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| Product | Description | |
|---|---|---|
| Nickel Chloride | Nickel Chloride. CAS No: 7718-54-9 |  Sarchem Laboratories New Jersey NJ |
| Nickel Chloride | Nickel Chloride. Grades: 98.% Very High (95-98%). CAS No. 7718-54-9. Pack Sizes: Gram Quantities: 50 gm, 250 gm. Order Number: 2677. |  www.prochemonline.com |
| Nickel Chloride | Nickel Chloride. Grades: 99.% Extremely High (>=99%). CAS No. 7791-20-0. Pack Sizes: Gram Quantities: 500 gm , 2 kg. Order Number: 2680. | www.prochemonline.com |
| Nickel Chloride | Nickel Chloride. Grades: Reagent. CAS No. 7791-20-0. Order Number: 2678. | www.prochemonline.com |
| Nickel Chloride Hexahydrate | Nickel Chloride Hexahydrate. CAS No. 7791-20-0. Molecular Formula NiCl2 * 6H2O. Chemical Reagents |  Cater Chemicals Corp. Illinois IL |
| Nickel chloride solution | Tin Plating IntermediatesZinc Plating Intermediates. CAS No. 7718-54-9. Molecular formula: NiCl2. Mole weight: 129.6. Catalog: ACEP7718549-2. |  |
| [1, 3-Bis (diphenylphosphino) propane]nickel (II) Chloride | [1, 3-Bis (diphenylphosphino) propane]nickel (II) Chloride is used as an effective catalyst for Kumada coupling and Suzuki reactions. It also catalyzes other reactions to convert enol ethers, dithioacetals and vinyl sulfides to olefins. Group: Biochemicals. Grades: Highly Purified. CAS No. 15629-92-2. Pack Sizes: 2.5g, 5g. Molecular Formula: C27H26Cl2NiP2, Molecular Weight: 542.04. US Biological Life Sciences. |  Worldwide |
| Bis(triphenylphosphine)(2-methylphenyl) Nickel(II) chloride | Bis(triphenylphosphine)(2-methylphenyl) Nickel(II) chloride is a precursor to the synthesis of an air-stable Ni-precatalyst developed by Buchwald and coworkers. Uses: Transition metal catalysts. Synonyms: Nickel, chloro(2-methylphenyl)bis(triphenylphosphine)-; Chloro (2-methylphenyl)bis (triphenylphosphine)nickel; Nickel, chloro-o-tolylbis(triphenylphosphine)-; Chloro (2-methylphenyl)bis (triphenylphosphine)nickel (II); Buchwald Nickel Cross-Coupling Catalyst Precursor; [Bis(triphenylphosphine)](o-tolyl)chloronickel; Bis(triphenylphosphino)(2-methylphenyl)chloronickel(II). Grades: ≥95%. CAS No. 27057-09-6. Molecular formula: C43H37ClNiP2. Mole weight: 709.85. |  |
| Chloride(triphenylphosphane)(N-benzyl-N-methyldithiocarbamate)nickel(II) | Nickel Complexes. CAS No. 1251468-61-7. Molecular formula: C27H25ClNNiPS2. Mole weight: 552.74. Purity: 0.98. Catalog: ACM1251468617. | |
| cis-[1,2-Bis(diphenylphosphino)ethane](2-methylphenyl)nickel(II) chloride | Nickel Catalysts. CAS No. 1256262-67-5. Mole weight: 583.69. Catalog: ACM1256262675. | |
| Methallylnickel chloride dimer | Nickel Complexes. Alternative Names: Chloronickel;2-methanidylprop-1-ene. CAS No. 12145-60-7. Molecular formula: C8H14Cl2Ni2. Mole weight: 298.49. Appearance: Crystal. Purity: 0.95. Canonical SMILES: CC(=C)[CH2-]. CC(=C)[CH2-]. Cl[Ni]. Cl[Ni]. Catalog: ACM12145607. | |
