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Names | |||
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IUPAC name
Propane-1,3-diol
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Other names
1,3-Dihydroxypropane
Trimethylene glycol |
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Identifiers | |||
504-63-2 | |||
3D model (Jmol) | Interactive image | ||
3DMet | B00444 | ||
Abbreviations | PDO | ||
969155 | |||
ChEBI | CHEBI:16109 | ||
ChEMBL | ChEMBL379652 | ||
ChemSpider | 13839553 | ||
DrugBank | DB02774 | ||
ECHA InfoCard | 100.007.271 | ||
EC Number | 207-997-3 | ||
KEGG | C02457 | ||
MeSH | 1,3-propanediol | ||
PubChem | 10442 | ||
RTECS number | TY2010000 | ||
UNII | 5965N8W85T | ||
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Properties | |||
C3H8O2 | |||
Molar mass | 76.10 g·mol−1 | ||
Appearance | Colourless liquid | ||
Density | 1.0597 g cm−3 | ||
Melting point | −27 °C; −17 °F; 246 K | ||
Boiling point | 211 to 217 °C; 412 to 422 °F; 484 to 490 K | ||
Miscible | |||
log P | −1.093 | ||
Vapor pressure | 4.5 Pa | ||
Refractive index (nD)
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1.440 | ||
Thermochemistry | |||
Std enthalpy of
formation (ΔfH |
−485.9–−475.7 kJ mol−1 | ||
Std enthalpy of
combustion (ΔcH |
−1848.1–−1837.9 kJ mol−1 | ||
Hazards | |||
Safety data sheet | sciencelab.com | ||
S-phrases | S23, S24/25 | ||
NFPA 704 | |||
Flash point | 79.444 °C (174.999 °F; 352.594 K) | ||
400 °C (752 °F; 673 K) | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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what is ?) | (|||
Infobox references | |||
1,3-Propanediol is the organic compound with the formula CH2(CH2OH)2. This three-carbon diol is a colorless viscous liquid that is miscible with water.
It is mainly used as a building block in the production of polymers such as polytrimethylene terephthalate.
1,3-Propanediol can be formulated into a variety of industrial products including composites, adhesives, laminates, coatings, moldings, aliphatic polyesters, copolyesters. It is also a solvent and used as an antifreeze and in wood paint.
1,3-Propanediol may be chemically synthesized by the hydration of acrolein, or by the hydroformylation of ethylene oxide to afford 3-hydroxypropionaldehyde. The aldehyde is hydrogenated to give 1,3-propanediol. Moreover, the bioconversion of glycerol to 1,3-propanediol is existent in certain bacteria.
Two other routes involve bioprocessing by certain micro-organisms:
1,3-Propanediol does not appear to pose a significant hazard via inhalation of either the vapor or a vapor/aerosol mixture.