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2-Amino-3-Cyano-4,5-Dimethylpyrrole

    • Product Name 2-Amino-3-Cyano-4,5-Dimethylpyrrole
    • Alias 2-amino-4,5-dimethyl-1H-pyrrole-3-carbonitrile
    • Einecs 'EINECS 620-508-5'
    • 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
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    Specifications

    HS Code

    732613

    Chemical Name 2-Amino-3-Cyano-4,5-Dimethylpyrrole
    Cas Number 871126-18-6
    Molecular Formula C7H9N3
    Molecular Weight 135.17
    Appearance Light yellow to brown solid
    Melting Point 89-92°C
    Purity ≥98%
    Solubility Soluble in DMSO, DMF; slightly soluble in water
    Storage Conditions Store at room temperature, protected from light and moisture

    As an accredited 2-Amino-3-Cyano-4,5-Dimethylpyrrole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 2-Amino-3-Cyano-4,5-Dimethylpyrrole, sealed with screw cap and clearly labeled for laboratory use.
    Shipping 2-Amino-3-Cyano-4,5-Dimethylpyrrole is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It must be handled with care and transported in accordance with local and international regulations for hazardous materials, ensuring proper labeling, documentation, and protection from excessive heat, light, and physical damage during transit.
    Storage 2-Amino-3-Cyano-4,5-Dimethylpyrrole should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, ideally in a chemical storage cabinet. Store away from strong oxidizers and acids. Properly label the container and follow standard laboratory safety protocols when handling or storing this compound.
    Application of 2-Amino-3-Cyano-4,5-Dimethylpyrrole

    Applications of 2-Amino-3-Cyano-4,5-Dimethylpyrrole in Industrial Manufacturing

    As a specialized producer of 2-Amino-3-Cyano-4,5-Dimethylpyrrole, we work closely with established customers across downstream sectors that rely on this intermediate for synthesis of advanced materials and functional molecules. Our industrial-grade material contributes to several high-value manufacturing streams where process reliability, quality protocols, and formulation precision are critical for downstream success. Below, we detail core application scenarios and specific integration points within contemporary manufacturing industries.

    1. Active Pharmaceutical Ingredient (API) Synthesis: Pyrrole-Based Drug Scaffolds

    Pyrrole derivatives featuring amino and cyano groups play a key role in the assembly of heterocyclic pharmaceutical intermediates, specifically for small-molecule APIs focused on anti-infective, anti-inflammatory, or kinase inhibitor research. Our raw material serves as a direct synthon in multi-step organic synthesis where defined substitution patterns impact biological activity and molecular targeting. Downstream pharma companies require tight specification alignment and batch traceability to align with regulatory compliance and strict impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. FDA 21 CFR Part 211 (where applicable)
    • European Pharmacopoeia monographs for heterocyclic intermediates
    • USP General Chapter <661> for residual solvents in synthesis

    Typical usage ratio

    • Usually 5–18% (w/w) in multi-component intermediate synthesis; adjusted per activity, yield optimization, and stepwise reactivity of coupling partners

    Downstream process integration

    • Added during heterocycle formation in batch reactors after prior halogenation/alkylation steps, or as a building block for Suzuki, Buchwald-Hartwig, or nucleophilic substitution coupling reactions

    Final product types

    • Branded and generic APIs for anti-cancer and anti-viral drugs
    • Precursor molecules for kinase inhibitors and research compounds
    • Advanced intermediates eligible for DMF registration

    2. High-Performance Dye and Pigment Intermediate Manufacturing

    Pyrrole-based compounds are essential for synthesizing high-performance dyes and specialty pigments, especially where strong electron-donating and -withdrawing groups improve color stability, lightfastness, and spectral properties for industrial inks and coatings. The material serves as a key monomer in condensation or cyclization reactions, supporting colorant formulations used by textile, packaging, and ink manufacturers who must align their final product safety and eco-compliance to international standards.

