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2,2,4,4-Tetramethylpentanoic acid, also known as TMPIA, is a synthetic organic compound characterized by its molecular formula C9H18O2. It is a colorless liquid with a strong odor, and it is recognized for its high flash point and stability under normal temperatures and pressures. This makes it a versatile chemical with a wide range of industrial applications, including its use as a corrosion inhibitor and in the production of fragrances and flavorings. Additionally, it serves as a precursor in the synthesis of other organic compounds and polymers, highlighting its importance in the chemical and manufacturing industries as a valuable building block for various products.

3302-12-3

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3302-12-3 Usage

Uses

Used in Chemical and Manufacturing Industries:
2,2,4,4-Tetramethylpentanoic acid is used as a versatile building block for the synthesis of various organic compounds and polymers, contributing to the development of a wide range of products in these industries.
Used as a Corrosion Inhibitor:
In the chemical industry, 2,2,4,4-Tetramethylpentanoic acid is utilized as a corrosion inhibitor, helping to prevent the degradation of materials and equipment, thereby extending their lifespan and improving efficiency.
Used in Fragrance and Flavoring Production:
2,2,4,4-Tetramethylpentanoic acid is employed in the production of fragrances and flavorings due to its strong odor, enhancing the sensory qualities of various consumer products.
Used in the Synthesis of Other Organic Compounds:
As a precursor, 2,2,4,4-Tetramethylpentanoic acid plays a crucial role in the synthesis of other organic compounds, enabling the creation of new materials and substances with diverse applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 3302-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3302-12:
(6*3)+(5*3)+(4*0)+(3*2)+(2*1)+(1*2)=43
43 % 10 = 3
So 3302-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O2/c1-8(2,3)6-9(4,5)7(10)11/h6H2,1-5H3,(H,10,11)

3302-12-3SDS

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 2,2,4,4-tetramethylpentanoic acid

1.2 Other means of identification

Product number -
Other names Pentanoic acid,2,2,4,4-tetramethyl

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:3302-12-3 SDS

3302-12-3Relevant academic research and scientific papers

Method for synthesizing trimethylacetic acid and 2,2,4,4-tetramethylvaleric acid through diisobutylene carbanyl group

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Paragraph 0024-0026, (2017/06/02)

The invention discloses a method for synthesizing trimethylacetic acid and 2,2,4,4-tetramethylvaleric acid through a diisobutylene carbanyl group, and belongs to the technical field of organic carboxylic acid synthesis. An oxo synthesis method is adopted, and the method for synthesizing trimethylacetic acid and 2,2,4,4-tetramethylvaleric acid through the diisobutylene carbanyl group comprises the following steps that 1, a carbonylation reaction is conducted, wherein diisobutylene, carbonic oxide and water serve as the raw materials, a sulfuric acid aqueous solution with the concentration ranging from 65% to 80% serves as a catalyst, pressurization is conducted under the condition of 20 DEG C to 30 DGE C for a reaction, and a mixture of pivalic acid sulfonate and 2,2,4,4-tetramethylvaleric acid sulfonate is obtained; 2, hydrolysis is conducted, wherein the obtained mixture of pivalic acid sulfonate and 2,2,4,4-tetramethylvaleric acid sulfonate in the first step is subjected to hydrolysis at 5 DEG C to 10 DEG C, standing is conducted for layering, an aqueous phase is subjected to extraction and concentration and then recycled, an organic phase is subjected to rectification, and trimethylacetic acid and 2,2,4,4-tetramethylvaleric acid are obtained. According to the method for synthesizing trimethylacetic acid and 2,2,4,4-tetramethylvaleric acid through the diisobutylene carbanyl group, diisobutylene is adopted to replace pure isobutylene in the prior art to react with sulfuric acid and carbonic oxide to produce trimethylacetic acid, and 2,2,4,4-tetramethylvaleric acid is generated simultaneously; the method is convenient and safe, and potential safety hazards are greatly reduced.

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