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2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is a synthetic chemical compound with the molecular formula C8H2F14O. It is a colorless, odorless liquid that is highly flammable and volatile.
Used in Industrial Applications:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used as a solvent for various industrial processes due to its ability to dissolve a wide range of substances.
Used in Research Settings:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used as a surfactant in research settings to lower the surface tension of liquids, enabling better dispersion and interaction of substances.
Used in Chemical Production:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used as an intermediate in the production of other chemicals, contributing to the synthesis of various compounds.
Used in Refrigeration Industry:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used as a refrigerant due to its high volatility and ability to absorb and release heat.
Used in Pharmaceutical Manufacturing:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used in the manufacturing of pharmaceuticals, potentially serving as a building block for the development of new drugs.
Used in Agrochemical Production:
2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is used in the production of agrochemicals, such as pesticides and herbicides, to improve their effectiveness and properties.

25065-50-3

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25065-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25065-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,6 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 25065-50:
(7*2)+(6*5)+(5*0)+(4*6)+(3*5)+(2*5)+(1*0)=93
93 % 10 = 3
So 25065-50-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F12O/c8-2(3(9,1-20)5(11,12)13)4(10,6(14,15)16)7(17,18)19/h2,20H,1H2

25065-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,4,5,5,5-hexafluoro-2,4-bis(trifluoromethyl)pentan-1-ol

1.2 Other means of identification

Product number -
Other names 1,1,3-trihydroperfluoro-2,4-dimethylpentan-1-ol

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:25065-50-3 SDS

25065-50-3Downstream Products

25065-50-3Relevant academic research and scientific papers

Radiochemical addition of alcohols to perfluoro-2-alkenes

Kurykin,German,Kartasheva,Pikaev

, p. 193 - 194 (1996)

Radical addition of aliphatic alcohols to internal perfluorinated olefins has been studied. The process occurs non-stereoselectively to give equimolar mixtures of diastereoisomers in all cases.

ESR SPECTRA OF SPIN-ADDUCTS OF HYDROXYALKYL RADICALS WITH PERFLUORO-4-METHYL-2-PENTENE

Tumanskii, B. L.,Kurykin, M. A.,Solodovnikov, S. P.,Bubnov, N. N.,German, L. S.

, p. 644 - 646 (1991)

A study was carried out on the ESR spectra of the spin-adducts of hydroxyalkyl radicals with perfluoro-4-methyl-2-pentene (I) formed upon the photolysis of alcoholic solutions of this perfluoroolefin.The stable conformational positions of the substituents in the spin-adducts depend on the structure of the hydroxyalkyl radicals.The spin-sadducts are annihilated as a consequence of hydrogen atom abstraction as indicated in a preparative experiment.

HYDROFLUOROETHER COMPOUNDS AND PROCESSES FOR THEIR PREPARATION AND USE

-

Page/Page column 22, (2008/06/13)

A hydrofluoroether compound comprises two terminal fluoroalkyl groups and an intervening substituted or unsubstituted oxymethylene group, each of the fluoroalkyl groups comprising only one hydrogen atom and, optionally, at least one catenated (that is, in-chain) heteroatom; with the proviso that the hydrogen atom is part of a monofluoromethylene moiety.

MANUFACTURE OF FLUORINATED ALCOHOLS

-

Page/Page column 3-4, (2008/06/13)

Present invention relates to a process for the manufacture of fluorinated alcohols as well as borates which are employed in the manufacture of the fluorinated alcohols. Fluorinated alcohols of the formulae HOCHRCF(CF3)CHFCF(CF3)2 and HOCHRCF(CF(CF3)2)CHFCF3, HOCHRCF(CF2CF3)CH(CF3)2 and HOCHRC(CF3)2CHFCF2CF3 are made by heating a mixture of a borate of the formula (RCH2O)3B, wherein R═H or a C1 to C7 alkyl group, with perfluoro-4-methyl-2-pentene or perfluoro-2-methyl-2-pentene and a free-radical initiator to form a mixture of borates, optionally separating the mixture of borates from any reactants, solvents, and by-products; hydrolyzing the mixture of borates to form a hydrolysis product mixture; and separating the alcohols from the hydrolysis product mixture.

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