fbpx
Wikipedia

Civetone

Civetone is a macrocyclic ketone and the main odorous constituent of civet oil.[1] It is a pheromone sourced from the African civet. It has a strong musky odor that becomes pleasant at extreme dilutions.[2] Civetone is closely related to muscone, the principal odoriferous compound found in musk; the structure of both compounds was elucidated by Leopold Ružička.[3] Today, civetone can be synthesized from precursor chemicals found in palm oil.[4]

Civetone
Names
Preferred IUPAC name
(9Z)-Cycloheptadec-9-en-1-one
Other names
cis-Civetone; 9-Cycloheptadecen-1-one; Cycloheptadeca-9-en-1-one; (Z)-9-Cyclohepta-decen-1-one
Identifiers
  • 542-46-1 Y
3D model (JSmol)
  • Interactive image
ChemSpider
  • 4475121 Y
ECHA InfoCard 100.008.013
EC Number
  • 208‐813‐4
  • 5315941
UNII
  • P0K30CV1UE Y
  • DTXSID80883434
  • InChI=1S/C17H30O/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-17/h1-2H,3-16H2/b2-1- Y
    Key: ZKVZSBSZTMPBQR-UPHRSURJSA-N Y
  • InChI=1/C17H30O/c18-17-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-16-17/h1-2H,3-16H2/b2-1-
    Key: ZKVZSBSZTMPBQR-UPHRSURJBS
  • O=C1CCCCCCC/C=C\CCCCCCC1
Properties
C17H30O
Molar mass 250.426 g·mol−1
Appearance Crystalline solid
Density 0.917 at 33 °C
Melting point 31 to 32 °C (88 to 90 °F; 304 to 305 K)
Boiling point 342 °C (648 °F; 615 K)
Solubility in oils soluble
Solubility in ethanol soluble
Solubility in water slightly soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YN ?)

Uses edit

Civetone is a synthetic musk used as a perfume fixative and flavor.

In order to attract jaguars to camera traps, field biologists have used the Calvin Klein-brand male cologne Obsession. It is believed that the civetone in the cologne resembles a territorial marking.[5]

See also edit

References edit

  1. ^ The Merck Index, 15th Ed. (2013), p. 418, Monograph 2334, O'Neil: The Royal Society of Chemistry. Available online at: http://www.rsc.org/Merck-Index/monograph/mono1500002334
  2. ^ Bedoukian, Paul Z. "Perfumery and Flavoring Synthetics", 2nd ed., p. 248, Elsevier, New York, 1967.
  3. ^ Sell, Charles S. (1999). "Ingredients for the Modern Perfumery Industry". In Pybus, David H.; Sell, Charles S. (eds.). The Chemistry of Fragrances (1st ed.). Royal Society of Chemistry Publishing. pp. 51–124. ISBN 9780854045280.
  4. ^ Yuen-May Choo, Kay-Eng Ooi and Ing-Hong Ooi (August 1994). "Synthesis of civetone from palm oil products". Journal of the American Oil Chemists' Society. 71 (8). Springer Berlin / Heidelberg: 911–913. doi:10.1007/bf02540473. ISSN 0003-021X. S2CID 85189919.
  5. ^ "You'll Never Guess How Biologists Lure Jaguars To Camera Traps". Scientific American Blog Network.

civetone, macrocyclic, ketone, main, odorous, constituent, civet, pheromone, sourced, from, african, civet, strong, musky, odor, that, becomes, pleasant, extreme, dilutions, closely, related, muscone, principal, odoriferous, compound, found, musk, structure, b. Civetone is a macrocyclic ketone and the main odorous constituent of civet oil 1 It is a pheromone sourced from the African civet It has a strong musky odor that becomes pleasant at extreme dilutions 2 Civetone is closely related to muscone the principal odoriferous compound found in musk the structure of both compounds was elucidated by Leopold Ruzicka 3 Today civetone can be synthesized from precursor chemicals found in palm oil 4 Civetone Names Preferred IUPAC name 9Z Cycloheptadec 9 en 1 one Other names cis Civetone 9 Cycloheptadecen 1 one Cycloheptadeca 9 en 1 one Z 9 Cyclohepta decen 1 one Identifiers CAS Number 542 46 1 Y 3D model JSmol Interactive image ChemSpider 4475121 Y ECHA InfoCard 100 008 013 EC Number 208 813 4 PubChem CID 5315941 UNII P0K30CV1UE Y CompTox Dashboard EPA DTXSID80883434 InChI InChI 1S C17H30O c18 17 15 13 11 9 7 5 3 1 2 4 6 8 10 12 14 16 17 h1 2H 3 16H2 b2 1 YKey ZKVZSBSZTMPBQR UPHRSURJSA N YInChI 1 C17H30O c18 17 15 13 11 9 7 5 3 1 2 4 6 8 10 12 14 16 17 h1 2H 3 16H2 b2 1 Key ZKVZSBSZTMPBQR UPHRSURJBS SMILES O C1CCCCCCC C C CCCCCCC1 Properties Chemical formula C 17H 30O Molar mass 250 426 g mol 1 Appearance Crystalline solid Density 0 917 at 33 C Melting point 31 to 32 C 88 to 90 F 304 to 305 K Boiling point 342 C 648 F 615 K Solubility in oils soluble Solubility in ethanol soluble Solubility in water slightly soluble Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesUses editCivetone is a synthetic musk used as a perfume fixative and flavor In order to attract jaguars to camera traps field biologists have used the Calvin Klein brand male cologne Obsession It is believed that the civetone in the cologne resembles a territorial marking 5 See also edit5 Cyclohexadecenone a related musk chemicalReferences edit The Merck Index 15th Ed 2013 p 418 Monograph 2334 O Neil The Royal Society of Chemistry Available online at http www rsc org Merck Index monograph mono1500002334 Bedoukian Paul Z Perfumery and Flavoring Synthetics 2nd ed p 248 Elsevier New York 1967 Sell Charles S 1999 Ingredients for the Modern Perfumery Industry In Pybus David H Sell Charles S eds The Chemistry of Fragrances 1st ed Royal Society of Chemistry Publishing pp 51 124 ISBN 9780854045280 Yuen May Choo Kay Eng Ooi and Ing Hong Ooi August 1994 Synthesis of civetone from palm oil products Journal of the American Oil Chemists Society 71 8 Springer Berlin Heidelberg 911 913 doi 10 1007 bf02540473 ISSN 0003 021X S2CID 85189919 You ll Never Guess How Biologists Lure Jaguars To Camera Traps Scientific American Blog Network Retrieved from https en wikipedia org w index php title Civetone amp oldid 1176329110, wikipedia, wiki, book, books, library,

article

, read, download, free, free download, mp3, video, mp4, 3gp, jpg, jpeg, gif, png, picture, music, song, movie, book, game, games.