36030
2,4-Dichloro-1-nitrobenzene
purum, ≥98.0% (GC)
Synonym(s):
1,3-Dichloro-4-nitrobenzene, asym.-Nitro-m-dichlorobenzene
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About This Item
Linear Formula:
Cl2C6H3NO2
CAS Number:
Molecular Weight:
192.00
EC Number:
210-248-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1451655
MDL number:
grade
purum
assay
≥98.0% (GC)
bp
258 °C (lit.)
mp
29-32 °C (lit.), 30-32 °C
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
signalword
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
WGK 3
flash_point_f
305.6 °F
flash_point_c
152 °C
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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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
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