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Inarigivir (Ori-9020, Sb-9000) CAS NO 475650-36-3


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CAS No.:475650-36-3

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Inarigivir (Ori-9020, Sb-9000) is a high-purity, small-molecule pharmaceutical intermediate and research compound. This compound is critical for advanced antiviral research and development programs, particularly in the field of hepatitis B therapeutics. It is primarily utilized by pharmaceutical R&D laboratories, biotechnology companies, and contract research organizations (CROs) engaged in the discovery and synthesis of novel antiviral agents.

Application

  • Antiviral Drug Development: Key intermediate in the research and synthesis of novel therapeutic agents targeting hepatitis B virus (HBV).
  • Pharmaceutical R&D: Used as a reference standard and building block in medicinal chemistry for structure-activity relationship (SAR) studies.
  • Biochemical Research: Employed in in vitro and in vivo studies to investigate mechanisms of action for immune modulation.
  • Preclinical Studies: Serves as an active pharmaceutical ingredient (API) intermediate for formulation development and toxicology assessments.
  • Contract Manufacturing: Supplied to CDMOs for the scale-up synthesis under cGMP conditions for clinical trial material production.

Basic Information

Product Name Inarigivir (Ori-9020, Sb-9000)
CAS No. 475650-36-3
Molecular Formula C19H21N5O7S2
Molecular Weight 495.53 g/mol
Synonyms SB 9000; SB-9000; Ori-9020; ORI-9020; Inarigivir sodium; 2-Amino-9-[(1S,3R,4S)-4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-3H-purin-6(9H)-one 5'-(methyl hydrogen sulfate) 3'-(hydrogen sulfate); GS-9900; GS 9900
EINECS Contact for details

Quality Control

Our Inarigivir is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for research and development. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We adhere to relevant guidelines for pharmaceutical intermediates, and specifications can be aligned with client requirements for preclinical and clinical development stages.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). This material is hygroscopic (moisture-sensitive) and must be kept under inert atmosphere or in a desiccator to maintain stability and prevent degradation.

Specification

Item Specification
Appearance White to off-white powder
Identification (HPLC) Conforms to reference standard
Identification (IR) Conforms to structure
Assay (HPLC) ≥98.0%
Water Content (KF) ≤1.0%
Residual Solvents (GC) Meets ICH Q3C guidelines
Heavy Metals <10 ppm
Single Unknown Impurity ≤0.5%
Total Impurities ≤2.0%

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

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Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.