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Sigma-Aldrich

5-Methylsalicylic acid

98%

Synonym(s):

2-Hydroxy-5-methylbenzoic acid, p-Cresotic acid

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About This Item

Linear Formula:
CH3C6H3(OH)CO2H
CAS Number:
Molecular Weight:
152.15
Beilstein:
1909076
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

mp

150-154 °C (lit.)

SMILES string

Cc1ccc(O)c(c1)C(O)=O

InChI

1S/C8H8O3/c1-5-2-3-7(9)6(4-5)8(10)11/h2-4,9H,1H3,(H,10,11)

InChI key

DLGBEGBHXSAQOC-UHFFFAOYSA-N

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General description

5-Methylsalicylic acid exhibits a significant cross-reactivity during fluorescent polarization immunoassay for salicylates in serum.

Application

5-Methylsalicylic acid was used in generation of o-sulfate conjugates in situ and their analysis by ultra-performance liquid chromatography-time-of-flight mass spectrometry.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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M Koel et al.
Journal of analytical toxicology, 13(6), 358-360 (1989-11-01)
We studied the recently developed Abbott Laboratories fluorescent polarization immunoassay (FPIA) for salicylates in serum. The cross-reactivity test of the assay was performed with 20 substances that showed a similar chemical structure as salicylic acid. A chemical substitution on the
John B Tyburski et al.
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Shabnam Najafi AsliPashaki et al.
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In this research, a simple, rapid, and efficient air assisted - vesicle based microextraction (AAVME) approach was developed for the extraction of phenolic compounds and their analysis in different Melissa officinalis L. samples. The extraction method is based injection an
Jong-Dae Jang et al.
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The phase behavior of amphiphilic Pluronic block copolymers in aqueous solution is of importance for a broad spectrum of practical applications but has not been fully exploited yet. Here, the phase behavior of the mixture of the Pluronic P65 and
Jennifer A Jacobsen et al.
Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced hit rates ranging from 29% to 43% for five matrix metalloproteases

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