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4-Phenyl-1(2H)-Phthalazinone

    • Product Name 4-Phenyl-1(2H)-Phthalazinone
    • Alias phenidone
    • Einecs 213-668-5
    • 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

    598920

    Chemical Name 4-Phenyl-1(2H)-Phthalazinone
    Cas Number 28315-44-8
    Molecular Formula C14H10N2O
    Molecular Weight 222.24 g/mol
    Appearance Off-white to yellow powder
    Melting Point 216-219 °C
    Solubility Slightly soluble in water; soluble in organic solvents
    Purity Typically ≥98%
    Storage Condition Store at room temperature, away from light and moisture
    Iupac Name 4-phenylphthalazin-1(2H)-one
    Smiles C1=CC=C(C=C1)C2=CN(N=C2)C3=CC=CC=C3=O

    As an accredited 4-Phenyl-1(2H)-Phthalazinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical, 4-Phenyl-1(2H)-Phthalazinone (25g), is supplied in a sealed amber glass bottle with a tamper-evident cap and labeling.
    Shipping 4-Phenyl-1(2H)-Phthalazinone is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be handled in compliance with regulatory guidelines, using proper labeling and documentation. Shipping requires appropriate packaging to prevent leaks or breakage, and all safety and hazard protocols must be strictly observed during transit.
    Storage 4-Phenyl-1(2H)-phthalazinone should be stored in a tightly closed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Store at room temperature unless otherwise specified. Keep away from incompatible substances such as strong oxidizers and acids. Appropriate chemical storage cabinets are recommended to prevent accidental contact and contamination.
    Application of 4-Phenyl-1(2H)-Phthalazinone

    Applications of 4-Phenyl-1(2H)-Phthalazinone in Industrial Manufacturing

    4-Phenyl-1(2H)-Phthalazinone, produced at industrial scale under stringent quality controls, brings high performance and reliability across several advanced manufacturing sectors. Below are the principal downstream application areas where this material plays a critical process role.

    1. Synthesis of High-Temperature Polyimides

    In specialty polymers manufacturing, especially high-temperature polyimides for the electronics and aerospace industries, 4-Phenyl-1(2H)-Phthalazinone acts as a heterocyclic monomer providing improved thermal resistance, dimensional stability, and low dielectric loss. Process engineers introduce this monomer during the polycondensation step with dianhydrides and diamines. Strict compliance with environmental and product safety standards is enforced from incoming raw material acceptance through polymerization and film, sheet, or fiber extrusion. These polyimides are used for flexible printed circuits, insulation for wires, and components exposed to demanding thermal cycles.

    Industry compliance standards

    • UL 94 V-0 (Flammability of Plastic Materials)
    • IEC 61249-2-21 for base materials in printed circuits
    • REACH Regulation (EC) No 1907/2006
    • RoHS Directive 2011/65/EU

    Typical usage ratio

    • 10–30% by mole of total monomeric content, adjusted according to polymer architecture, target Tg, and mechanical requirements

    Downstream process integration

    • Charged to polycondensation reactor after dehydration stage; reacts with selected dianhydrides under inert atmosphere, followed by imidization (thermal or chemical) to yield precursor films or resins

    Final product types

    • PI flexible circuit substrates
    • Wire enamel insulations
    • Heat-resistant films for flexible electronics
    • Polymide-based aerospace structural composites

    2. Intermediate for Pharmaceutical Active Compounds

    Our 4-Phenyl-1(2H)-Phthalazinone serves as a key intermediate in the synthesis of several investigational and commercial drug substances containing the phthalazinone core. Medicinal chemists leverage its structure to construct anti-cancer, anti-inflammatory, and central nervous system compounds through site-selective modification and coupling. Stringent control under cGMP and ICH Q7 requirements covers API manufacturing. All product handling adheres to national pharmacopeia and registration guidelines before downstream formulation into dosage forms.

