
Confirm identity & composition
Establish what a material is and whether it's what it should be — chemical identity, composition, purity, and elemental makeup.

These are the questions an analytical program usually starts from.
Five defined stages, from the brief to the report. Enter at any of them.
The material, its known history, the analytical objective, and the decision the data must support.
Confirm sample format, quantity, preparation, handling, comparison groups, and acceptance criteria.
Choose an established capability, or define the method-development work the objective requires.
Document preparation and run the agreed testing under defined analytical conditions.
Evaluate results, comparisons, anomalies, and limitations, and deliver a technical report with recommended next steps.
Every capability area and instrument, in one place. Filter to an area or search the full inventory by method, property, instrument, or model.
64 analytical instruments and systems
Separate, identify, quantify, and compare chemical components, molecular-weight distributions, impurities, and volatile or ionic species.
Imaging and elemental analysis used to examine morphology, surfaces, defects, interfaces, particles, and structures across multiple length scales.
Assess thermal transitions, stability, degradation, flow behavior, viscosity, reaction behavior, and processing-relevant properties.
Quantify elemental composition to support material identification, purity evaluation, and formulation analysis.
Evaluate wettability, surface energy, roughness, thickness, porosity, profilometry, and film or coating behavior.
Investigate molecular structure, functional groups, optical behavior, composition, and chemical environments.
Evaluate strength, modulus, deformation, fatigue, wear, friction, impact, thermal transport, and behavior under controlled conditions.
Quantify water content, acidity, alkalinity, amine values, and other chemistry-dependent properties.
Examine conductivity, resistivity, impedance, dielectric behavior, semiconductor performance, electrochemical behavior, piezoelectric properties, and charge transport.
Characterize particle size, shape, distribution, stability, surface area, powder flow, and electrokinetic behavior.
Model configuration, detector availability, sample compatibility, and measurement range are confirmed for each engagement during scoping.
Beyond the physicochemical suite above, the laboratory evaluates biocompatibility and skin safety in-house — essential for on-body, wearable, and medical materials.
Assays, endpoints, and applicable standards are scoped to the material and its intended use.
Contract characterization for the materials and industries that need trustworthy data — regulated or not.
Myant's operating systems are independently certified. Where accredited testing or a specific standard is required, that's confirmed per engagement — this laboratory is not ISO/IEC 17025 accredited.
Where the lab differs from a standalone testing service.
The lab sits inside a development and manufacturing partner — so the data feeds directly into R&D, prototyping, and scale-up, carrying methods and criteria into the next decision.
Chromatography to electrical characterization, all in-house — so a program's comparisons stay consistent instead of fragmenting across separate vendors and shipments.
When no standard test fits, we build one — shaped to the decision you need to make, so the analysis answers your actual question.
Not seeing your question? Talk to the team that would run your program.
Discuss a projectLiquids, powders, films, coatings, polymers, particles, yarns, textiles, components, and more. The quantity needed depends on the material, method, and replicates — we confirm requirements before you ship anything.
Both. We run established methods, and when none fits we develop one for the material and the decision it must support — approach, sample preparation, repeatability, and a useful measurement range.
Where the method and capability are available, we can run it as written or adapt it for the program. Availability and any deviations are confirmed up front; formally accredited testing is scoped where required.
Yes — biocompatibility and skin-safety evaluation is available in-house for on-body, wearable, and medical materials. The assays, endpoints, and standards are scoped to the material and its intended use.
Hazards, storage, and shipping are reviewed before a sample is accepted. Confidentiality, data access, and IP are set in the agreement; sample retention, return, or disposal is defined during scoping.
Tell us what the material is and what the results need to answer. The laboratory team will help define the analytical path.