|
HS Code |
176839 |
| Cas Number | 203987-58-4 |
| Molecular Formula | C6H5N5 |
| Molecular Weight | 147.14 g/mol |
| Appearance | Off-white to light yellow powder |
| Purity | Typically >98% |
| Melting Point | 178-182°C |
| Solubility | Slightly soluble in water, soluble in DMSO and DMF |
| Storage Conditions | Store at 2-8°C, dry place |
| Synonyms | 5-Amino-4-cyano-3-(cyanomethyl)pyrazole |
As an accredited 5-Amino-4-Cyano-3-Cyanomethylpyrazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a sealed, amber glass bottle containing 25 grams, labeled "5-Amino-4-Cyano-3-Cyanomethylpyrazole" with safety information. |
| Shipping | 5-Amino-4-Cyano-3-Cyanomethylpyrazole is shipped in tightly sealed containers to prevent moisture and contamination. The package is clearly labeled as a laboratory chemical, and it is handled according to standard chemical safety protocols. Transport is conducted via regulated carriers, ensuring compliance with all local and international shipping regulations for chemicals. |
| Storage | **5-Amino-4-Cyano-3-Cyanomethylpyrazole** 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 acids and oxidizers. Protect from moisture, light, and direct sunlight. Clearly label the container, and ensure access is restricted to qualified personnel. Use secondary containment to prevent spills. |
Applications of 5-Amino-4-Cyano-3-Cyanomethylpyrazole in Industrial Manufacturing5-Amino-4-Cyano-3-Cyanomethylpyrazole serves as a specialized intermediate in several industrial segments requiring high-purity heterocyclic compounds. Below, we detail the main application scenarios based on real downstream industrial demands, precise integration steps, and established compliance frameworks. 1. Pharmaceutical Intermediate for Pyrazole-Based Drug SynthesisThis pyrazole derivative is widely used in manufacturing active pharmaceutical ingredients (APIs), especially for novel kinase inhibitors and anti-inflammatory drugs. The material acts as a core building block during the initial heterocyclic ring assembly. Our customers implement this intermediate primarily in the early steps of API production, which demands well-defined impurity control and consistent physical properties. Production batches are traceable and sampled according to pharmaceutical GMP requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Agrochemical Intermediate in Novel Herbicide SynthesisManufacturers in the agrochemical sector utilize this compound to produce advanced post-emergence herbicides. The compound’s dual cyano groups and amino functionality facilitate site-selective modifications, especially in the construction of pyrazole-linked carbamates and amides. These transformations require strict QC for impurity profiles to meet regulatory residue limits in crop applications. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Intermediate for High-Temperature Dye ManufactureThe material functions as a key pyrazole intermediate during the synthesis of disperse dyes intended for high-performance polyester and acetate fibers. Manufacturers utilize its dual cyano-reactive sites to enhance dye chromophore intensity and heat resistance properties. Process engineers integrate this intermediate into multi-step condensation and diazotization sequences, ensuring batch reproducibility and stability for the textile sector, which faces strict heavy metal and contaminant regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Active Intermediate in Explosives ManufacturingWithin the energetic materials industry, this compound serves as a precursor for pyrazole-based high explosives. Its cyano and amino functionalities allow for efficient nitration and ring modification critical in synthesizing insensitive energetic compounds. The production strictly adheres to hazardous material management and process safety standards, with a focus on avoiding unintended detonation during synthesis, granulation, and mixing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 5-Amino-4-Cyano-3-Cyanomethylpyrazole 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
Flexible payment, competitive price, premium service - Inquire now!
In the realm of advanced heterocyclic chemistry, 5-Amino-4-Cyano-3-Cyanomethylpyrazole emerges as a powerful intermediate that holds significance far beyond just its chemical formula. Our facility has devoted years of focused research and hands-on manufacturing expertise to navigating the subtle challenges involved in producing this compound at scale, without compromise on consistency or integrity.
5-Amino-4-Cyano-3-Cyanomethylpyrazole features a pyrazole ring system carrying both cyano and amino substituents. This structure creates a robust scaffold for applications that demand both electronic activation and diverse functionalization. Achieving high purity—typically not below 98%—defines our production process. Our analytical chemists routinely verify every batch using HPLC and NMR. Moisture and trace impurity controls remain a daily priority, not a checkbox.
Smooth crystallization during synthesis signals effective reaction control, but it is just one milestone. A slight offset in reaction temperature or solvent ratio can yield unwanted byproducts or cause troublesome isomerization. Our attention to detail starts on the bench and scales up all the way through industrial reactors. Years of process adjustment, solvent recovery, and purification have taught us that unchecked trace impurities, such as aldehyde variants or dimeric byproducts, can disrupt later-stage synthetic reactions for our customers.
