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288225

Sigma-Aldrich

Chloro(triethylphosphine)gold(I)

97%

Synonym(s):

(Triethylphosphine)gold(I) chloride

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About This Item

Linear Formula:
(C2H5)3PAuCl
CAS Number:
15529-90-5
Molecular Weight:
350.58
EC Number:
239-572-3
MDL number:
MFCD00013205
UNSPSC Code:
12161600
PubChem Substance ID:
24857327
NACRES:
NA.22

Assay

97%

form

solid

reaction suitability

core: gold
reagent type: catalyst

bp

210 °C/0.03 mmHg (lit.)

mp

84-86 °C (lit.)

SMILES string

Cl[Au].CCP(CC)CC

InChI

1S/C6H15P.Au.ClH/c1-4-7(5-2)6-3;;/h4-6H2,1-3H3;;1H/q;+1;/p-1

InChI key

SYBBXLKWGHAVHP-UHFFFAOYSA-M

Pictograms

Skull and crossbones
GHS06

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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F Märki et al.
Arzneimittel-Forschung, 42(3), 328-333 (1992-03-01)
The effect of several gold complexes on the activity of phospholipase C from human blood platelets was studied in vitro. Aurothiomalate and auranofin--2 agents used for the chrysotherapy of rheumatoid arthritis--, gold chloride, (triethylphosphine)gold chloride, and 5 newly synthesized (triethylphosphine)gold
31P nuclear-magnetic-resonance studies at 24 and 162 MHz of blood containing an anti-arthritic gold phosphine: relaxation via chemical-shift anisotropy.
N A Malik et al.
Biochemical Society transactions, 8(5), 635-636 (1980-10-01)
R M Snyder et al.
Biochemical pharmacology, 36(5), 647-654 (1987-03-01)
Auranofin (AF) is an orally active chrysotherapeutic agent whose precise mechanism of action with its putative target cell, the macrophage, is not known. In a previous paper, we described a sequential thiol exchange mechanism that explained auranofin's molecular mechanism of
N A Malik et al.
Journal of inorganic biochemistry, 12(4), 317-322 (1980-07-01)
Contrasting reactions of the antiarthritic complexes ClAuPEt3 and ClAu(PEt3)2 with blood have been studied by 31P nmr spectroscopy. The monophosphine complex has two binding sites in erythrocytes, probably at the SH groups of glutathione and haemoglobin. The bis complex solidifies
Cellular and molecular pharmacology of auranofin and related gold complexes.
S T Crooke et al.
Biochemical pharmacology, 35(20), 3423-3431 (1986-10-15)
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