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Nicotinoyl Chloride Hydrochloride

    • Product Name Nicotinoyl Chloride Hydrochloride
    • Alias Nicotinoyl chloride hydrochloride
    • Einecs 243-813-6
    • 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

    402021

    Cas Number 16016-39-0
    Molecular Formula C6H5Cl2N2O
    Molecular Weight 191.03 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 174-176°C
    Solubility Soluble in water and organic solvents
    Storage Condition Store at 2-8°C, keep container tightly closed
    Purity Typically ≥98%
    Synonyms 3-Pyridinecarbonyl chloride hydrochloride
    Hazard Class Corrosive

    As an accredited Nicotinoyl Chloride Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Nicotinoyl Chloride Hydrochloride, 25g, is packaged in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping Nicotinoyl Chloride Hydrochloride should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It must be handled as a hazardous material, with appropriate labeling and documentation, and transported under temperature-controlled conditions if required. Ensure compliance with local, national, and international regulations for chemical transportation.
    Storage Nicotinoyl Chloride Hydrochloride should be stored in a tightly closed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases and oxidizing agents. Store at room temperature or refrigerated, as specified on the manufacturer’s label. Always follow local regulations and safety guidelines for handling hazardous chemicals.
    Application of Nicotinoyl Chloride Hydrochloride

    Applications of Nicotinoyl Chloride Hydrochloride in Industrial Manufacturing

    Nicotinoyl Chloride Hydrochloride serves as a critical intermediate in specialized chemical manufacturing processes. We supply this material directly from our production facility for use in several focused downstream industries. Below we detail principal industrial applications, addressing real compliance requirements, recommended formulation ratios, integration methodology, and representative final product outcomes in each scenario.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers use Nicotinoyl Chloride Hydrochloride for synthesizing nicotinic acid derivatives, including new generation pyridine-containing APIs. During multi-step synthesis, this compound acts as an efficient acylating agent under controlled anhydrous conditions. QC protocols demand careful monitoring of residual chlorides, pyridine-related impurities, and compliance with international pharmacopoeial monographs. High purity is essential for meeting GMP batch release.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • United States Pharmacopoeia (USP)
    • European Pharmacopoeia (EP)
    • 21 CFR Part 211 (FDA cGMP for finished pharmaceuticals)

    Typical usage ratio

    • 0.85–1.05 molar equivalents per target pyridine ring in route-specific batch protocols
    • Ratio adjusts based on impurity control requirements and step yield optimization

    Downstream process integration

    • Introduced post-nitration and pre-amidation in pyridine core assembly
    • Reacts under low-moisture, temperature-controlled conditions in glass-lined reactors
    • Followed by hydrolysis, amination, or esterification steps depending on the route

    Final product types

    • Nicotinic acid-based active pharmaceutical ingredients (APIs)
    • Intermediate compounds for anti-tuberculosis, cardiovascular, and neuroprotective drugs
    • Pyridine amide derivatives registered in regulatory filings

    2. Agrochemical Intermediate Production

    Major agrochemical synthesis chains utilize this material for the construction of pyridine carboxamide frameworks. Vendors employ it as an acylating reagent when making complex herbicide and fungicide intermediates. Production lines specify input purity and batch traceability records, as strict compliance with agrochemical manufacturing guidelines and European and US chemical safety directives is mandatory.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for agricultural chemicals
    • REACH (EC No 1907/2006) Registration and Evaluation of Chemicals
    • EPA FIFRA (for United States-purposed agrochemicals)

    Typical usage ratio

    • 1.0–1.2 molar equivalents per target functional group in the carboxamide synthesis step
    • Batch chemists sometimes elevate dosage up to 1.3 equivalents to drive full conversion

    Downstream process integration

    • Added following initial ring chlorination to form activated pyridine intermediates
    • Used in closed-system reactions with regulated emissions capture
    • Further processed by amination or cyclization to yield final actives

    Final product types

    • Pyridine-based herbicide intermediates (e.g., for synthesis of picolinamide herbicides)
    • Fungicide actives containing a nicotinoyl moiety
    • Synthesis blocks for insecticide formulations

    3. Specialty Dye and Pigment Manufacturing

    In colorant manufacturing, this intermediate enables the targeted functionalization of pyridine rings in the design of high-performance dyes and organic pigments. Producers use it in acylation reactions to modify chromophoric groups under tightly controlled temperatures. Compliance with colorant-grade purity specifications as well as regional ecological and workplace safety directives remains essential throughout production.

