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N-Dodecyl Cyanide

    • Product Name N-Dodecyl Cyanide
    • Alias Lauronitrile
    • Einecs 246-148-0
    • 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

    807910

    Product Name N-Dodecyl Cyanide
    Cas Number 2437-25-4
    Molecular Formula C13H25N
    Molecular Weight 195.34 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 290-292°C
    Density 0.833 g/cm³ (at 20°C)
    Solubility In Water Insoluble
    Flash Point 127°C (closed cup)
    Refractive Index 1.4380-1.4400
    Melting Point -5°C
    Purity Typically ≥ 98%

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

    Packing & Storage
    Packing N-Dodecyl Cyanide is packaged in a 500 mL amber glass bottle with a secure screw cap and hazard labeling.
    Shipping N-Dodecyl Cyanide should be shipped in tightly sealed containers, protected from moisture and incompatible substances. It requires labeling as a hazardous chemical and should be handled following relevant regulations, including those for toxic and irritant substances. Transport under appropriate temperature conditions with spill containment measures is recommended to ensure safety during transit.
    Storage N-Dodecyl Cyanide should be stored in a cool, dry, well-ventilated area, away from sources of ignition and incompatible materials such as strong acids and oxidizers. Store in a tightly closed, clearly labeled container made of compatible material. Avoid exposure to heat, direct sunlight, and moisture. Ensure proper containment to prevent leaks, and keep away from food and drink. Use appropriate personal protective equipment when handling.
    Application of N-Dodecyl Cyanide

    Applications of N-Dodecyl Cyanide in Industrial Manufacturing

    As a dedicated manufacturer of N-Dodecyl Cyanide, we support specialized industries with a consistent and quality-assured supply for sophisticated downstream uses. Below, we detail the specific industrial application scenarios where our raw material integrates directly into modern formulations and processing routes, with a focus on regulatory needs, dosage optimization, production workflow, and targeted end products.

    1. Surfactant Intermediate for Specialty Chemical Synthesis

    N-Dodecyl Cyanide plays a critical role as a key intermediate in the production of specialty surfactants used for emulsion polymerization and high-performance detergents. Its nitrile group undergoes controlled chemical transformation, enabling the refinement of longer-chain surfactant molecules that meet precise application requirements in advanced industrial cleaning and polymer manufacturing.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006
    • OECD Guidelines for Testing of Chemicals
    • ISO 9001:2015 Quality Management System
    • Responsible Care Global Charter

    Typical usage ratio

    • 2.5–7.0% by weight, adjusted according to molecular weight targets for downstream alkyl surfactant synthesis

    Downstream process integration

    • Introduced in the batch reactor during nitrile-to-amide or amine group transformations prior to quaternization or sulfonation stages in surfactant manufacturing

    Final product types

    • Alkylamine-based surfactants for detergents
    • Quaternary ammonium compounds for textile auxiliaries
    • Polymerizable emulsifiers for emulsion resins

    2. Precursor for Long-Chain Fatty Amine Synthesis in Flotation Reagents

    This nitrile compound serves as a primary precursor for the reductive synthesis of dodecylamines, which function as selective flotation collectors in the mining industry. Reagent formulators rely on its controlled conversion to produce high-purity amines required for the beneficiation of non-ferrous ores and mineral separation efficiency.

    Industry compliance standards

    • ISO 12743:2006 Sampling of Processed Ferrous and Non-Ferrous Ores
    • U.S. EPA 40 CFR Part 261 - Identification and Listing of Hazardous Waste
    • China GB/T 22105-2008 Standards for Flotation Reagents
    • ISO 9001:2015 Quality Management System

    Typical usage ratio

    • 3.0–6.0% by mass within the overall collector formulation, depending on ore mineralogy and pH profile

    Downstream process integration

    • Fed into anhydrous hydrogenation reactors for conversion to long-chain primary amines, followed by blending with secondary components before final formulation of flotation collectors

    Final product types

    • Dodecylamine-based collectors for iron ore flotation
    • Cationic surfactant reagents for phosphate mineral upgrades

    3. Oilfield Corrosion Inhibitor Component

    Downstream oilfield chemical manufacturers utilize N-Dodecyl Cyanide as a hydrophobic building block for formulating corrosion inhibitors suitable for harsh downhole and pipeline environments. Its transformation to long-chain amines and subsequent derivatization ensures compatibility with a wide range of crude oils, saline environments, and high-pressure conditions often present in oil and gas operations.

