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1,7-Phenanthroline

    • Product Name 1,7-Phenanthroline
    • Alias Phenanthroline-1,7
    • Einecs 208-658-4
    • 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
    • CONTACT NOW
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    Specifications

    HS Code

    935129

    Chemicalname 1,7-Phenanthroline
    Molecularformula C12H8N2
    Molecularweight 180.21 g/mol
    Casnumber 473-18-7
    Appearance White to light yellow crystalline powder
    Meltingpoint 153-155 °C
    Solubility Slightly soluble in water, soluble in ethanol and benzene
    Density 1.21 g/cm3
    Pubchemcid 102582
    Synonyms Phenanthrene-1,7-diamine; 1,7-Phen
    Chemicalstructure Three fused benzene rings with nitrogens at positions 1 and 7
    Iupacname Phenanthroline-1,7-diamine
    Storagetemperature Store at room temperature

    As an accredited 1,7-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 1,7-Phenanthroline (10g) is a sealed amber glass bottle with a secure screw cap, labeled with safety information.
    Shipping **Shipping Description for 1,7-Phenanthroline:** 1,7-Phenanthroline should be shipped in tightly sealed containers, protected from light and moisture. Transport under ambient conditions unless otherwise specified. Ensure compatibility with packaging materials and comply with local, state, and international chemical shipping regulations. Proper hazard labeling and documentation must accompany the package. Handle with standard chemical safety precautions.
    Storage 1,7-Phenanthroline should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, and well-ventilated area. Keep it away from incompatible substances such as strong oxidizing agents. Proper chemical storage protocols should be followed, including clear labeling and access limited to trained personnel. Ensure that the storage area is equipped for spill containment and emergency response.
    Application of 1,7-Phenanthroline

    Applications of 1,7-Phenanthroline in Industrial Manufacturing

    As a direct producer of 1,7-Phenanthroline, we support several advanced chemical sectors that depend on this specialty intermediate. The following segments highlight distinct downstream industries where consistent quality, precise ratios, and controlled integration into processes ensure reliable finished products for demanding international markets.

    1. Analytical Reagents Manufacturing for Metal Ion Detection

    1,7-Phenanthroline undergoes large-scale formulation into colorimetric reagents, where it serves as a sensitive ligand for transition metal ions analysis. Commercial laboratories and industrial QC units depend on its chelating properties in photometric assays to quantify metals such as Fe(II) and Cu(II). Routine synthesis involves dissolving our material in buffers at controlled pH levels, with downstream partners emphasizing traceability and low impurity profiles. Strict compliance with analytical method validation requires absolute control over raw material lot-to-lot consistency, which we guarantee by batch release analytical data aligned with customer QC demands.

    Industry compliance standards

    • ISO/IEC 17025:2017 Laboratory Accreditation
    • European Pharmacopeia guidelines for analytical reagents
    • ASTM D1068 – Standard Test Methods for Iron in Water

    Typical usage ratio

    • 0.5–2.0 g/L in buffer systems for colorimetric assays, adjusted according to required detection limits and sample matrix complexity

    Downstream process integration

    • Direct dissolution into aqueous assay reagents, followed by filtration and standardized bottling for laboratory use

    Final product types

    • Pre-formulated colorimetric reagent kits
    • Analytical test strips
    • Water quality testing solutions
    • Metal ion assay standards

    2. Catalysis and Ligand Production for Chemical Synthesis

    Chemical manufacturers integrate 1,7-Phenanthroline as a building block ligand in homogeneous catalytic systems, particularly for the complexation of transition metals in fine chemical and pharmaceutical synthesis. Its robust chelation character, when matched to specific catalytic cycles (e.g., cross-coupling, oxidation), achieves targeted conversion rates. Formulation and metal incorporation protocols require controlled temperature, solvent choices, and, in continuous processes, precise feed ratios to maintain product yield and downstream safety.