    Industry compliance standards

    • EN 71-3 (Migration of certain elements in toys and pigments)
    • German BfR Recommendations (Colorants for Food Contact Materials)
    • ISO 9001 for pigment manufacturing process control

    Typical usage ratio

    • 0.9–1.1 equivalents per functional group in pigment precursor synthesis
    • Range may be increased up to 1.15 in high-purity dye batches

    Downstream process integration

    • Fed during late-stage chromophore functionalization or pigment precursor acylation
    • Requires controlled ventilation and solvents to limit occupational exposure
    • Intermediates undergo further purification, crystallization, or granulation after modification

    Final product types

    • Pyridinyl-based organic pigments for plastics, coatings, and inks
    • Specialty dyes for textile and digital printing industries
    • Colorant intermediates used in high-stability automotive or industrial formulations

    4. Fine Chemical & Research Reagent Formulations

    Research institutes and custom synthesis firms rely on this raw material for constructing pyridine-derived ligands, catalyst components, and research reagents. Highly specialized documentation, batch homogeneity, and impurity profile control are required to meet both research-grade and semi-industrial reagent specifications. International shipment mandates additional hazard communication and documentation for laboratory use.

    Industry compliance standards

    • ISO 17034 Reference Material Producer standards
    • OECD Test Guidelines (for research use only chemicals)
    • GHS/CLP Regulation (EC) No 1272/2008 labeling and SDS requirements

    Typical usage ratio

    • Typically 0.95–1.1 molar equivalents, adjusted to minimize excess and cleanup time
    • For highly selective ligand synthesis, precise stoichiometry is enforced

    Downstream process integration

    • Charged into custom synthesis steps for ligand or pyridine complex assembly
    • Applied within glovebox or inert atmosphere setup for air-sensitive reactions
    • Reaction byproducts managed by validated laboratory disposal streams

    Final product types

    • Pyridine-derived metal ligands for catalytic processes
    • Analytical-grade research reagents
    • Small-batch custom fine chemical building blocks
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    Certification & Compliance
    More Introduction

    Nicotinoyl Chloride Hydrochloride: A Closer Look from the Manufacturer’s Floor

    Understanding the Substance in Context

    Within our chemical production facilities, Nicotinoyl Chloride Hydrochloride has established its reputation as a specialty intermediate, playing an irreplaceable part in custom synthesis and API manufacturing. This compound, known within trusted technical circles as 3-Pyridinecarbonyl chloride hydrochloride, stands apart from its analogs through its relational chemistry. Over the years, our process technicians and chemical engineers have observed that while nicotinic acid and its derivatives attract wide attention in the market, their transformation paths often center around coupling, amidation, and acylation. Nicotinoyl Chloride Hydrochloride emerges as the reactive bridge, reliably granting access to new compounds without the process headaches seen with many other chlorides.

    Process Consistency and Quality Considerations

    Direct feedback from production and quality control underscores why this intermediate remains a mainstay. Batch after batch, our controlled process ensures a crystalline, off-white to pale yellow solid—easily handled in standard atmospheric conditions, despite its reactivity. Our typical specification centers on purity not less than 98 percent, tailored to advanced synthetic routes. The hydrochloride salt form holds strategic advantages. Free-base nicotinoyl chloride presents storage and handling risks, with greater sensitivity to moisture and potential for rapid hydrolysis. As the hydrochloride, stability improves, risking less during shipment or in extended storage. Our operators find that this makes it possible to deliver material that matches closely the requirements of demanding downstream synthesis lines, whether destined for API precursors or specialty agricultural applications.

    Sitting Between Academia and Industry

    Chemists, whether in a drug discovery group or a process plant, look for pragmatic tools to push molecular modifications. Nicotinoyl Chloride Hydrochloride fills this need at scale. Its elegance stems from the ease with which it forms nicotinamide bonds, making it an essential building block for synthesizing modified vitamin B3 derivatives, bioactive heterocyclic molecules, and a range of complex amides. Secondary and tertiary amine chemistries exploit this acidity and reactivity, frequently gaining high conversion rates and lower side-product profiles compared to using free acids or other acid chlorides. Lab accounts highlight how this intermediate outperforms other acylating reagents in clean reaction workups and manageable byproducts.

    Practical Aspects of Handling and Usage

    Experience on our manufacturing lines makes clear the importance of maintaining dry, inert conditions, especially at transfer points. Freshly prepared Nicotinoyl Chloride Hydrochloride, handled under nitrogen and packed in high-barrier containers, retains reactivity and reduces dusting, keeping losses within minimal thresholds. Chemists consistently report rapid acylation, especially with amines and alcohols, even at mild temperatures. Unlike benzoyl chloride or isonicotinoyl chloride, reactions proceed with softer profiles, which matters for protecting sensitive functional groups.

