Description

Glaucogenin C Mono-D-Thevetoside is a specific cardiac glycoside derivative, a high-purity reference standard and key intermediate in pharmaceutical research and development. Its precise chemical structure makes it invaluable for studying cardiac activity and for the synthesis of novel therapeutic agents. This compound is primarily sought by research institutions, pharmaceutical developers, and manufacturers of high-grade active pharmaceutical ingredients (APIs) for cardiovascular applications.

Application

• Pharmaceutical Reference Standard: Used as a certified standard for quality control, method validation, and regulatory submissions in drug development.
• Cardiac Drug Research: Serves as a critical intermediate or lead compound in the research and synthesis of new cardioprotective and cardiotonic agents.
• Biochemical Studies: Employed in pharmacological assays to investigate mechanisms of action related to Na+/K+-ATPase inhibition and cardiac contractility.
• Natural Product Isolation & Analysis: Used as a marker compound for the identification and quantification of related glycosides in plant extracts and herbal formulations.
• Academic Research: Utilized in university and institutional labs for studies in medicinal chemistry, pharmacology, and natural product chemistry.
• API Manufacturing: Acts as a high-purity building block or intermediate in the multi-step synthesis of complex active pharmaceutical ingredients.

Basic Information

Product Name	Glaucogenin C Mono-D-Thevetoside
CAS No.	849201-84-9
Molecular Formula	C36H56O13
Molecular Weight	696.83 g/mol
Synonyms	Glaucogenin C monothevetoside; Glaucogenin C D-thevetoside; (3β,5β,14β)-3-[(6-Deoxy-3-O-methyl-α-L-glucopyranosyl)oxy]-14-hydroxycard-20(22)-enolide; Glaucogenin C α-L-Thevetoside; 849201-84-9; Glaucogenin C mono-D-thevetoside; Glaucogenin C-α-L-thevetoside
EINECS	Contact for details

Quality Control

Every batch of Glaucogenin C Mono-D-Thevetoside is produced and tested under strict quality management systems. We provide comprehensive analytical data to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical research. A detailed Certificate of Analysis (COA) including HPLC purity, identification by spectroscopic methods (IR, NMR, MS), and related substance analysis is supplied with each 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). This product is hygroscopic (moisture-sensitive) and must be kept under anhydrous conditions. For long-term storage, consider storing under an inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (IR)	Conforms to reference spectrum
Identification (HPLC)	Retention time matches reference standard
Purity (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0%
Single Unknown Impurity	≤ 0.5%
Residual Solvents (GC)	Complies with ICH Q3C guidelines
Water Content (KF)	≤ 1.0% w/w

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