Gentiopicroside 10
- Assay
- 10%
- Appearance
- Brown-yellow powder
- Test
- HPLC
PH-NP 003 · PRODUCT DATA
Botanical Active Ingredient Supplier
Gentiana species derived ingredient
A botanical ingredient supplied in 10%, 80% and 98% grades. Appearance changes from brown-yellow to pale yellow and white as the listed grade changes, with assay measured by HPLC.
This page describes ingredient identity, specification and technical review points. It does not establish a finished-product efficacy or regulatory claim.
QUICK ANSWER
PINHONBIO supplies Gentiopicroside as product PH-NP 003 in 10% / 80% / 98% grades. It is supplied as brown-yellow, pale-yellow or white powder according to grade and reviewed using HPLC. Confirm the selected grade against the current Specification and corresponding batch COA.
IDENTITY & PROPERTIES
Product name, code, grade, label and batch documents should point to the same material. This is the foundation for technical, quality and purchasing review.
The product name, listed INCI and selected assay grade should be checked together. Do not infer that an extract name and a defined constituent name are interchangeable in every market.
GRADE SELECTION
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 |
|---|---|---|
| 10% grade | 10%; brown-yellow powder | HPLC |
| 80% grade | 80%; pale-yellow powder | HPLC |
| 98% grade | 98%; white powder | HPLC |
| Solubility | Soluble in ethanol, methanol and water | Conditions confirmed in TDS and trial |
| Odor | Characteristic | Sensory inspection |
COMPOSITION & ACTIVE CONTENT
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.
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
These are starting points for technical screening. Final suitability depends on the complete system, process, packaging and stability program.
SOLUBILITY, COMPATIBILITY & STABILITY
Supplier information supports initial screening. Compatibility and stability must still be demonstrated in the customer's formula, process and packaging.
QUALITY & REGULATORY SUPPORT
Availability and applicability vary by ingredient, grade, batch and intended market. A document being available does not by itself establish finished-product compliance.
Review the product code, grade, test method, current Specification and corresponding batch COA together.
Request applicable microbiology, heavy metals, residual solvents, pesticides or other risk-based controls for the selected ingredient.
IECIC, REACH, TSCA and other inventory or notification questions are confirmed for the specific material and destination market upon request.
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
After the target specification is confirmed, PINHONBIO provides the corresponding available TDS, Specification, SDS, batch COA or testing files.
Confirm Specification & Request Documents →PACKAGING
1 kg per bag or 25 kg per drum. Inner pack, outer case and label details are confirmed with the order.
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
Confirm the grade, quantity, destination market, formula format, required documents, lead time and acceptance terms in writing.
FAQ
Answers describe the current information boundary. Project-specific decisions should use written confirmation and current official documents.
Browse the buyer and formulator FAQ →They differ in listed assay and appearance. The current source maps 10% to brown-yellow powder, 80% to pale-yellow powder and 98% to white powder.
The listed grades are tested by HPLC. Purchase and acceptance should use the current specification and the COA for the corresponding batch.
Use level, solvent choice, temperature and addition order must be confirmed in the current TDS and through a trial in the customer's complete formula.
Available files may include the current TDS, Specification, SDS and a COA for the corresponding Gentiopicroside batch. Additional regulatory or testing files depend on the selected grade and project scope.
Send PINHONBIO the product code PH-NP 003, required grade, quantity, destination market and intended formulation format. Sample availability, quotation terms and documents are then confirmed in writing.
PROJECT REQUEST
Request a quotation, sample or current technical documents. Include the destination market and formulation conditions when available.