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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:2026-02-02 18:10:39
Product description Number Pack Size Price
1,3-Propanediol 98% P50404 100g $96.3
1,3-Propanediol pharmaceutical secondary standard, certified reference material PHR3167 1ML $200
1,3-Propanediol for synthesis 8.07481 250ML $93.6
1,3-Propanediol for synthesis 8.07481 1L $316
1,3-Propanediol United States Pharmacopeia (USP) Reference Standard 1570483 1ml $506
More product size

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℃)
Relative density, gas (air=1) 1,053 g/mL
Viscosity 44.923mm2/s
explosive limit 2.5%(V)
Water Solubility 100 g/L
Merck 14,9714
BRN 969155
Dielectric constant 35.0(20℃)
Cosmetics Ingredients Functions SOLVENT
VISCOSITY CONTROLLING
InChI 1S/C3H8O2/c4-2-1-3-5/h4-5H,1-3H2
InChIKey YPFDHNVEDLHUCE-UHFFFAOYSA-N
SMILES OCCCO[H]
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)
UNSPSC Code 41116107
NACRES NA.24

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
PPE Eyeshields, Gloves
Hazard Codes  Xi
Risk Statements  38
Safety Statements  23-24/25
WGK Germany  1
RTECS  TY2010000
Autoignition Temperature 405 °C
TSCA  TSCA listed
HS Code  29053980
Storage Class 10 - Combustible liquids
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(33)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich P50404 1,3-Propanediol 98% 504-63-2 100g $96.3 2025-07-31 Buy
Sigma-Aldrich PHR3167 1,3-Propanediol pharmaceutical secondary standard, certified reference material 504-63-2 1ML $200 2025-07-31 Buy
Sigma-Aldrich 8.07481 1,3-Propanediol for synthesis 504-63-2 250ML $93.6 2025-07-31 Buy
Sigma-Aldrich 8.07481 1,3-Propanediol for synthesis 504-63-2 1L $316 2025-07-31 Buy
Sigma-Aldrich 1570483 1,3-Propanediol United States Pharmacopeia (USP) Reference Standard 504-63-2 1ml $506 2025-07-31 Buy
Product number Packaging Price Buy
P50404 100g $96.3 Buy
PHR3167 1ML $200 Buy
8.07481 250ML $93.6 Buy
8.07481 1L $316 Buy
1570483 1ml $506 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.

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

1,3-Propanediol /PDO/ is mainly used for making polytrimethylene terephthalate polymer, which is used in fibers and fabrics, for example, carpets, textiles, engineering thermoplastics, nonwovens, films, and monofilaments. PDO finds also use as chain extender in thermoplastic polyurethanes, where it contributes to improved thermal, hydrolytic and dimensional stability. In adipate polyesters with other diols these diols are partly substituted by 1,3-propanediol 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.

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 2026-02-10 1,3-Propanediol
504-63-2
0.99 RongNa Biotechnology Co.,Ltd
1,3-Propanediol pictures 2026-02-01 1,3-Propanediol
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US $29.00 / mL 99.00% 10g TargetMol Chemicals Inc.
1 3 Propanediol pictures 2026-01-30 1 3 Propanediol
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US $10.00 / kg 1kg 99.5% 100 TON Hebei Chuanghai Biotechnology Co., Ltd
  • 1 3 Propanediol pictures
  • 1 3 Propanediol
    504-63-2
  • US $10.00 / kg
  • 99.5%
  • Hebei Chuanghai Biotechnology Co., Ltd
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