Ammine

3-Amino-4-bromophenol is an industrial chemical that is used in the diazotization and reduction reactions. 3-Amino-4-bromophenol can be synthesized by reacting hydrazine with iron oxide and nitrite in a condition of acetone and sodium nitrite. The product yield for this reaction is about 90%. 3-Amino-4-bromophenol crystallizes from acetone as a white powder.

2-(3,4,5-Trimethoxyphenyl)ethylamine (TMPEA), also known as 3,4,5-trimethoxyamphetamine or 3,4,5-trimethoxyphenethylamine is a psychoactive agent that is structurally related to amphetamine and mescaline. It is a precursor to TMA which is an hallucinogenic drug. TMPEA has been shown to have dose-dependent effects on locomotor activity in mice and rats. In addition, it has been found to bind with high affinity to 5HT2A receptors in the rat brain. This compound can be prepared by reacting trifluoroacetic acid with 2-(3,4,5-trimethoxyphenyl)ethanamine. The sample preparation of this compound may be performed using human serum or lophophora plants.

<p>2-(2,3-Dimethylphenoxy)ethylamine is a versatile building block that can be used for the synthesis of various complex compounds. It has been used as a reagent in research and as a speciality chemical. 2-(2,3-Dimethylphenoxy)ethylamine is useful in the synthesis of pharmaceuticals, agrochemicals, and other chemicals. This product is also a high quality intermediate that can be used for the production of active pharmaceutical ingredients (APIs). 2-(2,3-Dimethylphenoxy)ethylamine can also be used to produce scaffolds for organic syntheses.</p>

Please enquire for more information about Ethyl 4-(((tert-butyl)amino)thioxomethyl)piperazinecarboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride is a versatile building block that can be used in the synthesis of complex compounds. This compound is also a useful reagent, speciality chemical, and reaction component. cis-(+/-)-2-[(N-Benzyl-N-methyl)aminomethyl]-1-(3-methoxyphenyl)cyclohexanol hydrochloride has been shown to be a valuable scaffold for research chemicals with high quality.</p>

<p>4-Amino-3-chlorobenzonitrile is a ligand that binds to the heme of cytochrome P450 (CYP) enzymes. It has been shown to have a pharmacokinetic profile in rats and mice with lung diseases, which is similar to that of 4-amino-2-bromobenzonitrile. This ligand inhibits CYP enzymes by competing with endogenous substrates for binding sites on the heme, leading to an increase in the metabolism of drugs such as carbonyl drugs. 4-Amino-3-chlorobenzonitrile also has potent inhibitory effects on efflux pumps in cells and may be used to treat drug resistant bacteria.</p>

2-[(2-Amino-5-methoxyphenyl)dithio]-4-methoxyaniline is a high quality chemical reagent that can be used as a useful intermediate in the synthesis of a variety of complex compounds. This compound has been shown to have a wide range of uses, including as a building block in the synthesis of speciality chemicals and research chemicals. 2-[(2-Amino-5-methoxyphenyl)dithio]-4-methoxyaniline is an important reaction component that can be used in many organic reactions, such as coupling, condensation, substitution, elimination, nucleophilic addition and reduction.

1,2,2,3,3,4,4,5,5,6,6-Undecafluoro-N,N-Bis(1,1,2,2,2-Pentafluoroethyl)Cyclohexan-1-Amine is an efficient mitochondrial respiratory uncoupler that has been shown to increase the rate of oxidative phosphorylation in rat liver. It is also a membrane permeable compound that can be incorporated into micelles. This drug has been shown to have suboptimal effects on morphology and mitochondrial function in mice. 1,2 2 3 3 4 4 5 5 6 6 -Undecafluoro-N N Bis (1 1 2 2 2 2 Pentafluoroethyl) Cyclohexan 1 Amine has potential applications as a therapeutic agent for patients with respiratory disorders such as cystic fibrosis or chronic obstructive pulmonary disease.

<p>Gamma-aminopropyl mercaptan is a versatile building block that is used in the synthesis of complex organic compounds. It can be used as a reagent for research and as a speciality chemical. Gamma-aminopropyl mercaptan has been found to be useful in the synthesis of drugs, pesticides, and other biologically active substances. The compound has also been found to have anti-inflammatory properties.</p>

<p>2-Amino-4-fluorobenzoic acid is a nitrogenous heterocyclic compound. It is an analog of the epidermal growth factor (EGF), which can bind to the EGF receptor and stimulate cell growth and differentiation. 2-Amino-4-fluorobenzoic acid has been shown to have anticancer activity in vitro, as well as in vivo. The synthetic process for this compound involves nitrous acid, hydrochloric acid, and frequency reactions. This product is used industrially for the preparation of other compounds.</p>

<p>4-Phenoxybenzylamine is a cardiac stimulant that belongs to the group of l-type calcium channel blockers. It is a highly potent and selective blocker of voltage-gated L-type calcium channels in myocytes, which are cells that make up the muscle tissue of the heart. 4-Phenoxybenzylamine has been shown to be effective against resistant strains and can be used to optimize sodium channels in recombinant cells. This drug also blocks potassium channels, which may lead to an antiseizure effect. 4-Phenoxybenzylamine is hydrophobic and can be given orally.<br>END&gt;&gt;</p>

