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D68401

Sigma-Aldrich

2,4-Dichloro-1-nitrobenzene

97%

Synonym(s):

1,3-Dichloro-4-nitrobenzene, asym.-Nitro-m-dichlorobenzene

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About This Item

Linear Formula:
Cl2C6H3NO2
CAS Number:
611-06-3
Molecular Weight:
192.00
Beilstein/REAXYS Number:
1451655
EC Number:
210-248-3
MDL number:
MFCD00007071
UNSPSC Code:
12352100
PubChem Substance ID:
24894055

assay

97%

form

solid

bp

258 °C (lit.)

mp

29-32 °C (lit.)

SMILES string

[O-][N+](=O)c1ccc(Cl)cc1Cl

InChI

1S/C6H3Cl2NO2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H

InChI key

QUIMTLZDMCNYGY-UHFFFAOYSA-N

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Muta. 2 - Skin Sens. 1B

Storage Class

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

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ8561
STBJ7474
STBH8136
STBH0558
STBG3891V

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Makoto Ohnishi et al.
The Journal of toxicological sciences, 34(2), 233-237 (2009-04-02)
Oral administration of 2,4-dichloro-1-nitrobenzene (2,4-DCNB) causes kidney tumors in the rat. The objective of the present study was to identify the chemical structure of 2,4-DCNB metabolites in urine. Urine from 2,4-DCNB fed rats was more yellow than urine from control
P A Botham et al.
The British journal of dermatology, 117(1), 1-9 (1987-07-01)
The fate of 2,4-dinitrochlorobenzene, a potent contact sensitizing chemical, and 2,4-dichloronitrobenzene, a non-sensitizer, was compared following their application to the skin of BALB/c mice. Although both chemicals were able to bind to protein in vitro and were capable of being
Maja Aleksic et al.
Toxicology in vitro : an international journal published in association with BIBRA, 22(5), 1169-1176 (2008-04-29)
A large proportion of allergic skin reactions are considered to be the result of skin exposure to small organic chemicals that possess the intrinsic ability to covalently modify skin proteins, either directly or following activation. In the absence of information
V Breinholt et al.
Cancer letters, 154(2), 201-210 (2000-05-12)
The administration of lycopene to female rats at doses ranging from 0.001 to 0.1 g/kg b.w. per day for 2 weeks was found to alter the drug-metabolizing capacity and antioxidant status of the exposed animals. An investigation of four cytochrome
Bruno Miguel Neves et al.
Toxicology letters, 177(1), 74-82 (2008-02-19)
The development of non-animal methods for skin sensitization testing is an urgent challenge. Some of the most promising in vitro approaches are based on the analysis of phenotypical and functional modifications induced by sensitizers in dendritic cell models. In this
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