D72603
2,3-二氯丙烯
98%
别名:
2,3-Dichloro-1-propene, 2,3-Dichloropropene, 2,3-Dichloropropylene, 2-Chloroallyl chloride
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关于此项目
线性分子式:
ClCH2CCl=CH2
化学文摘社编号:
分子量:
110.97
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
201-153-8
Beilstein/REAXYS Number:
1361491
MDL number:
Assay:
98%
Form:
liquid
InChI
1S/C3H4Cl2/c1-3(5)2-4/h1-2H2
InChI key
FALCMQXTWHPRIH-UHFFFAOYSA-N
SMILES string
ClCC(Cl)=C
vapor density
3.8 (vs air)
vapor pressure
44 mmHg ( 20 °C)
assay
98%
form
liquid
expl. lim.
7.8 %
Quality Level
bp
94 °C (lit.)
density
1.204 g/mL at 25 °C (lit.)
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Dam. 1 - Flam. Liq. 2 - Muta. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
50.0 °F - closed cup
flash_point_c
10 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
E Eder et al.
Drug metabolism and disposition: the biological fate of chemicals, 16(1), 60-68 (1988-01-01)
At the present time, comprehensive metabolism studies of 2,3-dichloro-1-propene (2,3-DCP) have not yet been reported. We have investigated the biotransformation of 2,3-DCP using female Wistar rats in order to elucidate the bioactivation mechanisms. 175 mg/kg, 1,3-14C-2,3-DCP in corn oil was
M A Medinsky et al.
Toxicology letters, 23(1), 119-125 (1984-10-01)
2,3-Dichloropropene (2,3-DCP), a component of commercial fumigants and nematocides, was mixed with [14C]2,3-DCP and given to rats by peroral (p.o.) or intraperitoneal (i.p.) administration. Urine, feces, and expired air were collected over 72 h. Excretion of radioactivity in urine predominated
Roland P H Schmitz et al.
Environmental science & technology, 41(21), 7370-7375 (2007-11-30)
The reductive dehalogenation of chlorinated propenes was studied with the tetrachloroethene reductive dehalogenase purified from Sulfurospirillum multivorans to obtain indications for a radical mechanism of this reaction. When reduced methyl viologen (MV), which is a radical cation, was applied as
I Cascorbi et al.
Ecotoxicology and environmental safety, 30(3), 252-258 (1995-04-01)
Previously the toxicity of 45 heterogeneous environmental chemicals on growth and membrane functions in Saccharomyces cerevisiae and Chinese hamster ovary (CHO) cells (Cascorbi et al., 1993) was examined. In this study the inhibitory effects of the same set of chemicals
T Neudecker et al.
Mutation research, 170(1-2), 1-9 (1986-04-01)
In the presence of S9 mix all allylic chloropropenes tested exert considerable indirect mutagenic activity which is most pronounced for 1,2,3-trichloropropene. Lower as well as higher chlorinated derivatives are clearly less mutagenic. Longer than standard incubation time (120 min instead
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