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Yuen-May Choo, Kay-Eng Ooi and Ing-Hong Ooi (August 1994). "Synthesis of civetone from palm oil products".
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507:. It has a strong musky odor that becomes pleasant at extreme dilutions. Civetone is closely related to
516:
732:
536:
55:
250:
618:
Bedoukian, Paul Z. "Perfumery and
Flavoring Synthetics", 2nd ed., p. 248, Elsevier, New York, 1967.
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73:
cis-Civetone; 9-Cycloheptadecen-1-one; Cycloheptadeca-9-en-1-one; (Z)-9-Cyclohepta-decen-1-one
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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-
201:
567:. It is believed that the civetone in the cologne resembles a territorial marking.
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288:
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-
551:
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519:. Today, civetone can be synthesized from precursor chemicals found in
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Except where otherwise noted, data are given for materials in their
27:
435:
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705:"You'll Never Guess How Biologists Lure Jaguars To Camera Traps"
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606:, O'Neil: The Royal Society of Chemistry. Available online at:
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http://www.rsc.org/Merck-Index/monograph/mono1500002334
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31 to 32 °C (88 to 90 °F; 304 to 305 K)
515:; the structure of both compounds was elucidated by
200:
632:. In Pybus, David H.; Sell, Charles S. (eds.).
630:"Ingredients for the Modern Perfumery Industry"
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511:, the principal odoriferous compound found in
663:Journal of the American Oil Chemists' Society
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669:(8). Springer Berlin / Heidelberg: 911–913.
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398:342 °C (648 °F; 615 K)
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638:Royal Society of Chemistry Publishing
281:Key: ZKVZSBSZTMPBQR-UPHRSURJSA-N
7:
495:and the main odorous constituent of
291:Key: ZKVZSBSZTMPBQR-UPHRSURJBS
191:
14:
554:, field biologists have used the
709:Scientific American Blog Network
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450:(at 25 °C , 100 kPa).
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1:
634:The Chemistry of Fragrances
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602:(2013), p. 418, Monograph
64:)-Cycloheptadec-9-en-1-one
628:Sell, Charles S. (1999).
579:, a related musk chemical
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312:O=C1CCCCCCC/C=C\CCCCCCC1
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738:Mammalian pheromones
546:In order to attract
56:Preferred IUPAC name
728:Perfume ingredients
640:. pp. 51–124.
577:5-Cyclohexadecenone
360: g·mol
18:
675:10.1007/bf02540473
477:Infobox references
368:Crystalline solid
41:
32:
16:
503:sourced from the
491:is a macrocyclic
485:Chemical compound
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440:slightly soluble
234:CompTox Dashboard
120:Interactive image
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558:-brand male
556:Calvin Klein
552:camera traps
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79:Identifiers
71:Other names
61:
733:Macrocycles
365:Appearance
321:Properties
158:100.008.013
722:Categories
584:References
535:used as a
499:. It is a
432:Solubility
418:Solubility
404:Solubility
353:Molar mass
222:P0K30CV1UE
131:ChemSpider
107:3D model (
86:CAS Number
683:0003-021X
564:Obsession
501:pheromone
497:civet oil
179:208‐813‐4
171:EC Number
17:Civetone
691:85189919
600:15th Ed.
571:See also
521:palm oil
489:Civetone
426:soluble
412:soluble
96:542-46-1
748:Ketones
560:cologne
548:jaguars
509:muscone
470:what is
468: (
422:ethanol
374:Density
358:250.426
202:5315941
189:PubChem
140:4475121
689:
681:
644:
541:flavor
493:ketone
465:verify
462:
305:SMILES
50:Names
687:S2CID
436:water
270:InChI
109:JSmol
679:ISSN
642:ISBN
604:2334
539:and
527:Uses
513:musk
408:oils
213:UNII
671:doi
550:to
434:in
420:in
406:in
239:EPA
192:CID
724::
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667:71
665:.
598:,
543:.
523:.
343:30
337:17
60:(9
711:.
693:.
673::
650:.
460:N
346:O
340:H
334:C
241:)
237:(
111:)
62:Z
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