103-61-7

Basic information

• Product Name: FEMA 2296
• Synonyms: TRANS-CINNAMYL BUTYRATE;3-PHENYLALLYL BUTYRATE;3-PHENYL-2-PROPEN-1-YL BUTYRATE;FEMA 2296;CINNAMYL BUTYRATE;CINNAMYL N-BUTYRATE;(2E)-3-Phenyl-2-propenyl butyrate;3-PHENYLALLYL BUTYRATE 96%
• CAS NO: 103-61-7
• Molecular Formula: C₁₃H₁₆O₂
• Molecular Weight: 204.26
• EINECS: 203-128-7
• Product Categories: Aromatic Esters
• Mol File: 103-61-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 300 °C(lit.)
• Flash Point: >230 °F
• Appearance: COA
• Density: 1.013 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.000504mmHg at 25°C
• Refractive Index: n20/D 1.526(lit.)
• Water Solubility: 22.29mg/L at 25℃
• CAS DataBase Reference: FEMA 2296(CAS DataBase Reference)
• NIST Chemistry Reference: FEMA 2296(103-61-7)
• EPA Substance Registry System: FEMA 2296(103-61-7)

Safety Data

• Hazard Codes: Xn
• Statements: 20/21/22-36/37/38
• Safety Statements: 26-36
• WGK Germany: 2
• RTECS: ES8815000
• Hazardous Substances Data: 103-61-7(Hazardous Substances Data)

Usage

Chemical Properties

Cinnamyl butyrate has a fruity, slightly floral odor and sweet taste reminiscent of honey. It is used in orange and citrus flavors.

Occurrence

Reported found in fresh apple and caja fruit (Spondias lutea L.).

Preparation

By esterification of cinnamic alcohol with n-butyric acid.

Flammability and Explosibility

Notclassified

InChI:InChI=1/C13H16O2/c1-2-7-13(14)15-11-6-10-12-8-4-3-5-9-12/h3-6,8-10H,2,7,11H2,1H3/b10-6+

Upstream product

• 104-54-1 3-Phenylpropenol 
• 123-72-8 butyraldehyde 
• 123-20-6 vinyl n-butyrate 
• 105-54-4 butanoic acid ethyl ester 
• 141-75-3 butyryl chloride 
• 107-92-6 butyric acid 
• 623-42-7 butanoic acid methyl ester 

Relevant articles and documents

Kinetics of Enzymatic Synthesis of Cinnamyl Butyrate by Immobilized Lipase

This work illustrates the enzymatic synthesis of cinnamyl butyrate by esterification of butyric acid and cinnamyl alcohol. Experiments were performed to study the various operating parameters such as molar ratio, enzyme concentration, temperature, and spe

Cinnamyl alcohol fatty acid ester derivative and application and preparation method thereof

The invention relates to a derivative and an application and a preparation method thereof, in particular to a cinnamyl alcohol fatty acid ester derivative and an application and a preparation method thereof. As application of a percutaneous absorption penetration enhancer, a percutaneous administration preparation is prepared, so that the percutaneous absorption of a drug is improved, and the cumulative penetration amount of the drug is increased. The cinnamyl alcohol fatty acid ester derivative is prepared into fatty acyl chloride, and the fatty acyl chloride reacts with cinnamyl alcohol to obtain the cinnamyl alcohol fatty acid ester derivative. The compound can be applied to the percutaneous administration preparation to enhance the drug permeability, can further be used as perfume to cover up the bad smell of the preparation, and has wide potential application prospects.

Solvent-free transesterification in a ball-mill over alumina surface

An efficient procedure for transesterification has been developed in a ball-mill in the absence of any solvent, acid/base or metal catalyst. A variety of methyl, ethyl, allyl esters have been transesterified to higher benzyl and other esters in high yields by this procedure.