    Industry compliance standards

    • cGMP (current Good Manufacturing Practice) for pharmaceutical intermediates
    • REACH Regulation (EC) No 1907/2006 for chemical substances
    • Process safety management protocols (OSHA 29 CFR 1910.119)

    Typical usage ratio

    • 0.2–1.5 molar equivalents relative to metal center, tailored based on catalyst turnover target and substrate concentration

    Downstream process integration

    • Premixing with metal precursor in anhydrous solvents under inert atmosphere; introduced during catalyst complex formation stage

    Final product types

    • Pharmaceutical intermediates
    • Fine chemicals
    • Cross-coupling catalyst complexes
    • Oxidation catalyst systems

    3. Electroplating Bath Formulation for Surface Treatment

    Leading electroplating facilities utilize 1,7-Phenanthroline in advanced bath formulations for selective complexation of metal ions, notably copper and silver, during deposition on electronic components. The material’s use ensures consistent metal ion concentration and stability, critical to achieving uniform deposit thickness and electrical properties. Bath operation parameters—including pH control, temperature, and agitator speed—demand rigorous initial formulation and periodic analysis of the ligand concentration to comply with certification for finished electronic parts.

    Industry compliance standards

    • IPC-4552 specification for ENIG (Electroless Nickel/Immersion Gold) processes
    • RoHS Directive (2011/65/EU) for restriction of hazardous substances
    • ISO 9001:2015 for quality management in electronics manufacturing

    Typical usage ratio

    • 0.1–0.6 g/L in plating bath solutions, optimized based on target metal ion load and bath operating cycles

    Downstream process integration

    • Incorporation during bath make-up; ligand concentration monitored and replenished in maintenance cycles

    Final product types

    • Printed circuit boards
    • Semiconductor lead frames
    • Connectors for electronic devices
    • Precision metal contacts

    4. Photographic Chemical Formulation

    Manufacturers of specialty fine chemicals for photographic industries use 1,7-Phenanthroline as a selective silver ion binding agent in photographic developer and fixing compositions. Its performance enhances the contrast and resolution of printed images, particularly in scientific and medical imaging. The formulation protocol involves combining pure grade material in sequential charge with reducing agents and stabilizers under controlled mixing. Final reagent concentrations and purity directly affect the reproducibility and clarity of processed images.

    Industry compliance standards

    • ISO 18902:2013 Imaging materials — Processed imaging materials — Albums, framing and storage materials
    • ANSI IT9.2 – Image stability standards
    • Internal QC protocols established by medical and research imaging suppliers

    Typical usage ratio

    • 0.3–1.0 g/L in developer/fixer solutions, precisely adjusted per emulsion type and desired speed/contrast characteristics

    Downstream process integration

    • Direct dosing to aqueous phase of developer or fixer solution after filtration and QC release testing

    Final product types

    • Photographic developer concentrates
    • Medical X-ray processing reagents
    • Scientific imaging chemicals
    • Industrial photo-developer kits

    5. Research-Grade Complex Preparation for Laboratory Synthesis

    Producers of research chemicals and laboratory supplies rely on 1,7-Phenanthroline for the in situ generation of transition metal complexes, integral to academic and industrial study of redox agents and electron transfer catalysts. Our batches offer high assay and low background impurities, ensuring reproducible results in kinetic and mechanistic research. Laboratories emphasize raw material certification and certificate of analysis (CoA) traceability to meet reporting and audit requirements for peer-reviewed studies.

    Industry compliance standards

    • ACS Reagent Grade specifications
    • ISO 17034:2016 for reference material producers
    • Institutional laboratory QA/QC protocols

    Typical usage ratio

    • 0.1–2.0 molar equivalents, tailored to experiment design and nature of metal–ligand interactions

    Downstream process integration

    • Formulated into custom synthesis protocols, often as a dissolved stock added in micromolar-to-millimolar scale reactions

    Final product types

    • Transition metal–phenanthroline complexes
    • Laboratory standard solutions
    • Teaching kits for universities
    • Redox system model compounds
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    Certification & Compliance
    More Introduction

    1,7-Phenanthroline: Experience from a Chemical Manufacturer’s Bench

    Direct Perspective on 1,7-Phenanthroline

    1,7-Phenanthroline is not the kind of chemical you see on every lab shelf, but over the years we’ve watched it enable real progress in chemical research and applied manufacturing. Drawing on extensive hands-on synthesis and formulation experience, we see clear differences between 1,7-phenanthroline and its more common cousins, notably 1,10-phenanthroline. Most standard references focus on 1,10 because that is a familiar ligand in coordination chemistry, with a track record as a colorimetric agent for metal ions, but 1,7-phenanthroline brings unique structural features that open the door for niche but important applications.

