Peptide Medix product catalog

ET
Editorial Team
August 16, 2026 5 min read

A peptide blend fixes the ratio between its components at the moment of manufacture; a multi-vial stack leaves that ratio to the study design. Everything else — COA interpretation, concentration math, purity claims — follows from that one difference. Choosing peptide blends vs single vials is a study-design decision before it is a purchasing decision, and the most common error in the category is treating a co-formulated vial as if it were a single molecule. This guide sets out the three formats, the ratio and molarity arithmetic a blend forces on you, how a blend's certificate of analysis should differ from a single-peptide one, and when each format is the right tool. Research use only.

Peptide blends vs single vials: three formats, not two

FormatWhat arrivesRatioCOA expectationBest for
Co-formulated blendOne vial, components lyophilized togetherFixed at manufacturePer-component mass plus per-component purityFixed-ratio protocols, fewer handling steps
Multi-vial stackSeveral sealed vials shipped as one itemSet by the researcherOne COA per vial, as for single peptidesVarying one component against a fixed background
Separate single vialsIndividually orderedFully independentOne COA per lotAny design where components vary independently or lots must be traced separately

The Wolverine blend and the Wolverine Stack illustrate the distinction cleanly: the first is one vial of co-lyophilized BPC-157 and TB-500 at a fixed 1:1 mass ratio, the second is three separately sealed vials of BPC-157, TB-500 and GHK-Cu whose ratio is entirely yours to set.

Reading the ratio off a blend label

Blend labels state total mass and, when the ratio is not equal, the per-component split. A variant labelled 10 mg (5/5) contains 5 mg of each of two components. A variant labelled simply 80 mg, as on the four-component KLOW Blend, requires the COA to tell you how those 80 mg are divided — the split is not equal in most four-component preparations, and a blend whose documentation will not state per-component mass cannot be used quantitatively.

Worked example: concentration per component

  1. Start with the blend. A 10 mg (5/5) Wolverine vial reconstituted with 2 mL of diluent gives a total peptide concentration of 10 ÷ 2 = 5 mg/mL.
  2. Split it. Because the vial is 5 mg BPC-157 and 5 mg TB-500, the solution is 2.5 mg/mL of each, not 5 mg/mL of either.
  3. Per-unit mass. On a U-100 syringe, 0.01 mL (1 unit) contains 25 mcg of BPC-157 and 25 mcg of TB-500. A 0.1 mL draw is 250 mcg of each, 500 mcg total peptide.
  4. Compare with single vials. Achieving the same 2.5 mg/mL of each from separate vials means reconstituting a 5 mg BPC-157 vial with 2 mL and a 5 mg TB-500 vial with 2 mL — two reconstitutions, two septum entries per transfer, and the freedom to change either concentration later.

The underlying mg/mL arithmetic is the same one used for any vial and is covered in peptide reconstitution math explained.

The molarity trap: equal mass is not equal moles

This is the part that catches experienced researchers. A 1:1 mass ratio is not a 1:1 molar ratio unless the components happen to share a molecular weight, and they rarely do.

  • BPC-157: 1,419.55 Da. At 2.5 mg/mL → 2.5 g/L ÷ 1,419.55 g/mol = 1.76 mM.
  • TB-500: 889.02 Da. At 2.5 mg/mL → 2.5 ÷ 889.02 = 2.81 mM.

The same mass of each delivers roughly 1.6 times more molecules of TB-500 than of BPC-157. For a receptor-occupancy or stoichiometry question, that is the number that matters, and a fixed-mass blend cannot be adjusted to correct it. Any design that needs equimolar components needs single vials.

What a blend COA should show

A single-peptide certificate reports one HPLC purity figure and one mass-spectrometry identity confirmation. A blend cannot be summarised that way, and the honest documentation looks different:

  • Per-component purity, measured before blending. Each peptide should be synthesised, purified and released against its own COA, then combined. "≥99% purity" on a blend normally means each input met that specification, not that the mixture has a single 99% peak.
  • A chromatogram that resolves the components. On a reversed-phase run, four peptides of different hydrophobicity elute at four different retention times. A blend chromatogram should show the expected number of peaks with the expected area ratios; a single broad peak is a red flag.
  • Per-component mass in the vial, established gravimetrically at fill or by quantitative amino-acid analysis.
  • An identity confirmation per component. A blend has several molecular weights, and MS should account for all of them.

