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3,4,7,8-Tetramethyl-1,10-Phenanthroline

    • Product Name 3,4,7,8-Tetramethyl-1,10-Phenanthroline
    • Alias tmphen
    • Einecs 227-651-4
    • 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
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    Specifications

    HS Code

    343964

    Chemical Name 3,4,7,8-Tetramethyl-1,10-Phenanthroline
    Cas Number 23620-04-4
    Molecular Formula C16H16N2
    Molar Mass 236.31 g/mol
    Appearance Yellow crystalline powder
    Melting Point 218-221 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.17 g/cm³ (approximate)
    Iupac Name 3,4,7,8-Tetramethyl-1,10-phenanthroline
    Pubchem Cid 17513
    Smiles Cc1cc2nc3cc(C)cc(C)c3nc2cc1C
    Inchi InChI=1S/C16H16N2/c1-7-5-11-13(9-8(2)3)17-15-12(6-10(11)4)14(18-15)16(7)9/h5-6H,1-4H3
    Storage Conditions Store in a cool, dry place, tightly closed

    As an accredited 3,4,7,8-Tetramethyl-1,10-Phenanthroline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams, secured with a screw cap, labeled with chemical name, formula, and hazard symbols.
    Shipping **Shipping Description:** 3,4,7,8-Tetramethyl-1,10-Phenanthroline is shipped in tightly sealed containers, protected from light and moisture. It is labeled according to chemical safety regulations and transported as a non-hazardous material under standard conditions. Ensure compliance with local, national, and international chemical shipping guidelines for safe handling and delivery.
    Storage Store 3,4,7,8-Tetramethyl-1,10-phenanthroline in a tightly sealed container, in a cool, dry, well-ventilated area, away from light and moisture. Keep it separate from strong oxidizing agents and acids. Ensure proper labeling and avoid sources of ignition. Recommended storage temperature is room temperature or below. Follow all applicable chemical handling and safety protocols.
    Application of 3,4,7,8-Tetramethyl-1,10-Phenanthroline

    Applications of 3,4,7,8-Tetramethyl-1,10-Phenanthroline in Industrial Manufacturing

    3,4,7,8-Tetramethyl-1,10-Phenanthroline plays a critical role as a functional ligand in key segments of the chemical industry. As a direct manufacturer, we supply this intermediate to a select range of downstream processes where proven performance, consistency, and regulatory-compliant production matter most. Below, we highlight its validated applications across practical manufacturing scenarios, referencing industry standards, formulation specifics, integration points, and the types of end-use products resulting from its use.

    1. Homogeneous Catalysis in Fine Chemicals Synthesis

    This compound serves as an advanced ligand supporting homogeneous transition metal catalysts, particularly in fine chemical synthesis where selectivity and activity are tightly controlled. Its unique tetradentate structure supports distinct complexation with metals such as copper and ruthenium, facilitating processes like C-H activation and oxidative coupling. Manufacturers value its reliable chelation profile for batch and continuous processing, particularly where strict metal residue and impurity specifications are mandatory.

    Industry compliance standards

    • REACH (EC No 1907/2006, EU)
    • ISO 9001:2015 certified production
    • ICH Q3D Elemental Impurities for active pharmaceutical ingredients (when used in pharmaceutical syntheses)
    • Local environmental control standards for catalyst waste management

    Typical usage ratio

    • 0.1–1.2 mol% relative to metal center, adjusted by substrate and desired reaction rate

    Downstream process integration

    • Ligand addition occurs during catalyst pre-complexation or directly into the fine chemical reactor after metal salt charging, followed by substrate and oxidant charge.

    Final product types

    • Specialty intermediates for agrochemicals and electronics
    • Active pharmaceutical ingredient precursors
    • Perfume and flavor compound intermediates
    • Complex polymers for advanced materials

    2. Photoredox Catalysis in Organic Synthesis

    In advanced organic synthesis, this ligand forms the basis for various metal–ligand photoredox catalyst systems used in light-driven transformations. Its electronic properties optimize visible-light absorption and electron transfer in ruthenium and iridium complexes, enhancing reproducibility for scale-up photochemical manufacturing. Production teams rely on this compound in both academic technology transfer and commercial custom synthesis for photoreactions.

