Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

W346101

Sigma-Aldrich

2-Isopropylphenol

≥98%, FG

Synonym(s):

2-propan-2-ylphenol, O-cumenol, Prodox 131

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
(CH3)2CHC6H4OH
CAS Number:
88-69-7
Molecular Weight:
136.19
FEMA Number:
3461
Beilstein:
1363322
EC Number:
201-852-8
Council of Europe no.:
11234
MDL number:
MFCD00002224
UNSPSC Code:
12164502
PubChem Substance ID:
24901714
Flavis number:
4.044
NACRES:
NA.21

biological source

synthetic

grade

FG
Fragrance grade
Halal

Agency

follows IFRA guidelines
meets purity specifications of JECFA

reg. compliance

EU Regulation 1223/2009
EU Regulation 1334/2008 & 872/2012
FDA

vapor pressure

<0.05 mmHg ( 25 °C)

Assay

≥98%

refractive index

n20/D 1.526 (lit.)

bp

212-213 °C (lit.)

mp

12-16 °C (lit.)

density

1.012 g/mL at 25 °C (lit.)

application(s)

flavors and fragrances

Documentation

see Safety & Documentation for available documents

food allergen

no known allergens

fragrance allergen

no known allergens

Organoleptic

medicinal

SMILES string

CC(C)c1ccccc1O

InChI

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

InChI key

CRBJBYGJVIBWIY-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

Looking for similar products? Visit Product Comparison Guide

Related Categories

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

224.6 °F - closed cup

Flash Point(C)

107 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
STBK3751
STBJ8630
STBJ6381
STBJ0046
STBG4614V

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

F Reichlin et al.
Applied and environmental microbiology, 60(12), 4587-4591 (1994-12-01)
Pseudomonas sp. strain HBP1 Prp grew on 2-isopropylphenol as the sole carbon and energy source with a maximal specific growth rate of 0.14 h-1 and transient accumulation of isobutyric acid. Oxygen uptake experiments with resting cells and enzyme assays with
Martin Barann et al.
Anesthesia and analgesia, 106(3), 846-857 (2008-02-23)
5-Hydroxytryptamine type 3 (5-HT3) receptors are excitatory ligand-gated ion channels which are involved in postoperative nausea and vomiting. They are depressed by the anesthetic propofol, which, in contrast, enhances the activity of inhibitory ligand-gated ion channels such as gamma-aminobutyric acid
Yongnian Ni et al.
Talanta, 76(3), 513-521 (2008-07-01)
The binding interaction of the pesticide Isoprocarb and its degradation product, sodium 2-isopropylphenate, with bovine serum albumin (BSA) was studied by spectrofluorimetry under simulated physiological conditions. Both Isoprocarb and sodium 2-isopropylphenate quenched the intrinsic fluorescence of BSA. This quenching proceeded
Kevin A Harvey et al.
Bioorganic & medicinal chemistry, 18(5), 1866-1874 (2010-02-16)
The present study describes the characterization and evaluation of novel anticancer conjugates, 2,6-diisopropylphenol-docosahexaenoate (PP-DHA), and its analogues including 2,4-diisopropylphenol-docosahexaenoate (DIPP-DHA), 2-isopropylphenol-docosahexaenoate (IPP-DHA), 2-cyclohexanephenol-docosahexaenoate (CHP-DHA) and phenol-docosahexaenoate (P-DHA) on breast cancer cell lines. Representative breast cancer cell lines, based on estrogen
Jerry O Ebalunode et al.
Bioorganic & medicinal chemistry, 17(14), 5133-5138 (2009-06-13)
Current anesthetics, especially the inhaled ones, have troublesome side effects and may be associated with durable changes in cognition. It is therefore highly desirable to develop novel chemical entities that reduce these effects while preserving or enhancing anesthetic potency. In
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service