Description
COA-BACKED BOTANICAL INGREDIENT
Cuscuta chinensis Seed Extract
Cuscuta Seed Extract Powder 10:1 is presented for B2B ingredient qualification using representative batch evidence and batch-specific analytical language.

COA-Backed Specification
| Botanical identity | Cuscuta chinensis |
|---|---|
| Plant part | Seed |
| Form and colour | Fine yellow-brown powder |
| Assay | Extract ratio 10:1; result complies |
| Particle size | 100% through 80 mesh |
| Loss on drying | <=5.0%; result 4.12% |
| Ash | <=5.0%; result 3.74% |
| Representative batch | LXTSZ230724 |
| Manufacture date | 24 September 2023 |
| Shelf life | Two years when stored properly |
Representative values do not replace the current shipment COA.

Buyer Decision Guide
Compare this Extract ratio 10:1; result complies ratio grade by botanical identity, plant part and physical specification; the ratio is not an active-marker percentage.
- Evaluation sample typically 10-20 g
- Regular MOQ typically 1 kg
- Typical lead time 7-15 working days

How This Grade Differs
Cuscuta Seed Extract Powder 10:1 is qualified using botanical identity: Cuscuta chinensis; plant part: Seed; offered grade: Extract ratio 10:1; result complies. Its purchasing definition is the stated ratio grade (Extract ratio 10:1; result complies), not a guaranteed active-compound concentration.
When an alternative to Cuscuta Seed Extract Powder 10:1 is required, compare it against this page’s identity, grade and batch-document requirements.
Browse ingredients related to Cuscuta Seed Extract Powder 10:1
For a Cuscuta Seed Extract Powder 10:1 substitution review, match botanical identity, plant part, grade-defining assay or ratio, analytical basis, physical form and offered-lot documentation.
Quality and Documentation
Representative batch LXTSZ230724 supports the specification table above. Current lot evidence and buyer-defined verification govern acceptance of the commercial shipment.
BUYER QUALIFICATION SNAPSHOT
Cuscuta Seed Extract Powder 10:1: What to Match Before Ordering
This page describes a defined ingredient grade. Use the fields below to prevent substitution between raw powder, ratio extract and standardised grades. The quotation, approved specification and current shipment COA should identify the same material.
| Botanical identity | Cuscuta chinensis |
|---|---|
| Plant part | Seed |
| Assay | Extract ratio 10:1; result complies |
| Particle size | 100% through 80 mesh |
| Loss on drying | <=5.0%; result 4.12% |
| Representative batch | LXTSZ230724 |
Confirm botanical source and plant part.
Match ratio or assay and its test method.
Review the current offered-batch COA.
Continue with Standardized Botanical Extracts, the grade comparison guide, or the COA review checklist.
Frequently Asked Questions
What specification defines Cuscuta Seed Extract Powder 10:1?
For Cuscuta Seed Extract Powder 10:1: Extract ratio 10:1; result complies.
What establishes the botanical source?
For Cuscuta Seed Extract Powder 10:1: Qualification starts with Cuscuta chinensis, Seed. The product name alone is not sufficient when species, plant part or grade differs.
What evidence is needed for the offered lot?
For Cuscuta Seed Extract Powder 10:1: The page cites representative batch LXTSZ230724. The sample, quotation and shipment COA should be traceable to the grade actually offered.
Should the COA be reviewed before sample approval?
For Cuscuta Seed Extract Powder 10:1: Yes. The commercial review should use the COA for the lot being offered, together with the matching quotation and specification.
Which quality data should be checked together?
For Cuscuta Seed Extract Powder 10:1: Review identity and Extract ratio 10:1; result complies together with the listed physical tests and applicable contaminant and microbiological limits.
How should buyers confirm supply timing?
For Cuscuta Seed Extract Powder 10:1: Commercial timing is finalised after quantity, packaging, document set and any additional testing have been agreed.
Can particle size or pack format be adjusted?
For Cuscuta Seed Extract Powder 10:1: Application-specific requests require technical review. Approved changes should be documented rather than treated as an informal substitution.





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