    Industry compliance standards

    • ICH Q7: GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: Current Good Manufacturing Practice for Finished Pharmaceuticals (FDA)
    • Ph. Eur., USP, and JP (relevant monographs for final APIs)
    • National Registration Authority requirements (CFDA, EMA, USFDA)

    Typical usage ratio

    • Variable: Usually 1.0 equivalents in core coupling reactions, final % w/w in API depends on molecular scaffold and synthetic yield

    Downstream process integration

    • Added during key condensation or cyclization stage. Isolated via crystallization or chromatography and used for subsequent derivatization into API

    Final product types

    • Cancer therapeutics with phthalazinone backbone
    • Neuroprotective agents
    • Experimental anti-inflammatory APIs
    • Reference standards and building blocks for medicinal chemistry

    3. High-Performance Engineering Adhesive Formulations

    In adhesives manufacturing for microelectronics assembly, photonics, and specialty structural bonding, 4-Phenyl-1(2H)-Phthalazinone functions as a toughening co-monomer in resin matrices. Its inclusion enhances temperature stability, chemical resistance, and adhesion to polyimide or glass fiber surfaces. The material enters the formulation blending stage and is dispersed thoroughly into epoxy, cyanate ester, or bismaleimide resins before curing. Customers use our in-house grade for adhesives that remain dimensionally stable during soldering, autoclave cycles, or sustained environmental exposure.

    Industry compliance standards

    • IPC-4101: Base Materials for Rigid and Multilayer Printed Boards
    • JIS K 6850: Adhesives for Electronics
    • ISO 9001:2015 (Quality Management for Manufacturing)
    • IEC 61249-2-21: Halogen-free laminate systems

    Typical usage ratio

    • 1–10 wt% of total resin system; adjusted based on required Tg, fracture toughness, and compatibility with filler systems

    Downstream process integration

    • Incorporated during initial resin mixing, followed by high-shear dispersion and degassing prior to addition of curing agents and fillers

    Final product types

    • Microelectronic die attach adhesives
    • Optical device potting materials
    • PCB assembly epoxy adhesives
    • Structural adhesives for aerospace and automotive electronics

    4. OLED and Photonic Material Intermediates

    In the development and scale-up of advanced organic electronic materials, particularly for organic light-emitting diodes (OLEDs), 4-Phenyl-1(2H)-Phthalazinone is applied as a key precursor enabling the construction of electron transport layers and host materials. Its molecular rigidity and extended π-system support high quantum efficiency and device lifespan. Integration occurs at the organic synthesis stage for specialty intermediates, followed by solution or vapor-phase purification prior to vacuum deposition or inkjet printing at device makers. Downstream quality management ensures absence of ionic contaminants and accurate molecular weight distribution for photonic application performance.

    Industry compliance standards

    • ISO 14644-1: Cleanroom standards
    • JEITA EM-3601: Reliability testing for OLEDs
    • RoHS and REACH legislation for finished display modules
    • CQC Mark Certification (China Quality Certification for electronic components)

    Typical usage ratio

    • Varies: 5–20 mol% in organic layer formulations, or as a stoichiometric intermediate at 1.0 equivalents during precursor synthesis

    Downstream process integration

    • Synthesized into target heterocycle; purified and supplied for layer deposition in OLED stack structure during display module fabrication

    Final product types

    • OLED emitter materials
    • Electron transport layer (ETL) compounds for displays
    • High-performance organic thin-film photonic components
    • Device-grade organic intermediate supply

    5. Chemical Synthesis Building Block for Agrochemical Discovery

    Agricultural biochemists and crop protection companies utilize 4-Phenyl-1(2H)-Phthalazinone as an advanced heterocyclic scaffold during lead compound optimization phases. In crop protection R&D, this ingredient enables targeted modification to discover new fungicides, insecticides, and herbicides with improved selectivity. It is handled within R&D and pilot synthesis labs under national chemical safety practices. After confirmation of biological activity, scale-up incorporates systematic analytical QC at each step to support downstream formulation trials of technical active ingredients in field applications.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • ISO 17025: Testing and calibration of chemical laboratories
    • FAO/WHO Guidelines for pesticide preparation
    • National Chemical Law for Handling Restricted Substances

