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D72603

Sigma-Aldrich

2,3-Dichloro-1-propene

98%

Synonym(s):

2,3-Dichloro-1-propene, 2,3-Dichloropropene, 2,3-Dichloropropylene, 2-Chloroallyl chloride

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About This Item

Linear Formula:
ClCH2CCl=CH2
CAS Number:
78-88-6
Molecular Weight:
110.97
Beilstein:
1361491
EC Number:
201-153-8
MDL number:
MFCD00000943
UNSPSC Code:
12352100
PubChem Substance ID:
24894096
NACRES:
NA.22

vapor density

3.8 (vs air)

Quality Level

100

vapor pressure

44 mmHg ( 20 °C)

Assay

98%

form

liquid

expl. lim.

7.8 %

refractive index

n20/D 1.461 (lit.)

bp

94 °C (lit.)

density

1.204 g/mL at 25 °C (lit.)

SMILES string

ClCC(Cl)=C

InChI

1S/C3H4Cl2/c1-3(5)2-4/h1-2H2

InChI key

FALCMQXTWHPRIH-UHFFFAOYSA-N

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Related Categories

Signal Word

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

50.0 °F - closed cup

Flash Point(C)

10 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW7162
MKCW7123
MKCX0389
MKCW5407
MKCS9660

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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
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
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
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
J S Dutcher et al.
Fundamental and applied toxicology : official journal of the Society of Toxicology, 5(5), 997-1005 (1985-10-01)
2,3-Dichloropropene (DCP) is an intermediate used in the manufacture of carbamate herbicides and there is potential for human exposure during the manufacturing process. DCP is a known mutagen in bacteria systems and some structural analogs of DCP are carcinogenic. Since
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