90357-58-7

Basic information

• Product Name: propyl hydroxyacetate
• Synonyms: acetic acid, 2-hydroxy-, propyl ester; Acetic acid, hydroxy-, propyl ester; Propyl glycolate
• CAS NO: 90357-58-7
• Molecular Formula: C₅H₁₀O₃
• Molecular Weight: 118.1311
• Mol File: 90357-58-7.mol

Chemical Properties

• Boiling Point: 169.2°C at 760 mmHg
• Flash Point: 65.5°C
• Density: 1.054g/cm³
• Vapor Pressure: 0.507mmHg at 25°C
• Refractive Index: 1.422
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
• CAS DataBase Reference: propyl hydroxyacetate(CAS DataBase Reference)
• NIST Chemistry Reference: propyl hydroxyacetate(90357-58-7)
• EPA Substance Registry System: propyl hydroxyacetate(90357-58-7)

Safety Data

• Hazardous Substances Data: 90357-58-7(Hazardous Substances Data)

Usage

Uses

Used in Cosmetic Industry:
Propyl hydroxyacetate is used as a skin conditioning agent for its ability to improve skin texture and appearance. It helps to exfoliate the skin, promoting cell turnover and reducing the appearance of fine lines and wrinkles.
Used in Pharmaceutical Industry:
Propyl hydroxyacetate is used as a pharmaceutical intermediate for the synthesis of various drugs and medications. Its hydroxyl group allows for further chemical reactions and modifications, making it a versatile building block in the development of new pharmaceutical compounds.
Used in Food Industry:
Propyl hydroxyacetate is used as a flavoring agent in the food industry. Its ester structure imparts a pleasant aroma and taste, making it suitable for use in a variety of food products.
Used in Agricultural Industry:
Propyl hydroxyacetate is used as a plant growth regulator in agriculture. It can help to control plant growth and development, improving crop yields and quality.

Upstream product

• 71-23-8 propan-1-ol 
• 502-97-6 glycolide 
• 79-14-1 glycolic Acid 
• 5396-24-7 n-propyl chloracetate 
• 615-98-5 dipropyl oxalate 

Downstream Products

• 79-14-1 glycolic Acid 
• 22665-54-9 Nitrooxyessigsaeurepropylester 

Relevant articles and documents

Retention Characteristics and Sorption Enthalpies of Esters of Natural Hydroxycarboxylic Acids on DB-1 Stationary Phase

Abstract: Sorption characteristics and retention of esters of glycolic, lactic, malic, and tartaric acids with C1?C8 alcohols of linear structure are studied by gas-liquid chromatography in the temperature range of 90?260°C on DB-1 nonpolar phase. The values of the retention indices of the compounds studied are obtained. On the basis of experimentally determined retention times, the thermodynamic characteristics of sorption under the conditions of limiting dilution are estimated. The dependences of the change in sorption enthalpies on the length of the linear alkyl substituent and on the value of the logarithmic retention index are found. The possibility of estimating the energy of intermolecular interactions of lactic acid esters in the liquid phase is shown on the basis of the obtained values of sorption enthalpies and vaporization enthalpies.

Synthesis and application of glycolic esters in methanol-gasoline as bifunctional additives

Summary : To explore new and multifunctional additives for methanol-gasoline, glycolic esters were synthesized and screened as phase stabilizer and saturation vapor pressure depressor. The effect of the esters' structure on the efficiency was discussed. It was found that the stability of the blends depend on the length of the glycolic esters' alkoxy group, and hexyl glycolic and octyl glycolic were found to be the most effective in various gasoline-methanol blends. Additionally, the glycolic esters can depress the saturation vapor pressure of methanol-gasoline effectively as well, and decyl glycolic is the most effective one. With these data, it can be concluded that the glycolic esters have the great potential to be used as bifunctional gasoline-methanol additives.

Preparation and application of Hydroxyacetic Acid Esters as Methanol-Gasoline additives

In this paper, hydroxyacetic acid esters (glycolic esters) were synthesized and used as phase stabilizer and saturation vapour pressure depressor of methanol-gasoline. The results show that the stabilities of the blends depend on the length of the glycoli

Bridging racemic lactate esters with stereoselective polylactic acid using commercial lipase catalysis

A productive and enantioselective hydrolysis of racemic mixtures of lactate esters with commercial Candida rugosa lipase was performed. This step contributes to a novel envisioned route for stereoselective PLA production by combining recent chemocatalytic developments with this biocatalytic contribution, foreseeing two separate l- and d-lactate enantiomer streams. A study of the hydrolysis kinetics identified an unexpected rate determining step at the origin of an unprecedented ester reactivity order.

HOMOGENEOUS CATALYTIC HYDROGENATION OF DICARBOXYLIC ACID ESTERS. II

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