Methylene Blue

Methylene Blue

Methylene Blue

Methylene Blue

Methylene Blue (Methylthioninium Chloride) is an autoxidizable electron cycler for mitochondrial bioenergetics and cellular respiration research. Operating as an alternative electron donor/acceptor in the mitochondrial electron transport chain (ETC), it bypasses blockade at Complexes I and III, directly reducing cytochrome c to accelerate ATP synthesis and suppress reactive oxygen species (ROS).

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Quantity Discounted Price
4 - 6 $32.64
7 - 9 $31.96
10 + $31.28

What is Methylene Blue?

Methylene Blue (known chemically as Methylthioninium Chloride or 3,7-bis(dimethylamino)phenothiazin-5-ium chloride) is a synthetic phenothiazine derivative and potent redox-active autoxidizable electron cycler. Originally synthesized in 1876 as an aniline dye, it serves as a unique metabolic modifier in cellular biology due to its ability to cycle between oxidized (blue) and reduced leucomethylene blue (colorless) states at low nanomolar concentrations.

Batch-verified for high analytical purity at Modern Aminos, Methylene Blue is offered in three versatile laboratory formats:

  • 10MG/mL aqueous liquid solution in 30ML Amber bottle with 1mL precision dropper
  • 5MG dry-fill solid capsules (60 units per bottle)
  • 10MG dry-fill solid capsules (60 units per bottle)

Laboratories evaluating mitochondrial electron flux, oxygen consumption rates (OCR), and inducible nitric oxide synthase (iNOS) inhibition utilize Methylene Blue alongside complementary neuro-energetic reference standards available on the site, such as 9-Me-BC, NSI-189 Phosphate, Alpha GPC, and CoQ10.

Chemical and Molecular Data

Compound Name Methylene Blue (Methylthioninium Chloride)
Quantity / Formats Offered 10MG/mL Liquid Dropper (30ML) | 5MG Dry-Fill Capsules (60 Count) | 10MG Dry-Fill Capsules (60 Count)
Synonyms / Alt Names Methylthioninium chloride, Swiss blue, Basic Blue 9, Urolene Blue
CAS Number 61-73-4 (Anhydrous) | 7220-79-3 (Trihydrate)
Chemical Formula C16H18ClN3S
Molecular Weight 319.85 g/mol (Anhydrous) | 373.90 g/mol (Trihydrate)
IUPAC Name [7-(dimethylamino)phenothiazin-3-ylidene]-dimethylazanium; chloride
InChIKey YAFRGMALAMOOHI-UHFFFAOYSA-M
SMILES Code CN(C)C1=CC2=C(C=C1)N=C3C=CC(=[N+](C)C)C=C3S2.[Cl-]

What are the Mechanisms of Action?

The biochemical pathways and cellular targets:

  • Mitochondrial Electron Transport Chain (ETC) Shuttling: At nanomolar concentrations, Methylene Blue accepts electrons directly from NADH (bypassing Complex I and Complex III blockades) and transfers them directly to cytochrome c. This catalytic cycling increases Cytochrome c Oxidase (Complex IV) activity, elevating O2 consumption rates and cellular ATP yield.
  • Reduction of Reactive Oxygen Species (ROS) Leakage: By shunting excess electrons away from dysfunctional Complex I and Complex III sites, Methylene Blue reduces the formation of superoxide radicals (O2•-) and hydrogen peroxide (H2O2), protecting mitochondrial membrane lipid integrity under oxidative stress.
  • Nitric Oxide Synthase (NOS) & Guanylyl Cyclase Inhibition: Methylene Blue directly inhibits inducible nitric oxide synthase (iNOS) and neuronal nitric oxide synthase (nNOS), while selectively binding the heme moiety of soluble guanylyl cyclase (sGC) to dampen excessive nitric oxide / cGMP signaling in inflamed tissue models.

What do Preclinical & Academic Studies Show for Methylene Blue?

When evaluating research efficacy and published scientific literature:

  • Mitochondrial Respiration & Neuroprotection (PMC): Comprehensive biomedical reviews cataloged on PMC (PMC5826781) document Methylene Blue’s capacity to restore mitochondrial electron transport efficiency, increase Cytochrome c Oxidase activity, and protect neuronal culture viability during metabolic inhibition.
  • Cytochrome c Oxidase Activation & Metabolic Kinetics (ScienceDirect): Kinetic studies published in ScienceDirect evaluate Methylene Blue’s hormetic action, verifying increases in cellular ATP output and reduction of lactic acid accumulation in hypoxic cell lines.
  • Chemical Profiling & Identification (PubChem): Official structural characterization maintained on PubChem confirms the 319.85 g/mol molecular weight, phenothiazine ring geometry, and HPLC spectrophotometric absorption peaks (664 nm and 610 nm) of CAS 61-73-4.

