Description

Uzarigenin-Glucoside-Canaroside is a specific cardiac glycoside derivative, a compound of significant interest in pharmaceutical research and development. Its value lies in its role as a reference standard and a key intermediate for the synthesis of more complex bioactive molecules. This high-purity compound is essential for researchers and manufacturers in the pharmaceutical, biotechnology, and phytochemical sectors who require reliable, well-characterized materials for analytical, pharmacological, and synthetic applications.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the quality control and quantification of related cardiac glycosides in raw materials and finished products.
• Biochemical Research: Serves as a crucial tool in studies investigating the structure-activity relationships, metabolism, and mechanism of action of cardiac glycosides.
• Active Pharmaceutical Ingredient (API) Intermediate: Acts as a high-purity building block in the multi-step synthesis of novel therapeutic agents targeting cardiovascular conditions.
• Phytochemical Analysis: Employed as an analytical standard for the identification and quantification of uzarigenin derivatives in plant extracts and herbal formulations.
• Drug Discovery & Development: Utilized in high-throughput screening (HTS) assays and preclinical studies to evaluate efficacy and toxicity profiles.

Basic Information

Product Name	Uzarigenin-Glucoside-Canaroside
CAS No.	100857-42-9
Molecular Formula	C29H44O9
Molecular Weight	536.66 g/mol
Synonyms	Canaroside; Uzarigenin glucoside; Uzarigenin 3-O-β-D-glucopyranoside; 3β-[(β-D-Glucopyranosyl)oxy]-14-hydroxy-5β,14β-card-20(22)-enolide; (3β,5β)-3-(β-D-Glucopyranosyloxy)-14-hydroxy-19-oxocard-20(22)-enolide; 14-Hydroxy-3β-[(β-D-glucopyranosyl)oxy]-5β-card-20(22)-enolide
EINECS	Contact for details

Quality Control

Our Uzarigenin-Glucoside-Canaroside is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity, IR and NMR for structural confirmation, and tests for residual solvents and heavy metals, to ensure it meets the stringent requirements for research and development use. A detailed Certificate of Analysis (COA) is provided with every shipment, guaranteeing traceability, consistency, and compliance with your specifications.

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 in a desiccated environment to maintain stability and purity.

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%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm

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