D-Tryptophan Methyl Ester Hydrochloride

D-Tryptophan Methyl Ester Hydrochloride

Category :

Active Pharmaceutical Ingredient (API)

Chemical Class :

Biguanide Antidiabetic Agent

CAS Number :

1115-70-4

Product Form :

White to off-white crystalline powder

Grade :

USP / BP / EP (as per requirement)

End Use :

Pharmaceutical formulations

Packaging :

25 kg HDPE Drum (Custom Packaging Available)

Description:

D-Tryptophan Methyl Ester Hydrochloride is a key pharmaceutical intermediate widely used in the synthesis of active pharmaceutical ingredients such as Tadalafil. It serves as an important building block in the development of amino acid-based compounds utilized in advanced pharmaceutical formulations.

This intermediate is commonly applied in multi-step organic synthesis processes where high purity, stereochemical integrity, and controlled reactivity are essential. It plays a crucial role in the production of Tadalafil, ensuring efficient and reliable pharmaceutical manufacturing. Due to its consistent performance, it is suitable for both laboratory-scale research and large-scale industrial applications.

As a trusted global supplier and exporter from India, we ensure high-quality material with consistent purity and performance. Our product is manufactured under stringent quality control standards and supplied to meet international pharmaceutical and export requirements.


Applications:

  • Intermediate for Tadalafil synthesis
  • Pharmaceutical API manufacturing
  • Amino acid derivative synthesis
  • Organic and medicinal chemistry research
  • Chiral compound development
  • Large-scale pharmaceutical production

Key Features:

  • High purity and consistent quality
  • Excellent stereochemical stability
  • Suitable for pharmaceutical-grade applications
  • Reliable performance in complex synthesis
  • Ideal for industrial and research use

Export & Quality Assurance:

Manufactured under strict quality control systems, this product is available with COA, MSDS, and TDS documentation. We ensure secure packaging, consistent batch quality, and compliance with international standards, making it suitable for global pharmaceutical markets.

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