How does Methylene Blue compare to other compounds?

To evaluate electron transport mechanisms, bioenergetic pathways, and cellular protection, researchers compare Methylene Blue against alternative reference standards available at Modern Aminos:

Compound / Reference Primary Target / Class Core Mechanism of Action Research Focus & Profile
Methylene Blue Phenothiazine Autoxidizable Electron Cycler Bypasses Complex I/III to transfer electrons to cytochrome c, boosting Complex IV activity and ATP yield Focuses on mitochondrial electron transport, ROS leakage reduction, Cytochrome c Oxidase kinetics, and iNOS/sGC inhibition
9-Me-BC Methylated β-Carboline Dopaminergic Agent Upregulates Tyrosine Hydroxylase (TH) gene expression, drives neurite outgrowth, and boosts Complex I activity Focuses on structural restoration of dopaminergic neurons, neurite arborization, and catecholamine pathway recovery
NSI-189 Phosphate Benzylpiperazine Aminopyridine Neurogenic Compound Stimulates neurogenesis and synaptic expansion in the hippocampal subgranular zone (SGZ) Focuses on hippocampal volume recovery and dentate gyrus neurogenesis rather than direct mitochondrial electron cycling
CoQ10 (Coenzyme Q10) Endogenous Benzoquinone Lipid Electron Carrier Transfers electrons from Complex I and II to Complex III within the lipid bilayer Focuses on endogenous membrane lipophilic electron transport and lipid peroxidation prevention

Frequently Asked Questions (FAQs)

1. Is Modern Aminos a reliable place to buy Methylene Blue?

Yes, Modern Aminos is a highly trusted vendor for high-purity research chemicals and reference compounds. Every batch of Methylene Blue undergoes strict third-party analytical testing (including HPLC and UV-Vis Spectrophotometry) to verify high USP grade chemical purity, exact active concentration, and complete absence of heavy metal contaminants (such as arsenic, lead, or zinc).

2. What is the molecular mechanism of Methylene Blue in mitochondrial respiration?

Methylene Blue functions as an autoxidizable electron cycler. At low nanomolar concentrations, it accepts electrons from reduced NADH and transfers them directly to cytochrome c, bypassing Complex I and III blockades to increase Cytochrome c Oxidase (Complex IV) activity and ATP production.

3. How does Methylene Blue’s electron cycling action differ from standard antioxidants?

Standard antioxidant compounds neutralize reactive oxygen species (ROS) stoichiometrically by consuming themselves. Methylene Blue acts catalytically as a repeatable electron shuttle, preventing ROS generation at the source by rerouting electron leakage away from Complex I and III back into the respiratory chain.

4. Why is high analytical purity essential in Methylene Blue research assays?

Industrial or dye-grade methylene blue frequently contains heavy metals (lead, cadmium, zinc, arsenic) and synthesis contaminants that induce cytotoxicity and interfere with enzyme kinetics. Modern Aminos supplies ultra-pure reference-grade material suitable for sensitive in vitro assays.

5. What available formats does Modern Aminos offer for Methylene Blue research?

Modern Aminos provides Methylene Blue in three standardized formats: a 30ML liquid solution with 1mL precision dropper (10MG/mL), pre-measured 5MG dry-fill solid oral capsules (60 units per bottle), and 10MG dry-fill solid oral capsules (60 units per bottle).

6. How does Methylene Blue compare to 9-Me-BC in cellular energy research?

Methylene Blue acts as a direct electron shuttle across the mitochondrial electron transport chain (Complex IV focus), while 9-Me-BC is a methylated β-carboline that upregulates Tyrosine Hydroxylase gene expression and stimulates dopaminergic neurite outgrowth alongside Complex I enhancement.

7. What role does Methylene Blue play in nitric oxide (NO) pathway inhibition?

Methylene Blue inhibits inducible nitric oxide synthase (iNOS) and binds the prosthetic heme group of soluble guanylyl cyclase (sGC). This blocks the conversion of GTP to cGMP, making it a valuable tool for studying inflammatory signaling and vascular smooth muscle tone.

8. What are the proper storage and light-protection parameters for Methylene Blue?

Methylene Blue solutions and capsule containers should be stored tightly sealed in amber glass containers at room temperature (15°C to 25°C). Protecting the compound from direct sunlight and UV radiation prevents premature photochemical reduction and preserves chemical stability over extended shelf lives.

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  • This product is not to be used as an active pharmaceutical ingredient (API) in compounding or manufacturing drugs for human or veterinary use.
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