Name | 1,3-Dichloropropene |
Synonyms | D-D 1,3-D TELONE NEMATOX TELONE(R) D-D mixture 1,3-DICHLOROPENE DICHLOROPROPYLENE 1,3-DICHLOROPROPENE 1,3-Dichloropropene TRANS-1,3-DICHLOROPENE 3-CHLOROALLYL CHLORIDE 1,3-dichloroprop-1-ene A-CHLOROALLYL CHLORIDE (1E)-1,3-Dichloro-1-propene TRANS-1,3-DICHLORO-1-PROPENE Dichloropropene,Dichloropropane |
CAS | 542-75-6 |
EINECS | 208-826-5 |
InChI | InChI=1/C3H4Cl2/c4-2-1-3-5/h1-2H,3H2 |
InChIKey | UOORRWUZONOOLO-OWOJBTEDSA-N |
Molecular Formula | C3H4Cl2 |
Molar Mass | 110.97 |
Density | 1.2 |
Melting Point | -60 °C |
Boling Point | 97-112°C(lit.) |
Flash Point | 78°F |
Water Solubility | <0.01 g/100 mL at 16.5 ºC |
Vapor Presure | E-isomer 3700 Pa,Z-isomer 3500 Pa at 25 °C |
Appearance | neat |
Color | Colorless to Light yellow to Light orange |
Exposure Limit | ACGIH: TWA 1 ppm (Skin)NIOSH: TWA 1 ppm(5 mg/m3) |
Merck | 14,3075 |
BRN | 1719556 |
Storage Condition | 2-8°C |
Refractive Index | n20/D 1.472(lit.) |
Physical and Chemical Properties |
Colourless, flammable liquid with chloroform-like odour. Exists as a mixture of cis and trans isomers. Above 35℃ explosive vapour-air mixtures may be formed. CHIP requirements also cover the pure (Z) isomer (CAS 10061-01-5, EC 233-195-8). |
Use | For the production of pesticides, herbicides, etc |
Risk Codes | R10 - Flammable R20/21 - Harmful by inhalation and in contact with skin. R25 - Toxic if swallowed R36/37/38 - Irritating to eyes, respiratory system and skin. R43 - May cause sensitization by skin contact R50/53 - Very toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment. R65 - Harmful: May cause lung damage if swallowed R24/25 - R20 - Harmful by inhalation |
Safety Description | S36/37 - Wear suitable protective clothing and gloves. S45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) S60 - This material and its container must be disposed of as hazardous waste. S61 - Avoid release to the environment. Refer to special instructions / safety data sheets. |
UN IDs | UN 1992 3/PG 3 |
WGK Germany | 3 |
RTECS | UC8310000 |
TSCA | Yes |
HS Code | 29032990 |
Hazard Class | 3 |
Packing Group | II |
(IARC) carcinogen classification | 2B (vol. 41, sup 7, 71) 1999 |
NIST chemical information | Information provided by: webbook.nist.gov (external link) |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
use | 1, 3-dichloropropene is a colorless and sweet volatile liquid, white or amber when impure, and can be used as an intermediate in organic synthesis. 1, 3-dichloropropene is an intermediate of the herbicide Yanyanwei, and is also a component in the soil fumigant drop mixture. Used as an intermediate in organic synthesis. Night can be used as a component of the dripping mixture, which has a strong nematicidal effect. A mixture of 1,3-dichloropropene 50-60%, 1,2-dichloropropane 25% and other chloride 15% is generally used. The mixture is a yellow-brown liquid with a pungent chlorine odor, which is corrosive and easy to absorb water. 1, 3-dichloropropene is also used in the synthesis of the herbicide Qingyanling. used to produce pesticides, herbicides, etc. |
production method | is obtained by the reaction of propylene and chlorine. The reaction is carried out at 500-550°C and is obtained by separation. In the process of high temperature chlorination of propylene to epichlorohydrin, the side reaction makes the reactant a mixture of chlorinated hydrocarbons. During the separation of chloropropene, 3-chloropropylene-1 was obtained at the top of the tower, and by-product drops of mixture were obtained in the tower kettle, in which dichloropropane and dichloropropene reached more than 80%. Production of 1t epichlorohydrin, can produce by-product drops of 230kg mixture. the preparation method is obtained by reacting propylene and chlorine at 500~550 ℃ and separating. When propylene is chlorinated to prepare epichlorohydrin, the side reaction produces 3-chloropropene, 1, 3-dichloropropene and 1, 2-dichloropropane, which can also be generated after separation. The reaction equation is shown in the figure: CH3CH = CH2 + Cl2 → CH2ClCH = CH2 + HClCH2ClCH = CH2 + Cl2 → ClCH = CHCH2Cl |
category | pesticide |
toxicity classification | highly toxic |
acute toxicity | oral-rat LD50: 470 mg/kg; Oral-mouse LD50: 640 mg/kg |
flammability hazard characteristics | it is more flammable when exposed to open flames, high temperatures, and oxidants; combustion produces toxic chloride fumes; heated decomposition of toxic phosgene |
storage and transportation characteristics | warehouse ventilation and low temperature drying; Store separately from oxidant; Not suitable for long storage to prevent polymerization |
fire extinguishing agent | dry powder, dry sand, carbon dioxide, foam, 1211 fire extinguishing agent |
occupational standard | TWA 5 mg/m3 |
toxic substance data | information provided by: pubchem.ncbi.nlm.nih.gov (external link) |