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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/REAXYS Number:
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

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

wgk_germany

WGK 3

flash_point_f

50.0 °F

flash_point_c

10 °C

ppe

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
F R Johannsen et al.
Journal of toxicology and environmental health, 33(3), 291-302 (1991-07-01)
Groups of 15 male and 15 female Sprague-Dawley rats were exposed to 1 of 3 chloropropene (2,3-Di = DCP; 1,2,3-Tri = TRCP; and 1,1,2,3-Tetra = TECP) vapors to provide information on repeated exposures and the potential for reproductive impairment by
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
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
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
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