16500-91-7

Usage

Physical state

Colorless liquid It is a liquid without any color, which indicates its relatively low volatility and boiling point.

Odor

Faint, sweet The compound has a mild and sweet smell, which may not be easily detectable at low concentrations.

Primary use

Intermediate for the synthesis of other chemicals It is mainly used in the production of other chemical compounds, particularly pesticides and plastics.

Hazardous substance

Yes 1-Propene, 2,3,3,3-tetrachlorois considered hazardous due to its potential health and environmental risks.

Health effects

Skin, eye, and respiratory tract irritation Exposure to high levels of 1-Propene, 2,3,3,3-tetrachloro- can cause discomfort and irritation in these body parts.

Carcinogenic potential

Yes It has been classified as a potential carcinogen, which means it may cause cancer with prolonged or high-level exposure.

Environmental impact

Harmful if released into air or water The compound can have negative effects on the environment if it is not handled and stored properly.

Handling and storage precautions

Handle and store with caution To minimize potential risks to human health and the environment, it is important to follow proper safety procedures when working with 1-Propene, 2,3,3,3-tetrachloro-.

Upstream product

• 21700-31-2 1,1,1,2,3-pentachloro-propane 
• 74-99-7 prop-1-yne 
• 16714-68-4 1,1,2,2,3-pentachloropropane 

Downstream Products

• 2730-62-3 2-chloro-1,1,1-trifluoropropene 
• 10436-39-2 1,1,2,3-Tetrachloropropene 
• 17078-21-6 1,1,2-trichloro-3-phenyl-propene 
• 38320-96-6 3-bromo-1,1,2,2-tetrachloro-propane 
• 6066-14-4 3-bromo-1,1,2-trichloro-propene 
• 16714-68-4 1,1,2,2,3-pentachloropropane 

Relevant academic research and scientific papers

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.

METHOD FOR PRODUCING 2-CHLORO-3,3,3-TRIFLUOROPROPENE

The invention relates to a method for producing 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf) from at least one compound A selected from the group consisting of halopropane of formulae CX3CHClCH2X or CX3CFClCH3, or halopropenes of formula CQX2CCNCH2 and CX2═CClCH2X where X independently represents a fluorine or chlorine atom, characterised in that it comprises bringing said at least one compound A into contact with HF in a gaseous phase in the presence of a fluorination catalyst AlF3 or fluorine-bearing alumina in order to form a gaseous flow B comprising 2-chloro-3,3,3-trifluoropropene (HCFO-1233xf) et 3,3,3-trifluoropropene (HFO-1243zf).

PROCESS FOR THE PRODUCTION OF CHLORINATED PROPANES AND/OR PROPENES

Processes for the production of chlorinated propanes and/or propenes are provided. The present processes make use of methylacetylene, a by-product in the production of ethylene and/or propylene, as a low cost starting material, alone or in combination with propadiene, propene and/or propane. In the latter embodiments, the processes may also be utilized to provide a substantially pure stream of propane.

PROCESS FOR PREPARING CHLORINE-CONTAINING FLUOROCARBON COMPOUND

The present invention provides a process for preparing at least one chlorine-containing fluorocarbon compound selected from the group consisting of chlorine-containing fluoropropane compounds represented by Formula (1): CFnCl3-nCHClCH2—Cl, wherein n is 1 or 2, and chlorine-containing fluoropropene compounds represented by Formula (2): CFnCl3-nCCl═CH2, wherein n is 1 or 2, wherein the process includes the step of contacting at least one chlorine-containing compound selected from the group consisting of 1,1,1,2,3-pentachloropropane, 1,1,2,3-tetrachloropropene, and 2,3,3,3-tetrachloropropene with hydrogen fluoride in the absence of a catalyst while heating. According to the present invention, the chlorine-containing propane and propene compounds having 1 or 2 fluorine atoms can be prepared by an industrially applicable, simple and effective process.

PROCESS FOR PREPARING 2-CHLORO-3,3,3-TRIFLUOROPROPENE

The present invention provides a process for preparing 2-chloro-3,3,3-trifluoropropene including subjecting, in the absence of a catalyst, at least one chlorine-containing compound selected from the group consisting of chloropropane represented by formula (1): CClX2CHClCH2Cl, wherein each X is the same or different and each represents Cl or F, chloropropene represented by formula (2): CClY2CCl=CH2, wherein each Y is the same or different and each represents Cl or F, and chloropropene represented by formula (3): CZ2=CClCH2Cl, wherein each Z is the same or different and each represents Cl or F, to a reaction with hydrogen fluoride under heating in a gas phase. According to the present invention, 2-chloro-3,3,3-trifluoropropene (HCFC-1233xf) can be effectively prepared by an easy and economically advantageous process that is suitable for industrial scale production.

PROCESS FOR PREPARING CHLORINE-CONTAINING FLUOROCARBON COMPOUND

The present invention provides a process for preparing at least one chlorine-containing fluorocarbon compound selected from the group consisting of chlorine-containing fluoropropane compounds represented by Formula (1) : CFnCl3-nCHClCH2Cl, wherein n is 1 or 2, and chlorine-containing fluoropropene compounds represented by Formula (2) : CFnCl3-nCCl=CH2, wherein n is 1 or 2, wherein the process includes the step of contacting at least one chlorine-containing compound selected from the group consisting of 1, 1, 1, 2, 3-pentachloropropane, 1, 1, 2, 3-tetrachloropropene, and 2, 3, 3, 3-tetrachloropropene with hydrogen fluoride in the absence of a catalyst while heating. According to the present invention, the chlorine- containing propane and propene compounds having 1 or 2 fluorine atoms can be prepared by an industrially applicable, simple and effective process.