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5,6-Dimethyl-1,10-Phenanthroline

    • Product Name 5,6-Dimethyl-1,10-Phenanthroline
    • Alias Bathocuproine
    • Einecs 224-210-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    560373

    Chemical Name 5,6-Dimethyl-1,10-Phenanthroline
    Cas Number 5737-69-7
    Molecular Formula C14H12N2
    Molecular Weight 208.26 g/mol
    Appearance Light yellow to off-white solid
    Melting Point 218-222 °C
    Solubility Slightly soluble in water, soluble in organic solvents (e.g., ethanol, chloroform)
    Smiles CC1=CC2=NC3=CC=CC=C3N=C2C=C1C
    Iupac Name 5,6-dimethyl-1,10-phenanthroline
    Synonyms Bathophenanthroline, DMP
    Storage Condition Store at room temperature, tightly closed, in a dry place

    As an accredited 5,6-Dimethyl-1,10-Phenanthroline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging for 5,6-Dimethyl-1,10-Phenanthroline (1 gram) is a tightly sealed amber glass vial with a secure screw cap.
    Shipping 5,6-Dimethyl-1,10-Phenanthroline is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. Packaging complies with chemical safety regulations to prevent leaks and contamination. Labels indicating chemical identity, hazards, and handling precautions are affixed. Transport is conducted by certified carriers in accordance with local, national, and international guidelines.
    Storage Store 5,6-Dimethyl-1,10-Phenanthroline in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Ensure storage in a chemical cabinet with clear labeling, and follow standard safety practices to prevent contamination or accidental contact.
    Application of 5,6-Dimethyl-1,10-Phenanthroline

    Applications of 5,6-Dimethyl-1,10-Phenanthroline in Industrial Manufacturing

    5,6-Dimethyl-1,10-Phenanthroline serves as a high-purity chelating ligand in sectors demanding reliable metal complexation, selectivity, and analytical sensitivity. Our integrated production capabilities ensure consistent batch quality tailored for downstream processes in key markets. Below are the verified application scenarios based on industry practices and compliance requirements.

    1. Analytical Chemistry: Photometric Iron Assay Reagents

    This material enables trace iron detection in environmental, clinical, and industrial laboratories by forming red-orange complexes with Fe(II), supporting both automated and manual assays. Our product meets stringent analytical purity standards to ensure reproducible performance in reference and routine testing workflows.

    Industry compliance standards

    • ISO 7899 for water analysis
    • ASTM D1068-15 for industrial water iron determination
    • GLP (Good Laboratory Practice) requirements for chemical reagents
    • EPA Method 315B for low-level iron analysis

    Typical usage ratio

    • 0.01–0.05% w/v in final aqueous reagent blends
    • Adjusted based on expected iron concentration in analytical matrices

    Downstream process integration

    • Dissolved in ethanol or acetonitrile for master batch preparation
    • Mixed with buffer salts and stabilizers during reagent set-up
    • Packaged as single-use vials or ready-to-use reagent kits

    Final product types

    • Ready-to-use iron diagnostic reagent kits
    • Photometric test strips and cuvette solutions
    • Automated biochemical analyzer reagent bottles
    • Reference calibration solutions for laboratory use

    2. Homogeneous Catalysis: Starter Ligand for Transition Metal Complexes

    As a bidentate ligand with high metal ion affinity, 5,6-dimethyl-1,10-phenanthroline supports the synthesis of copper and ruthenium catalysts applied in cross-coupling, radical polymerization, and oxidative transformations. These processes require strict control over ligand-to-metal ratios to ensure catalytic efficiency and selectivity.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for substance registration
    • ISO 9001:2015 for quality documentation and process traceability
    • Internal catalyst batch testing in accordance with end-users’ QC protocols

    Typical usage ratio

    • 0.5–2.5 mol% relative to metal precursor in catalyst assembly
    • Fine-tuned for target reaction selectivity and catalyst lifetime

    Downstream process integration

    • Ligand added during in situ metal complex formation
    • Used in glovebox or inert atmosphere step to avoid metal center oxidation
    • Final catalyst isolated, purified, and distributed to synthesis or polymerization lines

    Final product types

    • Custom homogeneous copper or ruthenium catalyst complexes
    • Pre-catalyst concentrates for polymer and fine chemical synthesis
    • Technical-grade ligand-metal complexes for research and development

    3. Electrochemical Sensing: Redox Probe Formulations

    Electroanalytical device manufacturers incorporate this compound as a core complexing partner to modulate redox mediator activity, particularly in sensors targeting ferrous ions and related analytes. Its precise molecular structure supports reproducible calibration and sensor batch consistency.