    Typical usage ratio

    • 0.5–1.0 equivalents in reaction schemes; variable depending on structure-activity relationship study requirements

    Downstream process integration

    • Introduced in early lead generation or functionalization stages; extended to pilot and pre-commercial synthesis as structure confirmed and biological data validated

    Final product types

    • New agrochemical technicals for field trials
    • Discovery-phase crop protection leads containing phthalazinone motif
    • Formulated pesticide research compounds
    • Analytical reference substances
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    Certification & Compliance
    More Introduction

    4-Phenyl-1(2H)-Phthalazinone: Reliable Performance in Pharmaceutical Synthesis

    Introduction to 4-Phenyl-1(2H)-Phthalazinone

    Every product coming out of our chemical plant reflects decades of hands-on manufacturing. 4-Phenyl-1(2H)-Phthalazinone stands out as one of the more versatile intermediates on our production lines, prized by pharmaceutical researchers for its clean performance in demanding syntheses. The daily work inside our facilities revolves around real-world challenges, and we know which reaction step can make or break a process. As a manufacturer, the care we take with every batch of this phthalazinone comes straight from repeat conversations with end-users, lab chemists, and procurement departments who rely on authenticity and reproducibility, not vague claims or regulatory lingo.

    We've focused considerable effort into this molecule, sometimes called 4-phenylphthalazinone or 4-PHP, to ensure it holds up under scrutiny from both bench chemists and process engineers. Its CAS number lines up directly with our established synthetic routes and purity specifications. Years back, when a partner company tried to streamline costs with a lower-grade alternative, their yields plummeted and troubleshooting took weeks. Design matters, and so does having tight grip on impurity profiles from raw material to final lot.

    Production Experience and Quality Focus

    Day-to-day production of 4-Phenyl-1(2H)-Phthalazinone relies on skilled technicians and robust analytical controls. Our reactors never run on automatic pilot. During scale-up, we found that even minor deviations in solvent quality could throw off the product's crystal habit and filterability. We've instituted incoming checks on all starting phenylhydrazine and phthalic anhydride streams, pinning down levels of colored byproducts. The impact of a hot spot in the jacket or a misjudged addition rate can show up directly in GC traces, and the market notices batch-to-batch inconsistency. We run side-by-side comparisons of new and established lots, and we don't hesitate to reject what doesn't match.

    Analytical chemists in our labs use a battery of techniques for quality verification. HPLC serves as our frontline check, but NMR and LC-MS give clear reads on isomer content and persistent trace impurities. Rigorous specification work takes more than hitting a set of numbers on a certificate; it calls for intimate knowledge of what affects downstream chemistry in customer applications. We've learned this by running customer-initiated trials on both small and multi-kilo scales. Each batch carries a traceable record, not just for regulatory reasons, but because a strong feedback loop protects both our customer’s synthesis and our own brand.

    Model, Purity, and Material Handling

    We offer 4-Phenyl-1(2H)-Phthalazinone in several defined grades. Each model is distinguished by controlled moisture, ash content, and the level of process-derived organics. A typical pharmaceutical-grade batch achieves over 99.5% purity by HPLC, and we routinely push tighter margins for specialty applications. On site, our team knows that even a barely perceptible off-white tint can signal trace contaminants. In response, material gets double-vacuum dried and sieved before any lot release.

    Packing the material correctly impacts handling throughout the supply chain. We have switched from standard fiber drums to high-density polyethylene liners, eliminating previous issues of static buildup and potential cross-contamination. Dust control and staff training play a big role during packaging, both for worker safety and supply integrity.

