Methyclothiazide API Manufacturer in India

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

Methyclothiazide API

Methyclothiazide is a synthetic thiazide diuretic used in pharmaceutical formulations for the management of conditions associated with excess fluid retention and elevated blood pressure. It promotes the excretion of sodium and water through the kidneys and belongs to the benzothiadiazine/thiazide class of diuretics.

Methyclothiazide acts primarily by inhibiting the sodium-chloride cotransporter (NCC) in the distal convoluted tubule of the nephron. This reduces sodium and chloride reabsorption and increases urinary excretion of water and electrolytes.

Methyclothiazide is supplied as an Active Pharmaceutical Ingredient (API) for qualified pharmaceutical manufacturing, formulation development, analytical testing and research applications.

Methyclothiazide API Key Features

  • Pharmaceutical-grade API
  • Thiazide diuretic
  • Antihypertensive pharmaceutical ingredient
  • Used in formulations for fluid-retention disorders
  • Suitable for pharmaceutical formulation development
  • Suitable for analytical and research applications
  • Molecular Formula: C11H15ClN4O2S2
  • Molecular Weight: 354.85 g/mol
  • CAS Number: 135-07-9

Mechanism of Action

Methyclothiazide inhibits the Na⁺/Cl⁻ cotransporter in the distal convoluted tubule of the kidney. This decreases sodium and chloride reabsorption and increases the urinary excretion of sodium and water.

Thiazide diuretics can also reduce urinary calcium excretion and produce a sustained reduction in blood pressure with continued use.

Pharmaceutical Applications

Methyclothiazide is associated with pharmaceutical applications including:

  • Hypertension management
  • Edema associated with selected medical conditions
  • Thiazide diuretic formulations
  • Antihypertensive pharmaceutical formulations
  • Cardiovascular pharmaceutical development
  • Pharmaceutical API manufacturing
  • Formulation development
  • Analytical research

The approved indication and dosage depend on the specific pharmaceutical formulation and applicable regulatory requirements.

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 0.5%
Individual Impurity NMT 0.5%
Total Impurities NMT 2.0%
Water Content NMT 1.0%
Melting Point Approximately 230–233 °C
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