| Identification | Back Directory | [Name]
ethyl 2,3-epoxy-3-p-tolylbutyrate | [CAS]
74367-97-8 | [Synonyms]
ETHYL METHYL-P-TOLYLGLYCIDATE
ETHYLMETHYL-PARA-TOLYLGLYCIDATE
ethyl 2,3-epoxy-3-p-tolylbutyrate
3-Methyl-3-(4-tolyl)-glycidic acid ethyl ester
ethyl 3-methyl-3-(4-methylphenyl)oxirane-2-carboxylate
3-Methyl-3-(4-methylphenyl)oxirane-2-carboxylic acid ethyl ester
Oxiranecarboxylic acid, 3-methyl-3-(4-methylphenyl)-, ethyl ester
2-Oxiranecarboxylic acid, 3-methyl-3-(4-methylphenyl)-, ethyl ester | [EINECS(EC#)]
277-844-3 | [Molecular Formula]
C13H16O3 | [MDL Number]
MFCD00467015 | [MOL File]
74367-97-8.mol | [Molecular Weight]
220.26 |
| Hazard Information | Back Directory | [Chemical Properties]
Ethyl methyl-p-tolylglycidate has mild deep fruity, slightly floral aroma | [Definition]
ChEBI: Ethyl methyl-p-tolylglycidate is a member of toluenes. | [Taste threshold values]
Taste characteristics at 25 ppm: sweet, floral, fruity and cherry with almond and vanilla nuances. |
| Questions And Answer | Back Directory | [Aroma]
Mild, deepfruity, slightly floral and woody
odor with "cooked fruit" undertones and very
great tenacity.
Fruity, but not distinctly sweet taste. Somewhat dry undertone. | [Uses in Perfume]
Ethyl 2,3-epoxy-3-p-tolylbutyrate, which is comparatively rare, finds
a little use in perfume compositions for its
lasting, fruity character, and for its ability to
blend and create pleasant blends with the
Ionones, Cedar-wood derivatives, Butylcyclohexanyl acetate and many other woody or
Orris-like materials. It has less tendency to
produce harsh topnotes than e.g. Ethyl methyl phcrtyl glycidate, but it does not offer any
very natural fruit notes, unless accompanied
by the conventional materials for such notes.
It has good fixative propmies for the volatile
fruit esters and may round off the rough or
harsh topnotes of many perfume chemicals. |
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