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2-N-HEXYLCYCLOPENTANONE

2-N-HEXYLCYCLOPENTANONE ??? ???
?? ??:
13074-65-2
???:
2-N-HEXYLCYCLOPENTANONE
???(??):
2-HEXYLCYCLOPENTANONE;JASMATONE;hexylcyclopentanone;2-hexyl-cyclopentanon;jasmin cyclopentanone;2-Hexylcyclopentan-1-on;2-N-HEXYLCYCLOPENTANONE;2-Hexylcyclopentanone>Cyclopentanone, 2-hexyl-;2-hexylcyclopentan-1-one
CBNumber:
CB6445247
???:
C11H20O
??? ??:
168.28
MOL ??:
13074-65-2.mol

2-N-HEXYLCYCLOPENTANONE ??

?? ?
108-110°C 10mm
??
0,89 g/cm3
???
2.1Pa at 20℃
???
1.4495
???
112°C
?? ??
2-8°C
??
100.00%??. ???? ??? ???
?? ??
???
???
59.5mg/L at 20℃
BRN
2041950
??? ?? ??
PERFUMING
LogP
3.9
CAS ??????
13074-65-2(CAS DataBase Reference)
EPA
Cyclopentanone, 2-hexyl- (13074-65-2)
??
  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
RTECS ?? GY4972000
TSCA TSCA listed
HS ?? 2914290090
????(GHS): Exclamation Mark (GHS07)
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? P264, P280, P305+P351+P338,P337+P313P
??????:
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P280 ????/???/???/?????? ?????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
1
0 0

2-N-HEXYLCYCLOPENTANONE C??? ??, ??, ??

??

2-N-hexylcyclopentanone is less spicy or Celery-like than Jasmone, more sharp-fruity or green, and not quite as powerful. Rather than considering it as a lowcost substitute for Jasmone, it would be better to use it as an individual fragrance material with effects of its own. It will lend considerable floral-herbaceous power to fragrances other than the typical floral ones, and itmay participate in giving Jasmin effect when blended with suitable components.

Synthesis Reference(s)

Journal of the American Chemical Society, 98, p. 248, 1976 DOI: 10.1021/ja00417a048

2-N-HEXYLCYCLOPENTANONE ?? ?? ? ???

???

?? ??


2-N-HEXYLCYCLOPENTANONE ?? ??

???( 87)?? ??
??? ?? ??? ?? ?? ? ??
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2-N-HEXYLCYCLOPENTANONE ?? ??:

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