    Industry compliance standards

    • API RP 14E: Recommended Practice for Design and Installation of Offshore Production Platform Piping Systems
    • ISO 15544:2000 Petroleum and natural gas industries—Offshore production installations—Requirements and guidelines
    • OECD Guidelines for Testing of Chemicals (Aquatic Toxicity)
    • REACH registration dossier for downstream intermediates

    Typical usage ratio

    • 1.0–3.5% by weight as a feedstock within organic inhibitor concentrate blends, fine-tuned according to target hydrocarbon composition and water salinity

    Downstream process integration

    • Processed via hydrogenation and functionalization in blending tanks for incorporation as primary alkylamine moieties into multi-component inhibitor packages

    Final product types

    • Corrosion inhibitor concentrates for offshore and onshore pipelines
    • Downhole protection additives for enhanced oil recovery

    4. Intermediate for Alkylated Benzyl Cyanide Compounds in Agrochemical Synthesis

    Agrochemical active ingredient manufacturers employ this raw material as an alkyl chain donor in multi-step synthesis routes for novel substituted benzyl cyanides, forming the backbone of select insecticidal and herbicidal agents. Process consistency and minimal trace impurity content remain critical for developing agrochemical intermediates.

    Industry compliance standards

    • FAO/WHO: Specification and evaluations for agricultural pesticides (JMPR)
    • ISO 9001:2015 for Agrochemical Supply Chains
    • EU Regulation (EC) No 1107/2009—Placing of Plant Protection Products on the Market
    • China GB 4839-2009 Safety specifications for pesticides

    Typical usage ratio

    • 0.8–1.6 equivalents per mole of benzyl halide substrate, adjusted based on desired alkylation yield

    Downstream process integration

    • Enters nucleophilic substitution reaction sequences under controlled temperature in batch or semi-batch reactors, yielding alkylated cyanide intermediates for further transformation

    Final product types

    • Precursor intermediates for pyrethroid insecticides
    • Alkyl cyanide-based active ingredients for herbicidal formulations

    5. Raw Material for Alkylated Quaternary Ammonium Salts in Antimicrobial Agents

    The long alkyl chain of this nitrile enables efficient manufacturing of quaternary ammonium salts after amination and quaternization, delivering cationic antimicrobial performance in industrial disinfectants and preservation solutions for treated materials and facilities. Downstream customers value the raw material traceability and batch consistency for demanding biocidal registration filings.

    Industry compliance standards

    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)
    • U.S. EPA 40 CFR §§ 150–189: Registration of Pesticides and Antimicrobial Products
    • China GB 38598-2020 Hygienic Standard for Disinfectants
    • ISO 14001:2015 Environmental Management System for Biocidal Agents

    Typical usage ratio

    • 1.8–4.2% of the total quaternary ammonium salt batch yield, subject to titration and purity requirements in the downstream process

    Downstream process integration

    • Converted to tertiary amine and fed to methylation/quaternization reactors before final dilution and blending steps for formulation of concentrate or ready-to-use solutions

    Final product types

    • Benzalkonium chloride analogues for surface disinfectants
    • Alkyl quaternary ammonium salts for industrial and institutional biocidal applications
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    Certification & Compliance
    More Introduction

    N-Dodecyl Cyanide: Product Introduction from a Chemical Manufacturer’s Perspective

    Getting to the Core of N-Dodecyl Cyanide

    Standing on the laboratory floor, you gain a strong respect for the purpose and performance of each fine chemical that leaves the vessel. N-Dodecyl Cyanide carries a value that shows up in the way it pushes forward the work of organic synthesis. The product doesn’t get much limelight, but over years in this industry, we’ve seen first-hand how critical it becomes once it enters a workflow, especially for specialty synthesis and complex molecular construction.

    N-Dodecyl Cyanide has a formula of C13H25N and most of the time, the better batches present as a faint, clear liquid—neutral in odor, but carrying the fingerprint appearance you look for when quality matters. We handle it with an eye for purity because downstream reactions rely on tight consistency. Model variations are mostly set by purity specification and trace moisture content, with specialty requirements for critical impurities kept in mind for sensitive processes. Most users in pharmaceutical and process chemistry will gravitate toward product in the >98% (GC) range since even one percent deviation can throw intermediates off-target. Trace halides, peroxide-formers, or remaining catalyst residues, even at parts-per-million levels, can end sequences before they start. We prioritize batch analytics for each drum, and after years of feedback from our partners, we keep levels lower than general commercial grades.

