Description

O(6)-Npe-Morpholino G(Ibu) Succinate, Tea Salt is a specialized, high-purity chemical intermediate designed for advanced pharmaceutical synthesis. This compound is critical for researchers and manufacturers requiring precise, reliable building blocks for complex drug development, particularly in the creation of novel therapeutic agents. It is primarily utilized by the pharmaceutical, biotechnology, and advanced fine chemical sectors for the research and production of targeted drug candidates.

Application

• Pharmaceutical Intermediate: Serves as a key building block in the synthesis of novel active pharmaceutical ingredients (APIs) and prodrugs.
• Proteolysis-Targeting Chimera (PROTAC) Development: Used in the construction of linker molecules for targeted protein degradation platforms.
• Peptide & Nucleotide Conjugation: Facilitates the site-specific modification and functionalization of biomolecules for enhanced therapeutic properties.
• Prodrug Synthesis: Enables the development of masked drug forms with improved bioavailability and targeted release profiles.
• Bioconjugation Chemistry: Applied in creating antibody-drug conjugates (ADCs) and other targeted delivery systems.
• Medicinal Chemistry Research: Provides a versatile scaffold for structure-activity relationship (SAR) studies and lead optimization in drug discovery.

Basic Information

Product Name	O(6)-Npe-Morpholino G(Ibu) Succinate, Tea Salt
CAS No.	2504201-88-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	O6-(4-Nitrophenethyl)-morpholino-G(Ibu) succinate triethylamine salt; 6-O-(4-Nitrophenethyl)-morpholino-Guanosine(Ibuprofen) Succinate TEA Salt; Npe-Morpholino G(Ibu) Succinate TEA Salt; O6-Npe-Morpholino-G(Ibu)-Succ TEA; PROTAC Linker Intermediate; Nucleoside-Ibuprofen Conjugate TEA Salt; Guanosine Derivative TEA Salt; Advanced Pharmaceutical Building Block
EINECS	Contact for details

Quality Control

Our O(6)-Npe-Morpholino G(Ibu) Succinate, Tea Salt is manufactured under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods (NMR, MS), to ensure it meets the high standards required for pharmaceutical R&D and cGMP applications. A comprehensive Certificate of Analysis (COA) detailing purity, impurities, and other critical parameters is provided with 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 material is hygroscopic (moisture-sensitive) and must be kept under an inert atmosphere (e.g., nitrogen or argon) after opening to prevent degradation. Keep the container tightly sealed in a desiccator when not in use.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (HPLC)	Conforms
Identification (NMR)	Conforms
Purity (HPLC)	≥ 95.0%
Single Impurity (HPLC)	≤ 1.0%
Total Impurities (HPLC)	≤ 5.0%
Water Content (KF)	≤ 2.0%
Residual Solvents (GC)	Meets ICH guidelines

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