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Merck
CN

D72182

1,2-Dichloropropane

99%

Synonym(s):

Propylene dichloride

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About This Item

Linear Formula:
CH3CHClCH2Cl
CAS Number:
78-87-5
Molecular Weight:
112.99
EC Number:
201-152-2
UNSPSC Code:
12352100
PubChem Substance ID:
24894090
Beilstein/REAXYS Number:
1718880
MDL number:
MFCD00000868
Assay:
99%
Form:
liquid

Key Documents

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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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flash_point_f

59.0 °F - closed cup

signalword

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 1B - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 3

flash_point_c

15.0 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBB2939V
STBB2939
S30075
08714BZ
01113DO

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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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