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Malononitrile

    • Product Name Malononitrile
    • Alias Propane-1,1-dinitrile
    • Einecs 202-861-1
    • 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

    219383

    CAS_number 109-77-3
    IUPAC_name propanedinitrile
    molecular_formula C3H2N2
    molecular_weight 66.06 g/mol
    appearance colorless to slightly yellow liquid or solid
    melting_point 32-34 °C
    boiling_point 220 °C
    density 1.10 g/cm³ at 20 °C
    solubility_in_water miscible
    flash_point 109 °C (closed cup)
    odor slightly bitter almond-like
    refractive_index 1.419
    pubchem_CID 7876

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

    Packing & Storage
    Packing Malononitrile is packaged in a 500g amber glass bottle with a secure screw cap, labeled with hazard symbols and product details.
    Shipping Malononitrile is shipped in tightly sealed containers to prevent moisture absorption and leakage. It is classified as a hazardous material and should be handled according to applicable regulations. Transport should occur in a cool, well-ventilated area, away from sources of ignition, with appropriate labeling and documentation to ensure safe, compliant delivery.
    Storage Malononitrile should be stored in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers and bases. The container must be tightly closed and clearly labeled. Avoid exposure to moisture and direct sunlight. Use proper chemical storage cabinets designed for flammable or toxic substances, and ensure the area has appropriate spill containment measures.
    Application of Malononitrile

    Applications of Malononitrile in Industrial Manufacturing

    As a core intermediate with dual nitrile functionality, malononitrile supports critical downstream synthesis in several specialized chemical sectors. Our production integrates tight process control to ensure consistent purity, addressing granular needs in high-value manufacturing environments. Below, we detail practical application scenarios where downstream clients leverage malononitrile, reflecting precise industrial usage, handling, and compliance considerations.

    1. Agrochemical Active Ingredient Synthesis

    Malononitrile plays a pivotal role in the production of crop protection agents, notably selective herbicides and insecticides. Its reactive methylene group enables efficient C–C bond formation in condensation reactions, supporting large-scale synthesis of key actives such as sulfonylureas and pyrimidine derivatives. Manufacturers can modulate input ratios according to the specific requirements of each active ingredient, aligning with regulatory tolerances for pesticide residuals and technical standards for agricultural chemistry.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 (Quality Management Systems)
    • National Registration Authorities (e.g., US EPA, EU REACH, GB 2763/GB 2767 for China)
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • 10–40 mol% relative to key aromatic aldehyde or amine substrates; adjusted based on reaction yield and downstream substrate reactivity
    • 30–80 kg per batch in multi-ton production of active ingredient intermediates

    Downstream process integration

    • Charged directly to condensation or cyclization reactors after base/final solvent charging
    • Integrated as a co-reactant in multi-step synthesis involving Knoevenagel or Biginelli-type reactions

    Final product types

    • Herbicidal sulfonylureas (e.g., metsulfuron-methyl, chlorsulfuron)
    • Insecticide intermediates (e.g., neonicotinoids, pyrimidinyl derivatives)
    • Fungicidal actives incorporating dinitrile motifs

    2. Pharmaceutical Intermediate Manufacturing

    The compound serves as an essential building block in the preparation of precursors for cardiovascular drugs, central nervous system agents, and antiviral small molecules. In pharmaceutical production, chemists utilize malononitrile’s bifunctional reactivity to construct heterocyclic ring systems under strictly controlled GMP environments. Dosage and purification standards reflect both efficiency requirements and strict impurity control to align with regulatory drug quality expectations.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP-NF, Ph. Eur., and ChP monographs for intermediates
    • FDA 21 CFR Part 210/211
    • Good Laboratory Practice (GLP) and process traceability requirements

    Typical usage ratio

    • 1.2–1.5 equivalents per cyclization or alkylation step, adjusted in multi-component assembly for step yield
    • 250–800 g per 1 kg output of heterocyclic API precursors

    Downstream process integration

    • Added to reaction vessels for nucleophilic aromatic substitution or Michael-type additions
    • Pre-purified via recrystallization or solvent extraction before pharmaceutical coupling reactions

    Final product types

    • Pyrimidine-based API intermediates (e.g., barbiturates, antiepileptic scaffolds)
    • Antiviral nucleoside analogues intermediates
    • Dihydropyridine calcium channel blocker precursors (e.g., nifedipine family intermediates)

    3. Dye and Pigment Intermediate Production

    Malononitrile supports the synthesis of chromophoric systems via condensation with various aromatic aldehydes, yielding intermediates for disperse and vat dye classes. Specialty pigment makers exploit its stabilization of conjugated systems, enhancing color intensity and bath fastness. Quality protocols ensure trace metal content and color development stability comply with downstream textile and plastics requirements.

