- E-1,3-Dichloropropene
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- $0.00 / 1g
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2024-03-12
- CAS:10061-02-6
- Min. Order: 1g
- Purity: 98% HPLC
- Supply Ability: 100kg
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| | trans-1,3-Dichloropropene Basic information |
| | trans-1,3-Dichloropropene Chemical Properties |
| Boiling point | 97-112 °C(lit.) | | density | 1.198 g/mL at 25 °C(lit.) | | vapor pressure | 79.1 at 50 °C, 523.5 at 100 °C (Wilding et al., 2002) | | refractive index | n20/D 1.472(lit.) | | Fp | 78 °F | | storage temp. | 0-6°C | | solubility | Miscible with acetone, benzene, carbon tetrachloride, heptane, methanol (Worthing and Hance,
1991), methylene chloride, chloroform, trichloroethylene, and 1,1,2,2-tetrachloroethane. | | color | Colorless to Light yellow to Light orange | | Specific Gravity | 1.217 | | Water Solubility | 2.8g/L(20 ºC) | | Merck | 14,3075 | | Henry's Law Constant | 1.3 x 10-3 atm?m3/mol (Pankow and Rosen, 1988)
0.793 x 10-3 atm?m3/mol at 20 °C, 1.87 at 40 °C (static headspace-GC, Kim et al., 2003) | | Exposure limits | ACGIH TLV: TWA 1 ppm for cis and trans isomers (adopted). | | Stability: | Stable. Flammable. Incompatible with strong oxidizing agents, aluminium, aluminium alloys, some metal salts and halogens. May be light sensitive. | | CAS DataBase Reference | 10061-02-6(CAS DataBase Reference) | | NIST Chemistry Reference | 1-Propene, 1,3-dichloro-, (E)-(10061-02-6) | | EPA Substance Registry System | trans-1,3-Dichloropropene (10061-02-6) |
| | trans-1,3-Dichloropropene Usage And Synthesis |
| Description | Trans-1,3-dichloropropene appears as a clear colorless liquid with chloroform odor. Flash point 95 °F. Density 1.225 g/cm3 and insoluble in water. Hence sinks in water. A strong irritant. Used as a soil fumigant. It is used as an intermediate in the manufacture of 3,3-dichloro-1-propene and other pesticides. | | Chemical Properties | colourless liquid | | Chemical Properties | 1,3-Dichloropropene is a colorless to strawcolored liquid. Sharp, sweet, irritating, chloroform-like odor. | | Physical properties | Colorless to pale yellow liquid with a chloroform-like odor. Evaporates quickly when spilled. | | Uses | The isomer mixture is used as a soil fumigant and a nematocide. | | Definition | ChEBI: (E)-1,3-dichloropropene is a 1,3-dichloropropene with a (E)-configuration. It has a role as a fumigant. It is a 1,3-dichloropropene and a chloroalkene. It derives from a hydride of a propene. | | General Description | A clear colorless liquid with chloroform odor . Flash point 95°. Density 1.225 g / cm3 and insoluble in water. Hence sinks in water. A strong irritant. Used as a soil fumigant. | | Air & Water Reactions | Highly flammable. Insoluble in water. | | Reactivity Profile | trans-1,3-Dichloropropene reacts with aluminum, aluminum alloys, with other active metals and with some metal salts and halogens. Can react vigorously with oxidizing materials. . | | Fire Hazard | Flash point data for trans-1,3-Dichloropropene are not available, however literature indicates that trans-1,3-Dichloropropene is flammable. | | Potential Exposure | Used as a soil fumigant prior to
planting crops, such as cotton, sugar beet, potatoes; used in
combinations with dichloropropanes as a soil fumigant.
Workers engaged in manufacture, formulation and application of this soil fumigant and nematocide. | | Environmental Fate | Biological. The isomeric mixture showed significant degradation with gradual adaptation
in a static-culture flask-screening test (settled domestic wastewater inoculum) conducted
at 25°C. At concentrations of 5 and 10 mg/L, percent losses after 4 weeks of
incubation were 85 and 84, respectively. Ten days into the incubation study, 7–19% was
lost due to volatilization (Tabak et al., 1981).
Chemical/Physical. Hydrolysis in distilled water at 25°C produced trans-3-chloro-2-
propen-1-ol and hydrochloric acid. The reported half-life for this reaction is only 2 days (Kollig, 1993; Milano et al., 1988). trans-1,3-Dichloropropylene was reported to hydrolyze
to 3-chloro-2-propen-1-ol and can be biologically oxidized to 3-chloropropenoic acid
which is further oxidized to formylacetic acid. Decarboxylation of this compound yields
carbon dioxide (Connors et al., 1990). Chloroacetaldehyde, formyl chloride and chloroacetic
acid were formed from the ozonation of dichloropropylene at approximately 23°C
and 730 mmHg. Chloroacetaldehyde and formyl chloride also formed from the reaction
of dichloropropylene and hydroxyl radicals (Tuazon et al., 1984).
The evaporation half-life of trans-1,3-dichloropropylene (1 mg/L) from water at 25°C
using a shallow-pitch propeller stirrer at 200 rpm at an average depth of 6.5 cm is 24.6
minutes (Dilling, 1977).
Emits chlorinated acids when incinerated. Incomplete combustion may release toxic
phosgene (Sittig, 1985). | | Solubility in water | Miscible with acetone, benzene, carbon tetrachloride, heptane, methanol (Worthing and Hance,
1991), methylene chloride, chloroform, trichloroethylene, and 1,1,2,2-tetrachloroethane. | | Shipping | UN2047 Dichloropropene, Hazard Class: 3;
Labels: 3-Flammable liquid. | | Incompatibilities | Vapor may form explosive mixture
with air. Incompatible with oxidizers (chlorates, nitrates,
peroxides, permanganates, perchlorates, chlorine, bromine,
fluorine, etc.); contact may cause fires or explosions. Keep
away from alkaline materials, strong bases, strong acids,
oxoacids, and epoxides. May accumulate static electrical
charges, and may cause ignition of its vapors. Incompatible
with strong acids; oxidizers, aluminum or magnesium compounds; aliphatic amines; alkanolamines, alkaline materials;
halogens, or corrosives. Note: Epichlorohydrin may be
added as a stabilizer. | | Waste Disposal | Incineration, preferably
after mixing with another combustible fuel. Care must be
exercised to assure complete combustion to prevent the
formation of phosgene. An acid scrubber is necessary to
remove the halo acids produced. In accordance with
40CFR165, follow recommendations for the disposal of
pesticides and pesticide containers. Must be disposed properly by following package label directions or by contacting
your local or federal environmental control agency, or by
contacting your regional EPA office. Consult with environmental regulatory agencies for guidance on
acceptable disposal practices. Generators of waste containing this contaminant (≧100 kg/mo) must conform with
EPA regulations governing storage, transportation, treatment, and waste disposal. |
| | trans-1,3-Dichloropropene Preparation Products And Raw materials |
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