6792-31-0

Basic information

• Product Name: Hexafluoropropene trimer
• Synonyms: TRIMERS OF HEXAFLUOROPROPENE;HEXAFLUOROPROPENE TRIMER;PERFLUOROPROPENE TRIMER MIXTURE OF ISO&;Hexafluoropropene trimer 97%;HEXAFLUOROPROPENE TRIMER (MIXTURE OF ISOMERS);Hexafluoropropylene trimer;Perfluoropropene[trimer]
• CAS NO: 6792-31-0
• Molecular Formula: C9F18
• Molecular Weight: 450.07
• EINECS: -0
• Product Categories: refrigerants;Alkenyl;Halogenated Hydrocarbons;Organic Building Blocks
• Mol File: 6792-31-0.mol
• Article Data: 67

Chemical Properties

• Boiling Point: 110-115 °C(lit.)
• Flash Point: 75 °F
• Appearance: colorless liquid
• Density: 1.83 g/mL at 25 °C(lit.)
• Vapor Pressure: 4.46mmHg at 25°C
• Refractive Index: 1.273
• Storage Temp.: 2-8°C
• CAS DataBase Reference: Hexafluoropropene trimer(CAS DataBase Reference)
• NIST Chemistry Reference: Hexafluoropropene trimer(6792-31-0)
• EPA Substance Registry System: Hexafluoropropene trimer(6792-31-0)

Safety Data

• Hazard Codes: Xn,Xi
• Statements: 10-20/21/22-36/37/38
• Safety Statements: 16-26-36/37/39
• RIDADR: UN 1993 3/PG 3
• WGK Germany: 3
• HazardClass: 3.2
• PackingGroup: III
• Hazardous Substances Data: 6792-31-0(Hazardous Substances Data)

Usage

Description

Hexafluoropropene trimer is a perfluorinated compound that consists of three hexafluoropropene molecules linked together. It is known for its unique properties, such as high thermal stability, chemical resistance, and low surface energy, which make it suitable for various applications in different industries.

Uses

Used in Photochromic Compounds:
Hexafluoropropene trimer is used as a key component in the preparation of photochromic spiroindolinonaphthoxazine derivatives. These compounds exhibit reversible color changes upon exposure to light, making them suitable for applications in smart materials and optical devices.
Used in Fluorochemicals:
Hexafluoropropene trimer is used as a starting material for the synthesis of various fluorochemicals, such as 2-trifluoromethyl-3-heptadifluoroisopropyl-2-perfluoropentene-4-(N′,N′-dimethylamino propyl) imino(I). These fluorochemicals have potential applications in the development of new materials with enhanced properties, such as improved thermal stability and chemical resistance.
Used in Coatings and Lubricants Industry:
Hexafluoropropene trimer is used as a component in the formulation of high-performance coatings and lubricants. Its low surface energy and chemical resistance contribute to the development of coatings with excellent non-stick properties, corrosion resistance, and durability.
Used in Electronics Industry:
Hexafluoropropene trimer is used in the electronics industry for the development of materials with high dielectric constants and low dissipation factors. These materials are essential for the fabrication of high-performance capacitors, sensors, and other electronic components.
Used in Medical Industry:
Hexafluoropropene trimer is used in the medical industry for the development of biocompatible materials and coatings. Its chemical resistance and non-stick properties make it suitable for applications in medical devices, implants, and drug delivery systems.

InChI:InChI=1/C9F18/c10-3(11,7(21,8(22,23)24)9(25,26)27)1(4(12,13)14)2(5(15,16)17)6(18,19)20

Upstream product

• 375-22-4 heptafluorobutyric Acid 
• 661-97-2 1,2-dichlorohexafluoropropane 
• 754-34-7 1,1,1,2,2,3,3-heptafluoro-3-iodo-propane 
• 378-90-5 perfluoro-4-heptanone 
• 917-54-4 methyllithium 
• 354-25-6 2-chloro-1,1,2,2-tetrafluoroethane 
• 677-69-0 perfluoroisopropyl iodide 
• 7553-56-2 iodine 
• 76-19-7 freon-218 
• 678-26-2 perfluoropentane 
• 355-25-9 perfluorobutane 
• 123-91-1 1,4-dioxane 
• 423-33-6 1-Nitro-heptafluor(n)propan 
• 116-14-3 polytetrafluoroethylene 

Downstream Products

• 54974-25-3 1-(2,2,3,4,4,4-Hexafluoro-butyl)-4-methyl-benzene 
• 65487-84-5 N-(2-Cyano-phenyl)-2,3,3,3-tetrafluoro-propionamide 
• 63099-85-4 2-(1,2,2,2-tetrafluoro-ethyl)-3H-quinazolin-4-one 
• 359-58-0 1-chloro-1,1,2,3,3,3-hexafluoro-propane 
• 51346-64-6 CF₃CClFCHF₂ 
• 108292-11-1 C₄F₉^(1-) 
• 56436-75-0 cis-1,2,3,3,3-Pentafluoro-1-phenoxypropene 
• 56436-73-8 trans-1,2,3,3,3-Pentafluoro-1-phenoxypropene 
• 56436-77-2 2,3,3,3-Tetrafluoro-1,1-diphenoxypropane 
• 131043-23-7 2-(Difluorophenoxymethyl)-2,3,3,3-tetrafluoropropanoic acid 
• 187737-37-7 propene 
• 57915-69-2 1,1,1,2,3,3-hexafluoropentane 
• 38310-59-7 trans-1,1,2-trifluoro-3-methyl-2-trifluoromethylcyclobutane 
• 38310-59-7 cis-1,1,2-trifluoro-3-methyl-2-trifluoromethylcyclobutane 

Relevant articles and documents

A novel and efficient synthetic route to perfluoroisobutyronitrile from perfluoroisobutyryl acid

A novel synthetic route to perfluoroisobutyronitrile from perfluoroisobutyryl acid which has mild conditions and low toxicity is described. This study introduces detailed synthetic protocols and characterization including GC-MS, 13C NMR and 19F NMR spectroscopy of perfluoroisobutyryl acid, perfluoroisobutyryl chloride, perfluoroisobutyl amide and perfluoroisobutyronitrile. Besides, this route is superior to the established patent and shows potential application in high voltage electrical equipment.

Novel synthetic route to perfluoroallyl cyanide (PFACN) reacting perfluoroallyl fluorosulfonate with cyanide

A novel synthetic method for the preparation of perfluoroallyl cyanide CF2[dbnd]CFCF2CN (PFACN) is presented. This includes the addition – elimination reaction of cyanide anion with perfluoroallyl fluorosulfate CF2[dbnd]CF

Reaction system for preparing tetrafluoroethane-β-sultone and preparation method using the same

The present invention relates to a reaction system for preparing tetrafluoroethane-andbeta;-sultone and to a preparation method using the same. By using the reaction system for preparing tetrafluoroethane-andbeta;-sultone and the preparation method using the same, tetrafluoroethane-andbeta;-sultone can be prepared safely and easily at a high yield and a high purity at normal temperature and normal pressure, rapid heat generation can be avoided and the risk of explosion in processes due to pressurization is reduced, so that the reaction system and the preparation method are usefully used to prepare energy-related materials such as fuel cell electrolytes and the like derived from tetrafluoroethane-andbeta;-sultone, and in particular, are usefully used to prepare fluorine-based ionomers.COPYRIGHT KIPO 2017