MITRA-X
MITRA-X, engineered kratom ingredient

For brands replacing affected 7‑OH and kratom‑derivative product lines

MITRA-X™ is kratom extract produced through solvent‑free extraction, with mitragynine incorporated into a proprietary structured polyol matrix designed for oral delivery.

Carrier technology designed for improved bioavailability.

U.S. regulatory context

Reformulation landscape

  • Botanical kratom

    Remains outside federal Controlled Substances Act scheduling.

  • Selected derivatives

    MGPI, MGM‑15 and MGM‑16 are temporarily Schedule I.

  • Concentrated 7‑OH

    DEA’s revised threshold-based scheduling proposal remains pending.

An ingredient platform for brands developing their next formulation.

For brands reassessing their kratom and derivative-based product lines.

U.S. position as of 29 October 2026. Product availability and permitted uses vary by jurisdiction.

The ingredient

Extraction and carrier, in one ingredient

Solvent-free kratom extraction

Made with kratom extract produced using a solvent-free extraction method.

Structured carrier technology

Mitragynine is incorporated into a proprietary structured polyol matrix designed for oral delivery.

Conceptual carrier illustration. Solid nodes stand for the active held across the carrier lattice.

Bioavailability

Designed to improve bioavailability

Up to

53%

Increase in bioavailability reported for the carrier platform

Designed for oral delivery

The structured carrier is designed to support dispersion and ingredient availability for oral absorption.

Carrier-platform result. Performance may vary by active ingredient and formulation.

Formulation

Four formulation advantages

Carrier design supports the properties that matter in product development.

PriorityDesign approachDevelopment value

Taste

Design approach

Manage immediate bitterness through the carrier

Development value

Greater flexibility for flavour development

Water dispersion

Design approach

Support rapid hydration and dispersion in water

Development value

Easier incorporation into aqueous formulations

Ingredient consistency

Design approach

Distribute active material throughout the matrix

Development value

Control of ingredient loading

Format flexibility

Design approach

Provide an engineered powder for oral systems

Development value

One ingredient platform across development programs

Taste and dispersion

Less bitterness, faster dissolution

>61%

Reduction in bitterness

Reported taste profiling of the carrier technology

83%

Faster dissolution

Reported versus raw crystals and powder blends

Carrier-platform results. Performance may vary by active ingredient and formulation.

Applications

Potential product formats

One ingredient platform for multiple formulation programs.

  • Tablets and oral melts

    Solid oral formulations

  • Capsules

    Powder fill systems

  • Powder formats

    Stick packs and blended powders

  • Other oral formats

    Drinks, concentrates and gummies

Applications are subject to formulation validation and applicable market requirements.

Development

How development works

A program moves through four stages, from the first brief to commercial supply.

  1. 01

    Product brief

    Define the product format, target market and ingredient requirements.

  2. 02

    Sample evaluation

    Assess taste, dispersion and processing behaviour in your formulation.

  3. 03

    Product validation

    Establish performance, ingredient uniformity and stability of the product.

  4. 04

    Commercial supply

    Discuss specifications, volumes and supply terms for your application.