Itopride, identified by CAS number 122898-67-3, is a benzamide derivative widely recognized for its prokinetic properties, making it a valuable intermediate in the pharmaceutical industry. For professionals involved in drug synthesis and formulation, understanding its chemical characteristics and the nuances of its production is essential. This article delves into the core properties of Itopride and offers insights from manufacturers regarding its synthesis and supply.

Chemically, Itopride possesses the molecular formula C20H26N2O4 and a molecular weight of 358.43. Its appearance is typically described as a white powder, a crucial characteristic for quality assessment by buyers. The synthesis of Itopride involves complex organic chemistry, often starting from precursors like 3,4-dimethoxybenzoic acid and specific amines. Manufacturers focus on optimizing reaction conditions, such as temperature, solvents, and catalysts, to achieve high yields and purity, ensuring the final product meets the stringent requirements for pharmaceutical use.

When considering the Itopride price, it's important to understand that it is influenced by several factors including the cost of raw materials, the complexity of the synthesis process, and the purity achieved. Buyers looking to purchase Itopride should engage with manufacturers to understand these dynamics and secure the best value. For instance, a transparent Itopride manufacturer will provide detailed specifications and lot-specific analysis to support the buyer's quality assurance efforts.

The primary application of Itopride lies in its role as an API precursor for medications aimed at enhancing gastrointestinal motility. This makes it a sought-after intermediate for companies developing treatments for conditions such as functional dyspepsia, acid reflux disease, and other related motility disorders. The demand for Itopride directly correlates with the growth in the gastrointestinal drug market.

Key aspects to consider from a manufacturer's perspective include:

  • Synthetic Route Optimization: Continuous refinement of synthetic pathways to improve efficiency and reduce environmental impact.
  • Quality Control: Rigorous testing at various stages of production to guarantee 99%+ purity.
  • Regulatory Adherence: Compliance with international quality standards and provision of necessary documentation.
  • Supply Chain Management: Ensuring consistent availability and timely delivery to global clients.

By understanding these chemical properties and manufacturing considerations, pharmaceutical professionals can make informed decisions when sourcing Itopride. Engaging with reputable Itopride suppliers who prioritize quality and transparency is fundamental to successful drug development and production.