<p>Rhodamine B isothiocyanate (RBITC) is a fluorescent dye that can be synthesized by reacting 2,4-dinitrobenzene with aniline. RBITC fluoresces in the visible spectrum, but has also been shown to fluoresce in the near infrared region of the electromagnetic spectrum. The microstructural and morphological properties of RBITC have been studied using simulations methods such as molecular dynamics and Monte Carlo techniques. RBITC has a spinodal decomposition behavior when heated or cooled, which can be used to study transport pathways in solids. These pathways are motivated by connectivity and topological techniques.</p>

<p>Please enquire for more information about [1-(Pyrrolidin-1-ylcarbonyl)propyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Ammonium oxalate monohydrate is a white crystalline solid that has a molecular weight of 104.096 g/mol and a melting point of 129°C. Ammonium oxalate monohydrate is a salt formed by the reaction of ammonium with oxalic acid. It is used as an experimental model for wastewater treatment, where it is able to remove ammonium ions from wastewater. This material also reacts with sodium salts to form hydrogen bonding interactions, which can be measured using analytical methods such as X-ray diffraction or electrochemical impedance spectroscopy.</p>

<p>D-alpha-Aminosuberic acid is a tetrapeptide with transcriptional regulatory properties. It has been shown to have minimal toxicity and lacks enzymatic inactivation, making it an attractive candidate as a drug for the treatment of cancer. D-alpha-Aminosuberic acid has been found to activate rat striatal cells in vitro and may have immunomodulatory effects that could be beneficial in infectious diseases. Clinical studies are needed before this drug can be used for these purposes.</p>

The molecular formula of methylamine is CH3NH2. It has an intramolecular hydrogen bond that stabilizes the molecule. Methanol is a good solvent for methylamine, and its ph optimum is 10. Methylamine reacts with hydrochloric acid to form a molecule consisting of two hydrogen atoms and one nitrogen atom (H3N-HCl). The locomotor activity of rats was reduced by methylamine after administration at doses greater than 200 mg/kg. The uptake of methylamine in human serum was increased by α-tocopherol, an antioxidant. Methylamine reacts with amines to form products with different properties, including alkanoic acid and fatty acid. Methylamine binds to the type strain receptor but not other strains or species of bacteria.

<p>3,4-Dimethyl-6-D-ribitylaminobenzene is a versatile building block that can be used as a reagent, speciality chemical, or useful scaffold in organic chemistry. 3,4-Dimethyl-6-D-ribitylaminobenzene is also known as 3,4-dimethylaniline and CAS No. 3051-94-3. It is an important intermediate in the production of polyurethanes and amines. This compound has been shown to be an effective building block for the synthesis of other compounds related to pharmaceuticals, pesticides, and agrochemicals.</p>

<p>3-Nitrobenzylamine HCl is an intermediate in the synthesis of peptides. This compound is used to produce polypeptides and can be immobilized on a solid support for high yield production. 3-Nitrobenzylamine HCl can be covalently linked to a solid support by reacting with an activated carboxyl group and can undergo conformational changes upon irradiation with ultraviolet light or azobenzene derivatives. 3-Nitrobenzylamine HCl has been used in solid phase peptide synthesis, a technique that produces polypeptides at high yields. It is also used as a substrate for NMR techniques, which are useful for determining the nature of the molecule and its potentials.</p>

<p>2-Amino-3-chloro-5-nitrobenzonitrile is a hydroxyalkyl compound. It is sensitive to light, sulfamic acid and heat. The compound has been expressed in E. coli, but it is not possible to crystallize it due to its sensitivity to ph changes and organic solvents. The substance can be used as a dyestuff or dye intermediate. Due to its stability in crystal form, this substance can also be used as a raw material for the production of nitrite.</p>

(1-tert-Butylcyclopropyl)amine hydrochloride is a ciprofloxacin analog that inhibits the growth of bacteria by binding to the enzyme DNA gyrase. It also prevents the cleavage of RNA and protein synthesis which blocks the production of new cells in bacterial colonies. The drug has a broad spectrum of activity against Gram-positive and Gram-negative organisms, including methicillin-resistant Staphylococcus aureus (MRSA). The drug has been shown to be effective against isolates resistant to ciprofloxacin, such as Enterobacteriaceae, Pseudomonas aeruginosa, Acinetobacter baumannii, and Klebsiella pneumoniae. (1-tert-Butylcyclopropyl)amine hydrochloride binds to microtubules and disrupts the cell division process during mitosis. This drug has been shown to inhibit spindle formation in

<p>3-Aminobenzanilide is an organic compound that is used as a starting material in the synthesis of other compounds. It is also used in the synthesis of ethylenediamine and benzamide, which are used in the production of rubber. 3-Aminobenzanilide can be synthesized by reacting benzoyl chloride with ammonia or ethylenediamine. The reaction with ammonia produces 3-aminobenzamide, while that with ethylenediamine produces 3-aminobenzene. This compound has been shown to induce pentylenetetrazol convulsions and to produce neurological symptoms when administered at high doses.</p>

1-Aminoindane HCl is an inhibitor of the enzyme aminotransferase, which is involved in the metabolism of amines. It binds to the active site of this enzyme and prevents it from catalyzing its usual reaction. 1-Aminoindane HCl has been shown to inhibit 5-hydroxytryptamine uptake and release in rat brain synaptosomes. This drug also inhibits the binding of a number of drugs (e.g., amphetamine) to their receptors on plasma membranes and blocks the binding of drugs such as pargyline and α-methylparatyrosine to their receptors on mitochondria. 1-Aminoindane HCl is also a competitive inhibitor for primary amines such as tyramine and phenylethylamine.

