Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

3-Methylenecyclobutanecarbonitrile

    • Product Name 3-Methylenecyclobutanecarbonitrile
    • Alias 3-methylenecyclobutanecarbonitrile
    • Einecs 611-754-8
    • 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

    802928

    Compound Name 3-Methylenecyclobutanecarbonitrile
    Chemical Formula C6H7N
    Molecular Weight 93.13 g/mol
    Cas Number 25363-56-6
    Appearance Colorless to pale yellow liquid
    Boiling Point 75-77°C at 30 mmHg
    Density 0.975 g/cm3
    Refractive Index 1.470
    Solubility In Water Slightly soluble
    Flash Point 77°C
    Smiles C=C1CC(C#N)C1
    Inchi InChI=1S/C6H7N/c1-5-2-6(3-5)4-7/h1-2,6H2

    As an accredited 3-Methylenecyclobutanecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle, 5 grams, with tamper-evident seal; labeled with hazard symbols, chemical name, CAS number, and handling instructions.
    Shipping 3-Methylenecyclobutanecarbonitrile is shipped in tightly sealed chemical containers, protected from moisture and light. It is packaged according to hazardous material regulations, typically inside secondary containment, with proper labeling and documentation. The shipment is handled by certified carriers and complies with all safety standards for transporting organic nitrile compounds.
    Storage 3-Methylenecyclobutanecarbonitrile should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it in a cool, dry, and well-ventilated area, separated from incompatible materials such as strong oxidizers and acids. Ensure proper labeling, and store in a chemical storage cabinet if possible. Access should be limited to trained personnel wearing appropriate protective equipment.
    Application of 3-Methylenecyclobutanecarbonitrile

    Applications of 3-Methylenecyclobutanecarbonitrile in Industrial Manufacturing

    3-Methylenecyclobutanecarbonitrile serves as a highly specialized intermediate for advanced synthesis in several chemical manufacturing sectors. As a manufacturer, we deliver this raw material to support innovative downstream production, ensuring purity and consistent quality for critical industrial processes. The following sections detail the primary, real-world industrial applications where our product is utilized at scale.

    1. Pharmaceutical Intermediate for Antiviral API Synthesis

    This compound acts as a building block in the synthesis of advanced pharmaceutical intermediates, specifically targeting antiviral active pharmaceutical ingredient (API) production. R&D and pilot-scale manufacturing utilize this material for constructing structurally unique molecular scaffolds in small-molecule drugs, leveraging its strained ring and nitrile group for subsequent selective functionalization. Direct input into the process provides high-yield transformation under controlled alkylation and hydrolysis reactions, critical for stringent pharmaceutical environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (cGMP for Finished Pharmaceuticals)
    • EU GMP Volume 4, Annex 8 (Pharmaceutical Starting Materials)
    • USP Monograph reference for related intermediates as required

    Typical usage ratio

    • Used at 0.8–2.0 molar equivalents per target intermediate, adjusted for reaction scale and catalyst yield profile

    Downstream process integration

    • Charged in early-stage reaction to serve as a cyclobutane ring donor and nitrile source
    • Involved before key cyclization and functionalization steps
    • Reacted in anhydrous organic solvents under closed system
    • Critical for high-purity API batch runs requiring clean room standards

    Final product types

    • Small-molecule antiviral APIs
    • Pharmaceutical intermediates for specialty antivirals
    • Precursor scaffolds for new drug discovery
    • Patented next-generation active pharmaceutical compounds

    2. Agrochemical Synthesis as Ring-Conjugated Nitrile Intermediate

    Large-scale agrochemical manufacturers utilize this compound for its capability to introduce strained ring systems and active nitrile groups in new herbicide and insecticide molecules. The raw material enters the synthetic route for cyclobutane-derived actives where the methylidene group allows regioselective functionalization. CROP protection R&D favors this intermediate for scalable pilot synthesis in target molecule pipelines.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • REACH Regulation (EC) No 1907/2006 for chemical registration
    • FAO/WHO Specification for Pesticide Intermediates
    • ISO 9001:2015 for production traceability and quality management

    Typical usage ratio

    • Typically dosed at 3–7% by mass relative to total batch reactants, with process-dependent variation for desired ring-content in active molecule

    Downstream process integration

    • Added during early-stage building block formation, before halogenation and substitution chemistry
    • Methylenation and nitrile functionality exploited in selective pathways
    • Batch fed into jacketed reactors equipped with automated metering
    • In-line QC verifies absence of ring-opened byproducts at each step

    Final product types

    • Pyridinium-derived herbicides
    • Cyclobutane-based insecticidal actives
    • Pre-emergence weed control agents
    • Intermediates for fungicidal molecule development

    3. Specialty Monomer Sourcing for Advanced Polymer R&D

    Research departments in specialty chemical companies select this raw material as a functional cyclobutane monomer source for designing novel high-performance polymers. The reactive nitrile and methylene functionalities enable co-polymerization via radical or ring-opening polymerization methods, delivering unique properties such as improved rigidity, solvent resistance, or optical clarity. The addition of this compound into monomer feedstock blends allows for fine-tuning polymer matrices at laboratory and pilot production scales.