    Where N-Dodecyl Cyanide Finds Its Role

    We have seen N-Dodecyl Cyanide used in routes that look delicate under the hood, like manufacturing specialty surfactants or as an intermediate for advanced liquid crystal compounds. One reliable transformation uses it as a precursor to amines, where the long alkyl chain pulls in lipophilicity without breaking the backbone of the molecule. You don’t see this every day in routine commodity production; most requests for N-Dodecyl Cyanide come from R&D labs or advanced custom synthesis groups working on fine-tuned pharmaceutical molecules or new material science prototypes. One of the more invisible but important applications lands in the functionality it adds to surfactant design, for detergents or wetting agents that tackle stubborn interface problems. Here, the length of the dodecyl chain makes a real, measurable difference.

    Unlike simpler nitriles, dodecyl cyanide brings a balance—for users who find butyronitrile or octyl cyanide too volatile or too solvent-exposed for their chemistry. Short-chain analogs shift too quickly into phase changes or lose integrity in longer processes. Dodecyl, by comparison, steadies the ship; you get enough hydrocarbon content for targeted hydrophobic modification, but not so much that viscosity climbs out of control or handling becomes awkward. It’s a trick we’ve found useful when supporting teams in pilot production, where downstream reactors require tight control over reactivity and material losses, and every gram of developed intermediate matters when scaling up toward registration.

    Insights from Practical Handling and Storage

    Some customers worry about stability, particularly with repeated opening and extended benchtop exposure. In our experience, and with regular in-house testing, N-Dodecyl Cyanide stores well under nitrogen, and real-world oxidation risk stays low if basic protocols are respected. What’s more, thanks to its longer hydrocarbon chain, evaporation loss is minimized compared to lighter nitriles. For anyone running continuous flow or multistep processes, this predictability removes a substantial risk. When preparing for large-scale batch work, control over vapor pressure and volatility counts for a lot—it’s not just a numbers game on a safety chart; those properties keep your reaction yields inside the predicted window.

    Packaging for N-Dodecyl Cyanide reflects the needs of downstream facilities: lined steel drums or HDPE containers handle exposure issues, and every closure is checked for chemical compatibility. We’ve traced container off-gassing rates in different climates, and adjusted our drum venting protocols so product stability is maintained from dock to final blend tank. Temperature cycling during shipment remains a nontrivial challenge as hot climates can nudge moisture uptake or trigger stress on closure seals. After collecting years of thermal cycling data, we now recommend structuring warehouse storage away from oxidizers and acids, and keeping drums sealed except during active use. Proper drum handling creates fewer headaches than any technical fix downstream.

    Performance Differences from Other Cyanides

    From a manufacturer’s view, lumping N-Dodecyl Cyanide into the same bucket as other long-chain nitriles overlooks its unique window—especially with regard to reactivity, downstream modification, and final product characteristics. Dodecyl falls into a middle space: lengthy enough to build structure in specialty molecules, but not so long as to become waxy or immobile at room temperature. Contrast this with hexadecyl cyanide or octadecyl cyanide, which introduce solubility or blending difficulties in many solvents, or sometimes even separate into two phases in multi-component reactions. N-Dodecyl Cyanide offers a smoother operating range.

    Compared to short-chain cyanides (acetonitrile, butyronitrile, or even valeronitrile), dodecyl delivers enhanced compatibility in systems that require low vapor pressure and resistance to fast evaporation. Our technical teams have flagged a secondary advantage: better safety margins in large-scale pharmaceutical applications owing to lower toxicity and fewer occupational safety flags than some of the more volatile or aromatic nitrile cousins. Chemists notice the improved handling procedures, too. Standard PPE protocols give more leeway, without sacrificing control or introducing unseen hazards.

    As far as performance in chemical synthesis, the longer alkyl chain stabilizes intermediate formation in reaction steps where thermal input varies or where the solvent system demands flexibility. N-Dodecyl Cyanide avoids the phase-change risks encountered with short chain nitriles, which, in a run lasting more than twelve hours, can shift volatility profiles unexpectedly—sometimes changing the kinetic profile and sometimes even risking condenser overload. In multi-kilo scale syntheses, such unplanned losses translate directly to batch yield reductions and setback orders. With dodecyl cyanide, we’ve documented tighter process controls from start to finish.

