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HS Code |
901955 |
| Cas Number | 2537-99-5 |
| Molecular Formula | C10H6N2 |
| Molecular Weight | 154.17 |
| Iupac Name | isoquinoline-1-carbonitrile |
| Appearance | Off-white to yellow solid |
| Melting Point | 95-98°C |
| Boiling Point | 343.1°C at 760 mmHg |
| Density | 1.19 g/cm3 |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | N#CC1=CC=CC2=NC=CC=C12 |
| Inchi | InChI=1S/C10H6N2/c11-7-9-4-2-1-3-8-6-12-5-9-8/h1-6H |
| Synonyms | 1-Cyanoisoquinoline |
| Storage Temperature | Store at 2-8°C |
| Flash Point | 161.8°C |
As an accredited 1-Isoquinolinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Isoquinolinecarbonitrile, 25g: Supplied in an amber glass bottle with tamper-evident cap and hazard labeling for chemical safety compliance. |
| Shipping | 1-Isoquinolinecarbonitrile is shipped in tightly sealed containers, away from incompatible substances, and stored in a cool, dry, well-ventilated area. It is handled as a hazardous chemical; packaging complies with international transport regulations. Ensure all relevant documentation, proper labeling, and safety protocols are in place during transit to prevent leaks or exposure. |
| Storage | 1-Isoquinolinecarbonitrile should be stored in a tightly sealed container in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers and acids. Protect the chemical from moisture and direct sunlight. Use appropriate chemical-resistant containers and label clearly. Ensure access to safety equipment in storage and handling areas. |
Applications of 1-Isoquinolinecarbonitrile in Industrial Manufacturing1-Isoquinolinecarbonitrile serves as a foundational intermediate within advanced chemical synthesis chains, supporting key downstream manufacturing sectors. As a direct manufacturer, we provide this compound to industrial producers rigorously controlling for composition, traceability, and regulatory certainty. Below, we specify practical scenarios where our material enables precision formulation and integration according to well-established compliance frameworks and process requirements. 1. Active Pharmaceutical Ingredient (API) Synthesis in Oncology Drug Manufacturing1-Isoquinolinecarbonitrile supports the synthesis of select heterocyclic anticancer agents, acting as a nitrile building block for the introduction of isoquinoline scaffolds in API molecules. Downstream pharmaceutical producers utilize our material during key condensation steps in multistage syntheses, particularly for small-molecule kinase inhibitors targeting solid and hematologic tumors. Precise addition rates ensure the desired purity and yield of the target substance, subject to stringent QC protocols and global pharmacopoeial standards. Industry compliance standards
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2. Agrochemical Intermediate Production – Synthesis of Fungicide ActivesThe compound functions as a cyclization component during the preparation of certain crop-protection agents with isoquinoline motifs. Industrial formulators in the agrochemical sector incorporate the material to create active intermediates for finished fungicide formulations. Compliance with agricultural chemical registration demands precise process documentation and control, and our supply chain ensures material consistency across global plant sites specializing in triazoles and strobilurins. Industry compliance standards
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3. Specialty Dye Synthesis for Advanced MaterialsThis nitrile intermediate is incorporated by advanced dye manufacturers developing functional pigments and optical brighteners containing isoquinoline units. Material purity and particle size distributions are monitored to meet tight quality frameworks in specialty colorant production, crucial for end-use sectors such as functional polymers, display technologies, and security printing. Industry compliance standards
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4. Electronic Chemical Intermediates for Liquid Crystal MaterialsProducers of liquid crystal displays (LCDs) and related electronic materials employ the compound as a precursor for tailored heterocyclic intermediates integrated into high-purity liquid crystal mixtures. The strict control of trace impurities and low metal content aligns with the material purity standards demanded within display supply chains, supporting the yield and stability of advanced LC devices. Industry compliance standards
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In the world of fine chemicals, clarity and consistency shape every outcome. Throughout years behind the reactors and within the QC lab, 1-Isoquinolinecarbonitrile has distinguished itself as a valued intermediate for developers and manufacturers looking for streamlined synthetic routes and dependable reactivity. The appeal doesn’t come from a marketing campaign—it comes from chemistry that stands up to repeated scrutiny, meeting the critical needs of R&D chemists and process engineers who know their reactions will only be as reliable as the building blocks poured into the flask.
