Description
STANDARDISED BOTANICAL ACTIVE
Phillyrin — 98.0%
Phillyrin is supplied as a standardised single-compound botanical active isolated from forsythia fruit, released at 98.0% by HPLC against a batch-specific certificate of analysis. The purchasing definition is the molecule and its declared purity rather than a plant-ratio extract, so the specification is agreed on assay, identity and impurity profile.
COA-Backed Specification
| Identity | Phillyrin |
|---|---|
| Form and colour | Fine white crystalline powder |
| Assay | 98.0% |
| Method | HPLC |
| Particle size | 98% through 80 mesh |
| Loss on drying | <=5.0%; result 4.60% |
| Ash | <=5.0%; result 3.30% |
| Heavy metals | Within the limits of the approved specification |
| Microbiological limits | Within the limits of the approved specification |
| Representative batch | LXLQ260519 |
| Manufacture date | 19 May 2026 |
| Shelf life | Two years when stored properly |
Representative values do not replace the current shipment COA.
Buyer Decision Guide
Buyers approving Phillyrin usually settle three points before the first order: the assay method and acceptance range, the identity of the compound as distinct from a same-named plant extract, and the physical form the buyer’s process needs. Phillyrin is offered at 98.0% by HPLC. Confirm those three against your own specification so the delivered batch is released to the right grade.
- Assay: 98.0% by HPLC, released against the batch COA.
- Identity: Phillyrin as a single compound, not a plant-ratio extract.
- Impurity profile and residual solvents reported per batch.
- Physical form and particle size agreed against the buyer’s process.
- COA, specification sheet and safety data sheet accompany each shipment.
- Regulatory status, permitted uses and labelling are the buyer’s responsibility for the destination market.
How This Grade Differs
Phillyrin is frequently quoted alongside a botanical extract of the same plant. The extract is standardised to a ratio or to a minimum marker content, while Phillyrin is a single purified compound at 98.0%. The two are not interchangeable: dosing calculations, solubility and the analytical method used to release them all differ. Compare quotations on the declared assay and method, not on the plant name.
For a substitution review, compare botanical identity, plant part, assay target, analytical method, physical form and the current offered-batch COA.
Application Areas
- Hard capsules and two-piece capsule filling
- Stick packs and single-serve sachets
- Powder blends and dry mixes
- Beverage and liquid concentrate systems, subject to the buyer’s process validation
Packaging and Delivery
- Evaluation sample typically 10-20 g, subject to stock
- Regular MOQ typically 1 kg
- 1 kg foil bag or 25 kg fibre drum with inner food-grade liner
- Custom packing and private-label options subject to confirmation
- Typical lead time 7-15 working days after deposit
Quality and Documentation
Representative batch LXLQ260519 supports the specification table above. Use the cited record for preliminary comparison and request the offered-lot COA for final technical approval. Batch COA, specification sheet, agreed third-party testing and export documents are available for buyer verification.
Frequently Asked Questions
What specification defines Phillyrin Powder 98%?
For Phillyrin Powder 98%: 98.0%, tested by HPLC.
Which identity details must remain consistent?
For Phillyrin Powder 98%: match Phillyrin across the quotation, specification and offered-batch COA. The offered grade is 98.0%.
How is batch-specific approval completed?
For Phillyrin Powder 98%: the page cites representative batch LXLQ260519. Final approval requires the current lot’s identity, specification results and relevant dates.
What forms part of the technical review?
For Phillyrin Powder 98%: do not assess 98.0% in isolation; particle size, moisture or drying data and market-relevant safety limits can also affect acceptance.
Are you a manufacturer or a trading company?
LongBio is Shaanxi Longsheng Biotechnology Co., Ltd., a direct manufacturer of botanical extracts and functional ingredients integrating R&D, production and export support. Factory review can be arranged by video or an on-site visit.
Can I request the current batch COA before ordering?
Yes. Request the applicable current or representative COA and compare product identity, method, limits and results before approving a purchase order.
What is the minimum order quantity?
The regular MOQ is typically 1 kg. An evaluation sample of 10-20 g can usually be arranged before a formal order, subject to stock.
Do you support custom specifications or packing?
Alternative assay targets, particle size, packing and private-label requirements can be reviewed case by case, subject to production feasibility and a revised written specification.
Request COA, Sample or Quotation
Send your target specification, application, order quantity, destination country and required test limits.
