336-06-1

Basic information

• Product Name: OCTAFLUOROADIPOYL CHLORIDE
• Synonyms: OCTAFLUOROADIPOYL CHLORIDE;PERFLUOROADIPOYL CHLORIDE;Octafluoroadipoyl chloride 97%;Octafluoroadipoylchloride97%;Octafluoroadipoyl dichloride
• CAS NO: 336-06-1
• Molecular Formula: C₆Cl₂F₈O₂
• Molecular Weight: 326.96
• Mol File: 336-06-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 42-45°C 2mm
• Appearance: /
• Density: 1.735±0.06 g/cm3(Predicted)
• CAS DataBase Reference: OCTAFLUOROADIPOYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: OCTAFLUOROADIPOYL CHLORIDE(336-06-1)
• EPA Substance Registry System: OCTAFLUOROADIPOYL CHLORIDE(336-06-1)

Safety Data

• Hazard Codes: C,Xn
• Statements: 34-22
• Safety Statements: 26-36/37/39
• RIDADR: 3265
• HazardClass: CORROSIVE
• Hazardous Substances Data: 336-06-1(Hazardous Substances Data)

Usage

General Description

OCTAFLUOROADIPOYL CHLORIDE is a chemical compound that is used in the production of fluorinated polymers and specialty chemicals. It is a colorless, liquid compound with a pungent odor, and is highly reactive with water and air. Its main application is as a building block in the synthesis of perfluorinated compounds, which are used in a wide range of industrial and consumer products such as non-stick coatings, lubricants, and fire extinguishers. OCTAFLUOROADIPOYL CHLORIDE is a highly hazardous substance that requires special handling and strict safety precautions during its production and use.

Upstream product

• 336-08-3 perfluoroadipic acid 
• 1548-07-8 1,2,7,8-tetrachloro-1H,2H,7H,8H-tetradecafluoro-octane 
• 355-66-8 octafluoro-adipic acid diamide 
• 812-97-5 perfluoro-1,7-octadiene 

Downstream Products

• 355-74-8 2,2,3,3,4,4,5,5-octafluoro-1,6-hexanediol 

Relevant articles and documents

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Method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin

The invention discloses a method for preparing fluorine-containing dihydric alcohol from fluorine-containing cycloolefin. The method comprises the following steps: oxidizing fluorine-containing cycloolefin serving as a raw material by using an oxidizing agent and treating the fluorine-containing cycloolefin by using a strong alkali to generate a solid mixed salt containing corresponding fluorine-containing dicarboxylate, and then generating corresponding fluorine-containing binary acyl chloride under the action of an acylating chlorination reagent; and finally, enabling the fluorine-containing binary acyl chloride and a reducing agent to be subjected to a reduction reaction under the action of a solvent and a catalyst to obtain the corresponding fluorine-containing dihydric alcohol. The specific organic solvent and catalyst are adopted, and other conditions are matched, so that the fluorine-containing cycloolefin can be effectively promoted to generate corresponding fluorine-containing dihydric alcohol with high efficiency and high yield. The method has the advantages of easily available raw materials, simple process, convenience in operation, low cost and the like, and is suitable for large-scale production of fluorine-containing dihydric alcohol.