488-17-5
488-17-5
Chemical Structure
3-Methylcatechol
- CAS No.: 488-17-5
- Formula:C7H8O2
- Molecular Weight:124.14
IUPAC Name: 3-methylbenzene-1,2-diol
InChIKey: PGSWEKYNAOWQDF-UHFFFAOYSA-N
SMILES: OC1=CC=CC(C)=C1O
Biological Activity: 3-Methylcatechol is a phenolic derivative that can be produced by Pseudomonas putida MC2. 3-Methylcatechol can serve as a molecular building block in chemical synthesis to produce other active compounds[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3-Methylcatechol | 98.18% | 3-Methylcatechol is a phenolic derivative that can be produced by Pseudomonas putida MC2. 3-Methylcatechol can serve as a molecular building block in chemical synthesis to produce other active compounds. | ||||||||||||||||||||
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3-Methylcatechol (Standard) | ≥98% | 3-Methylcatechol (Standard) is the analytical standard of 3-Methylcatechol (HY-W012815). This product is intended for research and analytical applications. 3-Methylcatechol is a phenolic derivative that can be produced by Pseudomonas putida MC2. 3-Methylcatechol can serve as a molecular building block in chemical synthesis to produce other active compounds. | ||||||||||||||||||||
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4-Chloro-2-methylphenol | 99.19% | 4-Chloro-2-methylphenol is an antibacterial agent that can be used as a pharmaceutical excipient. | ||||||||||||||||||||
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3-Aminobenzene-1,2-diol | 98.0% | 3-Aminobenzene-1,2-diol (compound C8) is a matrix metalloproteinase (MMP) inhibitor with IC50 values of 20, 26, 16 and 16.3 μM for MMP-2, MMP-8, MMP-9 and MMP-14, respectively. | ||||||||||||||||||||
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Pyrogallol | 99.86% | Pyrogallol is a polyphenol compound, which has anti-fungal and anti-psoriatic properties. Pyrogallol is a reductant that is able to generate free radicals, in particular superoxide anions. | ||||||||||||||||||||
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3-Fluorocatechol | 99.32% | 3-Fluorocatechol is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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4-Methylcatechol (Standard) | 97.58% | 4-Methylcatechol (Standard) is the analytical standard of 4-Methylcatechol. This product is intended for research and analytical applications. 4-Methylcatechol is an intermediate in the degradation of some alkylbenzenes and an orally active suicide inhibitor of catechol 2,3-dioxygenase (C23O). 4-Methylcatechol induces apoptosis in melanoma cells through oxidative stress, but some studies have also shown that 4-Methylcatechol is carcinogenic. In addition, 4-Methylcatechol has antiplatelet and blood pressure-lowering activities. 4-Methylcatechol can also inhibit protein oxidation in beef but does not disulfide formation. | ||||||||||||||||||||
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2-Methylresorcinol | 2-Methylresorcinol is a tripyrrane analog. 2-Methylresorcinol is a cosmetic ingredient with endocrine activity. 2-Methylresorcinol combined with Butylhydroxyanisole (HY-B1066) and Avobenzone (HY-B0316) has anti-glucocorticoid-like activity. 2-Methylresorcinol combined with Avobenzone only has anti-androgen-like activity. 2-Methylresorcinol can be used as for cosmetic industry. | |||||||||||||||||||||
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Methylhydroquinone (Standard) | ≥98% | Methylhydroquinone (Standard) is the analytical standard of Methylhydroquinone. This product is intended for research and analytical applications. Methylhydroquinone is an orally active COX inhibitor with IC50s of 480.7 μM and 52.2 μM for ovine COX-1 and human recombinant COX-2, respectively. Methylhydroquinone has potential DNA damaging effects: 1) inhibiting COX-1 to reduce prostaglandin synthesis and exert anti-inflammatory activity; 2) inducing DNA single-strand breaks. Methylhydroquinone exerts its effects by competitively binding to the active sites of COX-1 (such as Tyr385, Met522) and non-covalent interactions. | ||||||||||||||||||||
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5-Amino-2-methylphenol (Standard) | ≥98% | 5-Amino-2-methylphenol (Standard) is the analytical standard of 5-Amino-2-methylphenol. This product is intended for research and analytical applications. | ||||||||||||||||||||
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3-Methoxycatechol | 99.98% | 3-Methoxycatechol is a catechol derivative with endothelium-dependent vasodilatory and antihypertensive activities. 3-Methoxycatechol activates GPR35, triggering dynamic mass redistribution and β-arrestin translocation. 3-Methoxycatechol inhibits tau self-interaction and scavenges free radicals such as DPPH. 3-Methoxycatechol combined with NaNO2 enhances forestomach proliferative lesions and papilloma formation, reduces glandular stomach lesions, and promotes esophageal lesion development. 3-Methoxycatechol can be used for research related to hypertension and papilloma. | ||||||||||||||||||||
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References
- [1]. L E Hüsken, et al. Integrated bioproduction and extraction of 3-methylcatechol. J Biotechnol. 2001 Jun 1;88(1):11-9. [Content Brief]
- [2]. Sun, et al. Ozonation of 3-methylcatechol and 4-methylcatechol in the atmosphere and aqueous particles: Mechanism, kinetics and ecotoxicity assessment. Chemical Engineering Journal 358 (2019): 456-466.
