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Merck
CN

59975

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
UNSPSC Code:
85151701
NACRES:
NA.24
PubChem Substance ID:
329758642
EC Number:
207-668-4
Beilstein/REAXYS Number:
1907713
MDL number:
MFCD00001402

Key Documents

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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

100

Related Categories

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

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

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

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Certificates of Analysis (COA)

Lot/Batch Number
1288284

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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
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
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
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
Tomonori Misaki et al.
Journal of the American Chemical Society, 127(9), 2854-2855 (2005-03-03)
Ti-crossed-Claisen condensation between a 1:1 mixture of carboxylic esters and acid chlorides promoted by TiCl4-Bu3N-N-methylimidazole proceeded successfully to give various beta-keto esters in good yields with excellent selectivities (19 examples, approximately 48-95% yield; cross/self-selectivity = approximately 96/4-99/1). The present method
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