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Merck
CN

46012

Pentachloroaniline

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H2Cl5N
CAS Number:
527-20-8
Molecular Weight:
265.35
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329757053
EC Number:
208-410-3
Beilstein/REAXYS Number:
2806732
MDL number:
MFCD00014769

Key Documents

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Product Name

Pentachloroaniline, PESTANAL®, analytical standard

InChI key

KHCZSJXTDDHLGJ-UHFFFAOYSA-N

InChI

1S/C6H2Cl5N/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H2

SMILES string

Nc1c(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
gas chromatography (GC): suitable

application(s)

agriculture
environmental

format

neat

Quality Level

100

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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

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK3697
BCBW9627
BCBW4600

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Yan Wang et al.
Ecotoxicology and environmental safety, 182, 109463-109463 (2019-07-28)
To eliminate pentachloronitrobenzene (PCNB) residue in PCNB-contaminated environment, the degradation potential of Pseudomonas putida QTH3 to PCNB was evaluated in this study. Peudomonas putida QTH3 could grow well in mineral salt medium (MSM) containing PCNB as sole carbon and was
Y Fushiwaki et al.
The Science of the total environment, 92, 55-67 (1990-03-01)
Environmental pollution by pentachloronitrobenzene (PCNB) was investigated at Tsumagoi, an intensive farming area, where a great amount of PCNB has been applied. High concentrations of PCNB were detected in river water near an area of cabbage cultivation. Further, pentachloroaniline (PCA)
Adriana Longoria et al.
Chemosphere, 72(3), 485-490 (2008-04-29)
Peroxidase transformations of widely distributed pollutants, tetra- and penta-chlorinated phenols and anilines, were studied using different peroxidases. Chloroperoxidase from Caldariomyces fumago was able to transform tetra- and penta-chlorinated phenols and anilines, while horseradish peroxidase, lignin peroxidase from Phanerochaete chrysosporium and
Didem Okutman Tas et al.
Environmental science & technology, 40(14), 4467-4472 (2006-08-15)
The microbial reductive dechlorination kinetics of pentachloroaniline (PCA) and less chlorinated anilines (CAs) were investigated with a mixed, fermentative/ methanogenic culture. Batch dechlorination assays were performed with all available CAs at an initial concentration of 3 microM, and an incubation
G Renner
Xenobiotica; the fate of foreign compounds in biological systems, 10(7-8), 537-550 (1980-07-01)
The metabolism of PCNB in rats was studied. Metabolites isolated from rat excreta and identified were: N-acetyl-S-(pentachlorophenyl)cysteine, pentachlorothiophenol, pentachlorothioanisole, 2,3,4,5-tetrachlorothiophenol, 2,3,4,5-tetrachlorothioanisole, 2,3,4,6- and/or 2,3,5,6-tetrachloro-thiophenol and -thioanisole, 1,4-bis(methylthio)tetrachlorobenzene, 1,4-dimercapto-tetrachlorobenzene and/or 4-methylthio-tetrachlorothiophenol, pentachlorophenol, pentachloroanisole, 2,3,4,5-tetrachlorophenol, 2,3,4,5-tetrachloroanisole, 2,3,4,6- and/or 2,3,5,6-tetrachloro-phenol and -anisole, pentachlorobenzene
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