    Industry compliance standards

    • ISO 9001:2015 for chemical production quality systems
    • REACH pre-registration for new monomer intermediates
    • ASTM D4762 for copolymer characterization
    • RoHS Directive (2011/65/EU) in case of electronic-grade polymers

    Typical usage ratio

    • Co-monomer loading between 0.5–10% by mole, variable by target polymer backbone and desired end-use properties

    Downstream process integration

    • Mixed with base monomer(s) before initiator addition in polymerization reactor
    • Fed through in-line dosing for continuous copolymer production
    • Post-polymerization purification under inert atmosphere, monitored for monomer conversion
    • Sampled for molecular weight distribution and end-group analysis

    Final product types

    • Specialty rigid plastics
    • High-clarity engineering polymers for optical applications
    • Pre-polymers for advanced resin systems
    • Functional coatings for industrial and electronic use

    4. Intermediate in Fine Chemical Synthesis for Advanced Materials

    This unique cyclobutane nitrile enters specialty organic syntheses for producing fine chemicals that demand precision structural integration. It supports the construction of customized ligands, specialty dyes, and catalytically active compounds. Custom molecule synthesis pathways utilize this intermediate for its compatibility with a wide range of nucleophilic additions and transition metal-catalyzed cross-coupling reactions, leading to highly defined end structures essential for material innovations in electronics and photonics.

    Industry compliance standards

    • ISO 9001:2015 certified production and batch traceability
    • Specialty chemical import/export regulatory filings (where applicable)
    • Internal Standard Operating Procedures for specialty feedstock handling
    • UN Globally Harmonized System (GHS) compliance on safety data management

    Typical usage ratio

    • Applied at 1–6% by mass, scaled to target structure’s requirement and downstream yield optimization

    Downstream process integration

    • Added in early or mid-synthesis to introduce constrained ring and nitrile group
    • Reacted under catalysis with metal complexes for further functionalization
    • Subjected to in-process analytical verification (LC-MS, NMR) at each transformation stage
    • Handled in closed systems to minimize volatile emissions

    Final product types

    • Specialty organic ligands for catalysis
    • Advanced monomer precursors for photonic materials
    • Performance dyes and pigments for device manufacturing
    • Small-molecule additives for high-tech coatings
    Free Quote

    Competitive 3-Methylenecyclobutanecarbonitrile prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    3-Methylenecyclobutanecarbonitrile: Hands-On Insights from the Manufacturing Floor

    Introducing Our Approach to 3-Methylenecyclobutanecarbonitrile

    Manufacturing 3-Methylenecyclobutanecarbonitrile isn’t about chasing a trend or following some industry formula. This compound plays a real, tangible role in specialty synthesis work, and we have rolled up our sleeves to make sure what we produce stands up where it counts—on your bench, in your plant, and through every synthesis path where reliability matters. We believe in speaking honestly about what goes into our processes, not just the product that comes out. Over the years, we have learned that producing this compound is more art than assembly line, a steady blend of experience, persistent improvement, and respect for the material itself.

    Detailed View: What Sets Our 3-Methylenecyclobutanecarbonitrile Apart

    This is not a warehouse secret; it’s a straightforward cyclobutane derivative with a nitrile functionality. Chemists often look for an intermediate that doesn’t stall a reaction, create ambiguous byproducts, or throw yields off. Success starts with purity and consistency, not with promises. Our team tests every lot with calibrated equipment – typically GC and NMR – to make sure you receive a colorless, crystalline solid, without surprise contaminants that could throw off a multi-step synthesis. Batch-to-batch consistency takes priority, avoiding headaches down the synthetic road.

    Specifications reflect the realities faced in the lab and on the plant floor. Moisture, trace metals, and thermal decomposition can sideline an entire order; we track those with every run. The melting range stands where it’s supposed to, and we listen when users tell us if traces affect downstream transformations. If a product starts to veer toward a yellowish tint or picks up off-odors, that’s when we double down on root cause, not just try to mask it. Customers have flagged that minute traces of polymeric byproducts can block later steps—so we developed purification regimes that go beyond usual chromatographic clean-up, focusing especially on cyclobutane ring stability and the methylene group's integrity.

