Rhodiola Rosea Extract

Main Active Ingredients:
Rhodiola Rosea Extract – CAS: 97404-52-9|Assay: 3% Rosavins / 1% Salidroside by HPLC
Application: Adaptogen & stress-support supplements, nootropic / cognitive formulas, sports-nutrition products
Ratio: 10:1, 20:1
Application: General-wellness supplements, functional foods & beverages, cost-effective formulations
MOQ: 1KG|US Warehouse Stock Available — ships within 2 business days for US customers
Certifications: ISO, HACCP, GMP, Kosher, Halal, Organic, BRC, FDA Registered Facility

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Rhodiola Rosea Extract (3% Rosavins / 1% Salidroside): Bulk B2B Wholesale Supplier

Written by Jonathan, Valeherb · Reviewed by Dr. Xiaoyan Qiu · Updated April 2026

Valeherb supplies standardized Rhodiola rosea extract — 3% rosavins / 1% salidroside by HPLC — for nootropic, sports nutrition, adaptogen supplement, and functional food formulations. Rhodiola is an adaptogen that has been studied in research for activity on the body’s stress-response pathways at the hormonal and neurochemical level, through mechanisms that research describes as distinct from stimulant-type compounds.[1] This dual-marker specification mirrors the phytochemical profile used across published clinical trials and is the baseline most buyers require to align a finished product with that trial evidence.


Active Compounds and Standardization

NOTE
The activity described in this section is drawn from published research on Rhodiola rosea and its marker compounds and is provided for informational purposes only — not a health or efficacy claim for any finished product. Any structure/function claim on a finished good must be self-substantiated by the marketer and carry the required FDA disclaimer; disease treatment or prevention claims require drug approval.

Rhodiola rosea (Arctic root, golden root) is a primary adaptogen native to high-altitude cold-climate regions of Siberia, Scandinavia, and the Tibetan Plateau. Its pharmacological activity comes from two compound classes that must be verified separately by HPLC:

Compound Activity Studied in Research Minimum Standard
Rosavins (Rosavin, Rosarin, Rosin) Studied for HPA-axis modulation and stress- and fatigue-related endpoints in research; species-specific to R. rosea — absent in R. crenulata and other cheaper substitutes, making rosavins the key authenticity marker[1] ≥3% by HPLC
Salidroside + Phenolic Complex Studied for neuroprotective and anti-fatigue activity in research. MAO-modulating activity is attributed to the full phenolic complex — rosiridin, rhodiocyanosides, and salidroside acting collectively — not to rosavins alone[3] ≥1% by HPLC
KEY POINT
The 3:1 rosavin-to-salidroside ratio mirrors the natural profile of wild-harvested Arctic root and is the specification used in the major published RCTs. Suppliers reporting only total saponin content — without separate HPLC values for rosavins and salidroside — cannot confirm equivalence to the trial material or species authenticity.

Available Grades and Specifications

Valeherb supplies Rhodiola rosea extract (CAS 97404-52-9) in two grade families. MOQ is 1 kg for both. The choice depends on whether your formulation needs marker-quantified material that matches the published trial profile, or a cost-effective concentration ratio for general-wellness positioning.

Grade Assay Identity Control Typical Application
Standardized Extract 3% Rosavins / 1% Salidroside by HPLC Dual-marker HPLC quantification; matches the profile used in published clinical trials Adaptogen & stress-support supplements, nootropic/cognitive formulas, sports-nutrition products
Ratio Extract 10:1 and 20:1 concentration ratio HPLC fingerprint for identity (not quantified to fixed rosavin/salidroside %) General-wellness supplements, functional foods & beverages, cost-effective formulations
KEY POINT
A concentration ratio (10:1, 20:1) describes how much raw herb was reduced into the extract — it is not a guarantee of rosavin or salidroside content. The published clinical trials used the standardized 3%/1% material; ratio grades are identity-verified by HPLC fingerprint but are not standardized to those marker levels and should not be represented as equivalent to the trial material. Specify which grade your claim strategy requires before ordering.

