2062-20-6

Basic information

• Product Name: DIMETHYL DODECAFLUOROSUBERATE
• Synonyms: DIMETHYL DODECAFLUOROSUBERATE;DIMETHYL PERFLUOROOCTANE-1,8-DIOATE;DIMETHYL PERFLUOROSUBERATE;Dimethyl dodecafluorooctanedioate~Perfluorosuberic acid dimethyl ester;Dimethyl dodecafluorooctanedioate;perfluorosuberic acid dimethyl ester;Dimethyl perfluorosuberate 98%;Dimethylperfluorosuberate98%
• CAS NO: 2062-20-6
• Molecular Formula: C₁₀H₆F₁₂O₄
• Molecular Weight: 418.13
• EINECS: -0
• Mol File: 2062-20-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 26°C
• Boiling Point: 152°C 60mm
• Flash Point: 152°C/60mm
• Appearance: /
• Density: 1,635 g/cm3
• Vapor Pressure: 0.0571mmHg at 25°C
• Refractive Index: 1.3425
• BRN: 1917354
• CAS DataBase Reference: DIMETHYL DODECAFLUOROSUBERATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL DODECAFLUOROSUBERATE(2062-20-6)
• EPA Substance Registry System: DIMETHYL DODECAFLUOROSUBERATE(2062-20-6)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 2062-20-6(Hazardous Substances Data)

Usage

Chemical Properties

White low melting solid

InChI:InChI=1/C10H6F12O4/c1-25-3(23)5(11,12)7(15,16)9(19,20)10(21,22)8(17,18)6(13,14)4(24)26-2/h1-2H3

Upstream product

• 678-45-5 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorooctanedioic acid 
• 1967-93-7 2,2,3,3,4,4,5,5,6,6,7,7-dodecafluorooctanedioyl dichloride 
• 67-56-1 methanol 
• 3601-05-6 1,8-Bis-methylmercapto-hexadecafluor-octan 
• 124-41-4 sodium methylate 

Downstream Products

• 3885-85-6 perfluorooctanedinitrile 
• 928307-63-5 4,4,5,5,6,6,7,7,8,8,9,9-dodecafluoro-1,12-di-naphthalen-2-yl-dodecane-1,3,10,12-tetraone 
• 3492-23-7 Dodecafluorsuberiadiamid 

Relevant articles and documents

PROCESSES FOR PRODUCTION OF FLUORINE-CONTAINING COMPOUNDS

This process for producing fluorine-containing compounds includes liquid-phase fluorination by introducing a raw material compound and fluorine gas into a solvent to replace hydrogen atoms in the raw material compound with fluorine atoms. More specifically, the process for producing fluorine-containing compounds includes (1) promoting fluorination by dissolving the raw material compound in anhydrous hydrofluoric acid and introducing into a liquid-phase fluorination solvent, or (2) promoting fluorination by dissolving the raw material compound in a perfluoro compound having a plurality of polar groups in a molecule thereof and introducing into a liquid-phase fluorination solvent. According to these processes, a fluorination reaction can be carried out at high yield and without containing hardly any isomers while using a hydrocarbon compound as is for the raw material.