Alcohols

3-Aminobutan-1-ol is an amine that is synthesized industrially by the reduction of soybean trypsin with borohydride. This chemical has been used as a substrate in asymmetric synthesis and can be detected by high detection sensitivity. 3-Aminobutan-1-ol binds to the carbonyl group of amino acid residues and causes a reaction with chloride ions for detection. The product of this reaction is an enantiomer, which can be separated from other reaction products by purified chiral stationary phases. 3-Aminobutan-1-ol is also involved in the biosynthesis of proteins and enzymes. It reacts with hydrochloric acid to form a salt, which can then be used as an enzyme inhibitor.

Nifurtoinol is a cross-linking agent that has antimicrobial properties. It is used to treat infectious diseases, such as sepsis and endocarditis, and autoimmune diseases, such as rheumatoid arthritis. It can be implanted into the eye to treat choroidal neovascularization due to age-related macular degeneration. Nifurtoinol binds to bacterial cell walls by forming covalent bonds with hydroxyl groups on the bacterial surface. This results in an inflammatory response that reduces the number of bacteria. Nifurtoinol is active against a wide range of microbes and is a broad-spectrum antimicrobial drug.

Please enquire for more information about 2,5,7-Trimethylquinolin-8-ol 1-oxide including the price, delivery time and more detailed product information at the technical inquiry form on this page

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cis-4-Cyclopentene-1,3-diol is a useful chemical intermediate that can be converted to diacetate, acetylation, or chloroacetate. It has a reactive functional group that can be used for synthesizing polymers and other compounds. cis-4-Cyclopentene-1,3-diol is also an excellent substrate for lipase reactions and it reacts with hydrogen fluoride to give desired products. This section has conformational properties that make it suitable for hydrogen bonding and can act as a ligand in coordination chemistry. cis-4-Cyclopentene-1,3-diol is also able to undergo substitution at the carbonyl carbon atom by various reagents such as fluorine.

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5-Hydroxyquinolin-2(1H)-one is a chalcone that can be synthesized from 2,5-dihydroxybenzaldehyde and quinoline. It is a bacteriostatic agent that inhibits bacterial growth by binding to the 50S ribosomal subunit, blocking the formation of an antibiotic-substrate complex with the enzyme cell wall synthesis that is required for cell wall biosynthesis, inhibiting protein synthesis and cell division. 5-Hydroxyquinolin-2(1H)-one has shown activity against methicillin resistant Staphylococcus aureus (MRSA) and methicillin resistant Enterococcus faecium. 5-Hydroxyquinolin-2(1H)-one also represses the expression of DNA topoisomerase II genes, which may be associated with its inhibitory effects on bacterial growth.