    Industry compliance standards

    • OEKO-TEX® STANDARD 100 for restricted substances in textile dyes
    • EN 71-3 (Toy Safety) for pigment leachability in coatings
    • ISO 9001:2015 Quality Management Systems for pigment manufacture
    • REACH Annex XVII entry 43 for pigment intermediates

    Typical usage ratio

    • Typically 3–12% (w/w base) in batch pigment condensation reactions; adjusted according to desired chromatic intensity and lightfastness target

    Downstream process integration

    • Incorporated during core chromophore synthesis by condensation with aromatic aldehydes under acidic conditions, then isolated and purified for pigment blending

    Final product types

    • High-stability organic pigments for plastics and coatings
    • Industrial dyes for cotton, wool, nylon, and paper
    • Colorant dispersions for inkjet and gravure printing

    3. Organic Semiconductor and OLED Material Production

    Specialty pyrrole units, including those with 2-amino and 3-cyano substitutions, support the design and fabrication of organic semiconductors, especially for organic light-emitting diodes (OLEDs) and conductive polymer electrodes. Manufacturers in the electronics sector require consistent monomer purity, reliable reactivity, and traceability throughout the integration of chemically synthesized building blocks into photonic device fabrication workflows.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in chemical electronics
    • IEC 61249-2-21 limit for halogen-free electronic materials
    • RoHS Directive 2011/65/EU for restricted substances in electronics
    • JEDEC J-STD-033D for handling moisture-sensitive device components

    Typical usage ratio

    • Varies from 4–9 mol% in the monomer blend for conductive polymer backbones; subject to optimization according to device layer thickness and target voltage thresholds

    Downstream process integration

    • Employed during solution polymerization or vacuum deposition for the synthesis and deposition of small-molecule films and conjugated polymers

    Final product types

    • OLED display layers for smartphones and televisions
    • Organic photovoltaic cell components
    • Polymer-based thin film transistors

    4. Agrochemical Intermediate Synthesis (Plant Protection Molecules)

    In the agrochemical sector, amino- and cyano-substituted pyrroles function as intermediates in the manufacture of certain herbicide and fungicide active substances. Downstream formulators depend on these molecular frameworks to achieve bioactivity targets for crop protection products, adhering to traceability and pesticide regulation requirements across global markets.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009 for plant protection products
    • U.S. EPA FIFRA guidelines for pesticide intermediate management
    • ISO 17025 for laboratory testing and batch validation

    Typical usage ratio

    • Between 6–15% (w/w), dictated by intended mode of biological action and desired concentration in downstream product synthesis

    Downstream process integration

    • Reacted with specific halogenated benzenes or alkylating agents in controlled batch synthesis to introduce the desired functional groups prior to formulation and micronization

    Final product types

    • Systemic fungicides for seed treatment
    • Pre- and post-emergent herbicide actives
    • Crop specific intermediate blends for further conversion

    5. Specialty Polymer Modifier in High-Temperature Engineering Plastics

    Certain engineering resins integrate functionalized pyrroles as chain modifiers to enhance thermal and oxidative stability, with downstream polymerizers incorporating these moieties to boost high-temperature performance and improve mechanical characteristics in end-use formulations. Stringent QC and documentation are essential throughout the blending and extrusion process to meet polyamide, imide, and related material specifications.

    Industry compliance standards

    • ISO 1043/1 for naming and coding of plastics
    • UL 94 flammability rating (V-0, V-1) for plastics
    • ASTM D3418 for DSC evaluation of thermal transitions
    • RoHS 2011/65/EU for restricted substances in electronic plastic parts

    Typical usage ratio

    • Ranges from 0.5–5% (w/w) as a co-monomer or functional chain extender, subject to assessments via melt-flow and impact resistance trials

    Downstream process integration

    • Compounded during polymerization in stirred jacketed reactors, or melt blended with base resins prior to extrusion and pelletization

    Final product types

    • High-performance polyimide and polyamide-imide engineering plastics
    • Injection molding grades for automotive and aerospace components
    • Specialty electrical insulators requiring enhanced heat resistance
    Free Quote

    Competitive 2-Amino-3-Cyano-4,5-Dimethylpyrrole prices that fit your budget—flexible terms and customized quotes for every order.

