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4-Pyridylacetonitrile Hydrochloride

    • Product Name 4-Pyridylacetonitrile Hydrochloride
    • Alias 4-(Cyanomethyl)pyridine hydrochloride
    • Einecs EINECS 204-746-0
    • 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

    387509

    Product Name 4-Pyridylacetonitrile Hydrochloride
    Cas Number 3619-56-9
    Molecular Formula C7H7N2Cl
    Molecular Weight 154.6 g/mol
    Appearance White to off-white solid
    Melting Point 195-200°C (dec.)
    Solubility Soluble in water and polar organic solvents
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms 4-(Cyanomethyl)pyridine hydrochloride
    Structure Pyridine ring with a cyanomethyl group at position 4 and a hydrochloride salt
    Inchi Key FUQXTQIKDIKXJA-UHFFFAOYSA-N

    As an accredited 4-Pyridylacetonitrile Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 4-Pyridylacetonitrile Hydrochloride is provided in a sealed amber glass bottle with a secure screw cap.
    Shipping 4-Pyridylacetonitrile Hydrochloride is shipped in tightly sealed, chemical-resistant containers to protect from moisture and light. Packaging complies with relevant safety and transportation regulations for chemicals. It is labeled with hazard, handling, and storage information, and shipped via certified carriers, ensuring temperature control and secure handling to maintain product integrity during transit.
    Storage 4-Pyridylacetonitrile Hydrochloride should be stored in a tightly sealed container, away from moisture and light, in a cool, dry, well-ventilated area. The chemical should be kept at room temperature (15–25°C) and separated from incompatible substances such as strong oxidizing agents. Proper labeling and secure storage are essential to prevent accidental exposure or contamination.
    Application of 4-Pyridylacetonitrile Hydrochloride

    Applications of 4-Pyridylacetonitrile Hydrochloride in Industrial Manufacturing

    As a manufacturer of high-purity 4-Pyridylacetonitrile Hydrochloride, we supply this specialty intermediate into a range of demanding industrial application fields. Our focus includes key downstream segments in agrochemicals, pharmaceuticals, specialty dyes, and advanced material synthesis, where strict compliance, established ratios, and precise process control are fundamental for consistent product quality.

    1. Agrochemical Intermediate Synthesis

    Major crop protection companies employ this compound as a pyridine-based building block for synthetic routes toward selective herbicides. The molecule’s nitrile functionality facilitates further functionalization, such as in cyclization or nucleophilic substitution reactions, unlocking access to diverse heterocyclic actives. Most integrated agrochemical plants incorporate it downstream from primary aromatics distillation, prior to the main active molecule assembly. It is sourced in lots sized for batch or continuous input, and must meet pesticide-grade specifications for purity, trace impurities, and moisture content for compliance with international agricultural standards.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 25157:2021 – Pesticides and Agrochemicals
    • REACH Registration (EC No. 1907/2006) for use as agrochemical intermediate
    • Chinese GB 20622 National Standard for Pesticide Intermediates

    Typical usage ratio

    • Batch processes: 0.95–1.15 equivalents relative to the core aromatic amine input
    • Ratio can vary based on target herbicide structure and impurity control measures

    Downstream process integration

    • Introduced immediately before heterocyclization or amidation step
    • Handled in closed reactors with nitrogen blanketing for moisture and oxygen control
    • On-line QC sampling for nitrile conversion rate and residual solvent removal

    Final product types

    • Pyridine-substituted herbicide actives
    • Pre-emergent weed control formulations
    • Intermediate salts for registered crop protection products

    2. Pharmaceutical API Intermediate

    Our material supports the synthesis of pyridine-containing pharmaceutical intermediates in regulated GMP environments. Many drug substances with central nervous system, anti-infective, or oncology action leverage this raw material at early or late-stage coupling. Operators must recertify each incoming lot against relevant pharmacopoeial monographs, and it is typically handled under controlled temperature and humidity to avoid hydrolysis. Multi-step active ingredient syntheses rely on its high reactivity in carbon–carbon bond-forming and further derivatization chemistries.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP-NF Monographs (if relevant intermediate listed)
    • European Pharmacopoeia General Chapters for intermediates
    • 21 CFR Part 211 – Current Good Manufacturing Practice for Finished Pharmaceuticals

    Typical usage ratio

    • 1.00–1.10 molar equivalents relative to primary amine coupling partner
    • Adjustment made based on impurity burden and step yield optimization