    Industry compliance standards

    • OEKO-TEX Eco Passport for dye intermediates
    • ZDHC MRSL Version 3.1 (for restricted substances in dye manufacture)
    • ISO 13321 for colorant characterization
    • REACH Regulation (EC) No 1907/2006 Annex XVII substances assessment

    Typical usage ratio

    • 15–25 wt% in condensation stages for aromatic dye precursor synthesis
    • Usage tuned based on chromophore extension and shade depth requirements

    Downstream process integration

    • Introduced to reactors at the condensation stage, typically under basic or acid-catalysed conditions depending on target pigment chemistry
    • Purified by washing and crystallization prior to coupling or azo dye formation steps

    Final product types

    • Disperse dyes for polyester fibers
    • Vat dyes used in cellulosic textile applications
    • Azo dye intermediates for use in plastics and inks

    4. Flavors and Fragrances Intermediate Preparation

    Specialty fragrance houses use malononitrile for the synthesis of musky and woody aroma molecules, including macrocyclic ketones and nitrile-containing aldehydes. During controlled condensation and reduction steps, it acts as a chain extender or as a precursor for further transformation in the construction of complex scent compounds. Manufacturers observe allergen controls and trace impurity monitoring in compliance with food and cosmetic regulatory requirements.

    Industry compliance standards

    • IFRA Standards (International Fragrance Association)
    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • ISO 9235:2013 for aromatic raw materials
    • FEMA GRAS (Flavor and Extract Manufacturers Association)

    Typical usage ratio

    • 8–18 wt% as a condensation nucleophile or chain unit per batch of aroma intermediate
    • Amount varied to balance scent profile and physical properties per formulation

    Downstream process integration

    • Dosed into reaction vessels during the Knoevenagel condensation or reductive cyclization stages
    • Used after preliminary distillation or filtration to remove trace off-odors before final transformation

    Final product types

    • Macrocyclic musks (e.g., civetone, muscone analogues)
    • Nitrile-based woody aroma precursors
    • Specialty intermediates for food and fine fragrance formulations

    5. Electronic Chemical and OLED Material Synthesis

    Advanced electronics and display sectors use malononitrile as a key reactant in crafting high-purity π-conjugated systems for organic light-emitting diodes and photonic materials. Its incorporation into aryl or vinyl frameworks facilitates enhanced charge transfer and color purity in emissive layers. Stringent materials testing and trace residue control are central to meeting the electrical, optical, and processability demands of the electronics value chain.

    Industry compliance standards

    • IEC 62684 for electronic chemical reliability
    • JEDEC JESD625 (Handling of Electrostatic Discharge Sensitive Devices)
    • ISO 9001 with electronic specialty chemical extensions
    • RoHS (Directive 2011/65/EU) substance restrictions

    Typical usage ratio

    • 5–20 mol% in aryl condensation reactions for precursor assembly
    • Quantity optimized for purity and optical property control in small-molecule and polymeric material synthesis

    Downstream process integration

    • Introduced after initial arylation or as a core unit in polymerization reactors for small-molecule OLED material production
    • Purified using column chromatography and high-vacuum drying to meet solvent and moisture contamination thresholds

    Final product types

    • Emission layer materials for OLED displays and panels
    • Charge transport materials for organic semiconductors
    • Photonic sensors for optical electronic applications
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    Certification & Compliance
    More Introduction

    Exploring the Significance of Malononitrile in Advanced Synthesis

    Introducing Malononitrile: Practical Application and Chemical Profile

    Decades of hands-on manufacturing experience keep showing the enduring value of malononitrile across the fine chemicals sector. Its chemical structure—CH2(CN)2—brings a rare double reactive group to synthetic chemists. We produce malononitrile in several lots, each tailored for reaction reliability and ease of storage, but always returning to the necessity for consistent melting point and controlled moisture levels. Purity comes out above 99.5% upon batch release, checked rigorously through gas chromatography and kept free from troublesome trace hydrolysis byproducts.

    Most of the world’s malononitrile ends up in the hands of customers seeking building blocks for pharmaceutical intermediate synthesis, agrochemicals, and specialty pigments. The market expects malononitrile to perform: immediate, clean reactions, little to no by-product formation, and a shelf life that stretches beyond seasonal demand cycles. The ease of handling, coupled with granule size uniformity and low dusting, matters during both bulk transport and fine pipetting work.

    What Sets Malononitrile Apart from Comparable Nitrile Products?

