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4-Amino-2-Methylpyrimidine-5-Carbonitrile

    • Product Name 4-Amino-2-Methylpyrimidine-5-Carbonitrile
    • Alias 4-AMPC
    • Einecs 628-679-2
    • 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

    429455

    Chemical Name 4-Amino-2-Methylpyrimidine-5-Carbonitrile
    Molecular Formula C6H6N4
    Molecular Weight 134.14 g/mol
    Cas Number 86138-39-6
    Appearance Off-white to light yellow solid
    Melting Point 180-185°C
    Solubility Slightly soluble in water, soluble in DMSO and methanol
    Purity Typically >98% (varies by supplier)
    Storage Conditions Store in a cool, dry place, tightly closed
    Synonyms 4-Amino-2-methyl-5-cyanopyrimidine
    Smiles CC1=NC=C(C#N)N=C1N
    Inchi InChI=1S/C6H6N4/c1-4-8-2-5(3-7)10-6(9)11-4/h2H,1H3,(H2,8,9,10,11)
    Hazard Class Non-hazardous (consult SDS for specifics)

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

    Packing & Storage
    Packing White, high-density polyethylene (HDPE) bottle containing 25g of 4-Amino-2-Methylpyrimidine-5-Carbonitrile, sealed, labeled with hazard and identification details.
    Shipping 4-Amino-2-Methylpyrimidine-5-Carbonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. Transport should comply with relevant chemical safety regulations, using proper labeling and documentation. Handle with care to avoid breakage or spillage. Suitable for shipping by air, sea, or land, depending on specific destination requirements and quantity.
    Storage Store 4-Amino-2-Methylpyrimidine-5-Carbonitrile in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat sources, and incompatible substances (such as strong acids or oxidizers). Protect from direct sunlight. Label the container clearly. Use in a chemical fume hood, and ensure appropriate personal protective equipment is available nearby. Follow all relevant safety and regulatory guidelines.
    Application of 4-Amino-2-Methylpyrimidine-5-Carbonitrile

    Applications of 4-Amino-2-Methylpyrimidine-5-Carbonitrile in Industrial Manufacturing

    4-Amino-2-methylpyrimidine-5-carbonitrile serves as a critical intermediate in specialty chemical manufacturing, supporting advanced synthesis in the pharmaceutical, agrochemical, and fine chemical sectors. Our manufacturing experience ensures consistent quality and regulatory alignment for all downstream applications across tightly regulated markets.

    1. Pharmaceutical API Intermediate Synthesis

    This compound functions as a key intermediate in the multi-step synthesis of thiamine derivatives and several anti-infective agents. Pharmaceutical manufacturers depend on its high purity for condensation reactions that produce essential pyrimidine-based active pharmaceutical ingredients. Process stability, compliant documentation, and validated analytics are crucial throughout production to satisfy medicinal chemistry and regulatory scrutiny.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211: Finished Pharmaceuticals
    • European Pharmacopoeia monographs where applicable
    • cGMP certification and full batch traceability requirements

    Typical usage ratio

    • Employed at 0.15–0.45 molar equivalents in intermediate step formulations, depending on target molecule pathway and reaction scale. Adjustment follows specific synthetic yield optimization and impurity control demands.

    Downstream process integration

    • Introduced to a condensation or aminopyrimidine ring formation stage under inert atmosphere, followed by purification via crystallization or chromatography before transition to final API coupling or derivatization.

    Final product types

    • Pharmaceutical grade thiamine analogues
    • Benzimidazole-based anti-infective APIs
    • Metabolic disorder drug intermediates
    • Nucleotide precursor molecules

    2. Agrochemical Active Compound Manufacturing

    The compound serves as a building block for synthesizing specialized herbicides, fungicides, and plant growth regulators, especially in products requiring pyrimidine moieties for enhanced bioavailability and target specificity. Agrochemical producers rely on its consistent input quality to sustain multi-ton batch production, reduce unwanted byproducts, and ensure stable formulation characteristics.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • Regulation (EC) No 1107/2009 (EU PPP Regulation)
    • ISO 17025: Testing and calibration for agrochemical analysis
    • REACH Annex II requirements for safety data provision

    Typical usage ratio

    • Implemented in 0.1–0.32 molar equivalent ranges, with optimization by molecular design and desired field application concentration. Precise ratio determined by downstream agrochemical synthetic procedure and targeted bioactivity.

    Downstream process integration

    • Combined at an early cyclocondensation step, often with aldehyde partners, followed by catalyst-assisted transformation to deliver the substituted pyrimidine scaffolds for further functionalization.

