Water-Soluble Kava Extract 99
- Assay
- 99% listed grade
- Appearance
- Off-white to pale-yellow powder
- Test
- HPLC
PH-NP 002 · PRODUCT DATA
Kava Extract
Botanical Active Ingredient Supplier
Extract of the dried root of Piper methysticum
A water-soluble Kava extract listed as a 99% grade, supplied as an off-white to pale-yellow powder and tested by HPLC. Third-party evaluation and pesticide-residue reports are available for document review.
- INCI
- To be confirmed in the current official file
- Grade
- 99% listed grade
- Form
- Off-white to pale-yellow powder
- Solubility
- Water-soluble
This page describes ingredient identity, specification and technical review points. It does not establish a finished-product efficacy or regulatory claim.
QUICK ANSWER
Kava Extract at a glance
PINHONBIO supplies Kava Extract as product PH-NP 002 in 99% listed grade grades. It is supplied as off-white to pale-yellow powder and reviewed using HPLC. Confirm the selected grade against the current Specification and corresponding batch COA.
IDENTITY & PROPERTIES
Confirm the product before evaluating the claim.
Product name, code, grade, label and batch documents should point to the same material. This is the foundation for technical, quality and purchasing review.
- Product name
- Kava Extract
- Product code
- PH-NP 002
- CAS
- 9000-38-8
- INCI
- To be confirmed in the current official file
- Source
- Extract of the dried root of Piper methysticum
- Form
- Off-white to pale-yellow powder
- Solubility
- Water-soluble
- Test method
- HPLC
The current source material does not confirm an INCI name. Buyers should verify the official TDS, composition and market-specific regulatory files before use.
GRADE SELECTION
Choose the grade, then check its batch.
Listed grades describe the commercial options in the current source material. Contract requirements and acceptance criteria belong in the current specification and purchase agreement.
| Review item | Listed requirement | Method or evidence |
|---|---|---|
| Listed grade | 99% | HPLC |
| Appearance | Off-white to pale-yellow powder | Visual inspection |
| Solubility | Water-soluble | Operating conditions confirmed in TDS and trial |
| Odor | Characteristic | Sensory inspection |
| Third-party reports | Match report number and tested sample | Document review |
COMPOSITION & ACTIVE CONTENT
Read composition in the context of the selected grade.
For a defined molecule, active content is normally expressed through identity and assay. For an extract or multi-component ingredient, marker content, carrier and composition need to be reviewed together.
- Material identity
- To be confirmed in the current official file
- Listed content
- 99% listed grade
- Analytical method
- HPLC
- Composition evidence
- Current Specification and corresponding batch COA
The listed assay or grade must not be interpreted as a finished-product efficacy claim. For extracts, request confirmation of the plant identity, plant part, marker definition, carrier and extraction information where applicable.
FORMULATION REFERENCE
Use the formula conditions to guide evaluation.
These are starting points for technical screening. Final suitability depends on the complete system, process, packaging and stability program.
Aqueous systemsSerumsEmulsionsCreamsOther water-phase formats
- Use level
- Confirm in the current TDS
- Addition conditions
- Confirm temperature, order of addition and system conditions through a formulation trial
- Compatibility
- Evaluate color, odor, clarity and interaction with the complete formula
- Before scale-up
- Complete compatibility and stability evaluation
SOLUBILITY, COMPATIBILITY & STABILITY
Confirm performance in the complete formulation.
Supplier information supports initial screening. Compatibility and stability must still be demonstrated in the customer's formula, process and packaging.
- Solubility
- Water-soluble
- pH window
- Confirm in the current TDS and formulation trial
- Process temperature
- Confirm the addition temperature and exposure time before scale-up
- Compatibility
- Evaluate with solvents, surfactants, electrolytes, preservatives and other actives in the complete system
- Stability checks
- Monitor appearance, odor, color, clarity, precipitation and active-content change under the intended program
- Packaging
- Include the intended primary pack in compatibility and stability evaluation
QUALITY & REGULATORY SUPPORT
Match quality evidence and regulatory review to the destination market.
Availability and applicability vary by ingredient, grade, batch and intended market. A document being available does not by itself establish finished-product compliance.
Identity and batch acceptance
Review the product code, grade, test method, current Specification and corresponding batch COA together.
Relevant contaminant controls
Request applicable microbiology, heavy metals, residual solvents, pesticides or other risk-based controls for the selected ingredient.
Market-specific status
IECIC, REACH, TSCA and other inventory or notification questions are confirmed for the specific material and destination market upon request.
Project-specific statements
Vegan, GMO, allergen, animal-testing and related declarations are supplied only when supported by the applicable product file.
Review PINHONBIO analytical capabilities, testing scope and third-party verification approach →
DOCUMENTATION
Confirm the grade before requesting documents.
After the target specification is confirmed, PINHONBIO provides the corresponding available TDS, Specification, SDS, batch COA or testing files.
Confirm Specification & Request Documents →01TDSTechnical data and formulation guidance
02SpecificationProduct acceptance criteria
03SDSSafety and handling information
04Batch COAResults for the corresponding batch
05Third-party reportsEvaluation and pesticide-residue reports, subject to sample and report matching
PACKAGING
Packaging
1 kg per bag or 25 kg per drum. Inner pack, outer case and label details are confirmed with the order.
STORAGE
Storage
Store sealed in a cool, dry place and protect from light. 24 months under the stated storage conditions. Reseal carefully after opening.
BEFORE ORDERING
Project confirmation
Confirm the grade, quantity, destination market, formula format, required documents, lead time and acceptance terms in writing.
FAQ
Common questions about Kava Extract
Answers describe the current information boundary. Project-specific decisions should use written confirmation and current official documents.
Browse the buyer and formulator FAQ →What identifies this Kava Extract product?
Check the PH-NP 002 code, Kava Extract name, CAS 9000-38-8, listed grade, water solubility, packaging label and corresponding batch COA together.
Is the INCI name confirmed?
Not in the current source material used for this page. The official product file and applicable market documentation must be checked before regulatory use.
How should third-party reports be reviewed?
Match the report number, tested sample, method, date and result scope. A third-party report should not be treated as proof for a different batch or an unsupported finished-product claim.
Which documents can buyers request for Kava Extract?
Available files may include the current TDS, Specification, SDS and a COA for the corresponding Kava Extract batch. Additional regulatory or testing files depend on the selected grade and project scope.
How can I request a Kava Extract sample or quotation?
Send PINHONBIO the product code PH-NP 002, required grade, quantity, destination market and intended formulation format. Sample availability, quotation terms and documents are then confirmed in writing.
PROJECT REQUEST
Ready to evaluate Kava Extract?
Request a quotation, sample or current technical documents. Include the destination market and formulation conditions when available.