2-Methoxy-4-(2-propenyl)phenol-acetat

Bezeichnung:2-Methoxy-4-(2-propenyl)phenol-acetat

CAS-Nr93-28-7

Englisch Name:EUGENOL ACETATE

CBNumberCB5107982

SummenformelC12H14O3

Molgewicht206.24

MOL-Datei93-28-7.mol

Synonyma

4-Allyl-2-methoxyphenylacetat

2-Methoxy-4-(2-propenyl)phenol-acetat

2-Methoxy-4-(2-propenyl)phenol-acetat physikalisch-chemischer Eigenschaften

Schmelzpunkt	26°C
Siedepunkt	281-286 °C(lit.)
Dichte	1.079 g/mL at 25 °C(lit.)
Dampfdruck	0.041Pa at 20℃
FEMA	2469 \| EUGENYL ACETATE
Brechungsindex	n20/D 1.518(lit.)
Flammpunkt	230 °F
storage temp.	under inert gas (nitrogen or Argon) at 2-8°C
Löslichkeit	Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly)
Aggregatzustand	Colourless to Light Yellow Oil to Semi-Solid
Farbe	White or Colorless to Light yellow
Geruch (Odor)	at 100.00 %. fresh sweet woody clove floral carnation malt spice
Geruchsart	spicy
Wasserlöslichkeit	407mg/L at 20℃
JECFA Number	1531
Stabilität	Stable. Combustible. Incompatible with strong oxidizing agents.
LogP	2.8 at 25℃
CAS Datenbank	93-28-7(CAS DataBase Reference)
NIST chemische Informationen	Phenol, 2-methoxy-4-(2-propenyl)-, acetate(93-28-7)
EPA chemische Informationen	Phenol, 2-methoxy-4-(2-propenyl)-, acetate (93-28-7)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22-38
S-Sätze:	36
WGK Germany	2
RTECS-Nr.	SJ4550000
HS Code	29147000
Toxizität	The acute oral LD₅₀ value in rats was reported as 1.67 g/kg (Jenner, Hagan, Taylor, Cook & Fitzhugh, 1964) and as 2.6 g/kg (2.3-2.9 g/kg) (Moreno, 1972b). The acute dermal LD₅₀ value in rabbits exceeded 5 g/kg (Moreno, 1972a).

Gefahreninformationscode (GHS)

EUGENOL ACETATE Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
R38:Reizt die Haut.
S-Sätze Betriebsanweisung:
S36:DE: Bei der Arbeit geeignete Schutzkleidung tragen.
Chemische Eigenschaften
Eugenyl acetate has a characteristic odor reminiscent of clove oil, with a burning, aromatic favor.
Chemische Eigenschaften
Eugenol Acetate occurs in clove oil, together with eugenol. It is a crystalline solid (mp 29°C) or yellowish liquid with a slightly fruity, clove odor. Eugenol acetate is prepared by acetylation of eugenol with acetic anhydride and is used in floral compositions to accentuate floral, spicy characters.
Occurrence
Reported found in the essential oils of Laurus nobilis, clove buds and leaves, cassia leaf and cinnamon leaf, root and bark
Verwenden
Eugenol Acetate is a constituent of Clove oil, an essential oil from the clove plant, Syzygium aromaticum. Clove oil is a natural analgaesic and antiseptic used primarily in dentistry for its main ingredient Eugenol. Clove oil can also be purchased in pharmacies over the counter, as a home remedy for dental pain relief, mainly toothache; it is also often found in the aromatherapy section of health food stores.
Application
Mild and sweet-spicy, balsamic-fruity odour, reminiscent of carnation. Earthy-fresh notes or leafy-floral notes are not uncommon. Used in perfumes to emphasize floralness in carnation, along with iso-eugenol, Amyl oxy-iso-eugenol, etc. Fresher than these, but also milder. Not stable in white soap or alkali. It is in flavors for berry, fruit, mint, spice, and vanilla types.
synthetische
By direct acetylation of eugenol using acetic anhydride.
Definition
ChEBI: Acetyleugenol is a member of phenols and a benzoate ester.
Flammability and Explosibility
Not classified
Sicherheitsprofil
Moderately toxic by ingestion. A skin irritant. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also EUGENOL, ALLYL COMPOUNDS, and ESTERS.

EUGENOL ACETATE Upstream-Materialien And Downstream Produkte

2-Methoxy-4-(2-propenyl)phenol-acetat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

93-28-7, EUGENOL ACETATE Verwandte Suche:

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