    Final product types

    • Systemic fungicides containing pyrimidine cores
    • Selective cereal herbicides
    • Plant growth regulatory agents
    • Seed treatment formulations

    3. Veterinary Drug Intermediate Production

    Manufacturers in the veterinary pharmaceutical industry apply this compound during the synthesis of molecules used in animal health therapies, exploiting its specificity for pyrimidine-based scaffolds that alter metabolic and immune response in livestock. Quality consistency, regulatory conformity, and lot uniformity are strictly monitored at every stage of animal drug production chains.

    Industry compliance standards

    • VICH GL2: Good Manufacturing Practice for Veterinary Products
    • US FDA Center for Veterinary Medicine (CVM) guidance
    • Ph. Eur. and USP Veterinary Supplement standards
    • ISO 9001:2015 for chemical process management

    Typical usage ratio

    • Utilized between 0.12–0.38 molar equivalents at intermediate coupling steps. Adjusted for animal species dosage sensitivity and target pharmacokinetics required in the terminal veterinary formulation.

    Downstream process integration

    • Mixed during the aminylation stage after initial ring assembly, followed by several purification and activation processes prior to conjugation to veterinary drug scaffolds.

    Final product types

    • Anti-parasitic veterinary drug intermediates
    • Pyrimidine-based livestock medications
    • Compounds for oral and injectable veterinary pharma products

    4. Fine Chemical and Specialty Dye Manufacture

    Chemists in the dye and pigment industry employ this pyrimidine-carbonitrile as a nucleophilic partner in producing select specialty dyes and optical brighteners. In these applications, performance hinges on chemical reactivity, narrow impurity specification, and compatibility with advanced dye-transfer technologies.

    Industry compliance standards

    • ISO 9001:2015 for colorant manufacturing
    • REACH Annex IV (substance-specific safety data requirements)
    • EU Council Directive 76/768/EEC on cosmetic colorants (for dyes used in cosmetic color formulations)
    • OECD Guidelines for the Testing of Chemicals (where applicable for dye safety assessment)

    Typical usage ratio

    • Dosed at 0.08–0.29 molar equivalents relative to chromophore core. Adjustments based on reactivity, desired tonality, and colorfastness specifications in finished dye material.

    Downstream process integration

    • Fed into a nucleophilic aromatic substitution or ring-closure reaction as an early precursor, then passed through color development, purification, and finishing lines to meet end-use performance criteria.

    Final product types

    • Pyrimidine-derived specialty dyes
    • Optical brighteners for textile applications
    • Organic pigments for plastics and coatings

    5. Chemical R&D and Reference Standards Production

    Research laboratories and analytical standards producers utilize this material as a primary reference standard and synthetic handle for structural elucidation studies, purity controls, and the custom synthesis of labelled analogues. Demand centers on documentation, consistent analytical profiles, and secure packaging for traceable distribution under certified conditions.

    Industry compliance standards

    • ISO 17034: General requirements for reference material producers
    • OECD GLP: Good Laboratory Practice for chemicals
    • ISO 17025: Analytical laboratory competence
    • Hazardous chemical transport under UN model regulations (for research shipment)

    Typical usage ratio

    • Exact quantity depends on required calibration standard concentration; commonly supplied in 10 mg to 500 mg aliquots formulated for HPLC, GC-MS, or NMR applications, matched to laboratory protocol specifications.

    Downstream process integration

    • Packed and securely sealed as analytical-grade solid or solution prior to dispatch for calibration or validation in synthetic and analytical research protocols.

    Final product types

    • Certified analytical reference materials
    • Labelled and deuterated chemical standards
    • Synthetic intermediates for method development
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    Certification & Compliance
    More Introduction

    Insight on 4-Amino-2-Methylpyrimidine-5-Carbonitrile: More Than a Reagent

    Practical Experience with a Core Intermediate

    Working with 4-Amino-2-Methylpyrimidine-5-Carbonitrile (commonly cataloged as model 2-ACN) takes you right into the heart of essential pyrimidine chemistry. At our manufacturing site, we see real demand from pharmaceutical researchers and fine chemical producers, who rely on this compound for its value as a versatile building block. Years of producing not just grams, but multi-ton lots, brings an appreciation for the subtleties behind this intermediate. It’s not simply another chemical; it’s a backbone component for developing complex molecules, often used in antiviral and antimalarial drug research.

