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Merck
CN

D72603

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24894096
EC Number:
201-153-8
Beilstein/REAXYS Number:
1361491
MDL number:
MFCD00000943
Assay:
98%
Form:
liquid

Key Documents

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Product Name

2,3-Dichloro-1-propene, 98%

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 %

refractive index

n20/D 1.461 (lit.)

bp

94 °C (lit.)

density

1.204 g/mL at 25 °C (lit.)

Quality Level

100

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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

危险化学品
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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ3532
MKCZ3531
MKCW7162
MKCW7123
MKCX0389

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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
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
J A Bond et al.
Toxicology and applied pharmacology, 78(1), 47-54 (1985-03-30)
2,3-Dichloropropene (2,3-DCP) is a constituent of some commercially available preplant soil fumigants for the control of plant parasitic nematodes. Human exposure potential exists during manufacture of the chemicals or during bulk handling activities. The purpose of this investigation was to
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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