Custom Botanical Ingredient Development

When standard grades don’t fit, we develop custom botanical extracts with our approved manufacturing partners, working on target markers, extract ratios and solubility from feasibility to scale-up.

Botanical extract standardization workflow showing markers, assay methods, specifications, stability, and batch consistency.

When Custom Development Makes Sense

It’s useful when no standard grade delivers the required assay, extract profile, solubility, physical property or application performance. Examples: a higher marker level, better dispersion, or a physical form that isn’t commercially available. A custom ingredient should solve a defined need and stay practical for repeat production. If an existing grade already fits, Specification & Grade Matching is the faster route.

Target→Feasibility→Prototype→Pilot→Verify→Scale

Botanical extract standardization workflow showing markers, assay methods, specifications, stability, and batch consistency.

Define the Target Profile

Many projects start with part of this: a reference COA, a benchmark material, a formulation problem or a target assay is often enough for a feasibility review. We then sort out which requirements are essential and which are flexible.

Evaluate the Botanical Source

Species, plant part, origin, natural marker level and material quality set what the extract can achieve. Raw materials vary between origins, harvests and lots, so the route must handle that variation. Availability and continuity of supply matter too; difficult starting materials can be sourced in parallel through Ingredient Sourcing.

Assess Feasibility

The question is whether the extract can be made consistently and at a practical scale. A viable processing route balances assay, yield, stability, physical properties, complexity, scalability and cost. Some targets are achievable but impractical because of low yield or cost; others need refining.

Botanical extract standardization workflow showing markers, assay methods, specifications, stability, and batch consistency.

Define the Specification

Marker and assay

For standardized extracts, a defined constituent such as polyphenols, flavonoids, anthocyanins, saponins or polysaccharides, always stated with the test method.

Extract ratio

Our listed extracts are 10:1, and other ratios can be developed. A ratio doesn't show active content, so a marker-based target is clearer where that matters.

Physical properties and solubility

Particle size, density, flow, carrier, dispersibility and solubility, evaluated in your formula, not in isolation. This matters especially for Functional Beverages.

Prototype, Pilot, Verify

01 Prototype

A bench-scale sample shows the gap between the first result and the target profile; analytical and formulation feedback guides refinement.

02 Pilot

Checks reproducibility as batch size grows. Extraction, concentration, drying, yield, handling and assay can all shift at scale.

03 Verify

Confirms identity, marker or assay, method, physical properties and project limits; results by different methods may not be comparable.

Once approved, the final specification becomes the reference for all production batches.

Scale Up for Commercial Production

The goal is a reproducible commercial ingredient, not a one-time sample. At this stage the question changes from “can it be made?” to “can it be made consistently?” Raw-material availability, operating conditions, yield and batch consistency become central. Approved ingredients move into Sample & Bulk Supply.

The same pathway supports new extracts, modified grades, application-specific ingredients and proprietary specifications.

Start Your Custom Ingredient Project

You don’t need a finished specification. A target assay, reference COA, benchmark sample or formulation challenge is enough for a first review.