33367
甲基五氯苯基硫醚
PESTANAL®, analytical standard
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关于此项目
经验公式（希尔记法）:
C7H3Cl5S
化学文摘社编号:
分子量:
296.43
EC Number:
217-363-8
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
2214412
MDL number:
InChI key
LGZZJTIUEJNNKV-UHFFFAOYSA-N
InChI
1S/C7H3Cl5S/c1-13-7-5(11)3(9)2(8)4(10)6(7)12/h1H3
SMILES string
CSc1c(Cl)c(Cl)c(Cl)c(Cl)c1Cl
grade
analytical standard
product line
PESTANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, NMR: suitable, gas chromatography (GC): suitable
mp
92-96 °C
suitability
passes test for identity (NMR)
application(s)
agriculture
environmental
format
neat
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Legal Information
PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
hcodes
Hazard Classifications
Aquatic Chronic 4
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
J A Gustafsson et al.
Nutrition and cancer, 2(4), 224-231 (1981-01-01)
The metabolism of four xenobiotics, pentachloromethylthiobenzene, 2-chloro-n-iso-propylacetanilide, 2-acetamido-4-(chloromethyl) thiazole and 2,4',5-trichlorobiphenyl, which are known to be metabolized via the mercapturic acid pathway, was examined in germfree and conventional rats. An essential role for the intestinal flora in the metabolism of
Cara L Ferreira et al.
Bioconjugate chemistry, 23(11), 2239-2246 (2012-10-06)
In this study, a bifunctional version of the chelate PCTA was compared to the analogous NOTA derivative for peptide conjugation, (68)Ga radiolabeling, and small peptide imaging. Both p-SCN-Bn-PCTA and p-SCN-Bn-NOTA were conjugated to cyclo-RGDyK. The resulting conjugates, PCTA-RGD and NOTA-RGD
Hexachlorobenzene (HCB) and some of its sulfur-containing metabolites: tissue retention and excretion routes in mice.
I Brandt et al.
Developments in toxicology and environmental science, 8, 627-630 (1980-01-01)
D J Mulford et al.
Xenobiotica; the fate of foreign compounds in biological systems, 21(5), 597-603 (1991-05-01)
1. The metabolism of pentachlorothioanisole to bis-(methylthio)tetrachlorobenzene was shown to involve turnover of about 50% of the original methylthio group. 2. Metabolites of the displaced methylthio group were methanesulphinic acid and sulphate in the urine, carbon dioxide in the expired
Y Kato et al.
Journal of pharmacobio-dynamics, 13(5), 278-284 (1990-05-01)
Effects of hexachlorobenzene (HCB) and its sulfur-containing metabolites on the heme metabolic enzymes in rat liver were investigated. A single injection of HCB caused the increase in activities of delta-aminolevulinic acid (ALA) synthetase and heme oxygenase, and contents of cytochrome
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