Description

Ganciclovir Sodium is the sodium salt form of the potent antiviral nucleoside analogue ganciclovir. This compound is critical for the formulation of injectable antiviral medications, offering enhanced solubility and stability for clinical use. It is primarily required by pharmaceutical manufacturers and research institutions developing and producing treatments for severe cytomegalovirus (CMV) infections, particularly in immunocompromised patients.

Application

• Active Pharmaceutical Ingredient (API) for injectable antiviral formulations.
• Treatment of CMV Infections, including CMV retinitis in AIDS patients and CMV disease in transplant recipients.
• Research and Development of novel antiviral therapies and drug delivery systems.
• Pharmaceutical Intermediates for the synthesis of more complex antiviral prodrugs.
• Reference Standard for quality control and analytical testing in pharmaceutical laboratories.
• Veterinary Pharmaceutical Applications for treating viral infections in animals.

Basic Information

Item	Detail
Product Name	Ganciclovir Sodium
CAS No.	107910-75-8
Molecular Formula	C9H12N5NaO4
Molecular Weight	277.21 g/mol
Synonyms	Ganciclovir Sodium Salt; Sodium Ganciclovir; 9-[(1,3-Dihydroxy-2-propoxy)methyl]guanine Sodium Salt; 2-Amino-1,9-dihydro-9-[[2-hydroxy-1-(hydroxymethyl)ethoxy]methyl]-6H-purin-6-one Sodium Salt; DHPG Sodium Salt; Cytovene Sodium; Cymevene Sodium; BMY-0940 (Sodium Salt)
EINECS	Contact for details

Quality Control

Our Ganciclovir Sodium is manufactured under strict quality management systems. Each batch is tested to ensure it meets high-purity standards suitable for pharmaceutical applications, with specifications aligned with major pharmacopoeial guidelines. A comprehensive Certificate of Analysis (COA) documenting identity, purity, and impurity profiles is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and must be kept in a dry environment to maintain stability and potency.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
pH (1% Solution)	10.5 - 11.5
Water Content (KF)	≤ 5.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Complies with ICH limits
Bacterial Endotoxins	< 0.1 EU/mg

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