Sennoside A CAS 81276 High Purity Factory Suppliers in China
Source high-purity Sennoside A CAS 81-27-6 from leading China factory suppliers. A premium dimeric anthraquinone glycoside used for pharmaceutical formulations, stimulant laxatives, and pharmacological research, meeting strict GMP standards for global delivery.
About this product
Product information from the supplier.
Sennoside A (CAS NO. 81-27-6) is a high-purity anthraquinone glycoside, widely recognized as a potent stimulant laxative and a critical pharmaceutical API. Extracted from Senna plants, this compound is essential for bowel preparation and the relief of acute constipation, serving as a vital precursor for the synthesis of Rhein Anthrone in advanced biochemical research.
Our Sennoside A is manufactured under rigorous quality control standards, ensuring a purity level of ≥95% (RP-HPLC). Designed specifically for industrial manufacturing, scientific research, and fine chemical applications, it provides the stability and reliability required for pharmacological studies, receptor binding assays, and the development of next-generation digestive health therapeutics.
Detailed Parameters
| Product Name | Sennoside A | CAS NO. | 81-27-6 |
|---|---|---|---|
| Appearance | Yellow to orange-yellow powder | Molecular Formula | C42H38O20 |
| Molecular Weight | 862.74 g/mol | Purity (RP-HPLC) | ≥95% |
| Solubility | Soluble in methanol, DMSO | Endotoxin | < 10 EU/mg |
| Storage Conditions | 2-8°C or room temperature | MOQ | 1g |
Key Advantages
Pharmaceutical Grade
Strict adherence to GMP-compliant production systems ensuring maximum product stability.
Rapid Logistics
Global delivery via DHL, FedEx, and UPS with advanced tracking and optimized transit times.
High Purity
Verified ≥95% purity via RP-HPLC, ideal for precision biochemical and pharmacological research.
Full Certification
Complete documentation provided, including COA, HPLC purity reports, and MS chromatograms.
Scalable Supply
Flexible capacity ranging from milligram research samples to ton-level industrial production.
Batch Traceability
Rigorous quality management system ensuring every batch is traceable and consistent.
Product Gallery
Management Platforms
GMP Synthesis
Standardized quality control covering raw material procurement and final synthesis.
Purification Lab
Advanced purification processes using HPLC and MS to ensure pharmaceutical grade purity.
Compliance Audit
Continuous monitoring of international trade standards and regulatory compliance.
Cold Chain Logic
Professional temperature-controlled storage and shipping for sensitive chemical APIs.
Inventory System
Strategic stock locations in the USA for rapid fulfillment and reduced lead times.
R&D Partnership
Collaboration with renowned universities for custom chemical synthesis and development.
Investment Return Comparison
| Comparison Metric | Standard Grade | GlobalTech Premium |
|---|---|---|
| Purity Level | ≥85% - 90% | ≥95% (Verified) |
| Documentation | Basic COA | COA, HPLC, MS, 3rd Party |
| Delivery Time | 14-21 Days | 3-7 Days (USA Stock) |
| Batch Stability | Variable | High Stability / Traceable |
| Regulatory Status | Uncertified | GMP / FDA Compliant Partners |
Frequently Asked Questions
Sennoside A is primarily used as an active pharmaceutical ingredient (API) for producing stimulant laxatives, aiding in bowel preparation and the treatment of chronic constipation.
We utilize Reverse-Phase High-Performance Liquid Chromatography (RP-HPLC) to ensure purity levels exceed 95%, provided via a detailed Certificate of Analysis (COA).
It should be stored at 2-8°C or room temperature, strictly protected from light and moisture in a tightly sealed container.
Yes, we support a flexible range of supply, from gram-level research samples to ton-level industrial quantities via our GMP-certified partners.
Yes, we maintain strategic stock in the USA to ensure the fastest possible transit times for our North American clients.
Absolutely. All our products are handled according to international shipping regulations, featuring secure packaging and complete regulatory documentation.