Description

1,3-Dihydro-3-Ethyl-1-(2-(4-Morpholinyl)Ethyl)-3-Phenyl-2H-Indol-2-One Monohydrochloride is a high-purity, synthetically derived organic compound primarily utilized as a critical pharmaceutical intermediate. Its value lies in its role as a key building block for the synthesis of complex active pharmaceutical ingredients (APIs), where consistent quality and reliable supply are paramount. This product is essential for research institutions and manufacturers in the pharmaceutical and fine chemical industries engaged in drug discovery and development processes. The compound is supplied with a Certificate of Analysis to ensure batch-to-batch consistency and traceability.

Application

• Pharmaceutical Intermediate: A key precursor in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
• Research & Development: Used in medicinal chemistry for structure-activity relationship (SAR) studies and lead optimization in drug discovery programs.
• Chemical Synthesis: Serves as a versatile building block for constructing complex heterocyclic compounds in organic synthesis.
• Reference Standard: Employed as an analytical standard for quality control and method validation in pharmaceutical analysis.

Basic Information

Product Name	1,3-Dihydro-3-Ethyl-1-(2-(4-Morpholinyl)Ethyl)-3-Phenyl-2H-Indol-2-One Monohydrochloride
CAS No.	37126-54-8
Molecular Formula	C22H26N2O2•HCl
Molecular Weight	386.92 g/mol
Synonyms	3-Ethyl-1-(2-morpholinoethyl)-3-phenylindolin-2-one hydrochloride; 3-Ethyl-1-[2-(morpholin-4-yl)ethyl]-3-phenylindolin-2-one hydrochloride; 3-Ethyl-1-(2-morpholin-4-ylethyl)-3-phenyl-1,3-dihydro-2H-indol-2-one hydrochloride; 2H-Indol-2-one, 1,3-dihydro-3-ethyl-1-[2-(4-morpholinyl)ethyl]-3-phenyl-, monohydrochloride; 3-Ethyl-3-phenyl-1-(2-morpholinoethyl)indolin-2-one HCl
EINECS	Contact for details

Quality Control

Our 1,3-Dihydro-3-Ethyl-1-(2-(4-Morpholinyl)Ethyl)-3-Phenyl-2H-Indol-2-One Monohydrochloride is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the stringent requirements for pharmaceutical intermediates. A detailed Certificate of Analysis (COA) documenting all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed to prevent degradation from atmospheric moisture. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
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 ≤ 0.5%

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