Description

Fingolimod Stearate Amide is a high-purity, chemically defined derivative of the active pharmaceutical ingredient Fingolimod. This compound is specifically engineered to offer enhanced stability and tailored physicochemical properties for advanced pharmaceutical research and development. It serves as a critical intermediate or reference standard for scientists developing novel formulations and delivery systems in the fields of immunology and neurology. The target industries for this specialized chemical are primarily pharmaceutical R&D, contract manufacturing organizations (CMOs), and academic research institutions focused on autoimmune and neurological disorders.

Application

• As a key pharmaceutical intermediate in the synthesis of novel Fingolimod analogs and prodrugs.
• As a reference standard for analytical method development and validation in quality control laboratories.
• For preclinical research investigating the structure-activity relationship (SAR) of sphingosine-1-phosphate (S1P) receptor modulators.
• In formulation studies aimed at improving the solubility, bioavailability, or controlled release profiles of therapeutic agents.
• As a starting material for process chemistry and scale-up optimization in active pharmaceutical ingredient (API) manufacturing.
• For use in academic research exploring new therapeutic pathways for multiple sclerosis and other autoimmune diseases.

Basic Information

Product Name	Fingolimod Stearate Amide
CAS No.	1242271-27-7
Molecular Formula	C41H78N2O2
Molecular Weight	631.1 g/mol
Synonyms	2-Amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol stearamide; FTY720 Stearamide; Fingolimod (FTY720) Stearic Acid Amide; (2R)-2-Amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol octadecanamide; 1-Stearamido-2-(4-octylphenethyl)-2-aminopropane-1,3-diol; FTY720-C18 Amide; S1P Receptor Modulator Derivative
EINECS	Contact for details

Quality Control

Our Fingolimod Stearate Amide is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing to ensure it meets the high-purity standards required for pharmaceutical research. Specifications typically include identity confirmation by spectroscopic methods, purity assessment by HPLC, and control of specific impurities. A comprehensive Certificate of Analysis (COA) detailing all test results is provided with every shipment to ensure full traceability and compliance with your research protocols.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry environment. The product is hygroscopic (moisture-sensitive) and should be handled under anhydrous conditions when opening to maintain stability and purity.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time corresponds to reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%

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