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16627-68-2

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16627-68-2 Usage

Description

1,1,2,2-Tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether (HFE-458) is a hydrofluoroether. Hydrofluoroether is a new type of lookchem chlorofluorocarbons (CFCs) substitute, ODP is zero, GWP is low, and the atmospheric residence time is very short. It is considered as one of the ideal substitutes for CFCs.

Uses

1,1,2,2-Tetrafluoroethyl-2,2,3,3-tetrafluoropropylether can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development processes and chemical production processes.

Synthesis

A system of a 6-L autoclave made of stainless steel was evacuated. The autoclave was charged with 401 g of potassium hydroxide (7.15 mol, 0.55 molar amount relative to 1 mol of a fluorine-containing alkyl alcohol), water (1604 mL), 2,2,3,3-tetrafluoro-1-propanol (boiling point of 109° C., specific gravity of 1.4) represented by HCF2CF2CH2OH (1716 g, 13 mol) as a fluorine-containing alkyl alcohol. Then, the system was evacuated and replaced with nitrogen 20 times at room temperature. After evacuated, the system was filled with tetrafluoroethylene to 0.1 MPa, and the reaction system was heated to 85° C. After the temperature in the system reached 85° C., tetrafluoroethylene was added thereto little by little so that the reaction pressure was kept at 0.5 to 0.8 MPa. The temperature in the system was adjusted so as to be kept at 75 to 95° C.Tetrafluoroethylene was added until the amount reached 0.5 molar relative to 1 mol of the fluorine-containing alkyl alcohol. The reaction was continuously carried out under stirring. When reduction in the pressure in the autoclave was stopped, the temperature in the autoclave was reduced to room temperature and unreacted tetrafluoroethylene was discharged, and the reaction was stopped. These steps took 5 hours to perform.The fluoroether of a lower phase of the production solution was HCF2CF2CH2OCF2CF2H (boiling point of 92° C., specific gravity of 1.52). Table 1 shows the composition of the fluoroether production solution of a lower phase resulting from GC analysis.

Check Digit Verification of cas no

The CAS Registry Mumber 16627-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,2 and 7 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 16627-68:
(7*1)+(6*6)+(5*6)+(4*2)+(3*7)+(2*6)+(1*8)=122
122 % 10 = 2
So 16627-68-2 is a valid CAS Registry Number.

16627-68-2 Well-known Company Product Price

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  • TCI America

  • (T3069)  1,1,2,2-Tetrafluoroethyl 2,2,3,3-Tetrafluoropropyl Ether  >98.0%(GC)

  • 16627-68-2

  • 5g

  • 290.00CNY

  • Detail
  • TCI America

  • (T3069)  1,1,2,2-Tetrafluoroethyl 2,2,3,3-Tetrafluoropropyl Ether  >98.0%(GC)

  • 16627-68-2

  • 25g

  • 690.00CNY

  • Detail
  • TCI America

  • (T3069)  1,1,2,2-Tetrafluoroethyl 2,2,3,3-Tetrafluoropropyl Ether  >98.0%(GC)

  • 16627-68-2

  • 100g

  • 1,390.00CNY

  • Detail

16627-68-2SDS

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 1,1,2,2-Tetrafluoroethyl-2,2,3,3-Tetrafluoropropylether

1.2 Other means of identification

Product number -
Other names 1,1,2,2-Tetrafluoroethyl 2,2,3,3-tetrafluoropropyl 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:16627-68-2 SDS

16627-68-2Downstream Products

16627-68-2Relevant articles and documents

METHOD FOR PRODUCING FLUORINE-CONTAINING ETHER WITH HIGH PURITY

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Page/Page column 4, (2012/04/11)

The present invention provides a method for efficiently producing a highly pure fluoroether containing remarkably low concentration of a fluorine-containing alkyl alcohol. The method is suited for scale-up and specifically includes performing countercurrent separation of a crude solution of fluoroether including a fluorine-containing alkyl alcohol as an impurity using water.

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