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5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One

    • Product Name 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One
    • Einecs 629-041-7
    • 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
    VTB
    Specifications

    HS Code

    532731

    Name 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One
    Molecular Formula C11H9ClN2O
    Molecular Weight 220.66 g/mol
    Cas Number 7599-26-2
    Appearance White to off-white solid
    Melting Point 162-166 °C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, away from moisture and light
    Synonyms 5-Chloro-2-methyl-6-phenyl-2,3-dihydro-3-pyridazinone
    Inchi Key SZBMTBSMSWMMQU-UHFFFAOYSA-N
    Smiles CC1NNC(=O)C(C2=CC=CC=C2)=C1Cl
    Usage Research chemical, intermediate in synthesis

    As an accredited 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g package is a sealed amber glass bottle, labeled with the chemical name, concentration, hazard warnings, and batch number.
    Shipping 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One is shipped in tightly sealed, chemical-resistant containers to prevent contamination and degradation. The package is clearly labeled, compliant with relevant regulations, and protected against moisture, heat, and physical damage. Transportation typically requires handling by trained personnel, with relevant safety documentation included.
    Storage 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One should be stored in a tightly closed container, kept in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances (such as strong oxidizers). Protect from moisture and excessive heat. Ensure the storage area is clearly labeled and complies with safety regulations for chemical storage. Use appropriate secondary containment to prevent spills.
    Application of 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One

    Applications of 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One in Industrial Manufacturing

    As an original producer of 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One, we supply this specialty intermediate to highly regulated segments where selective synthesis and predictable performance are critical. On this page, we detail real-world industrial use cases, with a focus on the unique chemistry, regulatory frameworks, formulation gradients, and integration into downstream workflows across our customers’ core sectors.

    1. Pharmaceutical Intermediate for Pyrazolone-based Drug Synthesis

    The pharmaceutical industry uses this compound as a key building block for the synthesis of pyrazolone-derivative APIs, especially in non-steroidal anti-inflammatory drugs and certain antipyretics. Manufacturers incorporate it at the heterocycle formation stage, enabling precise introduction of the chloro and phenyl substituents crucial for target activity. Production lines demand strict raw material characterization and compliance controls due to stringent regulatory oversight on finished medicines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • Ph. Eur. Monograph standards for relevant APIs
    • Chinese Pharmacopoeia standards for corresponding intermediates

    Typical usage ratio

    • Used at 1.1–1.4 molar equivalents relative to target API precursor, adjusted to reaction yield and stoichiometry constraints
    • Batch variation is generally less than ±5%, controlled via in-process analytical release

    Downstream process integration

    • Introduced during initial condensation or cyclization steps in multi-stage synthesis
    • Undergoes purification via crystallization prior to coupling reactions in API formation
    • Integrated into both continuous and batch process lines with internal QC checkpoints

    Final product types

    • Antipyretic and analgesic API (e.g., metamizole sodium derivatives)
    • Non-steroidal anti-inflammatory drug precursor substances
    • Combination pharmaceutical therapy intermediates
    • Contract-manufactured custom fine chemicals for drug development pipelines

    2. Agrochemical Intermediate for Selective Herbicide Development

    In agrochemical synthesis, this compound’s unique dihydropyridazinone structure serves as a precursor for various selective herbicide formulations, imparting specific activity against broadleaf weeds. Producers introduce it at the final heterocycle formation step, allowing control over molecular substitution patterns. Consistency in raw material specifications directly influences downstream formulation stability and field application efficacy.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO JMPR guidelines for pesticide ingredient purity
    • CropLife International technical standards
    • REACH registered for use in closed systems and integrated pest management

    Typical usage ratio

    • Formulated at 0.5–1.3 mol equivalent relative to active herbicide skeleton
    • Final use ratio determined by downstream transformation and residual analysis targeting ≤0.05% w/w carryover

    Downstream process integration

    • Enters as the dihydropyridazinone scaffold in late-stage condensation
    • Synthesized in solvent-controlled reactors, then subjected to chromatographic separation
    • Staged for further derivatization to produce the target crop protection agent

    Final product types

    • Selective post-emergent herbicide actives
    • Precursor intermediates for weed resistance management blends
    • Advanced agrochemical formulation components
    • Tech-grade material for downstream granule or liquid herbicide preparation

    3. Specialty Intermediate in Dyes and Pigments Manufacturing

    Dyestuff manufacturers employ this compound as a tailored intermediate in the synthesis of azo and heterocyclic pigment molecules, particularly for high-performance coloration applications in plastics and textiles requiring stability and specific absorbance profiles. The integration point is typically a coupling reaction, which exploits the aromatic and halogenated rings to generate custom shade profiles with improved fastness and light stability properties required by end users in automotive and industrial coatings.