    Industry compliance standards

    • 21 CFR Part 211 (US FDA cGMP for finished pharmaceuticals, where relevant to API synthesis)
    • ISO 14001:2015 for environmental, health, and safety in photochemical labs
    • RoHS Directive 2011/65/EU (for chemicals entering electronics value chain)
    • Specific photostability test protocols (ICH Q1B for relevant pharmaceutical products)

    Typical usage ratio

    • 0.01–0.50 mol% relative to metal, depending on light intensity, throughput, and batch vs. flow design

    Downstream process integration

    • Ligand is charged during metal complexation step prior to irradiation setup (batch reactor or flow photoreactor), with solution transfer under inert or low-oxygen atmosphere.

    Final product types

    • Sterically complex pharmaceutical building blocks
    • Photoactivated cross-coupling products for organic electronics
    • High-value fine chemicals prepared by visible-light catalysis
    • Polyaromatic compounds for OLED materials

    3. Analytical Reagents for Transition Metal Quantification

    3,4,7,8-Tetramethyl-1,10-Phenanthroline is widely adopted for laboratory and industrial-scale colorimetric assays, especially iron(II) and copper(I) quantification in water treatment, metallurgy, and environmental quality control. The compound's ability to form distinctive colored complexes allows sensitive and selective endpoint determination, supporting method reproducibility from high-throughput screening to certified reference material protocols.

    Industry compliance standards

    • ISO 17025:2017 for analytical laboratories
    • Standard Methods for the Examination of Water and Wastewater (APHA, AWWA, WEF: 3500-Fe D, 4500-Cu B)
    • EPA Method 365.2 (US) and EU Drinking Water Directive (98/83/EC) if used in regulatory water testing
    • USP <643> Total Organic Carbon, when used in pharmaceutical-grade water analysis

    Typical usage ratio

    • Reagent stock solution concentrations typically range from 0.01 to 0.10% w/v; final test sample addition is determined by method validation and sample matrix.

    Downstream process integration

    • Preparation of standard solutions for manual or automated photometric analysis; reagent is introduced directly into sample flow or batch container at analysis step.

    Final product types

    • Certified analytical kits for laboratory and field testing
    • Consumable reagent packs for industrial water treatment monitoring
    • Test cartridges for automated in-line monitors in metallurgy
    • Quality assurance reference standards

    4. Ligand in Electrocatalytic Material Manufacturing

    In the field of energy conversion and storage, this compound functions as a ligand in the fabrication and research of metal–organic electrocatalytic materials. The tailored tetramethyl substitution protects key nitrogen coordination sites, ensuring stability under oxidative and reductive cycling typical in fuel cell and sensor manufacture. Our customers incorporate it into electrode material synthesis and surface modification protocols to support high-sensitivity and durability requirements.

    Industry compliance standards

    • IEC 62282 series for fuel cell technologies
    • ISO 13485:2016 for electrochemical biosensors in medical diagnostics
    • ASTM D7981-21 (Electron Transfer Mediator Evaluation)
    • RoHS Directive for materials in electronics export channels

    Typical usage ratio

    • Typically 0.2–2.0 weight% relative to total catalyst layer, with adjustments based on electrode surface area and support material mass

    Downstream process integration

    • Ligand complexation with transition metals performed in solution, followed by deposition on substrate via drop casting, spin coating, or layer-by-layer assembly before electrode fabrication.

    Final product types

    • Electrocatalyst-coated electrodes for hydrogen fuel cells
    • Chemical sensors for heavy metal and VOC detection
    • Redox-active films in energy storage devices
    • Medical diagnostic microelectrodes

    5. Building Block in Coordination Polymer Synthesis

    Manufacturers engaged in advanced materials science utilize this ligand for constructing highly defined coordination polymers and metal-organic frameworks (MOFs). Its methyl-substituted backbone enables unique network topologies and robust porosity for applications in catalysis, gas separation, and molecular sensing. Careful adherence to controlled crystallization protocols underpins reliable scale-up and reproducibility of the resulting framework architecture.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical synthesis
    • ASTM E2439-05 (Standard Guide for MOF Characterization)
    • REACH Annex XVII, if frameworks are used in regulated consumer products
    • Local occupational health regulations for laboratory-scale advanced material synthesis

    Typical usage ratio

    • Typically 1:1 to 2:1 molar ratio with metal ions; precise ratio determined by desired framework pore size and crystallinity

    Downstream process integration

    • Material charged during MOF assembly via solution crystallization (solvothermal or hydrothermal); stoichiometry measured precisely prior to nucleation and growth phases.