<p>Please enquire for more information about 2-[[(4-Acetylphenyl)amino]methylene]-5,5-dimethyl-1,3-cyclohexanedione including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>5-Amino-4,6-dichloropyrimidine is a fluorescent probe that can be used in the detection of nucleophiles. It has been shown to inhibit the growth of cells infected with herpes simplex virus and hl-60 cells. This compound has also been shown to have nicotinic acetylcholine receptor activity and can be used as an analog for purines. The nitrogen atoms in this molecule are responsible for its anti-cancer properties. 5-Amino-4,6-dichloropyrimidine binds to epidermal growth factor (EGF) and blocks its binding site on the cell surface, reducing cancer cell proliferation. Benzyl groups on either end of this molecule act as a protective group against acid hydrolysis, making it stable in acidic environments such as stomach acid. This drug also contains chlorine atoms that make it easy to synthesize and purify by reacting with trifluoroacetic acid.</p>

[2-(3-Methylphenoxy)ethyl]amine hydrochloride is a fine chemical that is a versatile building block. It can be used as a reaction component in the synthesis of complex molecules and as a reagent for the synthesis of speciality chemicals and research chemicals. This compound has been shown to react with nitric acid to form an amine salt, which is useful for the manufacture of pharmaceuticals. [2-(3-Methylphenoxy)ethyl]amine hydrochloride can also be reacted with chloroacetic acid to form an amine salt, which is useful for the manufacture of pesticides. The high quality and versatility of this compound make it a useful scaffold for many types of reactions.

Please enquire for more information about 2-[Amino(2-oxo-2H-1-benzopyran-3-yl)methylene]propanedinitrile including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>tert-Butyl ((1S,2R)-2-aminocyclopentyl)carbamate is a fine chemical with versatile uses as a building block in the synthesis of more complex compounds. It is used as an intermediate in the production of pharmaceuticals and research chemicals. This compound has a CAS number of 445479-01-6. The tert-butyl group can be removed from this molecule in order to form a variety of different building blocks. Tert-butyl ((1S,2R)-2-aminocyclopentyl)carbamate is a high quality reagent that can be used for many reactions, such as amination, amidation, and carbamoylation.</p>

<p>4-Aminoquinaldine is a metastable redox potential compound that has been shown to reversibly reduce the mitochondrial membrane potential in leishmania. It also has been shown to have antimicrobial properties and is able to inhibit the growth of bacteria through hydrogen bonding interactions. 4-Aminoquinaldine is most effective against gram-positive bacteria and has an acidic pH, with a pKa of 3.4. The reaction mechanism for 4-aminoquinaldine involves nucleophilic attack at the C5 position of the quinolinium ring followed by elimination of H2O from the S2 position.</p>

<p>Tris(hydroxymethyl)aminomethane acetate is a compound that binds to antigen binding molecules in biological samples. It is a polymerase chain reaction (PCR) reagent and is used to prepare samples for PCR analysis. Tris(hydroxymethyl)aminomethane acetate has been shown to bind with receptor activity in the treatment of infectious diseases and metabolic disorders, such as alopecia areata and diabetes mellitus. Tris(hydroxymethyl)aminomethane acetate also stabilizes DNA templates for PCR analysis by preventing dNTPs from hydrolyzing prematurely. This prevents the formation of stable complexes with nucleotides, which may be useful in clinical pathology or plant physiology.</p>

The heptafluoro-N,N-bis(1,1,2,2,2-pentafluoroethyl)propane-1-amine is a chemical compound that is used as an additive. This additive has been shown to be efficient in the removal of organic compounds such as benzene and toluene from water. It can also be used for the treatment of biofuel waste water. The heptafluoro-N,N-bis(1,1,2,2,2-pentafluoroethyl)propane-1-amine has shown to have a wavelength absorbance profile with a maximum at 370 nm in the ultraviolet region of the electromagnetic spectrum. This compound can also be used for barcoding and identification purposes in applications where human contact is required.

