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Supelco

3,4-Dichloroaniline

PESTANAL®, analytical standard

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About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
Molecular Weight:
162.02
Beilstein/REAXYS Number:
636837
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:

grade

analytical standard

product line

PESTANAL®

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

272 °C (lit.)

mp

69-71 °C (lit.)

application(s)

agriculture
environmental

format

neat

SMILES string

Nc1ccc(Cl)c(Cl)c1

InChI

1S/C6H5Cl2N/c7-5-2-1-4(9)3-6(5)8/h1-3H,9H2

InChI key

SDYWXFYBZPNOFX-UHFFFAOYSA-N

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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 - Eye Dam. 1 - Skin Sens. 1

Storage Class

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

wgk_germany

WGK 3

flash_point_f

275.0 °F - closed cup

flash_point_c

135.00 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges


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Ashley D Sawle et al.
Toxicological sciences : an official journal of the Society of Toxicology, 118(1), 128-139 (2010-08-13)
Large-scale toxicogenomic screening approaches offer great promise for generating a bias-free system-wide view of toxicological effects and modes-of-action of chemicals and ecotoxicants. However, early applications of microarray technology have identified relatively small groups of responding genes with which to define
Xie-Feng Yao et al.
Microbiology (Reading, England), 157(Pt 3), 721-726 (2010-12-18)
An efficient 3,4-dichloroaniline (3,4-DCA)-mineralizing bacterium has been isolated from enrichment cultures originating from a soil sample with a history of repeated exposure to diuron, a major metabolite of which is 3,4-DCA. This bacterium, Bacillus megaterium IMT21, also mineralized 2,3-, 2,4-
Yoshie Ito et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 152(2), 189-194 (2010-04-20)
Arylhydrocarbon receptor (Ahr) and cytochrome P4501a1 (Cyp1a1) are members of the Ahr/Cyp1a1 pathway that oxygenates various toxic chemicals including aryl hydrocarbons. To elucidate Ahr/Cyp1a1 pathway responses in teleost fish tissues, we examined the effects of 3,4-dichloroaniline (3,4-DCA), a reference toxic
Benjamin T Martin et al.
Ecotoxicology (London, England), 22(3), 574-583 (2013-02-23)
Individual-based models (IBMs) predict how dynamics at higher levels of biological organization emerge from individual-level processes. This makes them a particularly useful tool for ecotoxicology, where the effects of toxicants are measured at the individual level but protection goals are
Philip Breugelmans et al.
Research in microbiology, 161(3), 208-218 (2010-02-12)
A proteomic approach was used to explore the metabolism of the phenylurea herbicide linuron and 3,4-dichloroaniline (3,4-DCA) in Variovorax sp. WDL1. This bacterium grows on linuron as sole source of carbon, nitrogen and energy, while it transiently accumulates 3,4-DCA as

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