    Why This Compound Matters in Organic Synthesis

    Anyone who has put in time on a research bench knows the frustration that comes with intermediates that are fussy, unpredictably reactive, or just plain inconsistent. 3-Methylenecyclobutanecarbonitrile carves out a niche in the synthetic world for its strained ring structure, useful in ring-opening studies and as a precursor to various pharmaceutical and agrochemical targets. Its nitrile group is a versatile handle for further transformation, often essential when aiming to introduce complexity into the carbon framework quickly. We have supplied this compound to groups focusing on new cyclobutane-bearing pharmaceuticals, as well as to manufacturers who scale up these transformations.

    We approach every synthesis with the perspective that a routine process on a small scale can turn into trouble during scale-up. Handling methylenecyclobutanes, especially with the electron-withdrawing nitrile, means respecting exothermic characteristics and potential runaway conditions. Our engineers have tuned both reactor conditions and purification to keep decomposition far below threshold levels. This focus translates to a cleaner, less reactive side-product slate that downstream chemists appreciate.

    Many users appreciate the well-defined reactivity: the strained ring opens smoothly under both thermal and catalytic conditions, while the nitrile transforms predictably under nucleophilic addition or reduction. Sometimes people overlook that a pure starting material saves much more time and cost than any cheap, cut-corner alternative. We have seen researchers uncover unexpected side routes when the starting nitrile is anything less than pure—so keeping impurities from creeping into the product stream is our obsession. It’s about more than numbers on a certificate; it’s the day-in, day-out reality of making things just work.

    Application Insights from Real Operations

    Our product’s journey doesn’t stop at our shipping dock. We keep in touch with users who stretch its utility, whether through scale-up campaigns, academic lab explorations, or process development efforts in custom synthesis outfits. Most project managers know that intermediates like 3-Methylenecyclobutanecarbonitrile play their part quietly, nestled inside the larger challenge of molecule-building. Sometimes, it winds its way through transformations that add functional groups, sometimes it’s incorporated as a bridging motif. We hear from dyestuff researchers who’ve used it to introduce rigidity into chromophores, as well as from polymer chemists tapping the strained ring for new backbone architectures.

    In these settings, minor lot-to-lot variability spells frustration. Two years ago, a pharmaceutical partner flagged that certain batches from external sources produced a sticky impurity that complicated separation on scale. After careful forensic work, it became clear that trace byproduct from incomplete cyclization steps—undetectable by routine TLC—could build up in kilo batches, fouling automated purification resins. We went back to our process, implemented deeper in-process testing, and added an extra crystallization step. Within three months, those issues faded out. We kept the fix, not because paperwork called for it, but because our customers’ results did.

    Differences That Really Show Up in the Lab

    Every manufacturer claims distinction—so we let our differences show up where they hit hardest: reliability, transparency, and technical honesty. Other products crowd the cyclobutane shelf, but some trade off chemical integrity for cost. Those unfamiliar with the quirks of synthesizing and isolating methylenecyclobutane nitriles often wind up with mixed oligomers, ring-opened residues, or brittle, difficult-to-handle solids. We rely on hands-on, direct analysis rather than batch averaging or loose, production-floor interpretations. Long experience making this compound has taught us not to cut steps or rush purifications.

    Standard-model nitrile intermediates—say, simple acrylonitrile or cyclobutanecarbonitrile—may share elemental formulas, but their reactivity profiles and downstream use cases diverge sharply. Direct substitution at the methylene site changes everything: where others tend to polymerize or break down, ours holds its structure and resists runaway polymerization under recommended reaction setups. That means fewer reworks for end-users, plus more reproducible results all around. Some manufacturers repackage from upstream suppliers or accept second-tier lots; we take ownership of each batch’s integrity because downtime, failed reactions, and scrapped material never offset small savings.

    Challenges and Solutions Learned Through Practice

    Production never stays on autopilot. Each technical glitch or odd-ball impurity profile forces hard questions. We see challenges in every stage, from raw material supply to finished packaging. Cyclobutane intermediates, especially with an exocyclic methylene, react sensitively to oxidative impurities and light. Years back, a shift in one solvent grade led to trace peroxides making their way into final product. Rather than mask the issue, we built new storage protocols, shielding all materials and intermediates from UV and atmospherics until ready for final crystallization and drying. Our vacuum filtration and inert-atmosphere handling now reflect those lessons learned.

    Disposal, too, means more than compliance. The highly strained ring system and nitrile group in spent material can interact in unpredictable ways during bulk waste processing. Some years ago, batch residues behaved stubbornly in incineration—generating minor off-gassing that caused local complaints. Tracking down the chemistry led us to institute a mild hydrolysis step before disposal, breaking the ring and neutralizing the nitrile safely. That process not only satisfied regulatory stakeholders but removed surprises from our environmental records. We pass on that real-world disposal advice to larger users scaling up, because nobody gains from a late-stage compliance headache.

