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ChemicalBook--->CAS DataBase List--->2566-89-4

2566-89-4

2566-89-4 Structure

2566-89-4 Structure
IdentificationBack Directory
[Name]

METHYL ARACHIDONATE
[CAS]

2566-89-4
[Synonyms]

Einecs 219-900-1
METHYL ARACHIDONATE
Arachidonic acid methyl
Methyl arachidonate (C20:4n6)
ARACHIDONIC ACID METHYL ESTER
METHYL ARACHIDONATE, >=99% (GC)
Methyl arachidonoate (5c,8c,11c,14c)
Methyl arachidonate (C20:4n6) Solution
C20:4 (ALL CIS-5,8,11,14) METHYL ESTER
ARACHIDONIC ACID METHYL ESTER APPROX. 99%
Methyl arachidonate@10.0 mg/mL in Heptane
Methyl all-cis-5,8,11,14-eicosatetraenoate
Methyl cis-5,8,11,14-Eicosatetraenoate(C20:4)
methyl cis-5,8,11,14-eicosatetraenoate solution
cis-5,8,11,14-Eicosatetraenoic acidmethyl ester
11,14-eicosatetraenoicacid,methylester,(all-z)-8
5Z,8Z,11Z,14Z-EICOSATETRAENOIC ACID, METHYL ESTER
Methyl arachidonate,Arachidonic acid methyl ester
methyl (5Z,8Z,11Z,14Z)-icosa-5,8,11,14-tetraenoate
(5Z,8Z,11Z,14Z)-Methyl icosa-5,8,11,14-tetraenoate
ALL CIS-5,8,11,14-EICOSATETRAENOIC ACID METHYL ESTER
(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraenoic acid methyl
5,8,11,14-Eicosatetraenoic acid, methyl ester, (all-Z)-
(5Z,8Z,11Z,14Z)-5,8,11,14-Icosatetraenoic acid methyl ester
(5Z,8Z,11Z,14Z)-5,8,11,14-Eicosatetraenoic acid methyl ester
5,8,11,14-Eicosatetraenoic acid, methyl ester, (5Z,8Z,11Z,14Z)-
DELTA 5 CIS 8 CIS 11 CIS 14 CIS EICOSATETRAENOIC ACID METHYL ESTER
Methyl cis-5,8,11,14-eicosatetraenoate Solution in Hexane/Toluene, 1000μg/mL
Methyl arachidonateQ: What is Methyl arachidonate Q: What is the CAS Number of Methyl arachidonate Q: What is the storage condition of Methyl arachidonate Q: What are the applications of Methyl arachidonate
[EINECS(EC#)]

219-900-1
[Molecular Formula]

C21H34O2
[MDL Number]

MFCD00016775
[MOL File]

2566-89-4.mol
[Molecular Weight]

318.49
Chemical PropertiesBack Directory
[Boiling point ]

200-205℃ (1-2 Torr)
[density ]

0.9168 g/cm3
[refractive index ]

1.4875 (589.3 nm 20℃)
[storage temp. ]

2-8°C
[solubility ]

chloroform: 50 mg/mL, clear, colorless
[form ]

Liquid
[color ]

Colourless
[BRN ]

1714445
[Stability:]

Light Sensitive
[LogP]

7.466 (est)
Safety DataBack Directory
[Hazard Codes ]

F,Xn,N
[Risk Statements ]

19-67-65-50/53-38-11
[Safety Statements ]

9-16-29-33-60-61-62
[RIDADR ]

UN 3183 4.2/PG 3
[WGK Germany ]

3
[F ]

10-21-23
[HazardClass ]

4.2
[PackingGroup ]

I
Raw materials And Preparation ProductsBack Directory
[Raw materials]

MQCWCUDQEBWUAM-AWVFLLPBSA-N-->2H-Pyran, 2-[(6-chloro-2-hexyn-1-yl)oxy]tetrahydro--->2-Hexyne, 1-bromo-6-chloro--->2-Hexyn-1-ol, 6-chloro--->magnesium,hept-1-yne,bromide. Fandachem-->5-Octenoic acid, 8-oxo-, methyl ester, (5Z)--->1,4-DECADIYNE-->METHYL CIS CIS-11 14-EICOSADIENOATE
[Preparation Products]

CIS-7,10,13,16,19-DOCOSAPENTAENOIC ACID METHYL ESTER
Hazard InformationBack Directory
[Uses]

Arachidonic acid is the keystone essential fatty acid at the origin of the arachidonic acid cascade. It is converted by cyclooxygenase, lipoxygenase, and epoxygenase enzymes into more than one hundred fifty different potent primary autacoid metabolites in species ranging from fungi to plants to mammals. Arachidonic acid is stored in tissue phospholipids in esterified form, where it comprises a small but critically controlled percentage of the polyunsaturated fatty acid pool. Arachidonic acid content is frequently measured by the saponification of the lipid fraction followed by methyl esterification and gas chromatographic analysis of the resulting FAME (fatty acid methyl ester) compounds. Arachidonic acid methyl ester can also be incorporated into dietary regimens or fed to cultured cells as a source of exogenous arachidonate.
[Definition]

ChEBI: A fatty acid methyl ester resulting from the formal condensation of the carboxy group of arachidonic acid with methanol.
[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.
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