1321-14-8
1321-14-8
Chemical Structure
Sulfogaiacol
- CAS No.: 1321-14-8
- Formula:C7H7O5S.K
- Molecular Weight:242.29
InChIKey: MXBYQSAGWRXDAC-UHFFFAOYSA-M
SMILES: OC1=CC=CC=C1OC.O=S(C)(O[K])=O
Biological Activity: Sulfogaiacol is a cough suppressant with expectorant properties, and it can be used for research on acute respiratory infections with oral activity[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Sulfogaiacol | 99.88% | Sulfogaiacol is a cough suppressant with expectorant properties, and it can be used for research on acute respiratory infections with oral activity. | ||||||||||||||||||||
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p-Cresyl sulfate potassium | 99.97% | p-Cresyl sulfate potassium is a uremic toxin that binds to a prototype protein. p-Cresyl sulfate potassium activates the JNK and p38 MAPK signaling pathways. p-Cresyl sulfate potassium has pro-inflammatory activity. | ||||||||||||||||||||
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Pyrocatechol sulfate | Pyrocatechol sulfate is a dietary phenolic metabolite and uremic toxin. Pyrocatechol sulfate can be derived from diet and gut Bacterial metabolism. Plasma levels of Pyrocatechol sulfate are sensitive to alcohol exposure and withdrawal, and are negatively correlated with anxiety, depression, and craving for alcohol in severe alcohol use disorder. Pyrocatechol sulfate can be used in studies related to chronic kidney disease and severe alcohol use disorder. | |||||||||||||||||||||
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Guaiacolsulfonate | Guaiacolsulfonate is an isomeric ingredient in potassium. Guaiacolsulfonate can be used for a variety of biochemical studies. | |||||||||||||||||||||
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Veratrole (Standard) | ≥98% | Veratrole (Standard) is the analytical standard of Veratrole. This product is intended for research and analytical applications. Veratrole (1,2-Dimethoxybenzene) is a key compound that widely exists in plants and attracts pollinators. The release of Veratrole has a circadian rhythm and plays an important role in plant reproduction, species differentiation, and interactions with pollinators. In addition, Veratrole can be demethylated by cytochrome P-450 in Streptomyces setonii. | ||||||||||||||||||||
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Guaiacol | 99.96% | Guaiacol, a phenolic compound, inhibits LPS-stimulated COX-2 expression and NF-κB activation. Anti-inflammatory activity. | ||||||||||||||||||||
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Guaiacol-13C6 | Guaiacol-13C6 is the 13C labeled Guaiacol. Guaiacol, a phenolic compound, inhibits LPS-stimulated COX-2 expression and NF-κB activation. Anti-inflammatory activity. | |||||||||||||||||||||
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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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Tamsulosin impurity 18 | 98.84% | Tamsulosin impurity 18 is an impurity of Tamsulosin. | ||||||||||||||||||||
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2-Ethoxyphenol | 99.90% | 2-Ethoxyphenol, also known as guaiacol ethyl ether, consists of a phenolic ring and an ethoxy group connected to the 2-position. The compound has a sweet, smoky flavor and is commonly used as a flavoring in foods such as baked goods, candy and beverages. | ||||||||||||||||||||
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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]. Armand C, et al. [Neocodion misuse: evolution between 1992 and 2002]. Therapie. 2004 Sep-Oct;59(5):547-53. [Content Brief]
- [2]. NGUYEN DUY TAN, et al. INVESTIGATION OF TOXICITY, ANTIMICROBIAL ACTIVITY AND COUGH TREATMENT OF PRODUCTS PRODUCED FROM Pouzolzia zeylanica PLANTS GROWING IN VIETNAM. Malays. Appl. Biol. (2020) 49(3): 43–51.
