1,3-Propanediol

Names
Preferred IUPAC name Propane-1,3-diol[1]
Other names 1,3-Dihydroxypropane Trimethylene glycol
Identifiers
CAS Number	504-63-2 Y
3D model (JSmol)	Interactive image
3DMet	B00444
Abbreviations	PDO
Beilstein Reference	969155
ChEBI	CHEBI:16109 Y
ChEMBL	ChEMBL379652 Y
ChemSpider	13839553 Y
DrugBank	DB02774 Y
ECHA InfoCard	100.007.271
EC Number	207-997-3
KEGG	C02457 Y
MeSH	1,3-propanediol
PubChem CID	10442
RTECS number	TY2010000
UNII	5965N8W85T Y
CompTox Dashboard (EPA)	DTXSID8041246
InChI InChI=1S/C3H8O2/c4-2-1-3-5/h4-5H,1-3H2 Y Key: YPFDHNVEDLHUCE-UHFFFAOYSA-N Y Key: YPFDHNVEDLHUCE-UHFFFAOYAS
SMILES OCCCO
Properties
Chemical formula	C3H8O2
Molar mass	76.095 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
Solubility in water	Miscible
log P	−1.093
Vapor pressure	4.5 Pa
Refractive index (nD)	1.440
Thermochemistry
Std enthalpy of formation (ΔfH⦵298)	−485.9–−475.7 kJ mol−1
Std enthalpy of combustion (ΔcH⦵298)	−1848.1–−1837.9 kJ mol−1
Hazards
NFPA 704 (fire diamond)	2 2 0
Flash point	79.444 °C (174.999 °F; 352.594 K)
Autoignition temperature	400 °C (752 °F; 673 K)
Safety data sheet (SDS)	sciencelab.com
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

1,3-Propanediol is the organic compound with the formula CH₂(CH₂OH)₂. This 3-carbon diol is a colorless viscous liquid that is miscible with water.

Products

It is mainly used as a building block in the production of polymers such as polytrimethylene terephthalate.^[2]

1,3-Propanediol can be formulated into a variety of industrial products including composites, adhesives, laminates, coatings, moldings, aliphatic polyesters, and copolyesters. It is also a common solvent. It is used as an antifreeze and as a component in wood paint.

Production

1,3-Propanediol is mainly produced by the hydration of acrolein. An alternative route involves the hydroformylation of ethylene oxide to form 3-hydroxypropionaldehyde. The aldehyde is subsequently hydrogenated to give 1,3-propanediol. Biotechnological routes are also known.^[2]

Two other routes involve bioprocessing by certain micro-organisms:

• Conversion from glucose effected by a genetically modified strain of E. coli by DuPont Tate & Lyle BioProducts (See: bioseparation of 1,3-propanediol). An estimated 120,000 tons were produced in 2007".^[3] According to DuPont, the Bio-PDO process uses 40% less energy than conventional processes,^[4][5] Because of DuPont and Tate & Lyle's success in developing a renewable Bio-PDO process, the American Chemical Society awarded the Bio-PDO research teams the "2007 Heroes of Chemistry" award.^[5]
• Conversion from glycerol (a by-product of biodiesel production) using Clostridium diolis bacteria and Enterobacteriaceae.^[6]

Safety

1,3-Propanediol does not appear to pose a significant hazard via inhalation of either the vapor or a vapor/aerosol mixture.^[7] However, like with any chemical exposure should be controlled and maintained.