    Industry compliance standards

    • IEC 61010 for electronic measurement devices
    • RoHS Directive 2011/65/EU for hazardous substance control
    • OEM-specific sensor quality assurance protocols

    Typical usage ratio

    • 0.02–0.10% w/w in sensing electrode formulation
    • Modified according to electrode sensitivity and target analyte range

    Downstream process integration

    • Blended into aqueous or organic conductive ink bases
    • Applied via screen printing or drop-casting onto electrode substrates
    • Sensor elements conditioned and aged for response stability

    Final product types

    • Disposable electrochemical test strips
    • Integrated biosensor arrays
    • Calibrated probe assemblies for analytical and environmental instruments

    4. Photoluminescent Material Synthesis: Coordination Polymers

    Downstream specialty chemical producers use 5,6-dimethyl-1,10-phenanthroline in constructing metal-coordination frameworks for optical and electronic material applications, favoring it for the fine-tuning of emission wavelength and intensity. Rigorous purity guarantees consistent photophysical properties in finished materials.

    Industry compliance standards

    • ISO 9001:2015 for manufacturing quality management
    • RoHS compliance in optoelectronic device materials
    • Customer-specific quality agreements for material purity and trace metals

    Typical usage ratio

    • 0.5–3.0 equivalents per metal ion in metal-organic framework synthesis
    • Adjusted to target emission profiles or lattice structures

    Downstream process integration

    • Added during batchwise crystallization under controlled pH and temperature
    • Combined with transition metal salts in solvent systems such as DMF or acetonitrile
    • Formed frameworks washed and purified for purity and photoluminescence checks

    Final product types

    • Photoluminescent powders and thin films
    • Precursor materials for light-emitting device assembly
    • Coating additives for optoelectronic components
    Free Quote

    Competitive 5,6-Dimethyl-1,10-Phenanthroline prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

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    Certification & Compliance
    More Introduction

    5,6-Dimethyl-1,10-Phenanthroline: An Industry Workhorse with Distinct Character

    From Raw Inputs to High Purity: The Manufacturing Perspective

    Every time a chemist selects 5,6-Dimethyl-1,10-phenanthroline from the shelf, the journey behind that powder traces back to the factory. Here, each batch earns its quality through control in synthesis and keen observation. Bringing this compound from raw materials to high purity involves close attention—those extra methyl groups at the 5 and 6 positions seem minor, but on the factory floor, they transform both the chemistry and behavior of the product. This is not just another ligand. It asks for careful recrystallization and patient drying to prevent the kind of trace impurities that can later trip up sensitive tests or catalysis work. Staff in production and QC walk the line daily, tracking not only purity but also moisture and trace metal content, since they know a persistent azeotrope or odd impurity can render a shipment useless for exacting research.

    Key Specifications: A Matter of Consistency

    Over the years, feedback from synthetic chemists and analytical labs has reinforced one lesson: reproducibility separates a reliable supplier from a hopeful contender. Our typical lot analysis hovers at purity levels above 99% (as per HPLC or NMR, depending on request), with threshold controls on volatile content and transition metal traces. Crystalline form matters—a batch can pass initial tests yet confound someone trying to dissolve it or use it for coordination chemistry if particle size strays too far. We've seen how a seemingly minor divergence in solubility or odor flags contamination or incomplete purification. Each kilogram shipped out carries a record of lot-specific results, not just a generic promise. This is not marketing—it's the result of years refining process steps, tweaking pH at key filtrations, and improving solvent recovery to keep each charge consistent with the last.

