Description
COA-BACKED BOTANICAL INGREDIENT
Rhodiola rosea L. Root Extract
Rhodiola Rosea Root Extract Powder 3% Standardized Assay is presented for B2B ingredient qualification using representative batch evidence and batch-specific analytical language.
COA-Backed Specification
| Botanical identity | Rhodiola rosea L. |
|---|---|
| Plant part | Root |
| Form and colour | Fine red-brown powder |
| Assay | Standardized assay >=3% by HPLC; result 3.24% (source COA does not name the analyte) |
| Particle size | 98% through 80 mesh |
| Loss on drying | <=5.0%; result 4.22% |
| Ash | <=5.0%; result 4.16% |
| Representative batch | LXHJ220312 |
| Manufacture date | 13 March 2021 |
| Shelf life | Two years when stored properly |
Representative values do not replace the current shipment COA.
Buyer Decision Guide
Compare this standardised grade by Standardized assay >=3% by HPLC; result 3.24% (source COA does not name the analyte), the stated method and the offered-lot result; raw material and ratio extracts are different purchasing specifications.
- Evaluation sample typically 10-20 g
- Regular MOQ typically 1 kg
- Typical lead time 7-15 working days
How This Grade Differs
Rhodiola Rosea Root Extract Powder 3% Standardized Assay is qualified using botanical identity: Rhodiola rosea L.; plant part: Root; offered grade: Standardized assay >=3% by HPLC; result 3.24% (source COA does not name the analyte). Its purchasing definition is anchored to Standardized assay >=3% by HPLC; result 3.24% (source COA does not name the analyte); alternatives must be compared on marker target and analytical basis.
Compare these related grades before approval:
For a substitution review, compare botanical identity, plant part, assay target, analytical method, physical form and the current offered-batch COA.
Quality and Documentation
Representative batch LXHJ220312 supports the specification table above. Confirm current batch results before release; the representative record remains supporting context rather than a shipment guarantee.
Frequently Asked Questions
What specification defines Rhodiola Rosea Root Extract Powder 3% Standardized Assay?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: Standardized assay >=3% by HPLC; result 3.24% (source COA does not name the analyte).
What botanical information supports comparison?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: Use Rhodiola rosea L., Root as the identity checkpoint, then confirm that the sample and commercial documents describe the same material.
What does the page's batch reference mean?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: The page cites representative batch LXHJ220312. Use it as an example of the tested grade, not as the release record for a future shipment.
Is current batch documentation part of qualification?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: Request the current COA before issuing approval so the offered lot can be checked against the agreed identity, grade and limits.
Which limits should match the destination market?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: Technical acceptance should cover identity, grade-defining data, physical quality and the safety tests required for the intended market.
How are order size and dispatch timing established?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: The quotation should state the applicable MOQ, pack format and lead time after current inventory and testing needs are reviewed.
How should customised requirements be documented?
For Rhodiola Rosea Root Extract Powder 3% Standardized Assay: Discuss pack format and relevant physical parameters before quotation; feasibility and any MOQ effect are confirmed for the exact request.
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