2033-89-8
2033-89-8
Chemical Structure
3,4-Dimethoxyphenol
- CAS No.: 2033-89-8
- Formula:C8H10O3
- Molecular Weight:154.16
IUPAC Name: 3,4-dimethoxyphenol
InChIKey: SMFFZOQLHYIRDA-UHFFFAOYSA-N
SMILES: OC1=CC=C(OC)C(OC)=C1
Biological Activity: 3,4-Dimethoxyphenol is a plant-derived phenylpropanoid compound and can use as a whitening agent in cosmetics. 3,4-Dimethoxyphenol exhibits broad-spectrum antimicrobial activity. 3,4-Dimethoxyphenol has tyrosinase-inhibiting activity. 3,4-Dimethoxyphenol has potent antioxidant effect isolated from the bacterial fermentation broth. 3,4-Dimethoxyphenol can be used for the study of infection[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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3,4-Dimethoxyphenol | 99.97% | 3,4-Dimethoxyphenol is a plant-derived phenylpropanoid compound and can use as a whitening agent in cosmetics. 3,4-Dimethoxyphenol exhibits broad-spectrum antimicrobial activity. 3,4-Dimethoxyphenol has tyrosinase-inhibiting activity. 3,4-Dimethoxyphenol has potent antioxidant effect isolated from the bacterial fermentation broth. 3,4-Dimethoxyphenol can be used for the study of infection. | ||||||||||||||||||||
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3,4-Dimethoxyphenol (Standard) | ≥98% | 3,4-Dimethoxyphenol (Standard) is the analytical standard of Lithocholic acid. This product is intended for research and analytical applications. 3,4-Dimethoxyphenol is a plant-derived phenylpropanoid compound and can use as a whitening agent in cosmetics. 3,4-Dimethoxyphenol exhibits broad-spectrum antimicrobial activity. 3,4-Dimethoxyphenol has tyrosinase-inhibiting activity. 3,4-Dimethoxyphenol has potent antioxidant effect isolated from the bacterial fermentation broth. 3,4-Dimethoxyphenol can be used for the study of infection. | ||||||||||||||||||||
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Veratryl alcohol | 99.98% | Veratryl alcohol (3,4-Dimethoxybenzyl alcohol) is a secondary metabolite of lignin-degrading fungi, commonly used as a substrate for lignin peroxidase (LiP) to measure lignin degradation activity. Veratryl alcohol protects LiP from inactivation by H2O2 and prevents the accumulation of LiP III compounds. Veratryl alcohol also acts as a stabilizer for manganese-dependent peroxidases (MnP). Veratryl alcohol is a quorum-sensing inhibitor (QSI) and exhibits antibacterial efficacy. | ||||||||||||||||||||
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Veratraldehyde (Standard) | ≥98% | Veratraldehyde (Standard) is the analytical standard of Veratraldehyde. This product is intended for research and analytical applications. Veratraldehyde is an important chemical used in perfumery, agrochemical, and pharmaceutical industries. | ||||||||||||||||||||
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3,5-Dimethoxyphenol (Standard) | ≥98% | 3,5-Dimethoxyphenol is a toxin metabolite, found in human consuming yew leaves. | ||||||||||||||||||||
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2,6-Dimethoxyphenol | 99.99% | 2,6-Dimethoxyphenol (Syringol) is a phenolic compound that scavenges free radicals and exhibits antioxidant activity. 2,6-Dimethoxyphenol is the substrate for determining laccase activity. | ||||||||||||||||||||
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2-Methoxyhydroquinone | 99.57% | 2-Methoxyhydroquinone is a phenolic compound that reduces TNF-α-induced production of chemokine (C-C motif) ligand 2 (CCL2) with an IC50 value of 64.3 µM. 2-Methoxyhydroquinone is also a precursor in the synthesis of the Hsp90 inhibitor Geldanamycin (HY-15230). | ||||||||||||||||||||
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1,2,4-Trimethoxybenzene | 97.0% | 1,2,4-Trimethoxybenzene is an orally active NLRP3 selective inhibitor. 1,2,4-Trimethoxybenzene can markedly suppress Nigericin (HY-127019) or ATP (HY-B2176)-induced NLRP3 inflammasome activation, thus decreasing caspase-1 activation and IL-1β secretion. 1,2,4-Trimethoxybenzene specifically inhibits the activation of NLRP3 inflammasome without affecting absent in melanoma 2 (AIM2) inflammasome activation. 1,2,4-Trimethoxybenzene inhibits oligomerization of the apoptosis-associated speck-like protein containing a CARD (ASC) and protein-protein interaction between NLRP3 and ASC, thus blocking NLRP3 inflammasome assembly. 1,2,4-Trimethoxybenzene can be used for the study of experimental autoimmune encephalomyelitis (EAE), multiple sclerosis, and type 2 diabetes. | ||||||||||||||||||||
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Homoveratrole | 99.36% | Homoveratrole is a phenolic compound and it is a volatile component of Juglans regia L.. | ||||||||||||||||||||
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Veratraldehyde-13C | Veratraldehyde-13C (3,4-Dimethoxy[7-13C]-benzaldehyde) is the 13C-labeled Veratraldehyde (HY-N1096). Veratraldehyde is an orally active aromatic compound and antibacterial agent. Veratraldehyde can be isolated from essential oils of plants such as peppermint and ginger. Veratraldehyde targets the PilY1 protein. Veratraldehyde has antibacterial activity against Pseudomonas aeruginosa. Veratraldehyde has a repellent effect against mosquitoes and ticks. Veratraldehyde can be used as a flavoring agent. | |||||||||||||||||||||
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Veratryl alcohol-13C | Veratryl alcohol-13C (3,4-Dimethoxybenzyl alcohol-13C) is the 13C-labeled Veratryl alcohol (HY-107858). Veratryl alcohol (3,4-Dimethoxybenzyl alcohol) is a secondary metabolite of lignin-degrading fungi, commonly used as a substrate for lignin peroxidase (LiP) to measure lignin degradation activity. Veratryl alcohol protects LiP from inactivation by H2O2 and prevents the accumulation of LiP III compounds. Veratryl alcohol also acts as a stabilizer for manganese-dependent peroxidases (MnP). Veratryl alcohol is a quorum-sensing inhibitor (QSI) and exhibits antibacterial efficacy. | |||||||||||||||||||||
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1-Bromo-2,4-dimethoxybenzene | 1-Bromo-2,4-dimethoxybenzene is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | |||||||||||||||||||||
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References
- [1]. Tanimoto S, et al. Synthesis and cosmetic whitening effect of glycosides derived from several phenylpropanoids. Yakugaku Zasshi. 2006 Mar;126(3):173-7. [Content Brief]
- [2]. Tomohiro Takaoa, et al. A Simple Screening Method for Antioxidants and Isolation of Several Antioxidants Produced by Marine Bacteria from Fish and Shellfish. Bioscience, Biotechnology, and Biochemistry. 1994, 58(10), 1780-1783.
- [3]. Lai J, et al. Transcriptome analysis reveals the inhibitory mechanism of 3,4-Dimethoxyphenol from Streptomyces albidoflavus strain ML27 against Xanthomonas oryzae pv. oryzae. Pestic Biochem Physiol. 2024 Jun;202:105913. [Content Brief]
