Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

2-Chloro-6-Phenylnicotinonitrile

    • Product Name 2-Chloro-6-Phenylnicotinonitrile
    • Alias 2-Chloro-6-phenyl-3-cyanopyridine
    • Einecs (EINECS) 682-056-6
    • 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

    481925

    Chemical Name 2-Chloro-6-Phenylnicotinonitrile
    Cas Number 57061-85-7
    Molecular Formula C12H7ClN2
    Molecular Weight 214.65 g/mol
    Appearance Off-white to light yellow solid
    Melting Point 116-120°C
    Solubility Insoluble in water; soluble in organic solvents
    Purity Typically >98%
    Smiles C1=CC=C(C=C1)C2=NC(=C(N=C2)Cl)C#N
    Inchi InChI=1S/C12H7ClN2/c13-11-10(7-14)8-15-12(16-11)9-5-3-2-4-6-9/h2-6,8H
    Storage Conditions Store at room temperature, away from moisture and light
    Usage Used as an intermediate in pharmaceutical and organic synthesis

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

    Packing & Storage
    Packing A 25g amber glass bottle, tightly sealed, labeled "2-Chloro-6-Phenylnicotinonitrile", with hazard symbols and batch information included.
    Shipping 2-Chloro-6-Phenylnicotinonitrile is securely packed in sealed containers and shipped according to standard chemical transport regulations. Protect from moisture, heat, and direct sunlight. Handle as a hazardous material, complying with all local, national, and international shipping guidelines, including proper labeling, documentation, and use of compatible packaging materials to prevent leaks or contamination.
    Storage 2-Chloro-6-Phenylnicotinonitrile should be stored in a tightly closed container in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Avoid exposure to direct sunlight and moisture. Handle with appropriate personal protective equipment and ensure proper labeling. Store at room temperature and keep away from ignition sources and acids to prevent hazardous reactions.
    Application of 2-Chloro-6-Phenylnicotinonitrile

    Applications of 2-Chloro-6-Phenylnicotinonitrile in Industrial Manufacturing

    2-Chloro-6-Phenylnicotinonitrile serves as a critical intermediate for advanced chemical synthesis across major industrial segments. Used primarily in specialized organic synthesis, this compound enables efficient downstream production of active pharmaceutical ingredients, complex crop protection molecules, and performance materials. Below, we detail key application scenarios relevant to real-world industrial practice, with focused data on compliance, formulation, processing, and commercial outcomes.

    1. Pharmaceutical Intermediate for Pyridine-Based API Synthesis

    Pharmaceutical manufacturers rely on this compound chiefly in the multi-step synthesis of select anti-inflammatory and neuroactive agents. Its chloro and phenyl substituents direct specific pyridine ring transformations, enabling subsequent coupling or derivatization into target pharmaceutical molecules. End users select this intermediate to streamline routes that demand precise reactivity or minimal by-product formation in commercial GMP settings.

    Industry compliance standards

    • Complies with ICH Q7 GMP for Active Pharmaceutical Ingredients
    • Must meet United States Pharmacopeia (USP) option where applicable for intermediate handling
    • Adheres to EMA (European Medicines Agency) guidelines for starting material traceability
    • Subject to internal quality systems aligned with ISO 9001:2015 certification

    Typical usage ratio

    • Usually dosed at 1.0–1.4 molar equivalents per synthesis batch
    • Adjusted according to stoichiometry of target API process (generally 0.9–1.2x theoretical, based on route efficiency)
    • Pilot runs may test 0.8–1.1 mol/mol for process development with recovery evaluation
    • Final scale-up uses ratio dictated by regulatory process registration

    Downstream process integration

    • Charged into the fluorination, Suzuki coupling, or Grignard reaction steps for substituted pyridine core assembly
    • Introduced after initial acylation or halogen exchange reactions to enable regioselective activation
    • Monitored by in-process HPLC/GC to confirm complete consumption before further modification
    • Isolation by controlled crystallization to guarantee batch purity

