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Felodipine-D5 CAS NO 1242281-38-4


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CAS No.:1242281-38-4

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Felodipine-D5 is a deuterated analog of the calcium channel blocker felodipine, specifically labeled with five deuterium atoms. This stable isotope-labeled compound is an essential reference standard and internal standard for precise quantitative analysis in bioanalytical and pharmacokinetic studies. It is primarily used by pharmaceutical R&D laboratories, contract research organizations (CROs), and analytical testing facilities to ensure accuracy and reliability in method development and validation.

Application

  • Internal Standard for LC-MS/MS: Critical for the accurate quantification of felodipine in complex biological matrices like plasma, serum, and urine.
  • Metabolite Tracing & Pharmacokinetics: Enables detailed studies of drug absorption, distribution, metabolism, and excretion (ADME) using mass spectrometry.
  • Method Development & Validation: Serves as a key component in developing and validating robust, regulatory-compliant bioanalytical assays.
  • Drug Impurity Profiling: Used as a reference marker in the identification and quantification of process-related impurities or degradants.
  • Clinical Research: Supports therapeutic drug monitoring and bioequivalence studies in clinical trial settings.
  • Quality Control in Manufacturing: Acts as a calibration standard to ensure the potency and purity of active pharmaceutical ingredient (API) batches.

Basic Information

Product Name Felodipine-D5
CAS No. 1242281-38-4
Molecular Formula C18H14D5Cl2NO4
Molecular Weight 387.28 g/mol
Synonyms Felodipine-d5; [2H5]-Felodipine; 4-(2,3-Dichlorophenyl)-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid 1-methylethyl 5-methyl ester-d5; Deuterated Felodipine; Felodipine (phenyl-d5); Felodipine Internal Standard; Isotopically Labeled Felodipine; Felodipine-D5 Standard
EINECS Contact for details

Quality Control

Our Felodipine-D5 is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for chemical purity and isotopic enrichment, NMR for structural confirmation, and mass spectrometry for identity verification. A detailed Certificate of Analysis (COA) is provided with every shipment, ensuring traceability and compliance with the stringent requirements of pharmaceutical R&D and regulatory submissions.

Storage

Preserve in a tightly closed container, protected from light. Store at controlled room temperature (15-25°C) in a dry, cool place. This product is hygroscopic (moisture-sensitive) and should be handled in a dry environment to prevent degradation.

Specification

Item Specification
Appearance White to off-white powder
Identification (IR) Conforms to structure
Identification (MS) Conforms to structure
Purity (HPLC) ≥ 98.0%
Isotopic Purity (MS) ≥ 98.0 atom % D
Chemical Purity ≥ 95.0%
Water Content (KF) ≤ 0.5%
Residue on Ignition ≤ 0.1%

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

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