    What Sets 1,7-Phenanthroline Apart

    Structurally, 1,7-phenanthroline positions nitrogen atoms further apart than the classic 1,10 form. This may look like a small change to the untrained eye, but anyone who’s actually performed comparative syntheses or UV-vis analyses appreciates the significance. The placement of nitrogen donors in different molecular positions influences how these molecules wrap around metal centers, change electronic properties, or act as building blocks for supramolecular assemblies. In our own laboratory, we have seen this reflected directly in binding behaviors and reaction kinetics.

    We produce 1,7-phenanthroline with high purity for specialized uses where this selectivity really matters, such as custom ligand design, catalysis control, or complexation studies that require a non-chelating geometry. When it comes to fine details, even a small impurity can exert unwanted effects, so our team puts extra effort into crystallization and purity assurance beyond commercially available grades to meet R&D demands.

    Production & Specification: Focusing on What Matters

    When we scale up 1,7-phenanthroline, quality control starts well before the molecule reaches the bottle. Over years of batch runs, process tweaking, and instrument checks, there’s one lesson that sticks: purity must be demonstrated, not simply stated. Typical trade-grade product often comes in at around 98% HPLC purity, but that last two percent can have a real impact. In our factory, we routinely push purity to 99% or above, both for internal projects and in direct response to requests from researchers who found trace contaminants causing reproducible artifacts.

    Particle size is another variable that influences user experience, though it tends to get overlooked by resellers who haven't handled bulk powders. Clumpy, poorly milled, or statically charged product might seem trivial in a paper spec sheet, but it slows down weighing and throws off solution preparation in the lab. Over time, we’ve refined our post-processing—through careful drying, sieving, and anti-static handling—to deliver smooth, manageable powder. Attention to packaging integrity keeps the product from absorbing moisture or undergoing coloration, which especially matters for those running spectroscopic experiments.

    Core Applications: The Reality of Usage and End-User Feedback

    In actual practice, most end-users working with 1,7-phenanthroline want to do more than just replicate textbook chemistry. We’ve supplied this product to industrial researchers probing novel photoactive complexes for LED materials, as well as academic groups engineering selective probes for trace-metal detection. Quite a few customers contact us after trying to work with the more common 1,10-isomer and finding its steric or electronic properties unsuited to their custom catalysts or analytical targets. Those who conduct extensive ligand screening usually note that 1,7-phenanthroline helps diversify test matrices without introducing excessive solubility or stability complications.

    From our side, feedback usually clusters around two main points: first, the advantage of the different nitrogen arrangement in tuning metal-ligand geometry, and second, product consistency from lot to lot. We’ve found, through repeated feedback cycles with both academic and commercial chemists, that control of very subtle defects—off-odor, inconsistent flowability, or even trace discoloration from side products—determines whether a powder sits unused, or becomes a preferred reagent. Those performing published research expect reliable NMR and MS results with a documented chain of identity; without real process transparency, all the certificates in the world do not make a product genuinely trustworthy.

    Comparing 1,7-Phenanthroline and 1,10-Phenanthroline in Real Use

    Every so often, someone asks, “Can 1,7-phenanthroline just substitute for 1,10-phenanthroline?” After years of hands-on batch production and customer dialogue, it’s clear the answer is no. The difference centers around chelation—the ability to form strongly bound, often stable, two-point contacts with transition-metal ions. 1,10-phenanthroline stands out as a classic chelating bis-nitrogen ligand. Its tightly positioned nitrogens create high-affinity complexes, so it’s favored in analytical and coordination chemistry for Fe(II), Cu(II), and similar cations. It’s practically the standard for iron detection by colorimetry.