    Industry compliance standards

    • EU REACH regulation (EC) No 1907/2006 for specialty chemicals
    • ZDHC Manufacturing Restricted Substances List (MRSL) for textile applications
    • EN ISO 105 series for color fastness in finished textiles
    • Chemical compliance for RoHS (for use in electronic coloring agents)

    Typical usage ratio

    • Represents 0.8–2% of final pigment batch mass, depending on target chromophore intensity
    • Adjusted up to 3% for specialty high-depth applications in HDPE or ABS plastics

    Downstream process integration

    • Added during diazo coupling or heterocycle synthesis in pigment plant synthesis blocks
    • Purified by precipitation or continuous filtration to remove residual reactants
    • Quality controlled for trace impurity profile affecting hue and fastness

    Final product types

    • Azo and heterocyclic pigments for industrial coatings
    • Colorants for spinning fiber and technical textiles
    • High-performance pigment dispersions for plastics processing
    • Batch dyes for automotive exterior and component color masterbatches

    4. Advanced Intermediate for Material Science and Organic Synthesis R&D

    Research teams in material science and commercial contract R&D utilize this compound as a foundational unit for the synthesis of complex organic frameworks, including ligands, functionalized monomers, and heterocyclic arrays. It provides a highly controlled start point for custom scaffold generation which is instrumental in the development of performance polymers and analytical standards.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation for analytical verification
    • ASTM E2879 for chemical purity in custom synthesis services
    • Client-driven material safety data review under GHS guidelines
    • OECD chemical testing guidelines for pre-commercial materials

    Typical usage ratio

    • Titrated at 0.1–2.5 mmol scale per mole of target test molecule
    • Scaled to pilot-level purity campaigns, subject to end-use validation protocols

    Downstream process integration

    • Acts as a starting structural unit for C-N or C-C bond formation in model compounds
    • Purification required through preparative HPLC or column chromatography prior to secondary modification
    • Fed into iterative parallel synthesis chains for library generation

    Final product types

    • Functionalized trial compounds for structure-activity studies
    • Polymer science monomer units for advanced material development
    • Chemical standards for analytical method validation
    • Ligand and catalyst scaffolds for academic and industrial R&D programs
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    Certification & Compliance
    More Introduction

    Introducing 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One: Experience, Precision, and Innovation on the Shop Floor

    At our chemical manufacturing plant, every product owes its existence to carefully chosen raw materials, experienced teams, and sound process controls. After many years in this business, experience tells us which compounds deliver reliability, cost-effectiveness, and adaptability during scale-up. Among such compounds, 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One proves itself in our lineup.

    Precise Chemistry with Every Batch

    Our engineers keep their eyes on the small stuff—moisture content, particle size, contaminants—because, in specialty chemicals, the smallest change can throw off an entire downstream batch. With 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One, we have refined production so the specifications stay tight. We regularly achieve highly consistent purity: modern chromatographic methods give us reproducible results for every shipment. We monitor for trace-level chlorinated byproducts and related substances, since these can impact both synthesis yield and regulatory standards in pharmaceutical and fine chemical applications.

    What Sets This Compound Apart

    Those who have worked in custom synthesis or active pharmaceutical ingredient (API) production will recognize our product as part of several key intermediate syntheses. Process chemists report consistent performance of our 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One, largely because we put time into minimizing batch-to-batch variation. It seems a simple claim, but such consistency in this field changes timelines for pharma pipelines. We don’t see this in competitors who buy material in bulk and resell it under their own brand; they simply lack visibility into each step, from reaction conditions to packing line cleaning protocols.

    A distinguishing feature is our approach to solvent removal and drying. Because this intermediate commonly advances to sensitive coupling or cyclization steps, residual solvents and excess water can reduce yields. Our team uses a staged vacuum drying process, supported by in-line NIR analyzers, so the product leaves our site with residual solvents below threshold levels. We do not rely on single-point sampling; instead, we maintain multiple sampling windows across each batch to catch inconsistencies early. Over time, this vigilance leads to fewer rejected blends and less troubleshooting at the customer’s facility.

