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
signalword
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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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
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
Xianli Wu et al.
Molecular nutrition & food research, 53 Suppl 1, S76-S84 (2009-02-10)
Black raspberries (BRB) contain high levels of polyphenols and have been demonstrated to be chemopreventive. In order to investigate the underlying mechanism and study the metabolism of anthocyanins, pigs were fed freeze-dried BRB powder or purified diet (control) and three
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
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