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Contents

   



(Top)
 


1 See also  





2 References  





3 Further reading  














Damascone






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From Wikipedia, the free encyclopedia
 


beta-Damascone[1]
Names
IUPAC name

(E)-1-(2,6,6-Trimethyl-1-cyclohexenyl)but-2-en-1-one

Other names

Rose ketones

Identifiers

CAS Number

3D model (JSmol)

3DMet
ChemSpider
ECHA InfoCard 100.041.660 Edit this at Wikidata
EC Number
  • 245-842-1

PubChem CID

UNII

CompTox Dashboard (EPA)

  • InChI=1S/C13H20O/c1-5-7-11(14)12-10(2)8-6-9-13(12,3)4/h5,7H,6,8-9H2,1-4H3/b7-5+ ☒N

    Key: BGTBFNDXYDYBEY-FNORWQNLSA-N ☒N

  • InChI=1/C13H20O/c1-5-7-11(14)12-10(2)8-6-9-13(12,3)4/h5,7H,6,8-9H2,1-4H3/b7-5+

    Key: BGTBFNDXYDYBEY-FNORWQNLBE

  • O=C(/C1=C(/CCCC1(C)C)C)/C=C/C

Properties

Chemical formula

C13H20O
Molar mass 192.30 g/mol
Density 0.934 g/mL
Hazards
GHS labelling:

Pictograms

GHS07: Exclamation markGHS09: Environmental hazard

Signal word

Warning

Hazard statements

H315, H317, H411

Precautionary statements

P261, P264, P272, P273, P280, P302+P352, P321, P332+P313, P333+P313, P362, P363, P391, P501

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

alpha-Damascone
Names
IUPAC name

(E)-1-(2,6,6-trimethyl-1-cyclohex-2-enyl)but-2-en-1-one

Other names

Rose ketones

Identifiers

CAS Number

3D model (JSmol)

3DMet

Beilstein Reference

2208707
ChEBI
ChemSpider
ECHA InfoCard 100.041.660 Edit this at Wikidata
EC Number

PubChem CID

CompTox Dashboard (EPA)

  • InChI=1S/C13H20O/c1-5-7-11(14)12-10(2)8-6-9-13(12,3)4/h5,7-8,12H,6,9H2,1-4H3/b7-5+

    Key: CRIGTVCBMUKRSL-FNORWQNLSA-N

  • C/C=C/C(=O)C1C(=CCCC1(C)C)C

Properties

Chemical formula

C13H20O
Molar mass 192.302 g·mol−1
Hazards
GHS labelling:

Pictograms

GHS07: Exclamation markGHS09: Environmental hazard

Signal word

Warning

Hazard statements

H302, H317, H411

Precautionary statements

P261, P264, P270, P272, P273, P280, P301+P312, P302+P352, P321, P330, P333+P313, P363, P391, P501

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

Damascones are a series of closely related chemical compounds that are components of a variety of essential oils. The damascones belong to a family of chemicals known as rose ketones, which also includes damascenones and ionones. beta-Damascone is a contributor to the aroma of roses, despite its relatively low concentration, and is an important fragrance chemical used in perfumery.[2]

The damascones are derived from the degradation of carotenoids.[3][4]

See also[edit]

References[edit]

  • ^ Biogeneration of C13-norisoprenoid compounds: experiments supportive for an apo-carotenoid pathway in grapevines. R. Baumes, J. Wirth, S. Bureau, Y. Gunata and A. Razungles, Analytica Chimica Acta, 29 April 2002, Volume 458, Issue 1, pages 3–14, doi:10.1016/S0003-2670(01)01589-6
  • ^ Volatile Compounds Released by Enzymatic Hydrolysis of Glycoconjugates of Leaves and Grape Berries from Vitis vinifera Muscat of Alexandria and Shiraz Cultivars. Jérémie Wirth, Wenfei Guo, Raymond Baumes and Ziya Günata, J. Agric. Food Chem., 2001, 49 (6), pages 2917–2923, doi:10.1021/jf001398l
  • Further reading[edit]

  • t
  • e

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Damascone&oldid=1073534207"

    Categories: 
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    This page was last edited on 23 February 2022, at 06:15 (UTC).

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