3107-98-0

Basic information

• Product Name: DIMETHYL OCTAFLUOROADIPATE
• Synonyms: DIMETHYL PERFLUOROADIPATE;DIMETHYL OCTAFLUOROADIPATE;Dimethyl perfluoroadipate~Octafluoroadipic acid dimethyl ester~Octafluorohexanedioic acid dimethyl ester;Dimethyl perfluorohexadionate;Octafluoroadipicaciddimethylester;Dimethyl octafluoroadipate 98%;Dimethyloctafluoroadipate98%;Dimethyl Octafluorohexanedioate
• CAS NO: 3107-98-0
• Molecular Formula: C₈H₆F₈O₄
• Molecular Weight: 318.12
• EINECS: -0
• Mol File: 3107-98-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 120 °C
• Flash Point: 120°C/15mm
• Appearance: /
• Density: 1,5 g/cm3
• Refractive Index: 1.3475
• BRN: 1916112
• CAS DataBase Reference: DIMETHYL OCTAFLUOROADIPATE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL OCTAFLUOROADIPATE(3107-98-0)
• EPA Substance Registry System: DIMETHYL OCTAFLUOROADIPATE(3107-98-0)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• HazardClass: IRRITANT
• Hazardous Substances Data: 3107-98-0(Hazardous Substances Data)

Usage

General Description

Dimethyl octafluoroadipate is a chemical compound characterized by its role as an anti-AID (autoimmune disease) agent and a metabolite. It is typically used in various industrial applications, specifically in the synthesis of other chemicals or as a component of chemical formulations. DIMETHYL OCTAFLUOROADIPATE contains octafluoroadipic acid, methyl ester, and two methyl groups. Its systematic name is Dimethyl 2,2,3,3,4,4,5,5-octafluoroadipate. The chemical's molecular formula is C8H6F8O4 and it has a molar mass about 350 g/mol. As with most chemicals, handling and usage of dimethyl octafluoroadipate should be done with care to avoid potential health risks. Its exact physical properties, such as boiling or melting points, as well as hazards, remain to be further defined.

Upstream product

• 67-56-1 methanol 
• 3492-11-3 1,6-Bis-methylmercapto-dodecafluor-hexan 
• 3872-27-3 2,2,3,3,4,4,5,5-octafluoro-hexanediimidic acid dimethyl ester 
• 54404-51-2 Monomethylester d.Perfluoradipinat 
• 124-41-4 sodium methylate 
• 67641-28-5 perfluoroallylfluorosulphate 
• 376-53-4 octafluoroadiponitrile 
• 37881-62-2 perfluoroadipic acid difluoride 

Downstream Products

• 355-74-8 2,2,3,3,4,4,5,5-octafluoro-1,6-hexanediol 
• 79865-19-3 2,2,3,3,4,4,5,5-Octafluoro-6-hydroxy-6,6-diphenyl-hexanoic acid methyl ester 
• 58191-54-1 C₁₈H₁₀F₈N₈O₈ 
• 85929-18-6 1,6-dimesityloctafluoro-1,6-hexanedione 
• 79865-34-2 2,2,3,3,4,4,5,5-Octafluoro-6-oxo-6-(2,4,6-trimethyl-phenyl)-hexanoic acid methyl ester 
• 79865-24-0 2,2,3,3,4,4,5,5-Octafluoro-6-hydroxy-6,6-di-m-tolyl-hexanoic acid methyl ester 
• 79865-31-9 2,2,3,3,4,4,5,5-Octafluoro-6-oxo-6-m-tolyl-hexanoic acid methyl ester 

Relevant articles and documents

FLUORINATION OF PERFLUOROALLYL FLUOROSULFATE

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PROCESS FOR PRODUCING FLUORINATED COMPOUND

To provide a process for producing a desired perfluorinated product at a high yield in a fluorination reaction of a partially fluorinated ester. A perfluorinated compound (4) is obtained by fluorinating in a liquid phase a compound (3) (wherein the fluorine content is at least 30 mass %) obtained by reacting a compound (1) and a compound (2), wherein the compound (1) is HOCH2—RA—CH2OH, the compound (2) is X1C(═O)—C(RB)(RC)(RD), RA is a bivalent saturated hydrocarbon group or the like which has no hetero atom such as an etheric oxygen atom, X1 is a halogen atom, and —C(RB)(RC)(RD) is a branched group.

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.