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Jasmone

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For Research Use Only | Not For Clinical Use
CATAP488108
CAS488-10-8
Structure
MDL NumberMFCD00001402
Molecular Weight164.24
EC Number207-668-4
InChI KeyXMLSXPIVAXONDL-PLNGDYQASA-N
REAXYS Number1907713
Descriptionanalytical standard
Density0.94 g/mL at 25 °C (lit.)
Assay≥99.0% (sum of isomers, GC)
BP134-135 °C/12 mmHg (lit.)
Formneat; gas chromatography (GC): suitable
Gradeanalytical standard
Impurity Content~6% trans-isomer
Refractive Indexn20/D 1.498 (lit.); n20/D 1.500
Size1ML
1

Attraction of New Zealand Flower Thrips, Thrips Obscuratus, to Cis-Jasmone, a Volatile Identified From Japanese Honeysuckle Flowers

A M El-Sayed, V J Mitchell, G F McLaren, L M Manning, B Bunn, D M Suckling

J Chem Ecol. 2009 Jun;35(6):656-63.

PMID: 19444522

1

Emerging Roles in Plant Defense for Cis-Jasmone-Induced Cytochrome P450 CYP81D11

Michaela Matthes, Toby Bruce, Keith Chamberlain, John Pickett, Johnathan Napier

Plant Signal Behav. 2011 Apr;6(4):563-5.

PMID: 21422824

1

Jasmone Hydroxylase, a Key Enzyme in the Synthesis of the Alcohol Moiety of Pyrethrin Insecticides

Wei Li, Fei Zhou, Eran Pichersky

Plant Physiol. 2018 Aug;177(4):1498-1509.

PMID: 29967096

1

New Roles for Cis-Jasmone as an Insect Semiochemical and in Plant Defense

M A Birkett, C A Campbell, K Chamberlain, E Guerrieri, A J Hick, J L Martin, M Matthes, J A Napier, J Pettersson, J A Pickett, G M Poppy, E M Pow, B J Pye, L E Smart, G H Wadhams, L J Wadhams, C M Woodcock

Proc Natl Acad Sci U S A. 2000 Aug 1;97(16):9329-34.

PMID: 10900270

1

Synthetic Cis-Jasmone Exposure Induces Wheat and Barley Volatiles That Repel the Pest Cereal Leaf Beetle, Oulema Melanopus L

Kevin J Delaney, Maria Wawrzyniak, Grzegorz Lemańczyk, Danuta Wrzesińska, Dariusz Piesik

J Chem Ecol. 2013 May;39(5):620-9.

PMID: 23588742

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