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343668

2-Hydroxy-3-isopropylbenzoic acid

Name: 2-Hydroxy-3-isopropylbenzoic acid
Brand: ALDRICH

98%

Synonym(s):

3-Isopropylsalicylic acid

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About This Item

Linear Formula:

(CH₃)₂CHC₆H₃(OH)CO₂H

CAS Number:

7053-88-5

Molecular Weight:

180.20

NACRES:

NA.22

PubChem Substance ID:

24861188

UNSPSC Code:

12352100

MDL number:

MFCD00075272

Assay:

98%

Form:

solid

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Properties

assay

98%

form

solid

mp

73-75 °C (lit.)

functional group

carboxylic acid

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)

Description

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

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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General anesthetic potencies of a series of propofol analogs correlate with potency for potentiation of gamma-aminobutyric acid (GABA) current at the GABA(A) receptor but not with lipid solubility.

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

The enzymic degradation of alkyl-substituted gentisates, maleates and malates.

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

Global Trade Item Number

SKU	GTIN
343668-5G	04061832619002