Dimethyl benzyl carbinol
DMBC ; 2-methyl-1-phenylpropan-2-ol ; Dimethyl benzene ethanol ; Benzyl dimethyl carbinol ; Benzyl propyl alcohol ; 2-benzyl-2-propanol ; Benzyldimethylcarbinol ; Dimethyl phenethanol ; Dimethyl phenethyl alcohol ; Dimethyl phenyl ethanol ; Dimethyl-2-phenyl ethanol ; 2-hydroxy-2-methyl-1-phenyl propane ; Phenyl-tert-butanol ; 1-phenyl-2-hydroxy-2-methylpropane
Photo credits: ScenTree SAS
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General Presentation
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CAS N° : : 100-86-7
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EINECS number : 202-896-0
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FEMA number : 2393
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Density : 0,976
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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 : 02.035
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JECFA number : 1653
Information on synthetic ingredients
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Acid Value : Lorem Ipsum
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Boiling Point : 95°C
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Detection Threshold : Donnée indisponible.
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Molecular formula : C10H14O
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Log P : Donnée indisponible.
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Molecular Weight : 150,22 g/mol
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Fusion Point : 24°C
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Flash Point : 82°C
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Vapor pressure : Lorem Ipsum
Uses
Other comments :
Comparing it with Dihydromyrcenol and Dimetol®, Dimethyl Benzyl Carbinol has a greener note.
Stability :
May crystalize through time
Most of the time, the occurrence of a benzenic cycle in a molecule causes a coloration of this molecule through time
Uses in perfumery :
Dimethyl Benzyl Carbinol is used in all types of perfumes, for reconstitutions of lilac, hyacinth, lily of the valley and jasmine. Useful in marine notes for a light and green effect.
Year of discovery :
Data not available.
Isomerism :
L-Carvone and Thymol are isomers of Dimethyl Benzyl Carbinol. Their smell is nevertheless very different: more minty for one and more aromatic for the other.
Synthesis precursor :
Dimethyl Benzyl Carbinol serves as a reagent in the synthesis of Dimethyl Benzyl Carbinyl acetate, and other esters that can be synthesized from this alcohol.
Natural availability :
Dimethyl Benzyl Carbinol is not available in its natural state.
Synthesis route :
Dimethyl Benzyl Carbinol (DMBC) is synthesized by a Grignard reaction using benzylmagnesium chloride reacting with acetone.
Regulations & IFRA
This ingredient is not restricted