    Manufacturers and end users keep asking the critical question: why favor malononitrile over competing nitrile reagents? The answer draws from hands-on experience on the factory floor and in process optimization meetings.

    Few compounds offer malononitrile’s combination of two active nitrile groups flanking a single methylene. That duality enables smooth Knoevenagel condensations, Michael additions, and cyclization reactions unlikely or inconvenient with mono-nitrile reagents like acetonitrile or benzonitrile. Acetonitrile delivers a single nitrile group, limiting diversity in C–C bond formation and often demanding harsher conditions or extra catalysts. Benzonitrile shares limited solubility and reactivity, making it less flexible in synthesis routes requiring multiple functionalizations or straightforward scale-up.

    Malononitrile’s molecular design permits the introduction of structural diversity, particularly in pharmaceutical and agrochemical synthesis, where speed and reliability justify its slightly higher raw cost over more basic alternatives. Nitrogen content in each mole enables downstream functionalization—critical in industries committed to green chemistry initiatives and minimization of waste. Compounds derived from malononitrile consistently show higher target yields in five- and six-membered ring synthesis, a claim tested repeatedly in benchtop runs and pilot plants.

    Direct Experience: Process Control and Downstream Impact

    Day in and day out at the plant, technicians and engineers keep malononitrile production running through continuous batch distillation and precise temperature control. Every degree Celsius of deviation risks forming side products. Reliable distillation columns and post-synthesis drying cabinets cut the chance of hydrolytic breakdown, which would otherwise spoil reactivity downstream and complicate purification columns for our customers.

    Our process skips lengthy solvent exchange steps, keeping the process greener and reducing water and energy input. Each drum or bag rolls off the line with lot and QC information verified against past analytical performances. No run leaves the gate without confirmation by infra-red and NMR checks—internal standards show retention of both nitrile groups, matching the theoretical spectrum closely.

    From a process engineering point of view, malononitrile requires less aggressive neutralization or quenching procedures after use, meaning customers face lower environmental impact and less frequent shutdowns for scrubber cleaning. Analysis in downstream workflows, especially flow chemistry units, demonstrates nearly quantitative conversion rates under mild base or acid catalysis. The reactivity profile supports applications ranging from small medicinal chemistry batches up to full-scale pesticide ingredient manufacture.

    Application Stories: From Field to Fine Chemicals

    Our malononitrile leaves the plant in demand by two main customer groups: those in pharmaceuticals and those in specialty chemicals. Pharmaceutical researchers use it to synthesize intermediates for barbiturate derivatives, antihypertensive compounds, and novel heterocycles. The medical sector depends on clean, pure batches because even 0.1% of residual impurity can foul downstream biological testing or jeopardize regulatory inspection. In agrochemicals, malononitrile underpins the creation of select herbicides and fungicides, where loss of reactivity or breakdown would cause batches to fail QC before ever reaching the field.

    Pigments and dye manufacturers see particular value in malononitrile’s capacity to introduce chromophore modifications without major changes to existing production lines. As global demand for specialty dyes with precise colorfastness and shade stability rises, the reliability of each malononitrile batch becomes essential.

    Specifications Backed by Data and Experience

    Beyond published literature, we track every lot through site-specific data collection. Melting range for standard product settles around 31–33°C. Water content, measured by Karl Fischer titration, must remain below 0.2% for reaction efficiency and long shelf life. Chloride and trace metal content stay far below regulated limits. Our plant’s history with malononitrile covers thousands of tons shipped annually, with real-time feedback informing continual adjustments—shortening crystallization time, reducing energy use, and keeping particles free-flowing through automated sieving.

    No process can eliminate every risk, but repeated reviews and strict in-process controls limit lot-to-lot variability. Chemists in charge of process optimization debate changes only after reviewing months’ worth of data embedded in each product lot’s digital trace.

    Challenges in Manufacturing and Handling

    Producing malononitrile challenges every unit operation it passes through. Chilled reaction vessels limit the rate of exothermic reactions, and any lapse in temperature control risks creating oily, low-purity residues. Even packaging comes with its own set of challenges; solid malononitrile must resist clumping, so operations run drying ovens on calibrated cycles and every liner receives anti-static treatment before bagging.

    Transport and storage generate a unique demand for chemical stability. Customers need sealed, inert atmosphere shipping—nitrogen blanket packing stops atmospheric moisture from reacting with the product during transit. We introduced a humidity analytics program at both loading and receiving ends. If moisture content rises above threshold, no shipment moves forward. That insistence on real metrics protects customers’ downstream syntheses and their people handling the substance in high-throughput labs or remote factory sites.

