Hydrazines

<p>Please enquire for more information about 4-Bromo-2-fluorophenylhydrazine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Beta-Naphthoylhydrazine is a chemical inhibitor that binds to the enzyme diacylglycerol, which is involved in the synthesis of cholesterol. It has been shown to inhibit the uptake of cholesterol by ovary cells and human serum lipase. Beta-Naphthoylhydrazine potently inhibits reactive oxygen species and may be used in the treatment of inflammation and cancer.</p>

<p>N-Phenylhydrazinecarbothioamide is a chemical compound that is used in wastewater treatment. It is an organic molecule that is composed of hydrophobic and hydrophilic parts. The hydrophobic part, which contains the phenyl group, binds to the hydrophobic region of the cell membrane and causes the cell to lyse. The hydrophilic part has an affinity for water and can be used as an electrode material in electrochemical impedance spectroscopy. N-Phenylhydrazinecarbothioamide also has been shown to have antibacterial properties against human pathogens, including Mycobacterium tuberculosis, Clostridium perfringens, and Escherichia coli O157:H7. The compound has been shown to inhibit cervical cancer cells by inhibiting protein synthesis through inhibition of ribosomal activity and fragmentation assay analysis showed that N-phenylhydrazinecarbothioamide binds to copper ions at a coordination geometry of</p>

<p>5-Bromo-2-hydrazinopyrimidine is a heterocyclic compound with the chemical formula C5H4N3Br. It is used as reagent, high quality, and complex intermediate in fine chemicals, research chemicals, and speciality chemicals. It is also a versatile building block for many reactions in synthesis of other compounds.</p>

<p>(4-Iodophenyl)hydrazine hydroiodide is a synthetic compound that has shown anti-viral activity against HIV and cytomegalovirus. It also has anticancer properties and can be used to treat colon cancer. The compound binds to the nucleic acid in a number of ways, including by forming reversible covalent bonds with functional groups on the nucleic acid. These interactions are primarily due to its pyrazole ring and hydrazine moiety. (4-Iodophenyl)hydrazine hydroiodide is structurally similar to phenyldiazenyl, which exhibits photochromism and fluorescence properties. This similarity may account for the observed photochemical changes in the molecule when exposed to light.</p>

<p>3-Benzyloxy-phenyl)hydrazine hydrochloride is a chemical used in the synthesis of other organic compounds. It is a versatile building block that can be used in the preparation of complex compounds and useful intermediates. 3-Benzyloxy-phenyl)hydrazine hydrochloride is an excellent reagent for reactions involving electron-deficient alkenes, alkynes, and cyclic ethers. This compound also has applications as a pharmaceutical intermediate and as an analytical reference standard for chemical analyses.</p>

<p>4-n-Butylphenylhydrazine hydrochloride is a chromatographic reagent used in the analysis of compounds. It is a colorless crystalline solid that can be dissolved in water, ethanol, acetone, and other organic solvents. The most common use of 4-n-butylphenylhydrazine hydrochloride is for reversed-phase liquid chromatography (LC) analysis. In this application, it is typically used as an internal standard to calibrate the LC system. This compound also has applications in mass spectrometry, where it is used as an ionization reagent for electrospray and electrospray ionization (ESI) mass spectrometry. ESIMS data can be obtained by using this compound to ionize the analyte and then measure the molecular weight of the resulting ions using a mass spectrometer with an orbitrap or quadrupole detector. 4-n-Butylphenylhyd</p>

<p>4-Bromophenylhydrazine hydrochloride is a hydroxylated phenylhydrazine derivative that is used as an inhibitor of the enzyme tyrosinase. It has been shown to have significant antiproliferative activity against various cancer cell lines in vitro. 4-Bromophenylhydrazine hydrochloride has undergone extensive chemical study and its molecular structure has been elucidated by means of computational methods. The compound inhibits human tyrosinase by cleaving the C-C bond between the hydroxyl group and the phenyl ring, inhibiting tyrosinase activity and preventing melanin production. This process is reversible, so it can be used to maintain skin pigmentation at a desired level. 4-Bromophenylhydrazine hydrochloride also inhibits other enzymes that are related to pigment production, such as chymotrypsin and trypsin.</p>

<p>4-Chlorophenylhydrazine hydrochloride is a chemical compound that contains a pyrazole ring, chlorine and anhydrous sodium. This substance is used as a reactant in the production of diazonium salts. 4-Chlorophenylhydrazine hydrochloride also inhibits the reaction of benzodiazepines with their binding site on the GABA receptor, which prevents the formation of reactive intermediates. It has been shown to have an inhibitory effect on wastewater treatment and can be used for the treatment of acidic water. 4-Chlorophenylhydrazine hydrochloride reacts with fluorescence probes to form intermolecular hydrogen bonds and hydrogen bonds that are used for determining pH values in solution.</p>

<p>3,4-Dimethylphenylhydrazine hydrochloride is a chemical compound with high quality, which is a useful intermediate for the synthesis of complex compounds. It also has potential as a building block for the synthesis of other compounds. 3,4-Dimethylphenylhydrazine hydrochloride is used in research and development.</p>

<p>2-(Trifluoromethyl)phenylhydrazine hydrochloride is a carbamic acid derivative that is used in the synthesis of other compounds. 2-(Trifluoromethyl)phenylhydrazine hydrochloride can be used to make carboxylic acids and their derivatives, such as esters, amides, and anhydrides. It also reacts with hydrogen fluoride to form trifluoroacetic acid and hydrogen gas. This compound is an isomerizing agent that converts alkyl halides into their corresponding carbonyls. Hydrogen fluoride reacts with 2-(trifluoromethyl)phenylhydrazine hydrochloride to form trifluoroacetic acid and hydrogen gas.</p>

