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Lanatoside D CAS NO 11030-31-2


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CAS No.:11030-31-2

Grade:Pharmacy Grade

Content:99.9%

Brand:Customizable

Packaging:Customizable

Description

Lanatoside D is a specific cardiac glycoside compound, a key intermediate in the biosynthesis of digoxin and other related therapeutic agents. Its precise chemical structure makes it a critical reference standard and starting material for pharmaceutical research and development. This high-purity compound is essential for laboratories and manufacturers focused on cardiovascular drug discovery, quality control, and metabolic studies.

Application

  • Pharmaceutical Reference Standard: Used as a high-purity calibrant in HPLC and LC-MS methods for the quantification of cardiac glycosides in raw materials and finished drug products.
  • Active Pharmaceutical Ingredient (API) Intermediate: Serves as a crucial precursor in the semi-synthetic production of digoxin and other cardiocative drugs.
  • Biochemical Research: Employed in studies investigating the mechanism of action, structure-activity relationships (SAR), and metabolism of cardiac glycosides.
  • Quality Control & Assurance: Essential for identity testing and impurity profiling in the manufacturing processes of digitalis-based medications.
  • Metabolite Studies: Used in research to identify and characterize the metabolic pathways and breakdown products of related therapeutic compounds.

Basic Information

Product Name Lanatoside D
CAS No. 11030-31-2
Molecular Formula C₄₉H₇₆O₂₀
Molecular Weight 985.1 g/mol
Synonyms Lanatoside D; 3β-[(O-β-D-Glucopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-O-2,6-dideoxy-β-D-ribo-hexopyranosyl-(1→4)-2,6-dideoxy-β-D-ribo-hexopyranosyl)oxy]-12β,14-dihydroxy-5β-card-20(22)-enolide; Digilanide D; Lanadigin; Digitalis Lanata Glycoside D
EINECS Contact for details

Quality Control

Our Lanatoside D is manufactured under strict quality management systems. Each batch is subjected to comprehensive analytical testing, including identity confirmation by spectroscopic methods and purity assessment by HPLC, to ensure it meets the stringent requirements for pharmaceutical research and development. 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 place at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed in a dry environment to prevent moisture absorption.

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%
Water Content (KF) ≤ 2.0%
Residue on Ignition ≤ 0.1%
Related Substances (HPLC) Total impurities ≤ 2.0% Any single impurity ≤ 1.0%

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

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