    Final product types

    • Metal-organic framework powders for catalyst carriers
    • Gas adsorption and storage media
    • Porous fillers in membrane separators
    • Sorbent materials for environmental remediation
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    More Introduction

    3,4,7,8-Tetramethyl-1,10-Phenanthroline: Insights from Chemical Production

    Understanding the Compound from a Manufacturer’s View

    Producing 3,4,7,8-Tetramethyl-1,10-Phenanthroline sits among the core specialties here at our plant. The chemistry behind this compound is simple to track for those of us who handle phenanthroline derivatives every day, but customers often ask what truly sets this variant apart. Often referred to in research as TMP or tmphen, 3,4,7,8-Tetramethyl-1,10-Phenanthroline builds on the foundational phenanthroline backbone by carrying methyl groups on both the 3, 4, 7, and 8 positions. This structural detail isn’t just a footnote—it drives real changes in physical properties, reactivity, and application range.

    Most people know standard 1,10-phenanthroline has a strong grip on metal ions, offering big value as a chelating ligand in coordination chemistry. We see a jump in interest, though, when extra methyl groups come into play. By blocking four positions, the tetramethyl version stops some side reactions in their tracks and locks in more stability for many transition metal complexes. Researchers comment on this increased selectivity, pointing to examples drawn from their work in catalysis and spectroscopy. In day-to-day production, the difference becomes apparent in the way our TMP forms crystals and handles humidity. Simply put, the extra methyls cut down on unwanted crystal aggregation and water uptake, translating into a smoother, more stable batch at scale.

    Pushing the Boundaries: What Good Chemistry Brings to Real Labs

    Preparation methods for 3,4,7,8-Tetramethyl-1,10-Phenanthroline have evolved over the years. We stepped away from older approaches that produced lower yields and generated significant waste streams. Our team, drawing on practical plant optimization, has tuned reaction conditions to boost selectivity and purity. Maintaining control over methylation steps makes a difference—not just in assay but also in batch reliability. Working with highly tuned glass-lined reactors, we can extend reaction durations and maintain product quality over runs. Our in-process checks confirm not only the presence of desired methylation but also catch residual solvents before final crystallization.

    Purity really changes the game for many end-users. Small differences in residual starting material or by-product content sometimes force a whole synthesis to be repeated downstream. Every time we tighten specifications—whether by more stringent chromatography or by refining workup conditions—reproducibility across lots improves. In some runs, we’ve logged measured purity above 99% by HPLC and NMR, with moisture content averaging below 0.1%. These details matter to researchers aiming for tightly controlled stoichiometric ratios in their metal-ligand systems or for those running sensitive electrochemical assays.

    Where 3,4,7,8-Tetramethyl-1,10-Phenanthroline Finds Its Niche

    Demand for TMP often comes from coordination chemistry, but its reach continues to expand. Early customers pushed for samples back when its main competition was unsubstituted 1,10-phenanthroline, targeting improved stability under oxidation or stronger discrimination among metal ions. Metal complex synthesis continues to drive raw material requests, as labs across the globe dig deeper into ruthenium, copper, and iron chemistry. They tell us that TMP offers new options for tuning ligand field strength, with observable changes in absorption spectra and redox potential.

    Aside from its ligand work, TMP steps into roles in electronics research, dye chemistry, and even DNA intercalation studies. In the context of organic light-emitting diode (OLED) research, engineers reach for TMP because its methyl groups can reduce unwanted excimer formation and lower quenching rates. Several academic labs reference its use in photoredox catalysis, highlighting improved turnover numbers. We notice that industrial users demand larger drum quantities seasonally, especially from research groups scaling up light-driven synthetic transformations.

