APIs para pesquisa e impurezas
Subcategorias de "APIs para pesquisa e impurezas"
- Aminoácidos e Derivados(12.322 produtos)
- Antraquinonas e Derivados(402 produtos)
- Derivados de Benzimidazol e Imidazol(10.402 produtos)
- Derivados das Benzodiazepinas(327 produtos)
- Carboidratos e Glicoconjugados(5.049 produtos)
- Ésteres e Derivados(42.242 produtos)
- Ácidos Graxos e Derivados Lipídicos(32.379 produtos)
- Flavonoides e Polifenóis(17.075 produtos)
- Radicais Livres e Agentes Oxidantes/Redutores(212 produtos)
- Cetonas e Derivados(2.399 produtos)
- Antibióticos Naturais e Semissintéticos(6.335 produtos)
- Nitrilas e Derivados Ciano(3.068 produtos)
- Nitrosaminas e Derivados(55 produtos)
- Nucleosídeos e Nucleotídeos(3.454 produtos)
- Fosfatos e Fosfonatos Orgânicos(1.195 produtos)
- Sulfonatos e Sulfatos Orgânicos(10.422 produtos)
- Compostos Organometálicos(4.418 produtos)
- Outros(6.272 produtos)
- Peptídeos e Proteínas(3.140 produtos)
- Polímeros e Derivados(99 produtos)
- Derivados de Purinas e Pirimidinas(8.907 produtos)
- Derivados de Quinazolina e Quinolina(65.744 produtos)
- Quinonas e Derivados(24.344 produtos)
- Sais e Derivados de API(81.161 produtos)
- Esteroides e Derivados(4.928 produtos)
- Sulfonamidas e Derivados(2.569 produtos)
- Terpenoides e Derivados(3.838 produtos)
- Tiazolidinedionas e Tiopiranos(2.753 produtos)
- Compostos β-Adrenérgicos(228 produtos)
Foram encontrados 58514 produtos de "APIs para pesquisa e impurezas"
Tofacitinib dihydro impurity
CAS:Tofacitinib dihydro impurity is a research and development impurity standard for the synthesis of Tofacitinib. It is a custom synthesis with high purity, pharmacopoeia grade, and synthetic. This product is also used in drug development for metabolism studies and analytical applications.
Fórmula:C16H22N6OPureza:Min. 95%Peso molecular:314.39 g/molOxacyclohexane open ring tacrolimus
CAS:Please enquire for more information about Oxacyclohexane open ring tacrolimus including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C44H71NO13Pureza:Min. 95%Peso molecular:822.04 g/molRef: 3D-IO183660
Produto descontinuadoN-Benzyl albuterol
CAS:N-Benzyl albuterol is a drug product that is custom synthesized to be of high purity with an analytical standard. It is used in research and development, pharmaceutical development, and as a pharmacopoeia or analytical standard. N-Benzyl albuterol has been found to be a metabolite of the drug product Albuterol Sulfate. It is also used in metabolism studies and natural product research. The CAS number for this compound is 24085-03-8.
Fórmula:C20H27NO3Pureza:Min. 95%Peso molecular:329.4 g/molIvermectin impurity I
CAS:Ivermectin impurity I is an analytical standard that is used for pharmacopoeia and custom synthesis. It is a natural metabolite of the drug Ivermectin, which has been shown to have anti-inflammatory properties in mice. Ivermectin impurity I binds to nicotinic acetylcholine receptors, leading to muscle paralysis and death. This compound is found in high purity for research and development purposes.
Fórmula:C48H74O14Pureza:Min. 95%Cor e Forma:PowderPeso molecular:875.09 g/molRef: 3D-II167729
Produto descontinuadoLinagliptin impurity G
CAS:Linagliptin impurity G is an impurity in the drug product Linagliptin. It is a natural substance and its CAS number is 668270-11-9. Impurity G can be synthesized from L-phenylalanine and cyclohexane carboxaldehyde in a two step process. The first step involves the reaction of L-phenylalanine with cyclohexane carboxaldehyde to yield methylcyclohexanecarboxylate, which then undergoes hydrolysis to give phenylcyclohexanol. In the second step, phenylcyclohexanol reacts with hydrochloric acid to produce phenylcyclohexanone, which is then oxidized with hydrogen peroxide to yield impurity G. Impurity G can also be found in the pharmacopoeia as a high purity HPLC standard for linagliptin.