    Understanding the Process: Hands-on Experience and Clean Transitions

    It’s easy for marketing gloss to obscure what really happens at a chemical plant floor. There are few shortcuts when scaling up finely tuned reactions. Our reactors operate under an automated batch control system, but our operators still make the call if exothermic events or pressure spikes crop up. That matters for 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One, which responds poorly to uncontrolled temperature ramps or delayed quenching steps. Overdosing reagents can form unwanted tars or side-products—mistakes an experienced operator avoids. Most quality stories in our industry don’t start with fancy promos, but with operators reacting smartly the night something looks off in Process Room C.

    Physical Characteristics: More Than Specification Sheets

    Regular samples from our plant show a pale to light yellow crystalline solid, with low-level polymorphic variability. Why does this matter? Because polymorphs affect melting point, filtration time, and overall reactivity in multi-step routes. We store extensive lot histories—melting behavior, particle size distributions, and stability assessments—since API manufacturers or researchers always want to know what’s changed, and why. Our transparency with these histories builds trust with customers eager to troubleshoot or adapt runs quickly.

    Handling characteristics, such as flowability and dusting, sit high on our watchlist. Our product remains free-flowing, even at low humidity, thanks to careful control of granulation and anti-caking agent blends. Packed in thick-walled, lined drums, material arrives safe from cross-contamination and environmental exposure. Customers notice this—the absence of lumps or clumping means easier transfers and more accurate weighing in their own labs or plants.

    Application Experience: Where This Compound Proves Itself

    This pyridazinone derivative earned its place among agrochemical and pharmaceutical researchers because of its unique substitution pattern. The chlorine at the 5-position and the methyl at 2 both discourage unwanted side-reactions during subsequent synthesis. As bulk manufacturers, we work with clients who go on to make heterocyclic derivatives, intermediate step APIs, or candidates used in medicinal chemistry screening. The phenyl group at 6 offers a versatile anchor point for further functionalization—clients who modify it with electron-withdrawing or electron-donating groups report reliable yields, helped by the purity and predictable reactivity of our intermediate.

    Drug development teams often value predictable scale-up most. Our material, characterized by narrow melting point ranges and minimal impurity profile, stands up to both kilo-lab and commercial reactor runs. Strict control of residual acid content and color ensures that purification steps downstream won’t run long, inflate costs, or compromise environmental compliance. R&D groups who’ve run into “hidden bits”—like trace halides, oxidized byproducts, or unknown tars—report clean runs with our product because we remove such pitfalls at the source. Lots come with detailed impurity profiles, letting those in development or regulatory submission teams provide straightforward documentation.

    Familiarity with export documentation and compliance rules means we can support partners wherever their work takes our compound, whether as an isolated intermediate or as part of a fast-moving research campaign. Our logistics team knows the hazards of delay: proper documentation, GHS-aligned labeling, and tamper-evident sealing back up our promise of regulatory readiness.

    Differences from Commodity Products and Reseller Channels

    Those who browse catalogs often find generic listings for pyridazinones. Our team stands by direct-from-plant operation. Unlike resellers, we don’t scramble for material during supply crunches or rely on assorted outside tollers. All steps—starting from core chlorination, methylation, and cyclization—remain indoors under full QA/ QC supervision. For each improvement in our molecule’s handling, stability, and purity, we keep data to share with clients because intellectual transparency means better outcomes for both sides.

    Some producers treat this molecule as “just another intermediate.” Our team invests in continuous monitoring of environmental impact, solvent use, and energy consumption per batch. Over several years, our waste reduction efforts in plant utilities—targeted recycling, solvent distillation, and closed handling—have lowered environmental footprint per ton. Waste minimization is no longer just compliance. It shapes how we improve synthesis lines and retain skilled staff who value responsible manufacturing. These factors build reliability into every drum shipped. Our approach carries through to sourcing: reagent and solvent traceability stays transparent, giving customers confidence every step feeds into their regulated or high-stakes processes without concern for off-spec surprises.

    Commitment to Safety and Manufacturing Integrity

    We take plant safety as seriously as product quality. We audit safety protocols frequently and talk openly with staff about improvement needs. Chemical manufacturing always carries inherent risk: chlorinated intermediates, strong bases, and multi-step exothermic reactions challenge any crew. Through cross-discipline training, we’ve reduced handling incidents and unplanned downtime. Real improvements—continuous scrubber upgrades, more fail-safe controls, and worker health monitoring—keep both staff safe and batches consistent. Customers who’ve walked our shop floors have seen everything from PPE upgrades to spill containment upgrades rolled out over the years, showing the long-term commitment to doing things right.

    Every change in our process, from recrystallization solvents to drum liners, undergoes both technical and regulatory assessment. Change control paperwork is not a box-ticking exercise. It has taught us that state-of-the-art quality systems cut both rework and complaints. When an improvement works, those benefits show up next month, not next year. Sustainable procedures reduce operator strain and, by extension, batch failure rates.