    Understanding Product Purity and Analytical Challenges

    Inside the plant, ensuring consistent purity at industrial scale calls for careful monitoring at every stage. Our analysts run GC-FID and GC-MS for every lot, targeting not just the major peak for N-Dodecyl Cyanide, but also fingerprinting for any byproducts or unreacted raw materials. From experience, a high-quality run gives a sharp, dominant N-dodecyl cyanide peak, and minor satellite peaks from side-channel alkylations or dehydration byproducts. Our internal practice demands that impurities (alkanes, alkenes, alcohols) are kept well below 0.5% each on area normalization, with water content tested with Karl Fischer titration and kept below 200 ppm for the tightest grades. Customers in pharmaceutical and electronics fields are particular about these metrics, since even trace levels of reactive impurities can throw off catalytic selectivity or cause side reactions.

    We observe more interest now in trace metal analysis, especially as downstream regulations tighten for end-user safety. For the strictest requirements, we run ICP-OES on every critical batch, checking for transition metals (nickel, palladium, copper)—residuals from classic cyanation catalysts and even certain workup stages. It’s a process with cost and time overhead, but feedback from advanced API manufacturers has shown it’s worth the investment. Inconsistent impurity profiles ruin batch validation, and heavy metal residuals prompt regulatory headaches later in the value chain. We learned this lesson during a period when a few lots showed higher-than-normal copper, caught in QC and intercepted before leaving our outbound dock. Our ongoing investment in trace analytics prevents such problems now.

    User Perspectives and Changing Applications

    N-Dodecyl Cyanide exists at a crossroads between established and emerging applications. In the early days, orders came mostly from industrial surfactant producers, securing alkyl chain length precursors for niche detergent modifications. Over time, orders have expanded, and today advanced material researchers reach out for specialties with dodecyl cyanide scaffolds in their synthetic blueprints. Some work involves the creation of lipophilic molecular building blocks for drug delivery carriers or molecular receptors. Researchers in universities and specialty manufacturers experiment with dodecyl cyanide for everything from stabilizing agents in emulsions, to backbone modifications in bio-inspired polymers, to intermediates for potentially novel agrochemical agents. We keep an eye on these trends, and often run custom purifications to support projects in early clinical or pre-commercial phases.

    A challenge sometimes arises from the specificity of end-use purity needs. Chemical R&D projects feature diverse solvent choices, side-chain modifications, and process conditions; a product that works for one application might not meet the color or impurity requirements for another. Our technical team invests in regular conversations with customers to tune batch parameters—sometimes pursuing extra distillation to meet color limits, or introducing extra carbon filtration to reduce trace organics that show up only in high-sensitivity assays.

    Balancing Production Efficiency and Sustainability Requests

    The industry now finds itself pulled in two directions: deliver chemically precise product, but with increasing scrutiny around environmental impact, resource efficiency, and regulatory compliance. The raw materials for N-Dodecyl Cyanide—dodecyl halides or alcohols, cyanide sources—raise clear safety and environmental questions. Our batch system design reflects this. We track cyanide consumption closely, run tight closed-system controls during synthesis, and have invested in reagent recovery and hydrolysis systems for byproduct capture. Over the past five years, incremental changes in plant design have dropped average cyanide use intensity by over 20%, with most captured residues returned for hydrolysis instead of external disposal. These operational choices take effort and investment, but they help address critical industry and regulatory concerns about hazardous process footprints.

    Solvent choice forms another axis of sustainability. In the past, many manufacturers favored classic solvents—toluene, chlorinated hydrocarbons, and recovery was less common. Modern process modifications allow for lower solvent consumption and safer alternatives, with recovery rates for our plant now exceeding 90% for key solvents. This approach tightens not only the environmental story but the cost basis for every kilogram produced. We’ve investigated use of alcohol-based solvents and continuous extraction units, with mixed success depending on batch size and product grade required. The reality is that each alternative introduces constraints in purity, process reliability, or downstream compatibility. The lessons collected from trial runs allow us to hit tighter cost and sustainability targets with each campaign.