    Working as both a ligand and an auxiliary agent, TMP holds value wherever selectivity and stability can impact selectivity or yield. It resists hydrolysis more persistently than its parent compound and delivers thermally robust complexes, helping downstream users dial in more predictive process controls. The consistency in our batches translates to fewer unknowns, which means smoother validation in R&D environments.

    Differences in Practice: What Sets TMP Apart from Other Phenanthrolines

    Rolling out metric tons of phenanthroline analogues every month gives us a clear look at what distinguishes a product. 3,4,7,8-Tetramethyl-1,10-Phenanthroline consistently separates itself from both 1,10-phenanthroline and other substituted versions through its methyl protection. We hear from process chemists that this modification blocks common oxidative degradation pathways, especially under ambient light or reactive solvent conditions. Laboratories using 2,9-dimethyl-1,10-phenanthroline or similar ligands report faster decomposition rates or recovery losses from their columns. By comparison, TMP preserves its integrity from synthesis to purification, allowing higher recoveries in both preparative and analytical workflows.

    Exploring chiral ligands or larger fused-systems can yield higher selectivity, but their cost and handling demands knock them out of contention for scale-up. TMP, on the other hand, strikes a practical middle ground. The methyl substituents keep the structure compact and manageable for both batch and continuous-flow setups. Physical handling in our facility feels familiar, as the compound flows well and maintains its color, without the need for excess stabilization additives or inert-gas blankets. End-users repeat this feedback, describing a consistently manageable solid—judged both by eye and by ease of transfer from bag to vessel.

    Not every batch of phenanthroline derivatives comes out clean—side-reaction products, unreacted starting material, and even polymorphic forms complicate downstream handling. Our experience shows that TMP, once dialed in, outperforms similar ligands for purity and reproducibility. Reliability from one run to the next often makes or breaks an industrial synthesis. We trace this back to disciplined synthetic planning and in-house control of every step, from methyl source selection to crystallization. Equipment maintenance may sound mundane, but without clean reactors and checks at each stage, even our best chemistry stumbles.

    Stability and Shelf Life: Less Downtime, Fewer Surprises

    Chemical users dread shelf-life issues. In TMP, the balance between hydrophobic methyls and ready metal binding makes storage relatively painless. We pack our finished bulk product under dry nitrogen for extra assurance, but real-world feedback suggests that the compound stands up to months—even years—on warehouse shelves. Comparing this to less stable ligands paints a sharp picture: one can reliably access high-performance ligand without risk of hydrolysis, clumping, or significant yellowing.

    Feedback loops from repeat customers keep us honest about what matters most in storage and handling. Some ligands require refrigeration, low-humidity glove boxes, or expensive desiccation. With TMP, open-bin storage in standard labs rarely leads to noticeable performance drop-off. Even after prolonged light exposure, 3,4,7,8-Tetramethyl-1,10-Phenanthroline resists oxidative breakdown more stubbornly than its non-methylated relatives. Long-term testing from our own QC labs supports these real-world testaments—with no major change in melting point, purity, or crystalline habit over extended monitoring periods.

    Addressing Process Challenges: Solubility, Handling, and Process Integration

    Anyone who’s scaled inorganic ligands encounters solubility headaches sooner or later. The four methyls in TMP slightly raise solubility in many organic solvents—an edge when pushing concentrated metal complex preparations. We measure higher concentrations with acetonitrile, dimethyl sulfoxide, and dichloromethane compared to unsubstituted phenanthroline under matched temperature and stirring conditions. This tweak supports users looking for efficiency in automated dosing or in-line monitoring, since less solid handling means less downtime.

    Solid TMP handles well in the plant: it doesn’t cake, becomes free-flowing with gentle agitation, and passes through simple filtration steps with little fines generation. This is not always true for other methylated ligands, especially those with less symmetrical substitution patterns or those derived from harsher methylation conditions. Customers tend to notice the difference most sharply in pilot plant operations—batch after batch, TMP comes out of bulk sacks and into reactors without painstaking prep or elaborate dust-control.