    Where Chemistry Happens: Usage in Lab and Industry

    Chemists reach for 5,6-Dimethyl-1,10-phenanthroline for its strong chelating ability. The diimine backbone, made more bulky and electron-rich at the 5 and 6 positions, shapes its interaction with metals in ways other phenanthrolines cannot match. We first saw high demand from academic research, especially in inorganic chemistry programs exploring redox-active metal complexes—copper, iron, ruthenium. Over time, industrial labs joined in, favoring this ligand for its unique ability to stabilize certain oxidation states for catalysis or to shift emission wavelengths in coordination complexes. Specialty dye makers use it to fine-tune fluorescence. Analytical labs use it in titrations and electrochemical determinations, often when classic 1,10-phenanthroline proves too plain or reactive. Sometimes, high-throughput screening setups need a batch made to strict purity and physical form, so our facility runs small-lot syntheses with custom parameters, learning each time where variations affect results.

    Differences That Matter: How Modifications Impact Real Outcomes

    On the surface, 5,6-Dimethyl and the parent 1,10-phenanthroline might seem close relatives, but practical experience says otherwise. The two added methyls bring real changes: solubility in nonpolar solvents increases, making it better suited in organic transformations or certain mixed-phase systems. Its steric bulk keeps some metal centers from overcrowding, discouraging the formation of oligomers and promoting discrete complexes—sometimes boosting selectivity, sometimes producing new emission colors in optical applications. Chemists working with photochemical catalysts have shown preference for the dimethyl version when they need to suppress certain ligand exchange processes. Years ago, a customer in advanced materials flagged batch-to-batch inconsistency as a problem—only after switching to our higher-purity dimethyl phenanthroline did their slow-growing crystals begin forming with reproducible habits.

    Anyone working with classic 1,10-phenanthroline knows it has a tighter melting range and tends to pick up impurities in storage—problems the dimethylated variant addresses through its more robust crystal packing and lower hygroscopic character. We hear from customers running automated synthesis robots or flow reactors that 5,6-Dimethyl-1,10-phenanthroline dissolves with fewer pre-treatments, reducing downtime and failed runs. These subtle improvements add up in research-intensive settings, and we keep seeking new tweaks—smaller particle size for easier dissolution, batch-specific solvent selection, or custom drying protocols.

    Trust Earned Through Experience

    One reason we see repeated orders is the trust developed from hands-on collaboration. We have spent time discussing protocols with customer labs, shipped test quantities with full CoA data, and invited feedback on what worked or failed for a particular reactor or analytical workflow. Some research teams care most about residual solvates, others about the IR spectrum or trace heavy metals—they get different answers out of products that, on paper, look identical. This input has shaped our adoption of high-sensitivity QA tools—ICP-MS for metal analysis, Karl Fischer titration for traces of moisture, and batch chromatograms held for years. Communication, patience, and persistence allow us to provide not just a chemical, but support and solutions for those unspoken variables in chemistry that make all the difference when scaling an experiment or launching a new diagnostic assay.

    Challenges in Scale-Up and Supply

    5,6-Dimethyl-1,10-phenanthroline brings its own manufacturing challenges. The methylation step, depending on method, can drift in regioselectivity, requiring careful monitoring to prevent unwanted isomers. Early on, we experienced batch loss from minor process contaminants—left unchecked, these would bleed into final product and frustrate users with unexplained color changes or side reactions. We have since tightened our raw material sourcing, running trial lots after each major supply chain shift. Small variations in reaction temperature or solvent quality show up not just in NMR spectra, but sometimes in customer productivity thousands of miles away. Over time, supply chain insights have taught us to anticipate bottlenecks, stock up ahead of seasonal outages, and prepare contingency plans for global shipping blackouts. Our in-plant teams know from experience that skip-level communication—buyers, QC, and bench chemists together—saves time and effort downstream.

    Packaging and shipment require as much care as synthesis. This product tolerates air exposure better than some ligands but does not benefit from rough handling; we use lined drums and lightweight containers with optional argon overlays, based on destination and likely storage conditions. We often receive feedback on packaging ease—those unsung technicalities influence how quickly a new project gets underway. Whether a client needs 500 grams or an industrial drum, we treat each order with the same focus on traceability and QA accountability. Maintaining a detailed lot history database allows us to address showing QA trends and provide replacement in rare cases of concern.

