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Perfluorotridecanoic Acid (PFTA) 97, also known as Perfluorinated Compound (PFC), is a perfluorinated alkyl acid (PFAA) that is considered a potential organic pollutant. It is characterized by its unique chemical structure, which consists of a fully fluorinated carbon chain, granting it specific properties such as high stability, resistance to degradation, and low surface tension.

72629-94-8

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72629-94-8 Usage

Uses

Used in Industrial Applications:
Perfluorotridecanoic Acid 97 is used as an additive in various industrial processes for its unique properties, such as its high chemical and thermal stability, and its ability to reduce surface tension. This makes it suitable for applications in the production of coatings, lubricants, and firefighting foams.
Used in Environmental Research:
PFTA 97 is also utilized in environmental research as a marker for studying the presence and behavior of perfluorinated compounds in the environment. Due to its persistence and potential for bioaccumulation, understanding its distribution and impact on ecosystems is crucial for assessing and managing environmental risks.

Check Digit Verification of cas no

The CAS Registry Mumber 72629-94-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,2 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72629-94:
(7*7)+(6*2)+(5*6)+(4*2)+(3*9)+(2*9)+(1*4)=148
148 % 10 = 8
So 72629-94-8 is a valid CAS Registry Number.
InChI:InChI=1/C13HF25O2/c14-2(15,1(39)40)3(16,17)4(18,19)5(20,21)6(22,23)7(24,25)8(26,27)9(28,29)10(30,31)11(32,33)12(34,35)13(36,37)38/h(H,39,40)

72629-94-8SDS

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 2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12,13,13,13-pentacosafluorotridecanoic acid

1.2 Other means of identification

Product number -
Other names 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,12,12-tricosafluorotridecanoic 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:72629-94-8 SDS

72629-94-8Downstream Products

72629-94-8Relevant academic research and scientific papers

OXYDATION ANODIQUE DE IODOPERFLUOROALCANES DANS LES ACIDES PERFLUOROALCANESULFONIQUES. PREPARATION DE NOUVEAUX ESTERS SULFONIQUES TOTALEMENT FLUORES RFSO3R'F A LONGUES CHAINES

Germain, A.,Commeyras, A.

, p. 487 - 492 (2007/10/02)

Perfluorinated sulphonic esters RFSO3R'F and fluorosulphates FSO3R'F, are easily obtained by anodic oxidation of iodoperfluoroalkanes R'FI in perfluoroalkene sulphonic acids RFSO3H (RF=CF3, C2F5, C4F9) and fluorosulphuric acid.With di-iodo compound I(CF2)4I, the mono and the diester can be selectively obtained.The alkaline hydrolysis of these esters produces perfluorinated carboxylic compounds.Polyfluorinated iodide R'FCH2CH2I are also oxidized in similar conditions.The mechanism of the electrolytic reaction is discussed.

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