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1-(PENTAFLUOROPROPIONYL)IMIDAZOLE, also known as PFPI, is a chemical compound that serves as a derivatizing reagent in the field of gas chromatography/mass spectrometry (GC/MS) analysis. It is effective in reacting with amino and hydroxyl functionalities, yielding distinctive products that can be easily analyzed. PFPI is known for providing a higher yield of products compared to pentafluoropropionic anhydride when preparing methyl ester/pentafluoropropionyl derivatives.

71735-32-5

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71735-32-5 Usage

Uses

Used in GC/MS Analysis:
1-(PENTAFLUOROPROPIONYL)IMIDAZOLE is used as a derivatizing reagent for enhancing the analysis of samples in GC/MS. It is particularly useful for the preparation of methyl ester/pentafluoropropionyl derivatives, as it provides a higher yield of products than other derivatizing agents.
Used in Analytical Chemistry:
In the field of analytical chemistry, 1-(PENTAFLUOROPROPIONYL)IMIDAZOLE is used as a reagent to improve the detection and quantification of specific compounds, such as d-chiro-Inositol, in various samples. This is achieved through the process of derivatization, which allows for better separation and identification of the target compounds during GC/MS analysis.
Used in Research and Development:
PFPI is utilized in research and development for the study of various chemical compounds and their interactions. Its ability to react with amino and hydroxyl functionalities makes it a valuable tool in the synthesis and analysis of new compounds, as well as in the investigation of their properties and potential applications.
Used in Pharmaceutical and Biomedical Industries:
In the pharmaceutical and biomedical industries, 1-(PENTAFLUOROPROPIONYL)IMIDAZOLE may be employed in the development of new drugs and therapies. Its role as a derivatizing reagent can aid in the identification and analysis of bioactive compounds, contributing to the advancement of drug discovery and the understanding of biological processes.
Used in Environmental and Food Analysis:
PFPI is also used in environmental and food analysis to identify and quantify specific contaminants or components in samples. The derivatization process facilitated by PFPI can improve the detection and analysis of these compounds, ensuring accurate and reliable results in various applications, such as monitoring pollution levels or assessing the quality of food products.

Check Digit Verification of cas no

The CAS Registry Mumber 71735-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,7,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71735-32:
(7*7)+(6*1)+(5*7)+(4*3)+(3*5)+(2*3)+(1*2)=125
125 % 10 = 5
So 71735-32-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H4Br2F3N/c8-3-1-4(7(10,11)12)6(13)5(9)2-3/h1-2H,13H2

71735-32-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (17281)  1-(Pentafluoropropionyl)imidazole  for GC derivatization, ≥98.5%

  • 71735-32-5

  • 17281-1ML

  • 452.79CNY

  • Detail

71735-32-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2,3,3,3-pentafluoro-1-imidazol-1-ylpropan-1-one

1.2 Other means of identification

Product number -
Other names N-(pentafluoropropionyl)imidazole

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:71735-32-5 SDS

71735-32-5Relevant academic research and scientific papers

Synthesis of novel 2-perfluoroacylcyclohexane-1,3-diones

Khlebnicova,Isakova,Baranovsky,Borisov,Lakhvich

, p. 1564 - 1569 (2008/09/18)

A one-pot synthesis of 2-perfluoroalkanoylcyclohexane-1,3-diones via C-acylation of cyclohexane-1,3-diones with N-perfluoroacylimidazole as an acylating agent is reported. A reaction was examined with isolated N-trifluoroacetylimidazole and with N-perfluoroacylimidazoles generated in situ from perfluorocarboxylic acid anhydrides or perfluorocarboxylic acids.

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