Literature DB >> 7075719

Deuterium isotope effects in the ninhydrin reaction of primary amines.

P H Yu, B A Davis.   

Abstract

The rate of development of Ruhemann's purple in the ninhydrin reaction of two deuterated primary amines, aa-d2-p-tyramine and aa-d2-beta-phenylethylamine, is significantly reduced. It appears to be a primary isotope effect and indicates that the cleavage of the carbon-hydrogen bond at the a-position is involved in the rate-determining step of the color reaction.

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Year:  1982        PMID: 7075719     DOI: 10.1007/bf01949352

Source DB:  PubMed          Journal:  Experientia        ISSN: 0014-4754


  3 in total

1.  Photometric ninhydrin method for use in the chromatography of amino acids.

Authors:  S MOORE; W H STEIN
Journal:  J Biol Chem       Date:  1948-10       Impact factor: 5.157

2.  Amino acid analysis: aqueous dimethyl sulfoxide as solvent for the ninhydrin reaction.

Authors:  S Moore
Journal:  J Biol Chem       Date:  1968-12-10       Impact factor: 5.157

3.  Deuterium isotope effects on the enzymatic oxidative deamination of trace amines.

Authors:  P H Yu; S Barclay; B Davis; A A Boulton
Journal:  Biochem Pharmacol       Date:  1981-11-15       Impact factor: 5.858

  3 in total

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