    Environmental and Regulatory Realities

    Stringent global standards govern every step of the malononitrile pipeline, from raw feedstock procurement to product shipment and waste management. Working with regulatory affairs and compliance staff, the factory design adheres to regional and national environmental guidelines. Yearly environmental impact reviews track emissions and containment procedures for any byproducts or off-gases. In-plant teams monitor cyanide levels, ensure secondary containment integrity, and train every operator to handle emergencies by simulation and hands-on drills.

    Our persistent investment in waste minimization—closed-loop water recycling, solvent recovery, and safe destruction protocols—reflects both evolving regulation and ethical responsibility. Factories want a clean record not just for certification, but to protect workers, local communities, and the environment surrounding the production site.

    Supporting Innovation: R&D and Strategic Partnerships

    Collaboration with academic and industrial partners has widened application potential for malononitrile. Internal R&D teams work alongside university laboratories to probe for novel reaction conditions, seeking efficiencies in atom economy and new end products. Intellectual property concerns receive careful attention, protecting partners’ discoveries without slowing the transfer of technology to the commercial plant. Joint pilot runs often yield process modifications—improvements trickle down to every production shift, as smaller footprint processes improve overall reaction throughput.

    In the last few years, we supported research on bio-based nitrile sources; equipment upgrades now enable partial substitution of legacy raw inputs. These steps often come with higher early-stage costs but pay off in long-term supply stability and compliance with greener supply chain initiatives.

    Supply Chain Lessons and the Future of Production

    Malononitrile’s supply traceability remains a constant target for improvement. Real-world events—weather disruptions, feedstock volatility, and regional instability—mean supply planning needs constant attention. We keep multiple procurement lines open and maintain buffer inventory at critical nodes. Every ton of malononitrile delivered ties back to a secure documentation chain.

    To support forward-planning customers, our teams now publish advance notice of any expected disruptions and build in supply planning support. Modular expansion in production lines allows for short-notice increases in output, protecting customers with just-in-time delivery needs.

    Global transportation has its own challenges. Shipping delays or lost containers can spoil product and damage supplier-customer trust built over long contracts. Consistent investment in packaging resilience, digital shipment tracking, and pre-vetted logistics partners keeps our delivered product within promised specification windows.

    Handling, Operator Awareness, and Safety

    Safe malononitrile use succeeds or fails on the experience of factory, warehouse, and lab staff. Pre-shift briefings, chemical-specific PPE distribution, and site-specific hazard protocols form the backbone of our daily routine. Anyone working near the product needs up-to-date safety data, responsible disposal instructions, and on-demand access to emergency support. Every person learns how to spot early signs of decomposition or contamination, reporting minor incidents quickly before they escalate to safety risks or product loss.

    Our investment in safety culture—routine drills, incident analyses, and continuous training—grows from the understanding that hazardous chemicals demand even closer attention than routine manufacturing operations. Every manager and operator recognizes that malononitrile’s correct handling means more than internal compliance; it preserves community trust and the reputation built over years of on-time, safe delivery.

    Pushing Innovation Beyond the Status Quo

    Each year, customer demand presses for new malononitrile-derived compounds, driving R&D and constant optimization of every process step. Interdisciplinary teams look for new catalysts, energy-saving technologies, and lower emission packaging. The core goal remains: deliver a building block that supports downstream innovation—more medicines, safer agrochemicals, more durable specialty pigments—all with less environmental impact, lower resource consumption, and maximum transparency.

    Production teams screen every process for waste and inefficiency, working closely with supply chain and logistics teams to close the loop on residual streams, seek knockout improvements in resource recovery rates, and extend the product’s application to new vertical markets.

    Customer feedback comes back to us in multiple forms—technical inquiries, claims for off-spec lots, and success stories from novel applications. All this information drives ongoing product improvement and keeps customer trust high. No amount of automation or data analytics replaces the daily communication between client technical teams and factory floor engineers.

    Malononitrile’s Ongoing Influence in Chemical Synthesis

    After years of manufacturing and supplying malononitrile, the importance of strong supplier-customer relationships stands out clearly. Repeat orders, continuous technical discussion, and honesty about process limitations steer the product’s evolution to meet changing industry demands. The story of malononitrile—more than its chemical formula or listing in a supply catalog—comes through in the cumulative experience gained by everyone touching the product on its journey from basic chemical to advanced end use, supporting industries that shape modern life.

    This experience, reinforced by decades of reliable supply, strict in-house testing, environmental responsibility, and constant open dialogue with users, has kept malononitrile as the backbone of hundreds of advanced syntheses. Attention to specification, care during production, and a focus on operator and environmental safety define both the product’s future and the future of our company in the shifting landscape of global chemical manufacturing.