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2,2-Dimethylcyclopropyl Cyanide

    • Product Name 2,2-Dimethylcyclopropyl Cyanide
    • Alias 2,2-Dimethylcyclopropylcarbonitrile
    • Einecs '252-088-4'
    • 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

    707169

    Iupac Name 2,2-Dimethylcyclopropanecarbonitrile
    Cas Number 930-55-2
    Molecular Formula C6H9N
    Molar Mass 95.146 g/mol
    Appearance Colorless to pale yellow liquid
    Density 0.858 g/cm³
    Boiling Point 141-143 °C
    Melting Point -8 °C
    Flash Point 38 °C (closed cup)
    Refractive Index 1.420
    Solubility In Water Slightly soluble
    Structure Cyclopropyl ring with two methyl groups at the 2-position and a nitrile group

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

    Packing & Storage
    Packing Amber glass bottle, 100 mL, with tamper-evident screw cap; chemical hazard labels, chemical name, and proper storage instructions displayed.
    Shipping 2,2-Dimethylcyclopropyl Cyanide should be shipped in tightly sealed containers under inert atmosphere, in accordance with local, national, and international regulations. Store and transport in a cool, well-ventilated place, away from sources of ignition and incompatible substances. Proper hazard labels, safety documentation, and protective measures must accompany the shipment.
    Storage 2,2-Dimethylcyclopropyl cyanide should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as acids and strong oxidizers. It should be kept out of direct sunlight and protected from moisture. Use appropriate chemical storage cabinets, and ensure proper labeling and access control to authorized personnel only.
    Application of 2,2-Dimethylcyclopropyl Cyanide

    Applications of 2,2-Dimethylcyclopropyl Cyanide in Industrial Manufacturing

    2,2-Dimethylcyclopropyl Cyanide serves as an essential intermediate in the synthesis of diverse advanced chemical products, supporting production chains in pharmaceuticals, crop protection, specialty fine chemicals, and materials science. As a direct manufacturer, we supply this compound to partners seeking stable supply, traceable quality, and product-specific technical documentation for these critical downstream applications.

    1. Pharmaceutical Intermediate Synthesis for Central Nervous System Agents

    Research-driven manufacturers employ this compound as a key building block for custom synthesis of CNS active pharmaceutical ingredients, including anticonvulsants and cognitive disorder medication precursors. In these applications, the compound’s cyclopropyl structure enables selective transformations and target molecule construction under controlled laboratory and production conditions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Current Good Manufacturing Practice (cGMP) – US FDA 21 CFR Parts 210, 211
    • China Pharmacopoeia and relevant EU Pharmacopoeia monographs for API synthesis
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) compliance for intermediate import/export

    Typical usage ratio

    • Common usage ranges from 0.8 to 1.2 molar equivalents relative to primary amine or carboxylic acid reactants, with batch charges precisely calculated based on the target API pathway and process yield analysis.

    Downstream process integration

    • Material is introduced in multi-step synthesis after initial halogenation or protection group installation, often via nucleophilic aromatic substitution or Grignard-type cyclopropanation, preceding hydrolysis or further cyclization stages.

    Final product types

    • Central nervous system API intermediates
    • Pyrrolidine-based pharmaceuticals
    • Precursor salts for final formulation and finishing
    • Research compounds for clinical candidate libraries

    2. Agrochemical Synthesis for Cyclopropane-Based Crop Protection Agents

    Crop protection manufacturers value this material for constructing active moieties in the latest generation of synthetic pyrethroid and cyclopropyl-substituted pesticides. It enables chemical structure modification that directly impacts product effectiveness and environmental degradation profiles, supporting both field efficacy and regulatory stewardship.

    Industry compliance standards

    • FAO/WHO Guidelines for the Quality Control of Pesticides
    • ISO 9001:2015 for process and quality management
    • Globally Harmonized System of Classification and Labelling of Chemicals (GHS)
    • Directive 91/414/EEC (EU Plant Protection Products Regulation) for active substance review

    Typical usage ratio

    • Formulators add 0.5 to 2.0 weight percent based on targeted substitution levels in organonitrile conversion, with scale-up parameters set through laboratory optimization and pilot plant validation data.

    Downstream process integration

    • The cyanide enters the process during cyclopropyl ring closure and subsequent cyanation step, following the initial preparation of aromatic or aliphatic precursors, and is distilled or crystallized prior to formulation blending.

