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Merck
CN

36319

2,3-Dichloro-1-propene

purum, ≥97.0% (GC)

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About This Item

Linear Formula:
ClCH2CCl=CH2
CAS Number:
78-88-6
Molecular Weight:
110.97
EC Number:
201-153-8
UNSPSC Code:
12352100
PubChem Substance ID:
24862353
Beilstein/REAXYS Number:
1361491
MDL number:
MFCD00000943

Key Documents

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vapor density

3.8 (vs air)

vapor pressure

44 mmHg ( 20 °C)

grade

purum

assay

≥97.0% (GC)

expl. lim.

7.8 %

refractive index

n20/D 1.461

bp

94 °C (lit.)

density

1.204 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

ClCC(Cl)=C

InChI

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

InChI key

FALCMQXTWHPRIH-UHFFFAOYSA-N

Disclaimer

may discolor to brown on storage

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

Storage Class

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

Regulatory Information

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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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