share

Deptropine Dihydrogen Citrate CAS NO 2169-75-7


Unit Price:

CAS No.:2169-75-7

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Deptropine Dihydrogen Citrate CAS NO 2169-75-7 is a high-purity pharmaceutical intermediate and active ingredient, recognized for its specific pharmacological activity. This compound is critical for ensuring the efficacy and consistency of final pharmaceutical formulations. It is primarily required by manufacturers in the pharmaceutical and life sciences sectors for research, development, and production of therapeutic agents.

Application

  • Pharmaceutical Active Ingredient (API): Serves as a key component in the synthesis of specific therapeutic medications.
  • Pharmacological Research: Used as a reference standard and investigational compound in preclinical and clinical studies.
  • Formulation Development: Employed in the development of stable and effective dosage forms such as tablets or injectables.
  • Biochemical Research: Utilized in studies exploring receptor interactions and biochemical pathways.
  • Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.
  • Analytical Standard: Acts as a high-purity standard for quality control and method validation in analytical laboratories.

Basic Information

Product Name Deptropine Dihydrogen Citrate
CAS No. 2169-75-7
Molecular Formula C₂₄H₃₃NO₈
Molecular Weight 463.52 g/mol
Synonyms Deptropine Citrate; Deptropine Dihydrogen Citrate; 3α-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yloxy)tropane Dihydrogen Citrate; 3α-(10,11-Dihydro-5H-dibenzo[a,d]cyclohepten-5-yloxy)-8-methyl-8-azabicyclo[3.2.1]octane Dihydrogen Citrate; Deptropine Hydrogen Citrate; Deptropine Acid Citrate; Deptrocin; BRN 4160995
EINECS 218-511-7

Quality Control

Our Deptropine Dihydrogen Citrate is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including identification, assay, and impurity profiling, to ensure it meets stringent pharmaceutical-grade specifications. A Certificate of Analysis (COA) detailing all test results is provided with every shipment to guarantee traceability and compliance.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). The product is hygroscopic (moisture-sensitive) and must be kept under dry conditions to prevent degradation.

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%
Loss on Drying ≤1.0%
Residue on Ignition ≤0.1%
Heavy Metals ≤20 ppm
Related Substances (HPLC) Total impurities ≤2.0% Any single impurity ≤0.5%

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

Complete Your RFQ

0/ 2000

Why choose US

Trusted Manufacturer

With our own production facilities, we ensure consistent quality, reliable supply, and full traceability.

Rigorous Quality Assurance

Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.

Advanced R&D Expertise

Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.