| Nickel(II) chloride | Nickel(II) chloride. Group: Biochemicals. Grades: Highly Purified. CAS No. 7718-54-9. Pack Sizes: 25g, 50g, 100g, 250g. US Biological Life Sciences. | Worldwide |
| Nickel (II) Chloride | NICKEL (II) CHLORIDE, ANHYDROUS, 99.99% pure, -10 mesh, (Synonym: Nickelous Chloride), Formula: NiCl2. CAS No. 7718-54-9. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| Nickel (II) Chloride | Nickel (II) Chloride. Grades: 99.95% Extremely High (>=99%). CAS No. 7791-20-0. Pack Sizes: Gram Quantities: 250 gm, 1 kg. Order Number: 2683. | www.prochemonline.com |
| Nickel (II) Chloride | NICKEL (II) CHLORIDE, HEXAHYDRATE, 99.5% pure, -20 mesh, (Synonym: Nickelous Chloride, Hexahydrate), Formula: NiCl2.6H2O. CAS No. 7791-20-0. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! | Texas TX |
| Nickel(II) chloride anhydrous 98+% | Nickel(II) chloride anhydrous 98+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 7718-54-9. Pack Sizes: 100g, 250g, 25g, 1Kg, 2.5Kg. US Biological Life Sciences. | Worldwide |
| Nickel(II) chloride anhydrous 99+% | Nickel(II) chloride anhydrous 99+%. Group: Biochemicals. Grades: Highly Purified. CAS No. 7718-54-9. Pack Sizes: 5g, 25g, 100g, 250g, 1Kg. US Biological Life Sciences. | Worldwide |
| Nickel (II)chloride hexahydrate | Nickel (II)chloride hexahydrate. CAS No: 7791-20-0 | Sarchem Laboratories New Jersey NJ |
| Nickel(II) chloride hexahydrate | Nickel(II) chloride hexahydrate. Group: Biochemicals. Grades: Highly Purified. CAS No. 7791-20-0. Pack Sizes: 100g. US Biological Life Sciences. | Worldwide |
| Nickel(II) chloride hexahydrate 98+% | Nickel(II) chloride hexahydrate 98+%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 7791-20-0. Pack Sizes: 100g. US Biological Life Sciences. | Worldwide |
| Nickel(II) chloride hexahydrate 99+.95% | Nickel(II) chloride hexahydrate 99+.95%. Group: Biochemicals. Grades: Reagent Grade. CAS No. 7791-20-0. Pack Sizes: 100g, 250g, 1Kg, 2.5Kg, 5Kg. US Biological Life Sciences. | Worldwide |
| Nickel(II) chloride hexahydrate ≥98.0% | Nickel(II) chloride hexahydrate ≥98.0%. Group: Biochemicals. Grades: Highly Purified. CAS No. 7791-20-0. Pack Sizes: 100g, 250g, 1Kg, 2.5Kg, 5Kg. US Biological Life Sciences. | Worldwide |
| Nickel (II) Chloride Hexahydrate, Reagent Grade, 100 g | Formula: NiCl2 6H2O. F. W: 237. 69. Characteristics: Green crystals or crystalline powder. Notes: Deliquescent. Storage Code: Blue; toxic. Alternative Names: Nickelous chloride hexahydrate. Grades: chem-grade reagent. CAS No. 7791-20-0. Product ID: 877142. -- SOLD FOR EDUCATIONAL USE ONLY -- |  |
| Nickel(II) Chloride Hydrate | Nickel(II) Chloride Hydrate. Group: Electrolytes. Alternative Names: Nickel(II) chloride. CAS No. 69098-15-3. Product ID: Dichloronickel; hydrate. Molecular formula: 147.61. Mole weight: Cl2H2NiO. O.Cl[Ni]Cl. InChI=1S/2ClH.Ni.H2O/h2*1H; 1H2/q; +2; /p-2. HGGYAQHDNDUIIQ-UHFFFAOYSA-L. 99%+. |  |