Much of the demand for 5-Amino-4-Cyano-3-Cyanomethylpyrazole flows from the pharmaceutical and agrochemical sectors. We see research groups and industrial formulators frequenting our order pipeline, seeking a reliable building block that brings both nitrogen reactivity and carbon-nitrile versatility. Take pharmaceutical intermediates as one case: pyrazole-based scaffolds often serve as the spines of kinase inhibitors or antiviral prototypes. The presence of both cyano and amino substituents opens two clear avenues for modification—either as sites for nucleophilic substitution or for coupling reactions that require high stability.
Our experience demonstrates that downstream success often ties back to how thoroughly manufacturers remove residual metal catalysts and how well they prevent batch-to-batch fluctuation. For years, clients described problems with earlier sources failing to control microimpurities, leading to side reactions under coupling conditions. In response, process improvements at our site focused on high-selectivity purification and repeated dry runs with larger pilot batches before scaling up. Reliability in physical attributes, like consistent melting point and crystal morphology, can determine whether a kilo-scale process runs smoothly or must halt for rework.
We focus our specification targets on real-world utility. Our standard particle size range—a midpoint between fine powder and free-flowing granules—came not from lab theory but from repeated dialogues with downstream formulators who needed ease of weighing and quick dissolution. Precise moisture content reduces the risk of clumping and facilitates integration with other intermediates or solvents. Analytical data—typically given as GC or HPLC chromatograms—reflect not only final purity but also the predictability of the compound’s reactivity profile. By maintaining lot-specific documentation and long-term batch tracking, we support both regulatory filings and internal quality assurance for our partners.
We are sometimes asked about the robustness of our process in dealing with seasonal humidity or batch scale increases. The answer is always found on the production floor: climate-controlled environments, continuous-loop solvent recovery, and real-time pH monitoring through all key synthetic stages. No shortcut can replace the value of cumulative production experience, especially when environmental factors and workforce training come into play.
Within the broader family of substituted pyrazoles, each variant carries subtle advantages and trade-offs. Our compound distinguishes itself by housing both the cyano and cyanomethyl groups along with an amino substituent. This combination offers reaction sites for both nucleophilic and electrophilic transformation, a duality not present in more symmetrical or less-substituted pyrazoles. The presence of an extra nitrile function can drastically expand downstream options—permitting, for example, conversion to amidines or offering anchor points for Suzuki or Sonogashira couplings.
Contrast this with 3,5-dicyanopyrazole or monocyano derivatives, which lack the same breadth of modification sites. Although those compounds can serve as neat intermediates for specific condensed ring systems or for highly selective deprotection reactions, they often fall short in flexible library synthesis or as broader building blocks for pharmacophores.
We’ve fielded customer questions about using simpler substituted pyrazoles for similar purposes, only to see that reaction yields and final product stability typically do not meet stricter pharmaceutical requirements. Our compound’s dual cyano and amino configuration supports more robust post-coupling transformations and offers a higher ceiling for researcher creativity.
Raw numbers rarely tell the whole story. The spectrum of customers who use this compound often share feedback about reproducibility, ease of workup, and compatibility with both aqueous and organic protocols. Routine feedback points to a clear demand: consistency under mild and moderate reaction conditions, and straightforward workup for scale-up. Dual reactivity permits broad compatibility with both polar and non-polar reagents, a clear edge when compared to mono-substituted relatives that tend to show selectivity under only one class of conditions.
Labs relying on small multigram bench synthesis care about quick, predictable dissolution, fast filtration, and tolerance to a variety of solvents. Bulk producers push for lower residual solvent percentages, reliable milling, and faster mixing without caking or lumping. Years refining our process have shown that theoretical purity has little meaning if the product fails in the practical steps that follow. For comprehensive downstream integration, attributes like minimal dusting, reproducible crystal habit, and controlled static electricity play just as important a role as the product’s chemical identity itself.
Producing 5-Amino-4-Cyano-3-Cyanomethylpyrazole involves more than just reacting two starting materials and watching a precipitate form. The synthesis requires careful tuning of base strength and solvent system; uncontrolled conditions can lead to polymerization, excessive byproduct formation, or incomplete ring closure. Early learning phases made the limits clear—excess base frequently generated tar-like residues that complicated filtration. Real progress arrived by overhauling reactor mixing and investing in in-line monitoring technology for both temperature and pressure.
Solvent selection emerged as both problem and solution. Typical organic solvents offered only partial solubility, slowing down purification and leading to inconsistent yields. Through trials, dimethylformamide and specialized polar aprotic systems produced sharper product precipitation and cleaner separation. Waste solvent recovery, an often overlooked piece, became a focus out of necessity when our volumes grew. Closed-loop distillation, routine reclamation, and real-time tracking of waste streams allowed us to reduce the environmental impact and operational costs while maintaining strict in-process controls.
