Hydrazines

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2-Hydroxy-4-hydrazinopyrimidine is a potential analog of the nucleoside 4-amino-2-chloropyrimidine. It has shown to be an active inhibitor of bacterial growth in vitro and in vivo, with a low efficiency. 2-Hydroxy-4-hydrazinopyrimidine is cytotoxic to mammalian cells at high concentrations, but not to bacterial cells.

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Methyl 1-methylhydrazinecarboxylate is a dione that can be thermolyzed to form acetaldehyde. It is proposed to initiate the acetylation of lead tetraacetate by an unknown mechanism, leading to fragmentation and the formation of a postulated tetrazane intermediate. Methyl 1-methylhydrazinecarboxylate has been shown to react with solvents such as tetrahydrofuran and pyridine in a way that produces phthalic acid derivatives. This reaction proceeds via deamination and pyridine hydrolysis. Methyl 1-methylhydrazinecarboxylate undergoes temperatures between 70°C and 100°C.

Benzyl 1-methylhydrazinecarboxylate is the benzyl ester of methylhydrazinecarboxylic acid. It is a white crystalline solid that is soluble in chloroform, acetone, and methanol but insoluble in water. This compound has been shown to inhibit the activity of elastase, an enzyme that breaks down elastin. Benzyl 1-methylhydrazinecarboxylate inhibits pancreatic enzyme activity by forming covalent bonds with amino acid residues on the active site of these enzymes. The high yield and relative ease of synthesis make this compound a promising inhibitor for the production of pharmaceuticals or other products that require proteolytic enzymes.

2-Hydrazin-4-methylbenzothiazole is a synthetic compound that can be used as a coagulant in wastewater treatment. It is also used to reduce the amount of chloride in industrial effluents. 2-Hydrazin-4-methylbenzothiazole can be synthesized from tetraphenyl, which is a byproduct of the synthesis of lanthanum metal. This compound has been shown to be an effective reducer for wastewater treatment and can be recycled for use in other chemical reactions. The synthetic process requires hydrochloric acid and an acid catalyst, such as hydrochloric acid or sulfuric acid, to produce 2-hydrazin-4-methylbenzothiazole. The byproducts are evaporated with the water vapor during the evaporation process.

4-tert-Butylphenylhydrazine hydrochloride is a chemical that belongs to the group of indole compounds. It is usually used as an intermediate in the synthesis of other chemicals. 4-tert-Butylphenylhydrazine hydrochloride can be synthesized by reacting cycloheptanone with sulfuric acid and hydrazine hydrochloride. The reaction produces a mixture of products, including 4-tert-butylphenol, 2,4-dinitrophenol, phenol, 3-methylindole, and 2-nitrobenzaldehyde.

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4-Chlorobenzyl)hydrazine dihydrochloride is a chemical compound that belongs to the group of organic compounds. It is an inorganic acid and an inorganic base with a chloride counterion. 4-Chlorobenzyl)hydrazine dihydrochloride has been used as a pharmaceutical excipient for the production of oral liquids, tablets, capsules, and other dosage forms. The interaction between 4-Chlorobenzyl)hydrazine dihydrochloride and aluminium may lead to toxic effects on the kidneys.

2-Ethoxyphenylhydrazine hydrochloride is a hydrazine compound with the chemical formula C6H8N2. It has an intense yellow colour, but is colourless in concentrated solution. 2-Ethoxyphenylhydrazine hydrochloride is soluble in water and ethanol, but insoluble in ether and benzene. The hydrazine group of this compound reacts with nitrous acid to form a selenious acid derivative, which then undergoes ion exchange reactions to form a selenious salt. 2-Ethoxyphenylhydrazine hydrochloride is sensitive to light and air, and can undergo oxidation reactions that produce a range of coloured compounds.

Please enquire for more information about DL-3-(3,4-Dimethoxyphenyl)-2-methyl-2-hydrazinepropionicacidalanine including the price, delivery time and more detailed product information at the technical inquiry form on this page

Stability Not determined Applications 2-Hydroxyethylhydrazine is a reagent that is used in the preparation of dichlorophenoxymethyl-substituted pyrazolones and analogs as neuroprotectors against cytoxicity from protein aggregation of mutant superoxide dismutase 1. Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package References Trippier, P. C., et al.: Bioorg. Med. Chem. Lett., 22, 6647 (2012); Rothstein, J., et al.: Anal. Nuerol, 65, S3 (2009)

4-(tert-Butyl)phenylhydrazine hydrochloride (BPHH) is a chemical compound that has been used as a synthetic precursor to indole. It has been shown to be synthesized from cycloheptanone and sulfuric acid, with the addition of hydrazine hydrochloride and sodium acetate. BPHH can also be synthesized from 4-nitrobenzaldehyde and hydrazine sulfate, which is then reacted with ethanolamine.

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2-Ethylphenylhydrazine hydrochloride is a diazonium salt that catalyzes the reaction of nitrite with acetonitrile to produce an organic solvent. This organic solvent can be used in the production of various products, such as anti-inflammatory drugs, which are generally made from organic solvents. 2-Ethylphenylhydrazine hydrochloride is not a non-steroidal drug, but it does have anti-inflammatory properties. The impurities in this product are mainly hydrochloric acid and 2-ethylphenol.

Pentafluorophenyl hydrazine is an organic compound with the formula CHC(F)NH. It is a reactive species that participates in chemical reactions involving free radicals, such as oxidative DNA damage. Pentafluorophenyl hydrazine reacts with fatty acids to form trifluoroacetyl esters and pentafluorophenyl esters, which can be analyzed by gas chromatography-mass spectrometry. Pentafluorophenyl hydrazine is also used for the preparation of hydrochloric acid and carbonyl group derivatives. This compound can be prepared by reacting trifluoroacetic acid with phenol or phenol ethers under acidic conditions. Pentafluorophenyl hydrazine is a reactive species that participates in chemical reactions involving free radicals, such as oxidative DNA damage. Pentafluorophenyl hydrazine reacts with fatty acids to form trifluoroacetyl esters and pentaf

Isopropylhydrazine hydrochloride is a synthetic compound that has two geometric isomers. The tautomeric form of the compound is the allosteric modulator of the enzyme, hydroxyphenylpyruvate dioxygenase. This inhibitor binds to tyrosine kinases and blocks their activity. Isopropylhydrazine hydrochloride also has anticancer activity against ba/f3 cells and inhibits protein synthesis by binding to c1-6 alkyl groups on phospholipids in cellular membranes.

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Hydrazine hydrochloride is an antimicrobial agent that belongs to the group of hydrazines. It is a fatty acid that has been esterified with hydrochloric acid and hydrogen fluoride to form the corresponding ester hydrochloride. Hydrazine hydrochloride has shown to be effective against a variety of microorganisms. The antimicrobial activity of this drug may be due to its ability to inhibit fatty acid synthesis by binding to the active site of the enzyme, acyl-CoA:malonyl-CoA acyltransferase (MCT). Hydrazine hydrochloride also inhibits the production of pyrazoles, which are compounds that are known to induce autoimmune diseases in mice.

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