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Merck
CN

36928

1,2,3,5-Tetrachlorobenzene

PESTANAL®, analytical standard

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About This Item

Empirical Formula (Hill Notation):
C6H2Cl4
CAS Number:
634-90-2
Molecular Weight:
215.89
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329755543
EC Number:
211-217-7
Beilstein/REAXYS Number:
1618864
MDL number:
MFCD00000543

Key Documents

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Product Name

1,2,3,5-Tetrachlorobenzene, PESTANAL®, analytical standard

InChI key

QZYNWJQFTJXIRN-UHFFFAOYSA-N

InChI

1S/C6H2Cl4/c7-3-1-4(8)6(10)5(9)2-3/h1-2H

SMILES string

Clc1cc(Cl)c(Cl)c(Cl)c1

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.

Other Notes

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.

Legal Information

PESTANAL is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation markEnvironment
GHS07,GHS09

signalword

Warning

hcodes

H302,H410

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
BCCG4657
BCBT5756

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Peter Kämpfer et al.
International journal of systematic and evolutionary microbiology, 54(Pt 3), 749-751 (2004-05-15)
A Gram-positive, rod-shaped, non-spore-forming bacterium (B5(T)) was isolated from an enrichment culture that contained 1,2,3,5-tetrachlorobenzene as the sole source of carbon. On the basis of 16S rRNA gene sequence similarity studies, strain B5(T) was shown to belong to the family
Mei Sun et al.
Environmental science & technology, 44(21), 8209-8215 (2010-10-01)
Sediment caps that degrade contaminants can improve their ability to contain contaminants relative to sand and sorbent-amended caps, but few methods to enhance contaminant degradation in sediment caps are available. The objective of this study was to determine if, carbon
W De Wolf et al.
Comparative biochemistry and physiology. C, Comparative pharmacology and toxicology, 100(1-2), 55-57 (1991-01-01)
1. Seven chlorinated anilines and one chlorinated benzene were tested for their ability to bioconcentrate in guppies (Poecilia reticulata) under different experimental conditions. 2. Interactions between compounds in a mixture influence the bioconcentration of some chlorinated anilines. These interactions result
Koji Ito et al.
Journal of pesticide science, 44(3), 171-176 (2019-09-19)
The substrate range of Nocardioides sp. strain PD653, capable of mineralizing hexachlorobenzene, was investigated based on the dissipation of substrates and the liberation of halogen ions. Strain PD653 dehalogenated 10 out of 18 halophenol congeners; however, it could dehalogenate only
B Z Fathepure et al.
Applied and environmental microbiology, 54(2), 327-330 (1988-02-01)
Hexachlorobenzene was dechlorinated to tri- and dichlorobenzenes in anaerobic sewage sludge. The complete biotransformation of 190 microM hexachlorobenzene (approximately 50 ppm) occurred within 3 weeks. The calculated rate of hexachlorobenzene dechlorination was 13.6 mumol liter-1 day-1. Hexachlorobenzene was dechlorinated via
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