Description

Ethyl Fingolimod Hydrochloride is a high-purity synthetic intermediate and active pharmaceutical ingredient (API) derivative of the immunomodulatory drug Fingolimod. This compound is critical for pharmaceutical research and development, particularly in the synthesis of novel sphingosine-1-phosphate (S1P) receptor modulators. It is primarily utilized by pharmaceutical manufacturers and advanced research institutions engaged in developing therapies for autoimmune diseases and organ transplantation.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of Fingolimod analogs and next-generation S1P receptor modulators.
• Active Pharmaceutical Ingredient (API) Research: Serves as a reference standard and starting material for the development and scale-up of new immunomodulatory drugs.
• Preclinical & Clinical Studies: Used in pharmacological and toxicological studies to investigate new therapeutic pathways.
• Process Chemistry & Optimization: Employed in route scouting and process development for more efficient API manufacturing.
• Academic & Institutional Research: Supports biochemical and pharmacological research into autoimmune disorders, multiple sclerosis, and transplant rejection mechanisms.
• Quality Control & Analytical Standards: Functions as a certified reference material (CRM) for assay validation and impurity profiling in regulatory submissions.

Basic Information

Product Name	Ethyl Fingolimod Hydrochloride
CAS No.	162361-23-1
Molecular Formula	C21H36ClNO2
Molecular Weight	369.97 g/mol
Synonyms	2-Amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol Ethyl Ester Hydrochloride; FTY720 Ethyl Ester Hydrochloride; (2-Amino-2-{2-[4-(1-oxooctyl)phenyl]ethyl}propane-1,3-diol) Ethyl Ester Hydrochloride; Ethyl 2-Amino-2-(2-(4-octylphenyl)ethyl)propane-1,3-diol Hydrochloride; UNII-8V71L2A7VQ; Fingolimod Ethyl Ester HCl
EINECS	Contact for details

Quality Control

Our Ethyl Fingolimod Hydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, identity confirmation by IR and NMR, and stringent control of residual solvents and related substances. We provide full traceability and Certificates of Analysis (COA) that detail compliance with in-house specifications developed for pharmaceutical research applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (NMR)	Conforms to structure
Assay (HPLC)	≥98.0%
Related Substances (HPLC)	Total impurities ≤2.0%
Single Unknown Impurity	≤0.5%
Residual Solvents (GC)	Complies with ICH Q3C
Water Content (KF)	≤1.0%
Heavy Metals	≤20 ppm

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