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Merck
CN

G4022

Gold(III) chloride trihydrate

ACS reagent, ≥49.0% Au basis

Synonym(s):

Hydrogen tetrachloroaurate(III), Tetrachloroauric(III) acid

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About This Item

Linear Formula:
HAuCl4 · 3H2O
CAS Number:
Molecular Weight:
393.83
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
240-948-4
MDL number:
Grade:
ACS reagent
Form:
powder, crystals or chunks
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grade

ACS reagent

Quality Level

form

powder, crystals or chunks

reaction suitability

reagent type: catalyst
core: gold

concentration

≥49.0% Au

impurities

≤0.1% Insoluble in ether

cation traces

alkalies and other metals (as sulfates): ≤0.2%

storage temp.

2-8°C

SMILES string

Cl[H].[H]O[H].[H]O[H].[H]O[H].Cl[Au](Cl)Cl

InChI

1S/Au.4ClH.3H2O/h;4*1H;3*1H2/q+3;;;;;;;/p-3

InChI key

XYYVDQWGDNRQDA-UHFFFAOYSA-K

Application

Gold(III) chloride trihydrate can be used as a gold precursor salt for the production of gold nanoparticles (AuNP) using various reducing agents.
It can also be used as a catalyst in the following processes:
  • HAuCl4 3H2O inPEG 400 is used to synthesize spirochromene derivatives via a one-pot three-component reaction of isatins/acenaphthoquinone, active methylene compounds, and cyclic 1,3-diketones/4-hydroxycoumarin.      
  • Au/CeO2 catalytic system is used in chemoselective oxidation of aromatic/aliphatic alcohols to corresponding carbonyl compounds.      
  • Used in the synthesis of allylnaphthalenes by ring-opening of 1,4-epoxy-1,4-dihydronaphthalenes with allyltrimethylsilane.



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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Met. Corr. 1 - Skin Corr. 1B - STOT RE 2 Oral

target_organs

Kidney

flash_point_f

Not applicable

flash_point_c

Not applicable

Storage Class

8A - Combustible corrosive hazardous materials



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Articles

Access gold precatalysts, silver salts, and unsaturated building blocks to accelerate research success in catalysis applications.


Sang Hui Jun et al.
Journal of nanoscience and nanotechnology, 14(8), 6202-6208 (2015-05-06)
Traditional medicinal plants possess diverse active constituents for exerting their biological activities. Recently, the innovative applications of plant extracts have revealed their promise as 'green' reducing agents for the reduction of metal ions during the synthesis of metallic nanoparticles. Herein
Jairo Pinto Oliveira et al.
Scientific reports, 9(1), 13859-13859 (2019-09-27)
Antibody-coated nanoparticles have recently attracted considerable attention, with the focus falling on diagnostics. Nevertheless, controlled antibody bioconjugation remains a challenge. Here, we present two strategies of bioconjugation with the aim of evaluating the best approach for the coupling of antibodies



Global Trade Item Number

SKUGTIN
G4022-10G04061835347759
G4022-1G04061835347766
G4022-5G04061835347780
G4022-25G04061835347773