Description

Ralitoline is a specialized organic compound with significant utility in advanced chemical synthesis and pharmaceutical research. Its unique molecular structure makes it a valuable intermediate for developing novel active pharmaceutical ingredients (APIs) and fine chemicals. This product is essential for research and development laboratories, pharmaceutical manufacturers, and chemical synthesis facilities focused on creating innovative therapeutic agents and high-value specialty compounds.

Application

• Pharmaceutical Intermediate: A key building block in the synthesis of novel active pharmaceutical ingredients (APIs) and drug candidates.
• Chemical Research: Used as a reagent or starting material in advanced organic synthesis and medicinal chemistry research programs.
• Fine Chemical Production: Serves as a critical intermediate in the manufacture of complex, high-purity specialty chemicals.
• Biochemical Studies: Employed in the development and study of compounds with potential biological activity.
• Process Development: Utilized in scaling up synthetic routes from laboratory to pilot and commercial production scales.

Basic Information

Product Name	Ralitoline
CAS No.	93738-40-0
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Ralitoline; 93738-40-0; 4-(2,6-Dimethylphenoxy)-1-piperidinecarboxamide; UNII-3R4P5Q5U4T; 3R4P5Q5U4T; 1-Piperidinecarboxamide, 4-(2,6-dimethylphenoxy)-; 4-(2,6-Dimethylphenoxy)piperidine-1-carboxamide
EINECS	Contact for details

Quality Control

Our Ralitoline is produced under stringent quality management systems to ensure batch-to-batch consistency and high purity. Each lot undergoes comprehensive analytical testing, including identity confirmation, purity assay, and impurity profiling, to meet the exacting standards required for pharmaceutical and research applications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (typically 15-25°C). Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Residual Solvents (GC)	Meets ICH guidelines
Loss on Drying	≤ 0.5%

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