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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/REAXYS Number:
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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Disclaimer

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

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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

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

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
09913DE
05118PD
13620TC
06418TB
00601CX

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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
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
J Raszyk et al.
Veterinarni medicina, 37(7), 379-391 (1992-07-01)
Four gilts, sisters from one litter, aged 70 days and weighing 20-24 kg, were used for a trial. Two experimental gilts (P) were administered an experimental feed mixture containing phenylmercury chloride (40 mg/kg). Two control gilts (K) were fed the
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