Triazinane

Not to be confused with triazene or triazane.

Triazinane

Identifiers
CAS Number	1,2,4: 942593-11-5 1,3,5: 110-90-7
3D model (JSmol)	1,2,3: Interactive image 1,2,4: Interactive image 1,3,5: Interactive image
Beilstein Reference	8477997
ChEBI	1,2,3: CHEBI:38040 1,2,4: CHEBI:38041
ChemSpider	1,2,3: 10613003 1,2,4: 11359397 1,3,5: 60330
ECHA InfoCard
E number
PubChem CID	1,2,3: 16048634 1,2,4: 16048633 1,3,5: 66971
CompTox Dashboard (EPA)	{{#property:P3117}}
InChI 1,2,3: InChI=1S/C3H9N3/c1-2-4-6-5-3-1/h4-6H,1-3H2 Key: OYWRDHBGMCXGFY-UHFFFAOYSA-N 1,2,4: InChI=1S/C3H9N3/c1-2-5-6-3-4-1/h4-6H,1-3H2 Key: VWKKSBDTNICZRS-UHFFFAOYSA-N 1,3,5: InChI=1S/C3H9N3/c1-4-2-6-3-5-1/h4-6H,1-3H2 Key: LKLLNYWECKEQIB-UHFFFAOYSA-N
SMILES 1,2,3: C1CNNNC1 1,2,4: C1CNNCN1 1,3,5: C1NCNCN1
Properties
Chemical formula	C3H9N3
Molar mass	87.126 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Triazinanes are a class of nitrogen-containing heterocycles. Triazinanes have six-membered cyclohexane-like ring but with three carbon centers replaced by nitrogen. The parent have the molecular formula (CH₂)₃(NH)₃. Three isomeric forms are possible, but only 1,3,5-triazinanes are common. 1,3,5-triazinane is a labile intermediate in the formation of hexamethylenetetramine from ammonia and formaldehyde.

Stable 1,3,5-Triorganotriazines are formed by condensation of primary amines and formaldehyde.

See also

• 6-membered rings with one nitrogen atom: Piperidine
• 6-membered rings with two nitrogen atoms: Diazinane
  • Hexahydropyrimidine
  • Hexahydropyridazine
• Triazine
• Borazine (borazole)
• Triazenes, organic compound with the formula RN=N−NR²