CAS 5568-90-1
:10H-Fenotiazina-10-etanamina, N,N,β-trimetil-, cloridrato (1:1)
- 10H-Phenothiazine-10-ethanamine, N,N,beta-trimethyl-, monohydrochloride (9CI)
- 10H-Phenothiazine-10-ethanamine, N,N,β-trimethyl-, hydrochloride (1:1)
- 10H-Phenothiazine-10-ethanamine, N,N,β-trimethyl-, monohydrochloride
- Isopromethazine hydrochloride
- Phenothiazine, 10-[2-(dimethylamino)-1-methylethyl]-, monohydrochloride
- Promethazine Impurity B (Isopromethazine) HCl
- Promethazine Impurity 2(EP Impurity B)
- N,N-dimethyl-2-phenothiazin-10-ylpropan-1-amine:hydrochloride
- Promethazine Impurity B
- PROMETHAZINE EP IMPURITY B HCL (ISOPROMETHAZINE HCL)
- ProMethazine EP IMpurity B
- N,N-dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amine
- Promethazine EP Impurity B/ Promethazine Related Compound B (Isopromethazine)
- Promethazine Impurity 2(Promethazine EP Impurity B)
- Vedi altri sinonimi
Promethazine Related Compound B (N,N-Dimethyl-2-(10H-phenothiazin-10-yl)propan-1-amine hydrochloride)
CAS:Compounds (excluding drugs) containing a phenothiazine ring-system (whether or not hydrogenated), not further fusedFormula:C17H20N2S·HClColore e forma:White PowderPeso molecolare:320.1114Promethazine EP Impurity B HCl (Promethazine USP Related Compound B, Isopromethazine HCl)
CAS:Formula:C17H20N2S·HClColore e forma:Gray SolidPeso molecolare:284.42 36.46Promethazine EP Impurity B (as Hydrochloride)
CAS:Prodotto controllatoFormula:C17H20N2S·ClHColore e forma:NeatPeso molecolare:320.88Iso Promethazine Hydrochloride
CAS:Impurity Promethazine EP Impurity B
Stability Hygroscopic
Applications Iso Promethazine Hydrochloride (Promethazine EP Impurity B) is a Promethazine (P757000) impurity.
References Gasco, M.R., et al.: J. Pharma. Sci., 68, 612 (1979),Formula:C17H20N2S·ClHColore e forma:White To Off-WhitePeso molecolare:320.88Promethazine related compound B
CAS:Promethazine is a phenothiazine derivative that is used as an antihistamine and antipsychotic. It has been found to bind to the H1 receptor, which may be the mechanism by which it inhibits histamine release. Promethazine also binds to the H2 receptor, which may be the mechanism by which it inhibits acid secretion in the stomach. Promethazine has been shown to have antiviral properties against herpes simplex virus type 1 (HSV-1) and human immunodeficiency virus (HIV). Promethazine can bind to metal ions and form a neutral complex that can inhibit receptors on cells. The drug has been shown to inhibit receptors for acetylcholine, dopamine, GABA, serotonin, histamine, and norepinephrine.
Formula:C17H20N2S•HClPurezza:Min. 95 Area-%Colore e forma:PowderPeso molecolare:320.88 g/molRef: ST-EA-CP-P86002
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