ChemicalBook--->CAS DataBase List--->7779-78-4

7779-78-4

7779-78-4 Structure

7779-78-4 Structure
IdentificationBack Directory
[Name]

4-METHYL-1-PHENYL-2-PENTANOL
[CAS]

7779-78-4
[Synonyms]

FEMA 2208
BENZYLISOBUTYLCARBINOL
ISOBUTYL BENZYL CARBINOL
4-methyl-1-phenylpentan-2-ol
4-METHYL-1-PHENYL-2-PENTANOL
α-Isobutylphenethyl alcohol
alpha-isobutyl-phenethylalcoho
ALPHA-ISOBUTYLPHENETHYL ALCOHOL
4-Methyl-1-phenyl-2-pentanol>
Benzeneethanol, α-(2-methylpropyl)-
Benzeneethanol, a-(2-methylpropyl)-
alpha-(2-methylpropyl)-benzeneethano
alpha-(2-methylpropyl)benzeneethanol
Benzeneethanol, alpha-(2-methylpropyl)-
.alpha.-(2-methylpropyl)-Benzeneethanol
[EINECS(EC#)]

231-939-6
[Molecular Formula]

C12H18O
[MDL Number]

MFCD00209515
[MOL File]

7779-78-4.mol
[Molecular Weight]

178.27
Chemical PropertiesBack Directory
[Boiling point ]

123 °C / 11mmHg
[density ]

0.95
[FEMA ]

2208 | ALPHA-ISOBUTYLPHENETHYL ALCOHOL
[refractive index ]

1.5030 to 1.5070
[Fp ]

110 °C
[storage temp. ]

Sealed in dry,Room Temperature
[solubility ]

slightly oily liquid. insoluble in water, miscible with alcohol and oils.
[form ]

clear liquid
[color ]

Colorless to Almost colorless
[Specific Gravity]

0.94
[Odor]

at 100.00 %. green floral herbal celery creamy
[Odor Type]

green
[JECFA Number]

827
[LogP]

3.12
[EPA Substance Registry System]

Benzeneethanol, .alpha.-(2-methylpropyl)- (7779-78-4)
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-36-52/53
[Safety Statements ]

26-36
[WGK Germany ]

2
[RTECS ]

DA0513300
[HS Code ]

2906290090
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Benzyl chloride-->Benzyl bromide-->Isovaleraldehyde
Hazard InformationBack Directory
[Description]

α-Isobutylphenethyl alcohol has a green, floral, somewhat herbaceous odor and a buttery, oily, caramellic flavor. May be prepared by reacting isobutyl aldehyde with benzyl magnesium chloride.
[Chemical Properties]

α-Isobutylphenethyl alcohol has a green floral, fresh, slightly sweet aroma.
[Uses]

α-Isobutylphenethyl alcohol is an excellent modifier in heavy and green floral fragrance types, in Oriental or Chypre bases, etc. It may form a significant basis of Honeysuckle, Freesia or variations of Rose or Muguet. It is used in flavor compositions for imitation Butter, Caramel, Chocolate, Fruit and Spice in concentrations equivalent to 50 ppm in the finished consumer product.
[Preparation]

By reacting isobutyl aldehyde with benzyl magnesium chloride.
[Aroma threshold values]

Aroma characteristics at 1.0%: herbaceous, warm celery-like, musk and creamy with a slight floral citrus nuance
[Taste threshold values]

Taste characteristics at 10 ppm: warm, amber sclarolide herbaceous celery-like with oily and creamy nuances.
[Biochem/physiol Actions]

Taste at 10 ppm
[Synthesis]

4-Methyl-1-phenyl-2-pentanol is prepared from benzyl chloride to benzyl magnesium bromide, and then hydrolyzed with isovaleraldehyde after Grignard reaction.
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