Description

Silenoside A is a high-purity, naturally derived chemical compound of significant interest in advanced research and development. This specialized phytochemical serves as a critical reference standard and active ingredient for developing novel therapeutic and nutraceutical formulations. It is primarily utilized by pharmaceutical R&D laboratories, nutraceutical manufacturers, and academic institutions focused on phytochemistry and natural product synthesis.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the identification, purity assessment, and quantification of Silenoside A in drug discovery and quality control processes.
• Active Pharmaceutical Ingredient (API) Intermediate: Serves as a key building block in the synthesis and development of new pharmaceutical compounds targeting specific biological pathways.
• Nutraceutical and Dietary Supplement Research: Investigated for its potential bioactive properties in the formulation of high-value, science-backed health supplements.
• Biochemical Research: Employed in in-vitro and in-vivo studies to explore its pharmacological activities, mechanism of action, and potential therapeutic benefits.
• Cosmeceutical Development: Evaluated for potential applications in advanced skincare formulations due to its natural origin and studied bioactivity.
• Analytical Chemistry: Used as an analytical standard in methods development and validation for HPLC, LC-MS, and other chromatographic techniques.

Basic Information

Product Name	Silenoside A
CAS No.	81655-86-9
Molecular Formula	Contact for details
Molecular Weight	Contact for details
Synonyms	Silenoside A; (3β,16α)-16-Hydroxy-13,28-epoxyursan-3-yl β-D-glucopyranoside; Urs-13-en-28-oic acid, 16-hydroxy-3-(β-D-glucopyranosyloxy)-, γ-lactone; Silenosidea A; Related triterpene glycoside from Silene species.
EINECS	Contact for details

Quality Control

Our Silenoside A is produced under strict quality management protocols to ensure batch-to-batch consistency and high purity. Each lot is accompanied by a comprehensive Certificate of Analysis (COA) detailing identity, purity, and impurity profiles. We support compliance with cGMP guidelines for pharmaceutical intermediates and reference standards. Certificates of Analysis (COA) are available upon request.

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 in a dry environment to prevent degradation. For long-term storage, consider desiccants or inert atmosphere.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC/IR)	Conforms to reference standard
Assay (HPLC)	≥95.0%
Loss on Drying	≤2.0%
Residue on Ignition	≤0.5%
Heavy Metals	≤20 ppm
Related Substances (HPLC)	Total impurities ≤5.0%
Solubility	Test solution should be clear

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