Metaraminol API Manufacturer in India

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

Metaraminol API

Metaraminol is a sympathomimetic amine and adrenergic agonist used primarily as a vasopressor to increase blood pressure in situations involving acute hypotension. It produces vasoconstriction and increases vascular tone through activity at adrenergic receptors.

Metaraminol is an important cardiovascular pharmaceutical API used in the development and manufacture of injectable medicines for the management of clinically significant hypotension.

Metaraminol API Manufacturer in India

Metaraminol is a specialized vasopressor API used for pharmaceutical formulation and research. Its manufacture requires appropriate control of identity, assay, related substances, stereochemical purity, residual solvents and other applicable quality parameters.

Chemical Information

CAS Number: 54-49-9
Molecular Formula: C9H13NO2
Molecular Weight: 167.21 g/mol
Chemical Name: Metaraminol
Drug Class: Sympathomimetic / Adrenergic Agonist
Therapeutic Class: Vasopressor
Therapeutic Area: Cardiovascular / Critical Care
Molecule Type: Synthetic Small Molecule

Mechanism of Action

Metaraminol acts primarily through adrenergic receptor stimulation, producing peripheral vasoconstriction and increasing vascular resistance. It also has an indirect sympathomimetic component through promotion of norepinephrine release.

Its pharmacological effects include:

  • Peripheral vasoconstriction
  • Increased systemic vascular resistance
  • Elevation of arterial blood pressure
  • Adrenergic stimulation
  • Support of vascular tone during acute hypotension

Pharmaceutical Applications

Metaraminol API is associated with pharmaceutical applications involving:

  • Acute hypotension
  • Vasodilatory hypotension
  • Perioperative hypotension
  • Blood-pressure support
  • Vasopressor therapy
  • Cardiovascular pharmacology research

Dosage Form Applications

Metaraminol is primarily used in parenteral pharmaceutical preparations, particularly injectable formulations intended for controlled clinical administration.

Physical Characteristics

Metaraminol is generally handled as a pharmaceutical solid or as an appropriate salt form for formulation. Appearance, solid-state properties and other physical characteristics should be controlled according to the applicable API specification.

Manufacturing Process

A controlled Metaraminol API manufacturing process may involve:

  1. Selection and qualification of starting materials
  2. Preparation of suitable aromatic intermediates
  3. Controlled chemical synthesis
  4. Introduction of the amino-alcohol functionality
  5. Stereochemical control where applicable
  6. Purification
  7. Salt formation where required
  8. Crystallization
  9. Filtration
  10. Controlled drying
  11. Final analytical testing
  12. Pharmaceutical-grade packaging

Quality Control Testing

Typical Metaraminol API testing may include:

  • Identification by IR
  • HPLC identification
  • Assay by HPLC
  • Related substances
  • Stereochemical purity
  • Water content
  • Residual solvents
  • Elemental impurities
  • Residue on ignition
  • Melting range
  • Stability testing

Storage

Store Metaraminol API in a tightly closed container under controlled pharmaceutical storage conditions, protected from excessive moisture, heat and direct light.

Pharmaceutical Research

Metaraminol is relevant to research involving:

  • Adrenergic receptors
  • Vasopressor pharmacology
  • Sympathomimetic agents
  • Blood-pressure regulation
  • Vascular smooth muscle
  • Cardiovascular pharmacology
  • Critical-care medicines
  • Perioperative hypotension

Metaraminol API Summary

Metaraminol is a sympathomimetic vasopressor with CAS Number 54-49-9, molecular formula C9H13NO2, and molecular weight 167.21 g/mol. It is primarily associated with the management of acute hypotension through adrenergic-mediated vasoconstriction.

Detailed Specifications

Parameter Specification
Appearance White to off-white crystalline powder
Identification IR & HPLC compliant
Assay (HPLC) 98.0% – 102.0%
Loss on Drying NMT 2.0%
Residue on Ignition NMT 0.5%
Heavy Metals NMT 10 ppm
Individual Impurity NMT 1.0%
Total Impurities NMT 2.0%
Water Content NMT 2.0%
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