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Butanoic acid, 4-(dimethylamino)-3-hydroxy-, also known as 4-(dimethylamino)-3-hydroxybutanoic acid, is an organic compound with the chemical formula C6H13NO3. It is a derivative of butanoic acid, featuring a hydroxyl group (-OH) at the 3-position and a dimethylamino group (-N(CH3)2) at the 4-position. Butanoic acid, 4-(dimethylamino)-3-hydroxy- is a colorless liquid with a molecular weight of 145.17 g/mol. It is soluble in water and has a melting point of approximately -35°C. The compound is used in the synthesis of various pharmaceuticals and agrochemicals, particularly as an intermediate in the production of certain drugs and pesticides. Due to its potential applications in the medical and agricultural fields, it is an important chemical in the development of new products.

542-06-3

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542-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 542-06-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 2 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 542-06:
(5*5)+(4*4)+(3*2)+(2*0)+(1*6)=53
53 % 10 = 3
So 542-06-3 is a valid CAS Registry Number.

542-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(dimethylamino)-3-hydroxybutanoic acid

1.2 Other means of identification

Product number -
Other names (+-)-4-Dimethylamino-3-hydroxy-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:542-06-3 SDS

542-06-3Relevant academic research and scientific papers

METHOD OF PREPARING AN ALKYLAMINE DERIVATIVE

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Page/Page column 6, (2012/03/10)

The present invention provides a method of preparing an alkylamine derivates which hardly generates impurities and enables mass production with high purity.

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