Skip to Content
Merck

Key Documents

View All Documentation

Skip To

343668

Sigma-Aldrich

2-Hydroxy-3-isopropylbenzoic acid

98%

Synonym(s):

3-Isopropylsalicylic acid

Sign Into View Organizational & Contract Pricing

Select a Size

5 G
₹23,100.00

₹23,100.00

Please contact Customer Service for Availability
Request a Bulk Order

Select a Size

Change View
5 G
₹23,100.00

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

₹23,100.00

Please contact Customer Service for Availability
Request a Bulk Order
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Quality Level

200

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)

Related Categories

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
527424135690219835
2-Hydroxy-3-isopropylbenzoic acid 98%

343668

2-Hydroxy-3-isopropylbenzoic acid

2-Hydroxy-3-nitrobenzaldehyde 98%

527424

2-Hydroxy-3-nitrobenzaldehyde

3,5-Diisopropyl-2-hydroxybenzoic acid 98%

135690

3,5-Diisopropyl-2-hydroxybenzoic acid

2-Hydroxy-3-methylbutyric acid 99%

219835

2-Hydroxy-3-methylbutyric acid

assay

98%

assay

98%

assay

98%

assay

99%

Quality Level

200

Quality Level

100

Quality Level

-

Quality Level

200

form

solid

form

-

form

powder

form

solid

mp

73-75 °C (lit.)

mp

105-109 °C (lit.)

mp

113-115 °C (lit.)

mp

86-87 °C (lit.)

functional group

carboxylic acid

functional group

aldehyde, nitro

functional group

carboxylic acid

functional group

carboxylic acid, hydroxyl

Gene Information

human ... GABRA1(2554)

Gene Information

-

Gene Information

-

Gene Information

-

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.[1]

Application

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

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

    • Choose from one of the most recent versions:

    Certificates of Analysis (COA)

    Lot/Batch Number
    BGBC1258V
    15918AO
    12901BO
    10615LI
    04513TG

    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

    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
    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

    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