25460
1-Chloro-2-nitrobenzene
purum, ≥99.0% (GC)
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About This Item
Linear Formula:
ClC6H4NO2
CAS Number:
Molecular Weight:
157.55
EC Number:
201-854-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
509273
MDL number:
vapor density
5.4 (vs air)
vapor pressure
0.04 mmHg ( 25 °C)
grade
purum
assay
≥99.0% (GC)
autoignition temp.
500 °F
expl. lim.
8.7 %
bp
246 °C (lit.)
mp
31-33 °C (lit.)
density
1.348 g/mL at 25 °C (lit.)
SMILES string
[O-][N+](=O)c1ccccc1Cl
InChI
1S/C6H4ClNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H
InChI key
BFCFYVKQTRLZHA-UHFFFAOYSA-N
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Oral
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
wgk
WGK 3
flash_point_f
258.8 °F - closed cup
flash_point_c
126 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
Regulatory Information
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Haizhen Wu et al.
Journal of environmental sciences (China), 21(1), 89-95 (2009-05-01)
A bacterial strain that utilized o-chloronitrobenzene (o-CNB) as the sole carbon, nitrogen and energy sources was isolated from an activated sludge collected from an industrial waste treatment plant. It was identified as Pseudomonas putida based on its morphology, physiological, and
Hong Liu et al.
Applied and environmental microbiology, 77(13), 4547-4552 (2011-05-24)
Pseudomonas stutzeri ZWLR2-1 utilizes 2-chloronitrobenzene (2CNB) as a sole source of carbon, nitrogen, and energy. To identify genes involved in this pathway, a 16.2-kb DNA fragment containing putative 2CNB dioxygenase genes was cloned and sequenced. Of the products from the
Enhanced catalytic degradation process of o-nitrochlorobenzene by palladium-catalyzed fe0 particles.
Xin-hua Xu et al.
Journal of environmental sciences (China), 17(5), 849-852 (2005-11-30)
Over Pd/Fe bimetallic catalyst, o-nitrochlorobenzene (o-NCB), at a concentration of 20 mg/L in aqueous solutions, is rapidly converted to o-chloroaniline (o-CAN) first, and then quickly dechlorinated to aniline(AN) and Cl-, without other intermediate reaction products. The aminated and dechlorinated reactions