1968 Volume 63 Issue 5 Pages 561-565
1. Tritiated uridine was degraded by the periodate and phenyl-hydrazine method to uracil without release of 3H from pyrimidine ring at the C5 position but, by treatment with 12 N perchloric acid, the C5-3H was completely eliminated.
2. The release of C5-3H from uracil and uridine by boiling with 1 N acid was first order and the velocity constants were calculated. The C6-3H was very stable to this acid treatment.
3. The distribution of 3H in commercial 5, 6-3H uracil and 5, 6-3H uridine, which were tritiated by catalytic exchange in 3H2O, was measured by bromination and by acid treatment. The percentage of III at C6 was 0.7-0.8% and 2-4 % of the total 3H bound in the pyrimidine ring of uracil and uridine, respectively.