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Butanoic acid, 2-(aminomethyl)-, also known as 2-(aminomethyl)butanoic acid or 2-amino-2-methylpropanoic acid, is an organic compound with the chemical formula C5H11NO2. It is a derivative of butanoic acid, featuring an aminomethyl group (-CH2NH2) attached to the second carbon atom. Butanoic acid,2-(aminomethyl)- is a white crystalline solid with a molecular weight of 117.15 g/mol. It is soluble in water and has a melting point of approximately 70-72°C. 2-(aminomethyl)butanoic acid is used in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds due to its unique functional groups, which include a carboxylic acid group and an amine group.

4385-92-6

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4385-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4385-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,3,8 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4385-92:
(6*4)+(5*3)+(4*8)+(3*5)+(2*9)+(1*2)=106
106 % 10 = 6
So 4385-92-6 is a valid CAS Registry Number.

4385-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(aminomethyl)butanoic acid

1.2 Other means of identification

Product number -
Other names 2-Aminomethyl-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 -
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More Details:4385-92-6 SDS

4385-92-6Relevant academic research and scientific papers

FLAME-INDUCED CARBOXYLATION OF UNSATURATED AMINES IN AN AQUEOUS FORMIC ACID SOLUTION

Nomoto, Shinya,Harada, Kaoru

, p. 145 - 148 (1985)

When a hydrogen-oxygen flame was kept in contact with an aqueous formic acid solution of unsaturated amines, carboxylation onto a double bond took place.This reaction revealed to be initiated by addition of a hydrogen atom to the double bond followed by coupling of the resulted substrate radical with a carboxyl radical.

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