Skip to Content
Merck
CN

Key Documents

View All Documentation

129526

2-Isopropylphenol

98%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
(CH3)2CHC6H4OH
CAS Number:
88-69-7
Molecular Weight:
136.19
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24847907
EC Number:
201-852-8
Beilstein/REAXYS Number:
1363322
MDL number:
MFCD00002224
Assay:
98%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

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)

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).

Still not finding the right product?

Explore all of our products under 2-Isopropylphenol

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

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

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

224.6 °F - closed cup

flash_point_c

107 °C - closed cup

ppe

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

Regulatory Information

危险化学品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
0001378083
1414604V
1378083V
1414604
1414605

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

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
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
View All Related Papers

Global Trade Item Number

SKUGTIN
129526-100G04061838726285
129526-5G04061837005404