    Looking beyond the plant floor, demand shifts as customers report changing regulatory frameworks—especially in Europe and North America, where new restrictions on downstream nitrite or cyanide carryovers have forced a review of all process steps. End-users ask for more thorough batch documentation. Our compliance workflow tracks the full set of process data, from reactivity logs to transport manifests, so customers undertaking regulatory submissions see a full chain of custody without surprises.

    Comparing N-Dodecyl Cyanide with Related Materials

    The unique chemical identity of N-Dodecyl Cyanide stands out in key areas: phase behavior, functional group reactivity, and user safety profile. Customers sometimes weigh decyl, tetradecyl or octadecyl analogs for similar applications, but real-world tests show that dodecyl’s balance of liquidity, melting point, and solvent compatibility beats the rest for practical work. We’ve run side-by-side reactivity screening in amine formation and downstream quaternization, where N-Dodecyl Cyanide shows consistent conversion rates in standard catalytic hydrogenation. Reaction predictability reduces troubleshooting labor, batch failures, and startup costs for new projects.

    Commercial supply chains influence product selection, as well. Supply for shorter-chain cyanides tends to be more robust, while longer-chain analogs introduce variable lead times and periodic shortages—especially as specialty applications spike. Our experience tracking global feedstock flows supports our decision to anchor supply to regionally available starting materials, which smooths price volatility and guarantees better delivery windows for our customers. These logistics and inventory choices offer stability in project planning and launch schedules for downstream users.

    Addressing Customer and Process Challenges

    Scaling production for N-Dodecyl Cyanide brings distinct technical challenges. One recurring question centers on batch-to-batch consistency, especially as customer volumes grow from kilos to multi-ton quantities. Chemical synthesis deals with small margins; minor deviations in reactor conditions or charge rates reveal themselves as unwanted isomerization, side-chain scission, or color formation. Our process engineers have invested substantial time in digital monitoring and audit trails, which allow root-cause analysis if off-spec lots appear. Historical data often tracks each deviation back to raw material batch variability or subtle changes in mixing time. Fast feedback from these production reviews underpins continuous process improvements.

    We often get requests for custom derivatization or downstream blending, particularly from users developing next-generation surfactants, emulsifiers, or pharmaceutical scaffolds. Experience shows that N-Dodecyl Cyanide tolerates a range of subsequent transformations: reduction to primary amines, introduction of functionalized aromatic rings, or extension to higher nitriles. Compared to other nitriles, dodecyl handles derivatization routes with fewer byproduct formation issues. This reliability comes from the uniformity of chain length and site reactivity built into the manufacturing method we use.

    From a plant safety view, dodecyl cyanide reduces operator exposure risk compared to more volatile nitriles. Its limited vapor pressure falls securely below most occupational safety limits under standard temperatures. Real-world leak simulations and personal monitoring in our facilities have shown lower airborne exposures with dodecyl than with more volatile alternatives, contributing to safer plant operation and a reduced personal protective equipment burden.

    Supporting Innovation in a Tight Market

    Manufacturing teams don’t just follow recipes; they solve complex puzzles. Product delivery involves chemical know-how, a practical sense of logistics, and clear communication with R&D partners. As a business, we invest in reliable, transparent supply of N-Dodecyl Cyanide, while committing to technical support and candid communication about potential limitations or batch deviations. This coordination has made a difference when supporting rapid scale-up for customers with urgent project timelines, particularly in the custom manufacturing space.

    Feedback loops with customers remain central. Every time a customer flags an issue—color, purity, residue, solvent incompatibility—it pushes the manufacturer to tighten routines or change plant settings. We welcome challenge runs, side-by-side validations, and even third-party audits of our analytical data packages. Over years, this open conversation has sharpened both our technical expertise and our ability to preemptively solve downstream obstacles. Customers exploring new downstream chemistry with our N-Dodecyl Cyanide benefit from tailored technical guidance, including specification charts and shipping documentation, to ensure their production lines run smoothly.

    Industry-wide knowledge grows through real trials, data exchange, and a shared understanding of application risks and payoffs. As new areas of fine chemical synthesis come into view—from advanced surfactants to preclinical pharmaceutical ingredients—N-Dodecyl Cyanide carves a place for itself through reliable performance, safe handling, and scalable supply. From our view, that’s the reason real-world chemistry depends on attention to detail, honest tracking of technical challenges, and a clear commitment to customer goals.