
Aminas
Subcategorías de "Aminas"
- Nitrosaminas(2.668 productos)
- Aminas primarias(30.948 productos)
- Cationes y sales de amonio cuaternario(1.099 productos)
- Aminas secundarias(20.886 productos)
- Aminas terciarias(17.195 productos)
Se han encontrado 8787 productos de "Aminas"
2-Aminomethyl-4-(4-fluorobenzyl)morpholine
CAS:2-Aminomethyl-4-(4-fluorobenzyl)morpholine (2AMFM) is a prokinetic agent that has been shown to be effective as a treatment for gastrointestinal motility disorders. This drug binds to the 5HT4 receptors, which are found on the enteric nervous system and in the gut. 2AMFM has been shown to increase the frequency of contractions in rat ileum and small intestine preparations. It also increases gastric emptying time and decreases postprandial acidity in dogs. 2AMFM is an enantiomeric mixture of two chiral molecules that are mirror images of each other. The racemic mixture is synthesized by reacting 2-aminomethyl-4-(4-fluorobenzyl)morpholine with chloroacetic acid ethyl ester.Fórmula:C12H17FN2OPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:224.27 g/molAmmonium chloride
CAS:Ammonium chloride is a salt of ammonium and chloride. It is used in wastewater treatment as a coagulant, to remove suspended solids from the water. In addition, ammonium chloride has been shown to have potent antitumor activity and is used in chemotherapy treatments. Ammonium chloride can be toxic if ingested or inhaled and should not be handled without proper safety precautions. Ammonium chloride also has an effect on the bowel disease, slowing down the rate at which it progresses. It is produced when trimethyl reacts with blood or water vapor. The surface methodology was used to obtain thermodynamic data for ammonium chloride. This method can be applied to other compounds that are difficult to analyze by other methods.Fórmula:NH4ClPureza:Min. 95%Forma y color:PowderPeso molecular:53.49 g/mol(S)-2-Azido isovaleric acid cyclohexylammonium
CAS:Please enquire for more information about (S)-2-Azido isovaleric acid cyclohexylammonium including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C6H13N•C5H9N3O2Pureza:Min. 95%Forma y color:PowderPeso molecular:242.32 g/mol2-Isopropyl-4-(methylaminomethyl)thiazole
CAS:2-Isopropyl-4-(methylaminomethyl)thiazole is a chemical compound that belongs to the group of halogenating agents. It is used as a precursor in the manufacturing process of pesticides and pharmaceuticals. 2-Isopropyl-4-(methylaminomethyl)thiazole is produced by the chlorination reaction of methylamine with chlorine. This chemical has a variety of industrial uses, including as an intermediate for herbicides, insecticides, and fungicides.Fórmula:C8H14N2SPureza:Min. 95%Peso molecular:170.28 g/mol4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine
CAS:4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine is a monoclonal antibody that binds to cancer cells. It has been shown to be effective in the treatment of leukemia, Hodgkin's disease, and non-Hodgkin's lymphoma. The binding of 4-Amino-1,3-dimethyl-2,6-dioxo-5-nitrosopyrimidine to cancer cells is due to the formation of a coordination geometry between the copper complex and the nitrogen atoms on the amino group. This drug has been shown to inhibit tumor growth by blocking the synthesis of DNA and RNA, which are key components in cell division. 4AADNP also inhibits cancer cells' ability to uptake glucose by inhibiting cellular glucose transporters. The binding affinity of 4AADNP for cancer cells is higher than for normal cells because cancer cells have more receptors for this drugFórmula:C6H8N4O3Pureza:Min. 95%Peso molecular:184.15 g/mol1,2-Diamino-2-methylpropane
CAS:Intermediate in the synthesis of anagliptin
Fórmula:C4H12N2Pureza:Min. 95%Peso molecular:88.15 g/molN-Hexylethylenediamine
