CAS 5568-90-1
:10H-Phenothiazine-10-ethanamine, N,N,β-trimethyl-, hydrochloride (1:1)
Description:
10H-Phenothiazine-10-ethanamine, N,N,β-trimethyl-, hydrochloride (1:1), commonly referred to as trimethobenzamide, is a chemical compound characterized by its phenothiazine structure, which consists of a tricyclic system containing sulfur and nitrogen atoms. This compound is typically encountered as a hydrochloride salt, enhancing its solubility in water and making it suitable for pharmaceutical applications. It exhibits properties as an antiemetic, primarily used to prevent nausea and vomiting associated with various conditions, including postoperative states and chemotherapy. The trimethylamine group contributes to its pharmacological activity, influencing its interaction with neurotransmitter receptors in the central nervous system. In terms of physical properties, it is usually a white to off-white crystalline powder, with a specific melting point range and solubility profile. Safety data indicates that, like many pharmaceuticals, it should be handled with care, as it may cause side effects or interactions with other medications. Overall, its unique structure and properties make it a significant compound in medicinal chemistry.
Formula:C17H21ClN2S
InChI:InChI=1/C17H20N2S.ClH/c1-13(12-18(2)3)19-14-8-4-6-10-16(14)20-17-11-7-5-9-15(17)19;/h4-11,13H,12H2,1-3H3;1H
InChI key:InChIKey=RISCHQYUHLQSBU-UHFFFAOYSA-N
SMILES:C(CN(C)C)(C)N1C=2C(SC=3C1=CC=CC3)=CC=CC2.Cl
Synonyms:- 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)
- See more synonyms
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Found 7 products.
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·HClColor and Shape:White PowderMolecular weight:320.1114Promethazine EP Impurity B HCl (Promethazine USP Related Compound B, Isopromethazine HCl)
CAS:Formula:C17H20N2S·HClColor and Shape:Gray SolidMolecular weight:284.42 36.46Promethazine EP Impurity B (as Hydrochloride)
CAS:Controlled ProductFormula:C17H20N2S·ClHColor and Shape:NeatMolecular weight:320.88Iso Promethazine Hydrochloride
CAS:<p>Impurity Promethazine EP Impurity B<br>Stability Hygroscopic<br>Applications Iso Promethazine Hydrochloride (Promethazine EP Impurity B) is a Promethazine (P757000) impurity.<br>References Gasco, M.R., et al.: J. Pharma. Sci., 68, 612 (1979),<br></p>Formula:C17H20N2S·ClHColor and Shape:White To Off-WhiteMolecular weight:320.88Promethazine related compound B
CAS:<p>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.</p>Formula:C17H20N2S•HClPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:320.88 g/mol







