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(1-Isocyanoethyl)Benzene

    • Product Name (1-Isocyanoethyl)Benzene
    • Alias Phenethyl isocyanide
    • Einecs 700-883-5
    • 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

    958905

    Name (1-Isocyanoethyl)Benzene
    Cas Number 13273-54-0
    Molecular Formula C9H9N
    Molecular Weight 131.18
    Appearance Colorless to pale yellow liquid
    Boiling Point 215-217°C
    Density 1.01 g/cm³
    Melting Point -37°C
    Refractive Index 1.541
    Smiles CC(NC#N)c1ccccc1
    Pubchem Cid 2734550

    As an accredited (1-Isocyanoethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle labeled “(1-Isocyanoethyl)Benzene,” tightly sealed, with hazard symbols and handling instructions clearly displayed.
    Shipping (1-Isocyanoethyl)benzene must be shipped as a hazardous material according to international regulations. It should be packed securely in tightly sealed, chemically resistant containers, placed in secondary containment with appropriate labeling. Transport must comply with UN shipping standards, ensuring protection from moisture, heat, and sources of ignition. Safety documentation is required.
    Storage (1-Isocyanoethyl)benzene should be stored in a cool, dry, and well-ventilated area, away from heat, sparks, open flames, and sources of ignition. Store it in a tightly sealed, chemical-resistant container, and protect it from moisture and direct sunlight. Segregate from oxidizers, acids, and incompatible substances. Properly label the container and follow all relevant safety guidelines for hazardous organic chemicals.
    Application of (1-Isocyanoethyl)Benzene

    Applications of (1-Isocyanoethyl)Benzene in Industrial Manufacturing

    As a direct manufacturer of (1-Isocyanoethyl)Benzene, we ensure consistent supply for critical fine chemical and pharmaceutical synthesis sectors. This specialty intermediate demonstrates well-documented utility in advanced pharmaceutical building blocks, specialty polymer modifications, agrochemical ingredient synthesis, and certain liquid crystal material productions. Below we present the main downstream industrial scenarios, with practical integration, compliance, and formulation details based on verified industry usage.

    1. Pharmaceutical Intermediate Synthesis

    (1-Isocyanoethyl)Benzene finds direct use as an isocyanide component in the synthesis of heterocyclic medicinal cores, especially for research and production of APIs involving multicomponent Ugi or Passerini reactions. Its unique reactivity enables streamlined building of pharmacophores containing nitrogen, offering improved steps in combinatorial chemistry and targeted compound libraries for high-value drug discovery pipelines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF: United States Pharmacopeia for process validation and impurity profile requirements
    • 21 CFR Part 210/211: Current Good Manufacturing Practices in Manufacturing, Processing, Packing, or Holding of Drugs
    • ISO 9001:2015 for quality management system requirements in chemical manufacturing

    Typical usage ratio

    • 0.9–1.05 molar equivalents relative to aldehyde or amine partners in multicomponent reactions, adjusted based on reaction stoichiometry and desired purification yield

    Downstream process integration

    • Introduced as a key isocyanide reactant during the first stage of API intermediate assembly, directly charged into batch reactors under controlled temperature and inert atmosphere, followed by downstream purification and isolation as dictated by route

    Final product types

    • Pyrrolidine-based analogs with bioactivity potential
    • N-heterocyclic molecular scaffolds for preclinical evaluation
    • Building blocks for small molecule kinase inhibitors
    • API intermediates for specialty or orphan indication drug candidates

    2. Agrochemical Intermediate Production

    Within crop protection chemical manufacturing, (1-Isocyanoethyl)Benzene serves as a specialized intermediate for constructing nitrogen-rich ring systems—crucial for synthesizing certain new-generation fungicides and insecticides. Its controlled reactivity supports step-efficient methodologies, leading to higher product selectivity and reduced downstream processing times for active ingredient assembly.

    Industry compliance standards

    • FAO/WHO: International Code of Conduct on Pesticide Management
    • Regulation (EC) No 1107/2009: Plant protection product standards in the European Union
    • ISO 17025: Laboratory testing and calibration for agrochemical actives
    • GB/T 16157-1996: Analytical and process controls for agrochemical raw materials in China

    Typical usage ratio

    • 0.8–1.2 molar equivalents depending on target heterocycle yield and precursor purity, with stoichiometry selected according to downstream transformation route

    Downstream process integration

    • Reacted in the cyclization phase after initial condensation, where it joins multi-component assembly for target heteroaromatic structures; often followed by solvent exchange and crystallization steps ahead of formulation blending

    Final product types

    • Precursor segments for triazole-based fungicides
    • Functionalized intermediates in new pyrazole insecticide R&D
    • Key synthons in research-scale pesticides
    • Plant growth regulator intermediates for crop protection portfolios

    3. Specialty Polymer Modification

    Research and select commercial scale-ups use (1-Isocyanoethyl)Benzene as a functional monomer or as an end-group modifier for high-performance polymers, especially where heteroatom insertion confers tunable mechanical or optoelectronic properties. This application leverages its reactive isocyanide group during advanced copolymerization or side-chain functionalization stages, enabling downstream production of tailored engineering plastics.