    Supporting Innovation Without Shortcuts

    Research and industrial syntheses set new bars for reliability every year. As green chemistry principles grow stricter and QC tollgates rise, we have adapted our process for both speed and sustainability. Short cuts might shave a day or two from throughput initially, but the price—in failed batches and loss of operator trust—far outweighs gain. Investing in improved process controls, digital batch tracking, and real-time impurity monitoring started as a way to keep our own costs down but evolved into an ongoing competitive advantage. Customers routinely ask for lot histories or analytical traces; we provide them with pride, knowing each reflects hard-won discipline.

    We have observed increased requests for high-purity 3-Methylenecyclobutanecarbonitrile, especially for applications setting new benchmarks in medicinal chemistry. Late-stage intermediates demand cleaner feedstocks, free from the kinds of haze or non-volatile residue sometimes tolerated in commodity-grade cyclobutanes. Our direct experience shows that meticulous fractionation and deep-vacuum dehydration produce cleaner end-product with sharper melting profiles. The extra effort may raise production costs, but feedback from the field confirms that reaction reliability more than justifies the attention.

    Reflections on Specific Use Cases

    We learn from each application field we support. Medicinal chemists rely on 3-Methylenecyclobutanecarbonitrile as a stepping-stone to functionalized cyclobutanes, valued for their pharmacological promise—particularly as ring size and geometry tuning can change molecular recognition and metabolic fate. Over the years, process chemists developing new routes to insecticidal or herbicidal compounds have flagged how our consistent melting range and low-odor profile translate into easier, more predictable scaling. In one agricultural project, a multi-tonne campaign ran on our material for over a year with no deviation in yields or product color—testament to why tight controls pay off in downstream consistency.

    Polymer researchers, meanwhile, come back because exocyclic methylene groups open up possibilities for novel cross-linking chemistries. Projects aiming for higher rigidity or altered persistence in polymer blocks find that minor shifts in purity or substitution pattern alter mechanical performance. The compound’s structural tension introduces new reactivity, making process control even more vital—especially where reactive extrusion or UV activation come into play. The lessons translate into our routine work: producing, testing, rechecking, and only shipping when each batch meets strict client and internal thresholds.

    Pilot plant managers and scale-up chemists frequently share cautionary stories about incoming lots that didn’t meet spec, causing days of lost time and labor. In the real world, recovery from fouled runs involves not only rework but also intensive maintenance—cleaning reactors, scrubbing trace residue, recalibrating analytical systems. These stories shape our culture; practicality and follow-through carry more weight than any abstract production metric.

    Feedback Response and Continuous Change

    Working directly with research scientists and production-scale partners gives us a feedback channel that shapes our daily routines. No batch leaves our facility before direct, multi-point QC. Trace moisture, minute isomer content, low-level refractive impurities—all flagged through direct analytics. A few years ago, a customer flagged color development after storage in certain packaging formats. We added improved HDPE containers with inner UV shields, controlled temperature logistics, and made post-shipment monitoring part of our standard service. Field notes inform our future process decisions—what worked yesterday shapes what we deliver tomorrow.

    We keep in close conversation with users about challenges percolating in the synthesis landscape. Regulatory expectations tighten; substrates become more complex; scale-up pressures mount. Each challenge pushes us to re-examine, tune, and sometimes overhaul established workflows. Sticking to the easy road only works until field results disagree—then repeat business disappears. That reality keeps our process dynamic, customer-centered, and open to improvement.

    Looking Ahead with Confidence in Proven Methods

    Seeing repeated project successes built on robust intermediates sharpens our resolve to double down on solid, ground-up manufacturing practice. Outsourcing critical steps or shelving responsibility only brings short-term gain and long-term loss— we’ve seen it too many times in other plants. By keeping our process in-house, from raw material sourcing to high-vacuum drying and careful packing, we ensure the compound users receive reflects the skill, discipline, and pride of our team. That commitment shows up as lower failure rates, clean downstream chemistry, and near-zero customer complaints.

    Our journey with 3-Methylenecyclobutanecarbonitrile has been shaped by the facts on the ground: synthesis quirks, scale-up realities, and the lived experience of chemists not afraid to tell us directly what worked, what didn’t, and what could be better. We move forward by acting on real feedback, innovations tested by day-to-day production, and a hands-on respect for both user and molecule. Each new challenge is a chance to do better, and each success a result of listening, adjusting, and delivering with integrity every time.