16714-68-4

Basic information

• Product Name: Pentachloropropane
• Synonyms: Pentachloropropane;1,1,2,2,3-pentachloropropane;Brn 1738270;Einecs 240-766-5;Propane, 1,1,2,2,3-pentachloro-
• CAS NO: 16714-68-4
• Molecular Formula: C₃H₃Cl₅
• Molecular Weight: 216.32092
• EINECS: 240-766-5
• Mol File: 16714-68-4.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 190.45°C (estimate)
• Flash Point: 78.1°C
• Appearance: /
• Density: 1.6330
• Vapor Pressure: 0.398mmHg at 25°C
• Refractive Index: 1.5061 (estimate)
• CAS DataBase Reference: Pentachloropropane(CAS DataBase Reference)
• NIST Chemistry Reference: Pentachloropropane(16714-68-4)
• EPA Substance Registry System: Pentachloropropane(16714-68-4)

Safety Data

• RIDADR: 2810
• HazardClass: 6.1(a)
• PackingGroup: II
• Hazardous Substances Data: 16714-68-4(Hazardous Substances Data)

Usage

Safety Profile

Moderately toxic by unspecified routes. When heated to decomposition it emits toxic fumes of Clí.

InChI:InChI=1/C3H3Cl5/c4-1-3(7,8)2(5)6/h2H,1H2

Upstream product

• 96-19-5 1,2,3-trichloropropene 
• 13116-53-5 1,2,2,3-tetrachloropropane 
• 107-05-1 3-chloroprop-1-ene 
• 78-88-6 2,3-Dichloroprop-1-ene 
• 16500-91-7 2,3,3,3-tetrachloropropene 
• 10035-10-6 hydrogen bromide 
• 94-36-0 dibenzoyl peroxide 
• 26198-63-0 1,2-Dichloropropane 
• 598-77-6 1,1,2-trichloropropane 
• 20589-85-9 1,2,3,3-tetrachloro-1-propene 
• 74-99-7 prop-1-yne 
• 18495-30-2 1,1,2,3-tetrachloropropane 
• 96-18-4 1,2,3-trichloropropane 
• 7791-25-5 sulfuryl dichloride 

Downstream Products

• 10436-39-2 1,1,2,3-Tetrachloropropene 
• 2730-62-3 2-chloro-1,1,1-trifluoropropene 
• 754-12-1 2,3,3,3-tetrafluoro-propene 
• 1814-88-6 1,1,1,2,2-pentafluoropropane 

Relevant articles and documents

Preparation method of 1,1,2,3-tetrachloropropene

The invention discloses a preparation method of 1,1,2,3-tetrachloropropene. The method comprises the steps of (1) reacting trichloromethane, 1,2-dichloroethylene and a first catalyst, cooling to room temperature after reaction is completed, adding water, carrying out vacuum rectification to obtain 1,1,2,3,3-pentachloropropane; (2) carrying out gas-phase catalytic dehydrochlorination reaction on the 1,1,2,3,3-pentachloropropane under the action of a second catalyst to obtain 1,2,3,3-tetrachloropropene; (3) carrying out gas-phase catalytic addition reaction on hydrogen chloride and the 1,2,3,3-tetrachloropropene under the action of a third catalyst to obtain 1,1,2,2,3-pentachloropropane; and (4) carrying out gas-phase catalytic dehydrochlorination reaction on the 1,1,2,2,3-pentachloropropane under the action of a fourth catalyst, collecting a reaction product and carrying out vacuum rectification to obtain the 1,1,2,3-tetrachloropropene. The preparation method is simple in process, available in raw materials, low in cost, high in yield, green and environment-friendly and is especially suitable for industrial production.

Compositions comprising 2,3,3,3-tetrafluoropropene, 1,1,2,3-tetra-chloropropene, 2-chloro-3,3,3-trifluoropropene, or 2-chloro-1,1,1,2-tetrafluoropropane

The present disclosure relates to compositions comprising 2,3,3,3-tetrafluoropropene that may be useful as heat transfer compositions, aerosol propellants, foaming agents, blowing agents, solvents, cleaning agents, carrier fluids, displacement drying agents, buffing abrasion agents, polymerization media, expansion agents for polyolefins and polyurethane, gaseous dielectrics, extinguishing agents, and fire suppression agents in liquid or gaseous form. Additionally, the present disclosure relates to compositions comprising 1,1,2,3-tetrachloropropene, 2-chloro-3,3,3-trifluoropropene, or 2-chloro-1,1,1,2-tetrafluoropropane, which may be useful in processes to produce 2,3,3,3-tetrafluoropropene.

PROCESS FOR THE PRODUCTION OF CHLORINATED ALKANES

Processes for the production of chlorinated alkanes are provided. The present processes comprise catalyzing the chlorination of a feedstream comprising one or more alkanes and/or alkenes with a catalyst system comprising one or more inorganic iodine salts and/or lower than conventional levels of elemental iodine and at least one Lewis acid. The processes are conducted in a nonaqueous media, and so, the one or more inorganic iodine salts are recoverable and/or reusable, in whole or in part.