3-Phenyl-2-propensäure-2-propenylester

Bezeichnung:3-Phenyl-2-propensäure-2-propenylester

CAS-Nr1866-31-5

Englisch Name:ALLYL CINNAMATE

CBNumberCB8304551

SummenformelC12H12O2

Molgewicht188.22

MOL-Datei1866-31-5.mol

Synonyma

Allylcinnamat

3-Phenyl-2-propensäure-2-propenylester

3-Phenyl-2-propensäure-2-propenylester physikalisch-chemischer Eigenschaften

Siedepunkt	150-152 °C15 mm Hg(lit.)
Dichte	1.053 g/mL at 25 °C(lit.)
Brechungsindex	n20/D 1.566(lit.)
FEMA	2022 \| ALLYL CINNAMATE
Flammpunkt	>230 °F
storage temp.	Keep in dark place,Sealed in dry,Room Temperature
Löslichkeit	Insoluble in water, soluble in alcohol and oils, almost insoluble in Propylene glycol.
Farbe	A colourless or pale straw-coloured liquid.
Geruch (Odor)	at 100.00 %. fruity balsamic pineapple spicy cinnamyl plum apricot peach
Geruchsart	fruity
JECFA Number	19
LogP	2.93
CAS Datenbank	1866-31-5(CAS DataBase Reference)
EPA chemische Informationen	2-Propenoic acid, 3-phenyl-, 2-propenyl ester (1866-31-5)

Sicherheit

Kennzeichnung gefährlicher	Xn
R-Sätze:	22
S-Sätze:	26-36
WGK Germany	3
RTECS-Nr.	GD8050000
HS Code	29163100
Toxizität	The acute oral LD₅₀ value in rats was reported as 1.52 g/kg and the acute dermal LD₅₀ value in rabbits as less than 5 g/kg(Levenstein, 1975).

Gefahreninformationscode (GHS)

ALLYL CINNAMATE Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:
R22:Gesundheitsschädlich beim Verschlucken.
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
A colorless liquid with peach- or apricot-like aroma. It is used as a flavoring agent or adjuvant.
Occurrence
Has apparently not been reported to occur in nature.
Verwenden
Allyl Cinnamate is a synthetic flavoring agent that is a fairly stable, hazy, colorless to light yellow colored liquid of cherry odor. it is used for its cherry note in flavors and has application in baked goods and candies at 1–2 ppm.
synthetische
By esterification of cinnamic acid with allyl alcohol in the presence of concentrated H2SO4.
Vorbereitung Methode
Allyl cinnamate is produced by the direct esterification of allyl alcohol with cinnamic acid.
Definition
ChEBI: Allyl cinnamate is a cinnamate ester.
Synthesis Reference(s)
Tetrahedron, 48, p. 1219, 1992 DOI: 10.1016/S0040-4020(01)90785-9
Tetrahedron Letters, 36, p. 113, 1995 DOI: 10.1016/0040-4039(94)02179-F
Sicherheitsprofil
Moderately toxic by ingestion. Human skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes. See also ALLYL COMPOUNDS and ESTERS
Stoffwechsel
Many esters, including benzyl cinnamate, are rapidly hydrolysed in vivo. Cinnamic acid is known to conjugate with glycine in the animal body, or it may be converted to benzoic acid(Williams, 1959). In the rabbit, cinnamic acid is almost entirely excreted as hippuric acid, without formation of cinnamoyl glycine(El Masry, Smith & Williams, 1956) . In the dog, Quick(1928) observed a large excretion of glucuronide, probably benzoylglucuronide. Dakin (1909) named B-phenyl-B-oxopropionic acid, cinnamoyl glycine and acetophenone as minor metabolites in the dog.
Solubility in organics
Allyl Cinnamate is soluble in alcohol and oils, almost insoluble in Propylene glycol.

ALLYL CINNAMATE Upstream-Materialien And Downstream Produkte

3-Phenyl-2-propensäure-2-propenylester Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

1866-31-5, ALLYL CINNAMATE Verwandte Suche:

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