Misplaced Pages

1,6-Hexanediol

Article snapshot taken from[REDACTED] with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.

This is an old revision of this page, as edited by Beetstra (talk | contribs) at 15:32, 19 October 2011 (Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'ChEMBL').). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Revision as of 15:32, 19 October 2011 by Beetstra (talk | contribs) (Script assisted update of identifiers for the Chem/Drugbox validation project (updated: 'ChEMBL').)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)
1,6-Hexanediol
Names
IUPAC name hexane-1,6-diol
Other names Hexamethylene glycol; 1,6-Dihydroxyhexane; 1,6-Hexylene glycol; Hexamethylenediol; HDO
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
DrugBank
ECHA InfoCard 100.010.068 Edit this at Wikidata
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C6H14O2/c7-5-3-1-2-4-6-8/h7-8H,1-6H2Key: XXMIOPMDWAUFGU-UHFFFAOYSA-N
SMILES
  • OCCCCCCO
Properties
Chemical formula C6H14O2
Molar mass 118.176 g·mol
Melting point 42 °C (108 °F; 315 K)
Boiling point 250 °C (482 °F; 523 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). ☒verify (what is  ?) Infobox references
Chemical compound

1,6-Hexanediol (HOCH2(CH2)4CH2OH) is a colorless crystalline solid that melts at 42 °C and boils at 250 °C. It is well soluble in water.

Production

1,6-Hexanediol is prepared industrially by the hydrogenation of adipic acid.

Uses

1,6-Hexanediol is widely used for industrial polyester and polyurethane production.

References

This article does not cite any sources. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed.
Find sources: "1,6-Hexanediol" – news · newspapers · books · scholar · JSTOR (June 2011) (Learn how and when to remove this message)
Category:
1,6-Hexanediol Add topic