Difference between revisions of "1,3-Dichloropropene"

Latest revision as of 10:01, 20 September 2010

1,3-Dichloropropene
Skeletal formula of the trans isomer	Skeletal formula of the cis isomer
Ball-and-stick model of the trans isomer	Ball-and-stick model of the cis isomer
IUPAC name 1,3-dichloroprop-1-ene
Systematic name 1-Propene, 1,3-dichloro-, (1E)-
Other names 1,3-D, Dorlone, Nematox, Telone, Nemex, cis-Dichloropropene, Di-Trapex CP, Vorlex 201, dichloro-1,3-propene, 1,3-dichloro-1-propene, 1,3-dichloro-2-propene, alpha-chloroallylchloride, chloroallylchloride, gamma-chloroallylchloride, chloroallyl chloride, chloroorpropenyl chloride, 3-dichloropropylene, 3-D, DCP
style="background: #F8EABA; text-align: center;" colspan="2" | Identifiers
CAS number	542-75-6 Y
PubChem	24726
ChemSpider	23117
EC number	208-826-5
KEGG	C06609
MeSH	1,3-dichloro-1-propene
ChEBI	18918
RTECS number	UC8310000
SMILES	Script error: No such module "collapsible list".
InChI	Script error: No such module "collapsible list".
InChI key	UOORRWUZONOOLO-OWOJBTEDBJ
style="background: #F8EABA; text-align: center;" colspan="2" | Properties
Molecular formula	C3H4Cl2
Molar mass	110.97 g/mol
Appearance	Colorless to straw-colored liquid, sweet chloroform-like odor
Density	1.217 g/mL (cis); 1.224 g/mL (trans)
Melting point	-84.5 °C
Boiling point	104 °C (cis); 112 °C (trans)
Solubility in water	2.18 g/L (cis) @ 25 °C; 2.32 g/L (trans) @ 25 °C
log P	1.82
Vapor pressure	34.4 mm Hg @ 25 °C (cis); 23.0 mm Hg @ 25 °C (trans)
style="background: #F8EABA; text-align: center;" colspan="2" | Hazards
EU Index	208-826-5
EU classification	T,N
R-phrases	10-20/21-25-36/37/38-43-50/53
S-phrases	(1/2-)-36/37-45-60-61
NFPA 704	75px 3 2 0
Flash point	28 °C
Autoignition temperature	> 500 °C
Explosive limits	5.3% - 14.5% (80 °C)
U.S. Permissible exposure limit (PEL)	1
Y (what is this?)  (verify) Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

1,3-Dichloropropene, also known as Telone or simply 1,3-D, is a colorless liquid with a sweet smell. It exists as a mixture of the geometric isomers cis-1,3-dichloropropene and trans-1,3-dichloropropene. It dissolves in water and evaporates easily. It is used mainly in farming as a pesticide, specifically as a preplant fumigant and nematicide. It widely used in the US and other countries, but in the process of being phased out in the European Union.^[1]

Effects

1,3-Dichloropropene (DCP) causes irritation at the point of contact. Inhalation can cause nausea, vomiting, irritation of the skin, eyes, and throat; breathing difficulties, headache, and fatigue. These effects generally occur at exposure levels that are much higher than the background levels found in air or water. Rats and mice that inhaled DCP repeatedly for about 2 weeks had damage to the lining of the nose, and mice had damage to the lung.

A man who accidentally ingested DCP died with severe damage to his stomach and surrounding organs, but little else is known about the effects of ingesting these substances in humans. Animal studies have reported damage to the stomach lining, lung congestion, difficulty walking, and effects on the liver and kidneys from ingesting high levels of DCP.^{[citation needed]}

A few workers who had skin contact with pesticides containing DCP developed blisters and an allergic reaction on their skin.^{[citation needed]}

It is not known whether DCP can cause birth defects in humans. Pregnant rats that inhaled 1,3-dichloropropene gave birth to fewer pups or pups with lower body weight. This occurred at exposures high enough to be toxic to the mothers.[3]

DCP is testable via blood and urine tests, although it is only detectable in the body for 1-2 after exposure. Exposure level estimates are possible with a blood sample.

Carcinogenicity

Evidence for the carcinogenicity of 1,3-dichloropropene in humans is inadequate, but results from several cancer bioassays provide adequate evidence of carcinogenicity in animals. The Department of Health and Human Services (DHHS) has determined that 1,3-dichloropropene may reasonably be anticipated to be a carcinogen. The International Agency for Research on Cancer (IARC) has determined that 1,3-dichloropropene is possibly carcinogenic to humans. The EPA has classified 1,3-dichloropropene as a probable human carcinogen.^[2]

Use

1,3-Dichloropropene is used as a pesticide in the following crops: [4]

Contamination

The ATSDR has extensive contamination information available.^[3]

References

1. ↑ COMMISSION DECISION of 20 September 2007 concerning the non-inclusion of 1,3-dichloropropene in Annex I to Council Directive 91/414/EEC and the withdrawal of authorisations for plant protection products containing that substance, Official Journal of the European Union, 25 September 2007.
2. ↑ [1]
3. ↑ [2]

• ATSDR ToxFAQs: Dichloropropenes
• ATSDR ToxFAQs: Dichloropropenes
• USGS Pesticide National Synthesis Project - Crop & Compound

Further reading

• ATSDR Toxicological Profile (9.2 MB)

de:1,3-Dichlorpropen et:1,3-dikloropropeen fr:1,3-dichloropropène nl:1,3-dichloorpropeen ja:1,3-ジクロロプロペン