Skip to Content
Merck
All Photos(2)

Documents

343668

Sigma-Aldrich

2-Hydroxy-3-isopropylbenzoic acid

98%

Synonym(s):

3-Isopropylsalicylic acid

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(CH3)2CHC6H3(OH)CO2H
CAS Number:
7053-88-5
Molecular Weight:
180.20
MDL number:
MFCD00075272
UNSPSC Code:
12352100
PubChem Substance ID:
24861188
NACRES:
NA.22

Assay

98%

form

solid

mp

73-75 °C (lit.)

SMILES string

CC(C)c1cccc(C(O)=O)c1O

InChI

1S/C10H12O3/c1-6(2)7-4-3-5-8(9(7)11)10(12)13/h3-6,11H,1-2H3,(H,12,13)

InChI key

XGAYQDWZIPRBPF-UHFFFAOYSA-N

Gene Information

human ... GABRA1(2554)

Related Categories

General description

2-Hydroxy-3-isopropylbenzoic acid is an analog of general anesthetic compound, propofol (2,6-diisopropylphenol). It was investigated for general anesthetic activity in Xenopus laevis tadpoles and for the ability to produce enhancement of submaximal GABA responses.

Application

2-Hydroxy-3-isopropylbenzoic acid may be used in the preparation of 3-isopropylgentisic acid.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

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

Visit the Document Library

D J Hopper et al.
The Biochemical journal, 122(1), 29-40 (1971-03-01)
1. Cell-free extracts, prepared from a non-fluorescent Pseudomonas grown on m-cresol, oxidized gentisate and certain alkyl-substituted gentisates with the consumption of 1 mol of oxygen and the formation of 1 mol of pyruvate from 1 mol of substrate. 2. In
M D Krasowski et al.
The Journal of pharmacology and experimental therapeutics, 297(1), 338-351 (2001-03-22)
A series of 27 analogs of the general anesthetic propofol (2,6-diisopropylphenol) were examined for general anesthetic activity in Xenopus laevis tadpoles and for the ability to produce enhancement of submaximal GABA responses and/or direct activation at recombinant GABA(A) receptors. Fourteen

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