Preparation of [14C]Musk Xylol
✍ Scribed by Dr. Anita H. Lewin; Usha Ramesh
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- French
- Weight
- 200 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-2135
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Carbonation of the aryl lithium obtained from 5‐t‐butyl‐3‐iodotoluene with carbon‐14 labeled carbon dioxide, followed by reduction gave [ArCH~3~‐^14^C]‐5‐t‐butyl‐m‐xylene. Nitration of this material gave [ArCH~3~‐^14^C]‐5‐t‐butyl‐2,4,6‐ trinitro‐m‐xylene, known as Musk Xylol. The overall yield was 32% and the product had specific activity 19.8 mCi/mmol (66 mCi/mg) and was > 99% pure.
📜 SIMILAR VOLUMES
## Abstract [^14^C]Acetamidino‐insulin was synthesized by acetamidination of insulin with methyl [^14^C]acetimidate hydrochloride. The acetamidino‐insulin contains two main components, which can be separated by DEAE‐cellulose column chromatography. They correspond to glycine^A‐1^ ‐ Phenylalanine^B‐
In response to a need for relative large amounts of highly labeled 14C p carotene, a search was made for a biological system which would supply an adequate amount of carotene with sufficient label. Methods previously described did not appear to be adequate appear to devote a greater part of their me
Oe~trone-4-~~C in dimethyl sulphoxide solutioii has been treated with lithium acetylide (ethylene diamine complex) to give ethynyl-oestradi01-4-~~C. ## INTRODUCTION. Ethynyloestradiol-4-14C of specific activity 40 pc/mg was required for clinical evaluation. Although the preparation of ethynyloest