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Analytical testing glossary

Definitions for laboratory documentation and research-material procurement. Research use only — not medical or dosing guidance.

Analytical report
A laboratory document summarizing methods and results for a sample or lot. A Certificate of Analysis is a common batch-linked form used in research procurement.

Related: How to read an analytical report · Understanding COAs

Batch verification
Looking up a lot number (or scanning a QR target) to open the corresponding batch documentation record for that container.

Related: Verify a batch · Understanding batch verification

Certificate of Analysis (COA)
A batch-linked laboratory document summarizing analytical results for a specific lot, typically including identity and/or purity methods, results, and dates. Used for research documentation—not as clinical authorization.

Related: Understanding COAs

Chromatogram
The detector signal recorded over time during a chromatographic run. Analysts integrate peaks to estimate relative abundance under the method’s rules.

Related: HPLC testing explained

HPLC
High-performance liquid chromatography. Separates components in a dissolved sample under pressure; used to report chromatographic purity for many research-material lots.

Related: HPLC testing explained

Identity testing
Analytical work that asks whether observed evidence is consistent with the expected compound. Mass spectrometry is commonly used for this purpose in research-material documentation.

Related: LC-MS identity testing · Purity versus identity

Impurity peak
An additional chromatographic signal integrated under the method rules and considered when reporting purity.
LC-MS
Liquid chromatography–mass spectrometry. Combines chromatographic separation with mass analysis; often used to support identity confirmation for research materials.

Related: LC-MS identity testing

Lot number (batch identifier)
A unique identifier tying a physical container to manufacturing or release documentation. Essential for traceability in laboratory quality systems.

Related: Batch verification · Research Vault

Main peak
The primary analyte signal used for purity calculations on a chromatogram, subject to the laboratory’s integration rules.
Orthogonal method
A second analytical approach that provides independent evidence about a material (for example, MS identity alongside HPLC purity). Used to strengthen documentation confidence.
Purity testing
Analytical work that estimates how much of a measured signal is attributable to the primary analyte under defined method conditions. HPLC is a common technique. Results are method-dependent and lot-specific.

Related: HPLC testing explained · Purity versus identity

Research Use Only (RUO)
Positioning that materials are supplied for laboratory research use and are not intended for human or veterinary use, diagnosis, or treatment. A disclaimer alone does not determine every regulatory outcome for every buyer.

Related: RUO policy · Compliance overview

Retention time
The time at which a peak elutes under stated chromatographic conditions. Useful for method context; not by itself a complete identity proof.
Storage documentation
Records of assigned storage conditions (temperature, light/moisture protection, location) tied to a lot or inventory entry under institutional SOPs.

Related: Laboratory storage reference · Storage documentation article

System suitability
Checks that confirm an analytical system is performing adequately before or during sample analysis. Often referenced in laboratory SOPs; may or may not appear on a supplier COA.
Target purity (catalog)
Catalog language describing the intended release specification for a SKU. Lot-specific measured values belong on the batch record or COA when available—not as a substitute for that certificate.

Related: Quality standards

Explore the research library, testing methodology, and Research Use Only policy.