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Butanoic acid, 3,3,4,4,4-pentafluoro-, also known as 3,3,4,4,4-pentafluorobutanoic acid, is a synthetic organic compound with the chemical formula C4H3F5O2. It is a derivative of butanoic acid, where five fluorine atoms replace hydrogen atoms in the molecule. Butanoic acid, 3,3,4,4,4-pentafluoro- is characterized by its strong, pungent odor and is used in various applications, such as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Due to its unique properties, it is also employed in the synthesis of fluoropolymers and as a reagent in organic synthesis. However, it is important to handle Butanoic acid, 3,3,4,4,4-pentafluoro- with care, as it may cause irritation to the eyes, skin, and respiratory system.

380-60-9

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380-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 380-60-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,8 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 380-60:
(5*3)+(4*8)+(3*0)+(2*6)+(1*0)=59
59 % 10 = 9
So 380-60-9 is a valid CAS Registry Number.

380-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3,4,4,4-pentafluoro-butyric acid

1.2 Other means of identification

Product number -
Other names 3,3,4,4,4-Pentafluor-buttersaeure

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:380-60-9 SDS

380-60-9Relevant academic research and scientific papers

An improved oxidation of an alcohol using aqueous permanganate and phase-transfer catalyst

Mahmood, Arshed,Robinson, Graham E.,Powell, Lyn

, p. 363 - 364 (2013/09/08)

The oxidation of a primary alcohol to the corresponding carboxylic acid via permanganate and phase-transfer catalyst has been modified to circumvent impurity formation incurred during the reaction. A safe, simple, and efficient process was developed which gave the required carboxylic acid in 77% isolated yield using sodium permanganate in the presence of tetraethylammonium hydrogen sulphate.

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