Identification | Back Directory | [Name]
2-BENZYL-2-BUTANOL | [CAS]
772-46-3 | [Synonyms]
2-BENZYL-2-BUTANOL 2-methyl-1-phenyl-2-butano Methylethylbenzyl carbinol 1-phenyl-2-methyl-butanol-2 2-methyl-1-phenylbutan-2-ol 2-Methyl-1-phenyl-2-butanol 1-Phenyl-2-methyl-2-butanol α-Ethyl-α-methylbenzeneethanol 2-Methyl-1-phenyl-2-butanol> Benzeneethanol, α-ethyl-α-methyl- alpha-ethyl-alpha-methyl-phenethylalcoho alpha-ethyl-alpha-methylphenethylalcohol | [EINECS(EC#)]
212-249-4 | [Molecular Formula]
C11H16O | [MDL Number]
MFCD01708473 | [MOL File]
772-46-3.mol | [Molecular Weight]
164.24 |
Chemical Properties | Back Directory | [Melting point ]
83.5-84 °C | [Boiling point ]
61 °C / 0.6mmHg | [density ]
0.97 | [refractive index ]
0.9 ° (C=neat) | [solubility ]
Almost insoluble in water, soluble in alcohoI and oils. | [form ]
clear liquid | [pka]
15.31±0.29(Predicted) | [color ]
Colorless to Almost colorless | [Specific Gravity]
0.97 | [Odor]
Peculiar green-floral, rather dry, mossy, almost leather-like odor |
Hazard Information | Back Directory | [Uses]
2-BENZYL-2-BUTANOL is used in perfume
compositions, partly for delicate floral fragrance types, part Iy for green-mossy or
Oriental types. It blends excellently with
Oakmoss and Vetiver, but also forms soft
and natural-green floral notes with Heliotropine, Anisylacetate etc. in Lilac or Lindenblossom. | [Preparation]
By Grignard type synthesis from
Benzyl magnesium bromide plus Methyl ethyl
ketone. | [Synthesis Reference(s)]
Synthetic Communications, 19, p. 293, 1989 DOI: 10.1080/00397918908050981 Tetrahedron Letters, 17, p. 993, 1976 |
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