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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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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.





