5454-19-3

Basic information

• Product Name: DECYL PROPIONATE
• Synonyms: FEMA 2369;DECYL PROPIONATE;Decylpropanoate;n-Decyl n-propionate;n-Decyl propanoate;Propanoic acid, decyl ester;Propanoicacid,decylester;Propionic acid, decyl ester
• CAS NO: 5454-19-3
• Molecular Formula: C₁₃H₂₆O₂
• Molecular Weight: 214.34
• EINECS: 226-703-4
• Product Categories: Alphabetical Listings;C-D;Flavors and Fragrances
• Mol File: 5454-19-3.mol
• Article Data: 5

Chemical Properties

• Melting Point: -31.6°C (estimate)
• Boiling Point: 123-124 °C8 mm Hg(lit.)
• Flash Point: 225 °F
• Appearance: /
• Density: 0.864 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.011mmHg at 25°C
• Refractive Index: n20/D 1.429(lit.)
• CAS DataBase Reference: DECYL PROPIONATE(CAS DataBase Reference)
• NIST Chemistry Reference: DECYL PROPIONATE(5454-19-3)
• EPA Substance Registry System: DECYL PROPIONATE(5454-19-3)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 5454-19-3(Hazardous Substances Data)

Usage

Chemical Properties

Decyl propionate has a slightly fatty, aldehyde-like odor reminiscent of cognac

InChI:InChI=1/C13H26O2/c1-3-5-6-7-8-9-10-11-12-15-13(14)4-2/h3-12H2,1-2H3

Upstream product

• 74-85-1 ethene 
• 112-30-1 1-Decanol 
• 201230-82-2 carbon monoxide 
• 802294-64-0 propionic acid 

Relevant articles and documents

Method for preparing organic carboxylic ester through combined catalysis of aryl bidentate phosphine ligand

The invention discloses a method for preparing organic carboxylic ester by combined catalysis of an aryl bidentate phosphine ligand. The method comprises the following steps: under the action of a palladium compound/aryl bidentate phosphine ligand/acidic additive combined catalyst, carrying out a hydrogen esterification reaction on terminal olefin, carbon monoxide and alcohol so as to generate theorganic carboxylic ester with one more carbon than olefin. According to the invention, by adoption of the palladium compound/aryl bidentate phosphine ligand/acidic additive combined catalyst, good catalytic activity and selectivity for the hydrogen esterification reaction of the olefin are achieved, and olefin carbonylation to synthesize organic carboxylic ester can be efficiently catalyzed. Thearyl bidentate phosphine ligand has a rigid skeleton structure of a rigid ligand and the flexibility of a flexible ligand, so the aryl bidentate phosphine ligand has proper flexibility due to the characteristic that the aryl bidentate phosphine ligand is soft and rigid, and a most favorable coordination mode and a stable active structure in space are favorably formed. In addition, the aryl bidentate phosphine ligand has the advantages of high stability, simple and convenient synthesis method and the like; and a novel industrial technology is provided for production of organic carboxylate compounds.

Cobalt(II)-catalyzed direct acetylation of alcohols with acetic acid

Cobalt(II) chloride hexahydrate (CoCl2·6H2O) efficiently catalyzes the acetylation of alcohols with AcOH in high yields. This protocol is also effective with other carboxylic acids, trifluoroacetic acid, propanoic acid, phenylacetic acid and benzoic acid, affording the corresponding acylated products in moderate to good yields. Removal of water is not necessary in these reactions. The catalyst can be filtered and recycled without loss of activity.

Carboxylic acids supported on silica: A smooth acylating agent for alcohols

An alternative procedure for the esterification of alcohols by short-chain carboxylic acids supported on silica is presented.