Description

Bacopaside X is a specific, high-purity saponin compound derived from the medicinal herb Bacopa monnieri. This compound is of significant interest for its role as a key analytical reference standard and active pharmaceutical ingredient in the development of nootropic and neuroprotective formulations. It is primarily sought by manufacturers and research institutions in the pharmaceutical, nutraceutical, and cosmeceutical industries for product standardization, quality control, and advanced R&D applications.

Application

• Pharmaceutical Reference Standard: Used as a primary standard in HPLC and LC-MS methods for the quantification of bacosides in raw materials and finished products.
• Nootropic Formulations: Incorporated into dietary supplements and functional foods aimed at enhancing cognitive function, memory, and learning.
• Neuroprotective Drug Development: Serves as a key active ingredient in preclinical and clinical research for conditions related to cognitive decline and neurological disorders.
• Nutraceutical Standardization: Ensures batch-to-batch consistency and potency in Bacopa monnieri extracts used in supplement capsules and tablets.
• Cosmeceutical Actives: Applied in premium skincare formulations for its potential antioxidant and anti-inflammatory properties that support skin health.
• Academic & Clinical Research: Utilized in biochemical, pharmacological, and toxicological studies to elucidate mechanisms of action and therapeutic efficacy.

Basic Information

Product Name	Bacopaside X
CAS No.	94443-88-6
Molecular Formula	C41H66O13
Molecular Weight	766.96 g/mol
Synonyms	Bacopaside X; Bacoside X; 3-O-[β-D-Glucopyranosyl-(1→3)-α-L-arabinopyranosyl] pseudojujubogenin; Jujubogenin isomer of bacopaside II; (3β,4α,20S,22R)-20-[(6-Deoxy-α-L-mannopyranosyl)oxy]-22-(β-D-glucopyranosyloxy)-3-[(2-O-β-D-glucopyranosyl-β-D-glucopyranosyl)oxy]-9-methyl-19-norlanost-5,24-dien-4-ol (IUPAC)
EINECS	Contact for details

Quality Control

Every batch of Bacopaside X is produced and analyzed under strict quality management protocols. Our products undergo rigorous identity, purity, and potency testing using advanced chromatographic (HPLC, UPLC) and spectroscopic (MS, NMR) techniques to ensure compliance with pharmaceutical-grade standards. Comprehensive Certificates of Analysis (COA) detailing all test parameters and results are provided to guarantee traceability and supply chain integrity for our global B2B clients.

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); the container must be kept tightly sealed in a dry environment to prevent degradation.

Specification

Item	Specification
Appearance	White to off-white powder
Identification (HPLC)	Conforms to reference standard
Identification (IR)	Conforms to structure
Assay (HPLC)	≥ 98.0%
Loss on Drying	≤ 2.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 10 ppm
Residual Solvents	Meets ICH guidelines

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