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H20008

Sigma-Aldrich

3-Hydroxybenzoic acid

ReagentPlus®, 99%

Synonym(s):

m-Salicylic acid

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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

Quality Level

200

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

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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’.

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2,3-Dihydroxybenzoic acid 99%

Sigma-Aldrich

126209

2,3-Dihydroxybenzoic acid

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)
Antioxidant and anti-inflammatory properties of 1, 2, 4-oxadiazole analogs of resveratrol.
Gobec M, et al.
Chemico-Biological Interactions, 240, 200-207 (2015)
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
Stefania Montersino et al.
Biochimica et biophysica acta, 1824(3), 433-442 (2011-12-31)
The genome of Rhodococcus jostii RHA1 contains an unusually large number of oxygenase encoding genes. Many of these genes have yet an unknown function, implying that a notable part of the biochemical and catabolic biodiversity of this Gram-positive soil actinomycete
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