Description

Milrinone Lactate is a high-purity pharmaceutical salt form of the potent cardiotonic agent, milrinone. This compound is critical for the formulation of injectable solutions used in acute cardiac care. It is primarily required by pharmaceutical manufacturers and research institutions engaged in cardiovascular drug development and production. The product is supplied under stringent quality controls to ensure batch-to-batch consistency for critical applications.

Application

• Active Pharmaceutical Ingredient (API) for intravenous formulations targeting acute heart failure.
• Reference Standard in analytical laboratories for quality control and method validation.
• Biochemical Research for studying phosphodiesterase III (PDE3) inhibition and cardiac contractility.
• Pharmaceutical Intermediates in the synthesis of specialized cardiovascular medications.
• GMP Manufacturing for the production of sterile injectable drugs under good manufacturing practices.

Basic Information

Product Name	Milrinone Lactate
CAS No.	100286-97-3
Molecular Formula	C12H9N3O • C3H6O3
Molecular Weight	303.27 g/mol
Synonyms	1,6-Dihydro-2-methyl-6-oxo-[3,4'-bipyridine]-5-carbonitrile lactate; Milrinone monohydrate lactate; WIN 47203 lactate; 2-Methyl-5-cyano-1,6-dihydro-6-oxo-[3,4'-bipyridine] lactate; Corotrope (associated brand); Primacor (associated brand)
EINECS	Contact for details

Quality Control

Our Milrinone Lactate is manufactured and tested to meet exacting standards suitable for pharmaceutical applications. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles. We adhere to ICH Q7 guidelines and can support documentation for regulatory submissions to agencies such as the FDA and EMA.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a low-humidity environment to prevent moisture absorption.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 1.5%
Specific Rotation	Contact for details

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.