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2-(decanamido)propanoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27167-48-2

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27167-48-2 Usage

Structure

Derivative of propanoic acid with an amide group attached to the second carbon atom and a decyl group attached to the nitrogen atom

Common uses

Surfactant
Emulsifier

Industrial applications

Used in various industrial products
Employed in personal care products

Surface tension reduction

Ability to lower the surface tension of liquids

Hair care applications

Conditioning agent
Provides smooth and soft texture to the hair

Check Digit Verification of cas no

The CAS Registry Mumber 27167-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,6 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 27167-48:
(7*2)+(6*7)+(5*1)+(4*6)+(3*7)+(2*4)+(1*8)=122
122 % 10 = 2
So 27167-48-2 is a valid CAS Registry Number.

27167-48-2Downstream Products

27167-48-2Relevant academic research and scientific papers

7-alkyl- and cycloalkyl-substituted imidazotriazinones

-

, (2008/06/13)

The present invention relates to 7-alkyl- and cycloalkyl-substituted imidazotriazinones, to processes for their preparation and to their use as medicaments, in particular as inhibitors of cGMP-metabolizing phosphodiesterases.

Enhancement of the rectal absorption of sodium ampicillin by N-acylamino acids in rats

Wu,Murakami,Higashi,Yata

, p. 508 - 512 (2007/10/02)

The promoting efficacies of N-acyl derivatives of amino acids on the rectal absorption of sodium ampicillin were investigated using the rat rectal loop technique. N-Acyl derivatives with longer carbon chains in the acyl moiety showed a greater promoting potency. The promoting potencies of N-acyl derivatives of phenylglycine and phenyl-alanine were greater than those of glycine and alanine derivatives when compared at the same length of carbon chain in their acyl moieties. The promoting action of N-acylamino acids was not influenced by the presence of N-ethylmaleimide or ouabain. The promoting potencies of N-acylamino acids were depressed in the presence of calcium chloride in the rectal loop. The contribution of the calcium ion sequestration capacity of N-acylamino acids to their promoting efficacies is discussed.

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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