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163702-07-6

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163702-07-6 Usage

Application

Methyl Perfluorobutyl Ether is a clear, colorless, low-odor, non-toxic, non-corrosive, non-flammable liquid substance with a chemical formula of C5H3F9O and a molecular weight of 250.06. Since it has low flammability, relatively low vapor pressure, low heat of vaporization, and low surface tension, it is considered to replace the chlorine-containing cleaning solvents such as 1,1,1-trichloroethane, CFC-113 (CF2ClCFCl2), and HCFC-141b (CH3CFCl2). Besides, it is a fluorinated ether solvent that is very compatible with many other ingredients, and is thought to have good sliding properties and serve as a good solvent in oil-based formulas.

Preparation

Because methyl perfluorobutyl ether contains perfluoroalkyl group (Rf) on one side and alkyl group (R) on the other side of ether linkage, it cannot be synthesized by selective partial fluorination of its hydrocarbon precursors. Instead, they may be prepared by coupling reactions of two reactants having Rf and R, coupling reactions of two reactants having Rf and R, respectively.

Chemical Properties

Clear colorless liquid

Uses

Different sources of media describe the Uses of 163702-07-6 differently. You can refer to the following data:
1. Nonafluorobutyl methyl ether (Methyl Nonafluorobutyl Ether, MFE) may be used to compose mixed-solvent electrolytes. Flash point, conductivity and NMR spectra of these solvent mixtures have been investigated.
2. Methoxyperfluorobutane can be used as a solvent: In the synthesis of various aryl fluoride derivatives via electrophilic fluorination of aryl and heteroaryl Grignard reagents. In grafting of fluorinated diblock copolymers onto silica particles.

General Description

consists of two inseparable isomers (CF3)2CFCF2OCH3 and CF3(CF2)3OCH3 with almost identical properties

Check Digit Verification of cas no

The CAS Registry Mumber 163702-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,3,7,0 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 163702-07:
(8*1)+(7*6)+(6*3)+(5*7)+(4*0)+(3*2)+(2*0)+(1*7)=116
116 % 10 = 6
So 163702-07-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H3F9O/c1-15-5(13,14)2(6,3(7,8)9)4(10,11)12/h1H3

163702-07-6 Well-known Company Product Price

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  • TCI America

  • (M1345)  Methyl Nonafluorobutyl Ether  >98.0%(GC)

  • 163702-07-6

  • 25g

  • 315.00CNY

  • Detail
  • TCI America

  • (M1345)  Methyl Nonafluorobutyl Ether  >98.0%(GC)

  • 163702-07-6

  • 500g

  • 2,500.00CNY

  • Detail

163702-07-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl Nonafluorobutyl Ether

1.2 Other means of identification

Product number -
Other names Perfluorobutyl Methyl Ether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:163702-07-6 SDS

163702-07-6Synthetic route

Dimethyl ether
115-10-6

Dimethyl ether

perfluorobutyryl fluoride
335-42-2

perfluorobutyryl fluoride

methyl nonafluorobutyl ether
163702-07-6

methyl nonafluorobutyl ether

Conditions
ConditionsYield
Stage #1: perfluorobutyryl fluoride With silver fluoride at 20℃; for 24h; Autoclave;
Stage #2: Dimethyl ether With water at 20℃; for 36h; Autoclave;
81.8%
perfluoropropylene
116-15-4

perfluoropropylene

1,3,3,3-tetrafluoro-1-methoxy-2-trifluoromethyl-propene
360-53-2

1,3,3,3-tetrafluoro-1-methoxy-2-trifluoromethyl-propene

methyl nonafluorobutyl ether
163702-07-6

methyl nonafluorobutyl ether

Conditions
ConditionsYield
With fluorine at -20℃; for 0.333333h; Inert atmosphere;72.5%
methanol
67-56-1

methanol

perfluoropropylene
116-15-4

perfluoropropylene

A

2,2,3,4,4,4-hexafluoro-1-butanol
382-31-0

2,2,3,4,4,4-hexafluoro-1-butanol

B

4H-octafluoro-2-difluoromethyl-butane
374-84-5

4H-octafluoro-2-difluoromethyl-butane

C

1,1,1,2,3,3-hexafluorobutane
76523-97-2

1,1,1,2,3,3-hexafluorobutane

D

methyl nonafluorobutyl ether
163702-07-6

methyl nonafluorobutyl ether

Conditions
ConditionsYield
Product distribution; Further Variations:; Reagents; Irradiation;A 20%
B n/a
C n/a
D n/a
nonafluoroisobutyl methyl ether
163702-08-7

nonafluoroisobutyl methyl ether

methyl nonafluorobutyl ether
163702-07-6

methyl nonafluorobutyl ether

A

C5H2ClF9O
205367-42-6

C5H2ClF9O

B

C5H2ClF9O
221617-86-3

C5H2ClF9O

C

C5HCl2F9O

C5HCl2F9O

D

C5HCl2F9O

C5HCl2F9O

Conditions
ConditionsYield
With chlorine for 4h; Irradiation;
With chlorine; 2,2'-azobis(isobutyronitrile) at 60℃; Heating / reflux;
methyl nonafluorobutyl ether
163702-07-6

methyl nonafluorobutyl ether

A

Carbonyl fluoride
353-50-4

Carbonyl fluoride

B

C5F10O2

C5F10O2

C

perfluoro-butyl formate

perfluoro-butyl formate

Conditions
ConditionsYield
With hydroxyl radical at 24.84℃; Kinetics; Temperature; Irradiation;

163702-07-6Downstream Products

163702-07-6Relevant articles and documents

Method for preparing fluorine-containing ether

-

Paragraph 0086-0087, (2019/07/29)

The invention relates to a 'method for preparing fluorine-containing ether', and belongs to the field of chemical synthesis. The method comprises the steps that under a nitrile solvent condition, carbonyl fluoride, trifluoroacetyl fluoride, pentafluoropropionyl fluoride, heptafluoro-n-butyryl fluoride, heptafluoro-iso-butyryl fluoride and other acyl fluorides are taken as raw materials to have anaddition reaction with metal fluorides to obtain perfluoroalkoxide, then under water catalysis, the perfluoroalkoxide and a low-toxic or even non-toxic harmless alkylating agent are subjected to an alkylation reaction to obtain the fluorine-containing ether. The method for preparing the fluorine-containing ether has the advantages that not only is the reaction condition mild, the yield of the fluorine-containing ether is high, but also the low-toxic or even non-toxic harmless alkylating agent is taken as a safe alkylation agent, the process is safe and reliable, and effective separation can beperformed by an ordinary distillation means in the industry.

Photolysis of perfluoropropylene-methanol mixture in vacuum ultraviolet

Fokanov,Pavlov,Semenov,Maksimov,Morozov

, p. 1275 - 1279 (2007/10/03)

The products of reaction of C3F6 with CH 3OH, initiated by vacuum ultraviolet, were determined. The kinetics scheme of the process was proposed. The parameters of the kinetic processes were calculated. The feasibility of p

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