Description
COA-BACKED BOTANICAL INGREDIENT
Lagerstroemia speciosa (L.) Leaf Extract
Banaba Leaf Extract Powder 1% Standardized Assay is presented for B2B ingredient qualification using representative batch evidence and batch-specific analytical language.

COA-Backed Specification
| Botanical identity | Lagerstroemia speciosa (L.) |
|---|---|
| Plant part | Leaf |
| Form and colour | Fine brown powder |
| Assay | Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA) |
| Particle size | 98% through 80 mesh |
| Loss on drying | <=5.0%; result 3.98% |
| Ash | <=5.0%; result 4.11% |
| Representative batch | LXHLB210721 |
| Manufacture date | 21 July 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 >=1% by HPLC; result 1.12% (analyte not identified on COA), 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
Banaba Leaf Extract Powder 1% Standardized Assay is qualified using botanical identity: Lagerstroemia speciosa (L.); plant part: Leaf; offered grade: Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA). Its purchasing definition is anchored to Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA); alternatives must be compared on marker target and analytical basis.
When an alternative to Banaba Leaf Extract Powder 1% Standardized Assay is required, compare it against this page’s identity, grade and batch-document requirements.
Browse ingredients related to Banaba Leaf Extract Powder 1% Standardized Assay
For a Banaba Leaf Extract Powder 1% Standardized Assay 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 LXHLB210721 supports the specification table above. Use the cited record for preliminary comparison and request the offered-lot COA for final technical approval.
Frequently Asked Questions
What specification defines Banaba Leaf Extract Powder 1% Standardized Assay?
For Banaba Leaf Extract Powder 1% Standardized Assay: Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA).
Which identity details must remain consistent?
For Banaba Leaf Extract Powder 1% Standardized Assay: Match Lagerstroemia speciosa (L.), Leaf across the quotation, specification and offered-batch COA. The differentiating target is Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA); confirm the marker, unit and stated analytical basis.
How is batch-specific approval completed?
For Banaba Leaf Extract Powder 1% Standardized Assay: The page cites representative batch LXHLB210721. Final approval requires the current lot's identity, specification results and relevant dates.
Can buyers verify the batch offered for sale?
For Banaba Leaf Extract Powder 1% Standardized Assay: Current batch documentation should be reviewed before purchase; a representative document is useful for screening but does not release a shipment.
What forms part of the technical review?
For Banaba Leaf Extract Powder 1% Standardized Assay: Do not assess Standardized assay >=1% by HPLC; result 1.12% (analyte not identified on COA) in isolation; particle size, moisture or drying data and market-relevant safety limits can also affect acceptance.
What commercial details belong on the quotation?
For Banaba Leaf Extract Powder 1% Standardized Assay: Confirm MOQ and timing on the live quotation because stock position, testing, packing and destination requirements can change both.
What happens when an application needs a modified parameter?
For Banaba Leaf Extract Powder 1% Standardized Assay: Alternative packing or selected parameters may be considered case by case, subject to production feasibility and a revised written specification.





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