    Final product types

    • Anti-inflammatory drug intermediates (e.g., pyridinecarboxamide APIs)
    • Antidepressant and neuroprotective pharmaceutical substances
    • Intermediates for kinase inhibitor active ingredients
    • Registration-grade fine chemicals for finished oral and parenteral pharmaceuticals

    2. Agrochemical Intermediate for Pyridine-Structured Crop Protection Agents

    Major agrochemical producers employ this material in synthetic routes toward pyridine-based active substances such as insecticides, herbicides, and fungicides. Its chemical structure provides the necessary reactivity for building blocks that undergo chlorination, nitrile conversion, or arylation in the manufacture of target agrochemicals, supporting precise molecular design in compliance-driven production environments.

    Industry compliance standards

    • Conforms to FAO/WHO specifications for pesticide intermediates
    • Must follow REACH registration for use in Europe (EC No. 1907/2006)
    • Guided by local EPA (Environmental Protection Agency) manufacturing practice standards
    • Subject to ISO 14001 for environmental management during synthesis

    Typical usage ratio

    • Dosed at 0.8–1.1 equivalence relative to primary reactant in batch and continuous processes
    • May range from 5–15% w/w of total reaction mass, depending on process step and crop-protection agent synthesized
    • Usage fine-tuned according to real-time NMR or LC-MS conversion monitoring
    • Development runs typically test 85–100% of theoretical dosing for process optimization

    Downstream process integration

    • Introduced in late-stage nitrile condensation or coupling steps within multi-step pesticide synthesis
    • Integrated into continuous flow reactors for high-throughput arylpyridine assembly
    • Purified by aqueous workup or extraction ahead of final formulation
    • Serves as a critical starting material in modular synthesis for new actives registration

    Final product types

    • Pyridine-based insecticidal actives (e.g., neonicotinoids and analogues)
    • Herbicide and fungicide intermediates
    • Precursor to pesticide formulation concentrates
    • Custom crop-protection molecule libraries for developmental screening

    3. Specialty Material Intermediate for Liquid Crystal and OLED Component Synthesis

    Materials science companies producing advanced display components select this intermediate for synthesizing substituted pyridine derivatives essential in liquid crystal and organic light-emitting diode (OLED) technologies. Its precise structure supports downstream functional group modification, impacting electrical and optical properties vital to high-performance displays. Manufacturing lines apply rigorous process control to ensure batch consistency required by the electronics industry.

    Industry compliance standards

    • Production meets ISO 9001 and IECQ QC 080000 (electronic component manufacturing process certification)
    • Adheres to RoHS Directive for restricted use of hazardous substances in electronics
    • Monitored under JIS (Japanese Industrial Standards) for LCD/OLED material purity
    • Complies with customer-specific supply chain audit protocols

    Typical usage ratio

    • Charged at 0.9–1.05 molar equivalents in precursor stage for LC or OLED material synthesis
    • Usage varies by targeted molecular modification, 3–10% by mass for functionalized derivatives
    • Development projects may adjust ratio to 1.1–1.3 for novel conjugated core assembly
    • Batch and continuous processes evaluated for optimal input with in-line spectroscopy feedback

    Downstream process integration

    • Added to palladium-catalyzed coupling or nucleophilic substitution steps for advanced liquid crystal monomers
    • Participates in cyclization and condensation protocols for OLED emitter material synthesis
    • Product isolated by column chromatography or thin-film distillation, depending on purity target
    • Process steps designed to minimize contaminant carryover critical for device-grade output

    Final product types

    • Liquid crystal display (LCD) alignment layers and switching monomers
    • Small-molecule OLED emitter materials
    • Functional dyes for photonic and optoelectronic devices
    • Conjugated intermediates for advanced display chemistry libraries

    4. Fine Chemical Building Block in Advanced Research Chemical Supply

    Leading research institutions and chemical suppliers incorporate this compound into the custom synthesis of high-value research molecules, especially where the phenyl-substituted pyridine core enables structure-activity relationship studies. Formulations demand lot-specific purity and documentation for reproducibility in R&D settings, impacting early discovery across pharmaceutical, agricultural and material science innovation pipelines.

