Services

Testing services & methods

Aletheia Labs provides analytical testing for research compounds, raw materials, and finished products. The 7× panel below is our standard certificate scope; individual assays can also be ordered on their own.

The 7× Certificate Panel
#TestMethodWhat it confirmsReporting
1IdentityLC-MS (ESI+)Observed molecular weight matches the expected compound.Consistent / not
2PurityRP-HPLC, UV 214 nmMain-peak purity relative to impurities and degradants.% area
3Net Peptide ContentHPLC vs. referenceActual quantity present vs. the labeled claim.mg/vial & %
4Acetate ContentRP-HPLC, UV 210 nmResidual acetate counter-ion from synthesis.% w/w
5Heavy MetalsICP-MS · USP ⟨232⟩/⟨233⟩Lead, arsenic, cadmium, mercury within elemental limits.ppm
6Bacterial EndotoxinKinetic chromogenic LAL · ⟨85⟩Endotoxin (pyrogen) load against acceptance limit.EU/mg
7SterilityMembrane filtration · BacT/ALERT · ⟨71⟩Absence of microbial growth over 14-day incubation.Growth / none

Methods are aligned with the general principles of the cited USP chapters. Acceptance criteria are set per analyte and agreed before testing.

Base tests

Included in every certificate

Purity Analysis (HPLC/UV)

Reversed-phase HPLC with UV detection separates components and quantifies the main compound relative to impurities and degradation products.

MethodRP-HPLC, UV-Vis
Turnaround5–7 business days
Sample1 vial minimum
Net Content & Identity (LC-MS)

Quantitation of the true peptide content against the label claim, plus mass-spec confirmation that the observed mass matches the expected molecular weight.

MethodHPLC quant + LC-MS (ESI+)
Turnaround5–7 business days
SampleAliquot from purity vial
Safety add-ons

Order individually or as part of the 7×

Heavy Metals (ICP-MS)

Part-per-billion elemental analysis for Pb, As, Cd, Hg and other regulated impurities, aligned with USP ⟨232⟩/⟨233⟩.

Turnaround5–7 days
SampleDedicated vial
Bacterial Endotoxin

Quantitative kinetic chromogenic LAL with product-specific spike-recovery validation, reported against limits per USP ⟨85⟩.

Turnaround5–7 days
Sample1 vial (partial)
14-Day Sterility

Membrane filtration into aerobic & anaerobic media with automated BacT/ALERT incubation; rapid read at day 2, final at day 14 (USP ⟨71⟩).

Turnaround2 days rapid / 14 final
Sample1 vial (destructive)
Pricing

Quotes are tailored to your panel & volume

Pricing depends on the tests selected and the number of batches. Tell us what you’re trying to confirm and we’ll send a testing plan and quote — volume rates available for vendors testing multiple lots.

Request a Quote Verify a COA