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1H,1H-Pentafluoropropyl methacrylate, with the molecular formula C7H5F5O2, is a fluoroalkyl-substituted methacrylate monomer. It is recognized for its exceptional thermal stability and chemical resistance, which are key attributes for its diverse applications across various industries.

45115-53-5

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45115-53-5 Usage

Uses

Used in Polymer and Coating Production:
1H,1H-Pentafluoropropyl methacrylate is used as a monomer in the production of polymers and coatings for its ability to enhance thermal stability and chemical resistance, making the resulting materials suitable for demanding environments.
Used in Textile Industry:
In the textile industry, 1H,1H-Pentafluoropropyl methacrylate is used as a component in the development of high-performance fabrics that are resistant to heat and chemicals, thus improving the durability and functionality of textiles.
Used in Electronics Industry:
1H,1H-Pentafluoropropyl methacrylate is utilized as a material in the electronics industry for the creation of coatings and components that require high thermal stability and protection against chemical degradation, ensuring the longevity and reliability of electronic devices.
Used in Automotive Industry:
Within the automotive sector, 1H,1H-Pentafluoropropyl methacrylate is employed as a component in the manufacturing of coatings and materials that can withstand the harsh conditions and chemical exposures typical in automotive applications, contributing to the performance and longevity of vehicles.
Used in Specialty Material Manufacturing:
1H,1H-Pentafluoropropyl methacrylate is used as a key ingredient in the production of specialty materials such as adhesives, sealants, and optical films, where its unique properties of thermal stability and chemical resistance are highly valued.
Safety Note:
It is crucial to handle 1H,1H-Pentafluoropropyl methacrylate with care due to its potential hazards. It can be harmful if inhaled or ingested and may cause skin and eye irritation upon contact, necessitating proper safety measures during its use.

Check Digit Verification of cas no

The CAS Registry Mumber 45115-53-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,5,1,1 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 45115-53:
(7*4)+(6*5)+(5*1)+(4*1)+(3*5)+(2*5)+(1*3)=95
95 % 10 = 5
So 45115-53-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H7F5O2/c1-4(5(13)14)2-3-6(8,9)7(10,11)12/h1-3H2,(H,13,14)/p-1

45115-53-5 Well-known Company Product Price

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  • (Code)Product description
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  • TCI America

  • (P2353)  2,2,3,3,3-Pentafluoropropyl Methacrylate (stabilized with TBC)  >98.0%(GC)

  • 45115-53-5

  • 5g

  • 290.00CNY

  • Detail
  • TCI America

  • (P2353)  2,2,3,3,3-Pentafluoropropyl Methacrylate (stabilized with TBC)  >98.0%(GC)

  • 45115-53-5

  • 25g

  • 1,290.00CNY

  • Detail
  • TCI America

  • (P2353)  2,2,3,3,3-Pentafluoropropyl Methacrylate (stabilized with TBC)  >98.0%(GC)

  • 45115-53-5

  • 100g

  • 4,990.00CNY

  • Detail
  • Alfa Aesar

  • (B24340)  2,2,3,3,3-Pentafluoropropyl methacrylate, 97%, stab.   

  • 45115-53-5

  • 5g

  • 403.0CNY

  • Detail
  • Alfa Aesar

  • (B24340)  2,2,3,3,3-Pentafluoropropyl methacrylate, 97%, stab.   

  • 45115-53-5

  • 25g

  • 1240.0CNY

  • Detail
  • Aldrich

  • (474193)  2,2,3,3,3-Pentafluoropropylmethacrylate  97%, contains 100 ppm 4-tert-butylcatechol as inhibitor

  • 45115-53-5

  • 474193-5ML

  • 1,953.90CNY

  • Detail

45115-53-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H,1H-Pentafluoropropyl methacrylate

1.2 Other means of identification

Product number -
Other names Methacrylic acid 2,2,3,3,3-pentafluoropropyl ester

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:45115-53-5 SDS

45115-53-5Downstream Products

45115-53-5Relevant academic research and scientific papers

Process for producing polyfluoroalkyl ester of unsaturated carboxylic acid

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

A polyfluoroalkyl ester of unsaturated carboxylic acid is produced in high yield in a more simple reactor and with much more reduction in the waste than the conventional process based on esterification reaction by subjecting a polyfluoroalkanol represented by the following general formula: [in-line-formulae]Rf-R—OH [/in-line-formulae] , where Rf is a polyfluoroalkyl group having 1-6 carbon atoms and R is an alkylene group having 1-6 carbon atoms, and an unsaturated carboxylic acid to dehydration reaction in a fluorine-containing solvent in the presence of an acid catalyst and a polymerization inhibitor.

Esterfication process for production of fluoroalkyl (meth)acrylate by pervaporation-aided membrane reactor

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

The present invention relates to a process for preparing fluoroacrylic acid ester using a pervaporation composite membrane, in particular, to a process for preparing fluoroacrylic acid ester performed in such a manner that water and unreacted fluoroalcohol generated in esterification between fluoroalcohol and (meth)acrylic acid in the presence of an acid catalyst are condensed and then passed through a pervaporation membrane to effectively remove water, followed by recycling the unreacted fluoroalcohol removed of water. The present process exhibits much higher conversion rate of fluoroacrylic acid ester, allows the decrease of energy consumption and could be performed in environment-friendly manner.

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