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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

Certificates of Analysis (COA)

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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)
James E Keller et al.
Neurochemical research, 28(3-4), 477-482 (2003-04-05)
Previous work had demonstrated that organomercurial-mediated modification of two cysteine residues in the vesicular acetylcholine transporter (VAChT) from Torpedo californica inhibits binding of vesamicol. The cysteines are protected by acetylcholine and vesamicol (Keller et al. 2000. J. Neurochem. 74:1739-1748). Modified
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