Folic acid and 6-formylpterin solutions of pH in the range 4.5-6.0 were pho
tolysed at 350 nm at room temperature. The photochemical reactions were fol
lowed by UV-VIS spectrophotometry, thin layer chromatography (TLC) and high
performance Liquid chromatography (HPLC). In the presence of oxygen, folic
acid is photochemically cleavaged yielding 6-formylpterin and p-aminobenzo
ylglutamic acid. As the photolysis proceeds, 6-carboxypterin arises from 6-
formylpterin, as observed when solutions only containing the latter compoun
d are irradiated in the presence of oxygen. In the absence of oxygen, folic
acid is not light-sensitive. However, when oxygen free solutions of 6-form
ylpterin are irradiated, a 'red intermediate' is observed, which is thermal
ly oxidised producing 6-carboxypterin on admission of oxygen. The quantum y
ields of substrates disappearance and of photoproducts formation are report
ed. (C) 2000 Elsevier Science S.A. All rights reserved.