    Standing Out in a Crowded Field

    With so many fine chemicals available, standing out takes more than meeting a minimum spec. The reputation for our 5,6-Dimethyl-1,10-phenanthroline rests on consistent quality, documented purity, and strong technical communication. Researchers in catalysis or material science sometimes report that generic-sourced chemicals contain noise—odd impurities that defy easy quantification but undermine yields or reproducibility. Continued collaborations with method developers at universities and in industry labs help us tune what really matters: color, solubility, reactivity, and detailed spectra.

    A few years ago, a pharmaceutical partner documented a minor UV-Vis absorption band their protocol flagged as a problem. Extra effort went into isolating the trace impurity responsible, then adjusting purification procedures—now, every kilo includes spectrum highlights to confirm absence. In another case, a large-scale materials producer spotted slumping yields traced to minor changes in water content; a switch to on-site drying and real-time moisture monitoring brought back consistency. The lesson: experience, not assumptions, drives improvement.

    Environmental and Responsible Manufacturing

    Even established chemicals face new scrutiny over their footprint and safety. By working with green chemistry experts, we keep solvent use efficient and reclaim or recycle as much as possible. After facing hazardous waste surges from an inefficient mother liquor handling step, we retrofitted our plant to recover more usable fractions, reducing both cost and environmental impact. We keep track of each waste stream, ensuring regulatory compliance while reducing impact at the point of use. Direct, ongoing customer dialogues give us insight into what matters: some researchers want detailed TDS and RoHS data, others care most about minimal packaging or local sourcing.

    Supporting Modern Application Demands

    Emerging fields such as photoredox catalysis, advanced diagnostics, and optoelectronics require tighter tolerances and documentation than even a decade ago. As standards shift and new analytical techniques probe ever-finer details in crystal structure or impurity profiles, our plant expands both capability and transparency. We have connections with labs and instrument makers, running off-schedule method development batches to ensure our product stays ahead of regulatory and technical expectations. Periodic customer audits or collaborations in method validation contribute to an evolving portfolio, not a static product.

    An important aspect of our role as manufacturer remains ongoing education. We review scientific journals and patent filings, learning where our product finds unexpected new roles, such as in bioinorganic modeling or next-generation molecular sensors. Several collaborators have published data showing why 5,6-Dimethyl-1,10-phenanthroline outperforms similar ligands when bound to transition metal centers under oxidative stress. This feedback closes the loop, guiding process improvement and spurring further dialogue.

    Path Forward: Quality, Collaboration, and Insight

    As research landscapes grow more complex, supplies of 5,6-Dimethyl-1,10-phenanthroline will remain crucial for those seeking innovation in catalysis, materials science, and analytical chemistry. Our experience guides not only production but also honest discussions about purity demands, logistical planning, and technical support. Each inquiry, each specification challenge, allows us to calibrate not only procedures but also how we communicate risk, capability, and opportunity to end users.

    Real value emerges over time—from early-morning QA checks to late-night consultation calls with a lab in another time zone, from pilot-scale tweaks to major process overhauls. We invest time and resources so each batch of 5,6-Dimethyl-1,10-phenanthroline can deliver results measured not only in purity points, but also in smooth experimental runs and published breakthroughs. This combination of technical rigor and listening to those at the bench keeps our chemical in demand and builds lasting relationships built on concrete results, not marketing slogans.

    Concluding Thoughts from the Factory Floor

    Supplying chemicals like 5,6-Dimethyl-1,10-phenanthroline means more than shipping off matched lots. It means knowing what a minor impurity or particle size difference will do in a reaction, tracking shifting application requirements, and responding to regulatory or logistical hurdles, day after day. Over time, close work with real users and scientists shapes not just products, but the methods and values by which we operate. This is how a molecule—with its distinct methyl groups and tested backbone—earns its place in the lab, the pilot plant, and beyond. By sharing experience and staying accountable at every step, we support those who depend on quality to drive their chemistry forward.