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Jasmone

analytical standard

Synonyme(s) :

cis-3-Methyl-2-(2-pentenyl)-2-cyclopenten-1-one

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About This Item

Formule empirique (notation de Hill):
C11H16O
Numéro CAS:
488-10-8
Poids moléculaire :
164.24
Numéro Beilstein :
1907713
Numéro CE :
207-668-4
Numéro MDL:
MFCD00001402
Code UNSPSC :
85151701
ID de substance PubChem :
329758642
Nomenclature NACRES :
NA.24

Qualité

analytical standard

Niveau de qualité

100

Pureté

≥99.0% (sum of isomers, GC)

Technique(s)

HPLC: suitable
gas chromatography (GC): suitable

Impuretés

~6% trans-isomer

Indice de réfraction

n20/D 1.498 (lit.)
n20/D 1.500

Point d'ébullition

134-135 °C/12 mmHg (lit.)

Densité

0.94 g/mL at 25 °C (lit.)

Application(s)

cleaning products
cosmetics
flavors and fragrances
food and beverages
personal care

Format

neat

Chaîne SMILES 

[H]\C(CC)=C(/[H])CC1=C(C)CCC1=O

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-

Clé InChI

XMLSXPIVAXONDL-PLNGDYQASA-N

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Catégories apparentées

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Autres remarques

This compound is commonly found in plants of the genus: mentha

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H315,H319,H335

Classification des risques

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Organes cibles

Respiratory system

Code de la classe de stockage

10 - Combustible liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

224.6 °F - closed cup

Point d'éclair (°C)

107 °C - closed cup

Équipement de protection individuelle

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificats d'analyse (COA)

Lot/Batch Number
1288284
1288284
1288284V
053416/1
53416/1

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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
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
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
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
A M El-Sayed et al.
Journal of chemical ecology, 35(6), 656-663 (2009-05-16)
This work was undertaken to identify floral compound(s) produced by honeysuckle flowers, Lonicera japonica (Thunberg), that mediate the attraction of New Zealand flower thrips Thrips obscuratus (Crawford). Volatiles were collected during the day and night and analyzed by gas chromatography-mass
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