The general framework for reading these documents is in how to read a peptide COA. If a supplier's blend COA reports a single purity number and a single mass with no per-component breakdown, the document does not describe the product.

When each format is the right choice

Choose a co-formulated blend when

  • The protocol specifies a fixed ratio you do not intend to vary — the case for CJC-1295 + Ipamorelin, where the two secretagogues act on different receptors converging on the same cell and the pairing is the established research configuration.
  • Handling steps are a meaningful source of error. Every reconstitution adds pipetting variance, a septum puncture and a contamination opportunity; a four-component blend removes three of each.
  • Total material cost per milligram matters and the ratio is acceptable as supplied.

Choose separate vials or a stack when

  • One component is being varied against the others — the defining requirement of a concentration–response design.
  • Equimolar rather than equal-mass comparison is required.
  • Components have materially different stability. Copper peptides, methionine-containing sequences and disulfide-bonded peptides degrade on different timelines; once co-formulated in solution, the whole vial is limited by its least stable member.
  • Lot traceability per component is required for publication or for internal QC.
  • Components need different diluents or different pH ranges to dissolve cleanly.

The NAD+ Longevity Stack is the archetype of the second column: three individually sealed vials priced as a kit, reconstituted independently.

Common mistakes

  • Treating total vial mass as per-component mass. An 80 mg four-component vial does not contain 80 mg of anything.
  • Assuming an equal mass split when the label does not state one.
  • Reporting molar concentrations for a blend without recalculating each component against its own molecular weight.
  • Accepting a single purity figure for a multi-component vial.
  • Splitting a blend to recover one component. Once co-lyophilized, the components cannot be separated without preparative chromatography; if you need one peptide alone, buy it alone from the lyophilized vial range.

The full co-formulated and multi-vial range sits in peptide blends and stacks.

Frequently Asked Questions

What does '10 mg (5/5)' mean on a blend label?
It means the vial holds 10 mg of total peptide split as 5 mg of each of two components. Reconstituted with 2 mL of diluent, the solution is 5 mg/mL total but 2.5 mg/mL of each component — the number that belongs in your calculations.
Is a 1:1 blend equimolar?
Only by coincidence. A 1:1 mass ratio is equimolar only if the two peptides share a molecular weight. BPC-157 is 1,419.55 Da and TB-500 is 889.02 Da, so 2.5 mg/mL of each gives 1.76 mM and 2.81 mM respectively — roughly 1.6 times more TB-500 molecules. Designs that need equimolar components require separate vials.
What should a blend certificate of analysis show?
Per-component purity measured before blending, a chromatogram resolving each component at its own retention time with the expected area ratios, per-component mass in the vial, and mass-spectrometry identity confirmation for every molecular weight present. A single purity figure and a single mass do not describe a multi-component product.
Can a blend be separated back into its components?
Not practically. Once co-lyophilized, separating the components requires preparative chromatography and a re-purification workflow. If a study needs one peptide on its own, order it on its own rather than attempting to fractionate a blend.
When is a blend the better choice?
When the protocol calls for a fixed ratio that will not be varied, when handling steps are a meaningful source of variance, and when the components are stable together. Each avoided reconstitution removes a pipetting error, a septum puncture and a contamination opportunity, which is a real advantage in a four-component preparation.
When should I use separate vials instead?
Whenever one component is being varied against the others, whenever equimolar rather than equal-mass comparison is needed, whenever components differ materially in stability, whenever per-component lot traceability is required, and whenever the components need different diluents or pH ranges to dissolve cleanly.
How does a stack differ from a blend?
A stack ships several individually sealed, individually tested vials as one catalogue item at a kit price. Nothing is co-formulated, so each vial carries its own certificate of analysis and each can be reconstituted at its own concentration. The pricing is bundled; the chemistry is not.
Does a blend degrade faster than single vials?
In solution it can. Once components share a vial, the working life of the whole preparation is set by its least stable member — copper complexes, methionine-containing sequences and disulfide-bonded peptides all follow different degradation timelines. Lyophilized and stored frozen, the difference is much smaller.

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