<p>2-Chloro-9-cyclohexyl-N-[4-(4-morpholinyl)phenyl]-9H-purin-6-amine is a synthetic chemical that has been used as a reaction component, reagent, and high quality research chemical. It has CAS No. 737005-53-7 and can be used as a useful scaffold for the synthesis of complex compounds. Other names for this compound are: 2C9H6N2ClN4P</p>

<p>Phenoxybenzamine hydrochloride is a drug with pharmacological properties, which is used in the treatment of carcinoid syndrome. It is a combination therapy group that can be used to treat patients with neurological disorders. Phenoxybenzamine inhibits the activity of the 5-HT2 receptors and has been shown to reduce neuronal death. In addition, it has been shown to increase chemiluminescence in cells infected with HIV. Phenoxybenzamine also has effects on cardiac function and can be used to treat congestive heart failure as well as high levels of natriuretic peptides in maternal blood during pregnancy. It has also been shown to be effective against infectious diseases, such as tuberculosis and malaria.</p>

Bromotrimethylammoniumbimane bromide is a fluorescent molecule that can be used as a probe for protease activity. It is also used to study the α1 subunit of the human histone deacetylase (HDAC) complex, which plays an important role in HIV infection and autoimmune diseases. The redox potential of Bromotrimethylammoniumbimane bromide has been shown to be dependent on its basic structure, with the disulfide bond being the most reactive. This chemical has been shown to have cytosolic Ca2+-dependent effects on cell signaling pathways, including induction of apoptosis and modulation of protein phosphatases.

4-(Methylsulfinyl)-1-butylamine is a fine chemical that is used as a versatile building block in the synthesis of complex compounds. It is also useful as a research chemical and reagent. 4-(Methylsulfinyl)-1-butylamine has been shown to be a high quality chemical with CAS number 187587-70-8.

m-Aminophenolsulfate is a sulfonated derivative of m-aminophenol. It has been used for wastewater treatment and as an analytical reagent for the determination of p2 group substances, such as sulfa drugs. It is also used in pharmaceutical preparations and human serum. m-Aminophenolsulfate may be activated by hydrochloric acid to form a reactive intermediate (m-aminophenoxy radical) that reacts with electron acceptors such as oxygen or nitrous oxide to generate reactive oxygen species. In this way, m-aminophenolsulfate can act as a broad-spectrum antimicrobial agent against both Gram negative and Gram positive bacteria. The mechanism of this reaction is adsorption on the bacterial cell wall, which leads to cell death through osmotic lysis or disruption of membrane integrity.

2-Amino-3-bromo-5-methylbenzoic acid is a fatty acid that belongs to the group of undescribed organic acids. It is found in soil as well as in organisms such as bacteria and fungi. The 2-Amino-3-bromo-5-methylbenzoic acid molecule has been shown to be an antibiotic, inhibiting the growth of bacterial strains belonging to the phyla Actinobacteria and Proteobacteria. It may also be present in plants, where it is channeled out through the roots. This fatty acid also has nucleobase properties, which are essential for DNA replication.br>br> span style="font-size: 12px;">2 Amino 3 bromo 5 methyl benzoic acid (2ABMB) was first isolated from soil samples collected from a site near Beijing, China. It is one of many undescribed organic acids that are found

<p>4-Diethylaminobenzaldoxime is a reaction component that is used in the synthesis of complex compounds. It has been shown to be a useful scaffold for the construction of novel chemical entities. It also has high quality, and can be used as a reagent in research or as a speciality chemical. 4-Diethylaminobenzaldoxime is versatile and can be used as an intermediate or building block in organic chemistry. This chemical has CAS No. 54376-65-7 and is classified as a fine chemical.</p>

<p>Please enquire for more information about 2-[Methyl[(tridecafluorohexyl)sulphonyl]amino]ethyl acrylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2-(4-Methyl-4H-1,2,4-triazol-3-yl)ethanamine dihydrochloride is a high quality chemical used as a building block in the synthesis of complex compounds. It is an intermediate in the manufacture of research chemicals, reagents and speciality chemicals. 2-(4-Methyl-4H-1,2,4-triazol-3-yl)ethanamine dihydrochloride is also a versatile building block that can be used in reactions to produce useful scaffolds. CAS No. 1158631-54-9</p>

<p>Didecyl dimethyl ammonium chloride is a quaternary ammonium compound. It has been used in toxicity studies on animals and as an analytical reagent for the detection of ammonium and chloride ions in the presence of copper chloride. Didecyl dimethyl ammonium chloride is also used as a disinfectant, with some reports of its use to treat infectious diseases. It has been found to have some effect on diptera larvae, but has no effect on epithelial mesenchymal cells. The phase transition temperature of this product is between -10°C and +20°C. This product can be purified by preparative high-performance liquid chromatography (HPLC).</p>

Ergotamine D-tartrate is a drug that belongs to the group of nonsteroidal anti-inflammatory drugs. It is used in the treatment of migraine and other headaches. Ergotamine D-tartrate inhibits the production of nitric oxide, which has been shown to be involved in the process of angiogenesis. This drug also has long-term efficacy for headaches and migraines, as well as an anti-migraine effect. Ergotamine D-tartrate binds to specific receptors on neurons called alpha2 adrenergic receptors, which are located on blood vessels in the brain and have been implicated in migraine pathophysiology. These receptors are not present on vessels elsewhere in the body, which makes ergotamine a more selective drug for migraine than other nonsteroidal anti-inflammatory drugs.

