Difference between revisions of "1,3,5-Trichlorohexahydrotriazine"
From Sciencemadness Wiki
(Created page with "{{Chembox | Name = 1,3,5-Trichlorohexahydrotriazine | Reference = | IUPACName = 1,3,5-Trichloro-1,3,5-triazinane | PIN = | SystematicName = | OtherNames = 1,3,5-Trichloro-[1,3...") |
(→Chemical) |
||
Line 113: | Line 113: | ||
==Properties== | ==Properties== | ||
===Chemical=== | ===Chemical=== | ||
− | + | The compound is flammable and burns releasing lots of smoke, leaving behind lots of tar. | |
===Physical=== | ===Physical=== |
Revision as of 20:32, 30 December 2023
1,3,5-Trichlorohexahydrotriazine, an unstable organic chloramine prepared from hexamine, acetic acid and sodium hypochlorite
| |
Names | |
---|---|
IUPAC name
1,3,5-Trichloro-1,3,5-triazinane
| |
Other names
1,3,5-Trichloro-[1,3,5]triazinane
1,3,5-Trichlor-hexahydro-[1,3,5]triazin 1,3,5-Trichlor-hexahydro-s-triazin 1,3,5-Trichlor-s-triazine 1,3,5-Trichlorohexahydro-[1,3,5]triazine 1,3,5-Trichlorotriazine | |
Properties | |
C3H6Cl3N3 | |
Molar mass | 190.46 g/mol |
Appearance | Colorless crystalline solid |
Melting point | 78 °C (172 °F; 351 K) (decomposes)[1] |
Boiling point | Decomposes |
Hazards | |
Safety data sheet | None |
Related compounds | |
Related compounds
|
Trichloroisocyanuric acid |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
1,3,5-Trichlorohexahydrotriazine or 1,3,5-Trichloro-1,3,5-triazinane is a chemical compound, poorly characterized in literature.[2] It has the chemical formula C3H6Cl3N3.
Contents
Properties
Chemical
The compound is flammable and burns releasing lots of smoke, leaving behind lots of tar.
Physical
1,3,5-Trichlorohexahydrotriazine is a colorless white solid.
Availability
There doesn't appear anyone selling this compound.
Preparation
1,3,5-Trichlorohexahydrotriazine can be prepared by from hexamine, acetic acid and sodium hypochlorite.[1]
Projects
- Chlorinating
Handling
Safety
There is little data regarding this compound.
Storage
In closed bottles.
Disposal
Neutralization with a reducing agent.
References
- ↑ 1.0 1.1 Delepine; Bulletin de la Societe Chimique de France; vol. <4> 9; (1911); p. 1025
- ↑ https://jcp.edpsciences.org/articles/jcp/abs/1972/01/jcp197269p104/jcp197269p104.html