Ethyllinoleat

Bezeichnung:Ethyllinoleat

Englisch Name:ETHYL LINOLEATE

CBNumberCB7676925

SummenformelC20H36O2

Molgewicht308.5

Synonyma

Ethyllinoleat

Ethyllinoleat physikalisch-chemischer Eigenschaften

Schmelzpunkt	<25℃
Siedepunkt	224 °C/17 mmHg (lit.)
Dichte	0.876 g/mL at 25 °C (lit.)
Brechungsindex	n20/D 1.455(lit.)
Flammpunkt	110°C
storage temp.	-20°C
Löslichkeit	Chloroform (Slightly), Ethyl Acetate (Slightly)
Farbe	Colourless
Geruch (Odor)	at 100.00 %. mild fatty fruity oily
Geruchsart	fatty
Merck	14,3820
BRN	1727827
LogP	8.173 (est)
CAS Datenbank	544-35-4(CAS DataBase Reference)
NIST chemische Informationen	Linoleic acid ethyl ester(544-35-4)
EPA chemische Informationen	9,12-Octadecadienoic acid (9Z,12Z)-, ethyl ester (544-35-4)

Sicherheit

Gefahreninformationscode (GHS)

S-Sätze Betriebsanweisung:
S23:Gas/Rauch/Dampf/Aerosol nicht einatmen(geeignete Bezeichnung(en) vom Hersteller anzugeben).
S24/25:Berührung mit den Augen und der Haut vermeiden.
Physiological effects
Ethyl linoleate (ELA) is an essential fatty acid used in many cosmetics for its anti-inflammatory properties.It inhibits the action of the reactive species of oxygen released by neutrophils due to an excess of bacteria, and prevents the hyperkeratinization induced by a lack of linoleic acid.
Verwenden
ethyl linoleate (vitamin F) is an emollient and an essential fatty acid.
Verwenden
Labelled Ethyl Linoleate (E924300). A fatty acid alkyl ester used in the vitamin industry.
Verwenden
Ethyl linoleate can be used as a drying agent for alkyd paints. It can also form N²,3-ethenoguanine via reaction with deoxyguanosine.
Definition
ChEBI: A long-chain fatty acid ethyl ester resulting from the formal condensation of the carboxy group of linoleic acid with the hydroxy group of ethanol.
Allgemeine Beschreibung
Ethyl linoleate can undergo auto-oxidation in the presence of the catalyst manganese(II)acetylacetonate.
Flammability and Explosibility
Non flammable
Biochem/physiol Actions
Ethyl linoleate solated from Oxalis triangularis inhibits forskolin-induced melanogenesis and tyrosinase activity in mouse B16 melanoma cells . This anti-melanogenic effect is mediated by inhibiting cAMP production.