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1,3-Propanediol

CAS No.
504-63-2
Chemical Name:
1,3-Propanediol
Synonyms
PDO;PROPANE-1,3-DIOL;1,3-PROPANDIOL;TRIMETHYLENE GLYCOL;1,3-PROPYLENE GLYCOL;PROPAN-1,3-DIOL;Dihydroxypropane;1,3-PROPANEDIOL FOR SYNTHESIS;1.3-PDO;nsc65426
CBNumber:
CB5853689
Molecular Formula:
C3H8O2
Molecular Weight:
76.09
MDL Number:
MFCD00002949
MOL File:
504-63-2.mol
MSDS File:
SDS
Last updated:2024-12-18 14:15:32

1,3-Propanediol Properties

Melting point -27 °C (lit.)
Boiling point 214 °C/760 mmHg (lit.)
Density 1.053 g/mL at 25 °C (lit.)
vapor pressure 0.8 mm Hg ( 20 °C)
refractive index n20/D 1.440(lit.)
FEMA 4753 | 1,3-PROPANEDIOL
Flash point >230 °F
storage temp. Store below +30°C.
solubility H2O: soluble
pka 14.46±0.10(Predicted)
form Oily Liquid
color Clear
PH 4.5-7.0 (100g/l, H2O, 20℃)
explosive limit 2.5%(V)
Relative density, gas (air=1) 1,053 g/mL
Viscosity 44.923mm2/s
Water Solubility 100 g/L
Merck 14,9714
BRN 969155
Dielectric constant 35.0(20℃)
InChIKey YPFDHNVEDLHUCE-UHFFFAOYSA-N
LogP -0.71 at 20℃
CAS DataBase Reference 504-63-2(CAS DataBase Reference)
FDA UNII 5965N8W85T
NIST Chemistry Reference 1,3-Propanediol(504-63-2)
EPA Substance Registry System 1,3-Propanediol (504-63-2)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H227
Precautionary statements  P501-P210-P264-P280-P302+P352-P370+P378-P362+P364-P332+P313-P403+P235
Hazard Codes  Xi
Risk Statements  38
Safety Statements  23-24/25
WGK Germany  1
RTECS  TY2010000
Autoignition Temperature 405 °C
TSCA  Yes
HS Code  29053980
Hazardous Substances Data 504-63-2(Hazardous Substances Data)
Toxicity LD50 orally in Rabbit: 15670 mg/kg LD50 dermal Rabbit > 20000 mg/kg
NFPA 704
0

1,3-Propanediol price More Price(29)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P50404 1,3-Propanediol 98% 504-63-2 100g $93.4 2024-03-01 Buy
Sigma-Aldrich PHR3167 1,3-Propanediol pharmaceutical secondary standard, certified reference material 504-63-2 1ML $186 2024-03-01 Buy
Sigma-Aldrich 8.07481 1,3-Propanediol for synthesis 504-63-2 250ML $88.9 2024-03-01 Buy
Sigma-Aldrich 8.07481 1,3-Propanediol for synthesis 504-63-2 1L $301 2024-03-01 Buy
Sigma-Aldrich 1570483 1,3-Propanediol United States Pharmacopeia (USP) Reference Standard 504-63-2 1ml $474 2024-03-01 Buy
Product number Packaging Price Buy
P50404 100g $93.4 Buy
PHR3167 1ML $186 Buy
8.07481 250ML $88.9 Buy
8.07481 1L $301 Buy
1570483 1ml $474 Buy

1,3-Propanediol Chemical Properties,Uses,Production

Chemical Properties

1,3-Propanediol, an isomer of propylene glycol, is a viscous, colorless, odorless, hygroscopic liquid that has a brackish irritating taste. miscible with various solvents such as water, ethanol, acetone, chloroform (chloroform) and ether, and is insoluble in benzene. Combustible.

Uses

1,3-Propanediol is used as a solvent for thin film preparations, in the production of polymers such as polytrimethylene terephthalate, adhesives, laminates, coatings, moldings, aliphatic polyesters, as an antifreeze and in wood paint. It also acts as a reagent for vinyl epoxide synthon, for epoxide ring-opening, for polymerization reactions and for natural product syntheses.

