1,5-Pentanediol
Chemical compound
From Wikipedia, the free encyclopedia
1,5-Pentanediol is the organic compound with the formula HO(CH2)5OH. 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.[3]
| Names | |
|---|---|
| Preferred IUPAC name
Pentane-1,5-diol | |
| Other names
Pentamethylene glycol 1,5-Dihydroxypentane | |
| Identifiers | |
3D model (JSmol) |
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| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.003.505 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C5H12O2 | |
| Molar mass | 104.14758 |
| Density | 0.994 g/mL at 25 °C |
| Melting point | â18 °C (0 °F; 255 K) |
| Boiling point | 242 °C (468 °F; 515 K) |
| Miscible | |
| Hazards | |
| GHS labelling:[2] | |
| Warning | |
| H302 | |
| P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Synthesis and reactions
1,5-Pentanediol is produced by hydrogenation of glutaric acid and its derivatives.[4] It can also be prepared by hydrogenolysis of tetrahydrofurfuryl alcohol.[5] 1,4-Pentadiene can be prepared from 1,5-pentadiol via the diacetate.[6]
Contamination of Bindeez
A toy called Bindeez (Aqua Dots in North America) was recalled by the distributor in November 2007 due to the unauthorized substitution of 1,5-pentanediol with 1,4-butanediol. The toy consists of small beads that stick to each other when sprinkled with water. 1,4-Butanediol, which when ingested is metabolized to gamma-hydroxybutyric acid, was detected by GC-MS.[7][8] ChemNet China lists the price of 1,4-butanediol at between US$1,350â2,800/tonne, while the price for 1,5-pentanediol is about US$9,700/tonne.[9]

