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1-(5-Chloro-1H-Indol-3-Yl)-2-Methylpropan-2-Amine CAS NO 833-05-6


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CAS No.:833-05-6

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

1-(5-Chloro-1H-Indol-3-Yl)-2-Methylpropan-2-Amine is a specialized indole derivative of significant interest in advanced organic synthesis. This compound serves as a crucial pharmaceutical intermediate and a versatile building block for the development of novel bioactive molecules. It is primarily utilized by research institutions and chemical manufacturers in the pharmaceutical, agrochemical, and life science sectors for the synthesis of complex chemical entities.

Application

  • Pharmaceutical Intermediate: Key precursor in the synthesis of novel drug candidates, particularly those targeting neurological and psychiatric disorders.
  • Agrochemical Research: Building block for developing new active ingredients in crop protection and pest management products.
  • Chemical Synthesis: Versatile reagent for constructing complex indole-based molecular frameworks in medicinal and process chemistry.
  • Life Science Research: Used in biochemical research as a tool compound for studying receptor interactions and enzyme inhibition.
  • Material Science: Potential monomer or intermediate for synthesizing specialty polymers and advanced organic materials.

Basic Information

Product Name 1-(5-Chloro-1H-Indol-3-Yl)-2-Methylpropan-2-Amine
CAS No. 833-05-6
Molecular Formula C12H15ClN2
Molecular Weight 222.71 g/mol
Synonyms 5-Chloro-α,α-dimethyl-1H-indole-3-ethanamine; 2-(5-Chloro-1H-indol-3-yl)-2-methylpropan-1-amine; 5-Chloro-α,α-dimethyltryptamine (5-Cl-α,α-DMT); 1-(5-Chloro-1H-indol-3-yl)-2-methyl-2-propylamine; 833-05-6; 5-Chloro-α,α-dimethyltryptamine; 5-Cl-DMT
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Quality Control

Our 1-(5-Chloro-1H-Indol-3-Yl)-2-Methylpropan-2-Amine is produced under strict quality management systems. Each batch undergoes rigorous analytical testing, including HPLC, NMR, and mass spectrometry, to ensure identity, purity, and consistency. Certificates of Analysis (COA) documenting all critical quality attributes are available upon request. We adhere to cGMP principles for the manufacture of pharmaceutical intermediates to support our clients' regulatory requirements.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). Keep the container tightly sealed in a dry environment to prevent moisture absorption. Store away from incompatible materials.

Specification

Item Specification
Appearance White to off-white crystalline powder
Identification (IR) Conforms to structure
Identification (HPLC) Conforms to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0%
Any single impurity ≤ 0.5%
Residual Solvents (GC) Complies with ICH guidelines
Heavy Metals ≤ 20 ppm
Loss on Drying ≤ 0.5%

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

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