Metoprolol Tartrate API Manufacturer in India

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

Metoprolol Tartrate API

Metoprolol Tartrate is the tartrate salt of metoprolol and a selective beta-1 adrenergic receptor antagonist (beta blocker). It is an established pharmaceutical active ingredient used in cardiovascular medicines. Metoprolol reduces beta-1 adrenergic activity in the heart, resulting in decreased heart rate and myocardial contractility.

Metoprolol Tartrate has the CAS Number 56392-17-7 and the molecular formula (C15H25NO3)2·C4H6O6, corresponding to a molecular weight of 684.81 g/mol. PubChem lists Metoprolol Tartrate as a salt consisting of two metoprolol molecules associated with one tartaric acid molecule.

Metoprolol Tartrate is widely relevant to pharmaceutical formulations intended for cardiovascular applications, including the management of hypertension, angina pectoris and certain cardiac conditions. The tartrate form is commonly associated with immediate-release metoprolol formulations.

Metoprolol Tartrate API Applications

Metoprolol Tartrate is used as an active pharmaceutical ingredient in formulations designed for cardiovascular therapy. Its pharmacological activity is primarily associated with selective blockade of beta-1 adrenergic receptors in cardiac tissue.

Key Features of Metoprolol Tartrate API

  • Selective beta-1 adrenergic receptor antagonist
  • Pharmaceutical API for cardiovascular formulations
  • CAS Number: 56392-17-7
  • Molecular weight: 684.81 g/mol
  • White crystalline powder
  • Very soluble in water
  • Applicable to pharmaceutical formulation and development
  • Available with product-specific analytical documentation

Metoprolol Tartrate API Manufacturer in India

Swapproop Drugs and Pharmaceuticals provides pharmaceutical APIs for formulation development and manufacturing requirements. Metoprolol Tartrate API can be offered for customers requiring a reliable pharmaceutical raw material for cardiovascular formulations.

Quality parameters, analytical documentation and release specifications should be evaluated according to the applicable pharmacopoeial standard and the batch-specific Certificate of Analysis (CoA).

Detailed Specifications

Parameter Specification
Appearance White crystalline powder or crystals
Identification IR & HPLC compliant
Assay (HPLC) 98.0% – 102.0%
Loss on Drying NMT 0.5%
Residue on Ignition NMT 0.1%
Individual Impurity NMT 0.5%
Total Impurities NMT 1.0%
Water Content NMT 0.5%
Specific Rotation +7.0° to +10.0° (αD20, after drying, C=2, H2O)
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