Description

Ganciclovir CAS NO 82410-32-0 is a synthetic nucleoside analogue and a potent antiviral agent. Its primary value lies in its selective inhibition of viral DNA polymerase, making it a critical active pharmaceutical ingredient (API) for treating severe cytomegalovirus (CMV) infections. This compound is essential for pharmaceutical manufacturers developing injectable formulations, oral medications, and ophthalmic solutions for immunocompromised patients, such as transplant recipients and individuals with HIV/AIDS.

Application

• Pharmaceutical API: Core active ingredient in antiviral medications for systemic CMV infections.
• Ophthalmic Formulations: Used in gels or implants for the treatment of CMV retinitis.
• Intravenous (IV) Solutions: Manufacture of sterile injectable drugs for hospital use.
• Oral Dosage Forms: Production of capsules or tablets for maintenance therapy.
• Research & Development: Reference standard and building block for novel antiviral compound synthesis.
• Veterinary Pharmaceuticals: Potential application in antiviral treatments for specific animal viruses.

Basic Information

Product Name	Ganciclovir
CAS No.	82410-32-0
Molecular Formula	C9H13N5O4
Molecular Weight	255.23 g/mol
Synonyms	9-[(1,3-Dihydroxy-2-propoxy)methyl]guanine; DHPG; BW-B759U; Cytovene; Cymevene; Ganciclovirum; Ganciclovir Sodium; GCV
EINECS	Contact for details

Quality Control

Our Ganciclovir is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, purity assay, and impurity profiling via HPLC, to ensure it meets high-grade pharmaceutical standards. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance with cGMP and ICH guidelines.

Storage

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

Specification

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

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