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L-Aspartic acid, N-(1-oxodecyl)-, also known as N-decanoyl-L-aspartic acid, is a chemical compound with the molecular formula C12H21NO4. It is a derivative of L-aspartic acid, an amino acid that plays a crucial role in various biological processes. In L-Aspartic acid, N-(1-oxodecyl)-, the L-aspartic acid molecule is modified by the attachment of a decanoyl group (a ten-carbon fatty acid chain) to its nitrogen atom. This modification can alter the properties and reactivity of the original amino acid, potentially affecting its solubility, stability, and interactions with other molecules. L-Aspartic acid, N-(1-oxodecyl)-, may be used in various applications, such as in the synthesis of pharmaceuticals, as a building block for more complex molecules, or in research to study the effects of fatty acid modifications on amino acid behavior.

1116-12-7

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1116-12-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1116-12-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1116-12:
(6*1)+(5*1)+(4*1)+(3*6)+(2*1)+(1*2)=37
37 % 10 = 7
So 1116-12-7 is a valid CAS Registry Number.

1116-12-7SDS

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 (2S)-2-(decanoylamino)butanedioic acid

1.2 Other means of identification

Product number -
Other names N-decanoyl-L-aspartic 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:1116-12-7 SDS

1116-12-7Downstream Products

1116-12-7Relevant academic research and scientific papers

Melting Behaviour of Some Pure N-Acyl Amino Acids and Peptides

Iyer, Venkataraman N.,Sheth, Geeta N.,Subrahmanyam, V. V. R.

, p. 856 - 859 (2007/10/02)

Fifty three tlc pure N-acyl amino acids were synthesized by Schotten-Baumann reaction from glc pure odd and even chain fatty acids and chromatographycally homogeneous amino acids and a few N-acyl peptides were prepared through the carboxylic carbonic anhydride intermediates.The melting points are reported and discussed.

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