Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine

    • Product Name N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine
    • Alias AMPP
    • Einecs 695-859-5
    • 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

    692252

    Chemical Name N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine
    Molecular Formula C16H15N5
    Molecular Weight 277.33 g/mol
    Appearance Solid (typically off-white to yellow)
    Cas Number 155270-99-8
    Purity Typically ≥98%
    Solubility Soluble in DMSO, slightly soluble in water
    Melting Point Approximately 220-222°C (may vary)
    Storage Conditions Store at 2-8°C, protect from light
    Synonyms 5-Amino-2-methyl-N-(4-(3-pyridyl)pyrimidin-2-yl)aniline
    Smiles Cc1ccc(N)cc1NC2=NC=NC(=C2)c3cccnc3
    Application Intermediate in pharmaceutical research

    As an accredited N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine is supplied in a sealed, amber glass bottle with tamper-evident cap.
    Shipping This chemical, N-(5-Amino-2-methylphenyl)-4-(3-pyridyl)-2-pyrimidineamine, will be shipped in compliance with applicable regulations for hazardous materials. It is securely packaged in a sealed container, cushioned to prevent breakage, and labeled appropriately for chemical transport. Shipping includes temperature control and tracking to ensure safe, prompt delivery to the recipient.
    Storage Store **N-(5-Amino-2-methylphenyl)-4-(3-pyridyl)-2-pyrimidineamine** in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as oxidizing agents. Keep the container tightly closed when not in use. Use appropriate safety measures to prevent dust or vapors. Recommended storage temperature is typically 2-8°C unless otherwise specified by the manufacturer or supplier documentation.
    Application of N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine

    Applications of N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine in Industrial Manufacturing

    As a direct manufacturer, we supply N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine for several high-value industrial applications requiring advanced workflow integration and consistent high-purity standards. Our material supports processes ranging from active pharmaceutical synthesis to performance materials, ensuring traceability and strict batch quality at each stage.

    1. Small Molecule Pharmaceutical API Synthesis

    This raw material functions as a key pyrimidine-based intermediate in multi-step syntheses for pharmaceutical actives, including kinase inhibitors and oncology-targeted APIs. Its structure allows targeted heterocyclic coupling, facilitating late-stage functionalization in cGMP-compliant active ingredient manufacture. Production operations require precise stoichiometric addition, managed under regulated environments for impurity control and traceability. Downstream integration occurs in GMP and FDA-audited facilities for high-volume oncology and immunology molecule development.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • EU GMP Volumes 1 & 4
    • FDA 21 CFR Part 211
    • US and EU Pharmacopeia Monographs (for intermediates)

    Typical usage ratio

    • Applied at 0.3–2.0 molar equivalents per final API batch, adjusted based on coupling step yield and process impurity profile

    Downstream process integration

    • Charged during late-stage or penultimate step amidation or cross-coupling reactions
    • Followed by purification via preparative chromatography or crystallization
    • Contaminant monitoring via HPLC and LC-MS according to QbD protocols

    Final product types

    • Advanced kinase inhibitor APIs
    • Structure-specific antitumor agents
    • Experimental immunology drugs

    2. Agrochemical Active Ingredient Synthesis

    In the agrochemical sector, this molecule acts as a pyrimidine building block for the manufacture of novel fungicides and selective herbicides. It undergoes nucleophilic substitution and further derivatization to deliver active agrochemical compounds that support resistance management and environmentally sound crop protection solutions. The process requires accurate reaction control to comply with regulatory impurity specifications for active agent registration both in domestic and export markets.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • OECD Principles of Good Laboratory Practice
    • US EPA 40 CFR Part 158 (Data Requirements for Pesticides)
    • China GB 4839-2009 Standard for Pesticides

    Typical usage ratio

    • Typically loaded at 0.6–1.5 molar equivalents in agrochemical synthesis steps, variable with yield and final purity demands

    Downstream process integration

    • Introduced as a core heterocycle in pyridine-pyrimidine hybrid molecule synthesis
    • Undergoes further acylation or ring modification to install bioactive side chains
    • Reaction monitored by GC and NMR for regulatory purity adherence

    Final product types

    • Pyrimidine-based cereal fungicide actives
    • Pyridyl herbicide intermediate compounds
    • Custom synthesized crop-protection agents

    3. Research Chemical and Custom Synthesis Services

    Leading chemical R&D institutions and contract development organizations select this compound for the synthesis of novel heterocyclic lead compounds in drug discovery and chemical biology. Its unique substitution pattern supports rapid late-stage diversification via palladium-catalyzed cross-coupling, allowing medicinal chemists to generate SAR libraries efficiently. The product’s high analytical purity facilitates reliable structure-activity relationship studies in regulated laboratory settings.

