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25065-50-3

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25065-50-3 Usage

General Description

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. 2,3,4,5,5,5-HEXAFLUORO-2,4-BIS(TRIFLUOROMETHYL)-1-PENTANOL is commonly used in industrial and research settings as a solvent, surfactant, and intermediate in the production of other chemicals. It is also used as a refrigerant and in the manufacturing of pharmaceuticals and agrochemicals. Due to its high volatility and potential health hazards, proper safety precautions must be taken when handling and storing this chemical.

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 articles and documents

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.

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.

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