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1,2-Propanediol
[CAS# 57-55-6]

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Identification
Classification Chemical pesticide >> Fungicide >> Azole fungicide
Name 1,2-Propanediol
Synonyms Propane-1,2-diol; Propylene glycol
Molecular Structure CAS # 57-55-6, 1,2-Propanediol, Propane-1,2-diol, Propylene glycol
Molecular Formula C3H8O2
Molecular Weight 76.09
CAS Registry Number 57-55-6
EC Number 200-338-0
FEMA 2940
SMILES CC(CO)O
Properties
Density 1.036
Melting point -60 ºC
Boiling point 187 ºC
Refractive index 1.431-1.433
Flash point 99 ºC
Water solubility miscible
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P305+P351+P338    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.4H302
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Skin sensitizationSkin Sens.1H317
Specific target organ toxicity - single exposureSTOT SE3H336
Chronic hazardous to the aquatic environmentAquatic Chronic2H411
SDS Available
up Discovory and Applicatios
1,2-Propanediol, also known as propylene glycol, is a versatile compound with important industrial, pharmaceutical, and consumer applications. 1,2-Propanediol was first synthesized in the mid-20th century by the hydration of propylene oxide, a process that remains the primary production method today. Propylene oxide undergoes catalytic hydrogenation under controlled conditions to produce 1,2-propylene glycol. This simple synthetic route ensures high purity and efficiency, making 1,2-propylene glycol readily available for a wide range of applications.

1,2-Propanediol is a clear, colorless, odorless liquid with a slightly sweet taste. Key properties include: It absorbs and retains water, making it useful in formulations where moisture control is required. It is completely miscible with water, facilitating its use in aqueous solutions. It has a low vapor pressure and does not evaporate readily at ambient temperatures. It is stable under normal conditions and does not undergo significant decomposition.

1,2-Propanediol is used in a wide range of industrial applications: Due to its lower toxicity, it is a safer alternative to ethylene glycol in automotive antifreeze formulations. Because of its ability to dissolve a wide range of substances, it is used as a solvent in paints, coatings, and industrial cleaners. It is a key ingredient in the production of polyesters, polyurethanes, and other polymers, where it acts as a precursor or plasticizer.

It can be used as a humectant and solvent in moisturizers, lotions, and creams, helping to retain moisture and improve product texture. It can be used as a solvent and stabilizer for active pharmaceutical ingredients (APIs) in oral, topical, and injectable formulations.

1,2-Propanediol has been approved by regulatory agencies such as the FDA and EFSA for use as a food additive (E1520): It can be used as a preservative in food and beverage products to extend shelf life by controlling water activity and microbial growth. It is also used to dissolve and deliver flavors and food colorings in processed foods and beverages.

1,2-Propanediol is considered environmentally friendly due to its biodegradability and low toxicity compared to other glycols. It is widely used in environmentally friendly formulations and products designed to minimize environmental impact. Ongoing research focuses on expanding the use of 1,2-Propanediol in sustainable technologies, such as renewable energy storage systems and biodegradable polymers. Advances in synthetic methods aim to improve efficiency and reduce production costs, further promoting its application in various industries.

References

1994. Ultrastructure of IVM-IVF Bovine Blastocysts Vitrified after Equilibration in Glycerol 1,2-Propanediol Using 2-Step and 16-Step Procedures. Cryobiology, 31(5).
DOI: 10.1006/cryo.1994.1051

1994. The Effect of Temperature at Which Slow Cooling Is Terminated and of Thawing Rate on the Survival of One-Cell Mouse Embryos Frozen in Dimethyl Sulfoxide or 1,2-Propanediol Solutions. Cryobiology, 31(5).
DOI: 10.1006/cryo.1994.1052
Market Analysis Reports
List of Reports Available for 1,2-Propanediol
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