Tranexamic Acid Cetyl Ester Not less than 98%
- Assay
- Not less than 98%
- Appearance
- White powder
- Test
- HPLC
PH-SynBio 003 · PRODUCT DATA
Tranexamic Acid Cetyl Ester
Cosmetic Active Ingredient Supplier
Oil-soluble synthetic ingredient
Tranexamic Acid Cetyl Ester is PINHONBIO product PH-SynBio 003, available in Not less than 98% grades as white powder and tested by HPLC. Confirm the selected grade against the current Specification and batch COA.
- INCI
- Tranexamic Acid listed in source material; identity confirmation required
- Grade
- Not less than 98%
- Form
- White powder
- Solubility
- Oil-soluble; listed for oil or emulsion systems
This page describes ingredient identity, specification and technical review points. It does not establish a finished-product efficacy or regulatory claim.
QUICK ANSWER
Tranexamic Acid Cetyl Ester at a glance
PINHONBIO supplies Tranexamic Acid Cetyl Ester as product PH-SynBio 003 in Not less than 98% grades. It is supplied as white 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
- Tranexamic Acid Cetyl Ester
- Product code
- PH-SynBio 003
- CAS
- Confirm in the current official file
- INCI
- Tranexamic Acid listed in source material; identity confirmation required
- Source
- Oil-soluble synthetic ingredient
- Form
- White powder
- Solubility
- Oil-soluble; listed for oil or emulsion systems
- Test method
- HPLC
The working product name describes a cetyl ester while the supplied INCI record states Tranexamic Acid. These identities are not automatically equivalent and must be resolved in official files before regulatory 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 | Not less than 98% | HPLC |
| Appearance | White powder | Visual inspection or current specification |
| Solubility | Oil-soluble; listed for oil or emulsion systems | Current TDS and formulation trial |
| Product identity | PH-SynBio 003 / Tranexamic Acid Cetyl Ester | Label, specification and batch documents |
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
- Tranexamic Acid listed in source material; identity confirmation required
- Listed content
- Not less than 98%
- 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.
SerumsEmulsionsCreamsAnhydrous or oil-phase systemsOther evaluated formats
- Grade selection
- Not less than 98%
- Use level
- Confirm in the current TDS
- Addition conditions
- Confirm solvent, temperature and order of addition through a formulation trial
- Before scale-up
- Complete compatibility and stability evaluation in the finished formula
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
- Oil-soluble; listed for oil or emulsion systems
- 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
05Regulatory and safety filesProvided according to product and project scope
PACKAGING
Packaging
1 kg per bag or 25 kg per drum. Final pack and label details follow the confirmed order.
STORAGE
Storage
Store sealed in a cool, dry place and protect from light. Shelf life and conditions follow the current label, TDS and SDS.
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 Tranexamic Acid Cetyl Ester
Answers describe the current information boundary. Project-specific decisions should use written confirmation and current official documents.
Browse the buyer and formulator FAQ →How should Tranexamic Acid Cetyl Ester be identified?
Check the PH-SynBio 003 code, product name, INCI or chemical identity, selected grade, packaging label and corresponding batch COA together.
Which Tranexamic Acid Cetyl Ester grade is listed?
The current source material lists Not less than 98%. Confirm the selected grade and acceptance criteria in the current Specification.
How are formulation conditions confirmed?
Use level, solvent, temperature, addition order and stability must be confirmed in the current TDS and in the customer's complete formula.
Which documents can buyers request for Tranexamic Acid Cetyl Ester?
Available files may include the current TDS, Specification, SDS and a COA for the corresponding Tranexamic Acid Cetyl Ester batch. Additional regulatory or testing files depend on the selected grade and project scope.
How can I request a Tranexamic Acid Cetyl Ester sample or quotation?
Send PINHONBIO the product code PH-SynBio 003, 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 Tranexamic Acid Cetyl Ester?
Request a quotation, sample or current technical documents. Include the destination market and formulation conditions when available.