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P27135

Sigma-Aldrich

Phenylmercuric chloride

Synonym(s):

Phenylmercury chloride

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About This Item

Linear Formula:
C6H5HgCl
CAS Number:
100-56-1
Molecular Weight:
313.15
Beilstein:
3536717
EC Number:
202-865-1
MDL number:
MFCD00000463
UNSPSC Code:
12352103
PubChem Substance ID:
24898355

mp

248-250 °C (dec.) (lit.)

SMILES string

Cl[Hg]c1ccccc1

InChI

1S/C6H5.ClH.Hg/c1-2-4-6-5-3-1;;/h1-5H;1H;/q;;+1/p-1

InChI key

AWGTVRDHKJQFAX-UHFFFAOYSA-M

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Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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J Chmielnicka et al.
Ecotoxicology and environmental safety, 7(2), 165-171 (1983-04-01)
The effect of sodium selenite on the activity of the selected enzymes in blood serum and on mercury concentration in some tissues of guinea pigs exposed to ethyl- (EtHg) or phenylmercuric chloride (PhHg) was investigated. Every second day for a
M Maretta et al.
Acta veterinaria Hungarica, 43(1), 153-161 (1995-01-01)
Phenylmercuric chloride was applied in three doses (5 ppm, 30 ppm Hg, and 30 ppm Hg + 4 ppm Se) via the food for 60 days. The effect of Hg with an without Se was studied histologically and the data
T Sorsa et al.
Medical biology, 63(2), 66-72 (1985-01-01)
Latent and active collagenase were extracted from human polymorphonuclear leukocytes. Separation of the two forms of the enzyme was performed by gel filtration on Sepharose 6 B. The latent form of the enzyme was detected from chromatographic fractions after a
Gelatinases/type IV collagenases in jaw cyst expansion.
O Teronen et al.
Annals of the New York Academy of Sciences, 732, 486-488 (1994-09-06)
V Lemau de Talancé et al.
Bioorganic & medicinal chemistry letters, 21(24), 7265-7267 (2011-11-15)
This study describes two novel synthetic procedures to prepare APM, a useful tool for the analysis and the purification of thiolated biomolecules. The methods developed are technically simple and robust and allowed the first full characterization of pure APM. Moreover
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