1-OCTEN-3-OL

Bezeichnung:1-OCTEN-3-OL

CAS-Nr3191-86-4

Englisch Name:1-OCTEN-3-OL

CBNumberCB2201397

SummenformelC13H16N2

Molgewicht200.28

MOL-Datei3191-86-4.mol

1-OCTEN-3-OL physikalisch-chemischer Eigenschaften

Siedepunkt	84-85 °C25 mm Hg(lit.)
Dichte	0.83 g/mL at 25 °C(lit.)
Brechungsindex	n20/D 1.437(lit.)
Flammpunkt	142 °F
Farbe	A colourless liquid.
CAS Datenbank	3191-86-4(CAS DataBase Reference)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-36/38
S-Sätze:	26-36
WGK Germany	3
RTECS-Nr.	RH3300000
Toxizität	The acute oral LD₅₀ in rats was reported as 0.34 g/kg and the acute dermal LD₅₀ in rabbits as 3.3 g/kg.

1-OCTEN-3-OL Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R36/38:Reizt die Augen und die Haut.
S-Sätze Betriebsanweisung:
S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Chemische Eigenschaften
1-OCTEN-3-OL is a colorless liquid. B.P. 175° C. Sp.Gr. 0.84. Very powerful, sweet-earthy, almost buttery and fungus- or fermentation-like odor with a strong herbaceous note, -suggestive of Lavender-Lavandin-Rose and Hay. Somewhat acridchemical undertone which is hardly perceptible at proper (high) dilution. Almost insoluble in water, soluble in alcohol and oils. Sweet-herbaceous, haylike-earthy taste.
Occurrence
Originally reported to be found in the mushroom Armillaria matsutake, a parasite growing on the radical hairs of Pinus densiflora in the forests of Japan. It has been isolated also from the essential oils of Mentha pulegium L., lavender and M. timjia.
Verwenden
1-OCTEN-3-OL has been identified in Lavandin and many other important essential oils, it has become extremely popular in the art and science of preparing artificial or "reconstituted" essential oils. This is where the alcohol finds its main outlet. It also used in flavors (and in artificial Spearmint), such as Spice, Fruit, etc. usuall> in very low concentration: 0.2 to 6 ppm in the finished consumer product.
synthetische
By a vinyl Grignard reaction on hexaldehyde or from amyl magnesium bromide and acrolein.
Stoffwechsel
In the animal body secondary alcohols can undergo either conjugation with glucuronic acid or oxidation to a ketone, which may be excreted in the urine or expired air or further oxidized or reduced back to the alcohol. Studies of secondary alcohols containing more than seven carbon atoms have been limited to octan-2-ol. The conjugation of this alcohol in rabbits is low and much of the alcohol may be excreted unchanged . A dilute solution of synthetic (dl)-locten-3-ol fed directly into the rumen of a cow produced after 2-4 hr a maximum concentration in the milk of 20 μg octenol/litre. This concentration did not give the milk an off-flavour, and was not reported to have any other effects.

1-OCTEN-3-OL Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

3191-86-4, 1-OCTEN-3-OL Verwandte Suche:

Send Inquriy