Photo credits: ScenTree SAS
Dimethyl benzyl carbinol
Floral > Fresh Flowers > Rosy > Green
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
| Company | Ingredient Name | ID | Comments | Naturality | Certifications | MOQ | Purity |
|---|---|---|---|---|---|---|---|
|
DIMETHYL BENZYL CARBINOL | - |
Visit website
|
- | 10 grs | - |
General Presentation
-
CAS N° :
100-86-7 -
EINECS number :
202-896-0 -
FEMA number :
2393 -
FLAVIS number :
02.035
-
JECFA number :
1653 -
Volatility :
Heart -
Price Range :
€€
Physico-chemical properties
-
Appearance :
Colorless liquid -
Density :
0,976 -
Refractive Index @20°C :
1.514 - 1.517 -
Optical rotation :
Data not available. -
Vapor pressure :
0.045 mmHg @20°C -
Flash Point :
82°C (179,6°F)
-
Molecular formula :
C10H14O -
Molecular Weight :
150,22 g/mol -
Log P :
Donnée indisponible. -
Fusion Point :
24°C (75,2°F) -
Boiling Point :
95°C (203°F) -
Detection Threshold :
Donnée indisponible.
Chemistry & Uses
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.
Natural availability :
Dimethyl Benzyl Carbinol is not available in its natural state.
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.
Synthesis route :
Dimethyl Benzyl Carbinol (DMBC) is synthesized by a Grignard reaction using benzylmagnesium chloride reacting with acetone.
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
Other comments :
Comparing it with Dihydromyrcenol and Dimetol®, Dimethyl Benzyl Carbinol has a greener note.
IFRA
IFRA 51th :
This ingredient is not restricted for the 51th amendment
