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Research Use Only · Reference compounds for in-vitro laboratory study · Not for human or animal consumption

Maison de Recherche

The Laboratory

Every vial that leaves this house is answerable to a ledger. Provenance is not a claim we make; it is a chain of custody we keep.

II
Chapter

Three pillars, in order.

Fmoc SPPS · cleanroom

Synthesis

Solid-phase peptide synthesis on automated coupling cycles, monitored for efficiency.

Prep RP-HPLC · ≥ 99%

Purification

Preparative reversed-phase HPLC with archived method files per SKU.

LC-MS · KF · LAL

Verification

Identity by mass spec, moisture by Karl Fischer, endotoxin by Limulus amebocyte lysate.

III
Chapter

From precursor to seal.

I

Raw Material

USP/EP reference precursors sourced under signed CoA. Every intake batch is logged and quarantined pending in-house verification.

II

Solid-Phase Synthesis

Fmoc chemistry on automated synthesizers in a controlled cleanroom. Coupling efficiency monitored per cycle.

III

Reversed-Phase HPLC

Preparative purification to a ≥ 99% purity floor. Method transfer files are archived for every SKU.

IV

Lyophilization

Freeze-drying under vacuum with programmed shelf-temperature ramps. Residual moisture verified by Karl Fischer.

V

Certificate of Analysis

Batch identity confirmed by LC-MS. Endotoxin, bioburden, and appearance recorded. COA hashed and signed.

VI

Cold-Chain Fulfillment

Vials stored at 2–8 °C, shipped with validated insulation. Every parcel carries a batch-linked seal.

IV
Chapter

The bench, itemized.

Purity determination

HPLC-UV

≥ 99.0% area/area at 220 nm

Identity confirmation

LC-MS (ESI)

Mass within 0.1% of theoretical

Residual moisture

Karl Fischer Titration

≤ 5.0% w/w

Pyrogen screening

Endotoxin (LAL)

< 0.5 EU/mg

Microbial limits

Bioburden

≤ 10 CFU/g

Composition verification

Amino-Acid Analysis

Ratios within ± 5% of theoretical

V
Chapter

Held to the mark.

  • ·ISO-class cleanroom conditions with monitored particulate, humidity, and pressure.
  • ·GMP-adjacent documentation for every intake, synthesis, and release step.
  • ·Reference standards traceable to USP / EP catalogs where established.
  • ·≥ 99% purity floor. No exceptions. No release below.
  • ·Batch-level COAs signed, hashed, and independently verifiable.
VI
Chapter

Recent batches.

Verify a batch →
BatchCompoundPurityReleased
AS-24-1108-BPCBPC-157 · 10 mg99.4%2024-11-08COA →
AS-24-1104-TB5TB-500 · 10 mg99.2%2024-11-04COA →
AS-24-1029-SEMSemaglutide · 10 mg99.6%2024-10-29COA →
AS-24-1022-TIRTirzepatide · 30 mg99.5%2024-10-22COA →
AS-24-1018-GLWGLOW · 70 mg99.3%2024-10-18COA →
AS-24-1012-IPAIpamorelin · 10 mg99.7%2024-10-12COA →
AS-24-1005-RETRetatrutide · 20 mg99.4%2024-10-05COA →
AS-24-0928-KLWKLOW · 80 mg99.3%2024-09-28COA →

Fin

Every vial answers to the ledger.