    On the other hand, 1,7-phenanthroline stretches out those two nitrogens, so bidentate chelation is not possible. This change means 1,7-phenanthroline either forms weaker complexes, or might only coordinate through one nitrogen. This property limits its use in typical chelation-driven colorimetric tests. Yet, for those who aim to intentionally break away from tight bidentate coordination—for example, when looking to create labile sites on a metal center in catalytic cycles—1,7-phenanthroline becomes a distinct asset. We’ve seen users in organometallic synthesis select it specifically to slow down or tune reaction pathways, or to steer the self-assembly of materials in ways that the rigid 1,10 variant would not allow.

    As a result, lab teams working with both compounds quickly learn not to generalize. 1,7-phenanthroline is not a fallback; it brings unique steric and electronic features that promote creativity in design. Our team regularly receives requests for side-by-side analysis, so we started logging comparative data: UV-vis curves, NMR profiles, and even solubility trends. This sort of “real numbers” comparison suits those building predictive models or troubleshooting scale-up. In the end, what matters isn’t redundancy but differentiation. Without wide production experience, it’s easy to miss the subtleties in function and performance.

    Purity Assurance in Hands-On Manufacturing

    Quality control for 1,7-phenanthroline starts with careful selection and verification of raw inputs. We’ve had to reject entire batches of crude, off-spec precursor because lower purity finds its way through to the final molecule in ways that even multiple recrystallizations can’t fully clean up. Vigilant monitoring of reaction endpoints, by TLC and real-time NMR, is a step learned from practical trial and error, not from theory alone. Final product checks rely on more than just analytical certificates; they reflect our full synthetic history for each lot.

    Troubleshooting crystallization defects has taught us that ambient humidity, batch temperature, and filtration rates impact the size and purity of final product crystals. With 1,7-phenanthroline, colored impurities from incomplete oxidation or cyclization can result in pale yellow or tan powders instead of the desired off-white solid. Our process engineers keep detailed records from drying oven to final jar, including environmental checks, pH logs, and all QC assay numbers. Customers have shared stories of significant experimental artifacts arising from “almost pure” starting material, so we stick close to the synthesis and never outsource these steps.

    Solubility and Handling: Practical Lessons

    Humid environments can cause even a few grams of 1,7-phenanthroline to clump or take on a faint color shift, especially during warmer seasons. Chemists who’ve worked with it in places lacking humidity control see this directly and often need to re-dry before weighing. We designed our packaging to use moisture-barrier materials, backed up with silica pouches, which shortened customer preparation time. A drier, flowable powder pours without static buildup or loss, so more ends up in the reaction vessel, less on the glove or benchtop.

    In terms of solvent compatibility, we have documented full dissolution in hot ethanol, methanol, and some polar aprotic solvents, with incomplete solubility in plain water at room temperature. We report these findings honestly with every shipment rather than promising universal “easy solubility” that can rarely be matched by actual powders. Handling advice drawn from customer feedback has taught us to recommend slow addition to the chosen solvent with consistent stirring and gentle warming, reducing the time required to get fully homogeneous solutions.

    Real User Innovation: New Application Frontiers

    We keep learning from the ways research teams develop new uses for 1,7-phenanthroline. A few years ago, a customer working on organic light-emitting diodes (OLEDs) demonstrated that our high-purity 1,7-phenanthroline gave improved stability in their custom emitter complexes versus the standard 1,10 variant. In another case, a water analysis team used the distinct non-chelating nitrogen layout to screen for “harder” metals that had previously eluded clear differentiation using standard detection chemistry. Neither project came from catalog recipes; both relied on bench-level experimentation and the know-how to safely handle and modify 1,7-phenanthroline in demanding workflows.

