Skip to Content
Merck
All Photos(1)

Key Documents

900127E

Avanti

14(15) EET

Avanti Research - A Croda Brand, ethanol solution

Synonym(s):

(±)14(15)-epoxy-5Z,8Z,11Z-eicosatrienoic acid

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C20H32O3
CAS Number:
Molecular Weight:
320.47
UNSPSC Code:
12352211
NACRES:
NA.25

Assay

99% (TLC)

form

ethanol solution

packaging

pkg of 1 × 500 μg (900127E-500UG)

manufacturer/tradename

Avanti Research - A Croda Brand

concentration

500 μg/mL (900127E-500UG)

lipid type

neutral glycerides

shipped in

dry ice

storage temp.

−20°C

General description

Epoxytrienoic acid (EET) is produced from arachidonic acid. 14(15) EET is an EET, which is produced by five cytochrome P450 (CYP) epoxygenases. It is a regioisomer of EET synthesized in mammalian tissues.

Biochem/physiol Actions

Epoxytrienoic acid (EET) plays a role as lipid mediator in the renal and cardiovascular systems. 14(15) EET activates many signal transduction pathways by binding to the membrane receptors. It possesses vasoactive properties.

Packaging

2ML Amber Glass Sealed Ampule (900127E-500UG)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Pictograms

FlameExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

55.4 °F

Flash Point(C)

13 °C


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Cytochrome P450 epoxygenase pathway of polyunsaturated fatty acid metabolism
Spector A A and Kim H Y
Biochimica et Biophysica Acta - Molecular and Cell Biology of Lipids, 1851(4), 356-365 (2015)
Cytochrome P450 and arachidonic acid bioactivation: molecular and functional properties of the arachidonate monooxygenase
Capdevila J H, et al.
Journal of Lipid Research, 41(2), 163-181 (2000)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service