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Ammonium 2-hydroxyisobutyrate (AHIB) is an organic compound with the chemical formula C4H9NO3 and a molecular weight of 119.12 g/mol. It is a white crystalline solid that is soluble in water and slightly soluble in ethanol. AHIB is a derivative of 2-hydroxyisobutyric acid, with an ammonium ion (NH4+) replacing the hydrogen atom in the carboxylic acid group. ammonium 2-hydroxyisobutyrate is used as a flavoring agent, a food additive, and a precursor in the synthesis of other chemicals. It is also known for its potential role in the production of bio-based plastics and as a building block for various pharmaceuticals. The compound is generally recognized as safe (GRAS) by the U.S. Food and Drug Administration for use in food products.

2539-76-6

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2539-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2539-76-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,3 and 9 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2539-76:
(6*2)+(5*5)+(4*3)+(3*9)+(2*7)+(1*6)=96
96 % 10 = 6
So 2539-76-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H8O3.H3N/c1-4(2,7)3(5)6;/h7H,1-2H3,(H,5,6);1H3

2539-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name azanium,2-hydroxy-2-methylpropanoate

1.2 Other means of identification

Product number -
Other names Ammonium a-hydroxyisobutyrate

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:2539-76-6 SDS

2539-76-6Downstream Products

2539-76-6Relevant academic research and scientific papers

Reactive Extraction of Free Organic Acids from the Ammonium Salts Thereof

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Page/Page column 11, (2010/08/22)

The invention relates to a process for converting ammonium salts of organic acids to the particular free organic acid, wherein an aqueous solution of the ammonium salt is contacted with an organic extractant and the salt is dissociated at temperatures and pressures at which the aqueous solution and the extractant are in the liquid state, and a stripping medium or entraining gas is introduced in order to remove NH3 from the aqueous solution and transfer at least a portion of the free organic acid formed to the organic extractant. The invention described here thus provides an improved process for releasing an organic acid, preferably a carboxylic, sulphonic or phosphonic acid, especially an alpha-hydroxycarboxylic acid or beta-hydroxycarboxylic acid, from the ammonium salt thereof by release and removal of ammonia and simultaneous extraction of the acid released with a suitable extractant from the aqueous phase. This process corresponds to a reactive extraction. The reactive extraction of an organic acid from the aqueous ammonium salt solution thereof can be improved significantly by the use of a stripping medium or entraining gas, for example nitrogen, air, steam or inert gases, for example argon. The ammonia released is removed from the aqueous solution by the continuous gas stream and can be fed back into a production process. The free acid can be obtained from the extractant by a process such as distillation, rectification, crystallization, re-extraction, chromatography, adsorption, or by a membrane process.

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