CAS 7640-51-9
:10H-Phenothiazine-10-ethanamine, N,N,α-trimethyl-, 5-oxide
Description:
10H-Phenothiazine-10-ethanamine, N,N,α-trimethyl-, 5-oxide, commonly referred to as a derivative of phenothiazine, is a chemical compound characterized by its phenothiazine backbone, which consists of a sulfur and nitrogen-containing heterocyclic structure. This compound typically exhibits properties such as being a solid at room temperature, with potential applications in pharmaceuticals, particularly as an antipsychotic or antihistamine agent due to its ability to interact with neurotransmitter systems. The presence of the trimethylamine group enhances its solubility and reactivity, making it useful in various chemical reactions. Additionally, the 5-oxide designation indicates the presence of an oxidized nitrogen atom, which can influence the compound's electronic properties and reactivity. Its molecular structure contributes to its biological activity, and it may exhibit fluorescence, making it useful in analytical chemistry. Safety data should be consulted for handling and exposure, as with all chemical substances, to ensure proper precautions are taken.
Formula:C17H20N2OS
InChI:InChI=1/C17H20N2OS/c1-13(18(2)3)12-19-14-8-4-6-10-16(14)21(20)17-11-7-5-9-15(17)19/h4-11,13H,12H2,1-3H3
InChI key:InChIKey=OWTCLFIFAFHQIX-UHFFFAOYSA-N
SMILES:C(C(N(C)C)C)N1C=2C(S(=O)C=3C1=CC=CC3)=CC=CC2
Synonyms:- 10-(2-(Dimethylamino)propyl)-10H-phenothiazine 5-oxide
- 10-(2-(Dimethylamino)propyl)-10H-phenothiazine5-oxide
- 10H-Phenothiazine-10-ethanamine, N,N,alpha-trimethyl-, 5-oxide
- 10H-Phenothiazine-10-ethanamine, N,N,α-trimethyl-, 5-oxide
- Diprazin sulfoxide
- N,N,alpha-Trimethyl-10H-phenothiazine-10-ethanamine 5-oxide
- N-[2-(Dimethylamino)propyl]phenothiazine S-oxide
- Phenothiazine, 10-[2-(dimethylamino)propyl]-, 5-oxide
- Promethazine 5-oxide
- Promethazine 5-sulfoxide
- Promethazine sulfoxide
- Romergan sulfoxide
- ProMethazine EP IMpurity D
- N,N,α-TriMethyl-10H-phenothiazine-10-ethanaMine 5-Oxide
- Promethazine Impurity 4(Promethazine EP Impurity D)
- N,N,a-Trimethyl-10H-phenothiazine-10-ethanamine 5-Oxide
- Promethazine Impurity 4(EP Impurity D)
- Promethazine EP Impurity D Dihydrochloride
- PROMETHAZINE EP IMPURITY D (PROMETHAZINE SULFOXIDE)
- (2RS)-N,N-Dimethyl-1-(10H-phenothiazin-10-yl)propan-2-amine S-oxide
- N,N-dimethyl-1-(5-oxophenothiazin-10-yl)propan-2-amine
- See more synonyms
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Found 12 products.
Promethazine sulfoxide
CAS:Promethazine sulfoxideFormula:C17H20N2OSColor and Shape:White SolidMolecular weight:300.4185Promethazine Sulfoxide
CAS:Compounds (excluding drugs) containing a phenothiazine ring-system (whether or not hydrogenated), not further fusedFormula:C17H20N2OSColor and Shape:Grey PowderMolecular weight:300.1296310-(2-(Dimethylamino)propyl)-10H-phenothiazine 5-oxide
CAS:Formula:C17H20N2OSPurity:95%Color and Shape:SolidMolecular weight:300.4185Promethazine EP Impurity D (Promethazine Sulfoxide)
CAS:Formula:C17H20N2OSColor and Shape:White To Off-White SolidMolecular weight:300.4210-(2-(Dimethylamino)propyl)-10H-phenothiazine 5-oxide
CAS:10-(2-(Dimethylamino)propyl)-10H-phenothiazine 5-oxidePurity:95%Molecular weight:300.43g/molPromethazine EP Impurity D
CAS:Controlled ProductFormula:C17H20N2OSColor and Shape:NeatMolecular weight:300.42Promethazine Sulfoxide
CAS:Controlled Product<p>Impurity Promethazine EP Impurity D<br>Applications Promethazine Sulfoxide (Promethazine EP Impurity D) is a metabolite of Promethazine (P757000).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Gottschalk, L., et al.: J. Pharm. Sci., 67, 155 (1978), de Jongh, G., et al.: Drug Metab. Dispos., 9, 48 (1981), Hale, P., et al.: Toxicol. Appl. Pharmacol., 86, 44 (1986), Delbressine, L., et al.: Xenobiotica, 22, 227 (1992),<br></p>Formula:C17H20N2OSColor and Shape:Light Red To PurpleMolecular weight:300.42Promethazine sulfoxide
CAS:<p>Promethazine sulfoxide is a phenothiazine derivative that is used in the treatment of allergies, colds, and motion sickness. It has been shown to inhibit peroxidases and reactions involving the production of hydrogen peroxide. Promethazine sulfoxide is metabolized by two pathways: one involving oxidation by cytochrome P450 enzymes and another involving hydrolysis by esterases or glucuronidases. The main metabolites are promethazine, promethazine sulfone, and N-methylpromethazine. When applied to urine samples, promethazine sulfoxide can be detected in concentrations of 1-10 ng/mL with an analytical method based on chromatography.</p>Formula:C17H20N2OSPurity:Min. 95%Color and Shape:PowderMolecular weight:300.42 g/mol











