H20008
3-Hydroxybenzoic acid
ReagentPlus®, 99%
Synonym(s):
m-Salicylic acid
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About This Item
Linear Formula:
HOC6H4CO2H
CAS Number:
Molecular Weight:
138.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-726-5
Beilstein/REAXYS Number:
508160
MDL number:
Product Name
3-Hydroxybenzoic acid, ReagentPlus®, 99%
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
SMILES string
OC(=O)c1cccc(O)c1
product line
ReagentPlus®
assay
99%
mp
200-203 °C (lit.)
Quality Level
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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
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Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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, 146(1-2), 20-29 (2007-01-11)
The removal of small trihalomethane precursors (THMPs) from aqueous solution by two commercial nanofiltration membranes (NF70 and NF270) was investigated. Resorcinol, phloroglucinol, and 3-hydroxybenzoic acid were selected as model compounds of small THMPs, while tannic acid was chosen as a
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