    Final product types

    • Pesticidal active ingredient intermediates
    • Synthetic pyrethroid base compounds
    • Herbicidal building blocks requiring cyclopropyl motifs
    • Stabilized field-ready pesticide technical concentrates

    3. Fine Chemical Synthesis for Advanced Fragrance Ingredients

    Producers of specialty aroma chemicals use the compound for introducing unique cyclopropyl groups into nitrile-based fragrance intermediates, which impart combinatorial odor profiles and molecular complexity sought by global fragrance houses, particularly in developing new green, woody, and fresh top-note ingredients.

    Industry compliance standards

    • IFRA (International Fragrance Association) Code of Practice
    • FEMA (Flavor and Extract Manufacturers Association) approved materials list
    • REACH regulation (EC 1907/2006) for fine fragrance chemicals
    • ISO 9001:2015 certified manufacturing processes for traceability

    Typical usage ratio

    • Fixative and intermediate synthesis recipes require 0.85 to 1.05 molecular equivalents per target aldehyde precursor, with fine-tuning for desired final olfactory impact and downstream functional group tolerances.

    Downstream process integration

    • Material is charged into closed reactors after solvent precharge during the nitrile addition step, followed by hydrogenation, distillation, and olfactory panel testing for batch release.

    Final product types

    • Novel nitrile-based fragrance intermediates
    • Green note aroma chemicals
    • Fine perfume fixatives with functional groups
    • Designer “nature-identical” fragrance bases

    4. Specialty Polymers and Advanced Materials Synthesis

    Materials science companies incorporate this cyclopropyl nitrile building block to engineer next-generation specialty polymers with controlled rigidity, barrier properties, or heat resistance. The cyclopropyl group enhances thermal stability, enabling the downstream manufacture of lightweight, chemically resistant films and molded parts for demanding end-user applications.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for polymer intermediates
    • EN ISO 1043-1 for plastics—abbreviations and terminology standardization
    • RoHS Directive 2011/65/EU (for electronic and automotive applications)
    • REACH Annex XVII restrictions evaluation where applicable

    Typical usage ratio

    • Process developers use 0.3 to 1.3 mol% of the compound as a comonomer or side-chain modifier in step-growth or radical polymerization, selecting ratios by desired mechanical and thermal properties of the final polymer.

    Downstream process integration

    • Monomer solution is polymerized via batch or continuous stirred tank reactors, entering the process at macromolecular chain initiation, then followed by addition of crosslinkers and further copolymerization adjustments based on viscosity monitoring.

    Final product types

    • Chemically resistant polymer films and sheets
    • Functional molded parts for electronics and automotive segments
    • Adhesive resins with improved heat distortion temperatures
    • Barrier coatings for specialty packaging
    Free Quote

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    Certification & Compliance
    More Introduction

    2,2-Dimethylcyclopropyl Cyanide: Practical Chemistry with Reliable Results

    Introduction to 2,2-Dimethylcyclopropyl Cyanide

    In the chemical manufacturing world, every choice of intermediate hinges on actual performance and trust. We have worked with 2,2-Dimethylcyclopropyl Cyanide through countless process runs, bench tests, and scaled-up campaigns. This compound, recognized for its cyclopropyl ring and robust nitrile functionality, stands out among the specialized building blocks useful across pharmaceutical, agrochemical, and materials synthesis.

    After years in the plant, we see the difference between what a product looks like on a paper and what it means for a customer when it moves through a real production line. Every batch of 2,2-Dimethylcyclopropyl Cyanide we make reflects this experience. The isomerically pure structure offers a compact, strained ring system, boosting reactivity in ring-opening reactions compared to typical linear nitriles. That translates to more control and less uncertainty for chemists aiming for specific targets.

    Specifications Proven in Real-World Chemistries

    Consistent quality matters, not only for paperwork but for yield and troubleshooting time. From our process, 2,2-Dimethylcyclopropyl Cyanide routinely achieves GC purity above 98%, with residual solvents falling well below standard assay limits. The physical state, pale liquid with a sharp nitrile odor, pours and measures without fuss in both production and R&D setups.

    Years of batch history taught us the practical values of stability. In normal storage – dry, cool areas – the material holds up for extended periods, resisting typical hydrolysis or polymerization pitfalls found in less robust nitriles. Packaging, whether in drums or specialized kegs, passes through rigorous quality checkpoints to ensure no contamination or evaporation. Customers appreciate pulling sample after sample with identical physico-chemical fingerprints.

    In our experience, working with 2,2-Dimethylcyclopropyl Cyanide has clear advantages during workups. The relatively low boiling point compared to bulkier cyclopropyl derivatives helps us streamline distillation, reducing both cycle time and energy needs. Downstream, users report clean extractions from aqueous systems and reproducible reactivity with nucleophiles or metallic catalysts.

