83-40-9

3-Methylsalicylic acid Chemical Structure
83-40-9

Chemical Structure

3-Methylsalicylic acid

Synonym(s): o-Cresotic acid; Hydroxytoluic acid

  • CAS No.: 83-40-9
  • Formula:C8H8O3
  • Molecular Weight:152.15

IUPAC Name: 2-hydroxy-3-methylbenzoic acid

InChIKey: WHSXTWFYRGOBGO-UHFFFAOYSA-N

SMILES: O=C(O)C1=CC=CC(C)=C1O

Biological Activity: 3-Methylsalicylic acid (o-Cresotic acid) is a derivative of salicylic acid. 3-Methylsalicylic acid exhibits significant fibrinolytic activity in human plasma by activating the fibrinolytic system. 3-Methylsalicylic acid can be used as an intermediate for the synthesis of other compounds. 3-Methylsalicylic acid inhibits the feeding of midges[1][2].

Cat. No. Product Name Purity Description Pricing
HY-B1399
3-Methylsalicylic acid 99.63% 3-Methylsalicylic acid (o-Cresotic acid) is a derivative of salicylic acid. 3-Methylsalicylic acid exhibits significant fibrinolytic activity in human plasma by activating the fibrinolytic system. 3-Methylsalicylic acid can be used as an intermediate for the synthesis of other compounds. 3-Methylsalicylic acid inhibits the feeding of midges.
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HY-B1399R
3-Methylsalicylic acid (Standard) ≥98% 3-Methylsalicylic acid (Standard) is the analytical standard of 3-Methylsalicylic acid. This product is intended for research and analytical applications. 3-Methylsalicylic acid (o-Cresotic acid) is a derivative of salicylic acid. 3-Methylsalicylic acid exhibits significant fibrinolytic activity in human plasma by activating the fibrinolytic system. 3-Methylsalicylic acid can be used as an intermediate for the synthesis of other compounds. 3-Methylsalicylic acid inhibits the feeding of midges.
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HY-204565
4-Methyl-3-hydroxyanthranilic acid 4-Methyl-3-hydroxyanthranilic acid (MHA) is a key precursor for the synthesis of Actinomycin D (HY-17559).
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HY-41494R
o-Toluic acid (Standard) ≥98% o-Toluic acid (Standard) is the analytical standard of o-Toluic acid. This product is intended for research and analytical applications. o-Toluic acid (2-Methylbenzoic acid) is a benzoic acid substituted by a methyl group at position 2. O-Toluic acid plays a role as a xenobiotic metabolite.
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HY-76375
2,3-Dimethylbenzoic acid ≥98.0% 2,3-Dimethylbenzoic acid is a transition metal catalyst.
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HY-78144
4-Methylsalicylic acid 99.97% 4-Methylsalicylic acid is a methyl derivative of Salicylic acid (HY-B0167). 4-Methylsalicylic acid derivatives inhibit the activity of alkaline phosphatases such as TNAP and IAP. 4-Methylsalicylic acid derivatives exhibit immunosuppressive activity.
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HY-78573
5-Methylsalicylic acid 99.78% 2-Hydroxy-5-methylbenzoic acid is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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HY-W002587R
4-Hydroxy-3-methylbenzoic acid (Standard) ≥98% 4-Hydroxy-3-methylbenzoic acid is a normal organic acid identified in urine specimens from a healthy population.
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HY-W002751R
6-Methylsalicylic acid (Standard) ≥98% 6-Methylsalicylic acid (Standard) is the analytical standard of 6-Methylsalicylic acid (HY-W002751). This product is intended for research and analytical applications. 6-Methylsalicylic acid is the secondary metabolite that could be isolated from some fungi. 6-Methylsalicylic acid can be used as building blocks for synthesis of antibacterial and anti-inflammatory agents.
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HY-W206016
3-Aminosalicylic acid 99.06% 3-Aminosalicylic acid (3-ASA) is a hydroxybenzoic acid compound. 3-Aminosalicylic acid serves as a building block for organic synthesis. It also acts as a potential impurity of 5-Aminosalicylic Acid (HY-15027).
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HY-Y0026
3-Hydroxy-4-methylbenzoic acid 99.75% 3-Hydroxy-4-methylbenzoic acid (3-Hydroxy-4-methylbenzoic acid) is a biological material or organic compound that can be used in life science research.
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HY-Y0202R
Pyrocatechuic acid (Standard) 99.62% Pyrocatechuic acid (Standard) is the analytical standard of Pyrocatechuic acid. This product is intended for research and analytical applications. Pyrocatechuic acid is a normal human benzoic acid metabolite found in plasma, and has increased levels after aspirin ingestion.
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References