Chemical Properties | Clear colorless to yellowish crystalline mass or liquid after meltin |
Chemical Properties | Benzyl Cinnamate occurs in
balsams and balsam oils. It forms white, sweet-balsamic-smelling crystals (mp
35-36°C). Benzyl cinnamate is used as a fixative in perfumes and as a component
of heavy, oriental perfumes. |
Chemical Properties | Benzyl cinnamate has a sweet, balsamic odor and a honey-like taste. |
Occurrence | Reported found in Peru and Tolu balsam, in Sumatra and Penang benzoin, and as the main constituent of
copaiba balsam. |
Uses | In artificial flavors, in perfumes, mainly as a fixative. |
Uses | Benzyl cinnamate has been employed as internal standard during the determination of compounds commonly added to personal care products such as UV filters and antimicrobial agents in environmental samples. |
Preparation | By heating benzyl chloride and excess sodium cinnamate in water to 100 to 115°C; by heating sodium cinnamate with an
excess of benzyl chloride in the presence of diethylamine. |
Definition | ChEBI: Benzyl cinnamate is the cinnamate ester derived from cinnamic acid and benzyl alcohol. Occuring in Balsam of Peru and Tolu balsam, in Sumatra and Penang benzoin, and as the main constituent of copaiba balsam, it is used in heavy oriental perfumes, as a fixative and as a flavouring agent. It has a role as a flavouring agent, a fragrance, a fixative, an antigen and an epitope. |
Production Methods | Benzyl cinnamate is produced by the direct esterification of
benzyl alcohol with cinnamic acid. |
Taste threshold values | Taste characteristics at 50 ppm: spicy, floral, fruity, balsamic. |
General Description | Benzyl cinnamate is widely used as a fragrance ingredient. |
Hazard | Moderately toxic. |
Flammability and Explosibility | Nonflammable |
Safety Profile | Moderately toxic by ingestion. Amild allergen and skin irritant. Combustible liquid. When heated to decomposition it emits acridsmoke and irritating fumes. |
target | Immunology & Inflammation related |
Metabolism | See monograph on Benzyl alcohol (p. 1011). |
Purification Methods | Recrystallise the ester to a constant melting point from 95% EtOH. It has the odour of balsam. Alternatively dissolve it in Et2O, wash it with 10% aqueous Na2CO3, H2O, dry (Na2SO4), evaporate and fractionate it under reduced pressure using a short Vigreux column (p 11). It decomposes when boiled at atmospheric pressure. [Eliel & Anderson J Am Chem Soc 74 547 1952, Bender & Zerner J Am Chem Soc 84 2550 1962, Beilstein 9 IV 2012.] |