Glycerol
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Names | |||
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Preferred IUPAC name
Propane-1,2,3-triol[1] | |||
Other names
Glycerin Glycerine Propanetriol 1,2,3-Trihydroxypropane 1,2,3-Propanetriol | |||
Identifiers | |||
3D model (JSmol) |
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
DrugBank | |||
ECHA InfoCard | 100.000.263 | ||
E number | E422 (thickeners, ...) | ||
KEGG | |||
PubChem CID |
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UNII | |||
CompTox Dashboard (EPA) |
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Properties | |||
C3H8O3 | |||
Molar mass | 92.094 g·mol−1 | ||
Appearance | Colorless hygroscopic liquid | ||
Odor | Odorless | ||
Density | 1.261 g/cm3 | ||
Melting point | 17.8 °C (64.0 °F; 290.9 K) | ||
Boiling point | 290 °C (554 °F; 563 K)[2] | ||
miscible[3] | |||
log P | -2.32[4] | ||
Vapor pressure | 0.003 mmHg (50 °C)[3] | ||
-57.06·10−6 cm3/mol | |||
Refractive index (nD) |
1.4746 | ||
Viscosity | 1.412 Pa·s (20 °C)[5] | ||
Pharmacology | |||
A06AG04 (WHO) A06AX01 (WHO), QA16QA03 (WHO) | |||
Hazards | |||
NFPA 704 (fire diamond) | |||
Flash point | 160 °C (320 °F; 433 K) (closed cup) 176 °C (349 °F; 449 K) (open cup) | ||
NIOSH (US health exposure limits): | |||
PEL (Permissible) |
TWA 15 mg/m3 (total) TWA 5 mg/m3 (resp)[3] | ||
REL (Recommended) |
None established[3] | ||
IDLH (Immediate danger) |
N.D.[3] | ||
Safety data sheet (SDS) | JT Baker | ||
Supplementary data page | |||
Glycerol (data page) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Glycerol (/ˈɡlɪsərɒl/),[6] also called glycerine in British English and glycerin in American English, is a simple polyol compound. It is a colorless, odorless, viscous liquid that is sweet-tasting and non-toxic. The glycerol backbone is found in lipids known as glycerides. Due to having antimicrobial and antiviral properties it is widely used in FDA approved wound and burn treatments. Conversely, it is also used as a bacterial culture medium.[7] It can be used as an effective marker to measure liver disease. It is also widely used as a sweetener in the food industry and as a humectant in pharmaceutical formulations. Owing to the presence of three hydroxyl groups, glycerol is miscible with water and is hygroscopic in nature.[8]