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    More Introduction

    2-Amino-3-Cyano-4,5-Dimethylpyrrole: The Practical Perspective from Our Lab

    From Our Process Lines: Bringing Reliable Chemicals to Everyday Synthesis

    At our manufacturing site, chemicals aren’t just catalogue listings—they are the products of years of effort in process optimization, strict batch-to-batch reproducibility, and countless troubleshooting logbooks filled by our teams. 2-Amino-3-cyano-4,5-dimethylpyrrole has become one of those essential compounds in our workflow that regularly makes its way to customers in pharmaceutical research, pigment development, and heterocyclic synthesis applications. Chemists in our labs work with this molecule nearly every week, so its role in modern lab settings comes with plenty of perspective from those who handle it and those who field calls when something unexpected comes up.

    What Sets 2-Amino-3-Cyano-4,5-Dimethylpyrrole Apart in Synthesis?

    Molecular tweaks make a substantial difference in downstream applications. In the case of 2-amino-3-cyano-4,5-dimethylpyrrole, those methyl groups on the pyrrole ring add more than just bulk—they drive unique reactivity and selectivity. The aminopyrrole core opens doors for creating fused rings, while the cyano group offers a reliable anchor for further functionalization. Some chemists prefer this compound over unsubstituted analogs because the extra methyl substituents improve solubility in a wider range of solvents and can steer reactions toward favored products. We have watched process teams in the dye sector choose this exact model for producing high-intensity pigments, while others in drug development favor it for the ease of derivatization into building blocks for heterocyclic libraries.

    This compound frequently comes up in inquiries about one-pot syntheses, and for good reason. The combination of electron-donating and electron-withdrawing groups leads to useful reactivity at the pyrrole ring for both nucleophilic and electrophilic reactions. Our technical team has seen research clients in Asia and Europe gravitate toward this model, citing reproducibility and clean purification steps as top reasons. Not all pyrrole derivatives deliver consistently smooth processability on scale, but this one’s profile tends to translate well from milligram to kilogram quantities. We’ve observed this in our own QA logs and from customer feedback over the past decade.

    The Difference Experience Makes in Consistent Production

    The chemists who scale up 2-amino-3-cyano-4,5-dimethylpyrrole in our facility measure more than purity with standard HPLC and NMR; yield consistency and freedom from trace byproducts matter just as much. Our teams have tuned the synthetic protocols over several years of iterative improvement. For example, one of our process engineers noticed that small changes in the amination step temperature had outsized effects on the formation of certain impurities—insights earned through close attention and repeated troubleshooting on plant lines.

    Not every manufacturer can deliver this molecule in high-purity, low-residue form, and we routinely hear from new research partners who switched suppliers after running into problems with off-color or low-activity lots elsewhere. We take pride in making a version that performs as expected with each shipment. That means handling raw material quality, precise distillation of intermediates, and even fine-tuning reaction workups before drying and packaging. These adjustments, based on our unique real-world experience, lead to a product that holds up under scrutiny in downstream reactions.

    Meeting Varied Industry Expectations

    People working in medicinal chemistry push hard for selective reactions at high throughput. Here, 2-amino-3-cyano-4,5-dimethylpyrrole shines. Its adaptability in palladium-catalyzed couplings and ring-closure strategies for bioactive heterocycles gives it an edge. Some clients have mentioned that batches sourced from less-experienced producers exhibit unpredictable impurity profiles, leading to troublesome purification bottlenecks in their own development cycles. We investigate these feedback details through direct technical exchanges rather than third-party resellers, and this has guided our refinements over time.

