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| ANISYL BUTYRATE Basic information |
| Product Name: | ANISYL BUTYRATE | | Synonyms: | ANISYL BUTYRATE;FEMA 2100;4-Methoxybenzyl butyrate;Butanoic acid, (4-methoxyphenyl)methyl ester;Butyric acid, p-methoxybenzyl ester;Anisylbutyrat;ANISYL BUTYRATE, NATURAL;Butanoic acid 4-methoxybenzyl ester | | CAS: | 6963-56-0 | | MF: | C12H16O3 | | MW: | 208.25 | | EINECS: | 230-163-5 | | Product Categories: | | Mol File: | 6963-56-0.mol |
| ANISYL BUTYRATE Chemical Properties |
| WGK Germany | 2 | | HS Code | 2915600000 | | toxicity | The acute oral LD50 value in rats was reported as 3.4 g/kg (3.02-3.78 g/kg) and the acute dermal LD50 value in rabbits exceeded 5 g/kg |
| ANISYL BUTYRATE Usage And Synthesis |
| Chemical Properties | Anisyl butyrate has a weak, floral, intensely sweet, plum-like odor | | Occurrence | Has apparently not been reported to occur in nature. | | Uses | Anisyl Butyrate is a synthetic flavoring agent that is a stable, color-
less liquid of sweet cassic odor. it should be stored in glass or tin
containers. it will intensify vanilla flavor and is used as a fixative.
it is used in ice cream, candy, and baked goods at 5–15 ppm. | | Preparation | From anisyl alcohol and n-butyric acid. | | Metabolism | Esters of benzyl alcohol, such as the acetate, are rapidly hydrolysed in vivo to benzyl alcohol, which is then oxidized. The expected general reaction of primary aromatic alcohols in the animal body is oxidation to the corresponding aromatic acid, which is usually excreted as a glycine conjugate and to a lesser extent as an ester glucuronide. In rabbits, benzyl alcohol is almost entirely converted to benzoic acid, which is excreted mainly as hippuric acid . In substituted anisoles with a carboxyl group or a potential carboxyl group attached to the aromatic ring, the ether link is relatively stable |
| ANISYL BUTYRATE Preparation Products And Raw materials |
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