Trithiolane

Trithiolane

Error creating thumbnail: structure of 1,2,3- and 1,2,4-trithiolane
Identifiers
CAS Number	1,2,3: 6669–39–2 1,2,4: 289–16–7
3D model (JSmol)	1,2,3: Interactive image 1,2,4: Interactive image
ChEBI	1,2,4: CHEBI:192387
ChemSpider	1,2,3: 504147 1,2,4: 8901
ECHA InfoCard
E number
PubChem CID	1,2,3: 579992 1,2,4: 9258
UNII	1,2,4: OF568IX8QZ
CompTox Dashboard (EPA)	{{#property:P3117}} 1,2,3: DTXSID90342229 1,2,4: DTXSID70183091
InChI 1,2,3: InChI=1S/C2H4S3/c1-2-4-5-3-1/h1-2H2 Key: LTTGPXZEANXUSL-UHFFFAOYSA-N 1,2,4: InChI=1S/C2H4S3/c1-3-2-5-4-1/h1-2H2 Key: QHGFEUAAQKJXDI-UHFFFAOYSA-N
SMILES 1,2,3: C1CSSS1 1,2,4: C1SCSS1
Properties
Chemical formula	C2H4S3
Molar mass	124.23 g·mol−1
Related compounds
Related compounds	Dithiolane
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

In the area of organosulfur chemistry, trithiolane refers to either of two families of heterocycles with the C₂S₃ rings:

• 1,2,3-trithiolanes with a C-C bond

parent: 1,2,3-trithiolane (registry number 6669–39–2), colorless liquid, boiling point = 224 °C

• 1,2,4-trithiolanes with only one S-S bond

parent: 1,2,4-trithiolane (registry number 289–16–7), colorless solid, melting point 74-75 °C

Occurrence

A 1,2,3-trithiolane arises from treating of norbornene with elemental sulfur. The same reaction also gives the pentasulfide (pentathiepane).

1,2,4-Trithiolanes are volatile components of many foods, especially after cooking. The frying of chicken produces 3,5-dimethyl-, 3,5-diisobutyl-1,2,4-trithiolane, 3-methyl-5-butyl-, and 3-methyl-5-pentyl-1,2,4-trithiolanes. Trithiolane itself contributes to the flavor of truffles. 3,5-Dimethyltrithiolane is a component of the intense odor of durian.