1,5-Pentanediol is the organic compound with the formula HO(CH2)5OH. Like other diols, this viscous colourless liquid is used as plasticizer and also forms polyesters that are used as emulsifying agents and resin intermediates.[3]
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| Names | |
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| 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 | −18 °C (0 °F; 255 K) |
| Boiling point | 242 °C (468 °F; 515 K) |
| Miscible | |
| Hazards | |
| GHS labelling:[2] | |
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| 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
edit1,5-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
editA toy called Bindeez (Aqua Dots in North America) was recalled by the distributor in November 2007 because of the unauthorized substitution of 1,5-pentanediol with 1,4-butanediol. The toy consists of small beads that stick to each other upon sprinkling 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 about US$1,350–2,800/tonne, while the price for 1,5-pentanediol is about US$9,700/tonne.[9]
References
edit- ^ 1,5-Pentanediol at Sigma-Aldrich
- ^ "1,5-Pentanediol". pubchem.ncbi.nlm.nih.gov.
- ^ Merck Index, 11th Edition, 7073.
- ^ Werle, P.; Morawietz, M. "Alcohols, Polyhydric". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a01_305. ISBN 978-3527306732.
- ^ Nakagawa, Yoshinao; Tomishige, Keiichi (2012). "Production of 1,5-Pentanediol from Biomass via Furfural and Tetrahydrofurfuryl Alcohol". Catalysis Today. 195: 136–143. doi:10.1016/j.cattod.2012.04.048.
- ^ R. E. Benson, B. C. McKusick, Oliver Grummitt, E. P. Budewitz, C. C. Chudd (1958). "1,4-Pentadiene". Organic Syntheses. 38: 78. doi:10.15227/orgsyn.038.0078.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ Wang, L. (2007-11-09). "Industrial Chemical Sullies Popular Children's Toy". Chemical & Engineering News.
- ^ Griffiths, J. (2008). "Government and Society: Scientific sleuthing: how GC/MS uncovered toy danger". Analytical Chemistry. 80 (1): 6. doi:10.1021/ac085987i.
- ^ "Mom: Chemical-laced toy made son 'drunk'". USA Today. Associated Press. 2007-11-09.