    Factories like ours don’t turn out 4-Amino-2-Methylpyrimidine-5-Carbonitrile in isolation; every batch stems from careful raw material selection, reaction condition control, and strict impurity management. Over time, experience has taught us that clients judge specifications not by a technicality on a data sheet but by performance in an actual synthetic workflow. Our batches regularly reach purity above 99%, with color and moisture content checked not just at QA benches but by our senior staff. Each lot’s reactivity comes into play when research chemists attempt to craft substitutions on the pyrimidine ring—or link the carbonitrile moiety during coupling reactions central to new drug candidates.

    How 2-ACN Stands Apart

    People often ask about differences between this compound and other substituted pyrimidines. From what we’ve seen, the presence of both the amino group at position 4 and the methyl at position 2 alters the electronic environment of the ring, and the nitrile at position 5 opens a path for additional derivatization. Chemists compare this to simpler pyrimidines like 2-methylpyrimidine, which lacks reactivity for some advanced routes, or 4-amino-5-chloropyrimidine, which leads down entirely different synthetic avenues. The combination of amino, methyl, and nitrile groups on a six-membered heterocycle isn’t a commodity derivative—it reflects years of development in designing intermediates suited for medicinal chemistry.

    Our practical take on this product’s difference comes from talking with customers who struggle with purity and isomer issues in certain pyrimidine analogues. They point out that 2-ACN’s structure enables predictable outcomes in amide coupling, nucleophilic aromatic substitution, and other core transformations. That reliability saves research teams time and resources, especially in scale-up. Having a statistically consistent impurity profile, minimal batch-to-batch coloring, and tightly controlled melting range sets apart a well-made 2-ACN sample from run-of-the-mill syntheses done at benchtop scale.

    Commitment to Consistency and Transparency

    From the manufacturing side, producing 4-Amino-2-Methylpyrimidine-5-Carbonitrile isn’t just a matter of executing a well-trodden route. Our feedstock quality directly impacts not only yield, but also downstream impurity burdens like homocyclic or dimeric side-products, which become clear problems for anyone working with analytical chromatograms or who attempts bioassays on finished bioactive molecules. Months of stability and packaging testing taught us to invest in barrier-lined packaging to protect against hydrolysis, especially in regions with high humidity, giving our clients more time to work with an uncompromised product.

    Transparency runs deeper than purity numbers. Our team’s routine includes batch-specific documentation—full HPLC trace, NMR verification, and moisture assay for every shipment. We also offer sample vials for new customers running their own process validations, so they can see in their workflow how a batch performs—no surprises, less requalification time. Visiting research labs and industrial plants showed us time and again that high-variability intermediates slow down project milestones, while predictable materials let scientists move forward with confidence.

    Real Usage and Downstream Applications

    Applications for 2-ACN stretch well beyond a narrow segment of pharmaceuticals. Some of our largest clients synthesize active ingredients for veterinary drugs where pyrimidine backbones support a range of APIs. Academic teams draw on our material to explore new cytidine analogs or build nucleotide mimics, since the amino and carbonitrile groups offer routes for extending or functionalizing the molecule. We’ve even shipped to labs researching agrochemicals and dyes, where the electron-withdrawing nitrile helps support stable pigment development.

    What sets this product’s usage apart is its convenience in downstream conversions. Compared to non-nitrile- or non-amino-substituted analogues, 2-ACN gets introduced early in a project’s synthetic development. This allows for late-stage modifications, letting researchers decide at pilot or production scale which substituents will maximize biological or physical properties. More than once we’ve seen clients try after-market modifications—only to discover that batch impurity or mislabelled material costs them validation cycles. With a clean feedstock, these problems get eliminated or at least held in check.

    Managing Quality From Crystallization Up

    Long-term experience with process development uncovered trouble spots in forming, purifying, and finishing this compound that rarely get discussed in literature. Many small-scale syntheses run into trouble during crystallization, producing sticky masses or off-spec colored crystals. On the manufacturing floor, we tackle the precipitation step with attention to solvent polarity, controlled temperature ramps, and rigorous seed charging. We’ve tested multiple mother liquor recycles, calibrated equipment for rapid separation, and introduced real-time monitoring for solvent residues in finished lots.

    Sheltering our batches from ambient moisture pays off in the final product. Uncontrolled exposure leads quickly to hydrolysis or clumping—something only those making multi-kg quantities fully appreciate. Even trace byproducts, like formyl- or acetonitrile-derivatives, are tracked in our in-house analytics to catch problems before clients have to.