    Downstream process integration

    • Charged during intermediate step of multi-stage synthesis, following initial purification under GMP isolation
    • Reaction performed in solvent systems (e.g., DMF, MeCN) with real-time HPLC monitoring
    • Post-reaction, mother liquors transferred for subsequent ring-closing or side-chain extensions

    Final product types

    • Pyridine-based pharmaceutical intermediates
    • Oncology drug building blocks
    • CNS active ingredient cores
    • Advanced intermediates for final step API syntheses

    3. Specialty Azo and Reactive Dye Manufacture

    4-Pyridylacetonitrile Hydrochloride is utilized by specialty dye manufacturers to introduce basic pyridyl groups into advanced azo and reactive dye structures. The intermediate’s controlled reactivity is advantageous in the diazotization and coupling stages for pigment products targeted toward high-end textile and paper applications. Dyehouses may require custom specifications for particle size, trace metal content, and aqueous solubility to improve blending and application properties during spray-drying or granulation steps.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textiles
    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • China GB 17592 National Textile Product Safety Technical Code
    • REACH Declaration of Safe Use, specifically for dye intermediates

    Typical usage ratio

    • 0.90–1.05 mole per mole of diazonium core, adjusted for shade control and purity retention

    Downstream process integration

    • Introduced at the coupling stage under controlled pH and temperature
    • Batch or continuous feeding ensures uniform color development
    • Followed by crystallization, filtration, and spray-drying as per end-use specification

    Final product types

    • Pyridine-substituted azo textile dyes
    • High-performance ink-jet printing pigments
    • Reactive dyes for cellulose-based fibers

    4. Electronic Materials and Conductive Polymer Precursors

    Advanced material producers exploit the pyridine core as a key intermediate in the design of precursors for conductive polymers and optoelectronic films. R&D and pilot-scale production lines employ stringent purity and residual inorganic specification to support high-value downstream applications. The compound is typically processed in air-free conditions, and batch traceability is essential for electronics-grade final products, which undergo extensive electrical and performance testing before end use.

    Industry compliance standards

    • IEC 60749-1 for semiconductor process chemical purity
    • IPC-4562 for base material controls in electronics
    • Chinese GB/T 39498 for electronic chemicals and specialty intermediates
    • Internal QC specifications for emissions and ionic contamination (major electronics houses)

    Typical usage ratio

    • Loaded at 1.00 equivalent relative to backbone monomer
    • Feed ratio modified for electrical property tuning and polymerization kinetics in pilot lines

    Downstream process integration

    • Metered into inerted reactors for precursor synthesis
    • Subjected to post-processing with acid/base treatment to stabilize desired moieties
    • Intermediate handled under dry box or controlled cleanroom conditions

    Final product types

    • Pyridine-containing conductive polymer prepolymers
    • Precursors for OLED and printable circuit materials
    • Photoresist additive intermediates
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    Certification & Compliance
    More Introduction

    4-Pyridylacetonitrile Hydrochloride: A Manufacturer’s Perspective

    Reshaping Fine Chemical Synthesis with High-Purity Pyridyl Reagents

    Within the chemical landscape, manufacturers know how subtle changes in structure and quality can reshape the entire project timeline. Speaking from the experience of years spent developing and scaling up challenging nitrogen-containing compounds, 4-Pyridylacetonitrile Hydrochloride has proven itself a workhorse in the hands of capable chemists. Its clear performance, reliability, and consistency have driven its adoption across a variety of applications.

    This compound, often abbreviated as 4-PAN HCl, brings an essential pyridine motif to a variety of synthetic strategies. The hydrochloride salt helps reduce volatilities compared to the free base, delivering a crystalline solid that simplifies handling, weighing, and reaction setup. In practical terms, our batches consistently achieve purity levels above 99%, cut after meticulous recrystallization, vacuum drying, and independent chromatographic verification.

    Solid Science, Dependable Outcomes

    Chemists have come to expect strict lot consistency and full transparency throughout the synthesis and isolation. 4-PAN HCl stands out by meeting those standards on a commercial scale. From the early R&D bench to hundred-kilo runs, our plant teams and QC chemists put every batch through full NMR, GC-MS, HPLC, and water content analyses. Any indications of starting material, isomeric contaminant, or unwanted side products prompt a review of catalyst charge, solvent volumes, and crystallization rates. Over time, this vigilance pays off in smoother downstream transformations and fewer setbacks from unexpected impurities.

