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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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
E Egaas
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 127(2), 117-122 (2000-11-18)
Atrazine (1,000 ppm), endosulfan (1 ppm) or butylated hydroxyanisole (BHA) (1,000 ppm) added to a semi-synthetic diet of Orthosia gothica for 2 days in the last instar did not change the soft tissue cytosolic glutathione-S-transferase (GST) activities towards 1-chloro-2,4-dinitrobenzene (CDNB)
Susila Sivapathasundaram et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 134(1), 169-173 (2003-01-14)
The ability of cattle and deer liver to catalyse xenobiotic conjugation reactions was investigated and compared with that of the rat. Marked differences in the activity of these enzymes were noted between the domestic animals and rats. Hepatic microsomal epoxide
M Arivazhagan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 79(2), 376-383 (2011-04-07)
The Fourier-transform infrared spectrum of 1,2-dichloro-4-nitrobenzene (DCNB) was recorded in the region 4000-400cm(-1). The Fourier-transform Raman spectrum of DCNB was also recorded in the region 3500-50cm(-1). Quantum chemical calculations of energies, geometrical structure and vibrational wavenumbers of DCNB were carried
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