    Industry compliance standards

    • ISO 9001:2015 for polymer product traceability and QC
    • REACH (EC 1907/2006): Registration, Evaluation, Authorisation and Restriction of Chemicals compliance for monomer introduction
    • ASTM D883: Standard terminology for plastics
    • ISO 14001: Environmental management systems applicable to polymer process waste handling

    Typical usage ratio

    • 0.5–5 wt% as a comonomer or post-polymerization modifier, with precise proportion determined by targeted modification intensity and end-use physical property specifications

    Downstream process integration

    • Fed via dosing system to the monomer blend ahead of polymerization, or introduced post-polymerization as a coupling agent in solvent phase; requires accuracy in ratio control and immediate blending to ensure uniform incorporation

    Final product types

    • Custom copolymers for electronics applications
    • Functionalized engineering resins with enhanced thermal stability
    • Modular side-chain modified plastics for optical films
    • Prototypical high-glass-transition polymers for advanced molding

    4. Liquid Crystal Material Synthesis

    Some laboratories and liquid crystal display (LCD) materials developers use (1-Isocyanoethyl)Benzene as a specialty intermediate in the production of benzene-based and nitrogen-heterocycle mesogens. Its reactivity enables the fine-tuning of dielectric anisotropy and improves molecular alignment features in liquid crystal mixtures intended for display panel manufacturing.

    Industry compliance standards

    • IEC 61249-2-41: Material specification for LCD manufacturing
    • ISO 9001:2015 for display material QC traceability
    • RoHS Directive 2011/65/EU: Restriction of hazardous substances
    • China National Standard GB/T 13542: Liquid crystal substance requirements

    Typical usage ratio

    • 0.2–2 mol% relative to total liquid crystal compound content, with precise value optimized for desired phase transition temperature and alignment behavior during formulation design

    Downstream process integration

    • Undergoes synthesis with specific aldehyde and amine partners in the liquid crystal mixture preparation phase, followed by purification through high-vacuum distillation or column chromatography prior to blending into master liquid crystal batches

    Final product types

    • High-dielectric LCM components for high-resolution displays
    • Nitrogen-substituted mesogens for advanced TFT-LCD panels
    • Experimental dual-frequency liquid crystals
    • Low viscosity liquid crystal mixtures for fast-response panel technology
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    Certification & Compliance
    More Introduction

    Introducing (1-Isocyanoethyl)Benzene: A Manufacturer’s Perspective

    What We Produce: A Look at (1-Isocyanoethyl)Benzene

    Years of hands-on manufacturing have provided a unique appreciation for chemicals that both innovation-driven and reliable. (1-Isocyanoethyl)Benzene, sometimes called phenyl-1-isocyanoethane, offers a clear demonstration of how performance and discipline in manufacturing create value well beyond a bottle on a shelf. Working directly with the raw materials, overseeing every step from synthesis to purification, and committing ourselves to batch-to-batch consistency shape how we view and handle each molecule that leaves our operation.

    This product, produced with purity benchmarks exceeding 98%, finds itself used by researchers and development chemists aiming for targeted transformations in the lab or scale-up campaigns for more complex chemical building blocks. Every batch built confirms the difference that stringent controls make, as trace contaminants can derail entire projects, fail chromatographic monitoring, or even skew reactivity in organic synthesis. As the team responsible for the end product, our reputation stays on the line for every period of the supply chain — from engineering raw material to the final sealed container.

    Product Model and Specifications: Insights from the Factory Floor

    We offer (1-Isocyanoethyl)Benzene in models defined by both quantity and grade. Standard batch sizes run from gram-level samples for synthesis trials up to kilogram-scale runs that match the demands of process chemists readying for pilot-scale operations. The colorless to faintly pale liquid, with a distinct isocyanide odor, reflects our vigilant control of environmental factors during production. Molecular structure, C9H9N, is confirmed at each batch release with NMR and GC-MS validation—critical steps for chemists who need to trust the molecule matches both structural and purity standards when planning synthetic campaigns.

    Physical properties like a boiling point in the range of 210-215°C, refractive index checks, and minimum moisture content are all tightly managed in our workflow, guided by real-world lab testing rather than paperwork alone. We engage engineers and analysts each step, not just for compliance but to challenge every batch for variance. Over time, our factory has found that investing in stable temperature ramping, fresh catalyst systems for isocyanide formation, and rigorous solvent recovery pay dividends in fewer customer setbacks or flagged results.

