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| Product | Description | |
|---|---|---|
| Ruthenium (III) Bromide | RUTHENIUM (III) BROMIDE, ANHYDROUS, 99.9% pure, -60 mesh, (Synonym: Ruthenium Tribromide, Anhydrous), Formula: RuBr3. CAS No. 14014-88-1. Noah Chemicals San Antonio, Texas. ISO 9001:2015 Certified. Request a Quote Today! |  Texas TX |
| 1,1'-Bis(diisopropylphosphino)ferrocene | 1,1'-Bis(diisopropylphosphino)ferrocene. Uses: Ruthenium- catalyzed hydrohydroxyalkylation of 1,1-disubstituted allenes ligand for palladium-catalyzed aminocarbonylation of pyridyl tosylates by means of ex situ generation of co. pd-catalyzed carbonylative ?-arylation of ketones with aryl iodides ligand for palladium-catalyzed alkoxycarbonylation of aryl bromides for the preparation of tertiary esters ligand for stereoselective palladium-catalyzed decarboxylative allylation ß-c-glycosylation ligand for ruthenium-catalyzed c-c coupling reactions of fluorinated alcohols with allenes. ligand for cobalt-catalyzed intermolecular formal hydroacylation reaction of olefins using n-3-picolin-2-yl aldimines as aldehyde equivalents. Additional or Alternative Names: 1,1-BIS(DIISOPROPYLPHOSPHINO)FERROCENE. Product Category: Organic Phosphine Compounds. Appearance: Orange-yellow powder. CAS No. 97239-80-0. Molecular formula: C22H36FeP2. Mole weight: 418.32. Purity: 0.98. IUPACName: 1,1-Bis(diisopropylphosphino)ferrocene. Product ID: ACM97239800. Alfa Chemistry ISO 9001:2015 Certified. Categories: 1,1\'-Bis(diisopropylphosphino)ferrocene. |  |
| Tetrabutylphosphonium Bromide | Tetrabutylphosphonium bromide (TBPB) is a quaternary salt which can be used: As a medium to disperse ruthenium catalyst for the synthesis of ethylene glycol from synthesis gas via ruthenium melt catalysis. As a catalyst supported on silica or alumina for the halogen exchange reaction to synthesize alkyl bromide from alkyl chloride. To synthesize various ionic liquids on mixing with different proportions of 1,3-dimethylurea for capturing NO gas. Uses: Metal plating, electropolishing, metal reprocessing, phase transfer media, batteries fuel cells, nanomaterials, industrial solvents, nuclear fuel red waste, enzymatic catalysis, lubricants heat transfer and solar energy conversion. Group: Battery materials polymerization reagents. Alternative Names: Tetra-n-butylphosphonium bromide; Phosphonium, tetrabutyl-, bromide; Phosphonium, tetrabutyl-, bromide (1:1). CAS No. 3115-68-2. Product ID: tetrabutylphosphanium; bromide. Molecular formula: 339.34. Mole weight: C16H36BrP. CCCC[P+](CCCC)(CCCC)CCCC.[Br-]. 1S/C16H36P. BrH/c1-5-9-13-17(14-10-6-2, 15-11-7-3)16-12-8-4; /h5-16H2, 1-4H3; 1H/q+1; /p-1. RKHXQBLJXBGEKF-UHFFFAOYSA-M. >99.0%(T). |  |
| Tricyclohexylphosphine | Tricyclohexylphosphine. Uses: Tricyclohexyl phosphine is a ligand catalyst used primarily in organometallic chemistry. ligand used in the pd-catalyzed coupling of malononitrile with aryl halides. suzuki reaction: bulky phosphine ligand used with a pd(0)-triolefinic macrocycle catalyst for suzuki coupling of aryl bromides and chlorides. this ligand is applied with ni as a key intermediate in the formation of cylcopentane compounds. as a reagent, tricyclohexylphosphine is used for a range of metal-catalyzed organic transformations. crabtree's catalyst is an organoiridium compound containing tricyclohexyl phosphine used for hydrogenation of mono-, di-, tri-, and tetra- substituted substrates and hydrogen transfer reactions. grubbs' catalysts consists of transition metal ruthenium and tricylohexyl phosphine utilized in olefin metathesis in synthetic organic chemistry. Additional or Alternative Names: Phosphine, tricyclohexyl-. Product Category: Promotional Products. Appearance: liquid. CAS No. 2622-14-2. Molecular formula: C18H33P. Mole weight: 280.44. Purity: 95+%. IUPACName: tricyclohexylphosphane. Product ID: ACM2622142-2. Alfa Chemistry ISO 9001:2015 Certified. | |
| Tri-tert-butylphosphonium tetrafluoroborate | Tri-tert-butylphosphonium tetrafluoroborate. Uses: Air-stable, non-pyrophoric precursor of the tri-t-butylphosphine ligand which is used in a variety of catalytic processes. ligand for suzuki cross-couplings. ligand for heck reactions. ligand for stille cross-couplings. ligand for α-arylation and vinylation of arylmandelic acid derivatives. ligand for direct arylation of hetercycles synthesis of benzocyclobutenes by c-h activation. cross-coupling of grignard reagents and aryl bromides. palladium catalyzed annulation of haloanilines. palladium-catalyzed acylation. palladium catalyzed carbonylative heck reaction. palladium-catalyzed aminosulfonylation. palladium-catalyzed intramolecular c-o bond formation. ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acid. Additional or Alternative Names: Fluoroboric Acid Tri-Tert-Butylphosphine Adduct. Product Category: Borate. Appearance: Solid. CAS No. 131274-22-1. Molecular formula: C12H28BF4P. Mole weight: 290.13. Purity: 0.98. IUPACName: tritert-butylphosphanium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F.CC(C)(C)[PH+](C(C)(C)C)C(C)(C)C. Product ID: ACM131274221-1. Alfa Chemistry ISO 9001:2015 Certified. | |
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