Description

Ozanimod is a potent and selective sphingosine-1-phosphate (S1P) receptor modulator, identified by the CAS registry number 1306760-87-1. This small molecule pharmaceutical is of critical importance for its targeted immunomodulatory action, offering a refined mechanism for managing autoimmune conditions. It is primarily required by pharmaceutical manufacturers and advanced research institutions engaged in the development and production of innovative therapeutics for immune-mediated diseases.

Application

• Active Pharmaceutical Ingredient (API): Primary use as the key therapeutic component in finished dosage forms for the treatment of relapsing forms of multiple sclerosis (MS).
• Clinical Research Material: Serves as a critical reference standard and bulk material for ongoing clinical trials exploring new indications and formulations.
• Pharmaceutical Development: Used in formulation studies for solid oral dosage forms such as capsules and tablets, focusing on stability and bioavailability optimization.
• Regulatory Submissions: Supplied as a high-purity compound for generating data required for regulatory filings (e.g., FDA, EMA) including stability, impurity profiling, and pharmacokinetic studies.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for the commercial-scale production of approved drug products.
• Mechanistic Studies: Utilized in preclinical and academic research to investigate S1P receptor biology and signaling pathways in immunology and neurology.

Basic Information

Product Name	Ozanimod
CAS No.	1306760-87-1
Molecular Formula	C23H28N2O3
Molecular Weight	380.48 g/mol
Synonyms	RPC-1063; CC-100044; 4-[(1E)-1-[[(4-Cyclohexyl-3-trifluoromethylphenyl)methoxyimino]ethyl]-2-ethyl-6,8-difluoro-1,2,3,4-tetrahydroquinolin-4-ol; 1-{4-[(1E)-1-({[4-Cyclohexyl-3-(trifluoromethyl)phenyl]methoxy}imino)ethyl]-2-ethyl-6,8-difluoro-3,4-dihydro-2H-quinolin-1-yl}ethanone; S1P Receptor Modulator RPC1063
EINECS	Contact for details

Quality Control

Our Ozanimod is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation, residual solvent analysis, and stringent control of specified impurities. We provide full traceability and support regulatory requirements with comprehensive documentation. Certificates of Analysis (COA) detailing all test results against agreed specifications are available for 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 under inert conditions or in a desiccated environment after opening to maintain stability and potency. 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)	≥98.5%
Related Substances (HPLC)	Total impurities ≤1.5% Any single unknown impurity ≤0.10%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤0.5%
Heavy Metals	≤20 ppm

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