Fórmula:C25H28N8O2Pureza:Min. 95%Cor e Forma:PowderPeso molecular:472.54 g/molDesfluoro ezetimibe
CAS:Desfluoro ezetimibe is a synthetic cholesterol-lowering drug that inhibits intestinal cholesterol absorption. It is chemically synthesized, and the process includes the introduction of fluorine at the 3-position of the C-ring. Desfluoro ezetimibe is not metabolized in humans, but it may be subject to oxidative degradation. The product is also subject to oxidation by light and air, which may result in formation of impurities. The drug substance has been validated as well as its isomers and efficiencies in mass spectrometry detection.
Fórmula:C24H22FNO3Pureza:Min. 95%Cor e Forma:White To Off-White SolidPeso molecular:391.43 g/molTerbinafine dihydrochloride
CAS:Terbinafine is a drug used in the treatment of onychomycosis, tinea versicolor and dandruff. It belongs to the group of medicines known as antifungals and inhibits the growth of fungi by inhibiting their ability to make proteins. Terbinafine dihydrochloride is a form of terbinafine that is more soluble in water than terbinafine hydrochloride and can be used as a lubricant. Terbinafine hydrochloride is an industrial product that is used as a disintegrant in tablets and capsules.
Fórmula:C36H40N2Pureza:Min. 95%Peso molecular:500.7 g/molTriethylene glycol flufenamate
CAS:Etofenamate impurity
Fórmula:C20H22F3NO5Pureza:Min. 95%Cor e Forma:Clear LiquidPeso molecular:413.39 g/molRef: 3D-IT58094
Produto descontinuadoD-6-Cyano-6-norlysergic acid methyl ester
CAS:Please enquire for more information about D-6-Cyano-6-norlysergic acid methyl ester including the price, delivery time and more detailed product information at the technical inquiry form on this page
Fórmula:C17H15N3O2Pureza:Min. 95%Peso molecular:293.32 g/molRef: 3D-FBA33404
Produto descontinuadoChlorthalidone impurity E
CAS:Chlorthalidone impurity E is an analytical standard for the HPLC analysis of chlorthalidone in pharmaceutical drug products and is a metabolite of chlorthalidone. Chlorthalidone impurity E is an API impurity that can be found in the synthesis of chlorthalidone, and it has been detected as a minor component in certain drug products. It is important to have an accurate specification for this compound, since it can affect the pharmacological properties of the drug product. The purity level of this compound must be at least 98% or greater to ensure that there are no contaminants present. This compound is also a metabolite of chlorthalidone and is used as a pharmacopoeia reference substance for testing equipment calibration.END>
Fórmula:C14H11ClN2O3SPureza:Min. 95%Peso molecular:322.77 g/molRef: 3D-IC76330
Produto descontinuadoAtorvastatin calcium trihydrate EP Impurity G
CAS:Atorvastatin is a drug that belongs to the class of statins. It is used for the treatment of high cholesterol levels and other related diseases, such as cardiovascular disease. Atorvastatin calcium trihydrate EP Impurity G is an impurity that may be present in atorvastatin calcium trihydrate. This compound has not been found to have any pharmacological activity.
Fórmula:C34H37FN2O5Pureza:Min. 95%Cor e Forma:PowderPeso molecular:572.67 g/molGS 441524 triphosphate
CAS:Triphosphorylated form of an antiviral nucleoside analog with activity against zoonotic feline infectious peritonitis virus (FIPV) and severe acute respiratory syndrome (SARS) virus from Coronaviridae family. The compound is the biologically active form of the GS 441524 prodrug and being triphosphorylated, it competes with natural nucleoside triphosphates in cells and interferes with viral RNA synthesis. Made to order.
Fórmula:C12H12N5O13P3·4NaPureza:(31P-Nmr) Min. 95 Area-%Cor e Forma:White PowderPeso molecular:531.20 g/molRef: 3D-FG167050
Produto descontinuado
