Description

Tiaramide is a pharmaceutical intermediate and active ingredient with significant therapeutic potential. This compound is valued for its role in the development of anti-inflammatory and analgesic agents, offering a pathway to advanced pharmaceutical formulations. It is primarily utilized by research institutions and manufacturers in the global pharmaceutical and life sciences sectors for drug discovery and production.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel anti-inflammatory drugs.
• Active Pharmaceutical Ingredient (API): Used in the formulation of finished dosage forms targeting specific inflammatory pathways.
• Biochemical Research: Employed in laboratory studies to investigate mechanisms of inflammation and pain.
• Preclinical Development: Serves as a critical material in the early-stage development and testing of new therapeutic candidates.
• Reference Standard: Used as an analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	Tiaramide
CAS No.	32527-55-2
Molecular Formula	C₁₅H₁₇ClN₂O₃S
Molecular Weight	340.83 g/mol
Synonyms	Tiaramide Hydrochloride; Farmacaina; FK-1160; 4-[(5-Chloro-2-oxo-3(2H)-benzothiazolyl)acetyl]-1-piperazineethanol; 1-(5-Chloro-2-oxobenzothiazolin-3-yl)acetyl-4-(2-hydroxyethyl)piperazine
EINECS	Contact for details

Quality Control

Our Tiaramide is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive Certificates of Analysis (COA) that detail identity, purity, and impurity profiles, supporting compliance with cGMP and ICH guidelines for pharmaceutical intermediates.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to minimize exposure to atmospheric moisture.

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%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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