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Aero Peptides

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Quality & testing

Every batch verified

Research only matters if the inputs are real. Here's exactly how we test, what we hold our suppliers to, and how you can verify any of it independently.

The Aero Peptide Process

Built around quality from production through fulfillment

01

Manufacturing

Solid-phase peptide synthesis by domestic US suppliers with documented supply-chain provenance.

02

Identity & purity

Quality remains our priority. Batches are supported by analytical testing and reviewed against strict standards before reaching production.

03

Release testing

An independent third-party lab issues a Certificate of Analysis covering identity, purity, endotoxin, residual solvents and water content. Lot numbers traceable from order to source.

04

Fulfilment

Tamper-evident vials, secure packaging, and discreet shipping. Order protection included.

The test panel

What we measure, and where the bar sits.

Identity verification

HPLC-MS

Each peptide is verified against its theoretical molecular weight using high-performance liquid chromatography coupled to mass spectrometry. Identity must match within 1 mass unit.

Purity

≥ 98%

Reverse-phase HPLC quantifies the target peptide against minor synthesis byproducts. We hold every batch to a minimum 98% area-percent purity threshold.

Endotoxin

< 0.1 EU/mg

Bacterial endotoxin is screened by LAL (Limulus Amebocyte Lysate) assay. Results well below the USP <85> compendial limits for parenteral research-grade material.

Residual solvents

< 0.5%

Gas chromatography quantifies residual TFA and synthesis solvents. ICH Q3C class-2 limits are the upper bound; our batches routinely run an order of magnitude lower.

Independent verification

Every result independently signed off

Release testing is performed by an external, ISO-accredited laboratory we don’t own. The Certificate of Analysis carries their stamp, their signatory, and the raw instrument data on request.

A note on standards. Aero Peptides products are sold strictly for in-vitro research and laboratory use. The internal quality thresholds described above are research-grade specifications; they are not pharmacopoeial release criteria and do not constitute approval for human or veterinary application. See our Research Use policy for the full scope of permitted use.