Description

Thiethylperazine Malate (200 Mg) is a high-purity pharmaceutical active ingredient, specifically the malate salt of thiethylperazine. This compound is critical for the formulation of antiemetic medications, offering reliable performance in therapeutic applications. It is primarily required by pharmaceutical manufacturers and research institutions engaged in the development and production of treatments for nausea and vertigo.

Application

• Pharmaceutical Active Ingredient (API): Primary use in the formulation of prescription antiemetic medications.
• Tablet and Capsule Manufacturing: Used as the key therapeutic component in solid oral dosage forms.
• Clinical Research & Development: Serves as a reference standard and raw material in preclinical and clinical studies for new anti-nausea therapies.
• Veterinary Pharmaceuticals: Potential application in veterinary medicine for managing emesis in animals.
• Analytical Reference Standard: Utilized in quality control laboratories for HPLC, GC, or spectroscopic assay calibration and method validation.

Basic Information

Product Name	Thiethylperazine Malate (200 Mg)
CAS No.	52239-63-1
Molecular Formula	C22H29N3O2S2 • C4H6O5
Molecular Weight	575.68 g/mol
Synonyms	Thiethylperazine Hydrogen Malate; Torecan; Norzine; 2-Ethylmercapto-10-[3-(4-methyl-1-piperazinyl)propyl]phenothiazine Malate; NSC-130046; 52239-63-1; Thiethylperazine (as malate)
EINECS	Contact for details

Quality Control

Our Thiethylperazine Malate is manufactured under strict quality systems. Each batch undergoes comprehensive analytical testing to ensure it meets high-purity standards suitable for pharmaceutical use. A detailed Certificate of Analysis (COA) is provided with every shipment, confirming identity, purity, and impurity profiles.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.