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Merck
CN

W239301

2-Methyl-1-phenyl-2-propanol

98%

Synonym(s):

1,1-Dimethyl-2-phenylethyl alcohol, Benzyl dimethyl carbinol

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About This Item

Linear Formula:
C6H5CH2C(CH3)2OH
CAS Number:
100-86-7
Molecular Weight:
150.22
Flavis number:
2.035
PubChem Substance ID:
329830480
UNSPSC Code:
12164502
FEMA Number:
2393
EC Number:
202-896-0
MDL number:
MFCD00004465
Beilstein/REAXYS Number:
1855608

Key Documents

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biological source

synthetic

reg. compliance

FDA 21 CFR 172.515

assay

98%

refractive index

n20/D 1.514 (lit.)

bp

94-96 °C/10 mmHg (lit.)

mp

23-25 °C (lit.)

density

0.974 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

documentation

see Safety & Documentation for available documents

food allergen

no known allergens

SMILES string

CC(C)(O)Cc1ccccc1

InChI

1S/C10H14O/c1-10(2,11)8-9-6-4-3-5-7-9/h3-7,11H,8H2,1-2H3

InChI key

RIWRBSMFKVOJMN-UHFFFAOYSA-N

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

13 - Non Combustible Solids

wgk

WGK 2

flash_point_f

177.8 °F - closed cup

flash_point_c

81 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBG9705V
01403BE

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Takao Raku et al.
Biotechnology letters, 26(8), 665-670 (2004-06-18)
For the purpose of developing a new synthetic polymer containing an asymmetric molecule branch, three racemic alcohols, i.e. 1-phenylethanol, 1-(4-methylphenyl)ethanol and 1-(2-naphthyl)ethanol, were esterified enzymatically with divinyladipate using a lipase from Pseudomonas cepacia. The enzymatic acylation of alcohols produced monoacylated

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