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12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID

CAS No.
169217-38-3
Chemical Name:
12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID
Synonyms
ETHEROLEIC ACID;12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID
CBNumber:
CB5229330
Molecular Formula:
C18H30O3
Molecular Weight:
294.43
MDL Number:
MFCD05864090
MOL File:
Mol file
Last updated:2023-06-08 09:03:08

12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID Properties

solubility Ethanol: soluble

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H225-H319
Precautionary statements  P210-P233-P240-P241-P242-P243-P264-P280-P303+P361+P353-P305+P351+P338-P337+P313-P370+P378-P403+P235-P501
NFPA 704
3
2 0

12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID Chemical Properties,Uses,Production

Description

Etheroleic acid is a divinyl ether oxylipin.1,2 It is a metabolite of linolenic acid that is formed in plants via 13-lipoxygenase-mediated formation of 13(S)-HpODE or (±)13-HpODE followed by conversion to the divinyl ether by divinyl ether synthase. Etheroleic acid (30 μM) is fungicidal against the powdery mildew B. graminis on the second leaves of barley seedlings.3

References

1. Grechkin, A.N., Ilyasov, A.V., and Hamberg, M. On the mechanism of biosynthesis of divinyl ether oxylipins by enzyme from garlic bulbs Eur. J. Biochem. 245(1),137-142(1997).
2. Hamberg, M. Biosynthesis of new divinyl ether oxylipins in Ranunculus plants Lipids 37(4),427-433(2002).
3. Cowley, T., and Walters, D. Local and systemic effects of oxylipins on powdery mildew infection in barley Pest Manag. Sci. 61(6),572-576(2005).

12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID Suppliers

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12-[1-L (E)-HEXENYLOXY]-9(Z),11(E)-DODECADIENOIC ACID ETHEROLEIC ACID 169217-38-3