    Clients in pigment R&D reflect a different set of requirements: color consistency, lightfastness, and reproducible reactivity. The methyl and cyano substitutions in this pyrrole structure enhance chromophore properties, yielding brighter and more stable colors for advanced pigment blends. We’ve had several collaborative trials with global partners that helped us push our models to match specific pigment property targets. Each batch undergoes hands-on testing by our analytical specialists before leaving our site—a practice that only a manufacturer really lives out every day.

    In material science applications, the molecule’s balanced profile of electronic effects makes it a common intermediate in synthesizing more complex structures, from advanced polymers to functional monomers. Research groups appreciate being able to draw upon direct, transparent answers about supply origin and processing adjustments. Unlike the vague promises found in much third-party marketing, our documentation and support reflect first-hand knowledge from every stage, starting with raw precursor purification.

    Why Not Every Pyrrole Derivative is Equal

    Some customers new to this chemistry ask why they should opt for 2-amino-3-cyano-4,5-dimethylpyrrole, rather than lean on more generic pyrrole templates. We highlight the unique reactivity profile imparted by its dual methyl and cyano groups. The methyls not only improve physical properties like solubility and melting range but real-world reports show they can block side reactions faced when using unsubstituted analogs. The presence of the amino group at the 2-position and cyano at 3-position creates a versatile fork in synthetic planning—clients designing libraries or seeking custom molecular scaffolds benefit from this tunability.

    We’ve seen cases in medicinal chemistry where attempts to substitute other pyrrole derivatives led to sluggish yield or complex mixtures. In pigments, alternative compounds might not deliver the deep hue or process stability required, especially at industrial scale. Using our own analytical data sets—built from years of batch QC—we consistently see tighter NMR and HPLC windows than commonly supplied products not made to the same standards. This isn’t just a marketing claim; it reflects differences that chemists notice under the lens of daily lab work or pilot plant scale-up.

    Operational Realities: What Matters in Daily Use?

    Ordering chemicals can seem routine, but from our manufacturing floor, we know small missteps in purity or packaging can derange weeks of R&D planning. We’ve experienced this firsthand with certain sensitive heterocycles, so every order of 2-amino-3-cyano-4,5-dimethylpyrrole goes through triple-stage moisture and oxygen controls before packaging. Research users have praised our approach of including actual batch analytical reports with every shipment—full chromatographic and spectroscopic output—so teams don’t have to gamble on blind purchasing. When feedback reaches us that a customer got repeatable, reliable building block performance in a key synthesis, our plant and QC team members take it as recognition for a job well done. Troubles are tracked down together, whether the challenge lies in a subtle reaction quirk or in packaging for long-distance transit.

    With this compound specifically, even minor trace impurities can impact sensitive cross-coupling or cyclization reactions. From our experience, gas-phase or liquid-phase synthetic routes yield subtle differences in byproduct profiles. Over the years, we’ve fine-tuned the reaction workup and purification to eliminate precursors and cross-contaminants that haunted early batches from less optimized protocols. Unlike some brokers, we report these technical details openly on request, because the chemist in us knows what it takes to troubleshoot a failed batch or pin down an unknown spot in a TLC plate.

    Quality Assurance: Our Practical Testing Measures

    Quality matters most when failures hit at the project stage, so our chemical manufacturing lab runs highly detailed pre-shipment analysis for every batch. Besides regular NMR and HPLC chemical purity checks, our team applies melting point analysis, moisture determination with Karl Fischer titration, and, when requested, solid-state purity characterization. For intermediate users, our process chemists are available for telephone support, sharing troubleshooting advice grounded in daily manufacturing practice.

    Across several production campaigns, we have compiled internal documentation that helps research clients optimize their own handling. For example, we recommend storage in cool, dry conditions based on real-world degradation studies, rather than just textbook statements. Shipment options are tailored based on climate and transit length, to minimize hydrolysis or discoloration in long-haul deliveries—an attention to detail that comes directly from seeing how actual field complaints occur and how recurring issues are prevented.

