Description

Pulmolin CAS NO 128523-74-0 is a high-purity pharmaceutical intermediate and active ingredient of significant importance in modern therapeutic development. Its primary value lies in its role as a key building block for synthesizing advanced respiratory and anti-inflammatory medications. This compound is essential for manufacturers and R&D teams in the pharmaceutical, biotechnology, and fine chemical sectors who require reliable, high-quality raw materials for drug formulation and clinical research.

Application

• Pharmaceutical Synthesis: A critical intermediate in the production of novel respiratory drugs and anti-inflammatory agents.
• Active Pharmaceutical Ingredient (API): Serves as the core active component in formulated pulmonary and bronchial medications.
• Biochemical Research: Used in preclinical and clinical studies to investigate mechanisms of action for lung-related conditions.
• Fine Chemical Manufacturing: Employed as a sophisticated precursor for complex organic syntheses in specialized chemistry.
• Contract Development and Manufacturing (CDMO): Supplied to CDMOs for scale-up and commercial production of finished dosage forms.
• Reference Standard: Utilized as an analytical standard for quality control and regulatory compliance testing.

Basic Information

Product Name	Pulmolin
CAS No.	128523-74-0
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Pulmolin; 128523-74-0; (2R,3aS,7aS)-1-[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-[[(2S)-2-Amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-3-hydroxypropanoyl]amino]-3-(1H-imidazol-5-yl)propanoyl]amino]-3-methylbutanoyl]amino]-5-guanidinopentanoyl]octahydro-1H-indole-2-carbonyl]pyrrolidine-2-carboxylic acid; UNII-7VMA8JE19P; 7VMA8JE19P
EINECS	Contact for details

Quality Control

Our Pulmolin is manufactured under strict quality management systems to ensure it meets the exacting standards required for pharmaceutical applications. Each batch is subjected to rigorous analytical testing, including identity confirmation, purity assay, and impurity profiling via advanced techniques like HPLC and mass spectrometry. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all relevant specifications to support your regulatory and quality assurance needs.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed in a dry environment to prevent degradation. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 2.0%
Residue on Ignition	≤ 0.5%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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