<p>(2S,6R)-2,6-Diaminoheptanedioic acid is an antimicrobial agent that inhibits bacterial growth by binding to the Toll-like receptor 2 (TLR2) and Toll-like receptor 4 (TLR4). It has been shown to inhibit the production of IL-12 in a dose-dependent manner. The crystal structure of the complex between (2S,6R)-2,6-diaminoheptanedioic acid and TLR4 reveals that this compound binds to TLR4 at the interface between its extracellular domain and transmembrane domain, which disrupts the interaction between TLR4 and its ligands. This compound also inhibits calcium uptake by gram-positive bacteria such as Staphylococcus aureus and Enterococcus faecalis. (2S,6R)-2,6-Diaminoheptanedioic acid may be used for wastewater treatment because it</p>

<p>Enisamium iodide is an antiviral agent synthesized from isonicotinic acid derivatives, which is a small molecule inhibitor of viral RNA polymerase. It interferes with the replication process of various viruses by inhibiting the activity of RNA-dependent RNA polymerase, crucial for viral genome synthesis. Enisamium iodide exhibits its antiviral properties by impeding the replication of single-stranded RNA viruses, thereby mitigating viral propagation in host cells.</p>

<p>O-(2,4-dinitrophenyl)hydroxylamine is a synthetic compound that binds to the enzyme bound site of the cap-dependent endonuclease. It is an inhibitor of influenza virus replication in vitro and has shown inhibitory activity against murine leukemia virus. O-(2,4-dinitrophenyl)hydroxylamine is also a model for the study of aminoglycoside antibiotics. The compound inhibits aminoglycoside-induced protein synthesis in eukaryotic cells and may be useful in understanding the mechanism of action and resistance to these antibiotics.</p>

N,O-Dimethylhydroxylamine hydrochloride is a methyl ketone that is used as an affinity ligand. It is synthesized by the reaction of hydrochloric acid and amide. N,O-Dimethylhydroxylamine hydrochloride has been shown to have growth factor β activity and can be used in the synthesis of analogs. The compound has been shown to have biological properties and can be used as a synthetic pathway for other compounds. N,O-Dimethylhydroxylamine hydrochloride reacts with hydroxyl groups in the presence of a base to form an ether linkage or with amines to form an amide linkage. This compound also has nmr spectra that are similar to those of growth factor.

4,6-Diamino-5-(formylamino)pyrimidine hydrochloride (4,6-dA-FAP) is a nucleic acid polymerase chain reaction probe that binds to damaged DNA. It can be used to identify the presence of nuclear DNA in human polymorphonuclear leukocytes. 4,6-Diamino-5-(formylamino)pyrimidine hydrochloride is also known as a redox indicator and has been shown to have antioxidant properties. This drug is not toxic at physiological levels, but it has been found to be an inhibitor of a number of enzymes. 4,6-Diamino-5-(formylamino)pyrimidine hydrochloride has been used in studies on cancer tissues and biological samples.

<p>3-Amino-pentanoic acid is a natural product that is synthesized by the biosynthesis of the amino acid valine. 3-Amino-pentanoic acid is an intermediate in the synthesis of cyclic lipopeptides, which are important for biological activity. The biological properties of this compound are not yet fully known, but it has been shown to bind to receptors and inhibit their function. Chronic treatment with 3-amino-pentanoic acid has been demonstrated to be effective against infectious diseases caused by mutant strains of bacteria such as Escherichia coli and Salmonella enterica serovar Typhimurium. This drug has also been shown to have an effect on bacterial DNA gyrase and protein synthesis. It is possible that 3-amino-pentanoic acid may be used as a pharmaceutical drug for the treatment of infectious diseases in humans.</p>

<p>(PEO)3-Mono-amine is a glucose analogue that is taken up by cells via glucose transporters. It has been shown to inhibit the growth of cancer cells in vitro and in vivo. This molecule can be conjugated with drugs, proteins, or other molecules for targeted delivery to tumor cells. The chemical stability of (PEO)3-Mono-amine makes it a potential candidate for use in on-line glucose sensing devices.</p>

<p>Carbonic acid ammonium zirconium salt is a high quality, complex compound that is used as a reagent and an intermediate. It has been shown to be useful in the synthesis of fine chemicals and speciality chemicals. Carbonic acid ammonium zirconium salt can also be used as a building block for research chemicals and versatile building blocks.</p>

2-[(4-Isopropylphenyl)amino]nicotinic acid is a fine chemical, useful building block, research chemicals, reagent, speciality chemical and a versatile building block. It is an intermediate in organic synthesis and can be used to form many types of compounds. This compound also has many applications in the field of chemistry including use as a reaction component or as a scaffold. 2-[(4-Isopropylphenyl)amino]nicotinic acid is used in the production of pharmaceuticals, pesticides and other industrial chemicals.

<p>2-(4-Bromophenyl)-1,3-benzoxazol-5-amine is an organic compound with a molecular formula of C14H10BrN2O and a molecular weight of 270.44 g/mol. 2-(4-Bromophenyl)-1,3-benzoxazol-5-amine is white to off white crystalline powder that is soluble in ether and ethanol but insoluble in water. It is a versatile building block for the synthesis of other fine chemicals. This compound has been used as a research chemical and as an intermediate in the synthesis of complex compounds.</p>

Please enquire for more information about 2-Amino-4-(trifluoromethyl)thiazole-5-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Propyloxybenzylamine is a high quality reagent, useful for complex compound synthesis. It is an intermediate in the production of other compounds and has been used as a building block for the synthesis of many diverse chemicals. 4-Propyloxybenzylamine is also a versatile building block that can be used in reactions to produce speciality chemicals and research chemicals. This compound can be used as a reaction component in the synthesis of a wide range of chemical compounds.