    Process Optimization and Sustainability in Production

    Environmental stewardship has become a major facet of how leading manufacturers operate. In our plant, not only do we ascribe to strong regulatory compliance, but we’ve invested in capturing and recycling waste streams during pyrrole synthesis. Over the last five years, we reduced solvent and raw material waste by optimizing process atom efficiency and implementing closed-loop solvent reclamation where feasible. Regulatory inspectors and client auditors frequently cite our clear process documentation and traceability as central strengths in supporting sustainable sourcing. This isn’t marketing lingo; it’s the practical result of years of ongoing improvement, tracking waste sheet logs, and periodic process reviews.

    We also collaborate directly with academic partners on greener catalysts and process aids for this class of heterocyclic intermediates. By substituting certain traditional reagents with less hazardous alternatives, we have cut hazardous byproduct generation and reduced caustic neutralization loads in waste streams. These efforts feed back to regulatory compliance and customer procurement requirements, but primarily, they are part of the evolving responsibility manufacturers hold for minimizing chemical impact while supporting sophisticated syntheses. This “shop floor” reality influences every batch of 2-amino-3-cyano-4,5-dimethylpyrrole you find sourced from a specialist rather than a bulk trader.

    Personal Experiences from Manufacturing Teams

    Our staff chemists and production operators bring a personal sense of ownership to every batch. Several team members have shared stories about overcoming unexpected plant glitches—whether it was a filtration apparatus failing just before a holiday shipment deadline or troubleshooting a hot-plate temperature calibration error that threatened product crystallinity. These challenges forged deep familiarity with real-world behaviors of pyrrole derivatives such as 2-amino-3-cyano-4,5-dimethylpyrrole, beyond what’s found in academic references.

    One memorable anecdote comes from a time our packaging engineer identified that using slightly thicker HDPE bottles prevented a run of minor shipping damage claims, prompted by observations that this molecule tended to show surface sensitivity under rough transit conditions. Collaboration across production, QC, and logistics ensures continuous improvement, and these practical adjustments show up in positive user experiences for both small-lot and bulk orders.

    Troubleshooting and Technical Support Based on First-Hand Practice

    As manufacturers, our technical advisory goes deeper than stock responses; support comes from hands-on troubleshooting and accumulated know-how. In the past, clients have reached out after running into unexpected chromatic shifts in pigment blends or stuck reactions in library synthesis campaigns. More often than not, quick exchanges with our process chemists uncover the solution—sometimes adjusting reaction solvent, other times clarifying optimal stoichiometry or reaction quenching strategy.

    We’ve also worked alongside university researchers scaling up new routes that utilize 2-amino-3-cyano-4,5-dimethylpyrrole as a key intermediate. In these collaborations, we deal directly with bench-level issues, leading to custom modifications in our product format (such as extended drying for moisture-critical steps or tailored particle sizing for maximized reaction rate). These solutions aren’t generic—they grow from a cycle of direct user feedback and in-house problem solving, creating a back-and-forth relationship rooted in shared aims and mutual respect for what’s at stake in complex synthesis work.

    Why Manufacturer Insight Matters

    For chemists who value consistency, transparency, and responsiveness, obtaining 2-amino-3-cyano-4,5-dimethylpyrrole directly from an experienced, reputable manufacturer confers clear advantages. The close link between synthesis control and technical feedback ensures chemists always receive product that is as intended—whether they are pursuing pharmaceutical innovation, pigment production, or cutting-edge material science. Our years of close interaction with research and industrial partners, combined with our persistent leaning on detail-oriented process control, shape every gram shipped from our plant to your lab bench.

    In chemical manufacturing, every compound earns its keep through application and reliability. 2-amino-3-cyano-4,5-dimethylpyrrole, as produced by our hands, shares a story of technical diligence, responsiveness to practical needs, and ongoing pursuit of quality informed by daily laboratory realities. This experience-driven focus speaks for itself wherever innovation, precision, and robustness are required.