𝔖 Bobbio Scriptorium
✦   LIBER   ✦

New adducts of 1,3,5-trinitro-1,3,5-triazacyclohexane (RDX)

✍ Scribed by W. Selig


Publisher
John Wiley and Sons
Year
1981
Tongue
English
Weight
447 KB
Volume
6
Category
Article
ISSN
0721-3115

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Relatively stable equimolar adducts of 1,3,5‐trinitro‐1,3,5‐triazacyclohexane were prepared with 2,6‐lutidine‐N‐oxide, 4‐hydroxy‐1‐butanesulfonic acid δ‐sultone (1,4‐butane sultone), and 2,2,6,6‐tetramethyl‐4‐piperidone‐1‐oxyl. Only the last adduct is selective for RDX; the others also form adducts with 1,3,5,7‐tetranitro‐1,3,5,7‐tetrazacyclooctane. A very labile RDX adduct is formed with tetrahydrothiophene‐1‐oxide. Some properties of the new adducts are presented.


📜 SIMILAR VOLUMES


Thermal decomposition of 1,3,5-trinitro-
✍ John C. Hoffsommer; Donald J. Glover 📂 Article 📅 1985 🏛 Elsevier Science 🌐 English ⚖ 525 KB

The kinetics of the thermal decomposition of RDX and the formation of three nitroso intermediates have been studied in hexaproteo (h6) benzene; hexadeutero (d6) benzene at 180"C and 200"C; and, as a melt at 210°C in sealed capillaries. Decomposition rates were determined by vapor-phase chromatograph

Spectrofluorimetric Determination of 1,3
✍ A. Lapat; L. Székelyhidi; I. Hornyák 📂 Article 📅 1997 🏛 John Wiley and Sons 🌐 English ⚖ 91 KB

RDX is one of the most important military explosives. It is a component of some plastic explosives which are frequently used in terrrorist attacks. Two fluorimetric methods have been described for the quantitative determination of RDX which are based on the detection of nitrite ions. After a basic

Synthesis of nitrogen-15 labeled 1,3,5-t
✍ S. Bulusu; J. Autera; T. Axenrod 📂 Article 📅 1980 🏛 John Wiley and Sons 🌐 French ⚖ 144 KB 👁 1 views

## Abstract Procedures are described for the synthesis of 1,3,5‐trinitro‐1,3,5‐triazacyclohexane (RDX), 1,3,5,7‐tetranitro‐1,3,5,7‐tetraazacyclooctane (HMX) fully labeled with nitrogen‐15.

Removal of 2,4,6-trinitrotoluene (TNT) a
✍ Y. Okamoto; E. J. Chou; M. Croce; D. Freeman; M. Roth; O. Colitti 📂 Article 📅 1982 🏛 John Wiley and Sons 🌐 English ⚖ 430 KB

## Abstract 2,4,6‐Trinitrotoluene (TNT) was found to react in aqueous solution with surfactants containing amino and quaternary ammonium groups at pH 10–11 at ambient temperature. The surfactants investigated included N‐tallow 1,3‐diaminopropane, trimethyl N‐tallow ammonium chloride and N,N,N′,N′,N

Synthesis of14C-labeled hexahydro-1,3,5-
✍ Károly Horváth; William L. Alworth 📂 Article 📅 1993 🏛 John Wiley and Sons 🌐 French ⚖ 184 KB 👁 1 views

## Abstract ^14^C‐labeled hexahydro‐1,3,5‐trinitro‐1,3,5‐triazine (2, RDX) was prepared by nitrolysis of hexahydro‐1,3,5‐tripropionyl‐1,3,5‐triazine (1) for bioenvironmental studies. 1 was synthesized from paraformaldehyde and propionitrile by a modified method reported earlier.