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1996-88-9

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1996-88-9 Usage

Chemical Properties

Colorless liquid

Uses

Perfluorooctylethyl Methacrylate was used to prepare fluorinated latexes by polymerization of miniemulsions as fluorinated monomers.Along with Perfluorodecylethyl Methacrylate (P286590), Perfluorooctylethyl Methacrylate was one of the pollutants from Great Lakes studied.

Check Digit Verification of cas no

The CAS Registry Mumber 1996-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1996-88:
(6*1)+(5*9)+(4*9)+(3*6)+(2*8)+(1*8)=129
129 % 10 = 9
So 1996-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C14H9F17O2/c1-5(2)6(32)33-4-3-7(15,16)8(17,18)9(19,20)10(21,22)11(23,24)12(25,26)13(27,28)14(29,30)31/h1,3-4H2,2H3

1996-88-9 Well-known Company Product Price

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  • Aldrich

  • (474223)  3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-Heptadecafluorodecylmethacrylate  contains MEHQ as inhibitor, 97%

  • 1996-88-9

  • 474223-25ML

  • 2,421.90CNY

  • Detail

1996-88-9SDS

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 3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodecyl 2-methylprop-2-enoate

1.2 Other means of identification

Product number -
Other names 1h,1h,2h,2h-perfluorodecyl methacrylate

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:1996-88-9 SDS

1996-88-9Downstream Products

1996-88-9Relevant articles and documents

Process for preparing fluorinated alkyl carboxylate esters

-

Page/Page column 5, (2008/06/13)

A process for preparing fluorinated alkyl carboxylate esters comprises reaction of a silver carboxylate or silver carboxylate precursor, such as silver (I) iodide with a fluorinated alkyl iodide and a carboxylic acid. Preferably the fluorinated alkyl iodide has the general formula CF3(CF2)nCH2CH2I, wherein n is an integer in the range of from 1 to 29 and the carboxylic acid is acetic acid, acrylic acid or methacrylic acid.

Synthesis and Mesoscopic Organization of Perfluoroalkyl-Alkylene Methacrylate Monomers

Hoepken, Jens,Faulstich, Sabine,Moeller, Martin

, p. 59 - 74 (2007/10/02)

Alcohols with perfluorinated segments, F(CF2)n-(CH2)m-OH; n = 8, 10, 12; m = 4, 6, 10; have been converted into methacrylates by a dicyclohexylcarbodiimide activated esterification reaction.The resulting methacrylates show two disordering transitions prior to isotropization.Polarization optical microscopy indicates the occurrence of smectic liquid crystal phases.Organic solutions of the amphiphilic methacrylates showed a strong decrease in the surface tension at low concentrations.Peculiar surface activity had already been observed for the compound with the shortest fluorocarbon segment.Needle shaped crystallites of the semifluorinated compounds are formed when hydrocarbon solutions of methacrylates with a perfluorododecyl substituent are cooled.The crystals can form a fine mesh network which encloses the solvent in the cavities.The size of the needle crystals and the internal dimensions of the network depend strongly on the crystallization conditions.

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