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129526

Sigma-Aldrich

2-Isopropylphenol

98%

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About This Item

Linear Formula:
(CH3)2CHC6H4OH
CAS Number:
88-69-7
Molecular Weight:
136.19
Beilstein:
1363322
EC Number:
201-852-8
MDL number:
MFCD00002224
UNSPSC Code:
12352100
PubChem Substance ID:
24847907
NACRES:
NA.22

vapor pressure

<0.05 mmHg ( 25 °C)

Quality Level

200

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.)

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)

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General description

2-Isopropylphenol is catabolized via a broad-spectrum meta cleavage pathway.

Application

2-Isopropylphenol was used to study the ability of 2-isopropylphenol to activate estrogen receptor (ER), androgen receptor (AR), progesterone receptor (PR) and estrogen-related receptor (ERR).

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

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Certificates of Analysis (COA)

Lot/Batch Number
0001378083
1414604V
1378083V
1414604
1414605

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Jian Li et al.
Toxicology in vitro : an international journal published in association with BIBRA, 24(1), 201-207 (2009-09-22)
Some phenols have been suspected to modulate the endocrine systems of wildlife and humans, but less is known about their interactions with different types of nuclear receptors. In this study, the ability of 2-tert-butylphenol, 2-isopropylphenol, 4-tert-octylphenol (4-t-OP), 2,4-dichlorophenol (2,4-DCP), 3,4-dichlorophenol
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
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
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
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
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