    Industry compliance standards

    • Manufactured under ISO 9001-certified quality management
    • Provided with batch-specific analytical data (NMR, HPLC, GC-MS traceability)
    • Meets internal trace metal and impurity benchmarks for research-grade intermediates
    • Documentation complies with GHS (Globally Harmonized System) MSDS and local transport regulations

    Typical usage ratio

    • Dosed between 1.0–2.0 equivalents in small-batch synthesis protocols, depending on screening target
    • Milligram to gram scale inputs adjusted based on lab-scale throughput needs
    • Excess equivalents may be used to drive reactions to completion in route scouting
    • R&D protocols document all formulation modifications for process transfer

    Downstream process integration

    • Utilized as early-stage scaffold in combinatorial library synthesis
    • Acts as arylation partner or nucleophile in exploratory coupling reactions
    • Subject to purification by prep-LC, recrystallization or distillation post-reaction
    • Reference standard for scalable synthesis route evaluation

    Final product types

    • Analytical reference molecules for pharmaceutical and agrochemical discovery
    • Building blocks for structure-activity relationship (SAR) campaigns
    • Intermediates for pilot synthesis of next-generation actives
    • Custom-synthesized compounds for academic and industrial research worldwide
    Free Quote

    Competitive 2-Chloro-6-Phenylnicotinonitrile prices that fit your budget—flexible terms and customized quotes for every order.

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

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    2-Chloro-6-Phenylnicotinonitrile: Practical Experience from the Production Floor

    Introduction to 2-Chloro-6-Phenylnicotinonitrile

    Among the many pyridine derivatives we have handled over the years, 2-Chloro-6-Phenylnicotinonitrile stands out for the combination of chemical stability and synthetic flexibility it delivers. We refer to its model number in the workshop as 2C6PNN—not a catchy name, but anyone who spends time in a real synthesis environment will tell you the value isn't in the product code, it's in the chemistry. In the plant, our team deals with ton-scale runs, high-purity isolations, and nuanced process control rather than small lab vials, and the differences become clear when batches need to meet the same targets week in and week out.

    Technical Details Come Alive in Production

    We manufacture 2-Chloro-6-Phenylnicotinonitrile by selective chlorination and aryl introduction steps that require strict process discipline. At an eye-level view, this chemical appears as a pale solid that blends a sharp chemical scent with notes familiar to anyone experienced with chlorinated aromatics. We validate every lot above the 99% mark using HPLC, with residual solvent limits that stand up to international scrutiny, because impurities come back to bite later in end-customer applications.

    Molecular formula is C12H6ClN2 and the molecular weight clocks in at 212.64 g/mol. Whenever a customer visits our plant, we emphasize how purity impacts downstream steps—whether you're working up an agrochemical intermediate or trying to launch a new pharmaceutical candidate, stray byproducts compound into headaches nobody wants.

    Real-World Applications from Those Who Make It

    In over a decade of making pyridine-based intermediates, the routes that use 2-Chloro-6-Phenylnicotinonitrile have proven robust for high-yield coupling and functional group manipulations. We see formulators order it for specialty pesticides and next-generation actives in crop science. Others pursue structure-activity relationships for pharmaceutical candidates, especially those looking for selective kinase inhibitors or anti-inflammatory agents. It's a backbone molecule where the benzonitrile motif plays a decisive role in potency and stability, not just decoration on a synthetic scheme.

    Our operators take pride in minimizing switch-over losses and batch variability, particularly for end-users working at metric ton scale where every pound of feedstock counts towards the bottom line. Having handled related compounds for years—from bare nicotinonitrile to its methyl, methoxy, and fluoro analogs—we're acutely aware of how subtle changes in ring or substituent affect solubility and reactivity. Our feedback from experienced R&D chemists shows 2-Chloro-6-Phenylnicotinonitrile performs better for Suzuki and Buchwald couplings when compared with more electron-rich or electron-poor pyridine variants, especially regarding side-product suppression.

