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1,1-ethanedithiol

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EntityQ4545644· pop 7· linked from 55 articles

1,1-ethanedithiol

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Ethane-1,1-dithiol is an organosulfur compound with formula CH3CH(SH)2. It is a colourless smelly liquid that is added to or found in some foods. The compound is an example of a geminal dithiol.

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Vinony's link graph records 55 inbound references to 1,1-ethanedithiol, and connects out to ethane-1,2-dithiol, sulfur and International Standard Book Number.

It sits within the topics Alkanethiols, Chembox having GHS data and Chembox image size set.

Vinony links it to 6 Wikipedia language editions.

Chemical data

Formula
C2H6S2
Molecular weight
94.2 g/mol
IUPAC name
ethane-1,1-dithiol
SMILES
CC(S)S
InChIKey
DHBXNPKRAUYBTH-UHFFFAOYSA-N
XLogP
1.3
Polar surface area
2 Ų
H-bond donors
2
H-bond acceptors
2
Formal charge
0

via PubChem

Wikidata facts

Has part
sulfur
Mass
93.991
Show 3 more facts
Commons category
Ethane-1,1-dithiol
chemical formula
C₂H₆S₂
canonical SMILES
CC(S)S
Sources (3)

via Wikidata · CC0

~3 min read

Encyclopedic overview

9 sections
Contents
  • Use
  • Identifiers
  • Natural occurrence
  • Properties
  • Reactions
  • Formation
  • See also
  • References
  • External links

Ethane-1,1-dithiol is an organosulfur compound with formula CH3CH(SH)2. It is a colourless smelly liquid that is added to or found in some foods. The compound is an example of a geminal dithiol.

==Use== Flavouring uses of ethane-1,1-dithiol may include drinks, oil, gravy, soup, meat, fruit, seasonings, and snacks. Maximum concentrations in use that are generally recognised as safe (GRAS) is five parts per million (ppm) but typical uses are around 0.2 ppm. It is supplied as a 1% solution in ethanol, due to its strong offensive smell. In the diluted form with 4% ethyl acetate and ethanol the CAS number is 69382-62-3. Toxicity may be due to metabolism products hydrogen sulfide and acetaldehyde, however as used it has a margin of safety of over 10,000,000. Other ways that it is modified in the body apart from hydrolysis is methylation to 1-methylsulfanyl-ethanethiol, oxidation of the sulfur to an ethyl sulfonate, glucuronidation of the sulfur, or combination with cysteine by way of a disulfide bridge.

Excerpted from Wikipedia’s “1,1-ethanedithiol” article, available under the CC BY-SA 4.0 licence.

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