Benzyl Acetate
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Benzyl Acetate
Benzyl acetate
Benzyl acetate-structure.svg
Benzyl acetate.gif
Names
Preferred IUPAC name
Benzyl acetate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.004.909 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C9H10O2/c1-8(10)11-7-9-5-3-2-4-6-9/h2-6H,7H2,1H3 checkY
    Key: QUKGYYKBILRGFE-UHFFFAOYSA-N checkY
  • InChI=1/C9H10O2/c1-8(10)11-7-9-5-3-2-4-6-9/h2-6H,7H2,1H3
    Key: QUKGYYKBILRGFE-UHFFFAOYAD
  • c1ccccc1COC(=O)C
  • CC(=O)OCc1ccccc1
Properties
C9H10O2
Molar mass 150.18 g/mol
Appearance Colourless liquid
Odor flowery
Density 1.054 g/ml
Melting point -51.5 °C (-60.7 °F; 221.7 K)
Boiling point 212 °C (414 °F; 485 K)
0.31 g/100 mL
Solubility Soluble in benzene, chloroform
Miscible with ethanol, ether, acetone
-93.18·10-6 cm3/mol
1.523
Hazards
NFPA 704 (fire diamond)
1
1
0
Flash point 102 °C (216 °F; 375 K)
461 °C (862 °F; 734 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Benzyl acetate is an organic ester with the molecular formula C9H10O2. It is formed by the condensation of benzyl alcohol and acetic acid.

Similar to most other esters, it possesses a sweet and pleasant aroma, owing to which, it finds applications in personal hygiene and health care products. It is a constituent of jasmin and of the essential oils of ylang-ylang and neroli. It has pleasant sweet aroma reminiscent of jasmine. Further as a flavoring agent it is also used to impart jasmine or apple flavors to various cosmetics and personal care products like lotions, hair creams etc..[1]

It is one of many compounds that is attractive to males of various species of orchid bees. It is collected and used by the bees as an intra-specific pheromone; In apiculture benzyl acetate is used as a bait to collect bees. Natural sources of benzyl acetate include varieties of flowers like jasmine (Jasminum), and fruits like pear, apple, etc.[2]

Industrially benzyl acetate is used as a medium of extraction in extraction of plastics, resin, cellulose acetate, cellulose nitrate, oils and lacquers.[]

References

  1. ^ "Benzyl acetate". The Good Scents Company.
  2. ^ Schiestl, F.P. & Roubik, D.W. (2004). "Odor Compound Detection in Male Euglossine Bees". Journal of Chemical Ecology. 29 (1): 253-257. doi:10.1023/A:1021932131526. PMID 12647866.

External links


  This article uses material from the Wikipedia page available here. It is released under the Creative Commons Attribution-Share-Alike License 3.0.

Benzyl_acetate
 



 



 
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