    On the academic side, research groups probing supramolecular assembly have leveraged 1,7-phenanthroline to guide selective assembly paths, using its lack of chelation to avoid crosstalk between parallel coordination sites. This approach has allowed synthesis of larger, more modular frameworks that would be impossible with aggressively binding chelators. Our technical team collaborates directly to troubleshoot process bottlenecks, offering real-life product performance data rather than pre-canned marketing claims.

    Some chemists have explored directed oxidation or functionalization on the phenanthroline core itself, using 1,7’s spatial arrangement to achieve otherwise unattainable substitution sites. We supply material for pilot-scale explorations, keeping production histories traceable so unexpected results can be traced back to a source batch if problems arise.

    Supporting Claims with Facts, Not Hype

    In the chemical industry, the proof is not in the brochure but in the beaker. Every claim about 1,7-phenanthroline’s differences or reliability stems from direct production experience, repeated QA cycles, and data supplied by the laboratories that use our products. Over time, we’ve gathered enough evidence to see which technical issues repeat—whether it’s erratic melting behavior due to residual solvents, or unexpected discoloration during storage. Sharing these findings openly promotes safer and smarter experimentation.

    Our own logs and external review data show that 1,7-phenanthroline generally remains stable under standard laboratory conditions for up to two years when kept dry and protected from light. Samples stored open to air, or at high ambient moisture, gradually turn tan and develop a characteristic musty odor that signals molecular breakdown and the presence of low-level oxidized byproducts. Technically, such changes reduce the ligand’s value for sensitive spectroscopic work and introduce trace background interference in catalytic screening. That is why our work includes ongoing shelf-life tracking and product recalls if new process defects are identified post-shipment.

    Accurate record-keeping and feedback collection allow us to learn from problems uncovered by users, not just our own teams. One large-scale customer flagged a packing material incompatibility that caused minor static buildup and product loss when dispensing larger quantities. This led to packaging process changes from our side. Over years of supplying the market, honest dialogue has yielded incremental but practical improvements in everything from product consistency to documentation clarity.

    Pursuing Better Outcomes: Solutions and Next Steps

    To address ongoing challenges, we have found practical success through proactive solutions, not generalized fixes. We take environmental monitoring inside the production workshop seriously, regularly calibrating sensors and recording deviations. This guards against batch-to-batch moisture differences, which can defeat even the best drying ovens if unchecked. Continued improvement in powder handling—through anti-static drum liners and controlled-environment packaging—has reduced end-user frustration and increased retrieval rates, especially in climates known for high dew points.

    For those encountering solubility or stability troubles with 1,7-phenanthroline, we advise thorough pre-dissolution trials tailored to specific solvents, avoiding assumptions carried over from past experience with other phenanthrolines. Extra filtration and small-volume tests highlight any batch-dependent residues or color changes before full-scale reactions. We provide detailed real-life test reports with every shipment, removing guesswork and increasing the chance of reproducible results.

    Direct engagement between manufacturers and users remains the best route to ongoing product refinement. By maintaining feedback loops—gathering direct experience from those using our material in synthesis, analysis, or scaling new technology—we adjust formulations and QC to keep pace with new technical demands. No product is ever “one-size-fits-all” in our view. 1,7-Phenanthroline’s real value emerges in the details: tightly-controlled purity, reliable handling, and openness about what sets it apart from better-known alternatives. We remain committed to supplying the most accurate, application-focused support grounded in actual production expertise, not empty generalities.

    Looking to the Future: Shared Progress by Practice

    Our experience as a chemical manufacturer shapes a different perspective on specialty compounds like 1,7-phenanthroline. This molecule may not dominate catalog pages, but its presence in targeted synthesis, sensor development, and new materials design tells its own story. We have seen the field’s shift, from routine colorimetric tests to cutting-edge research, driven by technical demands that challenge standard manufacturing processes.

    By focusing on direct quality control, honest feedback, and collaborative troubleshooting, we support the real needs of working chemists. We build upon what comes back from the bench—consistency, performance, transparency. For those shaping new chemistry frontiers, 1,7-phenanthroline brings another tool to the table, and our hands-on production commitment supports real scientific progress every day.