𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The synthesis of 18O multilabeled anhydrous nitric acid

✍ Scribed by A. C. Scott; J. H. McReynolds; M. Anbar


Publisher
John Wiley and Sons
Year
1976
Tongue
French
Weight
170 KB
Volume
12
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

^18^O‐multilabeled anhydrous nitric acid (89 atom % ^18^O) was prepared by exchange with H~2~^18^O, neutralization with NH~3~, and distillation from methane sulfonic acid. The use of trifluoromethane sulfonic acid, sulfuric acid, and oleum was also investigated, but these acids were found unsuitable due to rapid oxygen exchange. The extent of exchange was. monitored by converting water to methanol, nitric acid to nitroanisole, and analyzing by field ionization mass spectrometry.


📜 SIMILAR VOLUMES


Synthesis of 13C and 15N multilabeled 5-
✍ Katsumi Iida; Masahiro Kajiwara 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 French ⚖ 78 KB

## Abstract 5‐[4‐^13^C,^15^N]‐ and 5‐[5‐^13^C,^15^N]Aminolevulinic acid (ALA) were simply synthesized in four steps by the condensation of [1‐^13^C,^15^N]‐ or [2‐^13^C,^15^N]glycine, respectively, with phthalic anhydride, followed by conversion to the chloride, coupling reaction with a three‐carbon

The synthesis of alanine multilabeled wi
✍ S. D. Dimitrijevich; M. D. Scanlon; M. Anbar 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 French ⚖ 463 KB

## Abstract The work presented illustrates a practical sequence requiring relatively simple and inexpensive aoparatus, and using the commercially available isotopic sources, to produce L‐alanine from M+3 (^13^C~2~, ^15^N) to M+12 (^13^C~3~, ^15^N, D~4~, ^18^O~2~).

Synthesis of Concentrated 18O-Labelled H
✍ Guido Grassi; Markus Oldani; Alfred Bauder 📂 Article 📅 1983 🏛 John Wiley and Sons 🌐 German ⚖ 311 KB 👁 1 views

A method is described for the preparation of concentrated solutions (50–70%) of ^18^O‐labelled H~2~O~2~ in water. All singly ^2^H‐, ^13^C‐ and ^18^O‐labelled species of peroxyformic acid have been synthesized by the reaction of appropriately labelled formic acid and H~2~O~2~.

Synthesis and spectroscopic characterisa
✍ Christine Bleasdale; Martin K. Ellis; Peter B. Farmer; Bernard T. Golding; Kevin 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 362 KB 👁 1 views

## Abstract 3‐Chloroperbenzoic acid‐^17^O,^18^O was prepared from 3‐chlorobenzoyl chloride and hydrogen peroxide‐^17^O,^18^O (obtained by subjecting water‐^17^O,^18^O. Nitrobenzene‐^15^N was reduced to aniline‐^15^N, which was oxidised by 3‐chloroperbenzoic acid to nitrosobenzene‐^15^N. ^15^N and ^