A lot gets said about purity, but in practice, only careful control of each step, from raw material sourcing to post-synthesis treatment, guarantees a compound like 1-Isoquinolinecarbonitrile to meet consistently high benchmarks. The solid—white to off-white in typical batches, thanks to the minimization of colored side products—demonstrates that transparency isn’t just visual. Analytical testing, including HPLC and NMR, routinely shows purity above 99%. Moisture content is stringently limited, and trace contaminants are managed through multiple recrystallizations.
Unlike with commoditized intermediates, in-house chemists and operators draw directly on decades of scale-up and batch-to-batch reproducibility experience. Every run tells a story: reaction rates shift with subtle pressure changes, oven dwell times determine bulk properties, and lot-to-lot comparisons drive process tweaks. These aren’t theoretical ambitions, but daily habits shaped by direct feedback from each finished product.
The product has seen several specification increments over its development. Research-grade batches reflect a higher purity threshold, tightly controlling for halide or amine residues that would quench precious metal-catalyzed reactions. For process-scale requirements, the focus shifts toward optimizing crystallite size for downstream filtration or adjusting the particle surface for solubility in tailored solvent systems. The feedback loop between applications—be it pharmaceuticals, agrochemical intermediates, or specialty material precursors—drives the improvement roadmap.
We learned early that multi-purpose grade labels hide the real differences that matter on the plant floor. For example, micron-scale control can prevent filter clogging downstream, which is critical for customers automating their isolation processes. These details, derived from practical challenges rather than desk reviews, set apart product batches that keep projects on timeline from those that stall investigations or risk compliance headaches.
In our own hands, we notice the robustness 1-Isoquinolinecarbonitrile brings to heterocyclic chemistry. The compound’s unique structure—cyano group attached to the isoquinoline nucleus—offers useful electronic effects for coupling strategies. Reactions like Suzuki or Buchwald-Hartwig aminations process more swiftly, with cleaner isolation thanks to the minimized formation of hard-to-separate byproducts.
Colleagues working in process R&D often remark that other nitrile intermediates, such as benzonitrile derivatives, rarely deliver the same combination of direct reactivity and selectivity, especially when aiming at complex pharmaceutical scaffolds. With 1-Isoquinolinecarbonitrile, the cyano group remains intact under a wider range of conditions, resisting hydrolysis or reduction, even under scale-up stress. Avoiding post-reaction cleanups for unwanted hydrolysis byproducts has proven a significant operating advantage.
This stability translates to fewer surprises, both at lab scale and during full production. Years of observation have shown this nitrile not only tolerates rigorous purification protocols but also confines side reactions that normally spike impurity profiles. Being hands-on with these batches over time, we recognize the real-world value of a chemical that rarely forces a rework, saving both material cost and line time.
A major concern for purchasing and manufacturing managers remains workflow integration. In customers’ experience, the onboarding of 1-Isoquinolinecarbonitrile has supported timelines for high-value syntheses, particularly as a starting point for kinase inhibitor libraries and CNS-active APIs. Our internal programs saw cycle times drop when switching out older intermediates for this nitrile—stirring times reduced, waste streams cleaned up, and less energy spent on purification.
Beyond pharmaceuticals, the compound’s uses branch into advanced materials where isoquinoline scaffolds form chromophores or charge-transport matrices. Crafting conductive polymers, color-fast organic pigments, or light-absorbing layers for photovoltaic devices all benefit from the stable core of this molecule. The feedback often ties to batch control—the right polymorph, the narrow melting range, or the tailored particle profile. Where necessary, we support collaborative solvent optimization or custom sieving. Adjustments may come from new regulatory filings, adjustments to downstream process design, or targeted improvements requested by development partners.
Pain points encountered at the customer interface often relate to compatibility with increasingly sensitive downstream steps. Modern API synthesis or functional materials assembly calls for tighter impurity control and more predictive reactivity. From batch histories, we saw earlier approaches that used broad-spectrum amine or nitrile intermediates introduce carryover impurities, posing both toxicity and compliance risks. Current specifications for 1-Isoquinolinecarbonitrile, by contrast, reflect direct learning from these case studies: shelf stability, manageable particle flow, and clean breakdown profiles during stress-testing all speak to the accumulated benefit of process and analytical investment.
