22636-32-4

Basic information

• Product Name: 3-Pentyloxypropane-1,2-diol
• Synonyms: 3-(Pentyloxy)-1,2-propanediol;3-Pentyloxypropane-1,2-diol
• CAS NO: 22636-32-4
• Molecular Formula: C₈H₁₈O₃
• Molecular Weight: 162.2267
• Mol File: 22636-32-4.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 285.7°Cat760mmHg
• Flash Point: 126.6°C
• Appearance: /
• Density: 0.999g/cm³
• Vapor Pressure: 0.000315mmHg at 25°C
• Refractive Index: 1.453
• CAS DataBase Reference: 3-Pentyloxypropane-1,2-diol(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Pentyloxypropane-1,2-diol(22636-32-4)
• EPA Substance Registry System: 3-Pentyloxypropane-1,2-diol(22636-32-4)

Safety Data

• Hazardous Substances Data: 22636-32-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H18O3/c1-2-3-4-5-11-7-8(10)6-9/h8-10H,2-7H2,1H3

Upstream product

• 110-62-3 pentanal 
• 56-81-5 glycerol 
• 71-41-0 pentan-1-ol 
• 109-52-4 valeric acid 
• 624-24-8 methyl valerate 

Downstream Products

• 140467-90-9 Phosphoric acid 3-bromomethyl-phenyl ester 2-methoxy-3-pentyloxy-propyl ester 
• 145048-78-8 1-[(4-Methoxy-phenyl)-diphenyl-methoxy]-3-pentyloxy-propan-2-ol 

Relevant articles and documents

Thermodynamic characteristics of the sorption of glycerol ethers on stationary phase OV-101

Retention characteristics, temperature dependences of the retention characteristics, and thermodynamic characteristics of sorption on the nonpolar OV-101 phase are determined for 33 glycerol mono-, di-, and triethers with linear and branched monobasic alc

Selective synthesis of 1-O-Alkyl(poly)glycerol ethers by catalytic reductive alkylation of carboxylic acids with a recyclable catalytic system

(Poly)glycerol monoethers were synthesized in good yield and selectivity by the catalytic reductive alkylation of glycerol, diglycerol, and triglycerol with readily available, cheap and/or bio-sourced carboxylic acids. The reaction was catalyzed by 1 mol % of Pd/C under 50 bar H2 using an acid ion-exchange resin as a recyclable cocatalyst. The catalytic system was recycled several times, and a mechanism is proposed for this transformation.

PROCESS FOR MAKING POLYOL ETHERS

The present invention generally relates to a process for making polyol ethers by reacting a polyol and a carbonyl compound together in the presence of hydrogen gas and a palladium hydrogenation catalyst on an acidic mesoporous carbon support.