Description

Deoxyschizandrin is a bioactive lignan compound primarily isolated from the fruit of *Schisandra chinensis*. This compound is valued for its role as a key chemical marker and active ingredient, contributing to the therapeutic and research interest in traditional botanical extracts. It is essential for manufacturers and researchers in the pharmaceutical, nutraceutical, and cosmeceutical industries who require high-purity, standardized botanical components for product development and quality control.

Application

• Pharmaceutical Reference Standard: Used as a certified reference material (CRM) for the identification, assay, and quality control of Schisandra chinensis extracts and related herbal formulations.
• Nutraceutical Ingredient: Incorporated into dietary supplements for its potential adaptogenic and hepatoprotective properties, serving as a marker compound for product standardization.
• Cosmetic Actives: Formulated into skincare products for its antioxidant benefits, helping to protect skin cells from oxidative stress.
• Biomedical Research: Employed in in vitro and in vivo studies to investigate mechanisms of action related to liver health, anti-inflammatory effects, and neuroprotection.
• Herbal Extract Standardization: Critical for calibrating analytical equipment (HPLC, LC-MS) to ensure batch-to-batch consistency and potency of commercial botanical extracts.
• Traditional Medicine Formulations: Used in the development and modernization of Traditional Chinese Medicine (TCM) products that leverage the pharmacological profile of Schisandra.

Basic Information

Product Name	Deoxyschizandrin
CAS No.	69176-53-0
Molecular Formula	C24H32O6
Molecular Weight	416.51 g/mol
Synonyms	Deoxyschisandrin; Schisantherin B; Wuweizisu B; (-)-Deoxyschizandrin; NSC 122180; Schisandrin B Derivative; 1,2,3,13b-Tetrahydro-2-hydroxy-1,2,3-trimethoxy-6,7-methylenedioxybenzo[a]cyclopenta[j]phenanthren-4(4aH)-one
EINECS	Contact for details

Quality Control

Our Deoxyschizandrin is produced under strict quality management systems. Each batch undergoes comprehensive analytical testing, including HPLC for purity verification and identity confirmation via spectroscopic methods (IR, MS). We provide Certificates of Analysis (COA) with detailed specifications to support your regulatory and R&D requirements. The product is suitable for use as a pharmaceutical secondary standard.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at a controlled room temperature (15-25°C). The compound is light-sensitive; prolonged exposure to light should be avoided to maintain stability and potency.

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	≤ 0.5%
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.