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(NONAFLUORO-N-BUTYL)EPOXIDE is a fluorinated epoxide compound characterized by a three-membered ring structure consisting of an oxygen atom and two carbon atoms, with the hydrogen atoms in the butyl group of n-butyl vinyl ether replaced by nonafluoro groups. This results in a highly fluorinated compound that serves as a building block for synthesizing various fluorinated compounds and polymers. Its unique fluorinated structure endows it with properties suitable for applications requiring unique surface properties and resistance to chemical and environmental degradation.

89807-87-4

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89807-87-4 Usage

Uses

Used in Surfactant Industry:
(NONAFLUORO-N-BUTYL)EPOXIDE is used as a surfactant for its ability to lower surface tension in liquids, enhancing the spreading and wetting properties of the surfactant solution. Its fluorinated nature provides unique surface properties, making it suitable for applications in industries where high-performance surfactants are required.
Used in Lubricant Industry:
(NONAFLUORO-N-BUTYL)EPOXIDE is used as a lubricant due to its low friction coefficient and resistance to chemical and environmental degradation. Its fluorinated structure allows it to maintain lubricating properties under extreme conditions, making it ideal for use in high-performance lubricants for various industrial applications.
Used in Inorganic Coating Industry:
(NONAFLUORO-N-BUTYL)EPOXIDE is used as a component in inorganic coatings to provide unique surface properties and resistance to chemical and environmental degradation. Its fluorinated nature contributes to the formation of a durable and protective coating, suitable for applications in various industries where coatings with high resistance to wear, corrosion, and environmental factors are required.

Check Digit Verification of cas no

The CAS Registry Mumber 89807-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,0 and 7 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89807-87:
(7*8)+(6*9)+(5*8)+(4*0)+(3*7)+(2*8)+(1*7)=194
194 % 10 = 4
So 89807-87-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F9O/c7-3(8,2-1-16-2)4(9,10)5(11,12)6(13,14)15/h2H,1H2

89807-87-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,1,2,2,3,3,4,4,4-nonafluorobutyl)oxirane

1.2 Other means of identification

Product number -
Other names Nonafluorobutylepoxide

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:89807-87-4 SDS

89807-87-4Relevant academic research and scientific papers

NOUVELLES METHODES DE PREPARATION DES F-ALKYL OXIRANES A PARTIR DES ACETATES DE BROMO-2 F-ALKYL-2 ETHYLE ET DES BROMO-2 F-ALKYL-2 ETHANOL

Chaabouni, Mm.,Baklouti, A.,Szonyi, S.,Cambon, A.

, p. 307 - 315 (1990)

F-alkyl oxiranes provide many interesting intermediates.Their synthesis from 2-bromo-2-F-alkylethyl acetates and from 2-bromo-2-F-alkylethanols was improved by two different methods which are very easy to apply.One requires the use of concentrated caustic soda and a phase transfer catalyst; the other one, potassium fluoride in triethylene glycol.

SYNTHESE DE F-ALKYL OXIRANNES

Coudures, C.,Pastor, R.,Cambon, A.

, p. 93 - 104 (1984)

The perfluoroalkyloxirans were obtained with good yields from the long chain perfluoroalkyl ethylenes RFCH=CH2.All the reaction intermediates were isolated and described.Their structure was determinated by the usual spectroscopy methods : N.M.R., infra-red, mass spectrometry and by microanalysis.

Nouveaux amphiphiles cationiques perfluoroalkyles derives des 1-monotosylate et 1-monobromoacetate de 2-F-alkyl 2-bromo ethanols. II

Nasreddine, M.,Szoenyi, S.,Cambon, A.

, p. 293 - 300 (2007/10/02)

Tosylation, esterification and etherification reactions have been investigated for 2-F-alkyl-2-bromo-ethanols.Intermediates containing a tosyl group or a bromine atom could be converted into corresponding F-alkylated cationic amphiphiles by means of secon

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