<p>4-(4-Hydrazinylbenzyl)-2-oxazolidinone is an ion-pair and a synthetic intermediate for the production of several pharmaceuticals. It is a white solid that can be crystallized from water or alcohol. The major impurities in this compound are diazotization and triphosgene, which are process-related impurities. 4-(4-Hydrazinylbenzyl)-2-oxazolidinone is used to produce butyraldehyde, which is used as a solvent in the production of pharmaceuticals. This compound undergoes hydrogenation reduction to form butyraldehyde after hydrolysis, which produces linearity. Hydrolysis can be carried out with either acidic or basic conditions.</p>

<p>2,3-Dimethylphenylhydrazine hydrochloride hydrate is a fine chemical that is used as a building block for research chemicals and speciality chemicals. It is also a high quality reagent and useful scaffold for the synthesis of complex compounds. 2,3-Dimethylphenylhydrazine hydrochloride hydrate is versatile, being able to be used in reactions involving nucleophilic substitution or elimination reactions. This product can be used in reactions involving the formation of carbon-carbon bonds.</p>

<p>2-Naphthylhydrazine is a synthetic chemical that has an affinity for substrate binding sites. It is used as an inhibitor of monoamine oxidase (MAO) and can be used to study the function of MAO. 2-Naphthylhydrazine binds to the enzyme MAO, preventing it from breaking down amines, an important class of neurotransmitters. 2-Naphthylhydrazine also inhibits the activity of cytochrome P450 reductase, which is involved in drug metabolism. This chemical can be used in the synthesis of indocyanine green and methylbenzene. The reactivity of hydrazines with carbonyl groups in amines and anhydrous sodium phosphate leads to bond cleavage and release of ammonia gas.</p>

<p>2-Nitrophenylhydrazine is a drug that is used as an anti-inflammatory agent. It is a nonsteroidal anti-inflammatory drug (NSAID) that acts by blocking the production of prostaglandins in the body, preventing inflammation and pain. 2-Nitrophenylhydrazine can be used to treat conditions such as arthritis, gout, and rheumatoid arthritis. This drug also has the ability to remove organic contaminants from water. 2-Nitrophenylhydrazine binds with fatty acids in wastewater treatment plants, forming an insoluble complex that precipitates out of solution. The compound inhibits the activity of hydrogen bond and methyl ethyl groups, which are needed for the biosynthesis of polyunsaturated fatty acids like phytanic acid and diphenyl ether.</p>

<p>3,5-Dimethylphenylhydrazine hydrochloride is a chemical compound that is used as a reagent in biochemistry and molecular biology. It reacts with proteins to form stable covalent bonds. This reaction can be used to modify the active site of an enzyme or to create affinity labels for protein purification. 3,5-Dimethylphenylhydrazine hydrochloride can also react with a pyrrole group on the side chain of phenylalanine residues to form an affinity label that allows it to bind specifically to myoglobin. The modification of myoglobin alters its structure and its ability to bind oxygen, which results in a shift in the wavelength at which it absorbs light.</p>

<p>4-Sulfonamidephenylhydrazine HCl is a sulfonamide that inhibits the enzyme Cox-2, which is involved in inflammation. It also has anti-inflammatory activity and has been shown to inhibit the growth of fungi. 4-Sulfonamidephenylhydrazine HCl is an antifungal agent used for the treatment of dermatophytic infections such as tinea pedis and tinea cruris. The chemical structure of 4-Sulfonamidephenylhydrazine HCl consists of a methyl sulfone group linked with a pyrazole ring and a hydrazine hydrate group. The carbonic acid moiety in this compound stabilizes the pyrazole ring by forming hydrogen bonds with the nitrogen atom and oxygen atom on either side of it. This allows for the formation of two resonance structures to be maintained, which make it more stable than other similar compounds without this moiety.</p>

<p>3-Chloro-6-hydrazinopyridazine is a redox potential probe that has high cytotoxicity. It is used in the detection of the redox potential of hydrogen peroxide and nitric oxide by a turbidimetric method. 3-Chloro-6-hydrazinopyridazine can be used as a fluorogenic probe for the detection of chlorine atoms in biological systems. 3-Chloro-6-hydrazinopyridazine has been shown to enhance cancer cell growth and inhibit matrix metalloproteinase (MMP) activity. The biological properties of this compound are due to its ability to form intermolecular hydrogen bonds with nitrogen atoms, which leads to a dihedral angle that favors its binding to proteins.</p>

<p>1-Boc-2-[4-(2-pyridinyl)benzylidene]hydrazine is a compound that is used in the recycling of organic compounds. The sodium formate, which is a byproduct of biodiesel production, can be recycled using this compound. It can also be used to recycle tert-butyl carbazate, which is an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-Boc-2-[4-(2-pyridinyl)benzylidene]hydrazine has been shown to be effective at high pressures and temperatures, which make it useful for synchrotron experiments on cell parameters. This compound has been shown to have anisotropic properties due to its coordination with magnesium.</p>

<p>4-Benzyloxyphenylhydrazine HCl is a pro-apoptotic agent that is used in the treatment of cancer. It induces apoptosis by binding to estrogen receptors and modulating their activity. This drug has been shown to induce apoptosis in breast cancer cells (MCF-7) and inhibit the growth of prostate cancer cells (LNCaP). 4-Benzyloxyphenylhydrazine HCl binds to the estrogen receptor, which causes it to dimerize with other estrogen receptors, resulting in increased transcription of genes that regulate programmed cell death. It also inhibits the production of proteins that are vital for cell division, leading to apoptosis. Hydrolysis by hydrochloric acid or chloride leads to phenylhydrazone formation, which may react with diazo compounds such as benzaldehyde and nitrosyl chloride to form an aromatic hydrocarbon product.</p>