Structure via PubChem · Public domain (PubChem)
thiodiglycol
Sign in to saveAlso known as 2-[(2-hydroxyethyl)sulfanyl]ethan-1-ol, beta,beta'-dihydroxyethyl sulfide, beta-thiodiglycol, beta,beta'-dihydroxydiethyl sulfide, beta-hydroxyethyl sulfid, beta-bis(hydroxyethyl) sulfide, bis(beta-hydroxyethyl) sulfide, Dihydroxyethyl sulfide
Thiodiglycol, or bis(2-hydroxyethyl)sulfide (also known as 2,2-thiodiethanol or TDE), is the organosulfur compound with the formula S(CH2CH2OH)2. It is miscible with water and polar organic solvents. It is a colorless liquid. It is structurally similar to diethylene glycol.
In the Vinony graph
Vinony's link graph records 236 inbound references to thiodiglycol, and connects out to solvent, water and urine.
Vinony files it under Chembox image size set, Diols and ECHA InfoCard ID from Wikidata.
Vinony links it to 12 Wikipedia language editions.
Chemical data
- Formula
- C4H10O2S
- Molecular weight
- 122.19 g/mol
- IUPAC name
- 2-(2-hydroxyethylsulfanyl)ethanol
- SMILES
- C(CSCCO)O
- InChIKey
- YODZTKMDCQEPHD-UHFFFAOYSA-N
- XLogP
- -0.6
- Polar surface area
- 65.8 Ų
- H-bond donors
- 2
- H-bond acceptors
- 3
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Max clinical phase
- Phase 2
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
265 papers- Toxicity assessment of thiodiglycol.International journal of toxicology · 2005
- Non-contact detection of thiodiglycol vapors and associated degradation products using atmospheric flow tube mass spectrometry.The Analyst · 2021
- Oral toxicity evaluation of thiodiglycol in Sprague-Dawley rats.International journal of toxicology · 2014
- Thiodiglycol, the hydrolysis product of sulfur mustard: analysis of in vitro biotransformation by mammalian alcohol dehydrogenases using nuclear magnetic resonance.Toxicology and applied pharmacology · 2006
- [Thiodiglycol metabolism in Alcaligenes xylosoxydans subsp. denitrificans].Mikrobiologiia · 2002
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- carbon
- Mass
- 122.04
Show 6 more facts
- chemical formula
- C₄H₁₀O₂S
- canonical SMILES
- C(CSCCO)O
- World Health Organisation international non-proprietary name
- thiodiglycol
- subject has role
- enzyme inhibitor
- melting point
- -16
- Commons category
- Thiodiglycol
Sources (2)
via Wikidata · CC0
~2 min read
Encyclopedic overview
2 sectionsContents
- References
- External links
Thiodiglycol, or bis(2-hydroxyethyl)sulfide (also known as 2,2-thiodiethanol or TDE), is the organosulfur compound with the formula S(CH2CH2OH)2. It is miscible with water and polar organic solvents. It is a colorless liquid. It is structurally similar to diethylene glycol.
Thiodiglycol is manufactured by reaction of 2-chloroethanol with sodium sulfide.
Excerpted from Wikipedia’s “thiodiglycol” article, available under the CC BY-SA 4.0 licence.