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β-Hydroxybutyramide, also known as 4-hydroxybutyramide, is a chemical compound with the molecular formula C4H7NO2. It is a derivative of butyric acid, featuring a hydroxyl group (-OH) and an amide group (-CONH2) attached to the β-carbon atom. This organic compound is of interest in the field of chemistry and biochemistry, particularly in the study of ketone bodies, which are produced during periods of low carbohydrate availability and are used as an alternative energy source by the body. β-Hydroxybutyramide is a synthetic analog that can be used in research to understand the metabolic pathways and potential therapeutic applications related to ketone bodies.

40482-53-9

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40482-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40482-53-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,4,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40482-53:
(7*4)+(6*0)+(5*4)+(4*8)+(3*2)+(2*5)+(1*3)=99
99 % 10 = 9
So 40482-53-9 is a valid CAS Registry Number.

40482-53-9SDS

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 β-Hydroxybutyramide

1.2 Other means of identification

Product number -
Other names 3-hydroxybutyric 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:40482-53-9 SDS

40482-53-9Upstream product

40482-53-9Relevant academic research and scientific papers

A high throughput screening strategy for the assessment of nitrile-hydrolyzing activity towards the production of enantiopure β-hydroxy acids

Coady, Tracey M.,Coffey, Lee V.,O'Reilly, Catherine,Owens, Erica B.,Lennon, Claire M.

, p. 150 - 155 (2013/10/01)

Nitrile hydrolysing enzymes have found wide use in the pharmaceutical industry for the production of fine chemicals. This work presents a strategy that facilitates the rapid identification of bacterial isolates demonstrating nitrile hydrolysing activity. The strategy incorporates toxicity, starvation and induction studies along with subsequent colorimetric screening for activity, further focusing the assessment towards the substrates of interest. This high-throughput strategy uses a 96 well plate system, and has enabled the rapid biocatalytic screening of 256 novel bacterial isolates towards β-hydroxynitriles. Results demonstrate the strategy's potential to rapidly assess a variety of β-hydroxynitriles including aliphatic, aromatic and dinitriles. A whole cell catalyst Rhodococcus erythropolis SET1 was identified and found to catalyse the hydrolysis of 3-hydroxybutyronitrile with remarkably high enantioselectivity under mild conditions, to afford (S)-3-hydroxybutyric acid in 42% yield and >99.9% ee. The biocatalytic capability of this strain including the variation of parameters such as temperature and time were further investigated and all results indicate the presence of a highly enantioselective if not enantiospecific nitrilase enzyme within the microbial whole cell.

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