Skip to Content
Merck
All Photos(1)

Documents

H20008

Sigma-Aldrich

3-Hydroxybenzoic acid

ReagentPlus®, 99%

Synonym(s):

m-Salicylic acid

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
HOC6H4CO2H
CAS Number:
99-06-9
Molecular Weight:
138.12
Beilstein:
508160
EC Number:
202-726-5
MDL number:
MFCD00002506
UNSPSC Code:
12352100
PubChem Substance ID:
24895493
NACRES:
NA.22

product line

ReagentPlus®

Assay

99%

mp

200-203 °C (lit.)

SMILES string

OC(=O)c1cccc(O)c1

InChI

1S/C7H6O3/c8-6-3-1-2-5(4-6)7(9)10/h1-4,8H,(H,9,10)

InChI key

IJFXRHURBJZNAO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

3-Hydroxybenzoic acid, being a component of structural skeleton of various biologically active small molecules, is used in the synthesis of medicinally important compounds such as tyrosine kinase Tie-2 inhibitor, amyloidogenesis inhibitor, antioxidant and anti-inflammatory agents based on oxadiazole analogs of resveratrol.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H315,H319,H335

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 3

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

Customers Also Viewed

Slide 1 of 1

1 of 1

2,3-Dihydroxybenzoic acid 99%

Sigma-Aldrich

126209

2,3-Dihydroxybenzoic acid

Antioxidant and anti-inflammatory properties of 1, 2, 4-oxadiazole analogs of resveratrol.
Gobec M, et al.
Chemico-Biological Interactions, 240, 200-207 (2015)
Evolution of a highly selective and potent 2-(pyridin-2-yl)-1, 3, 5-triazine Tie-2 kinase inhibitor.
Hodous B L, et al.
Journal of Medicinal Chemistry, 50(4), 611-626 (2007)
Biochemical and structural evaluation of highly selective 2-arylbenzoxazole-based transthyretin amyloidogenesis inhibitors.
Johnson S M, et al.
Journal of Medicinal Chemistry, 51(2), 260-270 (2007)
Fredrik L Nordström et al.
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences, 28(5), 377-384 (2006-06-20)
Solution and solid-state properties of m-hydroxybenzoic acid have been investigated. Two polymorphs were found where the monoclinic modification exhibits a higher stability than the orthorhombic form. The solubility of the monoclinic polymorph was determined between 10 and 50 degrees C
Yi-Li Lin et al.
Journal of hazardous materials, 137(1), 324-331 (2006-04-11)
This research is dedicated to determine the rejection ratios of disinfection by-products (DBPs) precursors including resorcinol, phloroglucinol, 3-hydroxybenzoic acid, and tannic acid solution in the presence of calcium by nanofiltration with NF70 membrane. The rejections of these model compounds also
View All Related Papers

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