A more focused starting material

A formulation project sometimes needs the botanical extract; another needs a concentrated, named active. PINHONBIO® Spilanthol 98% addresses the latter brief. Its development value is the ability to define the test material and active loading clearly before exploring the finished cosmetic.

For an eye-area or facial-care concept, frame the evaluation around the intended appearance and sensory experience. A high assay makes the raw material more concentrated; it does not establish the strength, speed or tolerability of a finished-product effect.

The confirmed technical profile

The supplier lists 98% Spilanthol as a separate purified active alongside its Acmella extract standardized to 5% Spilanthol. These are distinct materials. The botanical extract’s INCI and prototype instructions should not be assigned to the purified option.

ItemPublished information
MaterialPurified Spilanthol; separate from the 5% standardized extract
CAS25394-57-4 — identifies Spilanthol
Assay98% Spilanthol by HPLC
AppearanceYellow-brown oily liquid
SolubilityPure Spilanthol is oil-soluble

Design the trial around active loading

When comparing concentrated and diluted materials, decide what the comparison is meant to isolate. Equal material additions answer a different question from equal nominal active additions. Record the selected grade, batch assay and material concentration so the calculation can be reconstructed.

Changing the grade also changes the accompanying material entering the base. Recheck the base composition and process after a substitution. A calculation can align nominal active loading, but it cannot demonstrate that two formulas behave alike.

Make incorporation a development variable

Oil solubility gives the formulator an initial direction for investigating incorporation. Build a small compatibility trial with the intended oil system, then observe how that trial behaves in the complete emulsion or other chosen format. Define the mixing sequence from grade-specific guidance and bench observations.

Look for changes in color, uniformity, separation and the sensory profile over time and in the intended pack. The documented eye-cream reference on the main site uses the 5% extract; it does not validate a use level or addition process for the 98% material.

Where the brief fits

An eye-area development brief can use a controlled prototype to explore the relationship between material choice and the finished formula. A facial-care development brief can investigate incorporation and sensory acceptance in its intended base. These are evaluation scenarios, rather than a claim that every such format has already been validated with this grade.

Keep tolerability and sensory observations separate. A noticeable sensation should not be used as a measure of cosmetic efficacy or as the sole criterion for accepting the formula.

Turn the sample into a useful decision

Send the intended format and process with the sample request. Review the 98% grade’s specification, TDS, SDS and corresponding batch COA. Agree on the observations that would support continuing the prototype before scaling the trial. The useful outcome is a reproducible formulation decision tied to a specific material.

Sources & scope

Supplier material reviewed October 4, 2026. General evaluation recommendations are editorial perspectives, not reported PINHONBIO test results.

Technical specifications & samples

Explore the Spilanthol 98% grade, request its technical files and discuss a sample for your formulation on PINHONBIO’s main website.

View technical specifications