Dimethylbenzylcarbinyl butyrate
Dimethylbenzylcarbinyl Butyrate ; (2-methyl-1-phenylpropan-2-yl) Butyrate ; Dimethylbenzylcarbinyl butanoate ; DMBC butyrate ; DMBC butanoate ; (2-methyl-1-phenylpropan-2-yl) butanoate ; Benzylpropyl butanoate ; Dimethylbenzene ethyl butyrate
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 10094-34-5
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EINECS number : 233-221-8
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FEMA number : 2394
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Density : 0,97
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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 : Heart
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Price Range : €€
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Appearance : Colorless liquid
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FLAVIS number : 09.232
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JECFA number : 1656
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 246°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C14H20O2
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Log P : 3,99
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Molecular Weight : 220,31 g/mol
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Fusion Point : <-70°C
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Flash Point : 94°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Hardly soluable in Propylene Glycol
Stability :
Esters may form their corresponding acid in stability
Uses in perfumery :
DMBC Butyrate is used in a large quantity in dry fruits and plum accords (major component of the Prunella® base). It can also be used in smaller quantity in more tasty notes as coffee, cocoa, apricot, in oriental perfumes and in floral-fruity-green rose, lily of the valley and hyacinth accords.
Year of discovery :
Data not available.
Isomerism :
Dimethyl Benzyl Carbinyl Butyrate has no known isomer used in perfumery.
Synthesis precursor :
Dimethyl Benzyl Carbinyl Butyrate is not a precursor to the synthesis of another compound of olfactory interest.
Natural availability :
Dimethyl Benzyl Carbinyl Butyrate is not available in its natural state.
Synthesis route :
Dimethyl Benzyl Carbinyl Butyrate 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
