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P27135

Sigma-Aldrich

Phenylmercuric chloride

Sinônimo(s):

Phenylmercury chloride

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About This Item

Fórmula linear:
C6H5HgCl
Número CAS:
Peso molecular:
313.15
Beilstein:
3536717
Número CE:
Número MDL:
Código UNSPSC:
12352103
ID de substância PubChem:

pf

248-250 °C (dec.) (lit.)

cadeia de caracteres SMILES

Cl[Hg]c1ccccc1

InChI

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

chave InChI

AWGTVRDHKJQFAX-UHFFFAOYSA-M

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Exoneração de responsabilidade

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

Palavra indicadora

Danger

Classificações de perigo

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

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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


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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
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
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
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

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