Ethyl cinnamate Chemical Properties

Melting point:

6-8 °C (lit.)

Boiling point:

271 °C (lit.)

Density 

1.049 g/mL at 20 °C (lit.)

vapor pressure 

6Pa at 20℃

refractive index 

n20/D 1.558(lit.)

FEMA 

2430 | ETHYL CINNAMATE

Flash point:

>230 °F

storage temp. 

2-8°C

solubility 

Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.

form 

Liquid

color 

Clear colorless to pale yellow

Odor

at 100.00 %. sweet balsam fruity spicy powdery berry plum

Odor Type

balsamic

Water Solubility 

insoluble

Merck 

14,2299

JECFA Number

659

BRN 

1238804

Dielectric constant

5.3（19℃）

Stability:

Stable. Incompatible with strong oxidizing agents, acids, bases, reducing agents. Combustible.

LogP

3.01 at 23.6℃

CAS DataBase Reference

103-36-6(CAS DataBase Reference)

NIST Chemistry Reference

trans-Ethyl cinnamate(103-36-6)

EPA Substance Registry System

Ethyl cinnamate (103-36-6)

Safety Information

Risk Statements 

20-22

Safety Statements 

23-24/25

WGK Germany 

1

RTECS 

GD9010000

TSCA 

Yes

HS Code 

29163990

Toxicity

The acute oral LD₅₀ value in rats was reported as 7.8 g/kg (7.41-8.19 g/kg) (Russell, 1973). The acute dermal LD₅₀ value in rabbits was reported as > 5 g/kg (Russell, 1973).

MSDS

• Language:English Provider:Ethyl 3-phenyl propenoate
• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS
• Language:English Provider:ALFA

Ethyl cinnamate Usage And Synthesis

Description

Ethyl cinnamate is the ester of cinnamic acid and ethanol, and is typically found in the essential oil of cinnamon. It is noteworthy that pure ethyl cinnamate has an aroma of cinnamon, complicated by balsamic and red fruit nuances,all of which can be characteristic of a fine Nebbiolo wine's aromatics.

Chemical Properties

Ethyl Cinnamate, ethyl 3-phenylacrylate, C6H5CH=CHCOOC2H5.Occurs naturally in storax and the volatile oil of Koempferia galanga.The commercial product is a colourless liquid, invariably prepared artificially. Has a sweet balsami honey-note odor of great persistence. Ethyl cinnamate is useful in Oriental bouquets, and in combination with clary sage and citrus oils will make delightful amber colognes.

Occurrence

Normally occurring in the trans-form; a cis-form also exists. Reported found in Oriental styrax, in the oil of Campheria galanga and in the rhizomes of Hedychium spicatum. Also reported found in cherry, American cranberry, pineapple, guava, strawberry, fresh blackberry, strawberry jam, soybean, yellow passion fruit juice, hybrid passion fruit juice, apple brandy, quince, prickly pear, strawberry wine, Bourbon vanilla, sea buckthorn, cinnamon leaf and root bark, clove, brandy, rum, sherry, grape wines, cocoa, soybean and other natural sources.

Uses

Ethyl cinnamate is used in medical intermediate, as a pharmaceutical intermediate and in organic synthesis.

Preparation

By heating to 100°C cinnamic acid, alcohol and sulfuric acid in the presence of aluminum sulfate; also by Claisen condensation of benzaldehyde and ethyl acetate

Definition

ChEBI: Ethyl cinnamate is an alkyl cinnamate and an ethyl ester.

Production Methods

Ethyl cinnamate is found in storax oil, Kaempferia galanga, and several other oils. It is produced by the direct esterification esterification of ethanol with cinnamic acid under azeotropic conditions or by Claisen-type condensation of ethyl acetate and benzaldeyde in the presence of sodium metal .

Aroma threshold values

Detection: 17 to 40 ppb

Taste threshold values

Taste characteristics at 20 ppm: balsamic, powdery, fruity, berry, punch, spice, sweet and green.

Synthesis Reference(s)

Journal of the American Chemical Society, 110, p. 2655, 1988 DOI: 10.1021/ja00216a053
Tetrahedron Letters, 30, p. 5153, 1989 DOI: 10.1016/S0040-4039(01)93472-0

General Description

Ethyl cinnamate can be used as a flavoring and fragrance ingredient. It is one of the key odor components reported in Burgundy Pinot noir wines.

Biochem/physiol Actions

Ethyl cinnamate inhibits the growth of Chlorella pyrenoidosa.

Safety Profile

Moderately toxic by ingestion. Combustible liquid. When heated to decomposition it emits acrid smoke and irritating fumes. See also ESTERS

Purification Methods

Wash the ester with aqueous 10% Na2CO3, then water, dry (MgSO4), and distil it. The purified ester is saponified with aqueous KOH, and, after acidifying the solution, cinnamic acid is isolated, washed and dried. The ester is reformed by refluxing for 15hours the cinnamic acid (25g) with absolute EtOH (23g), conc H2SO4 (4g) and dry *benzene (100mL), after which it is isolated, washed, dried and distilled under reduced pressure [Jeffery & Vogel J Chem Soc 658 1958]. [Beilstein 9 IV 2006.]

Ethyl cinnamate(103-36-6)Related Product Information

• Ethyl acetate
• Ethanol
• Octyl 4-methoxycinnamate
• Trinexapac-ethyl
• Ethyl formate
• Ethyl propionate
• 2-Ethoxyethanol
• Phenyl salicylate
• Diphenyl ether
• Cinnamyl cinnamate
• Ethylparaben
• Methyl cinnamate
• Propyl cinnamate
• PHENYL VALERATE
• ISOXADIFEN-ETHYL
• Cinnamic acid
• Benzyl cinnamate
• Cinnamaldehyde