    Operators notice this difference as soon as they monitor the reaction: the hydrolysis rate drops, giving more time for careful addition and improved scale-up prospects. Issues such as byproduct formation and hydrogen chloride evolution receive comprehensive mitigation thanks to the solid form, which generates less fuming than its liquid counterparts. The hydrochloride salt’s manageable reactivity eases the path to high-purity products, reducing cycle times in purification stages downstream. Wastewater treatment teams also record fewer spikes in volatile organic loads during both production and end-user blending.

    Why Substitution Matters

    In pharmaceutical and agrochemical synthesis, the demand for selective, high-conversion coupling steps never fades. Some research teams gravitate toward alternatives, such as isonicotinoyl chloride, hoping for positional differences or better compatibility. Yet, close trials show that the para-positioned isomer imparts unique properties, often favoring electron-donating partners, sometimes at the expense of yield or solubility. Nicotinoyl Chloride Hydrochloride’s ortho- and meta-reactions build richer scaffolds, especially when aiming for tailored heterocycles or unique flavor and fragrance agents. For seasoned synthetic chemists, these differences hold genuine utility, not just on paper but in actual batch yields and product consistency.

    With access to full analytical capabilities on-site, including HPLC, GC-MS, and NMR, our team supports customer discoveries about this molecule’s reactivity. Feedback confirms that this intermediate opens new doors in peptide coupling, modified nucleoside synthesis, and the preparation of sophisticated insecticides or fungicides. One group of medicinal chemists, reporting after a challenging kinase inhibitor project, pointed to sharper N-acylation efficiency and significant reductions in column purification steps—leading to higher batch throughput and lower solvent usage.

    Real-World Logistics and Customer Requirements

    Shipping and storage standards matter far more than most realize when working with moisture-sensitive intermediates like Nicotinoyl Chloride Hydrochloride. Pure acid chlorides risk partial decomposition even during short journeys through humid zones. Years in export taught our logistics team the importance of double-lined drums, low-permeability bags, and date-stamped outgo records. Customers rarely see these steps, but the unmistakable product consistency on arrival makes a real business case.

    Shelf life remains robust under recommended conditions—usually at least 18 months—making inventory turns predictable for both the manufacturer and end user. Formulation chemists in fine chemicals appreciate the ability to pull from stock without concern for degradation or altered melting points. End-use reports often describe material arriving in free-flowing crystalline form, without the caking or yellowing seen if exposed to excess moisture or heat.

    Driving Innovation and Cost Efficiency

    In our own laboratories, we constantly probe new routes—sometimes finding alternatives to classic acyl chloride chemistry. Yet the truth remains: Nicotinoyl Chloride Hydrochloride delivers reliable results and streamlines scale-up from gram to multi-ton levels. Our R&D chemists point to the shortened reaction times and fewer side reactions, enabling easier process validation in regulated pharma sectors. In one toll manufacturing campaign, switching from traditional carbodiimide activation to direct acylation using this intermediate trimmed several hours off the process, lowered input costs for solvents, and met strict impurity profiles demanded by customers.

    Production floor teams, who run large-scale reactors, value the controlled exotherms and lower gas evolution during charge. Maintenance staff benefit from reduced corrosion on lines and valves because the hydrochloride salt offers less aggressive fuming than other chlorides or acid anhydrides. Such practical realities influence process economics and maintenance schedules more than most theorists calculate.

    Comparisons to Other Chloride Intermediates

    Direct experience underscores the subtle but real distinctions between Nicotinoyl Chloride Hydrochloride and other acyl chlorides handled in our facilities. Benzoyl chloride, while powerful, comes with a much harsher fume profile and offers limited selectivity for heterocyclic synthesis. Acetyl chloride, though cost-effective, falls short in building more elaborate frameworks or structures needed in complex APIs.

    Nicotinoyl Chloride Hydrochloride’s gentle handling, ability to generate high-purity acylated products, and improved storage profile set it apart in both plant operations and synthetic outcomes. Our team’s cross-comparisons reveal that this intermediate delivers more reproducible batch yields in targeted applications, especially where N-heterocycles or functionalized pyridines rank as key goals. End-users in industrial biotech comment favorably on its compatibility with biocatalytic and chemoenzymatic processes—a spreading trend in greener, more sustainable production.

    Downstream Impact and Environmental Perspective

    Every step from raw materials sourcing to effluent treatment builds the full picture of an intermediate’s value. Our stewardship programs track input waste and process byproduct streams. Use of Nicotinoyl Chloride Hydrochloride often minimizes waste acid, requiring only simple neutralization, lessening regulatory burdens and disposal costs. Plant data over successive campaigns confirm that swapping from anhydrous free chlorides to the hydrochloride salt cut vent scrubber loads by over 25 percent—translating to real energy savings and lowered carbon impact.

