535346
Pentachlorothiophenol
96%
Synonym(s):
Pentachlorobenzenethiol
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About This Item
Linear Formula:
C6Cl5SH
CAS Number:
Molecular Weight:
282.40
EC Number:
205-107-8
UNSPSC Code:
12352100
MDL number:
Product Name
Pentachlorothiophenol, 96%
InChI key
LLMLGZUZTFMXSA-UHFFFAOYSA-N
InChI
1S/C6HCl5S/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H
SMILES string
Sc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
assay
96%
mp
223-227 °C (lit.)
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Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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J To-Figueras et al.
Toxicology letters, 56(1-2), 87-94 (1991-04-01)
The appearance of sex-related differences in the excretion of sulphur derivatives of hexachlorobenzene (HCB) and pentachloronitrobenzene (PCNB) was studied in vitro and in vivo. Sexually immature rats given HCB showed initially no differences in the excretion of N-acetyl-S-(pentachlorophenyl)cysteine, but 5-8
M D'Amour et al.
Toxicology and applied pharmacology, 112(2), 229-234 (1992-02-01)
Hexachlorobenzene (HCB) induces hepatic porphyria and liver cancer in female rats, whereas toxicity is minimal in male rats. HCB is biotransformed to sulfur-containing metabolites originating from conjugation to glutathione (GSH). This study aimed to assess differences in GSH conjugation of
Conversion products of hexachlorobenzene and their role in the disturbance of the porphyrin pathway in rats.
G Koss et al.
The International journal of biochemistry, 12(5-6), 1003-1006 (1980-01-01)
N Legault et al.
Biochemical pharmacology, 54(1), 19-25 (1997-07-01)
Hexachlorobenzene (HCB) is porphyrinogenic in adult female but not in male rats. This study aimed to assess the role of 17beta-estradiol in the induction of porphyria by HCB in both sexes by adding or removing the hormone. Groups of intact
Ramadan A Abuknesha et al.
Analytical and bioanalytical chemistry, 379(3), 411-418 (2004-04-23)
A polyclonal antiserum to pentachlorothiophenol-acetic acid-KLH was generated in sheep and assessed by solid phase ELISA. The assessment procedure included use of double checkerboard analysis in the absence and in the presence of analyte loads, estimation of cross reactivities of
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