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Key Documents

P30802

Sigma-Aldrich

2-Phenyl-2-propanol

97%

Synonym(s):

α,α-Dimethylbenzyl alcohol, Dimethyl phenyl carbinol

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About This Item

Linear Formula:
(CH3)2C(OH)C6H5
CAS Number:
Molecular Weight:
136.19
Beilstein:
1905012
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

powder

refractive index

n20/D 1.5196 (lit.)

bp

202 °C (lit.)

mp

28-32 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

SMILES string

CC(C)(O)c1ccccc1

InChI

1S/C9H12O/c1-9(2,10)8-6-4-3-5-7-8/h3-7,10H,1-2H3

InChI key

BDCFWIDZNLCTMF-UHFFFAOYSA-N

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Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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[Photometric determination of dimethylphenylcarbinol in water].
Z A Shcherbakova
Gigiena i sanitariia, (1)(1), 71-72 (1982-01-01)
[Information from the Soviet Toxicology Center].
Gigiena truda i professional'nye zabolevaniia, (8)(8), 53-56 (1982-08-01)
T Cvrk et al.
Archives of biochemistry and biophysics, 389(1), 31-40 (2001-05-24)
A putative binding region for cumene hydroperoxide in the active site of cytochrome P4501A1 was identified using photoaffinity labeling. Thr501 was determined as the most likely site of modification by azidocumene used as the photoaffinity label (T. Cvrk and H.
J Scognamiglio et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 50 Suppl 2, S130-S133 (2011-10-29)
A toxicologic and dermatologic review of 2-phenyl-2-propanol when used as a fragrance ingredient is presented. 2-Phenyl-2-propanol is a member of the fragrance structural group Aryl Alkyl Alcohols and is a tertiary alcohol. The AAAs are a structurally diverse class of
Jiafeng Geng et al.
Journal of inorganic biochemistry, 167, 60-67 (2016-12-03)
The diheme enzyme MauG utilizes H

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