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10483-16-6

δ-Amino-α-methylvaleric acid, also known as δ-Aminovaleric acid or δ-AIV, is an organic compound with the chemical formula C6H13NO2. It is a non-proteinogenic amino acid, meaning it is not one of the 20 amino acids that make up proteins in living organisms. δ-AIV is a white crystalline solid that is soluble in water and has a molecular weight of 131.17 g/mol. It is structurally similar to the amino acid valine, but with an additional methyl group on the α-carbon and an amino group on the δ-carbon. δ-Amino-α-methylvaleric acid has been studied for its potential applications in various fields, including pharmaceuticals and chemical synthesis, due to its unique structure and properties.

10483-16-6

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10483-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10483-16-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10483-16:
(7*1)+(6*0)+(5*4)+(4*8)+(3*3)+(2*1)+(1*6)=76
76 % 10 = 6
So 10483-16-6 is a valid CAS Registry Number.

10483-16-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-amino-2-methyl-valeric acid

1.2 Other means of identification

Product number -
Other names .5-amino-2-methylvaleric 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:10483-16-6 SDS

10483-16-6Downstream Products

10483-16-6Relevant articles and documents

Production of 6-aminocaproic acid

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Page column 8-9, (2008/06/13)

A process for making 6-aminocaproic acid by hydroformylating 3-pentenenitrile to produce 3-, 4-, and 5-formylvaleronitrile (FVN mixture), oxidizing the FVN mixture to produce 3-, 4-, and 5-cyanovaleric acid; hydrogenating the resulting product to produce 6-aminocaproic acid, 5-amino-4-methylvaleric acid, and 4-amino-3-ethylbutyric acid; and isolating 6-aminocaproic acid from the reaction product. The resulting 6-aminocaproic acid can be cyclized to produce caprolactam.

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