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Pentafluoroethylphosphonic acid, also known as PFPA, is a strong, fluorinated phosphonic acid compound with the molecular formula C2HF5O3P. It is characterized by its high reactivity and ability to form stable complexes with a wide range of metals, making it a versatile chemical used in various industries and research applications.

103305-01-7

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103305-01-7 Usage

Uses

Used in Organic and Inorganic Synthesis:
PFPA is utilized as a reagent in organic and inorganic synthesis processes, contributing to the formation of a variety of chemical compounds.
Used in Pharmaceutical Production:
Pentafluoroethylphosphonic acid is employed in the production of pharmaceuticals, where its unique properties aid in the development of new drugs and medicinal compounds.
Used in Agrochemical Production:
PFPA is used in the synthesis of agrochemicals, playing a role in the creation of pesticides, herbicides, and other agricultural chemicals to improve crop protection and yield.
Used in Materials Science:
Pentafluoroethylphosphonic acid is applied in materials science for the development of new materials with enhanced properties, such as improved durability or specific chemical resistance.
Used as a Building Block for Specialty Chemicals:
PFPA serves as a key building block for the synthesis of specialty chemicals, which are used in various high-value applications across different industries.
Used in the Production of Fluorinated Polymers:
Pentafluoroethylphosphonic acid is employed in the production of fluorinated polymers, which are known for their exceptional chemical stability, thermal resistance, and non-stick properties.
It is important to handle PFPA with care due to its corrosive and toxic nature, ensuring proper safety measures are in place during its use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 103305-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,3,0 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103305-01:
(8*1)+(7*0)+(6*3)+(5*3)+(4*0)+(3*5)+(2*0)+(1*1)=57
57 % 10 = 7
So 103305-01-7 is a valid CAS Registry Number.
InChI:InChI=1/C2H2F5O3P/c3-1(4,5)2(6,7)11(8,9)10/h(H2,8,9,10)/p-2

103305-01-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,2-pentafluoroethylphosphonic acid

1.2 Other means of identification

Product number -
Other names Pentafluoroethylphosphonic acid

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:103305-01-7 SDS

103305-01-7Relevant academic research and scientific papers

COMPOUNDS WITH (PERFLUOROALKYL) FLUOROHYDROGENPHOSPHATE ANIONS

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Page/Page column 15, (2012/10/23)

The present invention relates to a process for the preparation of compounds with (perfluoroalkyl)fluorohydrogenphosphate anion, and to compounds containing (perfluoroalkyl)fluorohydrogenphosphate anion and to the use thereof.

PROCESS FOR THE PREPARATION OF BIS(FLUOROALKYL)PHOSPHINIC ACID OR FLUOROALKYLPHOSPHONIC ACID

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Page/Page column 3-4, (2011/06/23)

The invention relates to a process for the preparation of bis(fluoroalkyl)phosphinic acid and/or fluoroalkylphosphonic acid by reaction of, monofluoroalkyltetrafluorophosphorane bis(fluoroalkyl)trifluorophosphorane or tris(fluoroalkyl)difluorophosphorane with water.

Reaction of perfluoroalkyl Grignard reagents with phosphorus trihalides: A new route to perfluoroalkyl-phosphonous and-phosphonic acids

Hosein, Adil I.,Le Goff, Xavier F.,Ricard, Louis,Caffyn, Andrew J. M.

experimental part, p. 1484 - 1490 (2011/04/23)

The reaction of perfluoroalkyl Grignard reagents with phosphorus(III) halides was explored. In the process a new convenient, one-pot, high yield method for the synthesis of (perfluoroalkyl)phosphonic acids has been developed. Perfluoroalkyl Grignard reagents react with phosphorus trichloride or phosphorus tribromide to form (perfluoroalkyl)phosphonous dihalides. Hydrolysis gives the corresponding (perfluoroalkyl)phosphonous acids. Oxidation of the phosphonous acids with H2O2 produces (perfluoroalkyl) phosphonic acids in 60-78% overall yields, based on the corresponding perfluoroalkyl iodide. The X-ray crystal structures of the toluidinium salts, [MeC6H4NH3]2[C2F 5PO3] and [MeC6H4NH 3][C8F17P(O)2OH], are reported.

Perfluoroalkanoic hydroformed mono-, bis (perfluorolefin alkyl) acid synthesis of salt and perfluorolefin alkylphosphonic

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Page/Page column 20, (2008/06/13)

The present invention relates to a process for the preparation of monohydroperfluoroalkanes, bis(perfluoroalkyl)phosphinates and perfluoroalkylphosphonates which comprises at least the treatment of at least one perfluoroalkylphosphorane with at least one base in a suitable reaction medium.

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