    Usage Built on Years of Application

    Our exposure covers multi-ton contract manufacturing for custom syntheses, but the chemistry we value most shows up in the reactions of real end-users. Medchem teams find 2,2-Dimethylcyclopropyl Cyanide essential for constructing high-value building blocks, particularly during the early design of cyclopropyl-bearing active pharmaceutical ingredients. Cyclopropyl rings bring metabolic stability and lipophilicity to drug candidates, and the dimethyl-substituted version creates steric bulk that can impact both potency and selectivity.

    We have supplied this reagent to crop protection companies designing new actives, where the rigid cyclopropyl core offers insecticidal and herbicidal candidates with new modes of action. When used as a cyanide source for ring opening or homologation steps, the compact structure helps introduce advanced motifs unavailable from linear nitriles or branched alternatives. Manufacturers aiming for high-throughput library synthesis appreciate how it cuts down purification steps compared to more reactive, less manageable nitriles.

    In custom synthesis and functional material projects, users ask for tight control over chirality and purity. The structure of 2,2-Dimethylcyclopropyl Cyanide, with its symmetric methyl groups, allows for predictable routes toward chiral intermediates, avoiding racemization issues sometimes experienced with cyclopropyl homologs. Our technical team regularly supports scale-up projects where customers need to translate bench chemistry directly to plant-scale, leading to fewer surprises during validation and regulatory submissions.

    What Sets 2,2-Dimethylcyclopropyl Cyanide Apart

    Over the years, we have tested other cyclopropyl nitriles, such as unsubstituted or mono-methyl derivatives. The addition of two methyl groups on the ring markedly changes the chemical landscape. Not only does it boost steric protection around the reactive center, but it also modifies volatility and solubility profiles. In practical terms, this means side reactions are less common, particularly those involving nucleophilic attack or excess heat.

    Compared to classic straight-chain nitriles, the three-membered ring presents unique strain-driven reactivity. This aspect makes certain reactions faster or easier to control, resulting in high yields or fewer byproducts. Our colleagues in synthesis report formation of cyclopropylamines, carboxylic acids, or heterocycles proceeding with cleaner profiles using the dimethyl-cyclopropyl variant than with open-chain competitors. The recovery rate in these conversions surpasses what you’d see from bulkier or more reactive nitriles, with less need for extensive purification by chromatography.

    We see clear environmental and handling benefits as well. 2,2-Dimethylcyclopropyl Cyanide’s moderate volatility and manageable hazard profile simplify worker training and plant scheduling. The compact molecular shape means less transport and storage volume for equivalent functional group content, reducing overhead in logistic chains.

    Price is another piece of the puzzle. Our scale and careful process development put this material within reach for most research and production groups, bridging the gap between high-end research compounds and cost-sensitive production units. Unplanned downtime and failed reactions due to side-product issues fall sharply compared with less refined alternatives.

    Another distinction appears at the regulatory level. Having supplied this product for regulated markets, we understand the compliance burdens facing our customers. We can provide not only reliable product but also documentation supporting REACH, TSCA, and country-specific regulations, removing barriers during audits and registrations.

    Lessons Learned from Daily Production

    Not every supplier has firsthand experience with the problems chemists face on the shop floor. We learned early that even small changes in upstream starting materials or process temperature deliver big swings in downstream yields. We control every step: raw material vetting, in-process sampling, and final product assays. This control results in a reproducible product, lot after lot.

    Shipping direct from our production floor gives our customers confidence that the product is not coming from a repackager or blending house. We see a marked difference in process efficiency and reproducibility for those who switch to direct-from-manufacturer supply. If issues ever occur, we work through joint root-cause analysis — actual people, not call center scripts. This way of working means our team understands both the chemistry and the operational headaches our customers face.

    Scaling up from grams to kilograms, or even multi-ton lots, throws curveballs. We have overcome challenges such as localized hot spots in reactors, byproduct formation from incomplete mixing, or equipment corrosion from nitrile exposure. Years of troubleshooting shape our approach to continuous improvement, keeping batch failures and waste generation low. This benefit doesn’t come from specs alone, but from hands-on, repetitive experience solving these issues.

    Supporting Customer Innovation with Practical Know-How

    Overseeing regular technology transfer projects has shown us the value of joining our customers’ teams early in the process. We often get invited to review synthetic plans before pilot runs, offering feedback on solvent selection, reaction temperatures, or product isolation ideas based on real plant results rather than textbook values. Users cite tangible improvements in yield or downstream throughput after adopting those suggestions.

    One example involves improving crystallization efficiency during intermediate isolation. Testing revealed that slight adjustments to antisolvent ratios delivered sharper, cleaner product cuts, reducing post-reaction workup times by hours per batch. Another case involved troubleshooting unexpected color formation — tracking it back to a trace-level impurity in a co-feedstock, now flagged at incoming quality check. These lessons, built from practice, sharpen our understanding of 2,2-Dimethylcyclopropyl Cyanide’s behavior across different chemistries.