| Nickel (II) Chloride Hydrate, 99.95% | Nickel (II) Chloride Hydrate, 99.95%. CAS No: 69098-15-3 | Sarchem Laboratories New Jersey NJ |
| Nickel(II) Chloride Hydrate 99.95% trace metals basis | Nickel(II) Chloride Hydrate 99.95% trace metals basis. CAS No. 7791-20-0. Molecular Formula Cl2Ni * 6H2O. Ultra High Purity Fine Chemicals | Cater Chemicals Corp. Illinois IL |
| trans-Bis(tricyclohexylphosphine)(2-methylphenyl)nickel(II) chloride | Nickel Catalysts. CAS No. 123839-28-1. Mole weight: 746.13. Catalog: ACM123839281. | |
| Tris(2,2'-bipyridine) Nickel dichloride | . Uses: Transition metal catalysts. Synonyms: Nickel(2+), tris(2,2'-bipyridine-κN1,κN1')-, chloride (1:2), (OC-6-11)-; Nickel(2+), tris(2,2'-bipyridine)-, dichloride; Nickel(2+), tris(2,2'-bipyridine-N,N')-, dichloride, (OC-6-11)-; Nickel(2+), tris(2,2'-bipyridine-κN1,κN1')-, dichloride, (OC-6-11)-; Tris(2,2'-bipyridine)nickel dichloride; Tris(2,2'-bipyridine)nickel(2+) dichloride. Grades: ≥95%. CAS No. 14751-84-9. Molecular formula: C30H24Cl2N6Ni. Mole weight: 598.15. | |
| 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. | |
| 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydroimidazolium Tetrafluoroborate | In-situ deprotonation leads to metal carbene species which acts as a catalyst in a variety of C-C and C-N bond forming reactions. Ligand used in the nickel or palladium-catalyzed coupling of aryl chlorides and amines. Ligand used for the palladium-catalyzed arylation of esters and amides. Ligand used for the palladium-catalyzed intermolecular amination of Csp3-H Bonds. Ligand used for the nickel-catalyzed hydrogenation of olefins. Group: Organic phosphine compounds. Alternative Names: 1,3-Bis(2,6-Diisopropylphenyl)-4,5-Dihydro-1H-Imidazol-3-Ium Tetrafluoroborate. CAS No. 282109-83-5. Molecular formula: C27H39BF4N2. Mole weight: 478.4. Appearance: White powder. Purity: 0.98. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dihydroimidazol-1-ium;tetrafluoroborate. Canonical SMILES: [B-] (F) (F) (F)F. CC (C)C1=C (C (=CC=C1)C (C)C)N2CC[N+] (=C2)C3=C (C=CC=C3C (C)C)C (C)C. Catalog: ACM282109835-1. | |
| 3,5,6,8-Tetrabromo-1,10-phenanthroline | 3,5,6,8-Tetrabromo-1,10-phenanthroline. Uses: 3,5,6,8-tetrabromo-1,10-phenanthroline can be used in the nickel-catalyzed amination of aryl and heteroaryl chlorides. Group: Ligands for functional metal complexessmall molecule semiconductor building blocks. Alternative Names: 66127-00-2; CTK1I0855; 3,5,6,8-tetrabromo-1,10-phenanthroline; BAPJVWLAFSQLNX-UHFFFAOYSA-N; 1,10-Phenanthroline, 3,5,6,8-tetrabromo-; ACMC-1B8M0; SCHEMBL7059861. CAS No. 66127-00-2. Product ID: 3,5,6,8-tetrabromo-1,10-phenanthroline. Molecular formula: 495.79. Mole weight: C12H4Br4N2. C1=C (C=NC2=C1C (=C (C3=C2N=CC (=C3)Br)Br)Br)Br. BAPJVWLAFSQLNX-UHFFFAOYSA-N. InChI=1S/C12H4Br4N2/c13-5-1-7-9 (15)10 (16)8-2-6 (14)4-18-12 (8)11 (7)17-3-5/h1-4H. 98%. | |