    End-Use: Why Chemists Prefer This Route

    Synthetic chemists and project managers come to us focused on specific goals — uniformity in reacting behavior, clean conversion to target structures, and consistency in solid-phase properties. 4-Phenyl-1(2H)-Phthalazinone excels especially in pharmaceutical intermediate synthesis, often forming the foundational core for antihypertensive, anticancer, and CNS drug projects. Where other aromatic scaffolds suffer from unpredictable reactivity, this phthalazinone shows stable resistance to side reactions during alkylation, acylation, and cyclization.

    Teams working on scale-up and technology transfer highlight the reliable melting point range and straightforward solubility characteristics of our product. In multi-step organic syntheses, especially those involving bifunctional nucleophiles, uncontrolled purity leads to costly rework. Our version lessens these worries, supporting both R&D and commercial demands without late-stage surprises. One of our pharma clients changed suppliers in the past and faced persistent haze in their crystallizations; reswitching to our material resolved their problem without further need for recrystallization.

    Distinguishing Our 4-Phenyl-1(2H)-Phthalazinone

    Our years of manufacturing have taught us where subtle differences appear in specialty intermediates. Competing offerings sometimes cut corners on precursor sourcing or drying cycles, and it shows up as “invisible” impurities that trigger batch failures for demanding users. Our own controls stem from direct accountability on the production floor, not just an audit or a paper certificate. This approach lets our partners chase higher-yielding transformations with reduced risk. The physical form from our reactors tends toward a manageable, free-flowing crystalline solid, avoiding clumping or excessive fines that complicate dispensing.

    What sets apart our 4-Phenyl-1(2H)-Phthalazinone isn’t just measured by raw data. Over years, our tech team has responded to troubleshooting calls, especially when customers uncovered low-level metal traces. Adjusting process water specs and switching to corrosion-resistant reactor elements paid off. Maintaining color stability and thermal performance round out the practical advantages we offer, especially where extended storage under varied climate conditions could otherwise degrade typical lots.

    Comparison with Other Structural Scaffolds

    Phthalazinone chemistry covers a stretch of research needs, but not all derivatives respond the same to handling and downstream modification. We see research groups who try to substitute simple phthalazinone or related phthalimide frameworks for cost reasons, only to find that electron distribution in the aromatic core and the presence of the 4-phenyl group strongly influence activity and functionalization. This specific isomer reduces the likelihood of uncontrolled N-alkylation, thanks to the rigid orientation conferred by the non-reactive phenyl substituent.

    Whether in heterocyclic annulation or selective reduction steps, our product’s predictability cuts development time for medicinal chemistry and process scale teams. Other suppliers exporting lower grade or broad-range phthalazinone blends run into solubility issues or co-crystallization with persistent minor isomers, which undercuts both yield and analytic clarity. Direct feedback from pilot runs proves to us that matching precise physical and chemical properties drives value far more than shipping generic “phthalazinone” stock.

    Safety, Logistics, and Storage Insights

    We treat logistic details as seriously as batch integrity. Over the years, we’ve seen how improper storage eats into a material’s lifetime and performance. 4-Phenyl-1(2H)-Phthalazinone, in our experience, remains stable only when shielded from moisture and light. A few seasons ago, a warehouse operator stacked inventory next to heat vents; thermal cycling led to yellowing and eventual clumping, forcing a costly product recall. That taught us to overhaul the storage and shipping regimen, including climate-controlled conditions and quick-turnaround scheduling in transit.

    Staff training on both the shipping and customer side reduces common mishaps. On engaging with groups new to the material, we walk teams through packaging opening and reseal practices, since atmospheric water can degrade some secondary properties over time. We’ve developed detailed, experience-backed guidance to keep all material as close to lab-fresh as practical through the entire chain of custody.