Please enquire for more information about 2-(3,4-dimethoxyphenyl)-3-((4-chlorophenyl)amino)inden-1-one including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>Please enquire for more information about Methyl 3-amino-6-methylthieno[2,3-b]pyridine-2-carboxylate including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

Fosfomycin is a broad-spectrum antibiotic that is effective against bacteria, especially those resistant to other antibiotics. Fosfomycin acts by inhibiting the synthesis of bacterial cell wall mucopeptides. It binds to the terminal amino acid residues of the peptidoglycan polymer and prevents cross-linking, which is essential for the formation of a functional cell wall. Fosfomycin also has low toxicity in humans and can be used as an alternative treatment for pandemic Covid-19 virus. This drug can be detected at very low concentrations in plasma samples using liquid chromatography with mass spectrometry (LCMS), which makes it useful for analysis of biological fluids. Fosfomycin can be prepared by reacting sodium carbonate and calcium carbonate with fosfomycin hydrochloride in water. The reaction products are then purified by liquid chromatography, leading to high detection levels. Fosfomycin phenylethylamine is an

<p>N,N'-Bis(2-hydroxyethyl)ethylenediamine is a chemical compound that has been used in the synthesis of a number of drugs. It is an alkanolamine that can be synthesized by the reaction of piperazine with hydroxyethylamine. In addition, N,N'-Bis(2-hydroxyethyl)ethylenediamine has been shown to have biological properties such as being able to stimulate the production of antibodies and citric acid in animals. It also has structural similarities to vitamin B12 and exhibits hydrogen bonding between its molecules. N,N'-Bis(2-hydroxyethyl)ethylenediamine is biodegradable and does not produce significant environmental effects when released into water or soil.</p>

<p>5-Carboxymethoxytryptamine hydrochloride (5CMT) is a chemical compound that belongs to the group of useful building blocks. It is a versatile intermediate that can be used in the synthesis of many important compounds. 5CMT reacts with amines and alcohols to form amides and esters. It also reacts with carboxylic acids to form acid halides and anhydrides. 5CMT has been shown to be a useful scaffold in organic synthesis, as it can be converted into various derivatives. 5CMT is soluble in water, methanol, ethanol, acetone, and dichloromethane.</p>

5,6-Diamino-1,3-dipropyluracil (DAU) is a synthetic drug that acts as an adenosine receptor antagonist. DAU binds to the adenosine receptors in the brain and inhibits the binding of adenosine, which may result in an anti-congestive effect. DAU has been found to be a potent inhibitor of the A2A adenosine receptor at nanomolar concentrations. This inhibition may be due to its ability to form covalent bonds with the receptor or its affinity for or blocking of agonist binding sites on the receptor. It also has been shown to have affinity for dopamine receptors, although it is not yet known if this activity contributes to its anti-congestive effects.

2,6-Diaminopurine hemisulfate salt is a fine chemical that can be used as a building block for research chemicals, reagents, and specialty chemicals. It has been shown to be useful in the synthesis of various types of complex compounds. 2,6-Diaminopurine hemisulfate salt is also versatile in the sense that it can be used as an intermediate in reactions or as a scaffold for chemical synthesis. This product has CAS number 69369-16-0.

N-tert-Butoxycarbonyl tyramine is a molecule that has been shown to have anti-tuberculosis properties. It is synthesized by reacting N-Boc-tyrosine with chloroform in the presence of an acid catalyst. The reaction product is a zwitterion, which can be converted to an ionic form by treatment with mineral acids or phosphoric acid. The chloride ion is released from the molecule and reacts with phosphate ions to form hydroxyapatite, which is used as a bone substitute. This compound also has potential for use in cancer treatments due to its ability to inhibit cell proliferation and induce apoptosis in cancer cells. The uptake of this drug was studied using caco-2 cells cultured on plastic membrane inserts in contact with phosphate buffered saline (PBS). The results showed that it had a high uptake rate and concentration in these cells. This compound was also found to have an inhibitory effect on phosphatase

<p>Initiates acrylamide polymerization in combination with ammonium persulfate</p>

Use as a positive control when detecting nitroreductase activity

Please enquire for more information about 4-(2,5-Dimethoxyphenyl)-1,3-thiazol-2-amine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>5,6-Diethyl-2,3-dihydro-1H-inden-2-amine hydrochloride is the salt form of a chemical compound that belongs to the group of acetylation agents. This chemical is highly soluble in water and is used as a reagent to acetylate amines. The industrial process for this compound begins with an acetone solution of 2,3-dihydroindene. Acetyl chloride reacts with 2,3-dithiobenzoyl chloride in an acid environment to produce 5,6-diethyl-2,3-dihydroindane. The product is treated with hydrogen chloride gas to produce 5,6-diethyl-2,3 dihydroindanamine hydrochloride. This compound has been shown to be toxic for aquatic life and can cause environmental pollution when released into the environment.</p>

