| Identification | Back Directory | [Name]
DIHYDRO-2,4,6-TRIMETHYL-1,3,5(4H)DITHIAZINE | [CAS]
638-17-5 | [Synonyms]
thialdin
FEMA 4018
THIALDINE
Thiaaldine
2,4,6-trimethyl-1,3,5-dithiazinane
2,4,6-Trimethylperhydro-1,3-dithiazine
2,4,6-trimethylperhydro-1,3,5-dithiazine
1,3,5-Dithiazine, perhydro-2,4,6-trimethyl
2,4,6-TRIMETHYLDIHYDRO-4H-1,3,5-DITHIAZINE
(4R,6S)-2,4,6-trimethyl-1,3,5-dithiazinane
DIHYDRO-2,4,6-TRIMETHYL-1,3,5(4H)DITHIAZINE
2,4,6-Trimethyl-1,3-dithia-5-azacyclohexane
Dihydro-2,4,6-trimethyl-1,3,5-(2H)dithiazine
2,4,6-trimethyl-1,3,5-dithiazine (thialdine)
5,6-dihydro-2,4,6-trimethyl-1,3,5-dithiazine
2,4,6-Trimethyl dihydro-4H-1,3,5- dithazinane
2,4,6-Trimethyl-5,6-dihydro-4H-1,3,5-dithiazine
2,4,6-trimethyldihydro-1,3,5-dithiazine (thialdine)
Dihydro-2,4,6-trimethyl-1,3,5(4H)-dithiazine (thialdine)
5-dithiazine,dihydro-2,4,6-trimethyl-,(2-alpha,4-alpha,6-alpha)-4h-3
3,5-Dithiazine,dihydro-2,4,6-trimethyl-,(2.alpha.,4.alpha.,6.alpha.)-4H-1 | [EINECS(EC#)]
211-323-3 | [Molecular Formula]
C6H13NS2 | [MDL Number]
MFCD00089205 | [MOL File]
638-17-5.mol | [Molecular Weight]
163.3 |
| Chemical Properties | Back Directory | [Melting point ]
46℃ | [Boiling point ]
261℃ | [density ]
1.011 | [FEMA ]
4018 | 2,4,6-TRIMETHYLDIHYDRO-4H-1,3,5-DITHIAZINE | [refractive index ]
1.4825 (estimate) | [Fp ]
112℃ | [storage temp. ]
Refrigerator | [solubility ]
Chloroform, Methanol (Slightly) | [form ]
solid | [pka]
6.35±0.70(Predicted) | [color ]
White to Pale Yellow | [Odor]
at 0.10 % in propylene glycol. sulfurous nutty hazelnut corn meaty earthy clam | [Odor Type]
meaty | [JECFA Number]
1049 | [LogP]
1.85 |
| Hazard Information | Back Directory | [Chemical Properties]
2,4,6-Trimethyldihydro-4H-1,3,5-dithiazine has a roasted, meaty odor. | [Definition]
ChEBI: Thialdine is an organonitrogen heterocyclic compound, an organosulfur heterocyclic compound and an organic heteromonocyclic compound. | [Preparation]
Reportedly prepared in a patented process by reacting the first aldehyde group with aqueous ammonia in a mixture of
acetaldehyde and alkanal (C4-C6) and reacting the resulting Schiff base with hydrogen sulfide. |
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