Measured with rigor.
Verified by design.
In-house analytical testing for research compounds, peptides, hormones, and related materials—with the measurement, units, scope, and limitations stated clearly.
Frequently requested
Four core testing categories.
Start with the most requested analytical scopes here, or open the complete service catalog for specialized and custom work.
Peptides, GLP-1 & proteins
Peptides
Sequence-informed identity, amount, chromatographic purity, net-content, and size-variant scopes for research peptides and related proteins.
Browse testsInjectable & oral formulations
Anabolic steroids
Targeted identity and quantitative testing for oil-based and oral anabolic steroid samples, with a stated result basis for every resolved target.
Browse testsTargeted identity & amount panels
SARMs & related compounds
Targeted identification and quantitative measurement for declared selective androgen receptor modulators and related research compounds.
Browse testsContaminant & microbiology scopes
Harm reduction
Complementary endotoxin, microbial-enumeration, elemental, and targeted contaminant testing for suitable sample matrices.
Browse testsResult language
Similar terms do not mean the same thing.
Each reported number answers a specific analytical question. RigorTrace keeps those questions separate so the result remains interpretable.
Identity
Evidence that a detected compound is consistent with the stated analyte, supported by the measurement types named in the report.
Amount
A quantitative result determined on a stated basis, such as mg/vial, mg/unit, or mg/mL, using a defined calibration and calculation model.
Chromatographic purity
The target peak’s relative area among method-defined detected peaks. It is not automatically total chemical purity or mass fraction.
Net peptide content
The sample-mass fraction attributed to peptide under a defined compositional model, distinct from chromatographic area percentage.
Microbial enumeration
Recovered culturable aerobic microorganisms, yeasts, and molds. It is not a sterility test.
Chain of custody
A controlled path from sample to report.
Five deliberate stages connect the submitted material to a reviewable, verifiable analytical record.
Define the scope
Tell us the compound, matrix, sample form, and question. The requested measurements and reporting basis are fixed before analysis.
Accession the sample
Each received item is logged against its unique submission identity, condition, and agreed analytical scope.
Analyze in-house
Our team performs the selected chromatographic, mass-spectrometric, elemental, or microbiological measurements.
Review the record
Data, calculations, units, qualifiers, and report language are reviewed before a document is released.
Issue & verify
The final report receives a document number, private verification key, revision, status, and SHA-256 record fingerprint.
Document integrity
Every released result has a trail.
A RigorTrace report is more than a PDF. Its identity and current status are anchored to a server-side record that can be checked independently.
Private verification key
Required with the document number to retrieve the matching record.
SHA-256 fingerprint
A deterministic fingerprint ties the displayed analytical data to its revision.
Revision & status
Verified, pending, or revoked is shown in text and color.
Uniform report schema
Every category uses the same core document architecture.
Verification record