Description

Isoprinosine is a synthetic immunomodulatory compound with antiviral properties, widely recognized for its role in supporting immune system function. This high-purity active pharmaceutical ingredient (API) is essential for the development and manufacture of advanced therapeutic formulations. It is primarily utilized by pharmaceutical companies and research institutions focused on immunology, virology, and antiviral drug development.

Application

• Pharmaceutical API: Core active ingredient in prescription antiviral and immunomodulatory medications.
• Clinical Research: Used in preclinical and clinical studies investigating treatments for viral infections and immune deficiencies.
• Immunology Formulations: Incorporated into specialized dosage forms designed to modulate and enhance immune response.
• Reference Standard: Serves as a high-purity analytical standard for quality control and method development in laboratories.
• Biochemical Research: A key reagent for studying cellular immune mechanisms and viral replication pathways.

Basic Information

Item	Details
Product Name	Isoprinosine
CAS No.	36703-88-5
Molecular Formula	C52H78N10O17
Molecular Weight	1115.22 g/mol
Synonyms	Inosine Pranobex; Inosiplex; Methisoprinol; Delimmun; Isoprinosin; Imunovir; 9-[(2-Hydroxyethoxy)methyl]guanine complex with 1-(Dimethylamino)-2-propanol 4-acetamidobenzoate (3:1:1); 36703-88-5
EINECS	Contact for details

Quality Control

Our Isoprinosine is manufactured under strict quality management systems, ensuring it meets the stringent requirements for pharmaceutical actives. Each batch is subjected to comprehensive analytical testing, including identification, assay, and impurity profiling via validated methods such as HPLC. A Certificate of Analysis (COA) documenting full compliance with agreed specifications is provided with every shipment.

Storage

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

Specification

Item	Specification
Appearance	White or almost white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Individual impurity ≤ 0.5%; Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Heavy Metals	≤ 20 ppm
Microbial Enumeration	Complies with Ph. Eur. 2.6.12/2.6.13

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