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Ketimipramine CAS NO 796-29-2


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CAS No.:796-29-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Ketimipramine CAS NO 796-29-2 is a tricyclic compound of significant interest in pharmaceutical research and development. This chemical serves as a key intermediate or reference standard in the synthesis and analytical profiling of active pharmaceutical ingredients (APIs). It is primarily utilized by research institutions and manufacturers in the pharmaceutical and life sciences sectors for drug discovery, process development, and quality control applications.

Application

  • Pharmaceutical Intermediate: Serves as a critical building block in the synthesis of complex drug molecules and active pharmaceutical ingredients (APIs).
  • Reference Standard: Used as a high-purity standard in analytical laboratories for method development, validation, and quality control testing via HPLC, GC, or spectroscopy.
  • Biochemical Research: Employed in life science research to study biological pathways, receptor binding, and pharmacological activity.
  • Process Chemistry: Integral to scale-up and optimization studies in pharmaceutical manufacturing for yield improvement and impurity profiling.
  • Contract Research & Manufacturing (CRAM): Supplied to CROs and CDMOs engaged in custom synthesis and development projects for clients.

Basic Information

Product Name Ketimipramine
CAS No. 796-29-2
Molecular Formula C₁₉H₂₀N₂
Molecular Weight 276.38 g/mol
Synonyms Ketimipramine; 5H-Dibenzo[b,f]azepine-5-propanamine, 10,11-dihydro-N,N-dimethyl-; 10,11-Dihydro-N,N-dimethyl-5H-dibenzo[b,f]azepine-5-propanamine; 3-(10,11-Dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1-amine; Desipramine Impurity; Desmethylimipramine; Norimipramine; G-35020
EINECS Contact for details

Quality Control

Our Ketimipramine is manufactured under a strict quality management system. Each batch undergoes comprehensive analytical testing, including identification (IR, NMR), purity assay (HPLC), and control of specified impurities, to ensure it meets the high standards required for research and pharmaceutical 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, and well-ventilated area at controlled room temperature (15-25°C). Keep the container tightly sealed to protect from moisture.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to reference spectrum
Identification (HPLC) Retention time corresponds to reference standard
Assay (HPLC) ≥ 98.0%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC) Complies with ICH Q3C guidelines
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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