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4-Hydroxy-3,5-dimethylbenzoic acid, 98%, Thermo Scientific Chemicals
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Catalog number A13051.14
also known as A13051-14
Price (USD)/ Each
539.00
-
Quantity:
25 g
Price (USD)/ Each
539.00
4-Hydroxy-3,5-dimethylbenzoic acid, 98%, Thermo Scientific Chemicals
Catalog numberA13051.14
Price (USD)/ Each
539.00
-
Chemical Identifiers
CAS4919-37-3
IUPAC Name4-hydroxy-3,5-dimethylbenzoate
Molecular FormulaC9H9O3
InChI KeyOMNHTTWQSSUZHO-UHFFFAOYSA-M
SMILESCC1=CC(=CC(C)=C1O)C([O-])=O
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream to pink or pale brown
FormCrystals or powder or crystalline powder
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Melting Point (clear melt)221.0-227.0?C
4-hydroxy-3,5-dimethylbenzoic acid is widely used as a reagent for potent TTR amyloidogenesis inhibitors. It plays an important role as an intermediate in agrochemicals and dyestuffs. It is also used in the preparation of mexiletine derivatives.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4-hydroxy-3,5-dimethylbenzoic acid is widely used as a reagent for potent TTR amyloidogenesis inhibitors. It plays an important role as an intermediate in agrochemicals and dyestuffs. It is also used in the preparation of mexiletine derivatives.
Solubility
Soluble in methanol.
Notes
Keep away from heat and avoid excessive light. Incompatible with oxidizing agents.
4-hydroxy-3,5-dimethylbenzoic acid is widely used as a reagent for potent TTR amyloidogenesis inhibitors. It plays an important role as an intermediate in agrochemicals and dyestuffs. It is also used in the preparation of mexiletine derivatives.
Solubility
Soluble in methanol.
Notes
Keep away from heat and avoid excessive light. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Demirkiran, O.; Sabudak, T.; Ozturk, M.; Topcu, G. Antioxidant and Tyrosinase Inhibitory Activities of Flavonoids from Trifolium nigrescens Subsp. petrisavi. J. Agric. Food Chem. 2013, 61 (51), 12598-12603.
- Khan, S.; Fatima, I.; Kazmi, M. H.; Malik, A. New Secondary Metabolites from Allium victorialis. Helv. Chim. Acta 2013, 96 (6), 1176-1181.