    R&D Collaboration and Real-World Problem Solving

    Our chemists partner closely with customer teams, sometimes long before the first order rolls in. Every year, new syntheses arrive from customers working on patent programs or trying to hit aggressive process yields. We support method development—providing variants with slight changes in crystallinity or hydration—so researchers can optimize reaction windows. This degree of cooperation proves invaluable when timelines run tight. We’ve lent out material for testing, participated in troubleshooting calls, and hosted visiting chemists more times than any sales presentation could count.

    In difficult process transitions, we deploy in-house knowledge—kinetics studies, impurity root cause analyses—so production meets not just the letter, but the spirit of our customer’s project requirements. Instead of chalking up outliers to “just process variability,” we look for repeatable corrections. These actions build customer loyalty and ensure repeat work. We store and share both batch and historical performance data, making handover to customer QA reliable and transparent. Unlike buyers or traders, we answer questions on-the-ground, from tank cleaning to lab method validations, because those details matter more than glossy catalogs.

    Environmental Stewardship—Toward Cleaner Chemistry

    Over the past decade, we’ve seen both customer expectations and regulatory floors shift. Clients watching their own carbon footprints are already asking suppliers about solvent consumption and waste ratios. Instead of slow catches to meet regulations, we try to think ahead: solvent recycling units keep our emissions in check, and energy recovery projects reduce process heating demands. These gains reduce operational costs and support clients who want to report the impact of every kilogram. Wastewater analysis data and recycling rates go into process reports we share upon request. This information supports transparent supply chains and show stakeholders compliance is no afterthought.

    By investing in equipment that captures air emission streams and supports solvent recovery, we advance both product purity and local environmental goals. Our operators understand how their work affects both immediate safety and long-term resource management, and we share process improvement milestones with our customers openly.

    Supply Chain, Timeliness, and Direct Communication

    We see delayed shipments and inconsistent lead times as bottlenecks for customers. Our policy runs on direct communication, so clients know their position in our queue, have live progress updates, and hear about anything causing a holdback. Years spent handling shipments in all climates taught our logistics staff plenty: liners, shock-absorbing packaging, and anti-moisture barriers matter more than promises on paper. Pre-cleared export paperwork, regular audits of freezer or hot-weather carriers, and a robust digital inventory tracking system keep us on schedule. This reduces transit surprises, minimizes storage costs for customers, and addresses one of the longest-standing headaches in chemical supply.

    Supply reliability goes beyond extra stock. Our proposal management team balances regular clients with new development orders, confirming realistic batch lead times and storage plans. This approach lets us adjust production for R&D surges or regulatory changes, all while maintaining the same product integrity. We talk directly to project leads or purchasing heads—no call centers or intermediaries stand between us and the end-users. Experience tells us this transparency keeps projects moving and trust intact.

    Continuous Investment in Analytical Infrastructure and Documentation

    Our investment in the latest chromatographic, spectroscopic, and impurity identification tools pays off daily. Consistent method validation, cross-checked results with customer analytics, and timely sharing of CoAs means labs get answers instead of questions. Traceability runs through everything we do: inventory lots, batch reports, and analytical data all link up in our ERP, not on scattered spreadsheets. We see the benefit reflected in customer ease during audits and regulatory submissions.

    We tailor additional documentation when necessary, offering impurity maps, extended stability reports, or bespoke containment recommendations aligned with the customer’s application. These are not afterthoughts; they result from two-way dialogue and attention to detail. Timely, accurate documentation reduces lost time in regulatory cycles and avoids rework for both us and our partners.

    Closing Thoughts from the Manufacturer’s Floor

    Chemical manufacturing rewards persistence and careful improvement. We have watched 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One develop from a niche research material into a dependable intermediate at scale, thanks to ongoing feedback and adaptation. Direct involvement in production and a willingness to improve, batch after batch, have created a robust process. Our connection to plant reality—raw material quality, real-time controls, skilled operators, and thoughtful logistics—sets us apart from parties who push paper or repackage someone else’s goods.

    For those developing new molecules, scaling up known routes, or seeking to cut troubleshooting and lead times, the difference between chemical sources comes down to integrity and experience. Every supplier talks about quality; those who can demonstrate process control, handling, responsiveness, and operational transparency prove it. Our journey with 5-Chloro-2-Methyl-6-Phenyl-2,3-Dihydropyridazin-3-One continues, not just because we make reliable product, but because we keep learning from every batch.