Description

Fty720 Octanoic Acid Hydrochloride is a high-purity chemical intermediate, primarily recognized for its role in the synthesis of Fingolimod (FTY720), an important immunomodulatory pharmaceutical agent. This compound is critical for ensuring the quality and efficacy of the final active pharmaceutical ingredient (API) in advanced therapeutic applications. It is essential for research institutions, pharmaceutical development laboratories, and manufacturers specializing in innovative immunosuppressant therapies and related fine chemical synthesis.

Application

• Pharmaceutical Intermediate: Key precursor in the multi-step synthesis of Fingolimod (FTY720) and its analogs.
• Immunology Research: Used in the development and study of novel S1P (sphingosine-1-phosphate) receptor modulators.
• Process Chemistry: Serves as a critical building block in GMP and non-GMP scale-up processes for API manufacturing.
• Reference Standard: Employed as an analytical standard for quality control and method validation in pharmaceutical analysis.
• Biochemical Synthesis: Utilized in the preparation of specialized probes and ligands for biological target studies.

Basic Information

Product Name	Fty720 Octanoic Acid Hydrochloride
CAS No.	896472-95-0
Molecular Formula	C28H48ClNO2
Molecular Weight	466.14 g/mol
Synonyms	2-Amino-2-[2-(4-octylphenyl)ethyl]propane-1,3-diol Hydrochloride; FTY720 Octanoate HCl; Fingolimod Octanoic Acid Ester Hydrochloride; (2-Amino-2-{2-[4-(octyl)phenyl]ethyl}propane-1,3-diol) Hydrochloride; FTY720 C8 Ester HCl; Octanoic Acid, Ester with FTY720, Hydrochloride; 2-Amino-2-(2-(4-n-octylphenyl)ethyl)-1,3-propanediol Hydrochloride
EINECS	Contact for details

Quality Control

Our Fty720 Octanoic Acid Hydrochloride is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. We provide comprehensive Certificates of Analysis (COA) with each shipment, detailing all critical quality attributes. Our production can align with cGMP guidelines for pharmaceutical intermediate applications upon request.

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). This material is hygroscopic (moisture-sensitive) and should be handled under dry conditions to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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