D68800
1,2-Dichloro-4-nitrobenzene
99%
Synonym(s):
3,4-Dichloronitrobenzene, asym.-Nitro-o-dichlorobenzene
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All Photos(2)
About This Item
Linear Formula:
Cl2C6H3NO2
CAS Number:
Molecular Weight:
192.00
Beilstein:
1818163
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
crystals
bp
255-256 °C (lit.)
mp
39-41 °C (lit.)
SMILES string
[O-][N+](=O)c1ccc(Cl)c(Cl)c1
InChI
1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H
InChI key
NTBYINQTYWZXLH-UHFFFAOYSA-N
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Related Categories
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
255.2 °F - closed cup
Flash Point(C)
124 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Shingo Arakawa et al.
Drug metabolism and disposition: the biological fate of chemicals, 38(9), 1545-1552 (2010-06-22)
A specific substrate to Mu class glutathione S-transferase (GST), 1,2-dichloro-4-nitrobenzene (DCNB), was administered to mice with a disrupted GST Mu 1 gene (Gstm1-null mice) to investigate the in vivo role of murine Gstm1 in toxicological responses to DCNB. A single
Toshiyuki Watanabe et al.
Archives of toxicology, 78(4), 218-225 (2003-12-20)
Liver and kidney glutathione S-transferase (GST) activities to 1,2-dichloro-4-nitrobenzene (DCNB) as a substrate (GST-D activities) were measured in 280 dogs from five different breeders, and significant individual differences in this activity were observed in both organs. Interestingly, 34 out of
V R Yoxall et al.
Archives of toxicology, 78(8), 477-482 (2004-03-23)
Rats were exposed to black tea (2.5% w/v) as their sole drinking liquid for either 1 day or 1 month, while controls were maintained on water. After this treatment period, all animals received a single oral dose IQ (2-amino-3-methylimidazo-[4,5-f]quinoline), and
Toshiyuki Watanabe et al.
Archives of toxicology, 80(5), 250-257 (2005-10-21)
We have reported the existence of low glutathione S-transferase (GST) dogs whose GST activity to 1,2-dichloro-4-nitrobenzene (DCNB) as a substrate (GST-D activity) is quite low, and have also reported significant individual differences in dog liver GST-D activity. The dogs were
L O Hansson et al.
Protein science : a publication of the Protein Society, 8(12), 2742-2750 (2000-01-13)
Two human Mu class glutathione transferases, hGST M1-1 and hGST M2-2, with high sequence identity (84%) exhibit a 100-fold difference in activities with the substrates aminochrome, 2-cyano-1,3-dimethyl-1-nitrosoguanidine (cyanoDMNG), and 1,2-dichloro-4-nitrobenzene (DCNB), hGST M2-2 being more efficient. A sequence alignment with
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