In countless campaigns, our chemists measure 1-Isoquinolinecarbonitrile directly against more routine aromatic nitriles or alternative heteroaromatic cores. Yield losses, labor hours, and energy overheads all come under comparison. While standard benzonitriles enter substitutions smoothly, they lack the enabling features for more demanding heterocycle synthesis or late-stage functionalization. Trying to adapt quinoline or naphthalene nitrile derivatives can introduce solubility headaches or unexpected reactivity. Isoquinoline fluoro- or amino-analogs offer different synthetic advantages, but the cyano substitution stands out in providing cross-coupling flexibility without preactivation or excessive protecting group strategies.
We work directly with bench teams and engineers to track not just isolated yield, but the total throughput improvement from reduced rework and downtime. Kinetic runs on pilot lines show direct time savings, and impurity profiles clarify with less operator intervention. Over the years, seeing fewer rejected batches or downgraded product tells the real story: operational risk drops when processes use intermediates that behave consistently and clean up easily.
Operators in our facilities handle metric tons of 1-Isoquinolinecarbonitrile across the year. Plant protocols have eliminated exposure risks traditionally seen with aromatic nitriles. Enclosure and dust collection systems keep airborne levels below occupational limits, while packaging in lined fiber drums mitigates both moisture pickup and cross-contamination. Regular feedback from the floor indicates direct-handling issues rarely emerge, owing to free-flowing solid properties and filtered final packaging. Unlike some analogs, our experience shows no tendency for sticky agglomeration or static clumping, even in high-humidity environments.
From a transportation perspective, we commit to regular hazard assessments but find no unexpected handling events compared to other solid organic intermediates. Downstream customers report similarly smooth transitions during storage and transfer, both in bulk and smaller packaging sizes for laboratory use.
Sustained access ranks among the most-cited customer requirements for key intermediates. Manufacturing this compound in-house allows for tight oversight of raw material stocks, utility inputs, and safeguard inventory. We resist external shocks by dual-sourcing core reagents and maintaining modular batch reactors. The operation has weathered global logistics volatility with less disruption compared to traders; we can flex lot sizes and stagger production for reliable lead times.
Process modifications, driven by both regulation and field learning, push us to refine each campaign, focusing not just on throughput but on risk mitigation for delayed fulfillment or process deviations. We keep sample libraries from each batch for retrospective QC, and maintain transparent communication with long-term customers during any operational adjustments.
Every kilogram of 1-Isoquinolinecarbonitrile tells a story shaped by years of hands-on development and tight integration with the demands of modern synthesis. The compound appears simple on a spec sheet, but its performance reflects a rarely achieved union: a robust intermediate that meets the technical demands of high-value product development while smoothing out practical hiccups in plant and laboratory environments.
Direct interaction with both the material and its users drives every improvement—minute solubility enhancements, incremental impurity reduction, and batch reproducibility. Whether in small pharma innovation labs, large-scale API production, or materials research facilities, the benefits show up on the ground: fewer reruns, faster process adoption, and confidence that intermediate lots match reaction needs yesterday, tomorrow, and the years ahead.
Keeping every aspect—from particle size through storage—to a tight specification, and allowing for project-by-project customization where feasible, keeps the product relevant for new applications as the boundaries of fine chemistry move forward. Our technical support and development teams remain embedded within the production effort, sharing learnings from pilot and commercial batches and drawing directly from customer problem-solving as new challenges arise.
We owe advances in our 1-Isoquinolinecarbonitrile offering to daily collaboration with customers and partners facing tightening regulatory controls, more aggressive efficiency targets, and ever-increasing purity requirements. The process never stands still: learning from both plant feedback and end-user outcomes means next-generation variants emerge ready to solve tomorrow’s bottlenecks.
As industry requirements evolve, we adapt by refining both the upstream chemistry and downstream handling. Staying close to the process—in the plant, at the customer’s bench, or inside the analytical lab—ensures no specification is set in stone when new demands or smarter processes come to light.
From direct synthesis improvements to smarter packaging logistics, every step in our production of 1-Isoquinolinecarbonitrile draws from experience, feedback, and a clear understanding of both what works and what doesn’t in real-world applications. The material may serve as a single intermediate, but the accumulated knowledge behind each shipment sets the foundation for our commitment to reliability, safety, and ongoing progress in the fine chemicals sector.