase | Contains thiamine diphosphate and [4Fe-4S] clusters. Acceptors include ferredoxin and the nickel-dependent carbon monoxide dehydrogenase (EC 1.2.7.4). Group: Enzymes. Enzyme Commission Number: EC 1.2.7.10. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-1224; oxalate oxidoreductase; EC 1.2.7.10. Cat No: EXWM-1224. | |
| (SP-4-4)-[N-[[5-Chloro-2-[[[ (1S, 2R)-1- (phenylmethyl)-2-pyrrolidinyl-κ N]carbonyl]amino-κ N]phenyl]phenylmethylene]glycinato (2-)-κ N, κ O]-nickel | Nickel Complexes. Alternative Names: 2- [ [ [2- [ (2R) -1-Benzylpyrrolidine-2-carbonyl] azanidyl-5-chlorophenyl] -phenylmethylidene] amino] acetate; nickel (3+). CAS No. 1021603-69-9. Molecular formula: C27H24ClN3NiO3. Mole weight: 532.64. Purity: 0.98. Canonical SMILES: C1CC (N (C1)CC2=CC=CC=C2)C (=O)[N-]C3=C (C=C (C=C3)Cl)C (=NCC (=O)[O-])C4=CC=CC=C4. [Ni+3]. Catalog: ACM1021603699. | |
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