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Key Documents

Altri documenti

D72603

Sigma-Aldrich

2,3-Dichloro-1-propene

98%

Sinonimo/i:

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

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About This Item

Formula condensata:
ClCH2CCl=CH2
Numero CAS:
78-88-6
Peso molecolare:
110.97
Beilstein:
1361491
Numero CE:
201-153-8
Numero MDL:
MFCD00000943
Codice UNSPSC:
12352100
ID PubChem:
24894096
NACRES:
NA.22

Densità del vapore

3.8 (vs air)

Livello qualitativo

100

Tensione di vapore

44 mmHg ( 20 °C)

Saggio

98%

Forma fisica

liquid

Limite di esplosione

7.8 %

Indice di rifrazione

n20/D 1.461 (lit.)

P. eboll.

94 °C (lit.)

Densità

1.204 g/mL at 25 °C (lit.)

Stringa SMILE

ClCC(Cl)=C

InChI

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

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Categorie correlate

Avvertenze

Danger

Classi di pericolo

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

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

3 - Flammable liquids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

50.0 °F - closed cup

Punto d’infiammabilità (°C)

10 °C - closed cup

Dispositivi di protezione individuale

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

Certificati d'analisi (COA)

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Allyl chloride reagent grade, 98%

Sigma-Aldrich

A30702

Allyl chloride

1,3-Dichloroacetone ≥95%

Sigma-Aldrich

168548

1,3-Dichloroacetone

1,3-Dichloro-2-propanol 97%

Sigma-Aldrich

184489

1,3-Dichloro-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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