Clinical Evidence

Rhodiola rosea is one of the few adaptogens with multiple peer-reviewed RCTs specifically examining stress-related fatigue and cognitive performance — not just general wellbeing. The trials below characterise the standardized extract; they are not claims for any finished product. Four references anchor the evidence base:

A randomized, double-blind, placebo-controlled trial by Olsson et al. (2009) dosed 576 mg/day of standardized extract (SHR-5) for 28 days in subjects with stress-related fatigue. The treatment group showed statistically significant reductions in fatigue and improvements in concentration, alongside a reduced cortisol response to awakening stress, versus placebo.[5]

Darbinyan et al. (2000) reported that a single dose of standardized Rhodiola extract significantly improved measures of mental fatigue, associative thinking, short-term memory, and calculation speed in physicians performing night-shift work — a real-world cognitive-load condition.[2]

De Bock et al. (2004) found that 200 mg taken one hour before exercise significantly increased time-to-exhaustion and reduced perceived exertion versus placebo in a double-blind crossover design — relevant to sports-nutrition applications.[4]

A systematic review by Ishaque et al. (2012) covering 11 RCTs reported a favorable safety profile across all included studies and improvements in physical and mental fatigue measures in most trials.[6]


Formulation Applications and Dose Reference

The doses below reflect amounts used in published research and are a formulation reference only — not therapeutic recommendations. Finished-product dosing and any associated claims are the responsibility of the marketer.

Application Dose Used in Studies Formulation Notes
Stress & adaptogen supplements 400–600 mg/day[5] Vegan capsule, split AM/midday. Pairs with Ashwagandha KSM-66, Eleuthero, Schisandra for comprehensive adaptogen stacks
Nootropic & cognitive formulas 200–400 mg/serving[2] Complements L-theanine, B vitamins, lion’s mane; commonly used alongside caffeine in cognitive blends
Sports nutrition 200 mg acute, 60–90 min pre-workout[4] Not listed on the WADA Prohibited List (verify the current list at sourcing). Compatible with powder blends, RTD beverages, and chew formats
Functional foods & beverages 100–200 mg/serving Heat-stable extract grades available. Mild bitter profile; natural flavor masking recommended at higher concentrations

Sourcing Criteria

Criterion What to Require
Dual HPLC Standardization Separate batch-level values for rosavins (≥3%) and salidroside (≥1%) — bundled total saponin readings are insufficient to confirm equivalence to the trial material
Species Authentication Rosavin presence confirms R. rosea. Request crenulatin testing by NMR or HPLC-UV — crenulatin is a coumarin unique to R. crenulata, detected in 2 of 4 commercial products in a 2020 analytical study, in which fewer than one quarter of products confirmed their labeled rosavin and salidroside amounts[7]
Third-Party COA Per-batch: rosavins, salidroside, heavy metals (USP <232>), pesticide residues, microbial limits (USP <2021>), moisture
Geographic Origin Siberia, Scandinavia, or high-altitude Tibetan Plateau preferred. Request harvest origin documentation — growing conditions directly influence bioactive concentration
Certifications ISO, HACCP, GMP, BRC, Kosher, Halal, and Organic available; manufactured in an FDA-registered facility for US DSHEA supply chains. Confirm Non-GMO and the specific certificate scope per batch/market
CAUTION
Dose-dependent side effects (dizziness, dry mouth, mild agitation) have been reported at >600 mg/day — mitigate by splitting doses and taking with food. Avoid late-evening dosing due to mild activating effects. Not recommended during pregnancy or breastfeeding. Consult a healthcare professional before combining with psychiatric medications — MAO-modulating activity is attributed to the full phenolic extract complex, not a single compound.[3]