    On the health and safety side, production teams comment on the improved air quality in areas where the hydrochloride salt prevails. Dust control and dermal exposure issues, perennial hazards with fine acids and basic powders, reduce sharply due to the compound’s solid crystalline nature and lack of volatile organics. This translates to lower occupational exposure levels and simplified compliance with workplace regulations.

    Feedback Loops and Technical Collaboration

    We listen closely to customer feedback and research partner questions. Regular technical exchanges with industrial users outline pain points in their processes, ranging from solvent compatibility to batch reproducibility. Production trials in-house actually shifted drying and milling protocols, boosting flow properties and reducing caking. Analytical chemists regularly refine the material’s fingerprint, ensuring each lot matches historical benchmarks—an output of the kind of longitudinal oversight that only manufacturers who touch every stage can provide.

    Several contract research organizations working with us praise the ease of integrating Nicotinoyl Chloride Hydrochloride into automated synthesis platforms. With automation picking up speed across all chemical fields, this predictability and stability mean less rework and higher confidence for both small-batch and continuous flow chemistry setups. If a batch diverges from standard, rapid communication from our QA lines to customers keeps everyone aligned, trimming downtime and surprises in external operations.

    Material Safety, Storage, and Sustainable Practice

    Historically, acid chlorides have posed persistent challenges for safe design and waste minimization at scale. Choosing the hydrochloride salt over alternatives with more dangerous profiles brings benefits beyond reactivity. Less off-gassing and better control of hydrolytic instability lighten the load on air emission controls. Field audits, conducted as part of both ISO and GMP programs, show better track records for container integrity and reduced spoilage across shipping routes. For our customers, this means less documentation of loss and lower risk of rejected shipments.

    Storing Nicotinoyl Chloride Hydrochloride needs only cool, dry conditions away from incompatible oxidizing agents, much like other specialty solids. There is no requirement for elaborate refrigeration or double-bund containment. In process room practice, charge teams find this translates into real, routine ease: evacuating drums involves minimal risk, and returned containers rarely fail integrity checks.

    The Human Element Behind the Molecule

    From R&D benches to shipping docks, people shape every ton of Nicotinoyl Chloride Hydrochloride moving out of our facilities. Chief process engineers, in consultation with synthesis and analytical chemists, drive workflow improvements and lead hazard reviews. Line operators handle day-to-day challenges during charging and packaging, intercepting problems before they reach customers. Maintenance and warehouse crews provide insight into drum storage layouts, ventilation needs, and container reuse programs.

    Every improvement, whether in lot-to-lot color stability or minor tweaks to drying cycle times, comes from direct observation and iterative problem-solving. Our plant schedules reflect a clear reality: customers expect a product they can trust on delivery and in their syntheses. The best supply partnerships grow out of consistent production, transparent communication, and a shared drive to solve evolving process demands.

    Learning Together—Evolution of a Specialty Intermediate

    Markets change, regulatory demands shift, and new research fronts continue to emerge across life sciences and materials engineering. Our longstanding involvement with Nicotinoyl Chloride Hydrochloride has shaped technical knowledge about pyridine-based intermediates and the requirements behind their selection. In pharma, crop protection, and advanced materials, application scientists increasingly favor flexible, predictably reactive intermediates. This compound’s synthesis, storage, and performance reinforce its profile across both established and evolving chemical sectors.

    Collaborative research projects highlight growth in demand for cleaner synthetic steps, less corrosive process agents, and flexible acyl group donors. Results like faster reaction monitoring, easier waste water management, and fewer off-spec lots reflect the shared gains of working in step with active feedback from users. For us, each drum shipped represents not just a commodity but a building block for new breakthroughs—delivered reliably, informed by years at the manufacturing front line.

    Looking Forward: Meeting New Challenges

    We balance decades of experience producing Nicotinoyl Chloride Hydrochloride with a commitment to innovation and adaptive scale-up. Our engineers invest time in refining process steps, while formulation teams test compatibility with newer solvents and reaction media, keeping pace with shifting customer preferences and sustainability targets. Scaling up to meet rising demand, without sacrificing batch consistency, means regular review of reactor designs, filtration technologies, and packaging logistics.

    As end-use trends drift toward green chemistry, less waste, and energy-smart operations, the unique combination of reactivity and manageability in this product continues to deliver practical advantages. Plant teams undertake regular training, updating both safety protocols and handling best practices as regulations or market expectations evolve. The human drive to improve efficiency, lower environmental footprint, and deliver on chemistry’s toughest challenges remains the core of our commitment to each customer—now and in the future.