Aldéhydes

Terephthalaldehyde chloride is a water-insoluble, white solid that is soluble in organic solvents. It forms a protective layer on metal surfaces and plastics, preventing corrosion and microbial growth. Terephthalaldehyde chloride has been shown to be effective against Escherichia coli, Klebsiella pneumoniae, Bacillus subtilis, Pseudomonas aeruginosa, Staphylococcus aureus, and Salmonella enterica. Terephthalaldehyde chloride's antimicrobial activity is attributed to its acid complex with phosphorus pentoxide and electrochemical impedance spectroscopy data indicate that it reacts with the anionic sites of bacterial cell walls. Terephthalaldehyde chloride does not react with human serum proteins or ester linkages; however, it has toxic effects on mice at high doses.

1-Benzyl-1H-imidazole-5-carboxaldehyde is a molecule that is reactive with other molecules. It is synthesized from 7-ethoxycoumarin and naphthalene, which are precursors to the benzyl group. 1-Benzyl-1H-imidazole-5-carboxaldehyde has been shown to be an aromatase inhibitor, and it may have potential as a cancer treatment. This molecule also inhibits the enzyme 7-ethoxycoumarin odeethylase, which results in an increase of 7-ethoxycoumarin levels in tissues. 1BICA has also been shown to inhibit calcium channels, which may be useful for treating heart arrhythmia or hypertension. The biological properties of this molecule are not well understood, but it has been found to inhibit liver microsomes and to be synthetized by rat liver enzymes.

Please enquire for more information about 8-Bromo-6-methylimidazo[1,2-a]pyridine-3-carbaldehyde including the price, delivery time and more detailed product information at the technical inquiry form on this page

Salicylaldehyde azine (SAZ) is a polymerized compound that has been shown to inhibit tyrosinase, an enzyme that catalyzes the oxidation of L-tyrosine to DOPA and dopaquinone. It can be used as a fluorescent probe for metal ions and has been used in the preparation of aluminium salts. The interaction of SAZ with protonated functional groups on tyrosinase leads to inhibition by blocking the active site. This inhibition is reversible and can be reversed by adding a reducing agent such as sodium dithionite.