    Upstream and Downstream Integration

    Tight integration with both our raw material sourcing and customer feedback shapes every adjustment made in production. Changes upstream—phenylhydrazine lots, alternative solvent vendors—translate directly into impurity patterns that show up in final product analytics. Upstream traceability reduces surprises on the customer end, something we’ve learned is vital to keeping long-term business. Not long ago, when a shift in phthalic anhydride grade crept into our process, we caught the anomaly in trial-scale runs. Customer input, combined with our internal analytics, resolved any drift before it reached a full-scale batch.

    Downstream applications drive further tweaks. Medicinal chemists continually share how compromised batches, even with slight off-spec readings, slow their compound screen rates or force reruns. That steady conversation keeps our QA team focused not just on “passing” specs, but tuning performance to address new incoming synthesis plans.

    Regulatory, Documentation, and Traceability

    Regulatory compliance, while essential, doesn’t overshadow good manufacturing practice. Our documentation covers full batch traceability, impurity profiles, and storage history. The push for transparency means sharing analytical methods, revision histories, and any observations on atypical reactions from previous campaigns.

    Adaptability comes into play as customer requirements evolve. More recently, requests for hazard statements or expanded impurity panels have grown, particularly from export customers. Instead of sticky legal disclaimers, we outfit our documentation with user-friendly, straight narrative about material characteristics, test results, and best-use cases. This reduces downstream confusion and supports regulatory ease in pharmaceutical and research development filings.

    Sustainability and Waste Management Considerations

    Over the years, we’ve reshaped our approach to sustainability in manufacturing 4-Phenyl-1(2H)-Phthalazinone. Waste management begins at the reaction design, not the end of the process. Recycling and distillation of solvents minimize environmental impact. A few years back, disposal issues from mother liquors prompted us to rethink water use and solvent recovery rates. Periodic audits and straightforward reporting ensure compliance with environmental standards. This experience-driven approach reduces not just our costs, but environmental risk passed onto customers handling waste streams.

    Variations in reaction efficiency and side-product profiles led us to rotate production schedules and adjust reactor cycles. For customers pursuing green chemistry and advanced pharmaceutical manufacturing, we openly share process enhancements that minimize by-products, not only to meet market demand but to drive the art and responsibility of specialty chemical manufacturing forward.

    Challenges and Continuous Improvement

    The real value of 4-Phenyl-1(2H)-Phthalazinone comes to light in problem-solving. Whether dropping out an unknown impurity or dialing in better crystallization kinetics, our plant thrives on direct user feedback and iterative improvements. Mistakes get made—deviations from standard operating procedure or instrument drift—yet rapid troubleshooting and corrective actions have kept production on track. Chemists visiting our plant routinely see our attention to detail, from material segregation to batch-specific logbooks updated after every operation.

    Failure to maintain these standards can have a ripple effect through a supply chain built on trust. One memorable instance involved a project deadline threatened by delayed customs clearance and lost shipment visibility; the team’s quick intervention and direct communication made all the difference. The lesson isn’t just logistical—it’s tied directly to product integrity and customer success. Our long record of re-examining older processes, adopting new in-house testing, and learning from real customer pain points ensures that each new lot of 4-Phenyl-1(2H)-Phthalazinone stands up to its reputation in the market.

    Looking Forward: Innovation Driven by Real-World Use

    Where this material finds new applications, we embrace the changes that come with updated research trends and industry standards. Collaboration with university labs, contract research organizations, and process development chemists pushes us to adapt, refine, and occasionally re-engineer our manufacturing methods. We keep laboratory-scale feedback at the center of our operation, allowing us to spot new use cases where the particular structure of 4-Phenyl-1(2H)-Phthalazinone introduces advantages over older heterocycles or less conformationally constrained scaffolds.

    Whether as a key node in a synthetic pathway, a reliability test for a new catalytic process, or a persistent core for specialty actives, our product reflects the relentless curiosity and practical wisdom that only direct, ongoing manufacturing imparts. We continue to invest in our plant and people, recognizing that the best solutions emerge from the intersection of science, experience, and honest problem-solving.