4-(Dimethylaminobenzylidene)rhodanine is a monosodium salt of the drug rhodanine. Rhodanine is a small-molecule, kinetically stable, and surface active agent that inhibits tumor growth by binding to sulfamoyl chloride, inhibiting the synthesis of DNA. Rhodanine has been shown to inhibit the growth of colon cancer cells in mice and human leukemia cells in vitro. This drug also inhibits the proliferation of erythrocytes and platelets. Rhodanine binds to chloride ions on cell surfaces and forms a complex with silver ions that can then be detected by electron microscopy or profiling studies using hydroxide solutions. The efficacy of 4-(dimethylaminobenzylidene)rhodanine as an anticancer agent is dependent on its concentration. A blood sample containing 4% dimethylaminobenzylidene rhodanine was found to have anti-t

<p>Please enquire for more information about 4,6-Diamino-2-nitro-m-xylene including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>3-Aminobenzamide is a drug that has been shown to be effective in the treatment of temozolomide-induced neuronal death. 3-Aminobenzamide inhibits the synthesis of ATP and blocks its binding to the atp-binding cassette transporter, which prevents the transport of this nucleotide into cells. This results in cell death due to insufficient energy metabolism and inability to repair DNA damage. 3-Aminobenzamide also increases production of reactive oxygen species, which are involved in reperfusion injury and myocardial infarcts. 3-Aminobenzamide is used as a model system for studying DNA repair and energy metabolism.</p>

<p>N-Ethylmethylamine is a compound that is used in the preparation of fatty acid methyl esters, which are used as biomarkers for assessing lipid metabolism. It has also been shown to be an effective antimicrobial agent against bacteria, such as Pseudomonas aeruginosa and Escherichia coli. N-Ethylmethylamine interacts with membranes by binding to phospholipids and amines. The mechanism of this interaction is not fully understood, but it may be due to steric interactions or hydrogen bonding. N-Ethylmethylamine reacts with chlorine atoms in solution to form chloramines, which are more stable than free chlorine molecules. This reaction can be catalyzed by ph optimum or activated carbon. The reaction between hydrochloric acid and methyl ethyl amine produces methylamine gas, which is toxic in high concentrations.</p>

<p>Dimethylphencyclidine is a potent analgesic with high affinity for opioid receptors. It is an agonist at the μ-opioid receptor and κ-opioid receptor. Dimethylphencyclidine may also act as a nociceptive agent and has been shown to modulate pain in animals. This drug has also been shown to be neuropathic, as it inhibits the development of chronic constriction injury (CCI) in rats by reducing the formation of reactive oxygen species and increasing the expression of brain-derived neurotrophic factor (BDNF). Dimethylphencyclidine has undergone clinical trials for the treatment of neuropathic pain and is currently in phase II clinical development.<br>The pharmacological properties of dimethylphencyclidine are due to its ability to act on opioid receptors and other neurotransmitter systems, including serotonin, dopamine, acetylcholine, glutamate, and glycine. The chemical name for this drug is 4-(Dimethylamino)-4-phen</p>

<p>2-Amino-4-(trifluoromethyl)benzoic acid (2ATB) is a fluorescent compound that is used in assays to study the function of cells. It is a functional theory that 2ATB binds to the skeleton of cells, which are then subjected to optical properties testing. Fluorescence resonance energy transfer has been shown to occur between 2ATB and retinoic acid molecules in the cell nucleus, which may be related to cellular senescence. The structure of 2ATB has been determined by X-ray crystallography and it has been synthesized by halogenation.</p>

<p>Aminomethylphosphonic acid has proven action as a mimetic of both D- and L-alanine; it acts as an inhibitor of cell wall enzymes such as D-Ala-D-Ala synthetase, alanine racemase (JAA02406), and UDP-N-acetylmuramyl-L-alanine synthetase</p>

O-(4-Nitrophenyl)hydroxylamine (OPH) is an enantioselective, catalytic, and thermal stable reagent for the synthesis of chiral methyl groups. OPH can be used as a nucleophile to convert electron-deficient alkenes into α-chloroalkenes. It also reacts with nitroarenes to give nitroalkenes in high yields. OPH has been shown to be effective in the asymmetric hydrolysis of esters and amides through its ability to oxidize the methyl group on the substrate. This reaction does not occur with other groups such as hydroxyl or hydrogen atoms. Methyl groups are important for many biological molecules, including proteins and nucleic acids, which form the backbone of cells that make up living organisms. The OPH reaction is catalyzed by enzymes called methyltransferases, which transfer one atom of methyl from S-adenosylmethionine (SAM)

<p>4-Hydroxy-3-methoxybenzylamine is a nonsteroidal anti-inflammatory drug (NSAID) that has been shown to inhibit the production of cytokines and prostaglandins. It is metabolized by cytochrome P450 enzymes in the liver to form an amide and anhydrous sodium methyl myristate, which are excreted in urine. The reaction solution was analyzed using kinetic energy spectroscopy, which showed that 4-hydroxy-3-methoxybenzylamine reacts with vanillylamine to create a polymerase chain reaction product. This compound also has specific binding affinity for toll-like receptor 2 with high affinity, suggesting that it may have immunomodulatory properties.</p>

3-Amino-5-nitro-2,1-benzisothiazole is a diazonium salt that is used in wastewater treatment. It reacts with hydrogen peroxide to produce an unstable amine and a stable glycol ether. This process is known as the 3ABA reaction. The amine can be cleaved by water to produce ammonia and nitrous acid. Nitrous acid can react with organic matter in wastewater to form nitrate salts, which are soluble and easily removed from the wastewater stream. 3-Amino-5-nitro-2,1-benzisothiazole is also used in the manufacture of polyethylene terephthalate (PET) plastics. PET plastics are resistant to staining and have excellent color clarity.

