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Methylene Blue 10mg/60caps
During our packaging transition, you may receive products with either our previous or updated label. Rest assured, the formulation, purity and quality remain exactly same as standards.
Methylene Blue is a heterocyclic aromatic chemical compound functioning as a redox indicator in research applications. The compound demonstrates selective inhibition of guanylate cyclase and modulation of nitric oxide-dependent pathways in experimental models. Methylene Blue exhibits electron transfer properties in oxidation-reduction reactions and serves as a photosensitizer in chemical analysis.
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- For Laboratory Research Use Only
3D Molecular Structure
Drag to rotate · scroll to zoom| Chemical Formula | C16H18ClN3S |
|---|---|
| Synonyms | Methylthioninium chloride, 3,7-Bis(dimethylamino)phenothiazin-5-ium chloride |
| Molar Mass | 319.85 g/mol |
| CAS Number | 61-73-4 |
| PubChem CID | 6099 |
| Total Compound Content | 600 mg (10 mg per capsule) |
| Shelf Life | 36 months |
Every batch is independently lab tested for identity, purity and potency. View our lab testing program →
How does Methylene Blue participate in electron transfer processes?
Methylene Blue possesses a reduction potential of approximately +11 mV and can reversibly cycle between oxidized and reduced states. This redox behavior enables participation in electron transfer reactions involving NADH/NADPH-dependent systems, cytochrome-associated pathways, and mitochondrial electron transport-related processes. These characteristics have made Methylene Blue a valuable research tool for investigating electron transport dynamics, oxidation-reduction mechanisms, and redox-regulated signaling networks.
What interactions have been reported between Methylene Blue and protein aggregation systems?
Experimental investigations have examined interactions between Methylene Blue and protein aggregation pathways, including studies of protein assembly dynamics, intermolecular association processes, and aggregation-related structural transitions. Its well-characterized molecular properties have established Methylene Blue as a useful compound for investigating aggregation mechanisms, protein interaction networks, and the physicochemical factors influencing protein organization.
Why is Methylene Blue widely used in redox chemistry research?
Methylene Blue combines well-defined electron transfer properties, reversible redox cycling, and established photochemical characteristics within a single molecular scaffold. These features have made it a widely utilized reference compound for studies involving redox signaling, electron transport mechanisms, oxidation-reduction reactions, photochemical processes, phenothiazine pharmacology, and molecular pathway characterization associated with redox-active compounds.
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