CAS:N-Hexylethylenediamine is a hydrophobic chemical compound that can be synthesized and used as a monomer. It has been shown to form gels when mixed with other compounds, such as acrylic acid. The specific interactions of N-hexylethylenediamine are due to its functional groups. These include amines, which protonate at low pH levels, and modifiers, which increase the viscosity of the gel. N-Hexylethylenediamine is often used in protein modelling because it has trifunctional groups that can interact with three different amino acids. This chemical also has an nmr spectrum and x-ray absorption data available for it.Fórmula:C8H20N2Pureza:Min. 95%Peso molecular:144.26 g/mol[2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride
CAS:Producto controladoPlease enquire for more information about [2-(5-Chloro-1H-indol-3-yl)-1-methylethyl]amine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C11H13ClN2Pureza:Min. 95%Peso molecular:208.69 g/mol4-Aminobicyclo[2.2.2]octane-1-carboxylic acid methyl ester
CAS:Please enquire for more information about 4-Aminobicyclo[2.2.2]octane-1-carboxylic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C10H17NO2Pureza:Min. 95%Peso molecular:183.25 g/mol1-(Methylamino)adamantane
CAS:1-(Methylamino)adamantane is a dopamine receptor ligand that has been shown to be neuroprotective in rodent models of ischemia-reperfusion injury. 1-(Methylamino)adamantane exhibits high affinity for the D2 subtype, with potency and efficacy that are comparable to those of dopamine. It also acts as an agonist at the D1 and D3 receptors, although it displays weaker binding affinity than dopamine. The neuroprotective effects of 1-(methylamino)adamantane have been demonstrated in wild-type mice following ischemia-reperfusion injury, but not in animals with a mutant form of the gene encoding dopamine receptors. These findings suggest that 1-(methylamino)adamantane may be able to provide protection against ischemia-reperfusion injury by acting on downstream pathways such as protein kinase C or nitric oxide synthase.Fórmula:C11H19NPureza:Min. 95%Peso molecular:165.28 g/mol3-Hydroxy-4-amino-butyric acid
CAS:Producto controlado3-Hydroxy-4-amino-butyric acid is a synthetase that catalyzes the formation of 3-hydroxy-4 amino butyric acid from 3-hydroxy butyric acid and ammonia. This reaction occurs in the presence of chloride ions, ethyl bromoacetate and butyric acid. The isolated yield of this reaction is 47%. The product can be converted to 3-amino butyric acid by dehydrating it with hydrochloric acid. 3-Hydroxy-4 amino butyric acid has been shown to have anticancer properties in vitro. It also has been shown to have antiinflammatory properties, which may be due to its ability to inhibit the production of prostaglandin E2, an inflammatory mediator.Fórmula:C4H9NO3Pureza:Min. 95%Forma y color:PowderPeso molecular:119.12 g/molN-Nitrosodicyclohexylamine
CAS:N-Nitrosodicyclohexylamine (NDCA) is a chemical that is used as a corrosion inhibitor. The stability of NDCA in the environment has been studied extensively and found to be resistant to many conditions including heat, light, and pH. NDCA is absorbed by the skin or ingested and has been shown to cause genotoxic effects in human lymphocytes. The genotoxic potential of NDCA has also been demonstrated in V79 cells. NDCA reacts with amines to form an intermediate that spontaneously decomposes into nitrosamines, which are carcinogenic. This reaction mechanism was confirmed using analytical methods such as gas chromatography-mass spectrometry (GC-MS).Fórmula:C12H22N2OPureza:Min. 95%Peso molecular:210.32 g/mol4-Methoxy-N-methylbenzylamine
CAS:4-Methoxy-N-methylbenzylamine is a synthesized compound that is structurally similar to piperazine. It has been synthesized using the Chloramine T method and has been shown to be active as an amine receptor ligand. This molecule binds to the amine receptor site of the GABAA receptor with high affinity, inhibiting chloride ion flow. The functional groups on this molecule are likely responsible for its binding activity. 4-Methoxy-N-methylbenzylamine may be useful in the treatment of scopolamine-induced amnesia, due to its ability to bind to specific receptors in the brain.Fórmula:C9H13NOPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:151.21 g/molBis(tert-butoxycarbonyl) Lisdexamphetamine
