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Rauwolscine 4-Aminophenylcarboxamide CAS NO 108206-13-9


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CAS No.:108206-13-9

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Rauwolscine 4-Aminophenylcarboxamide is a specialized organic compound belonging to the class of indole alkaloid derivatives. This high-purity intermediate is of significant interest for advanced pharmaceutical research and development, particularly in the study of neurological pathways. It is primarily utilized by research institutions and pharmaceutical companies engaged in the synthesis of novel therapeutic agents. The compound is supplied under stringent quality control to ensure reliability for critical applications.

Application

  • Pharmaceutical Intermediate: Serves as a key building block in the synthesis of complex molecules for preclinical and clinical research.
  • Neurological Research: Used in biochemical studies targeting adrenergic and serotonergic receptors to investigate potential treatments for CNS disorders.
  • Reference Standard: Employed as a high-purity analytical standard in method development and quality control laboratories.
  • Academic Research: Utilized in university and institutional labs for pharmacological studies and chemical synthesis projects.
  • Process Development: Acts as a critical material for scaling up synthetic routes in process chemistry within API (Active Pharmaceutical Ingredient) development.

Basic Information

Product Name Rauwolscine 4-Aminophenylcarboxamide
CAS No. 108206-13-9
Molecular Formula C24H26N4O2
Molecular Weight 402.49 g/mol
Synonyms 4-Aminophenylcarboxamide Rauwolscine; Rauwolscine-4-Aminophenylcarboxamide; 16-Epi-α-Yohimbine 4-Aminophenylcarboxamide; α-Yohimbine derivative; (16α,17α)-16,17-Didehydro-19-methyloxayohimban-16-carboxylic acid 4-aminophenylamide; Rauwolscine carboxamide derivative; Contact for additional synonyms.
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Quality Control

Our Rauwolscine 4-Aminophenylcarboxamide is manufactured under a quality management system and undergoes rigorous analytical testing to ensure identity, purity, and consistency. Standard quality control includes chromatographic purity analysis (HPLC), identity confirmation (IR, NMR), and residual solvent screening. A comprehensive Certificate of Analysis (COA) detailing batch-specific results is provided with each shipment. Specifications can be aligned with client requirements for research or cGMP applications.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (typically 15-25°C). The product may be hygroscopic (moisture-sensitive); therefore, the container should be kept tightly sealed in a dry environment. For long-term storage, consider inert atmosphere conditions.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time matches reference standard
Purity (HPLC) ≥ 98.0%
Loss on Drying ≤ 1.0%
Residue on Ignition ≤ 0.1%
Heavy Metals ≤ 20 ppm
Residual Solvents (GC) Complies with ICH guidelines

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

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