𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Excretion of tritiated 3–2′ dimethyl-4-diphenylamine

✍ Scribed by Paul Lo Gerfo; Frederic P. Herter


Publisher
John Wiley and Sons
Year
1972
Tongue
English
Weight
329 KB
Volume
4
Category
Article
ISSN
0022-4790

No coin nor oath required. For personal study only.

✦ Synopsis


Tritiated 3-2'Dimcthyl4diphenylaminc was prepared by catalytic cxchangc and studics were carricd out in Wistar-Furth rats following subcutaneous injection. Blood levels reachcd their peak in 12 hours and this correlated closely with thc peak lcvels of label in thc urine and bile.

Ninety per cent of labelled compound was excreted within 5 days, less than 3% uf the tritium excreted was in thc form of tritiated water. Sixty-five per cent of cxcrctcd labcl appeared in the stools, and 35%) in the urine of intact animals. In animals with bile fistula, 85%) of the label appeared in the bile and 15% appeared in the urine. This data suggcstcd recirculation of the compound and radioautographs were done at 10 and 20 hours after injection of labelled carcinogen, to see if there was any preferred site of absorption in the G I . tract. None WJS found. Kadioautographs failcd to show any prcfcrrcd localization of thc labcl in the cells of the G.I. tract, liver, kidney, or bladder.

.


📜 SIMILAR VOLUMES


Excretion of tritium after therapeutic i
✍ Barbara Chipperfield 📂 Article 📅 1967 🏛 John Wiley and Sons 🌐 French ⚖ 678 KB

This paper describes investigations on the excretion of tritium in the urine, breath and faeces after therapeutic injections of tritiated tetra-sodium 2-methyl-I :I-naphthaquinol diphosphate in patients suffering from advanced malignant disease. Most of the tritiated material is excreted in the urin

Tritiation of 1,2,3-benzenetriol (pyroga
✍ D. M. Dulik; W. H. Soine 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 French ⚖ 360 KB

## Abstract The synthesis of 4,6‐^2^H~2~‐1,2,3‐benzenetriol from 1,2,3‐benzenetriol was possible under both acid and base catalyzed conditions. However, under simulated physiological conditions it was observed that the label underwent exchange and was lost. Using a three step synthesis, 5‐^2^H‐1,2,

Synthesis of 2,4-diamino-6-piperidinylpv
✍ Terry J. Gilbertson 📂 Article 📅 1976 🏛 John Wiley and Sons 🌐 French ⚖ 154 KB

## Abstract Minoxidil‐3′,4′,;5′‐^3^H(N), 25.6 Ci/mM. has been synthesized by the reaction of piperidine‐3,4,5‐^3^H(N) with 2,4‐diamino‐6‐chloro‐pyrimidine‐3‐oxide. Purification was by paper chromatography. Minoxidil prepared in this way was shown to be suitable for radioimmunoassay and was stable f

Photoelectron-Spectroscopic Characteriza
✍ Evi Honegger; Yang Zhong-zhi; Edgar Heilbronner; William V. E. Doering; John C; 📂 Article 📅 1984 🏛 John Wiley and Sons 🌐 German ⚖ 709 KB

## Abstract The He(Ia) photoelectron (PE) spectra of the (__E,E__)‐, (__E,Z__)‐ and (__Z,Z__)‐isomers of the title compound have been recorded to obtain information about their conformation in the gas phase. For a valid correlation with the PE data of other dienes it is necessary to take the potent

Über 2,4-dimethyl-furan-3-aldehyd
✍ Tadeus Reichstein; Heinrich Zscchkke 📂 Article 📅 1932 🏛 John Wiley and Sons 🌐 German ⚖ 369 KB

effectuant l'essai au papier amido-iodurb. Lorsque la diazotstion est terminbe, on verse la solution sur de la glace et ajoute imm6diatement une solution aqueuse -de 3,5 'gr. d'iodure de potassium; il se produit un abondant dbgagement d'azote et l'acide iodb se dbpose sous forme d'un prbcipitd jsune