Propylene glycol
Appearance
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| Names | |||
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| Preferred IUPAC name
Propane-1,2-diol | |||
Other names
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| Identifiers | |||
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3D model (JSmol) |
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| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.000.307 | ||
| EC Number |
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| E number | E1520 (additional chemicals) | ||
| KEGG | |||
PubChem CID |
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| RTECS number |
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CompTox Dashboard (EPA) |
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| Properties | |||
| C3H8O2 | |||
| Molar mass | 76.10 g·mol−1 | ||
| Appearance | colourless liquid | ||
| Odor | odorless | ||
| Density | 1.036 g/cm3 | ||
| Melting point | −59 °C (−74 °F; 214 K) | ||
| Boiling point | 188.2 °C (370.8 °F; 461.3 K) | ||
| Miscible | |||
| Solubility in ethanol | Miscible | ||
| Solubility in diethyl ether | Miscible | ||
| Solubility in acetone | Miscible | ||
| Solubility in chloroform | Miscible | ||
| log P | −1.34[2] | ||
| Vapor pressure | 10.66 Pa (20 °C) | ||
| Thermal conductivity | 0.34 W/m·K (50% H2O @ 90 °C (194 °F)) | ||
| Viscosity | 0.042 Pa·s | ||
| Thermochemistry | |||
| Specific heat capacity, C | 189.9 J/(mol·K) [3] | ||
| Pharmacology | |||
| QA16QA01 (WHO) | |||
| Hazards | |||
| GHS labelling:[4] | |||
| Template:HPhrases | |||
| Template:PPhrases | |||
| NFPA 704 (fire diamond) | |||
| Related compounds | |||
Related glycols |
Ethylene glycol, 1,3-propanediol | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| Infobox references | |||
Propylene glycol, also called 1,2-propanediol or α-propylene glycol, is an organic compound. The chemical formula of propylene glycol is CH3CH(OH)CH2OH. Propylene glycol is used as a food additive, an ingredient in polymers, and a solvent. Mixtures of propylene glycol and water are used as antifreeze.[6] It is mixed with glycerin to make liquid for e-cigarettes.[7]
It is the second-simplest vicinal diol, a type of chemical where two hydroxy groups are attached to a pair of neighbouring carbon atoms. It is a positional isomer of trimethylene glycol, which is sometimes also called β-propylene glycol.
Sources
[change | change source]- ↑ The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals. Merck & Co. 1989. ISBN 978-0-911910-28-5.
- ↑ "Propylene Glycol_msds".
- ↑ Zaripov, Z.I. (1982). Experimental study of the isobaric heat capacity of liquid organic compounds with molecular weights of up to 4000 a.e.m.
- ↑ GHS: "Kein gefährlicher Stoff nach GHS" GESTIS 013620
- "Propylene Glycol - Cameo Chemicals". NOAA Office of Response and Restoration. NOAA. Retrieved 3 October 2018.
- ↑ Freeman, Andrew I.; Surridge, Ben W.J.; Matthews, Mike; Stewart, Mark; Haygarth, Philip M. (2015). "Understanding and managing de-icer contamination of airport surface waters: A synthesis and future perspectives". Environmental Technology & Innovation. 3: 46–62. Bibcode:2015EnvTI...3...46F. doi:10.1016/j.eti.2015.01.001.
- ↑ Carpenter, Matthew J.; Cummings, K Michael; Wahlquist, Amy E.; Heckman, Bryan W.; Smith, Tracy T. (2020). "The Impact of E-liquid Propylene Glycol and Vegetable Glycerin Ratio on Ratings of Subjective Effects, Reinforcement Value, and Use in Current Smokers". Nicotine & Tobacco Research. 22 (5): 791–797. doi:10.1093/ntr/ntz130. PMC 7171278. PMID 31403695.