    TMP works best where high-throughput processes demand reliable inputs. As producers, we see a steady trend toward larger-volume, high-purity orders destined for integrated continuous-flow metal complex synthesis. Our plant responds by keeping inventory tight and ensuring quick lot turnover, so each drum delivers the freshly prepared product. This approach minimizes age-related variability and lines up with customer expectations for hassle-free integration.

    Meeting Regulatory and Environmental Standards in TMP Production

    Keeping within environmental and safety benchmarks isn’t hype for us—it’s a daily obligation. Regulations control solvent emissions, waste by-products, and even packaging materials for substances moving across borders. Our approach focuses on reducing chlorinated hydrocarbons and minimizing waste streams by re-tooling our methylation strategies. Year after year, these changes cut waste output per unit product and reduce our downstream disposal needs. Compliance checks run alongside batch testing for every shipment, with traceability right back to raw material sources.

    Our team built experience through collaborations with academic labs and industry partners who care about green chemistry. Some have requested custom batches using alternative methylating agents or greener solvents—challenges we tackle through ongoing R&D. Documentation follows every order, supporting downstream regulatory needs and customer certification processes. We keep auditor access open, so every inspection runs fast, smooth, and transparent.

    Sustainability initiatives extend into process utilities. Energy use in purification stages has dropped since we installed targeted condensers and recycling loops for key solvents. Data from utility meters reflect lower energy draw per kilogram produced, measurable not only in company reporting but in the bottom-line price for buyers. We feel this sort of accountability improves trust and forges partnerships that last beyond the one-time sale.

    Customer-Driven Development: Listening and Responding to Lab Needs

    Technical teams on the customer side never shy from sharing both pain points and successes with our TMP. Their field experience joins our plant data to paint a wider picture of where improvements hold value. Some labs order material for catalyst development, facing sudden new analytical requirements as their processes mature. In these cases, we adjust packaging, provide extended certificates of analysis, or even support method transfer by supplying detailed impurity profiles.

    Through years in the field, feedback ranges from tactile concerns—product slip, color consistency, and dusting behavior—to deep analytical demands, such as tight limits on trace organics. Questions about compatibility with analytical standards arise as application fields evolve. Our solution comes down to flexibility: whether producing smaller custom batches for trial projects, or scaling up to match a customer’s growing throughput, the focus rests on delivering the TMP they trust, in the form they rely on.

    We also support joint troubleshooting. If solubility falls short under new process conditions, chemists reach out and we propose pre-dissolution steps, solvent changes, or blending aids that have worked for production-grade TMP. Every customer faces a unique constellation of requirements, and sharing on-the-ground experience bridges the gap between plant and lab. These partnerships feed improvements on both sides—in optimized production on ours, and in less trial-and-error on theirs.

    Looking Forward: Future Directions for TMP and Ligand Chemistry

    TMP finds itself at an interesting transition in the market. As our own team tracks the growing shift toward sustainable, cost-transparent chemicals, we spot an opening for continued process upgrades. Industry partners express growing interest in renewable raw material inputs, lower energy consumption, and real-time digital batch tracking. In response, our plant targets closed-loop solvent management and explores new methyl sources derived from bio-based streams.

    On the materials science front, customers bring up next-gen applications—such as advanced sensors, photoactive arrays, and biomedical imaging systems. The reliability of TMP plays to these uses. R&D collaborations, both within our own technical group and in external partnerships, shape the evolution of our product line. Every improvement in TMP feeds into an ecosystem where cleaner, more robust chemistry supports both scientific progress and responsible manufacturing.

    In closing, our daily business goes beyond bulk delivery. Satisfying technical teams means responding to real problems, adapting to new requirements, and supporting innovation in practical terms. The steady performance of 3,4,7,8-Tetramethyl-1,10-Phenanthroline, grounded in hard-won experience and continuous feedback from the field, has proven to be an enabling force in both small-scale experimentation and high-throughput industrial synthesis. As new applications call for even tighter quality, improved handling, and greener standards, we welcome every chance to build tomorrow’s chemistry in partnership with the people who put these molecules to work.