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Safety Information

12-1430

Sigma-Aldrich

Gold(III) chloride

SAJ special grade (dihydrate), ≥98.5%

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About This Item

Linear Formula:
AuCl3
CAS Number:
13453-07-1
Molecular Weight:
303.33
EC Number:
236-623-1
MDL number:
MFCD00014172
UNSPSC Code:
12352300
PubChem Substance ID:
329749639

grade

SAJ special grade (dihydrate)

Assay

≥98.5%

reaction suitability

reagent type: catalyst
core: gold

availability

available only in Japan

SMILES string

Cl[Au](Cl)Cl

InChI

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

InChI key

RJHLTVSLYWWTEF-UHFFFAOYSA-K

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

PDSCL

Deleterious substance

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

12-1430-1-1G-J:

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Certificates of Analysis (COA)

Lot/Batch Number
U8671
U4631
U0457
U0364
U5236

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Ahmed A Elzatahry et al.
International journal of nanomedicine, 7, 2829-2832 (2012-06-30)
This report concerns nanofiber composites that incorporate N-heterocyclic carbenes and the use of such composites for testing antimicrobial and antifungal activities. The nanofiber composites were produced by electrospinning mixtures of the gold chloride or gold acetate complexes of a bis(imino)acenaphthene
Vanajakshi Gudla et al.
The Journal of organic chemistry, 76(24), 9919-9933 (2011-10-28)
An intramolecular approach to generate compounds containing an arylnaphthalene lignan scaffold in high yields is presented. It involves a sequential intramolecular electrophilic attack of carbonyl on arylalkyne followed by benzannulation catalyzed by gold salt. AuCl(3) in combination with AgSbF(6) works
Zhi-Xiong Ma et al.
Organic letters, 14(22), 5736-5739 (2012-11-06)
An imino-Nazarov cyclization using α-aryl-substituted allenamides is described. This gold(I)-catalyzed cascade is efficient and regioselective in constructing a diverse array of synthetically useful aromatic-ring fused cyclopentenamides. The success in this transformation represents a solution to the challenge in establishing an
Muthu Irulappan Sriram et al.
Methods in molecular biology (Clifton, N.J.), 906, 33-43 (2012-07-14)
Owing to the wide-ranging applications of noble metal nanoparticles in diverse areas of science and technology, different methods have been proposed for their synthesis. Here, we describe the methods for the intracellular biosynthesis of silver and gold nanoparticles using the
Yuanjing Xiao et al.
Organic letters, 14(17), 4662-4665 (2012-08-25)
The cyclic α-imino gold carbene intermediate B is most likely generated in situ via regioselective nitrene transfer from an azido group to a tethered terminal alkyne in the presence of a gold catalyst and at ambient temperature. This highly electrophilic
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