Skip to main content

Frequently Asked Questions about Benzyl Cinnamate


What is Benzyl Cinnamate?



Benzyl cinnamate (molecular formula C16H14O2) is the chemical compound which is the ester derived from cinnamic acid and benzyl alcohol. It is a white to pale yellow solid or crystal substance that has a sweet balsamic odor. Benzyl cinnamate is used as a fragrance ingredient in a wide variety of cosmetics and personal care products, including aftershaves, perfumes and colognes, skin care and hair care products.

What else is Benzyl Cinnamate called?

This chemical can be identified by different names, including:
3-Phenyl 2-propenoic acid benzyl ester, Benzylester kyseliny skoricove, Benzyl 3-phenyl propenoate, Phenyl Methyl, 3-phenyl-2-propenoate, Benzyl beta-Phenylacrylate, Phenyl Methyl 3-phenyl propenoate, Benzylcinnamoate, Cinnamein
This may not be a complete list as manufacturers introduce and delete chemicals from their product lines

Where is Benzyl Cinnamate found?

This chemical is a commonly used sweet and floral flavoring agent. It is used in perfumes and fragrances. Further research may identify additional product or industrial usages of this chemical.

Why is Benzyl Cinnamate used in cosmetics and personal care products?

Benzyl cinnamate is used to impart an odor to cosmetics and personal care products. It is used as a fragrance ingredient in a wide variety of cosmetics and personal care products, including aftershaves, perfumes and colognes, skin care and hair care products.

How to store and handle Benzyl Cinnamate safely?

Storage
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.

Handling
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation.

Comments

Popular posts from this blog

Properties, Synthesis and Applications of 3-Phenyl-1-propanol

3-Phenyl-1-propanol belongs to the class of organic compounds known as benzene and substituted derivatives. These are aromatic compounds containing one monocyclic ring system consisting of benzene. 3-Phenyl-1-propanol is found in alcoholic beverages. 3-Phenyl-1-propanol occurs in storax and fern balsam. Also present in Vaccinium species fruits, guava fruit and peel, blackberry, other fruits, rum, white wine, shitake mushroom, matsutake mushroom and peated malt. Synonyms of  3-Phenyl-1-propanol: 3-Phenylpropan-1-ol; 3-Phenyl-n-propanol; Hydrocinnamic alcohol; 3-Phenylpropyl alcohol; Phenylpropyl alcohol; Phenylpropylic alcohol; (3-Hydroxypropyl)benzene Chemical properties of 3-Phenyl-1-propanol: 3-Phenyl-1-propanol is colorless viscous liquid with a sweet scent of flowers and sweetmeat and the flavor of fresh fruit after dilution. Its boiling point is at 236 °C, flash point at 109 °C. It is soluble in ethanol, propylene glycol and most of the non-volatile oil...

Carboxylic Acids and Esters Available at Landmark

Carboxylic acids are compounds containing a functional group called the carboxyl group (-COOH). The general molecular formula for carboxylic acids is CnH2n+1COOH. An ester is an organic compound where the hydrogen in the carboxyl group is replaced with a hydrocarbon chain. Esters are derived from carboxylic acids and (usually) an alcohol. The chemical formula of an ester is RCO2R ′ , where R is the hydrocarbon parts of the carboxylic acid and R ′ is the introduced group. Both carboxylic acids and esters contain a carbonyl group with a second oxygen atom bonded to the carbon atom in the carbonyl group by a single bond.  In a carboxylic acid, the second oxygen atom also bonds to a hydrogen atom. In an ester, the second oxygen atom bonds to another carbon atom. The names for carboxylic acids and esters include prefixes that denote the lengths of the carbon chains in the molecules and are derived following nomenclature rules similar to those for inorganic acids and sa...