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59975

Supelco

Jasmone

analytical standard

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C11H16O
CAS Number:
488-10-8
Molecular Weight:
164.24
Beilstein:
1907713
EC Number:
207-668-4
MDL number:
MFCD00001402
UNSPSC Code:
85151701
PubChem Substance ID:
329758642
NACRES:
NA.24

grade

analytical standard

Quality Level

100

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

SMILES string

[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-

InChI key

XMLSXPIVAXONDL-PLNGDYQASA-N

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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

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

224.6 °F - closed cup

Flash Point(C)

107 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

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

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Toby J A Bruce et al.
Proceedings of the National Academy of Sciences of the United States of America, 105(12), 4553-4558 (2008-03-22)
It is of adaptive value for a plant to prepare its defenses when a threat is detected, and certain plant volatiles associated with insect damage, such as cis-jasmone (CJ), are known to switch-on defense metabolism. We used aphid and aphid
John A Pickett et al.
Phytochemistry, 68(22-24), 2937-2945 (2007-11-21)
The challenges and opportunities for protecting agricultural production of food and other materials will be met through exploiting the induction of defence pathways in plants to control pests, diseases and weeds. These approaches will involve processes that can be activated
Walter P Suza et al.
Planta, 227(6), 1221-1232 (2008-02-06)
The Arabidopsis thaliana (L.) Heynh. JASMONATE RESISTANT 1( JAR1) locus is essential for pathogen defense, but its role in wound response has not been investigated. JAR1 encodes an enzyme that conjugates jasmonic acid (JA) to isoleucine, which was recently shown
Munenori Suzuki et al.
Bioscience, biotechnology, and biochemistry, 68(7), 1617-1620 (2004-07-28)
Coronatine (1), its synthetic analogs (6-13) and jasmonic acid induced various volatiles in rice leaves. In the range of 0.01-0.1 mM, dihydrocoronatine (7) exhibited 4-687 times higher activity for linalool emission than that of 1. The radioactive derivative of 7
Sarah Y Dewhirst et al.
Pest management science, 68(10), 1419-1429 (2012-06-15)
Two important pests of the sweet pepper, Capsicum annuum, are the peach potato aphid, Myzus persicae, and the glasshouse potato aphid, Aulacorthum solani. Current aphid control measures include the use of biological control agents, i.e., parasitic wasps, but with varying
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