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{{ChemicalSources}} {{ChemicalSources}}


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[[Category:Simple aromatic rings}}

Revision as of 02:05, 14 February 2007

1,3,5-Triazine
1,3,5-Triazine 1,3,5-Triazine
General
Systematic name 1,3,5-Triazine
Other names sym-Triazine
s-Triazine
Cyanidine
Hydrogen cyanide trimer
Vedita
Molecular formula C3H3N3
SMILES C1=NC=NC=N1
Molar mass 81.08 g/mol
Appearance White crystalline solid
CAS number
Properties
Density and phase ? g/cm³, ?
Solubility in water ? g/100 ml (? °C)
Melting point 81-83 °C (355 K)
Boiling point ? °C (? K)
Structure
Molecular shape planar
Dipole moment zero
Hazards
MSDS External MSDS
Main hazards Sensitive to water
NFPA 704
Flash point ? °C
R/S statement R: ?
S: ?
RTECS number XY2957000
Supplementary data page
Structure and
properties
n, εr, etc.
Thermodynamic
data
Phase behaviour
Solid, liquid, gas
Spectral data UV, IR, NMR, MS
Related compounds
Related ? ?
Related compounds ?
Except where noted otherwise, data are given for
materials in their standard state (at 25 °C, 100 kPa)
Infobox disclaimer and references

The chemical compound 1,3,5-triazine, also called s-triazine, is an organic chemical compound whose chemical structure has a six-membered heterocyclic aromatic ring consisting of three carbon atoms and three nitrogen atoms. It is a common reagent, and readily form derivatives, which are used as pharmaceutical products and herbicides.

Chemistry

The atoms in triazine rings are analogous to those in benzene rings, which makes triazines aromatic compounds like benzene.

The most common derivative of 1,3,5-triazine is 2,4,6-triamino-1,3,5-triazine, commonly known as melamine or cyanuramide. Another important derivative is 2,4,6-trihydroxy-1,4,5-triazine better known as cyanuric acid.

Isomers

The 1,3,5-triazine is one of three triazines, the two other isomers being 1,2,3-triazine and 1,2,4-triazine.

All three triazines. The small blue numbers represent the numbering of the atoms in the ring structure.


External links

Template:ChemicalSources [[Category:Simple aromatic rings}}

Category: