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Merck
CN

196037

4-Isopropylbenzyl alcohol

97%

Synonym(s):

Cumic alcohol

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About This Item

Linear Formula:
(CH3)2CHC6H4CH2OH
CAS Number:
536-60-7
Molecular Weight:
150.22
NACRES:
NA.22
PubChem Substance ID:
24851732
UNSPSC Code:
12352100
EC Number:
208-640-4
MDL number:
MFCD00004663

Key Documents

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Product Name

4-Isopropylbenzyl alcohol, 97%

InChI key

OIGWAXDAPKFNCQ-UHFFFAOYSA-N

InChI

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

SMILES string

CC(C)c1ccc(CO)cc1

assay

97%

form

liquid

refractive index

n20/D 1.519 (lit.)

bp

135-136 °C/26 mmHg (lit.)

solubility

alcohol: miscible
diethyl ether: miscible
water: insoluble

density

0.982 g/mL at 25 °C (lit.)

functional group

hydroxyl

Quality Level

100

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General description

4-Isopropylbenzyl alcohol has mosquito repellent properties and has been isolated from Eucalyptus camaldulensis. Oxidation of 4-isopropylbenzyl alcohol over TiO2-supported nano gold catalyst has been investigated.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302,H315

Hazard Classifications

Acute Tox. 4 Oral - Skin Irrit. 2

Storage Class

10 - Combustible liquids

wgk

WGK 2

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKBX9498V
MKBV0111V
MKBR2679V
MKBB8834V
MKBB8834

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New mosquito repellent from Eucalyptus camaldulensis.
Watanabe K, et al.
Journal of Agricultural and Food Chemistry, 41(11), 2164-2166 (1993)
Selective oxidation of alcohols to aldehydes and ketones over TiO2-supported gold nanoparticles in supercritical carbon dioxide with molecular oxygen.
Wang X, et al.
Applied Catalysis A: General, 349(1), 86-90 (2008)
Annemieke Strijkstra et al.
Applied and environmental microbiology, 80(24), 7592-7603 (2014-09-28)
The betaproteobacteria "Aromatoleum aromaticum" pCyN1 and "Thauera" sp. strain pCyN2 anaerobically degrade the plant-derived aromatic hydrocarbon p-cymene (4-isopropyltoluene) under nitrate-reducing conditions. Metabolite analysis of p-cymene-adapted "A. aromaticum" pCyN1 cells demonstrated the specific formation of 4-isopropylbenzyl alcohol and 4-isopropylbenzaldehyde, whereas with

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