Home  

Random  

Nearby  



Log in  



Settings  



Donate  



About Wikipedia  

Disclaimers  



Wikipedia





Pentyl butyrate





Article  

Talk  



Language  

Watch  

Edit  


(Redirected from Amyl butyrate)
 


Pentyl butyrate, also known as pentyl butanoateoramyl butyrate, is an ester that is formed when pentanol is reacted with butyric acid,[1] usually in the presence of sulfuric acid as a catalyst. This ester has a smell reminiscent of pearorapricot. This chemical is used as an additive in cigarettes.

Pentyl butyrate
Pentyl butyrate
Names
Preferred IUPAC name

Pentyl butanoate

Other names

Pentyl butyrate

Identifiers

CAS Number

3D model (JSmol)

ChemSpider
ECHA InfoCard 100.007.946 Edit this at Wikidata
EC Number
  • 208-739-2

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C9H18O2/c1-3-5-6-8-11-9(10)7-4-2/h3-8H2,1-2H3 ☒N

    Key: CFNJLPHOBMVMNS-UHFFFAOYSA-N ☒N

  • InChI=1/C9H18O2/c1-3-5-6-8-11-9(10)7-4-2/h3-8H2,1-2H3

    Key: CFNJLPHOBMVMNS-UHFFFAOYAQ

  • CCCCCOC(=O)CCC

Properties

Chemical formula

C9H18O2
Molar mass 158.24 g/mol
Odor Apricot
Density 0.86 g/cm3
Melting point −73.2 °C (−99.8 °F; 200.0 K)
Boiling point 186 °C (367 °F; 459 K)

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

☒N verify (what is checkY☒N ?)

Infobox references

References

edit
  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Pentyl_butyrate&oldid=1207009103"
     



    Last edited on 13 February 2024, at 18:47  





    Languages

     


    تۆرکجه
    Bosanski
    Català
    Deutsch
    Español
    Esperanto
    فارسی
    Français

    Polski
    Português
    Српски / srpski
    Srpskohrvatski / српскохрватски
    ி
    Tiếng Vit

     

    Wikipedia


    This page was last edited on 13 February 2024, at 18:47 (UTC).

    Content is available under CC BY-SA 4.0 unless otherwise noted.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Terms of Use

    Desktop