Description

Camellia sinensis var. assamica · Ripe Tea Extract
Pu-erh Tea Extract Powder
A ripe Pu-erh tea ingredient for beverage, food and supplement formulation. The 10:1 ratio and any tea-polyphenol target are confirmed against the selected grade and shipment batch COA.



PRODUCT OVERVIEW
Pu-erh Tea Extract Powder for B2B Formulation
A ripe Pu-erh tea ingredient for beverage, food and supplement formulation. The 10:1 ratio and any tea-polyphenol target are confirmed against the selected grade and shipment batch COA. Final suitability, use level, sensory performance and regulatory status must be confirmed for the destination market.
TYPICAL SPECIFICATION
Supply Parameters
| Source | Pu-erh ripe tea from Camellia sinensis var. assamica |
|---|---|
| Specification | 10:1 extract ratio; selected tea-polyphenol grades require separate specification confirmation |
| Appearance | Reddish-brown fine powder |
| Quality controls | Confirmed by approved specification and shipment batch COA |
| Shelf life / storage | Confirmed on the current specification and product label |
Final commercial supply is governed by the approved order specification and shipment batch COA.
AVAILABLE OPTIONS
Specification and Packing Options
10:1 extract ratio; selected tea-polyphenol grades require separate specification confirmation
Particle size, dispersibility or handling parameters confirmed per project.
Alternative targets require technical and analytical confirmation.
Evaluation, 1 kg, bulk and private-label options.
BUYER DECISION GUIDE
Pu-erh Tea Extract Buyer Decision Guide
Choose this grade when the project calls for a ripe Pu-erh tea identity and a ratio extract. Confirm whether the formula needs a general 10:1 extract or a separately standardised tea-polyphenol grade; these are not interchangeable purchasing specifications.
For qualification, send the application, target claim-neutral specification, annual volume, destination market and required analytical limits. LongBio will match the quotation and document set to the selected grade.
APPLICATION AREAS
Ingredient for Product Development
Discuss beverage, dry-blend, capsule and tablet development. Colour, flavour, solubility, stability and process compatibility should be tested in the final formula.
QUALITY & DOCUMENTATION
Evidence Matched to the Offered Grade
Current specification and batch COA are available for buyer review. Other technical, origin, allergen, GMO, irradiation, safety or certification documents are supplied only when available and applicable to the chosen grade, facility and destination market.
PACKAGING & SERVICE
Sample, Bulk Supply and OEM / ODM Support
- Evaluation sample: typically 10–20 g, subject to stock
- Regular MOQ: 1 kg
- Standard packing confirmed for product form and order
- Typical lead time: 7–15 working days, subject to stock, testing and customisation

FREQUENTLY ASKED QUESTIONS
Pu-erh Tea Extract Purchasing FAQ
What specification is available?
10:1 extract ratio; selected tea-polyphenol grades require separate specification confirmation. Final limits are confirmed in the approved specification.
Can I review a COA?
Request the applicable specification and a current or representative COA before purchase.
What is the MOQ and sample policy?
Regular MOQ is 1 kg. A 10–20 g sample may be available subject to stock and courier arrangements.
Can you customise specification or packing?
Targets, physical properties, packing and private-label needs can be reviewed before quotation.
What information should I send?
Provide application, target specification, quantity, destination market, packing and required analytical limits.
How is the offered-batch COA used for order approval?
The buyer should compare the product name, botanical identity, grade, analytical method, limits and batch details with the approved order specification. The shipment-batch COA is the controlling quality record.
Does the website replace batch qualification or formulation testing?
No. Website information supports sourcing review only. Buyers should qualify the current documents and sample, verify the final formulation and confirm regulatory suitability in the destination market.
Request Documentation and Quotation
Send your specification, application, order quantity and destination market.
COA Evidence Status
The page presents a 10:1 offered option. The exact ratio, tea-polyphenol target, test method and acceptance limits must be matched to the current offered-batch COA before order approval; no unrelated tea COA is used as evidence.
Source, Applications and Quality Review
Use these product-specific views together with the written specification and the current offered-batch COA. Images illustrate ingredient identity, application context and quality-control workflow; final acceptance is document and sample based.



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