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D72603

Sigma-Aldrich

2,3-Dichlor-1-Propen

98%

Synonym(e):

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

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About This Item

Lineare Formel:
ClCH2CCl=CH2
CAS-Nummer:
78-88-6
Molekulargewicht:
110.97
Beilstein:
1361491
EG-Nummer:
201-153-8
MDL-Nummer:
MFCD00000943
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24894096
NACRES:
NA.22

Dampfdichte

3.8 (vs air)

Qualitätsniveau

100

Dampfdruck

44 mmHg ( 20 °C)

Assay

98%

Form

liquid

Expl.-Gr.

7.8 %

Brechungsindex

n20/D 1.461 (lit.)

bp

94 °C (lit.)

Dichte

1.204 g/mL at 25 °C (lit.)

SMILES String

ClCC(Cl)=C

InChI

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

InChIKey

FALCMQXTWHPRIH-UHFFFAOYSA-N

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Verwandte Kategorien

Signalwort

Danger

Gefahreneinstufungen

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

Zielorgane

Respiratory system

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 3

Flammpunkt (°F)

50.0 °F - closed cup

Flammpunkt (°C)

10 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Allylchlorid reagent grade, 98%

Sigma-Aldrich

A30702

Allylchlorid

1,3-Dichloraceton ≥95%

Sigma-Aldrich

168548

1,3-Dichloraceton

1,3-Dichlor-2-propanol 97%

Sigma-Aldrich

184489

1,3-Dichlor-2-propanol

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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