The density of the product is not validated, however, a density of 0.9168 g/mL has been reported in the literature.
Fortfahren mit
A9298
Methyl-Arachidonat
≥99% (GC)
Synonym(e):
Methyl-arachidonat
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| Packungsgröße | SKU | Verfügbarkeit | Preis |
|---|---|---|---|
| 50 mg | Warenkorb auf Verfügbarkeit prüfen | € 253,00 | |
| 100 mg | Warenkorb auf Verfügbarkeit prüfen | € 431,00 |
Über diesen Artikel
Empirische Formel (Hill-System):
C21H34O2
CAS-Nummer:
Molekulargewicht:
318.49
UNSPSC Code:
12352211
NACRES:
NA.25
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1714445
Technischer Dienst
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Unterstützung erhaltenbiological source
Mortierella alpina
Quality Level
assay
≥99% (GC)
form
liquid
functional group
ester
lipid type
omega FAs
shipped in
dry ice
storage temp.
−20°C
SMILES string
CCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)OC
InChI
1S/C21H34O2/c1-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21(22)23-2/h7-8,10-11,13-14,16-17H,3-6,9,12,15,18-20H2,1-2H3/b8-7-,11-10-,14-13-,17-16-
InChI key
OFIDNKMQBYGNIW-ZKWNWVNESA-N
Application
- Lipid peroxidation products mediate the formation of 8-hydroxydeoxyguanosine in DNA.: This article explores the role of lipid peroxidation products, specifically those involving methyl arachidonate, in causing oxidative DNA damage, indicating the compound′s influence on cellular aging and disease processes (Park JW et al., 1992).
Biochem/physiol Actions
Unlike most unsaturated fatty acid methyl esters, methyl arachidonate is a potent activator of protein kinase C at 5–50 μM. At the low end of the effective concentration range, the effect is due to cyclooxygenase products, while lipoxygenase products mediate the effect at higher concentrations.
Unlike most unsaturated fatty acid methyl esters, methyl arachidonate is a potent activator of protein kinase C.
Packaging
Sealed ampule under vacuum.
1 of 1
Dieser Artikel | |||
|---|---|---|---|
| functional group ester | functional group ester | functional group ester | functional group ester |
| biological source Mortierella alpina | biological source - | biological source fungus | biological source synthetic (organic) |
| assay ≥99% (GC) | assay ≥99% (capillary GC) | assay ≥98.5% (GC) | assay ≥99% |
| storage temp. −20°C | storage temp. −20°C | storage temp. −20°C | storage temp. −20°C |
| form liquid | form powder | form liquid | form solid |
| shipped in dry ice | shipped in ambient | shipped in ambient | shipped in ambient |
Lagerklasse
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)
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Wenjia Tang et al.
Bioresource technology, 196, 559-565 (2015-08-22)
A novel two-step enzymatic method is described in this study to synthesize symmetrical triacylglycerols (TAGs) with arachidonic acid (ARA) at the sn-2 position. The processes included the synthesis of 2-monoacylglycerols (2-MAGs) rich in 2-arachidonoylglycerol (2-AG) by enzymatic ethanolysis and the
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A9298-50MG | 04061833402290 |
| A9298-100MG | 04061838254696 |
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Wie ist die Dichte von A9298. Ich muss eine Stammlösung herstellen und benötige dringend diese Auskunft!!
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