Methoxamine API Manufacturer in India

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

Methoxamine API

Methoxamine is a direct-acting alpha-adrenergic agonist and sympathomimetic compound used as a vasopressor. It produces peripheral vasoconstriction primarily through stimulation of alpha-1 adrenergic receptors, resulting in increased vascular resistance and elevation of blood pressure.

Methoxamine is mainly associated with cardiovascular and critical-care pharmaceutical applications, particularly the management of hypotension.

Methoxamine API Manufacturer in India

Methoxamine is a specialized vasopressor pharmaceutical API used in pharmaceutical research and formulation development. The hydrochloride salt, Methoxamine Hydrochloride, has been used in injectable pharmaceutical preparations.

Chemical Information

CAS Number: 390-28-3
Molecular Formula: C11H17NO3
Molecular Weight: 211.26 g/mol
IUPAC Name: 2-amino-1-(2,5-dimethoxyphenyl)propan-1-ol
Synonyms: Methoxamin, Methoxamedrine, Pseudomethoxamine
Drug Class: Sympathomimetic / Alpha-Adrenergic Agonist
Therapeutic Class: Vasopressor / Antihypotensive Agent
Therapeutic Area: Cardiovascular / Critical Care
Molecule Type: Synthetic Small Molecule

Mechanism of Action

Methoxamine acts directly on alpha-adrenergic receptors, with selectivity for the alpha-1 receptor subtype. Its stimulation of peripheral alpha receptors causes vasoconstriction and increases systemic vascular resistance.

Pharmaceutical Applications

Methoxamine is associated with:

  • Acute hypotension
  • Blood-pressure support
  • Vasopressor therapy
  • Perioperative hypotension
  • Cardiovascular pharmacology
  • Adrenergic receptor research
  • Vasoconstrictor drug development

Dosage Form Applications

Methoxamine Hydrochloride has historically been supplied as an injectable solution, including preparations containing 10 mg/mL or 20 mg/mL.

Physical Characteristics

Methoxamine free base has the molecular formula C11H17NO3 and molecular weight 211.26 g/mol.

The hydrochloride salt is reported as colorless or white plate-like crystals / white crystalline powder, with a reported melting point of 212–216 °C.

Quality Control Testing

Typical Methoxamine API testing may include:

  • Identification by IR
  • HPLC identification
  • Assay
  • Related substances
  • Water content
  • Residual solvents
  • Elemental impurities
  • Optical / stereochemical purity
  • Residue on ignition
  • Melting point
  • Stability testing

Detailed Specifications

Parameter Specification
Appearance White crystalline powder or crystals
Identification IR & HPLC compliant
Assay (HPLC) 98.0% – 102.0%
Loss on Drying NMT 1.0%
Residue on Ignition NMT 0.2%
Individual Impurity NMT 0.5%
Total Impurities NMT 1.0%
Water Content NMT 1.0%
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