    Product Differences: A Manufacturer’s Perspective

    Direct comparison with other substituted nicotinonitriles shows the value in the 2-chloro, 6-phenyl arrangement. If you remove the phenyl group, nucleophilic aromatic substitution slows down measurably, affecting process yields and costs for the end user. In cases where the chlorine isn't present, the site for cross-coupling all but disappears. Products with methyl at the 6-position instead of phenyl turn out to have lower stability in transit and occasionally pack poorly, a lesson we learned after field complaints during summer storage in high-humidity regions.

    Incorporating a phenyl at the 6-position balances electron density, supporting targeted reactivity in palladium-catalyzed transformations. We see purer profiles in finished goods from downstream customers, which translates into easier regulatory compliance and smoother scale-up. That isn't something you'll read in a generic catalog blurb—it's real feedback from ongoing technical support calls and joint troubleshooting when something gums up the customer’s reactor.

    Another difference comes in how 2-Chloro-6-Phenylnicotinonitrile handles in bulk. After optimizing our crystallization step, the bulk powder flows with minimal caking, easing handling for continuous dosing systems. Comparisons with similar pyridine intermediates from other manufacturers confirmed a tighter particle size distribution, which matters for facilities automating their slurry feeds. Particle engineering does not show up in a chemical formula, but it changes the job for everyone from the warehouse operator to the research chemist.

    Our Experience Shaping Production and End-Use

    Many years ago, our pilot plant struggled with color impurities in this compound. After investigating, we traced the culprit to trace oxidized byproducts from a chlorine bleed that ran too hot. A shift in carrier gas flow and a stepwise cooling schedule fixed the problem, drastically reducing byproduct formation. Lower color means easier further purification for our customers, especially where light-sensitive downstream processes run the risk of introducing discoloration that might trigger unnecessary batch rejections.

    Our team regularly talks to end-users dissatisfied with off-the-shelf material that claims identical purity but behaves unpredictably in their processes. Some blame it on batch-to-batch variation. Our batch logs tell the tale—slight deviations during the exotherm or crystallization cause shifts in particle size or incorporate trace impurities. Sticking to a rigid, validated process reduces the chance of those headaches rediscovering themselves in a customer's facility. Anyone who's lost a week to plugging valves or reprocessing material understands the value of consistent, high-purity feedstocks.

    From a manufacturing oversight standpoint, our equipment must hold up to both corrosive chlorination stages and aggressive organic workups. Higher-grade alloys used in reaction and storage vessels don’t just protect our capital, they keep contaminants from seeding impurity growth—yielding a cleaner product for our customers. Stainless steel imparts no flavor, so to speak, but anyone who has dealt with rusty residues knows the nightmare of trying to clean up after a substandard reactor. Reliability counts at every scale.

    Sustainability and Safety Practices as Daily Routines

    Most of the push for “green” comes from policy and regulation, but as producers we learn quickly that minimizing waste cuts real operating costs. With 2-Chloro-6-Phenylnicotinonitrile, recapturing solvents pays back within a year. Proper scrubbing of chlorinated off-gases doesn’t just keep in line with emissions rules, it keeps our neighbors happy and reduces unplanned shutdowns triggered by environmental complaints.

    Safety isn’t a buzzword in the plant. Chlorination reactions mean a single oversight invites acid formation or runaway exotherms. Our teams receive annual retraining on process hazards, emergency shutdown procedures, and respirator use specific to every process step. Small changes—better draining points or extra cooling jackets—make the difference between smooth production and emergency interventions. Real-world safety goes beyond paperwork to culture and vigilance, day in and day out.