    Industry compliance standards

    • ISO 9001:2015 for Research Chemical Production
    • GLP (Good Laboratory Practice, OECD 21)
    • REACH (EC 1907/2006) substance registration
    • Material traceability as per ICH Q11 Process Development guidelines

    Typical usage ratio

    • Used at 10–20 mmol scale for screening libraries, up to 200 g batch for preclinical scale-up; adjusted upon reaction pathway and purity required

    Downstream process integration

    • Enters as a core fragment in Suzuki and Buchwald-Hartwig coupling sets
    • Purified via automated flash chromatography or preparative HPLC
    • QC performed using NMR, LC-MS, and elemental analysis

    Final product types

    • SAR screening libraries for drug discovery
    • Patented heterocyclic scaffold custom syntheses
    • Advanced starting materials for lead optimization projects

    4. Electronic and Optoelectronic Material Precursors

    The advanced aromatic and nitrogen-rich structure of this molecule makes it a suitable intermediate for synthesizing specialty ligands and crosslinkers in optoelectronic applications, particularly in OLED emitting layer development and organic semiconductor fabrication. Clean downstream performance requires low-conductivity, trace-metal control, and stable batch-to-batch purity. Production integrates into formulation reactors using high-purity solvents with inert gas blanketing, supporting end-user requirements for defect-free film-forming solutions.

    Industry compliance standards

    • ISO 9001:2015 for Electronic Material Production
    • IEC 62655:2013 for organic electronic chemicals
    • RoHS Directive 2011/65/EU (restrictions on hazardous substances in electronics)
    • QC validated per SEMI C3 standards

    Typical usage ratio

    • Employed at 0.1–0.5 wt% in emitting layer precursor blends; ratio may be tweaked by film thickness and emission wavelength design needs

    Downstream process integration

    • Integrated into small molecule ligand synthesis as a core framework component
    • Subjected to one-pot derivatization for substitution on the pyrimidine or pyridyl group
    • Material purified to >99.5% by sublimation or continuous crystallization

    Final product types

    • OLED emitting layer molecules
    • Organic thin-film transistor semiconductors
    • Custom ligands for electronic inks

    5. Specialty Dye and Pigment Intermediates

    Our product serves as a robust foundation for producing specialty dyes and organic pigments, especially those intended for advanced printing, textile coloration, and photoactive coatings. The aromatic and pyrimidine motifs enable efficient diazotization and coupling chemistry, supporting lightfastness and thermal stability in downstream pigments. Manufacturers apply strict color index controls and impurity monitoring to comply with international textile and printing standards.

    Industry compliance standards

    • OEKO-TEX Standard 100 for textile chemicals
    • EN 71-3:2019 (Safety of Toys - Migration of certain elements)
    • ISO 12040:2004 for organic pigment testing
    • Restriction of hazardous substances per EU and US regulations

    Typical usage ratio

    • Filled at 3–8 mol% in pigment synthesis batches; level adjusted based on shade, fastness goals, and end-use application

    Downstream process integration

    • Diazotized and coupled with phenolics or amines for dyestuff core formation
    • Incorporated in multi-step pigment synthesis trains followed by filtration and milling
    • Final physical properties tuned by post-synthesis treatment

    Final product types

    • Textile and polymer-compatible pigments
    • High-color-density offset printing dyes
    • Photoactive imaging layer coatings

    6. Analytical Reference Standard Manufacture

    Due to its complex structure, the material is in demand as a reference standard for quantitative HPLC and LC-MS calibration in pharmaceutical and chemical analysis. We supply certified lots to analytical laboratories, requiring high-purity, full COA traceability, and batch-specific impurity profiling. End users apply the standard in method validation for regulated product testing, ensuring result consistency and regulatory acceptance in global markets.

    Industry compliance standards

    • ISO 17034:2016 for Reference Material Producers
    • ISO/IEC 17025:2017 for Testing Laboratories
    • Ph. Eur., USP, and JP reference standard section requirements
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation

    Typical usage ratio

    • Prepared as 1–10 mg/mL standard solutions for calibration routines; quantity based on instrument detection limit and QC SOP

    Downstream process integration

    • Packed in ampoules or vials under inert conditions to prevent degradation
    • Released alongside complete impurity profile and stability data
    • Integrated into laboratory QC systems and method validation kits

    Final product types

    • Certified reference standards for HPLC calibration
    • LC-MS/MS method validation controls
    • System suitability reagents in pharmaceutical QC
    Free Quote

    Competitive N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine 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

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine: Lifting the Standards of Modern Synthesis

    Real Work, Real Chemistry: Meeting the Demands of a Precise Molecule

    We produce N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine in our own facilities, not through intermediaries or badge engineering. Over the past decade, our crews have worked through hundreds of production cycles with this molecule. They’ve seen every quirk and stubborn challenge this compound brings to the reactor. It’s a small-molecule solid, crystalline and stable under ambient conditions, based on both in-house and external verification. Our technicians can recognize its distinctive physical outline at sight.

