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Merck
CN

450235

Potassium gold(III) chloride

99.995% trace metals basis

Synonym(s):

Potassium tetrachloroaurate(III), Gold potassium chloride

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About This Item

Linear Formula:
KAuCl4
CAS Number:
13682-61-6
Molecular Weight:
377.88
NACRES:
NA.23
PubChem Substance ID:
24868232
UNSPSC Code:
12352302
EC Number:
237-190-1
MDL number:
MFCD00043088
Assay:
99.995% trace metals basis
Form:
powder
Solubility:
H2O: soluble, alcohol: soluble, ethanol: soluble

Key Documents

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InChI key

JMONCQYBAMKVQQ-UHFFFAOYSA-J

InChI

1S/Au.4ClH.K/h;4*1H;/q+3;;;;;+1/p-4

SMILES string

[K+].Cl[Au-](Cl)(Cl)Cl

assay

99.995% trace metals basis

form

powder

reaction suitability

core: potassium

impurities

≤55.0 ppm Trace Metal Analysis

solubility

H2O: soluble, alcohol: soluble, ethanol: soluble

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General description

The yellow crystals of potassium gold chloride are soluble in water. 1,2

Application

Key raw material for synthesis of new gold(III) dithiolate complexes for luminescence studies or possible uses as photosensitizers or photocatalysts.1

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCN9534
MKCM9764
MKCM0319
MKCL4363
MKCG5004

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M. Adnan Mansour et al.
Inorganic chemistry, 37(18), 4625-4632 (2001-10-24)
Two Au(III) dithiolate complexes, [Au(dbbpy)(tdt)]PF(6) and Au(eta(2)-C,N-ppy)(tdt), (dbbpy = 4,4'-di-tert-butyl-2,2'-bipyridine; tdt = 3,4-toluenedithiolate; ppy = C-deprotonated 2-phenylpyridine), have been prepared and structurally characterized by X-ray crystallography. The complexes have low-energy absorption bands that exhibit mild solvatochromism (lambda(max) = 444 nm
Sergey S Zalesskiy et al.
Journal of the American Chemical Society, 135(9), 3550-3559 (2013-01-02)
Soluble gold precatalysts, aimed for homogeneous catalysis, under certain conditions may form nanoparticles, which dramatically change the mechanism and initiate different chemistry. The present study addresses the question of designing gold catalysts, taking into account possible interconversions and contamination at
R Balagurunathan et al.
Indian journal of biochemistry & biophysics, 48(5), 331-335 (2011-12-15)
Biosynthesis of gold nanoparticles by Streptomycetes from Himalayan Mountain was undertaken for the first time. Out of 10 actinomycete strains tested, four strains (D10, HM10, ANS2 and MSU) showed evidence for the intracellular biosynthesis of gold nanoparticles, among which the
Xianqing Tian et al.
Talanta, 93, 79-85 (2012-04-10)
Graphene decorated with gold nanoparticles (AuNPs-β-CD-Gra) has been synthesized by in situ thermal reduction of graphene oxide and HAuCl(4) with β-cyclodextrin (β-CD) under alkaline condition. The AuNPs-β-CD-Gra product was well characterized by infrared spectroscopy, X-ray powder diffraction, scanning electron microscopy
Andrew R Garcia et al.
Colloids and surfaces. B, Biointerfaces, 105, 167-172 (2013-02-05)
Fluorescent insulin fibrils gold nanoclusters (Au NCs) have been synthesized through the reduction of gold by human insulin in fibrillated form. Likewise, nanocluster formation has been regulated by insulin, working as a protein-based template. Environment- and surface-controlled experiments have shown
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