| (4,4'-dMeObpy)NiCl2 | . Uses: Transition metal catalysts. Synonyms: 4,4'-Dimethoxy-2,2'-bipyridine nickel (II) chloride; Nickel, dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-; Dichloro(4,4'-dimethoxy-2,2'-bipyridine-κN1,κN1')-Nickel; 4,4'-dimethoxy-2,2'-bipyridine Nickel dichloride. Grades: ≥95%. CAS No. 1303613-81-1. Molecular formula: C12H12Cl2N2NiO2. Mole weight: 345.84. | |
| ATP | A Class I Brightener which is primarily improves tolerance metallic purities, ductility and covering power at low current densities. Suitable in Cu, Ni and Ni-Fe alloy electroplating baths. Group: Nickel plating intermediates. Alternative Names: S-Carboxyethylisothiuronium chloride;Carboxyethylisothiuronium chloride; ATP. CAS No. 5425-78-5. Molecular formula: C4H9ClN2O2S. Mole weight: 184.64446. Appearance: White or yellowish powder. ECNumber: 231-010-5. Catalog: ACEP5425785. | |
| Bis(triphenylphosphino)(2-methylphenyl)chloronickel(II), 99% | This complex is used as an air-stable nickel precatalyst for the amination of aryl chlorides, sulfamates, mesylates, and triflates. This nickel precatalyst is used for the polymerization of halothiophenes. Group: Nickel catalysts. Alternative Names: MFCD28144558; Bis(triphenylphospino)(2-methylphenyl)chloronickel(II); 27057-09-6. CAS No. 27057-09-6. Molecular formula: C43H39ClNiP2+. Mole weight: 711.876g/mol. IUPACName: chloronickel; methylbenzene; triphenylphosphanium. Canonical SMILES: CC1=CC=CC=[C-]1. C1=CC=C (C=C1)[PH+] (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)[PH+] (C2=CC=CC=C2)C3=CC=CC=C3. Cl[Ni]. Catalog: ACM27057096. | |
| BrettPhos | Ligand for palladium-catalyzed cross-coupling reactions using aryl mesylates with electron-deficient anilines. Ligand for palladium-catalyzed cross-coupling of primary arylamines at low catalyst loading. Ligand for palladium-catalyzed cross-coupling of aryl iodides and primary amines. Ligand for the Suziki-Miyaura coupling of tosylates and mesylates. Ligand for the palladium-catalyzed trifluoromethylation of aryl chlorides. Ligand for the palladium-catalyzed formation of aryl-SCF3 compounds from aryl bromides. Ligand for the nickel-catalyzed cross-coupling of styrenyl epoxides with boronic acids. Ligand for the palladium-catalyzed intramolecular CH difluoroalkylation. Group: Organic phosphine compounds. Alternative Names: C35H53O2P; dicyclohexyl-(2',4',6'-triisopropyl-3,6-dimethoxy-biphenyl-2-yl)-phosphane; BrettPhos; 2-(Dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl; ZINC43220891; ST24046493; 2-DICYCLOHEXYLPHOSPHINO-2',4',6'-TRIISOPROPYL-3,6-DIMETHOXYBIPHENYL; AS-19342; 2-(Dicyclohexylphosphino)3,6-dimethoxy-2 inverted exclamation marka,4 inverted exclamation marka,6 inverted exclamation. CAS No. 1070663-78-3. Molecular formula: C35H53O2P. Mole weight: 536.781g/mol. IUPACName: dicyclohexyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=C (C=CC (=C2P (C3CCCCC3)C4CCCCC4)OC)OC)C (C)C. Catalog: ACM1070663783. | |
| 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. | |
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