Mass over volume
Labeled milligrams divided by milliliters of solvent. Units mg/mL. That is the concentration of the stock you just made.
Methods
CAS and sequence on the catalog page are public identity. Peak area, observed mass, and net peptide content are lot data. They sit on the COA that matches the vial.
Overview
Bench calculation
Labeled milligrams divided by milliliters of solvent. For preparing an in-vitro stock. Not a protocol and not a purity figure.
5.00 mg/mL
10 mg labeled ÷ 2 mL solvent
In-vitro stock concentration. Research use only.
Labeled milligrams divided by milliliters of solvent. Units mg/mL. That is the concentration of the stock you just made.
This box does not use HPLC area percent, net peptide content, or observed mass. Those remain on the lot COA.
A stated mg/mL lets later dilutions be written into the notebook. Identity and purity are still the COA.
01 · HPLC

Detector signal with only mobile phase flowing. A stable baseline is required before a peak can be integrated. Drift and noise are method notes.
Each UV-active species leaves the column at a characteristic time under a stated method. Retention time depends on that method. It is not identity on its own.
The dominant peak is assigned to the listed compound after identity work, not instead of it. Other peaks are other UV-active species at that wavelength.
HPLC purity is main-peak area divided by total detected peak area at a stated wavelength. An area ratio, not a weighing of the vial.
The calculation is:
HPLC purity = (main-peak area) ÷ (sum of detected peak areas) at a stated λ
Related peptides, leftover protecting groups, and process impurities appear as extra UV peaks when they elute and absorb at that wavelength. They are other species, not a second purity number.
Counter-ions and residual water are often invisible at 214 nm. A high area percent can still sit on a cake that is partly TFA and moisture. Net peptide content is a separate measurement (typically amino-acid analysis or nitrogen) and belongs on the COA when it is run.
02 · HPLC and MS

A complete lot record answers two questions.
What share of the UV-active material is the main peak? Chromatography (typically reversed-phase HPLC). It does not name the molecule.
Is that species the listed compound? Mass spectrometry: theoretical mass from the public formula versus observed mass. Agreement supports identity. A mismatch is not rescued by area percent.
Purity of the wrong molecule is still the wrong molecule. Theoretical and observed mass, with the ionization method, belong on the COA.
03 · Certificate of analysis
A certificate of analysis is a laboratory record for one lot. These five fields make it usable as a record, not a brochure.
The same identifier as the vial label. If the PDF and the label disagree, the record is not matched.
Test date or report date. A sheet with no year is incomplete.
The laboratory that ran the work. A table without a lab is not a certificate.
HPLC column and wavelength, MS ionization mode, residual-solvent method when reported. A percentage with no method is not an HPLC result.
The chromatogram, or a table of retention times and area percent. Without one of those, the integration is not visible.
A COA is incomplete when it is missing:
04 · Net peptide
Schematic. Bar lengths are teaching marks, not lot measurements, and not a purity claim for any SKU.
Lyophilized peptide is a cake of sequence plus counter-ion plus residual water. HPLC at 214 nm usually does not see the salt or the moisture.
Two numbers can sit on one certificate: HPLC area percent for the main UV peak, and net peptide content for the fraction of weighed mass that is peptide. They answer different questions. A single homepage percentage collapses them.
See also HPLC area percent vs net peptide content.
05 · Chemical identity
CAS, sequence, and formula below are literature identity for the named listing. Lot confirmation is the observed mass on that lot’s COA.
Literature identity for the pentadecapeptide. Lot confirmation is observed mass on the COA.
Open the SKU →A dinucleotide cofactor. There is no peptide sequence.
Open the SKU →Published fragment identity. Unmodified hGH 177–191 starts with Phe, not Tyr. Identity note.
Open the SKU →Heptapeptide fragment, not the 43-residue protein. TB-500 vs Tβ4.
Open the SKU →A blend is two molecules. The COA should show both observed masses. Identity note.
Open the SKU →Curcuminoids complexed with phospholipid. Curcumin CAS 458-37-7. Not a peptide. Identity note.
Open the SKU →06 · Catalog
USD list prices for the SKUs below. The bar length is price, not purity.
AOD-9604 $95 · BPC-157 $110 · NAD+ $120 · Curcumin Phytosome $140 · Tesamorelin / Ipamorelin $155 · BPC-157 / TB-500 Blend $185. Catalog prices, not a quality ranking.
07 · FAQ
Research Use Only. These materials are sold for in-vitro and laboratory research. They are not approved medicines, not supplements, and not for human consumption, self-administration, or therapeutic use.
No. No body-weight charts, injection instructions, or treatment advice. The calculator on this page is bench arithmetic (mg/mL) for in-vitro stocks.
HPLC reports how UV-active peak area splits. Mass spectrometry checks whether the species matches the expected mass. A complete lot record uses both.
A percentage without lot, method, and wavelength is not a result. Those figures are issued on the COA for that lot.
A manufacturing batch. The lot on the vial should match the lot on the certificate. Different lots of the same SKU are different records.
Temperature-sensitive compounds ship with cold-chain packaging rather than as ambient shelf stock. Packaging method, not a stability claim for a named lot.
References
Method literature and public registries. Lot HPLC, MS, and net peptide figures remain on the matching COA.
Research use only. Not FDA approved. Not for human consumption, self-administration, or therapeutic use. Chromatograms and bar charts on this page are schematics. Sequences, CAS numbers, and molecular weights are public literature identity. Lot HPLC, MS, and net peptide content are issued on the matching COA.
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