Published November 1970 | Version v1
Journal article

The preparation of α-oxo acid derivatives suitable for specific-radioactivity determination

  • 1. Edinburgh Univ. (UK)

Description

1. Conditions favouring the condensation of o-phenylenediamine with α-oxo acids to form substituted quinoxalines have been investigated. The best yields (85–100%) are obtained by incubation of the reagents in 2m-hydrochloric acid. Substitution of acetic acid for hydrochloric acid, or of halogen-substituted 1,2-diaminobenzenes for phenylenediamine, increases the initial rate of reaction, but not the yield of quinoxalines. 2. The quinoxaline derivatives are insoluble in water and can be readily purified. They are very suitable for determination of the specific radioactivities of radioactively labelled α-oxo acids because they are colourless, soluble in dioxan-based scintillators, and their strong absorption of u.v. light facilitates their chemical determination. As little as 1 nmol can be accurately determined by means of the blue fluorescence produced by absorption of light at 340–360nm. 3. Optimum conditions for preparation, purification and separation by paper and thin-layer chromatography are described.

Additional details

Identifiers

Publishing Information

Journal Title
Biochemical Journal
Journal Volume
120
Journal Issue
1
Series
Biochem. J.
Journal Page Range
171-175
ISSN
0306-3283

INIS

Country of Publication
United Kingdom
Country of Input or Organization
United Kingdom
INIS RN
2006950
Subject category
S07: ISOTOPES AND RADIATION SOURCES;
Resource subtype / Literary indicator
Progress Report
Descriptors DEI
ORGANIC ACIDS; AMINES; PHENYLENE RADICALS; DETERMINATION; RADIOACTIVITY; LABELLED COMPOUNDS; DIOXANE; SCINTILLATORS; ULTRAVIOLET RADIATION; ABSORPTION; FLUORESCENCE; PREPARATION; SEPARATION PROCESSES; THIN-LAYER CHROMATOGRAPHY; CHEMICAL REACTIONS; SOLUBILITY; WATER

Optional Information

Notes
Updated automatically by Metadata and Full-Text Enrichment Agent