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关于此项目
线性分子式:
Cl2C6H3NO2
化学文摘社编号:
分子量:
192.00
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-764-2
Beilstein/REAXYS Number:
1818163
MDL number:
Assay:
99%
Form:
crystals
InChI key
NTBYINQTYWZXLH-UHFFFAOYSA-N
InChI
1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H
SMILES string
[O-][N+](=O)c1ccc(Cl)c(Cl)c1
assay
99%
form
crystals
bp
255-256 °C (lit.)
Quality Level
mp
39-41 °C (lit.)
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
255.2 °F - closed cup
flash_point_c
124 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
危险化学品
此项目有
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, 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
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, 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
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
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