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?????
????? ??? ???
?? ??:
488-10-8
???:
?????
???(??):
?????;??-???
???:
Jasmone
???(??):
CIS-JASMONE;(Z)-JASMONE;JASMONE;FEMA 3196;cis-Jasmon;Aids032327;cis-Jabarme;Aids-032327;Cis jasmine;JASMONE, CIS-
CBNumber:
CB0251161
???:
C11H16O
??? ??:
164.24
MOL ??:
488-10-8.mol
MSDS ??:
SDS

????? ??

?? ?
134-135 °C12 mm Hg(lit.)
??
0.94 g/mL at 25 °C(lit.)
???
0.91Pa at 20℃
???
n20/D 1.498(lit.)
FEMA
3196 | 3-METHYL-2-(2-PENTENYL)-2-CYCLOPENTEN-1-ONE
???
225 °F
?? ??
Sealed in dry,Room Temperature
??? ??
Liquid
??
Colorless to Light orange to Yellow
??
????? ??? ? 10.00%.?? ?? ? ??? ??? ??? ?
?? ??
???
???? ??
synthetic
???
1.48g/L at 20℃
Merck
14,5259
JECFA Number
1114
BRN
1907713
InChIKey
IVLCENBZDYVJPA-ARJAWSKDSA-N
LogP
2.8 at 35℃
CAS ??????
488-10-8(CAS DataBase Reference)
NIST
2-Cyclopenten-1-one, 3-methyl-2-(2-pentenyl)-, (Z)-(488-10-8)
EPA
2-Cyclopenten-1-one, 3-methyl-2-(2Z)-2-pentenyl- (488-10-8)
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  • ?? ? ?? ??
  • ?? ? ???? ?? (GHS)
??? ?? Xi
?? ???? ?? 36/37/38
????? 26-37/39
WGK ?? 2
RTECS ?? GY7301000
TSCA Yes
HS ?? 29142990
?? ?? ??? 488-10-8(Hazardous Substances Data)
?? rabbit,LD50,skin,> 5gm/kg (5000mg/kg),Food and Cosmetics Toxicology. Vol. 17, Pg. 845, 1979.
???? ?? KE-24774
????(GHS): GHS hazard pictograms
?? ?: Warning
??·?? ??:
?? ??·?? ?? ?? ?? ?? ?? ? ?? ?? P- ??
H315 ??? ??? ??? ????? ?? ????? ?? 2 ?? GHS hazard pictograms P264, P280, P302+P352, P321,P332+P313, P362
H319 ?? ?? ??? ??? ?? ? ?? ?? ??? ?? ?? 2A ?? GHS hazard pictograms P264, P280, P305+P351+P338,P337+P313P
H335 ?? ???? ??? ? ?? ?? ???? ?? - 1? ??;???? ?? ?? 3 ?? GHS hazard pictograms
??????:
P261 ??·?·??·???·??·...·????? ??? ????.
P264 ?? ??? ?? ??? ????.
P264 ?? ??? ?? ??? ????.
P271 ?? ?? ??? ? ?? ???? ?????.
P280 ????/???/???/?????? ?????.
P302+P352 ??? ??? ??? ?? ????.
P305+P351+P338 ?? ??? ? ?? ?? ???? ????. ???? ?????? ?????. ?? ????.
NFPA 704
1
2 0

????? MSDS


Jasmone

????? C??? ??, ??, ??

??

This has a jasmine odor.

??? ??

Jasmone has a floral, fruity, jasmine odor. cis-Jasmone is widely used in the creation of high quality florals like jasmine and tuberose. Also used in the reconstitution of synthetic essential oils.

??

The cis-form is reportedly occurring naturally; it is found in the essential oils of jasmine (3%), jonquil, and Pittosporum glabratum, in neroli oil, in peppermint (Mentha piperita), and in bergamot, apricot, raspberry, cinnamon, corn mint and spearmint oils, beer, tea, soybean and heated beans.

??

Traces, often mere fractions of one percent in a perfume oil may introduce just that wanted warmth and deep floral note almost unobtainable with other chemicals.
Jasmone's flavor power is even greater. Concentrations of about 1 ppm have perceptible effect in many fruit flavors, while naturally, concentrations in Mint flavors are higher.

??

A ketone found in jasmine oil and other flower oils.

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