Uses

As a diol, 1,3-propanediol is subject to many of the same polymeric applications as other low molecular mass diols (e.g., ethylene glycol, propylene glycol, and 1,4-butanediol). However, its relatively high price limits its use to applications requiring very specific performance characteristics. It is a raw-material source for 1,3-dioxanes. 1,3-Propanediol-bis(4-aminobenzoate) can be used as a chain extender in polyurethane elastomers. This bisbenzoate, which can also be synthesized from 1,3-dichloro-propane, finds other applications as a cross-linking agent in epoxy formulations and as a rubber additive.

Definition

ChEBI: Propane-1,3-diol is the simplest member of the class of propane-1,3-diols, consisting of propane in which one hydrogen from each methyl group is substituted by a hydroxy group. A colourless, viscous, water-miscible liquid with a high (210℃) boiling point, it is used in the synthesis of certain polymers and as a solvent and antifreeze. It has a role as a protic solvent and a metabolite.

Application

In adipate polyesters with other diols these diols are partly substituted by 1,3-propanediol (PDO) to break crystallinity in order to obtain liquid polyester polyols. In polyesters for powder coatings PDO improves the flexibility but lowers the glass transition temperature somewhat. PDO finds also uses in cosmetics and personal care products, engine coolants, and solvents for ink-jet and screen inks.

Application

1,3-Propanediol is prepared as a by-product in the manufacture of glycerin by the saponification of fat. It is used to lower the freezing point of water and as a chemical intermediate. Industrial exposure is limited. It is also used to Solvent for thin film preparations, Vinyl epoxide synthon and reagent for epoxide ring-opening and polymerization reactions, Reagent for natural product syntheses.
A new large market for 1,3-propanediol will be in polyester coatings and in the production of poly(trimethylene terephthalate), a new material for the production of high quality carpet fibers.

Biosynthesis

1,3-Propanediol (1,3-PDO) can be produced by fermentation from glycerol, with different strains such as Klebsiella pneumoniae, Clostridium butyricum, Clostridium pasteurianum, and Citrobacter freundii. Drawbacks of industrial fermentation using these strains are strong inhibition of 1,3-PDO production and by-products during fermentation.

Flammability and Explosibility

Non flammable

Synthesis

1,3-Propanediol is produced commercially by Degussa starting from acrolein.
CH2CHCHO + H2O → HOHCH2CH2CHO
HOHCH2CH2CHO + H2 → HOHCH2CH2CH2OH
The addition of water under mild acidic conditions gives 3-hydroxypropionaldehyde with high selectivity. Preferentially buffer solutions with a pH 4-5 or weak acidic ion exchange resins are used as catalysts. Further hydrogenation of this aqueous solutions gives 1,3-propanediol. There is an alternative route via hydroformylation of ethylene oxide and subsequent hydrogenation of the intermediate 3-hydroxypropionaldehyde.

Purification Methods

Dry this diol with K2CO3 and distil it under reduced pressure. More extensive purification involves conversion with benzaldehyde to 2-phenyl-1,3-dioxane (m 47-48o) which is subsequently decomposed by shaking with 0.5M HCl (3mL/g) for 15minutes and standing overnight at room temperature. After neutralisation with K2CO3, the benzaldehyde is removed by steam distillation and the diol is recovered from the remaining aqueous solution by continuous extraction with CHCl3 for 1day. The extract is dried with K2CO3, the CHCl3 is evaporated and the diol is distilled. [Foster et al. Tetrahedron 6 177 1961, Beilstein 1 IV 2493.]

2453-03-4
504-63-2
Synthesis of 1,3-Propanediol from 1,3-Dioxan-2-one
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View Lastest Price from 1,3-Propanediol manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,3-Propanediol  pictures 2024-12-20 1,3-Propanediol
504-63-2
US $6.00 / kg 1kg 99% 2000KG/Month HebeiShuoshengImportandExportco.,Ltd
1,3-Dihydroxypropane pictures 2024-12-20 1,3-Dihydroxypropane
504-63-2
US $70.00 / kg 1kg 99 5000 Hebei Zhuanglai Chemical Trading Co.,Ltd
Trimethyleneglycol; propane-1,3-diol pictures 2024-12-20 Trimethyleneglycol; propane-1,3-diol
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US $70.00 / kg 1kg 99 5000 Hebei Zhuanglai Chemical Trading Co.,Ltd
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