    Instead of seeing the hydrochloride as a mere alternative to the free base, our customers recognize its enhanced shelf stability. Moisture pickup and atmospheric degradation pose less trouble, allowing extended storage without drifting purity or troublesome decomposition. Production managers appreciate that this reduces requalification testing and lowers cost-of-goods for projects with long supply timelines. This isn’t possible with less stable, more sensitive analogs or with lots sourced from inconsistent suppliers.

    The Pursuit of Reliability

    Consistency matters in the hard world of scale-up. Analysts look for crisp melting points and straightforward peak overlays, and 4-PAN HCl delivers. Each lot receives a unique tracking number, pulled directly from our controlled walk-in storage. Material stays double-bagged in sealed fiber drums, limiting exposure to air and low-level organic vapors. Our laboratory staff audit long-term stability by re-testing reserve samples from years-old productions, confirming that this salt remains chemically sound well beyond the typical shelf-life window.

    Experience tells us users return to reliable reagents not out of habit, but because months of project work hinge on each input’s reproducibility. Project scientists and procurement managers alike contact our technical team about meeting custom assay requests, adapting volumes, or accelerating documentation. Handling those needs smoothly comes from the discipline of doing one thing well, over and over, until every blind spot is addressed. As the original manufacturer, we remain close enough to the process to maintain those margins.

    Broader Utility in Modern Synthesis

    Within medicinal chemistry, heterocyclic scaffolds form the backbone of modern therapeutics. The demand for nitrogen scaffolds, particularly those featuring pyridyl rings, keeps growing. 4-Pyridylacetonitrile Hydrochloride fills a niche: introducing a cyanomethyl group para to the nitrogen atom. This opens direct access to a wealth of custom derivatives, including amides, amines, and carboxylic acids.

    Most use cases exploit its reactivity in either alkylations, condensations, or reductions. Medicinal chemists employ it for rapid SAR campaigns that demand grams to tens of kilograms, whether for library buildouts, pilot clinical batches, or intermediate production. Because we optimize for high solubility and a robust crystal form, the hydrochloride salt coefficients linearly from small flask runs through to glass-lined reactor campaigns. This keeps productivity high while safely limiting volatilization and trace impurity buildup, both of which have sabotaged competing salts or less-controlled free bases.

    Clear Differences From Competing Materials

    Some compounds exist in a market saturated by indistinguishable versions from multiple sources. 4-PAN HCl hasn’t reached quite that level. Direct analogs such as 2-Pyridylacetonitrile or the parent acetonitrile derivatives display valuable reactivity, but the para-nitrile arrangement in 4-PAN toggles distinct electronics over the heterocycle. This simple difference guides downstream selectivity. For teams working on novel kinase inhibitors, antibacterial frameworks, or agrochemical candidates, that selectivity means new lead structures and less time spent re-optimizing protecting group schemes.

    Our own synthetic routes favor high-atom economy and negligible formation of unwanted regioisomers. The main impurities—primarily traces of 3-PAN, dimerized byproducts, or chloride analogs—are quantified to below 0.2%, supported by updated certificates of analysis for each delivery. Scalability doesn’t cost us purity or crystalline size uniformity. Teams running kilogram orders appreciate that the process holds up at both pilot and commercial scale, with similar filtration and drying profiles at every increment.

    Process Development and Manufacturing Challenges

    In the old days of custom nitrogen chemistry, new compounds often brought headaches: color impurities, hydrolysis, and poor batch repeatability. Those pain points taught us hard lessons about water content, solvent polarity, and time standing solutions at different temperatures. At early stages, moisture intrusion could force complete batch rejection. Setting up temperature tracks and sealed reactors, along with regular validation of desiccant beds, let us minimize those risks well ahead of shipping.

    Trace metals and residual solvent loads often trigger regulatory flags in regulated pharma routes. Thorough validation of each batch, confirmed by ICP-MS for metals and Karl Fischer titration for water, has kept clients’ compliance teams satisfied year after year. Our plant engineers have also cut cycle times, lowering waste load and solvent carryover by reformulating wash and mother liquor streams. These hard-won process optimizations matter more than theoretical ideals; they decide which supplier gets picked for the next multi-tonne long-term contract.

