Structure via PubChem · Public domain (PubChem)
1,5-pentanediol
Sign in to saveAlso known as pentane-1,5-diol, pentylene glycol, pentamethylene glycol, 1,5-dihydroxypentane
1,5-Pentanediol is the organic compound with the formula HO(CH)OH. Like other diols, this viscous, colorless liquid is used as a plasticizer and also forms polyesters, which are used as emulsifying agents and resin intermediates.
In the Vinony graph
Vinony's link graph records 122 inbound references to 1,5-pentanediol, and connects out to International Standard Book Number, mass density and digital object identifier.
It sits within the topics Alkanediols, Chembox having GHS data and ECHA InfoCard ID from Wikidata.
Vinony links it to 17 Wikipedia language editions.
Chemical data
- Formula
- C5H12O2
- Molecular weight
- 104.15 g/mol
- IUPAC name
- pentane-1,5-diol
- SMILES
- C(CCO)CCO
- InChIKey
- ALQSHHUCVQOPAS-UHFFFAOYSA-N
- XLogP
- -0.1
- Polar surface area
- 40.5 Ų
- H-bond donors
- 2
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Wikidata facts
- Subclass of
- alkanediols
- Mass
- 104.084
Show 6 more facts
- has characteristic
- bitterness
- chemical formula
- C₅H₁₀O₂
- canonical SMILES
- C(CCO)CCO
- melting point
- -18
- Commons category
- 1,5-Pentanediol
- boiling point
- 239
Sources (2)
via Wikidata · CC0
~1 min read
Encyclopedic overview
3 sectionsContents
- Synthesis and reactions
- Contamination of Bindeez
- References
1,5-Pentanediol is the organic compound with the formula HO(CH)OH. Like other diols, this viscous, colorless liquid is used as a plasticizer and also forms polyesters, which are used as emulsifying agents and resin intermediates.
==Synthesis and reactions== 1,5-Pentanediol is produced by hydrogenation of glutaric acid and its derivatives. It can also be prepared by hydrogenolysis of tetrahydrofurfuryl alcohol. 1,4-Pentadiene can be prepared from 1,5-pentadiol via the diacetate.
Excerpted from Wikipedia’s “1,5-pentanediol” article, available under the CC BY-SA 4.0 licence.