    We maintain closed transfer lines and double-sealed pumps to keep area concentrations below occupational exposure limits. Even apparently low-concern compounds like nicotinonitriles call for solid containment policies, as lessoned from handling generations of analogs. Process byproducts require treatment, whether liquid or vapor—a lesson no manufacturer forgets after dealing with local water utility inspections, especially with the persistent attention drugs and pesticides attract in global supply chains.

    Global Supply, Regulations, and Traceability

    Cross-border shipments for active intermediates bring complexity, because material origin and traceability can affect regulatory submissions, registration times, and final launch timings. Our systems record each step from sourcing of starting pyridines through dispatch of final drums, time-stamped and ready for audit. Auditors often arrive thinking documentation hides gaps, only to discover that digital logs lay out every charge, evacuation, temperature adjustment, and inspection—in effect, a chemical’s biography that matches the reality on the floor.

    Customers working on regulatory filings emphasize the importance of up-to-date impurity profiles and batch histories for compliance with authorities from the US FDA to the EU REACH system. We respond by running full panels on heavy metals, residual solvents, and relevant trace byproducts. Only experience teaches how a “minor” unknown peak at sub-ppm range can scuttle a new product introduction or trigger inquiries down the supply chain. We have learned to get in front of these challenges by systematic, repeated impurity tracking and timely communication to our partners, saving months of regulatory back-and-forth.

    Long-term traceability becomes more than an afterthought—a recall or investigation years down the line draws on records, product identification, and chain-of-custody controls. We grew our electronic systems organically, anchored in actual queries and requests from end-users, not hypothetical "best practices" promoted by consultants. A robust traceability system isn’t just for the legal department; it proves essential every time a nonstandard impurity crops up and the source must be pinpointed without delay.

    Perspectives from Decades in the Plant

    Over the years, requests for specialized blends or adjusted particle sizes have shaped the way we approach the market. Some customers required dust-free granules, others wanted micronized powder for direct dissolution. In every case, close contact between our process team and the customer’s formulation group saw us running lab, pilot, and production trials on both sides. Years ago, a client required a dechlorinated variant mid-development—a problem that, due to shared technical input, we resolved within a month by creating an offshoot process still in use today.

    Sometimes challenges come from logistics, not formulation. An overseas partner experienced caking under humid port conditions, so we retooled our packaging and modified desiccant loading schedules. The improvements cut damage claims by more than half, taught us all to never take “standard” warehouse conditions for granted, and led to tighter partnerships built on real-world solutions, not sales pitches. Handling feedback from operators as well as plant engineers, we learn to anticipate problems before they escalate.

    We track color, flow, and stability scores from every batch in the last ten years, seeking variances and predicting trends. Barcodes and RFID enabled us to create forensics-level batch reconstruction, allowing our operators to work more intelligently and keep efficiency high. Meal breaks, unusual weather patterns, and even time-of-day cooling cycles appear in batch logs—a level of detail inspired not by regulation, but by experience chasing down root causes for outlier results.

    Opportunities and Challenges Ahead

    As more sectors adopt data-driven process control, the need for traceable, high-purity intermediates only increases. Customization now extends past just functional group placement—it covers everything from regulatory alignment to advanced supply planning. The experience we’ve built making 2-Chloro-6-Phenylnicotinonitrile over hundreds of production lots now forms the backbone of our approach to problem-solving for new and existing partners.

    Rising expectations around clean chemistry and circular supply chains continue to push technology inside the plant. New filtration units, online impurity monitors, and alternative energy inputs promise to keep this product compatible with both customer requirements and the planet. What never changes is the need to match technical performance with commercial realities—bulk availability, on-schedule delivery, and responsive support.

    Having lived through cycles of surplus and shortage, the best surprise remains a reliable, high-quality supply that eliminates process interruptions downstream. As producers, we value long-term customer relationships grounded in technical trust, shared transparency, and the cumulative knowledge gained through solving real-world problems together. The story of 2-Chloro-6-Phenylnicotinonitrile is one of constant adaptation—balancing chemical rigor with operational flexibility, always rooted in the realities of production and end-user satisfaction.