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[10- (2, 5-Dihydroxy-3, 4-dimethylphenyl) decyl]triphenyl-phosphonium Bromide is a plastoquinone derivative used as a tool to interrupt execution of the aging program. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 25mg, 250mg. Molecular Formula: C36H44ClO2P. US Biological Life Sciences.
[ (Methoxy) methyl] triphenylphosphoniumChloride is used in the synthesis of Cephalotaxine (C261050), an antiviral and antitumor agent. Also used in the synthesis of Taxol A fragment. Group: Biochemicals. Alternative Names: (Methoxymethyl) triphenylphosphoniumChloride; (Methoxymethyl) triphenylphosphoniumChloride; NSC 49223; Triphenyl (methoxymethyl) phosphoniumChloride. Grades: Highly Purified. CAS No. 4009-98-7. Pack Sizes: 10g. US Biological Life Sciences.
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(Phenylthio) methyl triphenylphosphoniumchloride
(Phenylthio) methyl triphenylphosphoniumchloride. Group: Biochemicals. Alternative Names: Triphenyl[ (phenylthio) methyl]phosphoniumchloride. Grades: Highly Purified. CAS No. 13884-92-9. Pack Sizes: 2g, 5g, 10g, 25g, 50g. Molecular Formula: C25H22ClPS. US Biological Life Sciences.
Trihexyltetradecylphosphoniumchloride 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: Tetradecyltrihexylphosphoniumchloride. 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)phosphoniumchloride
Trihexyltetradecylphosphoniumchloride 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: Tetradecyltrihexylphosphoniumchloride. 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.
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).
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: Phosphonium ionic liquids. Alternative Names: Tetra-n-butylphosphonium bromide;Phosphonium, tetrabutyl-, bromide;Phosphonium, tetrabutyl-, bromide (1:1). CAS No. 3115-68-2. Molecular formula: C16H36BrP. Mole weight: 339.34. Appearance: White to Almost white powder to crystal. Purity: >99.0%(T). IUPACName: tetrabutylphosphanium;bromide. Canonical SMILES: CCCC[P+](CCCC)(CCCC)CCCC.[Br-]. ECNumber: 221-487-8. Catalog: ACM3115682.
Trihexyltetradecylphosphonium bis(2,4,4-trimethylpentyl)phosphinate is a phosphonium-based ionic liquid. It can be prepared by reacting trihexyl(tetradecyl)-phosphoniumchloride with bis(2,4,4-trimethylpentyl)phosphinic acid in the presence of a base. 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: Electrolytes. Alternative Names: Tetradecyltrihexylphosphoniumbis(2, 4, 4-trimethylpentyl)phosphinate. CAS No. 465527-59-7. Product ID: bis(2,4,4-trimethylpentyl)phosphinate; trihexyl(tetradecyl)phosphanium. Molecular formula: 773.27. Mole weight: Linear Formula [CH3(CH2)5]3P[N(SO2CF3)2](CH2)13CH3. CCCCCCCCCCCCCC[P+] (CCCCCC) (CCCCCC)CCCCCC. CC (CC (C) (C)C)CP (=O) (CC (C)CC (C) (C)C)[O-]. 1S / C32H68P. C16H35O2P / 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; 1-13 (9-15 (3, 4) 5) 11-19 (17, 18) 12-14 (2) 10-16 (6, 7) 8 / h5-32H2, 1-4H3; 13-14H, 9-12H2, 1-8H3, (H, 17, 18) / q + 1; / p-1. ZKQLVOZSJHOZBL-UHFFFAOYSA-M. ≥90.0%.
WIN 64338 hydrochloride
WIN 64338 hydrochloride is a potent, non-peptide and competitive bradykinin B2 receptor antagonist. In organ bath studies, WIN 64338 inhibits [3H]-bradykinin binding on guinea pig trachea with nanomolar affinity but is not active in the rabbit aorta (the classical bradykinin B1 preparation). Synonyms: WIN 64338 hydrochloride; WIN 64338 HCl; WIN 64338; WIN64338; WIN-64338. (S)-4-[2-[Bis(cyclohexylamino)methyleneamino]-3-(2-naphthalenyl)-1-oxopropylamino]benzyl tributyl phosphoniumchloride hydrochloride. CAS No. 163727-74-0. Molecular formula: C45H68ClN4OP.HCl. Mole weight: 783.95.
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