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170275

Sigma-Aldrich

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
Beilstein:
1855608
EC Number:
202-896-0
MDL number:
MFCD00004465
UNSPSC Code:
12352100
PubChem Substance ID:
24850290
NACRES:
NA.22

Assay

98%

form

solid

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.)

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

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Application

2-Methyl-1-phenyl-2-propanol was used in the preparation of 2-methyl-1-phenyl-2-propyl bromide.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

177.8 °F - closed cup

Flash Point(C)

81 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

170275-100G:
170275-5G:
170275-BULK:
170275-500G:
170275-VAR:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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David C Magri et al.
Organic & biomolecular chemistry, 1(19), 3418-3429 (2003-10-31)
Two dialkyl peroxides, devised as kinetic probes for the heterogeneous electron transfer (ET), are studied using heterogeneous and homogeneous electrochemical techniques. The peroxides react by concerted dissociative ET reduction of the O-O bond. Under heterogeneous conditions, the only products isolated
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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