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BAM15 35mg

BAM15 35mg

35mg • 50 Capsules
$185.00$225.00-18%

BAM15 is a mitochondrial protonophore uncoupler studied for its effect on cellular respiration and substrate oxidation without the membrane depolarisation associated with older uncouplers. Supplied as pre-dosed capsules.

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Product Details
FormOral capsules — pre-dosed, no reconstitution
Purity≥99% (verified)
StorageCool and dry, sealed; protect from light
BatchCOA available on request
Why Choose BAM15 35mg?

BAM15 is a mitochondrial protonophore uncoupler studied for its effect on cellular respiration and substrate oxidation without the membrane depolarisation associated with older uncouplers. Supplied as pre-dosed capsules.

Key Benefits
  • Mitochondrial uncoupler — metabolic research
  • Pre-dosed capsules — no reconstitution
  • Third-party tested — COA available on request
  • Ships from the USA in discreet packaging
⚠️ Products are sold for laboratory and research use only. Not for human consumption. Not evaluated by the FDA.

About BAM15 35mg

BAM15 is a mitochondrial protonophore — a small molecule that carries protons across the inner mitochondrial membrane, dissipating the proton gradient that would otherwise drive ATP synthesis. The energy is released as heat instead, which is what the term 'uncoupler' describes.

Chemical uncouplers are not new. What made BAM15 a subject of renewed research is selectivity: earlier compounds in this class, most notoriously 2,4-dinitrophenol, also depolarise the plasma membrane, which is where their well-documented toxicity comes from. BAM15 was characterised as acting on the mitochondrial membrane with substantially less plasma membrane effect.

Supplied as pre-dosed capsules for laboratory research use only. Not for human consumption.

Research background

Mitochondrial selectivity

The defining published claim is that BAM15 depolarises the mitochondrial membrane without the plasma membrane depolarisation seen with older protonophores. That selectivity is the reason it is studied at all rather than being of purely historical interest.

Substrate oxidation and energy expenditure

Uncoupling increases substrate oxidation because the electron transport chain runs without the constraint of ATP demand. Animal studies have examined fat oxidation and energy expenditure using this as the mechanism.

Insulin sensitivity models

A related strand examines glucose handling in diet-induced obesity models, on the hypothesis that reducing lipid accumulation in muscle and liver alters insulin signalling.

Comparison with older uncouplers

Much of the published work is explicitly comparative, measuring BAM15 against DNP and FCCP to characterise the safety margin that motivated its development.

The literature is preclinical — cell culture and rodent models. BAM15 has not completed human clinical trials and is not an approved drug. Mitochondrial uncouplers as a class have a serious historical safety record, which is precisely why selectivity is the central research question.

Storage and stability

StateTemperaturePractical shelf life
Sealed bottle, room temperature15–25 °CTo printed expiry
Sealed bottle, refrigerated2–8 °CTo printed expiry
Opened bottle, tightly closed15–25 °CMonths, if kept dry
Exposed to humidityanyDegrades — discard

Oral dosage forms are considerably more forgiving than lyophilized peptides. Capsules and tablets are stable at room temperature and require no cold chain, in transit or in storage.

Moisture is the real enemy rather than temperature. Keep the bottle tightly closed, leave the desiccant sachet in place, and avoid storing in a bathroom or anywhere humidity swings. Protect from direct light.

Purity and verification

Every lot is tested by an independent laboratory before release. HPLC establishes purity as a percentage of total content, separating the target compound from synthesis by-products; mass spectrometry confirms molecular identity.

For an encapsulated product there is a second question a vial does not raise: content uniformity. A capsule can be the right compound at the right purity and still be filled inconsistently, so BAM15 is checked for fill weight consistency across the batch as well as for identity and purity.

The certificate of analysis references the lot number printed on your bottle label. Request it at [email protected].

Frequently asked questions

What does 'mitochondrial uncoupler' mean?
Normally the proton gradient across the inner mitochondrial membrane drives ATP synthesis. An uncoupler lets protons cross without passing through ATP synthase, so the gradient dissipates as heat instead of being captured as chemical energy. The mitochondrion keeps burning substrate but produces less ATP.
How is BAM15 different from DNP?
Both are protonophores, but 2,4-dinitrophenol also depolarises the plasma membrane, which underlies its narrow margin between effect and serious harm. BAM15 was characterised as acting far more selectively on the mitochondrial membrane. That distinction is the entire basis of the research interest.
Is BAM15 a peptide?
No. It is a small molecule — a fluorinated diarylamine — and is unrelated structurally to the peptides in this catalogue. It appears alongside them because it is studied in overlapping metabolic research.
Does this need refrigerated shipping?
No. Capsules and tablets are stable at ambient temperature, so no cold chain is needed in transit or on arrival. Keep the bottle sealed and dry.
Is a certificate of analysis available?
Yes, per lot. The COA corresponds to the lot number printed on your bottle. Email [email protected] with that number and we will send it.
Do capsules need any preparation?
No. These are pre-dosed oral dosage forms — no reconstitution, no bacteriostatic water, no measuring. That is the practical difference from the lyophilized vials.

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