Salidroside Powder Cas No.10338-51-9
Source: Extracted from the roots and rhizomes of Rhodiola rosea L.
Purity: ≥99%
CAS No.: 10338-51-9
Molecular Formula: C₁₄H₂₀O₇
Molecular Weight: 300.30 g/mol
Testing Method: HPLC
Active Ingredient: Salidroside
Product Characteristics: White to off-white crystalline powder
Packaging: 1 kg/aluminum foil bag, 25 kg/cardboard drum; customizable
Storage Conditions: Store sealed in a cool, dry place away from light
Shelf Life: 24 months
This product is intended for use as a pharmaceutical raw material, health food ingredient, and research reagent only. It is strictly prohibited for use in cosmetics or direct consumption.
Products Description
High-Purity Salidroside API Powder | CAS 10338-51-9
Salidroside (CAS No. 10338-51-9) is a potent, bioactive phenylethanoid glycoside systematically extracted and purified from the premium roots and rhizomes of Rhodiola rosea. Operating at the intersection of botanical extraction and pharmaceutical synthesis, Xi'an Tihealth provides a highly standardized Salidroside API powder with an HPLC-validated purity of ≥99.0%. By employing advanced chromatographic separation techniques, we meticulously eliminate solvent residues and heavy metals, delivering a reliable, consistent raw material designed for rigorous biomedical research, pharmaceutical intermediates, and high-end adaptogenic nutraceutical formulations.
Technical Data Sheet (TDS) & Core Specifications
| Testing Item | Specification Limit |
|---|---|
| Botanical Source | Rhodiola rosea L. (Roots and Rhizomes) |
| Assay (HPLC, Salidroside) | ≥ 99.0% |
| Appearance | White to off-white fine powder |
| Moisture (Loss on Drying) | ≤ 1.0% |
| Heavy Metals (Total) | ≤ 10 ppm (Complies with USP standards) |
| Solvent Residue | Complies with Eur. Ph. limits |
*Batch-specific Certificate of Analysis (COA) and HPLC chromatograms are strictly provided with every commercial shipment.
Pharmacological Mechanism & Bioactivity
As an isolated, highly purified adaptogenic compound, Salidroside exerts multi-targeted cellular effects documented in advanced preclinical models:
- Cellular Energy & Metabolic Regulation: Modulates key energy-sensing pathways, notably the AMPK/mTOR and SIRT1/PGC-1α axes, thereby promoting mitochondrial biogenesis and enhancing resistance to cellular hypoxia and fatigue.
- Neuroprotective Dynamics: Exhibits significant free radical scavenging capacity, protecting neuronal integrity against oxidative stress and modulating neuroendocrine responses (e.g., the HPA axis) related to mood and cognitive endurance.
- Cardiovascular Support R&D: Investigated for its potential in maintaining vascular endothelial function and regulating localized inflammatory cytokine production (anti-inflammatory properties).
Applications & Formulation Suitability
- Pharmaceutical Intermediates: Acts as a standardized active ingredient for the development of targeted therapeutics addressing chronic fatigue, cognitive decline, and metabolic imbalances.
- Premium Nutraceuticals: Ideal for formulating high-end, clean-label dietary supplements (capsules, tablets, and functional beverages) requiring precise dosage and guaranteed adaptogenic efficacy.
- Academic & Biomedical Research: Serves as a highly reliable reference standard and bioactive agent for in-vitro and in-vivo pharmacological studies.
Regulatory Notice: This product is classified as a botanical API/raw material intended strictly for industrial manufacturing, formulation, and laboratory research. Formulators are responsible for ensuring final product compliance with regional authorities (e.g., FDA, EFSA).
Frequently Asked Questions (FAQ)
Standard Rhodiola rosea extracts typically contain 1% to 3% Salidroside alongside rosavins and other plant matrices. Our ≥99% Salidroside API is a highly purified, single-molecule compound, ensuring exact dosing and eliminating the variability and impurities found in crude botanical extracts.
2,Is this Salidroside powder soluble in water?
Yes, due to its glycoside structure, highly purified Salidroside exhibits excellent solubility in water and ethanol, making it exceptionally versatile for liquid formulations, functional beverages, and sterile R&D solutions.
3,How do you ensure the absence of solvent residues from the extraction process?
Our extraction and purification facility operates under strict GMP protocols. We utilize advanced macroporous resin separation and vacuum drying techniques. Every batch is tested via Gas Chromatography (GC) to ensure solvent residues comply with stringent Eur. Ph. and USP limits.
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