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481823

Sigma-Aldrich

Mercury(II) thiocyanate

99.99% trace metals basis

Synonym(s):

Mercuric isothiocyanate, Mercuric sulfocyanide, Mercuric thiocyanate, Mercury di(thiocyanate), Thiocyanic acid, mercury(II) salt

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About This Item

Linear Formula:
Hg(SCN)2
CAS Number:
592-85-8
Molecular Weight:
316.75
Beilstein/REAXYS Number:
3561344
EC Number:
209-773-0
MDL number:
MFCD00011039
UNSPSC Code:
12352302
PubChem Substance ID:
24871785
NACRES:
NA.23

assay

99.99% trace metals basis

form

powder

technique(s)

NMR: suitable

impurities

≤110 ppm Trace Metal Analysis

mp

165 °C (dec.) (lit.)

density

3.71 g/mL at 25 °C (lit.)

SMILES string

N#CS[Hg]SC#N

InChI

1S/2CHNS.Hg/c2*2-1-3;/h2*3H;/q;;+2/p-2

InChI key

GBZANUMDJPCQHY-UHFFFAOYSA-L

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Application

Increasing interest in solid state NMR of heavy-metal nuclei results in the preparation of several Hg-thiocyanate and selenocyanate compounds as potential models.

Disclaimer

For U.S. Customers: Contains mercury; Do not place in trash - dispose according to local, state, or federal laws.

signalword

Danger

Hazard Classifications

Acute Tox. 1 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

supp_hazards

EUH032

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

248.0 °F - closed cup

flash_point_c

120 °C - closed cup

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Certificates of Analysis (COA)

Lot/Batch Number
SLCB0955
SLBV8862
SLBM5557V
SLBC0937
SLBC0936

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M A Koupparis et al.
Journal of pharmaceutical sciences, 75(8), 800-804 (1986-08-01)
An automated flow-injection determination of chloride salts of drugs, based on the colorimetric mercurothiocyanate determination of chloride counterion is described. The majority of these drugs can be determined, using chloride ion standards, with a coefficient of variation less than 1%
Bowmaker, G.A. et al.
Inorganic Chemistry, 37, 1734-1734 (1998)
Ajit Kumar et al.
World journal of microbiology & biotechnology, 31(8), 1211-1216 (2015-05-11)
Xanthobacter autotrophicus GJ10 has been widely studied because of its ability to degrade halogenated compounds, especially 1,2-dichloroethane (1,2-DCA), which is achieved through chromosomal as well as plasmid pAUX1 encoded 1,2-DCA degrading genes. This work described the gene expression and enzyme

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