Proper safety management matters, especially when intermediates can carry reactive groups. The combined presence of the amino and dual cyano functional groups creates a potential for unwanted side reactions if storage and transit conditions slip out of line. Climate-controlled storage and oxygen-exclusion containers now form part of our standard shipping process, based on experience with early shipments that suffered quality loss due to excessive temperature fluctuation en route.
For customers aiming to file regulatory dossiers or develop patented pharmaceuticals, our production documentation stands up under scrutiny. We provide comprehensive batch records, impurity profiles, and retrospective process improvement charts. These go beyond legal compliance—they help partners anticipate scale-up challenges, identify optimal reaction windows, and trace any deviation in physical properties back to its production stage. Our openness with process history and results has fostered long-term supply relationships, as regulatory teams focus heavily on reproducibility and full impurity disclosure.
Intellectual property considerations often frame the use of this compound. Our team frequently works with patent attorneys and technical consultants to ensure that modifications and derivatives stay within regulatory and legal lane markers. This foresight shields our partners from both legal pitfalls and technical surprises down the line.
Ongoing engagement with customers acts as our R&D feedback loop. We listen when synthetic chemists describe sticking points—like slow crystallization under specific solvent mixtures or unmanageable foaming during scale-up filtration. In some cases, those comments become the seed for our own process improvements, such as adjusting seeding protocols for crystal formation or fine-tuning the rate of reagent addition to eliminate hot spots in the reactors.
We balance stability with agility in how we modify our process. Real-life customer challenges prompt incremental changes: investing in finer mesh sieves to enhance convenience for glovebox weighing or developing moisture management solutions that reduce caking for bulk shipments delivered during monsoon months. Maintaining an open channel for end-user suggestions helped us standardize some product features that now set us apart, such as batch-specific certificates showing not only standard purity data but also real-life solubility and dissolution rates in common reaction solvents.
Supply chain resilience goes well beyond simple inventory management. We commit to continuous monitoring of raw material sourcing, making adjustments before disruptions ripple through to our customers. Our procurement specialists work directly with upstream suppliers to ensure a constant supply of both core chemicals and packaging materials. In years past, shortages of precursor nitriles forced us to verify long-range contracts and invest in multiple-source networks that buffer us against solitary supplier failure.
Investments in environmental controls now shape our routine operations. Solvent recovery, energy use optimization, and waste minimization influence every scale-up decision. Operators receive regular training to identify points of waste and implement corrective actions without waiting for top-down directives. By internalizing these lessons, we not only meet regulatory demands but also set a foundation for long-lasting operational consistency, easier audits, and lower costs.
Many of the organizations we supply use this product to seed further transformations—often in the synthesis of complex target molecules, prodrugs, or advanced agrochemicals. Open and ongoing dialogue between our production teams and our partners’ engineering, procurement, and quality staff helps us preempt disruptions and stick to mutually agreed delivery timelines, even during periods of unplanned downtime or market fluctuation. Our team holds regular technical review sessions with key accounts, sharing both successes and troubleshooting data to help everyone move up the learning curve, step by step.
Where special handling or packaging adaptations suit a partner’s automated equipment or particular clean-room requirements, we adapt our batch packaging strategy. Lessons learned from pharma, biotech, and specialty materials clients all flow back into our continual process refinement, which leads to further gains in reliability and user satisfaction. Flexibility in documentation approach, labeling languages, and shipping conditions all stem from direct feedback and shared success metrics.
The versatility of 5-Amino-4-Cyano-3-Cyanomethylpyrazole fuels fresh lines of investigation among academic groups and corporate R&D teams. Novel derivatives see ongoing exploration for use as antibacterial and antifungal precursors, as well as in crop protection products targeting resistant pest species. Several research partnerships focus on customizing the functionalization sites, where the amino and cyano substituents act as levers for tuning activity profiles or binding affinity.
Our own innovation cycles run in parallel. We have invested in data analytics and high-throughput screening for next-generation reaction optimizations. Process improvements on our drawing boards aim to lower energy usage, increase throughput, and minimize manual handling—improving both safety and product uniformity.
With regulatory landscapes in flux and new activity profiles emerging from the latest research, we keep our development roadmaps open for rapid response. Our integrated understanding of production, logistics, and downstream chemistry helps our partners to go from idea to kilogram with fewer headaches and greater confidence.
5-Amino-4-Cyano-3-Cyanomethylpyrazole stands as more than just a molecular entity in our catalog. It is a case study in how process discipline, responsiveness to end-user needs, and long-term technical investment join forces to power both innovation and reliability. Our team makes this compound not only to meet demand, but to support customers shaping the future of medicine, agriculture, and materials science. Each batch carries forward our commitment to transparency, scientific rigor, and actionable collaboration.