    Understanding the Downstream Impact

    Every manufacturer supplies a certificate of analysis, but our operation spends much more time following up on actual downstream test results. More than a few chemists told us poorly crystallized or contaminated batches disrupt scale-up, costing thousands in rework for filtration and solvent stripping. Learning from these headaches, we built feedback loops with core users—so if a batch gives trouble with solubility or yield in an unusual reaction, we hear about it fast.

    We provide technical support for custom derivatives, sometimes running joint pilot reactions to help client teams expedite intermediate validation. In one project, a multinational pharma group wanted a custom-graded 2-ACN for a unique route to a nucleoside inhibitor. We applied an extra round of solvent exchange and low-temperature crystallization, hitting their desired melting point and color spec. That collaborative work underscores why experience matters at a manufacturing scale.

    Why Specification Details Matter

    In the world of pyrimidine intermediates, seemingly minor differences in specification reveal themselves to be critical at commercial scale. Companies who have switched from competitors to our material often cite smoother filtration, lower residual solvent, and better handling properties. For instance, our QA data reflects true process conditions, not only the best-case scenario. Over years, we gathered customer feedback on solubility profiles and polymorphic behavior, leading us to refine drying protocols. Moisture content is kept below half a percent, and even trace heavy metals—often ignored in general-purpose grades—are tracked in final release, avoiding failures in GMP and regulated workflows.

    We’ve also had production runs customized to address end-use-specific needs, such as tailoring particle size for microfluidization or providing large crystalline agglomerates for certain continuous processes. Our partnerships with downstream formulators taught us that a “one-size-fits-all” approach leads to bottlenecks as projects advance from lab to kilo labs and, finally, to ton-scale plants.

    Learning From Client Challenges

    Not every order is straightforward. Requests come from startups with limited technical support, academic researchers searching for a very pure sample, or major manufacturers scaling new chemical entities. Some struggle with polymorphic forms or solvate stability when blending 2-ACN with bases or acids. Others require unconventional packaging for unusually reactive workups. We listen to these concerns and run parallel stability tests to replicate client handling conditions. Over time, this hands-on approach prevents disruption and builds trust—two things a certificate of analysis can’t fully capture.

    A recent example involved a lab that experienced out-of-spec melting points after shipping to a tropical climate. Investigating with them, we found standard drums absorbed excess moisture. Switching to double-lined, airtight containers fixed the issue for their next order. It’s experiences like these that shape how we, as producers, think about not just pure chemical synthesis but real-world delivery and usability.

    Responsible Manufacturing Practices

    Quality and safety always come with environmental responsibility. Our facility incorporates solvent recycling and adheres to strict waste minimization plans. Over years, regulations governing chemical manufacturing tightened, especially for cyanated aromatics like 2-ACN. Installing abatement equipment for off-gassed byproducts, running regular air and effluent monitoring, and following best-practice containment keeps our operation in good standing—not only with agencies, but with our neighbors and employees.

    Employee training rounds out responsible production. We train operators in batch-specific protocols, hands-on impurity recognition, and troubleshooting equipment. In-house safety audits ensure every batch meets the standards required for export or local use. We’ve learned, over decades, that a well-trained team not only protects itself but looks out for the chemists down the line who will handle the compound in their own facilities.

    Looking Ahead With Continued Innovation

    The market for functionalized pyrimidines continues to evolve. Where early demand centered on generic API synthesis, partnerships are now shifting to novel analog screening and combinatorial chemistry. As medicinal chemistry grows more sophisticated, so do requests for tighter impurity specs, fully traceable supply chains, and on-demand modification of core intermediates like 4-Amino-2-Methylpyrimidine-5-Carbonitrile.

    We respond by investing in more robust in-line analytics and rapid-cycle development with R&D. Whenever a client presents a new downstream demand—such as a chiral variant, a distinct crystalline form, or a solvent-free appearance—we engage directly to design better processes. Each new challenge brings opportunities for improvement, from upstream raw material vetting to tailored delivery schedules that fit modern global supply chains.

    Final Thoughts From the Factory Floor

    Putting out consistently reliable 4-Amino-2-Methylpyrimidine-5-Carbonitrile means more than lab synthesis or transactional sales. For our team, every order testifies to a production philosophy that values hands-on experience, open dialogue, and the everyday details that only come from living with the molecule from raw materials through crystallization and shipment.

    Stories from customers rarely focus on the molecule’s formula or systematic name. They talk about ease of integration into their next step, the relief when a new batch runs smoothly, and the value of direct access to real factory insights. By bridging what we know from making the compound with the real concerns of those using it, each shipment starts a new chain of discovery—from technical solutions to the next generation of synthetic achievement.