• Source: Butyl propionate

Butyl propionate is a butyl ester of propionic acid. This ester has the chemical formula CH3CH2COO(CH2)3CH3.




Occurrence in nature


Butyl propionate is a plant metabolite, a human metabolite and an insect attractant. Butyl propionate is a natural ester found in Armenian apricot.




Preparation


Butyl propionate is derived by esterification of propionic acid with butanol.

CH3CH2COOH + CH3(CH2)3OH ⇌ CH3CH2COO(CH2)3CH3 + H2O




Properties


Butyl propionate is a colorless liquid with a pear drops-like or apple-like odor. The liquid is less dense than water. Its vapor is 4.5 times denser than the air at the mean ocean level.




Uses


Butyl propionate is used to make fragrances, perfumes and as a flavoring. It is also used in paints and primers for auto body or engine, appliance coatings (paints designed specifically for painting household items and vehicles like microwave ovens, refrigerators and automobiles), enamels, lacquers, and printing inks, as a solvent for adhesives and nitrocellulose, and in polymerization reactions for acrylic resins.




Hazards and toxicity


Butyl propionate may irritate skin and eyes. Exposure to its vapor may cause eye and respiratory system irritation. Upon ingestion, causes abdominal pain and nausea. This chemical is very flammable. It may ignite even at ambient temperatures. Above 32 °C (90 °F), explosive mixtures with air may be formed. Strong oxidizing acids may cause a violent reaction that is sufficiently exothermic to ignite this chemical and the reaction products. Upon catching a fire, irritating, toxic and suffocating gases may be produced, such as carbon dioxide and carbon monoxide.




References

Kata Kunci Pencarian:

• Butil hidroksitoluen
• Butyl propionate
• C7H14O2
• Ester
• Clobetasol propionate
• Fluticasone propionate
• Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)propionate
• Aldol reaction
• Pentaerythritol tetrakis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate)
• Butylated hydroxytoluene
• C5H10O2