Description

Indantadol is a high-purity pharmaceutical intermediate and research chemical of significant interest in medicinal chemistry. Its value lies in its role as a key building block for the synthesis of novel therapeutic agents targeting neurological pathways. This compound is primarily needed by pharmaceutical R&D laboratories, contract manufacturing organizations (CMOs), and academic institutions engaged in drug discovery programs.

Application

• Pharmaceutical Intermediate: A critical precursor in the multi-step synthesis of potential central nervous system (CNS) active drugs.
• Medicinal Chemistry Research: Used as a scaffold or starting material for structure-activity relationship (SAR) studies to develop new pharmacologically active molecules.
• Reference Standard: Serves as an analytical standard for quality control and method development in API (Active Pharmaceutical Ingredient) manufacturing.
• Biochemical Research: Employed in vitro studies to investigate specific biological targets and mechanisms of action.

Basic Information

Product Name	Indantadol
CAS No.	202844-10-8
Molecular Formula	C17H16N2O2
Molecular Weight	280.32 g/mol
Synonyms	1-(4-Chlorophenyl)-3,3-dimethyl-1,3-dihydro-2H-indol-2-one; CHR 2797; Tosedostat; (4-Chlorophenyl)(3,3-dimethyl-2-oxoindolin-1-yl)methanone; Indantadol hydrochloride (salt form); UNII-6Q4WX5M2H5
EINECS	Contact for details

Quality Control

Our Indantadol is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical research applications. A detailed Certificate of Analysis (COA) providing specifications for assay, related substances, and residual solvents is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to maintain stability.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Loss on Drying	≤ 0.5%
Residue on Ignition	≤ 0.1%

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