Methyltrosine API Manufacturer in India

Swapnroop Pharma · WHO-GMP Certified · +91 87670 62101

Methyltrosine API Manufacturer in India

Methyltrosine, commonly known as metyrosine, is a synthetic amino-acid derivative and tyrosine hydroxylase inhibitor used in pharmaceutical applications involving catecholamine production. It reduces the synthesis of catecholamines such as dopamine, norepinephrine and epinephrine by inhibiting the enzyme tyrosine hydroxylase.

Methyltrosine is primarily associated with the management of pheochromocytoma, particularly when reduction of excessive catecholamine production is required. It is an important pharmaceutical ingredient for specialized endocrine and cardiovascular applications.

Methyltrosine API is used for qualified pharmaceutical manufacturing, formulation development, analytical testing and research applications.

Methyltrosine API Key Features

  • Pharmaceutical-grade active pharmaceutical ingredient
  • Tyrosine hydroxylase inhibitor
  • Catecholamine synthesis inhibitor
  • Associated with pheochromocytoma treatment
  • CAS Number: 672-87-7
  • Molecular Formula: C10H13NO3
  • Molecular Weight: 195.22 g/mol
  • Small-molecule pharmaceutical ingredient
  • Suitable for pharmaceutical formulation development
  • Suitable for analytical and research applications

Mechanism of Action

Methyltrosine inhibits tyrosine hydroxylase, the rate-limiting enzyme in catecholamine biosynthesis. By reducing the conversion of tyrosine to L-DOPA, it decreases the subsequent production of dopamine, norepinephrine and epinephrine.

This reduction in catecholamine synthesis makes methyltrosine useful in pharmaceutical management of conditions involving excessive catecholamine production.

Pharmaceutical Applications

Methyltrosine API is associated with:

  • Pheochromocytoma-related pharmaceutical formulations
  • Catecholamine excess management
  • Endocrine pharmaceutical development
  • Tyrosine hydroxylase inhibition research
  • Cardiovascular pharmaceutical research
  • Pharmaceutical formulation development
  • API manufacturing
  • Analytical development
  • Drug-substance research

The approved indications and dosage forms depend on the specific pharmaceutical product and applicable regulatory jurisdiction.

Detailed Specifications

Parameter Specification
Appearance White crystalline powder or crystals
Identification IR & HPLC compliant
Assay (HPLC) 98.0% – 102.0%
Loss on Drying NMT 2.0%
Residue on Ignition NMT 0.5%
pH (1% Solution) 5.0–8.0
Individual Impurity NMT 2.0%
Total Impurities NMT 2.0%
Water Content NMT 2.0%
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