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D55792

Sigma-Aldrich

3,5-Dichloroaniline

≥97%

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About This Item

Linear Formula:
Cl2C6H3NH2
CAS Number:
626-43-7
Molecular Weight:
162.02
Beilstein:
636492
EC Number:
210-948-9
MDL number:
MFCD00007774
UNSPSC Code:
12352100
PubChem Substance ID:
24893944
NACRES:
NA.22

Quality Level

200

Assay

≥97%

form

crystals

bp

259-260 °C/741 mmHg (lit.)

mp

46-52 °C (lit.)

SMILES string

Nc1cc(Cl)cc(Cl)c1

InChI

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

InChI key

UQRLKWGPEVNVHT-UHFFFAOYSA-N

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Signal Word

Danger

Hazard Classifications

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

Target Organs

Kidney

Storage Class Code

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

WGK

WGK 3

Flash Point(F)

271.4 °F - closed cup

Flash Point(C)

133 °C - closed cup

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Multiresidue determination of fungicides in wine.
M A García et al.
Bulletin of environmental contamination and toxicology, 62(6), 717-722 (1999-06-03)
H H Lo et al.
Journal of applied toxicology : JAT, 14(6), 417-422 (1994-11-01)
Chloroanilines are widely used chemical intermediates for the manufacture of dyes, agricultural chemicals and industrial compounds. Nephrotoxicity occurs as one toxicity following intraperitoneal (i.p.) administration of chloroaniline hydrochlorides to rats. The purpose of this study was to examine the effect
Reversed-phase high-performance liquid chromatography of pesticides. VII. Analysis of Vinclozolin, Iprodione, Procymidone, Dichlozolinate and their degradation product 3,5-dichloroaniline on white must and wine extracts.
P Cabras et al.
Journal of chromatography, 256(1), 176-181 (1983-01-28)
M A Valentovic et al.
Toxicology letters, 78(3), 207-214 (1995-08-01)
3,5-Dichloroaniline (3,5-DCA), a derivative needed in the manufacture of dyes, pesticides and industrial compounds has been reported to induce renal damage. This study investigated whether pretreatment with inducers or inhibitors of P450 altered 3,5-DCA toxicity. P450 levels were induced in
Christian H Lindh et al.
Rapid communications in mass spectrometry : RCM, 21(4), 536-542 (2007-01-25)
The fungicides vinclozolin and iprodione are widely used in agriculture. These pesticides are dicarboximide fungicides containing the common moiety 3,5-dichloroaniline (3,5-DCA). It has been suggested that low-level exposures to such compounds may be associated with adverse health effects such as
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