CAS:Producto controladoPlease enquire for more information about Bis(tert-butoxycarbonyl) Lisdexamphetamine including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C25H41N3O5Pureza:Min. 95%Peso molecular:463.61 g/molFmoc-TOAC-OH
CAS:Fmoc-2,2,6,6-tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid (FMOC) is a highly reactive nitroxide that reacts with oxygen to form superoxide radicals. FMOC has been used to study the effects of radiation on proteins and peptides. It can be synthesized by reacting an amino acid with the reagent N-(3-(dimethylamino)propyl)-N'-methylcarbodiimide hydrochloride (EDC). The product then reacts with 4-(2,2,6,6,-tetramethylpyridinium) perchlorate in acetonitrile to create a fluorescent compound. When FMOC is labeled with a heavy metal such as gadolinium or manganese it becomes paramagnetic and can be detected using magnetic resonance imaging (MRI). FMOC also binds to the sarcoplasmic reticulumFórmula:C25H29N2O5Pureza:Min. 95%Peso molecular:437.51 g/mol[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine
CAS:[1,2,4]Triazolo[1,5-a]pyrimidin-7-amine is a competitive inhibitor of tumor growth. It has been shown to inhibit the synthesis of DNA and RNA by binding to the N7 nitrogen atom in the nucleotide base. The compound also has a trifluoromethyl group that can be used as an assay for enzymatic activity. [1,2,4]Triazolo[1,5-a]pyrimidin-7-amine can be synthesized from 2-(3'-hydroxypropoxy)phenylamine by reaction with hydroxylamine and formaldehyde in the presence of sodium cyanide. This drug inhibits tumor growth in vitro and in vivo and is active against infectious diseases such as hepatitis B virus (HBV).Fórmula:C5H5N5Pureza:Min. 95%Peso molecular:135.13 g/mol2-(Diphenylphosphino)ethylamine
CAS:2-(Diphenylphosphino)ethylamine is a palladium complex that is used as a catalyst for the oxidation of alcohols to aldehydes and ketones. However, this compound can also be used in the synthesis of molybdenum complexes. 2-(Diphenylphosphino)ethylamine has been shown to catalyze the oxidation of aliphatic alcohols to corresponding aldehydes and ketones in homogeneous solution. This reaction proceeds by a transfer mechanism, with an irreversible oxidation at the metal center. The reaction products are not observed due to the high reactivity of hydrogen peroxide and its decomposition products. Control experiments showed that 2-(diphenylphosphino)ethylamine does not oxidize other substrates such as benzene or nitrobenzene, which are more stable than alcohols.
Fórmula:C14H16NPPureza:Min. 95%Forma y color:Clear LiquidPeso molecular:229.26 g/mol1-Boc-4-aminopiperidine-4-carboxylic acid
CAS:Please enquire for more information about 1-Boc-4-aminopiperidine-4-carboxylic acid including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C11H20N2O4Pureza:Min. 95%Forma y color:White To Beige SolidPeso molecular:244.29 g/molN-Butyl nor scopolamine hydrochloride
CAS:Please enquire for more information about N-Butyl nor scopolamine hydrochloride including the price, delivery time and more detailed product information at the technical inquiry form on this pageFórmula:C20H28ClNO4Pureza:Min. 95%Peso molecular:381.89 g/mol2-(2-Chlorophenyl)ethylamine
CAS:Producto controlado2-(2-Chlorophenyl)ethylamine is an amine that inhibits the production of proteins vital for cell division. It binds to bacterial 16S ribosomal RNA and inhibits protein synthesis, leading to cell death by inhibiting the production of proteins vital for cell division. 2-(2-Chlorophenyl)ethylamine has been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Clostridium perfringens, although is not active against acid-fast bacteria such as Mycobacterium tuberculosis or Mycobacterium avium complex. 2-(2-Chlorophenyl)ethylamine has shown anti-inflammatory properties, which may be due to its inhibition of prostaglandin synthesis.Fórmula:C8H10ClNPureza:Min. 95%Peso molecular:155.62 g/mol
