21379-33-9

  • Product Name:1,3-Butanediol, 4,4,4-Trifluoro-3-(Trifluoromethyl)-
  • MF:C5H6F6O2
  • Purity:99%
  • Molecular Weight:212.092
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Product Details

Cost-effective customized wholesale 1,3-Butanediol, 4,4,4-Trifluoro-3-(Trifluoromethyl)- 21379-33-9

  • Molecular Formula:C5H6F6O2
  • Molecular Weight:212.092
  • Vapor Pressure:0.322mmHg at 25°C 
  • Refractive Index:1.3411 
  • Boiling Point:177.032oC at 760 mmHg 
  • PKA:9.35±0.29(Predicted) 
  • Flash Point:60.867oC 
  • PSA:40.46000 
  • Density:1.527g/cm3 
  • LogP:1.22450 

1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)-(Cas 21379-33-9) Usage

General Description

1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)- is a colorless organic compound that is commonly used as a solvent in various industries. Its chemical structure features butanediol, a four-carbon molecule with two hydroxyl groups. The addition of three fluorine atoms and a trifluoromethyl group to the butanediol molecule increases its stability and alters its physical and chemical properties. 1,3-Butanediol, 4,4,4-trifluoro-3-(trifluoromethyl)- is utilized as a solvent in the production of resins, coatings, and adhesives, as well as in the synthesis of pharmaceuticals and agricultural chemicals. Its low toxicity and high solvency make it a valuable ingredient in a wide range of industrial applications.

InChI:InChI=1/C5H6F6O2/c6-4(7,8)3(13,1-2-12)5(9,10)11/h12-13H,1-2H2

21379-33-9 Relevant articles

Methods for Producing Fluorine-Containing Hydroxyaldehyde, Fluorine-Containing Propanediol, and Fluorine-Containing Alcohol Monomer

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Paragraph 0213-0214, (2015/12/30)

As shown by the following reaction formu...

PROCESS FOR PREPARING FLUORINATED DIOLS

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Page/Page column 7, (2012/09/10)

A process for preparing a fluorinated di...

THE REACTION OF SOME 3- AND 4-FLUOROOXETANES WITH ACIDS

Tarrant, Paul,Bull, R. N.

, p. 201 - 216 (2007/10/02)

Several oxetanes prepared from hexafluor...

21379-33-9 Process route

4,4,4-Trifluor-3-hydroxy-3-(trifluormethyl)butanal
21379-32-8

4,4,4-Trifluor-3-hydroxy-3-(trifluormethyl)butanal

4,4,4-trifluoro-3-(trifluoromethyl)butane-1,3-diol
21379-33-9

4,4,4-trifluoro-3-(trifluoromethyl)butane-1,3-diol

Conditions
Conditions Yield
With tert-butyl methyl ether; hydrogen; palladium on activated charcoal; at 170 ℃; under 517.162 Torr;
99%
With 5% active carbon-supported ruthenium; hydrogen; In di-isopropyl ether; at 70 ℃; under 13501.4 Torr; Autoclave;
acetaldehyde
75-07-0,9002-91-9

acetaldehyde

Hexafluoroacetone
684-16-2

Hexafluoroacetone

4,4,4-trifluoro-3-(trifluoromethyl)butane-1,3-diol
21379-33-9

4,4,4-trifluoro-3-(trifluoromethyl)butane-1,3-diol

Conditions
Conditions Yield
acetaldehyde; Hexafluoroacetone; With cesium fluoride; at -78 - 20 ℃; for 5h; Autoclave; Inert atmosphere;
With lithium aluminium tetrahydride; In diethyl ether; Cooling with ice;
50 %Spectr.

21379-33-9 Upstream products

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    2,2-bis(trifluoromethyl)oxetane

  • 21379-32-8
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    4,4,4-Trifluor-3-hydroxy-3-(trifluormethyl)butanal

  • 75-07-0
    75-07-0

    acetaldehyde

  • 684-16-2
    684-16-2

    Hexafluoroacetone

21379-33-9 Downstream products

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