Our Standards

Quality Assurance & Testing

Rigorous testing protocols ensure every batch meets strict purity and identity standards for research-grade compounds.

Testing Methodology

Identity Verification

High-Performance Liquid Chromatography (HPLC) confirms molecular identity and structural integrity for every compound.

Purity Analysis

Liquid Chromatography-Mass Spectrometry (LC-MS) detects and quantifies impurities. Target purity: >99%.

Residual Solvent Testing

Testing for residual solvents and synthesis byproducts ensures compounds meet laboratory safety standards.

Testing Process

1

Incoming Screening

All raw materials undergo identity verification and purity screening.

2

Post-Synthesis

Each batch tested for identity, purity, and contaminants.

3

Third-Party Verification

Independent ISO/IEC 17025 accredited lab confirmation.

4

Final Release

Released only after passing all tests and verification.

Third-Party Lab Verification

All certificates of analysis (CoA) are reviewed and confirmed by Research Analytics Labs, an ISO 17025-accredited third-party laboratory specializing in peptide and small molecule analysis.

This independent verification ensures transparency and confidence in the quality of research materials provided to our scientific community.

Certificate of Analysis (CoA)

Every product lot ships with a CoA that includes:

  • • Compound name and CAS number
  • • Lot number for traceability
  • • Test date and laboratory name
  • • Test method (HPLC, LC-MS)
  • • Results with purity percentages
  • • Lab identity and accreditation

For Research Use Only. All products are intended for laboratory research purposes only. Not for human or animal use. Not for diagnostic, therapeutic, or clinical purposes.