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1,5-pentanediol

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EntityQ161557· pop 18· linked from 122 articles

1,5-pentanediol

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Also 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 sections
Contents
  • 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.

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