Regulatory Status

FDA NOTICE
These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease.
  • US (DSHEA): Rhodiola rosea extract is a lawful dietary-supplement ingredient. Structure/function claims (e.g., stress support, mental performance) must be self-substantiated by the marketer and carry the FDA disclaimer; published RCTs on the standardized extract can contribute to that substantiation. Disease treatment or prevention claims require drug (NDA) approval
  • EU: Registered as a traditional herbal medicinal product under Directive 2004/24/EC; traditional-use registration covers indications such as temporary symptoms of stress and fatigue. Claims beyond the traditional-use scope require full marketing authorization
  • Canada (NHPs): A Health Canada NNHPD monograph exists for Rhodiola, with permitted claims in the area of stress tolerance and mental performance, subject to meeting the monograph conditions

References

[1] Panossian A & Wikman G. (2010). Effects of adaptogens on the central nervous system and the molecular mechanisms associated with their stress-protective activity. Pharmaceuticals, 3(1), 188–224. PMID: 27713248

[2] Darbinyan V et al. (2000). Rhodiola rosea in stress-induced fatigue: a double-blind cross-over study. Phytomedicine, 7(5), 365–371. PMID: 11081987

[3] van Diermen D et al. (2009). Monoamine oxidase inhibition by Rhodiola rosea L. roots. Journal of Ethnopharmacology, 122(2), 397–401. PMID: 19168123

[4] De Bock K et al. (2004). Acute Rhodiola rosea intake can improve endurance exercise performance. Int J Sport Nutr Exerc Metab, 14(3), 298–307. PMID: 15256690

[5] Olsson EMG et al. (2009). A randomised, double-blind, placebo-controlled, parallel-group study of the standardised extract SHR-5 of Rhodiola rosea in stress-related fatigue. Planta Medica, 75(2), 105–112. PMID: 19016404

[6] Ishaque S et al. (2012). Rhodiola rosea for physical and mental fatigue: a systematic review. BMC Complement Altern Med, 12, 70. PMID: 22643043

[7] Marchev AS et al. (2020). Authenticity and quality evaluation of different Rhodiola species and commercial products based on NMR-spectroscopy and HPLC. Phytochemical Analysis, 31(6), 756–769. PMID: 32311178

FAQ

A1:It is the dual HPLC standardization spec: the extract is verified to contain at least 3% rosavins and at least 1% salidroside, measured separately. Both numbers matter because they come from different compound classes — rosavins are the marker unique to true R. rosea, while the salidroside/phenolic complex carries separate activity. The 3:1 ratio mirrors wild Arctic root and matches the profile used in the major published trials, which is why buyers use it as the baseline rather than a single “total” figure.
A2:Rosavins are species-specific to Rhodiola rosea and absent in cheaper substitutes like R. crenulata, so a confirmed rosavin value is the primary proof of authenticity, not just potency. A supplier reporting only “total saponins” or salidroside alone cannot demonstrate the material is genuine R. rosea. In a 2020 analytical study, fewer than a quarter of commercial products confirmed their labeled rosavin and salidroside amounts, and an adulteration marker (crenulatin) was found in 2 of 4 products — so per-batch HPLC rosavin testing is the key sourcing safeguard.
A3:They are different species with different chemistry. R. rosea (Arctic/golden root) contains rosavins and is the species used in most published Western clinical research; R. crenulata lacks rosavins and instead carries the coumarin crenulatin, which is used as a marker to detect adulteration. R. crenulata is cheaper and common in China — note that the Chinese Pharmacopoeia lists R. crenulata, not R. rosea — so for R. rosea formulations, confirm the species by rosavin presence and crenulatin testing.
A4:Request a per-batch third-party Certificate of Analysis covering: separate HPLC values for rosavins (≥3%) and salidroside (≥1%); species authentication (rosavin confirmation, with crenulatin testing to rule out R. crenulata); heavy metals (USP ); pesticide residues; microbial limits (USP ); and moisture. Harvest-origin documentation (Siberia, Scandinavia, or high-altitude Tibetan Plateau) and an FDA-registered facility for US supply are also worth confirming.

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