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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:
InChI key
QUIMTLZDMCNYGY-UHFFFAOYSA-N
InChI
1S/C6H3Cl2NO2/c7-4-1-2-6(9(10)11)5(8)3-4/h1-3H
SMILES string
[O-][N+](=O)c1ccc(Cl)cc1Cl
grade
purum
assay
≥98.0% (GC)
bp
258 °C (lit.)
mp
29-32 °C (lit.), 30-32 °C
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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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
Maja Aleksic et al.
Toxicology in vitro : an international journal published in association with BIBRA, 21(4), 723-733 (2007-02-24)
Covalent modification of skin proteins by electrophiles is a key event in the induction of skin sensitisation but not skin irritation although the exact nature of the binding mechanisms has not been determined empirically for the vast majority of sensitisers.
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
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