About Auralen
Reference standards, made for the bench.
We produce lyophilized peptide reference standards for in-vitro laboratory research. Every lot is third-party assayed, sealed under nitrogen, and traceable from synthesis through fill.
The why
The catalog is the product.
The data is the proof.
We started Auralen because too much of the research-peptide market regards documentation as an afterthought. A vial without a certificate is a guess. A certificate without a method is a marketing document.
A reference standard is only worth what its certificate says it is.
Auralen lots ship with HPLC and mass-spectrometry data from a third-party laboratory. Synthesis source and lot numbers are traceable end-to-end. Fill, capping, and labeling happen in an ISO-class controlled environment. None of this is novel — it is what a reference standard should be.
What we commit to
Four standards, every lot.
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Independent assay
Every lot is tested by a third-party laboratory we do not own. The certificate of analysis includes identity by mass spectrometry and purity by reverse-phase HPLC.
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Documented purity
≥ 99% peptide content for our standard catalog. Lots that fall short of spec do not ship — they are destroyed and the batch is re-synthesized.
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Traceable origin
Synthesis source and lot number are recorded for every vial and archived for the life of the batch. If you ask which facility produced lot #2407B, we can tell you.
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Cleanroom fill
Reconstitution, fill, capping, and labeling happen in an ISO-class controlled environment. Stoppers and seals are USP-grade.
By the numbers
Documented, every lot.
- 2024 Founded
- 31 Compounds
- 55 SKU variants
- ≥99.5% Avg purity
- 100% Per-lot QC
- 0 Lots shipped without COA
In-vitro research only.
Auralen products are reference materials. They are not drugs, supplements, or medical devices. They are not for human or animal consumption. Sale is restricted to qualified researchers and laboratory professionals.
- Lab tested
- Third-party verified
- 99%+ purity
- Pharma grade