D72182
1,2-二氯丙烷
99%
别名:
二氯化丙烯
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关于此项目
线性分子式:
CH3CHClCH2Cl
化学文摘社编号:
分子量:
112.99
EC Number:
201-152-2
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1718880
MDL number:
Assay:
99%
Form:
liquid
InChI key
KNKRKFALVUDBJE-UHFFFAOYSA-N
InChI
1S/C3H6Cl2/c1-3(5)2-4/h3H,2H2,1H3
SMILES string
CC(Cl)CCl
vapor density
3.89 (vs air)
vapor pressure
40 mmHg ( 19.4 °C)
assay
99%
form
liquid
autoignition temp.
1035 °F
expl. lim.
14.5 %
bp
95-96 °C (lit.)
mp
−100 °C (lit.)
density
1.156 g/mL at 25 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Flam. Liq. 2
存储类别
3 - Flammable liquids
wgk
WGK 3
flash_point_f
59.0 °F - closed cup
flash_point_c
15.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
J C Hage et al.
Applied microbiology and biotechnology, 57(4), 548-554 (2002-01-05)
Pseudomonas sp. strain DCA1, which is capable of utilizing 1,2-dichloroethane (DCA) as sole carbon and energy source, was used to oxidize chlorinated methanes, ethanes, propanes, and ethenes. Chloroacetic acid, an intermediate in the DCA degradation pathway of strain DCA1, was
Aaron J Oakley et al.
Biochemistry, 41(15), 4847-4855 (2002-04-10)
The hydrolysis of haloalkanes to their corresponding alcohols and inorganic halides is catalyzed by alpha/beta-hydrolases called haloalkane dehalogenases. The study of haloalkane dehalogenases is vital for the development of these enzymes if they are to be utilized for bioremediation of
Kirsti M Ritalahti et al.
Applied and environmental microbiology, 70(7), 4088-4095 (2004-07-09)
1,2-Dichloropropane (1,2-D), a widespread groundwater contaminant, can be reductively dechlorinated to propene by anaerobic bacteria. To shed light on the populations involved in the detoxification process, a comprehensive 16S rRNA gene-based bacterial community analysis of two enrichment cultures derived from
Piotr Cysewski et al.
Chemosphere, 63(1), 165-170 (2005-09-09)
Studies on oxidation of tert-butyl ethers in the presence of chloride ions proved that acid medium favoured formation of chloro organic compounds. 1,2-Dichloro-2-methylpropane, 3-chloro-2-chloromethylpropene were identified among the reaction products. Presence of these compounds was identified both in the case
Kelly E Fletcher et al.
Environmental science & technology, 43(18), 6915-6919 (2009-10-08)
The isotope fractionation of 1,2-dichloropropane (1,2-D) during dichloroelimination to propene by Dehalococcoides populations was explored in laboratory experiments in order to provide data for the characterization of the fate of 1,2-D in heterogeneous subsurface systems. Compound specific stable carbon isotope
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