59975
茉莉酮
analytical standard
别名:
(Z)-3-甲基-2-(2-戊烯基)-2-环戊烯-1-酮
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关于此项目
经验公式（希尔记法）:
C11H16O
化学文摘社编号:
分子量:
164.24
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
EC Number:
207-668-4
Beilstein/REAXYS Number:
1907713
MDL number:
产品名称
茉莉酮, analytical standard
InChI key
XMLSXPIVAXONDL-PLNGDYQASA-N
InChI
1S/C11H16O/c1-3-4-5-6-10-9(2)7-8-11(10)12/h4-5H,3,6-8H2,1-2H3/b5-4-
SMILES string
[H]\C(CC)=C(/[H])CC1=C(C)CCC1=O
grade
analytical standard
assay
≥99.0% (sum of isomers, GC)
technique(s)
HPLC: suitable
gas chromatography (GC): suitable
impurities
~6% trans-isomer
refractive index
n20/D 1.498 (lit.)
n20/D 1.500
bp
134-135 °C/12 mmHg (lit.)
density
0.94 g/mL at 25 °C (lit.)
application(s)
cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care
format
neat
Quality Level
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Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Other Notes
This compound is commonly found in plants of the genus: mentha
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
10 - Combustible liquids
wgk
WGK 2
flash_point_f
224.6 °F - closed cup
flash_point_c
107 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
Anna Pawełczyk et al.
European journal of medicinal chemistry, 44(7), 3032-3039 (2008-09-06)
Taking the rising interest in jasmone structure based fragrant compounds into account it has been decided to take up an attempt to synthesize the new heterocyclic derivatives of this 2,3-disubstituted cyclopentenone, which could be characterized by the ability of interaction
Stefan Dötterl et al.
Journal of chemical ecology, 38(12), 1539-1543 (2012-11-13)
Many plants attract their pollinators with floral scents, and these olfactory signals are especially important at night, when visual signals become inefficient. Dynastid scarab beetles are a speciose group of night-active pollinators, and several plants pollinated by these insects have
Anna Pawełczyk et al.
European journal of medicinal chemistry, 41(5), 586-591 (2006-03-28)
cis-Jasmone, from jasmonoid group, is an important jasmine odor fragrance compound. The syntheses of new heterocyclic analogues of jasmone were described. Five analogues of this compound were prepared under microwave irradiation and the results of the microwave assisted syntheses were
Michaela C Matthes et al.
Planta, 232(5), 1163-1180 (2010-08-17)
cis-jasmone (CJ) is a plant-derived chemical that enhances direct and indirect plant defence against herbivorous insects. To study the signalling pathway behind this defence response, we performed microarray-based transcriptome analysis of CJ-treated Arabidopsis plants. CJ influenced a different set of
Laxmi Yeruva et al.
Experimental lung research, 32(10), 499-516 (2006-12-16)
The jasmonates, cis-jasmone (CJ) and methyl jasmonate (MJ), were investigated for their effects against NSCLC cell lines A549 and H520. CJ or MJ inhibited the proliferation of both cell lines in a dose-dependent manner as well as induced cell cycle
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