    People working on novel or proprietary chemistries often worry about supply chain security. We address concerns by keeping multi-month stocks and flexible production campaigns, backed by real data and transparent scheduling. If customers require tailored purification, dry solvent addition, or alternate container formats, our plant adapts quickly so research timelines and process campaigns stay on track.

    IP-sensitive projects often call for confidentiality. As a manufacturer, we keep everything in house, ensuring information security and minimizing the risk of leaks or unauthorized product movement. Long-term partners value the assurance that process data and supply arrangements remain sealed within our direct relationship.

    Real-World Challenges and Approaches to Solutions

    No chemical process runs without hiccups. Over time, we’ve found that monitoring for micro-impurity buildup and cross-contamination is key. Our plant employs parallel testing on input, in-line, and output samples, using GC-MS and NMR as needed. If a batch shows trace-level problems, our teams trace it down to raw material lots, blending tanks, or even valve seals, rapidly swapping out faulty inputs to restore performance.

    Efficient waste management emerges as another area where real-world experience shapes outcomes. Handling of spent solvents and residual process wastes follows strict onsite treatment protocols. Our environmental compliance team works closely with process engineering to fine-tune solvent recovery ratios, recover valuable cyclic intermediates, and lower effluent loads well beneath regional limits. Hard-won success here helps our customers meet their own sustainability targets and audit requirements.

    Loading and packaging subjects every drum and keg to thorough inspection for leaks or headspace vapor build-up. Product traceability from batch to drum gives customers visibility straight to plant batch logs. We work with third-party labs only for verification, as all main analysis happens under our roof, performed by operators and analysts trained onsite.

    Process safety carries special importance when handling nitriles. We value the lessons learned from early incidents — well-contained due to vigilant monitoring and clear SOPs, but instructive. Safety reviews address not only flammability but also skin, inhalation, and environmental routes of exposure, shaping our procedures for plant personnel and shipping partners. Sharing these insights with customers means new users avoid past pitfalls.

    Opportunities and Directions for the Future

    One area where we see growth lies in asymmetric synthesis. Researchers actively explore enantioselective routes for cyclopropyl intermediates. Understanding the stereochemistry of 2,2-Dimethylcyclopropyl Cyanide enables development of new ligands, catalyst technologies, and greener processes. We invest in pilot-scale campaigns to refine chiral resolution steps and regularly update customers on new findings, closing the loop from early feasibility to plant-ready options.

    Digitalization impacts even the world of commodity chemicals. We now use integrated batch tracking, real-time analytics, and predictive maintenance for reactors and distillation columns. This data-driven approach cuts down downtime, boosts right-first-time outcomes, and allows us to flag abnormal results before they enter the next processing chain. Customers appreciate faster response times for COAs or deviation reports, streamlining their own regulatory and operational needs.

    We are constantly improving our synthetic route to raise atom economy and energy efficiency, lowering our environmental footprint per kilogram produced. Customers needing expanded supply for late-stage development or commercial launch benefit from reliable forecast planning rooted in actual production data, not marketing estimates or external projections.

    The growing need for sustainable supply chains leads many partners to re-examine their vendor lists. As the direct producer, we accommodate requests for increased supply resilience, green chemistry metrics, and multi-source validations. This adaptability anchors our relationships and helps customers with new green procurement targets or LCA reporting for their own clients.

    Open Dialogue and Real Solutions

    Niches like the one filled by 2,2-Dimethylcyclopropyl Cyanide rarely follow a perfect script. Customer needs change with project goals or regulatory shifts. We keep our conversations direct, fielding technical questions from bench chemists, process engineers, and supply managers alike. Our goal stays the same every time: deliver a product that works as intended, with no hidden surprises, and back it up with actual process know-how.

    This approach strengthens our partnerships, not only through formal agreements but also in the daily details — such as advice on handling, lessons learned from previous inquiry cycles, and honest feedback if a new chemistry seems better suited to another reagent. That authenticity forms the backbone of our work with 2,2-Dimethylcyclopropyl Cyanide. No shortcuts, no up-selling, just science, manufacturing, and shared results.

    Summary

    Manufacturing 2,2-Dimethylcyclopropyl Cyanide has taught us respect for the process and for the user. We see each batch as more than a tally on the board, but as a critical component in our customers’ progress, whether toward launching a new medication or unlocking an innovative material. Through steady investment, technical transparency, and ongoing dialogue, we commit ourselves to delivering a cyclopropyl nitrile that meets both today’s demands and tomorrow’s opportunities.