13116-58-0

Basic information

• Product Name: (1E)-1,2,3-Trichloro-1-propene
• Synonyms: (1E)-1,2,3-Trichloro-1-propene;(E)-1,2,3-Trichloro-1-propene
• CAS NO: 13116-58-0
• Molecular Formula: C₃H₃Cl₃
• Molecular Weight: 0
• Mol File: 13116-58-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 142°Cat760mmHg
• Flash Point: 65.5°C
• Appearance: /
• Density: 1.376g/cm³
• Vapor Pressure: 7.14mmHg at 25°C
• Refractive Index: 1.487
• CAS DataBase Reference: (1E)-1,2,3-Trichloro-1-propene(CAS DataBase Reference)
• NIST Chemistry Reference: (1E)-1,2,3-Trichloro-1-propene(13116-58-0)
• EPA Substance Registry System: (1E)-1,2,3-Trichloro-1-propene(13116-58-0)

Safety Data

• Hazardous Substances Data: 13116-58-0(Hazardous Substances Data)

Usage

General Description

(1E)-1,2,3-Trichloro-1-propene is a chemical compound with the molecular formula C3H3Cl3. It is a colorless liquid with a pungent odor that is primarily used in the production of agricultural and consumer products. (1E)-1,2,3-Trichloro-1-propene is classified as a hazardous substance, as exposure to high concentrations can cause irritation to the eyes, skin, and respiratory system. Prolonged or repeated exposure may also lead to more serious health effects, including damage to the liver and kidneys. The compound is also harmful to aquatic life and can persist in the environment for an extended period. Therefore, it is essential to handle and dispose of (1E)-1,2,3-Trichloro-1-propene with caution and in compliance with safety regulations.

InChI:InChI=1/C3H3Cl3/c4-1-3(6)2-5/h1H,2H2/b3-1+

Upstream product

• 78-88-6 2,3-Dichloroprop-1-ene 
• 36712-42-2 (E)-2,3-dichloroallyl alcohol 
• 13116-53-5 1,2,2,3-tetrachloropropane 
• 7782-50-5 chlorine 
• 142-28-9 1,3-Dichloropropane 
• 627-30-5 1-chloro-3-hydroxypropane 
• 18495-30-2 1,1,2,3-tetrachloropropane 
• 2736-73-4 2,3-dichloro-2-propene-l-ol 

Downstream Products

• 7069-38-7 trans-1,3-dichloropropylene 
• 2736-73-4 2,3-dichloro-2-propene-l-ol 

Relevant articles and documents

PROCESSES FOR PREPARING PENTACHLOROPROPANE AND TETRACHLOROPROPENE FROM DICHLOROPROPENE

A processes for preparing 1,1,2,3-tetrachloropropene, 2,3,3,3-tetrachloropropene, or a mixture thereof from 1,3-dichloropropene. The process may include a two successive chlorination and dehydrochlorination reactions. In a first chlorination reaction 1,3-dichloropropene is reacted with a chlorination agent to form a first chlorination reaction product including 1,1,2,3-tetrachloropropane. This first chlorination reaction product is reacted with a dehydrochlorination reagent in a first dehydrochlorination reaction to form a first dehydrochlorination reaction product including a trichloropropene. The trichloropropene containing reaction product is reacted with a chlorination agent in a second chlorination reaction to form a second chlorination reaction product including at least one of 1,1,1,2,3-pentachloropropane or 1,1,2,2,3-pentachloropropane. This reaction product is reacted with a dehydrochlorination reagent in a second dehydrochlorination reaction to form a second dehydrochlorination reaction product having 1,1,2,3-tetrachloropropene or a 2,3,3,3-tetrachloropropene.

MANUFACTURE OF DICHLOROPROPANOL

Manufacture of dichloropropanol Process for manufacturing dichloropropa nol wherein a glycerol-based product comprising at least one diol containi ng at least 3 carbon atoms other than 1,2- propanediol, is reacted with a chlorinati ng agent, and of products derived from dichloropropanol such as ep ichlorohydrin and epoxy resins. No figure.