Description

3-Amino-1-(2,3-Dihydro-1H-Indol-1-Yl)-1-Propanonehydrochloride is a high-purity, advanced pharmaceutical intermediate with a distinct indole-based structure. This compound is critical for the synthesis of complex active pharmaceutical ingredients (APIs) and novel chemical entities in medicinal chemistry research. It is primarily utilized by pharmaceutical R&D laboratories and fine chemical manufacturers focused on developing new therapeutic agents, particularly in the areas of central nervous system and oncology research.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel drug candidates and active pharmaceutical ingredients (APIs).
• Medicinal Chemistry Research: Used in structure-activity relationship (SAR) studies and lead optimization for new therapeutic targets.
• Organic Synthesis: Serves as a versatile precursor for constructing complex heterocyclic compounds and indole derivatives.
• Biochemical Research: Potential use as a tool compound or probe in biochemical and pharmacological assays.
• Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for custom synthesis projects.
• Academic Research: Utilized in university and institutional labs for advanced organic synthesis and drug discovery programs.

Basic Information

Product Name	3-Amino-1-(2,3-Dihydro-1H-Indol-1-Yl)-1-Propanonehydrochloride
CAS No.	1220039-03-1
Molecular Formula	C11H15ClN2O
Molecular Weight	226.70 g/mol
Synonyms	1-(2,3-Dihydro-1H-indol-1-yl)-3-aminopropan-1-one hydrochloride; 3-Amino-1-(indolin-1-yl)propan-1-one hydrochloride; 1-(Indolin-1-yl)-3-aminopropan-1-one HCl; 3-Amino-1-indolin-1-ylpropan-1-one hydrochloride; 3-Amino-1-(2,3-dihydroindol-1-yl)propan-1-one hydrochloride; 1-(2,3-Dihydro-1H-indol-1-yl)-3-oxopropylamine hydrochloride
EINECS	Contact for details

Quality Control

Our 3-Amino-1-(2,3-Dihydro-1H-Indol-1-Yl)-1-Propanonehydrochloride is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via spectroscopic methods, to ensure it meets the stringent requirements for pharmaceutical R&D. Certificates of Analysis (COA) detailing batch-specific results are available upon request, supporting regulatory documentation needs.

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 nature, the container must be kept tightly sealed to minimize exposure to 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.