    Export, Packaging, and Documentation

    Chemical transportation is rarely simple, especially when products move from one region’s regulatory system to another’s. We work directly with shipping agents to ensure all critical documentation, including proper labeling, full lot traceability, and certificates of analysis, travels ahead of the physical product. Polyethylene-lined fiber drums or sealed HDPE bottles protect the hydrochloride salt from ambient humidity and accidental spillage. Our teams have pre-cleared most common Incoterms, shaving days from delivery schedules domestically and abroad.

    Each packaging lot travels with original manufacturer's sealed QA reports, MSDS, and, if necessary, clearance for residual solvents. Over the years, we’ve learned that even a perfect product will fail end-use screens if paperwork lags or contains inconsistencies. For custom formulations or derivative screening, bulk packaging formats as large as 50 kg and as small as 100 g allow R&D teams as well as production groups to source efficiently. Whether shipping by air, sea, or express, feedback from logistics veterans steers packaging design and labeling refinement.

    Research Feedback and Ongoing Development

    Commercial clients and academic laboratories have pushed us to innovate beyond simple batch staging. Adjustments in particle size, batch blending, and even polymorph control have come about through active dialog with project leads from multiple continents. Once, a project in advanced API synthesis flagged subtle crystallization challenges at a 20-kilogram batch threshold. Shadowing their operators during mixing and filtration, we detected temperature-dependent microseeding issues that we ultimately solved by reformulating cooling rates and adjusting seed loadings. That kind of field feedback comes only to manufacturers with skin in the game and the willingness to adjust process windows in real time.

    Analytical chemists appreciate the support in troubleshooting. Shielded from routine QC, we maintain a technical support line for interpreting NMR and mass spectral quirks, especially as new process intermediates appear. These conversations sometimes yield upgrades that cascade into improved impurity profiles or tighter isomeric control for subsequent lots. Countless detail changes stem from these close research relationships: adjusted drying parameters, flagged glassware interaction issues, or new downstream solubility protocols. Most of all, our own team’s pride in being makers, not just packagers, speaks through the consistency and reliability of our lots.

    Sustainability Initiatives and Worker Safety

    Any manufacturer working with nitrile and pyridine intermediates recognizes their environmental and safety implications. Routine air scrubbing, closed-system halide handling, and advanced solvent recovery underpin daily operations. Our plant operators and technicians run ongoing training—simulation drills for spills, regular respirator fit assessments, and real-time gas detector checks. Over the last decade, meaningful reductions in both energy load and waste output have emerged from relentless process tuning and a willingness to reinvest savings in safer, greener infrastructure.

    We audit solvent use and minimize waste streams by recovering and reusing acetonitrile and pyridine fractions wherever feasible. Waste minimization for halide byproducts plays into broader reductions of dissolved organic wastes and cuts regulatory risk during expansions. Safety metrics tie directly to staff retention: operators and chemists who feel protected on the job drive lower turnover, which further bolsters institutional memory of historical troubleshooting and success strategies.

    Future Directions and Customer Collaboration

    Looking years ahead, 4-Pyridylacetonitrile Hydrochloride stands poised to underpin not just familiar medicinal and agrochemical syntheses, but the new wave of advanced materials, electronic chemicals, and specialty dyes. Process improvement never stops, and neither do quality targets. Customers have suggested everything from solventless crystallization methods to fully recyclable packaging, and every idea goes into the technical pipeline for pilot studies. Partnerships with university researchers on tailored derivatives are putting our own legacy expertise to the test, as the need for even cleaner, more selective intermediates grows.

    From bench researchers to global R&D heads, feedback cycles between manufacturer and end user continually shape how 4-Pyridylacetonitrile Hydrochloride is made, handled, and delivered. With the increasing complexity of new molecular entities and rising sensitivity to trace contaminants, the bar moves perpetually higher. Only manufacturers with full transparency, hands-on process knowledge, and a clear commitment to improvement can keep up.

    The Manufacturer’s Commitment to Evolving Demands

    In the end, success for a compound like 4-Pyridylacetonitrile Hydrochloride comes down to a mix of reliability, openness to improvement, and direct experience on the plant floor and in end users’ labs. Quick-fix solutions fall short of what R&D pipelines demand today. Backed by the collective problem-solving of hundreds of production batches, recall management protocols, long-term partnerships, and a company-wide culture of accountability, this is one product that continues to prove its value every day, batch after batch. It’s the sum of small details, hard-earned process insights, and honest communication with users that keeps our material in front of demanding chemists year after year, project after project.