Quality Assurance

Testing & Verification

Every compound is independently verified before it reaches you. Here's exactly how we ensure purity, identity, and sterility.

100%
Third-Party Tested
99%+
Purity Standard
0%
In-House COAs

Why independent testing matters

Most suppliers rely on Certificates of Analysis provided by the manufacturer—the same company that profits from higher purity claims. This creates an obvious conflict of interest.

We take a different approach. Every batch we produce is sent to an independent, third-party laboratory that has no financial stake in the results. If a compound doesn't meet our standards, we don't ship it.

Independent verification isn't just a marketing claim—it's the foundation of research integrity.

Three pillars of verification

Each compound undergoes three distinct types of analysis before release.

01

Purity Analysis

High-Performance Liquid Chromatography (HPLC) separates the target compound from impurities and calculates exact purity percentage.

METHODHPLC
02

Identity Confirmation

Mass Spectrometry (MS) verifies the molecular weight and structure to confirm you're getting the exact compound ordered.

METHODLC-MS
03

Sterility Testing

Endotoxin and microbial contamination testing ensures products meet pharmaceutical-grade sterility standards.

METHODLAL/USP

Our Testing Partners

Eurofins
Scientific Analysis

ISO 17025 accredited. Primary lab for HPLC purity analysis.

SGS
Global Testing

Mass spectrometry and identity confirmation.

Charles River
Biotech Services

Endotoxin testing and sterility verification.

See the data yourself

Download full COAs for every product. Batch-specific results from independent labs.