3-(2-Aminoethyl)-5-methoxy-1H-indole-2-carboxylic acid is a fine chemical that is used as a building block for research chemicals, reagents, and specialty chemicals. It has the CAS No. 52648-13-2. 3-(2-Aminoethyl)-5-methoxy-1H-indole-2-carboxylic acid is also a versatile building block for synthesis of complex compounds with high quality and is a reaction component in many reactions. This compound can serve as an intermediate or scaffold in chemical synthesis.

N-Acetyl fluvoxamine acid is a versatile building block that can be used as a reagent, speciality chemical, or useful scaffold. It has uses in research and as a building block for complex compounds. N-Acetyl fluvoxamine acid is also a useful intermediate and reaction component. This compound has CAS number 88699-87-0.

Please enquire for more information about 5,5-dimethyl-2-(((3-nitrophenyl)amino)methylene)cyclohexane-1,3-dione including the price, delivery time and more detailed product information at the technical inquiry form on this page

4-Amino-2-methylbenzoic acid ethyl ester is a versatile building block that can be used in the synthesis of complex compounds. It has been shown to have a number of useful applications, such as in the synthesis of pharmaceuticals, research chemicals, and speciality chemicals. 4-Amino-2-methylbenzoic acid ethyl ester is also an important reagent for the production of high quality pharmaceuticals and intermediates. This chemical is also a useful scaffold for organic reactions.

2-Amino-3-nitrobenzoic acid (2ABN) is a peroxide that is used as an antiviral. 2ABN has been shown to inhibit the formation of reactive oxygen species in cancer cells, leading to apoptosis. It also inhibits the growth of carcinoma cell lines and tissues. 2ABN reacts with chloral hydrate to form a particle that can be encapsulated for delivery and release in vivo. This drug has been expressed in Escherichia coli, which may lead to improved stability and ease of production. 2ABN is thought to have anti-inflammatory properties due to its ability to inhibit the production of prostaglandins. The reactivity of 2ABN with surfactants such as sodium laureth sulfate (SLES) has been shown, which leads to it being used as an emulsifying agent for topical application.

<p>Useful chiral building block</p>

<p>2-Amino-N-methylbenzamide is a benzodiazepine receptor antagonist that has been shown to inhibit the proliferation of cancer cells in vitro. 2-Amino-N-methylbenzamide binds to the benzodiazepine receptor, which is found in cell nuclei and is involved in controlling the process of cell division. Benzodiazepines are a class of drugs that work by increasing the activity of GABA, which reduces neuronal excitability. 2-Amino-N-methylbenzamide prevents this activity by binding to the benzodiazepine receptor, preventing GABA from binding to its receptors and thereby inhibiting neuronal excitability. This drug has also been shown to inhibit cancer growth through an anthranilic acid derivative, methyl anthranilate. Methyl anthranilate inhibits DNA synthesis and induces apoptosis in cancer cells, leading to cell death.</p>

Please enquire for more information about 1-((2,5-dichlorophenyl)sulfonyl)-5-methylthio-1,2,4-triazole-3-ylamine including the price, delivery time and more detailed product information at the technical inquiry form on this page

<p>2-(Methylamino)acetohydrazide is a cross-linking agent that is used in the production of chitosan quaternary ammonium citrate. 2-(Methylamino)acetohydrazide also has antimicrobial properties. The monoclonal antibody reacts with the aldehyde groups on the polymer film, forming a disulfide bond. This inhibits bacterial growth by preventing cell wall synthesis, which is required for bacterial replication and survival. In addition, 2-(methylamino)acetohydrazide can be combined with malic acid or glyoxal to form polycarboxylic acid films that have antimicrobial activity.</p>

4-Aminobenzhydrazide is a reactive chemical that can be used to study the kinetics of reactions. It is used in vitro as an antimicrobial agent against human eosinophils, HL-60 cells, and K562 cells. 4-Aminobenzhydrazide has been shown to inhibit the production of eosinophil peroxidase by inhibiting mmp-9 activity. This drug also inhibits the growth of bacteria such as Staphylococcus aureus and Escherichia coli in vitro. 4-Aminobenzhydrazide is chemically stable and does not decompose at high temperatures or react with sodium ferulate (a common oxidant).

<p>1-Phenylcyclohexanamine hydrochloride is a secondary amine that binds to the nicotinic acetylcholine receptor. It has been shown to inhibit the activity of rat liver microsomes and dopamine, with a primary amino group. The analogs of 1-phenylcyclohexanamine hydrochloride are active and have been shown to inhibit acetylcholinesterase in rat brain tissue. This inhibition leads to an increase in the neurotransmitter acetylcholine, which causes an excitatory effect on the central nervous system. 1-Phenylcyclohexanamine hydrochloride is also used as a molecular model for studying glutamate receptors because of its similar structure.</p>