EurekaMag.com logo
+ Site Statistics
References:
53,214,146
Abstracts:
29,074,682
+ Search Articles
+ Subscribe to Site Feeds
EurekaMag Most Shared ContentMost Shared
EurekaMag PDF Full Text ContentPDF Full Text
+ PDF Full Text
Request PDF Full TextRequest PDF Full Text
+ Follow Us
Follow on FacebookFollow on Facebook
Follow on TwitterFollow on Twitter
Follow on Google+Follow on Google+
Follow on LinkedInFollow on LinkedIn

+ Translate

Preparation of methyl carbon 14 labeled docosa 7 10 13 16 tetraenoate


Journal of Labelled Compounds & Radiopharmaceuticals 19(9): 1063-1070
Preparation of methyl carbon 14 labeled docosa 7 10 13 16 tetraenoate
Methyl[1-14C]docosa-7,10,13,16-tetraenoate [important to the development of testicular tissue] was prepared from [1-14C]arachidonic acid by 2 successive Arndt-Eistert syntheses which could also be used for the step-wise homologation of other labeled fatty acids. After purification by gas chromatography the specific activity was 6.16 mCi/mmol, and the radiochemical purity was 97%.

(PDF 0-2 workdays service: $29.90)

Accession: 006173473



Related references

The synthesis of 1 carbon 14 arachidonate and 3 carbon 14 docosa 7 10 13 16 tetraenoate. Lipids 6(12): 889-894, 1971

Lithiated intermediates in the synthesis of carbon 11 labeled compounds the preparation of carbon 11 labeled d l alpha methyl ornithine and carbon 11 labeled d l alpha methyl valine. International Journal of Applied Radiation & Isotopes 35(6): 559-562, 1984

A semi automated synthesis system for routine preparation of carbon 11 labeled ym 09151 2 and carbon 11 labeled pyrilamine from carbon 11 labeled methyl iodide. Applied Radiation & Isotopes 42(2): 202-205, 1991

The synthesis and metabolism of hexadeca-4,7,10-trienoate, eicosa-8,11,14-trienoate, docosa-10,13,16-trienoate and docosa-6,9 12,15-tetraenoate in the rat. Biochim Biophys Acta 152(3): 519-530, 1968

Preparation of carbon 11 labeled methyl iodide and l s methyl carbon 11 labeled methionine by an automated continuous flow process. International Journal of Applied Radiation & Isotopes 33(5): 363-370, 1982

The synthesis of 1-14C-arachidonate and 3-14C-docosa-7,10,13,16-tetraenoate. Lipids 6(12): 889-894, 1971

Preparation of carbon 14 labeled tetra methyl cyclo propanecarboxylic acid and insecticidal carbon 14 labeled terallethrin from it. Radioisotopes 30(8): 452-454, 1981

Semi automated preparation of a carbon 11 labeled antibiotic carbon 11 labeled n methyl erythromycin a lactobionate. International Journal of Applied Radiation & Isotopes 35(2): 103-110, 1984

Regeneration of a steroid carbon 13 angular methyl group from a functionalized precursor application to the preparation of carbon 18 deuterium labeled steroids and carbon 18 deuterium labeled d homo steroids. Australian Journal of Chemistry 32(10): 2327-2330, 1979

Comparison of the rates of expired carbon 13 labeled carbon di oxide following administration of carbon 13 labeled methoxy phenacetin and carbon 13 labeled di methyl aminopyrine to smokers and nonsmokers and the effect of hepatic alterations on expired carbon 14 labeled carbon di oxide kinetics following carbon 14 labeled methoxy phenacetin to rats. Clinical Research 28(2): 541A, 1980