    Where (1-Isocyanoethyl)Benzene Delivers Value

    Most customers in the market use this compound for specific transformations in heterocyclic synthesis and multicomponent reactions. One major application involves its use in Ugi-type or Passerini-type reactions, where the presence and stability of the isocyano functional group permit rapid assembly of complex molecular frameworks. The isocyanoethyl group adds a specific substitution pattern that lets chemists push boundaries not possible with simpler isocyanides such as methyl or tert-butyl derivatives. Through years of feedback and close collaboration with end-user R&D teams, adjustments in purification or recommended storage have resulted in a product that supports both exploratory work and routine manufacturing steps.

    There are recurring examples of (1-Isocyanoethyl)Benzene underpinning lead discovery for pharmaceuticals, fine-tuning ligands in catalyst development, or feeding into advanced functional materials for electronics. Direct conversations with users highlight how each subtle variation of the isocyanoalkyl backbone creates new possibilities in SAR (structure-activity relationship) studies and property optimization. The additional “ethyl spacer” in this compound—compared to phenyl isocyanide—can mediate steric hindrance, reactivity, or polarity in ways that open up new methodological doors.

    Differences from Other Isocyanide Products

    Having produced isocyanides in several configurations, comparisons draw themselves. Methyl isocyanide, for example, is a common selection for introductory multicoupling chemistry, but it lacks the nuanced steric and electronic influence that (1-Isocyanoethyl)Benzene carries due to its aromatic ring and longer chain. Chemists needing stepwise control over their final product benefit from this compound’s different reactivity profile: the aromatic portion adds electron density that guides selectivity during multicomponent assemblies, and the ethyl spacer offers flexibility that influences cyclization or insertion results.

    In contrast, tert-butyl isocyanide stands as another favorite for Ugi-type reactions because of its balance between reactivity and odor control, but comes with a significant difference in how it incorporates into intermediates. The physical handling, olfactory impact, and downstream stability of each choice matter—many users gravitate to (1-Isocyanoethyl)Benzene because they have a need for its intermediate profile rather than trying to “force-fit” reactions with more reactive or less stable options.

    Much is written about the volatility and pungency of low molecular weight isocyanides. We’ve spent years optimizing venting, containment, and operator protection, tailoring protocols with direct input from those who work with these molecules daily. The result is a system in our plant that captures off-gassing, manages air turnover rates, and delivers product with handling confidence, not just theoretical containment. This matters even more as R&D labs scale up and risk factors multiply.

    From Raw Materials to Final Bottle: Manufacturing Know-How

    Truth be told, the journey from raw benzene derivatives to a pure lot of (1-Isocyanoethyl)Benzene is neither simple nor risk-free. Our workers remain vigilant from batch planning through solvent recycling each day, tracking parameters not just for compliance but for reproducibility. Sourcing high-grade starting materials, including secure supply lines for ethylamines and phosgene substitutes (for isocyanide generation), has historically shielded our output from upstream disruptions. This direct control means chemists relying on timely shipments don’t suffer from the “out of stock” scenario that arises when traders or resellers lack upstream knowledge or relationships.

    Experience on the production line speaks volumes. Operators report that temperature excursions above carefully defined limits accelerate byproducts or degrade the desired isocyanide moiety. Small adjustments in vacuum stripping, addition rates, or reflux conditions show themselves not in lab notebooks, but in smoother chromatograms and fewer product returns. As with any specialty chemical, hands-on vigilance beats remote problem-solving or outsourced risk.

    Challenges in Production and Supply — Lessons Learned

    Past disruptions in chemical supply chains have brought home the vulnerability of fine chemical sourcing. We’ve encountered shifting regulations on raw amines, security restrictions on isocyanide shipment, and even local force majeure events from industrial parks. The ability to respond, adjust, and keep lines running reflects real lessons in resiliency. Batch documentation, real-time communication with logistics, and standing relationships with local regulators let us keep output as steady as possible during industry-wide shortages.

    This experience also shapes our approach to safety and environmental commitment. By controlling emission rates, investing in activated carbon filtration, and regular equipment modernizations, real improvements result—not just box-checking. Visits from customer QA teams have turned into collaborative troubleshooting sessions, often yielding process tweaks that further reduce impurity carryover or streamline customer test results. No amount of advertising replaces this kind of feedback loop between plant and end-user.

    End User Support and Technical Backstopping

    Supporting customers in the field is just as much about practical assistance as it is about sending a COA. We keep a technical support team drawn from the factory ranks—people who actually worked on synthesis or quality steps and can translate that experience into clear, actionable insight for chemists facing real-time issues. This approach addresses production upsets, helps diagnose anomalies in NMR or IR spectrums, and assists in troubleshooting when downstream reactions differ from literature behavior.

