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Methyl nonafluorovalerate, a fluorinated organic compound with the chemical formula C5H2F9O2, is a colorless liquid characterized by a strong odor. It is insoluble in water and serves as a crucial building block in the synthesis of various fluorochemicals and pharmaceuticals. Due to its unique properties, it also finds applications as a solvent and intermediate in the production of agrochemicals and specialty chemicals. While it is considered to have low toxicity, ongoing research is essential to comprehensively assess its environmental and health impacts.

13038-26-1

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13038-26-1 Usage

Uses

Used in Fluorochemical Production:
Methyl nonafluorovalerate is used as a key building block for the synthesis of various fluorochemicals. Its fluorinated nature contributes to the unique properties of these compounds, making them suitable for a wide range of applications, including refrigerants, surfactants, and fire suppressants.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, methyl nonafluorovalerate serves as an intermediate in the production of certain medications. Its chemical structure allows for the development of drugs with specific therapeutic properties, potentially enhancing the efficacy and safety of these pharmaceuticals.
Used as a Solvent:
Methyl nonafluorovalerate's solvent properties make it a valuable component in various industrial processes. Its ability to dissolve a wide range of substances, combined with its low toxicity, positions it as a preferred choice for applications where traditional solvents may pose environmental or health risks.
Used in Agrochemical Manufacturing:
As an intermediate in the production of agrochemicals, methyl nonafluorovalerate plays a vital role in the development of effective and environmentally friendly pesticides, herbicides, and other agricultural products. Its unique properties contribute to the creation of agrochemicals with improved performance and reduced environmental impact.
Used in Specialty Chemicals Production:
Methyl nonafluorovalerate's versatility extends to the specialty chemicals industry, where it is used as an intermediate in the synthesis of high-performance materials. These materials, which may include polymers, coatings, and adhesives, benefit from the compound's fluorinated nature, resulting in enhanced properties such as chemical resistance, thermal stability, and non-stick characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 13038-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13038-26:
(7*1)+(6*3)+(5*0)+(4*3)+(3*8)+(2*2)+(1*6)=71
71 % 10 = 1
So 13038-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H3F9O2/c1-17-2(16)3(7,8)4(9,10)5(11,12)6(13,14)15/h1H3

13038-26-1 Well-known Company Product Price

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  • TCI America

  • (M1912)  Methyl Nonafluorovalerate  >97.0%(GC)

  • 13038-26-1

  • 5g

  • 1,200.00CNY

  • Detail

13038-26-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl Nonafluorovalerate

1.2 Other means of identification

Product number -
Other names Methyl Perfluoropentanoate

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:13038-26-1 SDS

13038-26-1Relevant academic research and scientific papers

Hydrophobic Effects on Photochemical and Photophysical Processes: Evidence for Aggregation of Perfluorocarbon in Aqueous-Organic Solvents

Tung, Chen-Ho,Ji, Hai-Feng

, p. 2761 - 2766 (1995)

The emission spectra and photodimerization of fluorinated alkyl 2-naphthoates (NpFCn) and 9-anthrylmethyl perfluoroalkanoates (AnFCn) in aqueous-organic binary solvents have been investigated.The fluorescence spectra of NpFCn in dimethyl sulfoxide-water (DMSO-H2O) are dominated by excimer emission.Addition of long chain fluorocarbon compounds to the solution results in a reduction in the excimer emission and an enhancement of monomer emission.Selective excitation of the naphthalene moiety in the mixture solution of NpFCn and AnFCn leads to strong emission from AnFCn.Photoirradiation of NpFCn yields a 'cubane-like' photodimer with a relatively high quantum yield.All these observations suggest that hydrophobic interactions force molecules with long fluorocarbon chains to form aggregates in aqueous-organic binary solvents.

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