Description

Convallatoxol is a high-purity cardiac glycoside derivative, a key intermediate in advanced pharmaceutical synthesis. This compound is valued for its specific biological activity and structural role in developing therapeutic agents. It is primarily utilized by research institutions and pharmaceutical manufacturers engaged in the development of cardiovascular drugs and biochemical studies.

Application

• Pharmaceutical Intermediate: A critical building block in the synthesis of novel cardiac glycosides and related therapeutic compounds.
• Biochemical Research: Used as a reference standard or active agent in studies of sodium-potassium ATPase inhibition and cardiac cell function.
• Academic & Discovery Chemistry: Serves as a starting material or model compound in medicinal chemistry programs targeting heart failure treatments.
• Reference Standard Production: Manufactured to high purity for use in analytical method development, validation, and quality control laboratories.

Basic Information

Product Name	Convallatoxol
CAS No.	3253-62-1
Molecular Formula	C29H42O10
Molecular Weight	550.64 g/mol
Synonyms	Convallatoxol; 3β,5,14-Trihydroxy-19-oxo-5β-card-20(22)-enolide; Strophanthidin 3-O-β-D-glucoside; Corchoroside A aglycone 3-O-β-D-glucoside; 19-Oxoconvallatoxin; 19-Oxoconvalloside; 5β-Card-20(22)-enolide, 3,5,14-trihydroxy-19-oxo-, 3-β-D-glucopyranoside; Convallatoxin 19-aldehyde
EINECS	Contact for details

Quality Control

Our Convallatoxol is produced under a strict quality management system. Each batch undergoes comprehensive analytical testing, including HPLC for purity and identity confirmation via IR and NMR spectroscopy, to ensure it meets the high standards required for pharmaceutical research and development. A Certificate of Analysis (COA) detailing all specifications 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 (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Loss on Drying	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm

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