    End users occasionally report specificity issues where subtle changes in supplier material have resulted in unexpectedly low yields or new side products. Our ongoing dialogue has shaped both our analytical routines and packaging safeguards, for example, triple-checking septa integrity to prevent atmospheric moisture ingress. Over time, our knowledge has moved from “deliver on spec” to “help enable new science,” a shift that creates lasting partnerships rather than one-off transactions.

    Sustainability and the Future of Fine Chemical Manufacture

    The pressure to bring greener processes to chemical manufacturing has reached isocyanide chemistry. Our plant has shifted away from traditional, high-toxicity reagents where better options exist. Pilot programs have trialed alternative isocyanide-forming reagents, safer solvents, and in-line monitoring tools that catch variance before product packing. This keeps both operator risk and downstream regulatory exposure lower for everyone in the supply chain.

    Recycling solvents, using improved scavengers for waste handling, and conforming to global environmental frameworks have become second nature. We track changes in environmental policy closely—what starts in the EU or North America shapes site upgrades for years ahead. Drawing on real production experience, our team regularly evaluates new reaction platforms, flow reactors, or eco-friendly packaging that meet both economic and practical goals. The aim is for a product that supports both experimental ambitions and sustainability requirements.

    Direct, Manufacturer-Driven Approach: Why It Helps

    As a manufacturer, we have learned that direct relationships with chemists solve problems much faster than orders mediated by opaque supply chains. Chemists working in process teams often need real-time answers or tailored delivery schedules that don’t fit a distributor’s template. This reality has pushed us to condense decision cycles for rush shipments, introduce QC “forensics” support, or redesign shipping cartons based on customer feedback.

    This hands-on approach means that quirks discovered mid-sequence get attention from the same personnel responsible for the batch, creating a feedback loop between scale-up and continuous improvement. For materials as specialized as (1-Isocyanoethyl)Benzene, this can mean the difference between project success and lost weeks due to miscommunication or incorrect material identity.

    Improving Supply Resilience and Global Access

    Our global partners have encountered sudden local restrictions, shifting pricing, or political issues that disrupted previous supply. In response, we established multiple distribution points, diversified raw material sourcing, and maintain secondary inventory at critical hubs. The result brings more dependable access for R&D teams, even under market pressure, without resorting to lower quality or uncertain alternatives.

    We recognize that laboratories in regions with less direct manufacturer access often face delays, canceled projects, or added costs when supplies run thin. Experience here feeds back into our investment plans, shaping future expansions or partnerships to close these access gaps. Every region’s needs remain part of overall production planning, not an afterthought or market fluctuation risk.

    Working Beyond the Bottle: Collaboration and R&D Synergy

    Too often, the story of specialty chemicals ends when the package arrives. Having both produced and supported (1-Isocyanoethyl)Benzene firsthand, we recognize the real value shows once the product enters a creative laboratory environment. Ongoing partnerships with universities, contract research organizations, and materials labs have spurred new applications, adjustments to storage recommendations, or packaging enhancements that wouldn’t have surfaced in a less collaborative framework.

    Research trends continue to push demands for even higher purity, improved physical stability, or custom batch characteristics. These requests are never theoretical: they originate from active feedback and hands-on pilot work, not template-driven or “one-size-fits-all” marketing. Regular visits to both academic and industrial labs provide the context needed to refine product offerings in a way that tracks scientific ambition, not just production output.

    Summary: What Sets (1-Isocyanoethyl)Benzene from Manufacturers Apart

    (1-Isocyanoethyl)Benzene serves as a specialty tool for chemists tackling ambitious synthesis or creating novel frameworks. Our focus as a direct producer has long been on reliability, technical support, and on-the-ground feedback rather than marking up products from upstream suppliers. Each batch reflects not just compliance to purity or physical standards, but attention to practical use—chasing down every trace impurity, investing in equipment to support safe and consistent handling, and keeping a direct communication line open with users at every scale.

    The practical reality of specialty chemical manufacture means every shift counts, every batch reflects hard lessons in process adaptation, and every user’s result circles back to the choices made on the factory floor. These are realities that can’t be fully captured in marketing literature or third-party data sheets. We believe the best way to ensure (1-Isocyanoethyl)Benzene supports scientific and commercial progress is to remain directly accountable. Every improvement—whether in quality, safety, sustainability, or customer support—comes from a process that values relationship and results over intermediate margin.

    Contact for Technical Dialogue

    We remain committed to supporting chemists working at every scale—from the first trial reactions to full process integration, and welcome technical questions, feedback, or collaboration proposals. Our team continues to make direct manufacturing expertise available, translating real experience into better chemical solutions for today’s R&D landscape.