Dimethyl benzyl carbinyl acetate
Dimethylbenzylcarbinyl acetate ; (2-methyl-1-phenylpropan-2-yl) acetate ; DMBC acetate ; Dimethylbenzylcarbinyl ethanoate ; (2-methyl-1-phenylpropan-2-yl) ethanoate ; DMBC ethanoate ; Benzylpropyl acetate ; Benzylpropyl ethanoate ; Dimethylbenzene ethyl acetate
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 151-05-3
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EINECS number : 205-781-3
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FEMA number : 2392
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Density : 0,998
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Optical rotation : Lorem Ipsum
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Allergens : This ingredient does not contain any allergen.
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Refractive Index @20°C : Lorem Ipsum
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Volatility : Head/Heart
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 09.227
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JECFA number : 1655
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 250°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C12H16O2
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Log P : 2,91
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Molecular Weight : 192,26 g/mol
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Fusion Point : Donnée indisponible.
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Flash Point : 103°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
In comparision to Dimethyl Benzyl Carbinol, Dimethyl Benzyl Carbinyl acetate has a more zesty-bergamot smell and is less rosy.
Stability :
Dimethyl Benyl Carbinyl acetate is relatively stable in perfumes and every kind of functional bases.
Uses in perfumery :
Dimethyl Benzyl Carbinyl acetate is used for a contribution of sweetness and a zesty note with fruity, rosy, lavender and fresh accords. Used in soaps and cosmetics.
Year of discovery :
1939
Isomerism :
Dimethyl Benzyl Carbinyl acetate has no known isomer used in perfumery.
Synthesis precursor :
Dimethyl Benzyl Carbinyl acetate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Dimethyl Benzyl Carbinyl acetate is not available in its natural state.
Synthesis route :
Dimethyl Benzyl Carbinyl acetate is obtained by an esterification reaction between acetic acid and Dimethyl Benzyl Carbinol, catalysed by a small amount of a strong concentrated acid such as sulfuric acid.
Regulations & IFRA
This ingredient is not restricted
