TESTING::DOCUMENTATION

Analytical
Rigor

Every compound we release has been subjected to independent multi-platform analytical verification. This page describes our testing methodology and documentation standards. Batch-specific COAs are available exclusively through the customer portal.

Analytical Methods

HPLC-UV/MS

HPLC Chromatography

High-Performance Liquid Chromatography with UV and mass spectrometric detection provides precise purity quantification. Identifies and quantifies impurities at the sub-0.1% level. All columns and mobile phases are calibrated against NIST-traceable reference standards.

≥ 99.0% Purity Threshold
Sub-0.1% Impurity Detection
NIST-Traceable Standards
ESI-MS/MS

Mass Spectrometry

Electrospray ionization tandem mass spectrometry confirms molecular weight and structural identity of every compound. Molecular weight verification to ±0.1 Da ensures correct compound identity and rules out structural isomers or synthesis byproducts.

Molecular Weight ± 0.1 Da
Structural Identity Confirmed
Isomer Discrimination
AAA-PITC

Amino Acid Analysis

PITC derivatization amino acid analysis validates sequence integrity and composition of peptide compounds. Provides a quantitative amino acid composition profile confirming sequence accuracy and peptide stoichiometry.

Sequence Accuracy 100%
Quantitative Composition
Full Stoichiometry Profile
ICP-MS

Heavy Metal Screening

Inductively Coupled Plasma Mass Spectrometry screens for trace heavy metal contamination across all batches. Ensures compounds meet strict residual metal limits consistent with pharmaceutical grade standards.

< 10 ppm Total Metals
Arsenic, Lead, Mercury, Cadmium
ICP-MS Multi-Element Panel

Batch Release Process

01

Synthesis & Initial QC

Compounds are synthesized under controlled conditions with in-process analytical checkpoints throughout the synthesis cycle.

02

Third-Party Submission

Completed batches are shipped directly to our independent ISO 17025 accredited testing partner with chain-of-custody documentation.

03

Multi-Platform Analysis

The independent lab conducts HPLC, MS/MS, AAA, and heavy metal screening as a complete analytical panel — results reported with raw data.

04

CoA Generation

Upon passing all analytical benchmarks, the lab issues a batch-specific Certificate of Analysis documenting all test results and methodology.

05

Internal Review & Release

Our scientific team reviews the independent results before releasing any batch for sale. Any batch failing threshold requirements is destroyed.

06

Customer CoA Access

The final CoA, chromatograms, and mass spectra are uploaded to the secure customer dashboard, accessible post-purchase to verified customers only.

Batch Documentation Is Private by Design

We do not publish Certificates of Analysis publicly. Each CoA, HPLC chromatogram, and mass spectrum report is available only to the verified customer who purchased that specific batch, through the authenticated customer portal. This protects documentation integrity and prevents misrepresentation.

Portal Access