    Specifications That Reflect True Processing Realities

    Customers who know their synthetic targets appreciate narrow impurity profiles in raw chemical inputs. The key with N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine comes down to tight control over the parent structure and consistent lot-to-lot performance. Analytical data supports a purity limit above 99 percent in our typical workshops. By keeping batch sizes and temperature ramps under supervision, 0.5 percent or less total impurities holds true across months of operation. Moisture comes in well below what’s tolerable for follow-on reactions, so chemists lose less time recalibrating conditions or troubleshooting failed coupling.

    Our production team follows validated routes for scale-up. Each crew member applies hands-on training and maintains proper documentation throughout every cycle. Regular in-house tests—such as HPLC, melting point ranges, and NMR spectral comparisons—show the reproducibility of each lot.

    Particle size distribution for the finished product arises not from theoretical aspirations, but from what the customer actually requests or demonstrates by trial. Most often, we produce it as a fine powder, good for dissolving into common organic solvents or for solid-phase transformations. Sometimes the customer’s own application tells us whether to leave the product as received, apply mild grinding, or process through further screening.

    How Users Leverage the Compound

    In the labs where drug discovery happens, the chemical crew holds N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine as a proven tool for building more complex molecules. The two aromatic rings, connected to the electron-rich and electron-poor heterocycles, open plenty of synthetic routes for combinatorial chemistry. Medicinal chemists find value in its versatility. They use it as a core scaffold, introduce it into kinase inhibitor templates, or apply selective modifications to test new functional group additions.

    Over the last few years, we’ve worked alongside in-house biologists and external partners to see how this scaffold contributes to enzyme inhibition, cell permeability, and downstream pharmacokinetics. Our plant doesn’t claim to develop the end application, but we do support researchers pushing closer to approved compounds.

    Some research outfits use this molecule at early lead optimization stages. Feedback from customers tells us about its solubility in DMSO, stability through long-term bench storage, and how smoothly it reacts in reductive amination, cross-coupling, and hydrogenation reactions. More than once, a partner chemist has called to say, “Your material just works. We don’t lose time chasing down weird byproducts or unpredictable reaction rates.” They value the small things: less chromatographic artifact, higher yields in the next step, and fewer unexplained delays.

    Comparing With Competing or Similar Products

    It’s a crowded field for chemicals that sit in the pyrimidine and pyridine families. Many producers or resellers offer lookalike compounds, switching out substituents or flipping the position of a methyl or amino group. From experience, subtle differences in molecular symmetry and electronic distribution can swing the synthetic outcome.

    Some buyers make the mistake of accepting substitutes based on generic descriptions or batch certificates, not on actual hands-on testing. Over time, they learn about invisible impacts. For example, a meta-methyl substitution versus an ortho-methyl in the aromatic ring can throw off binding affinity or interfere with the downstream boronic acid coupling steps. Our version of N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine is the specific isomer—the one that matches well-cited journal procedures and peer-verified synthesis plans.

    We do not push unnecessary purification (such as laborious recrystallization past what’s beneficial), nor add stabilizers or carriers just to hit mass targets. This approach grew out of technical feedback loops. Inconsistent suppliers in the early years of this compound saw solvent residues or degradation products pile up. Reproducibility is everything.

    Companies focused only on reselling lack true knowledge of the reaction’s bottlenecks and potential byproduct traps. Because our workforce carries experience from reaction kettle to final packaging, we pick up on root causes that don’t show up in lab data alone. Some customers come to us tired of unexplained micro-impurities in competitor material that disrupt analytical profiles or toxicology results. After switching, those same groups report sharper NMR peaks and more reliable preclinical testing.

    Supporting Application-Specific Demands

    N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine doesn’t slot neatly into commodity or bulk intermediates. Researchers working on targeted therapies, enzyme screening, or agricultural analogs want clean, traceable raw material, and batches that match what their process chemists expect. In our experience, groups using the compound in kinase inhibition projects comment on low baseline background in their screens, a point that sometimes gets ignored in catalog entries.

    Each year, customer feedback shapes how we refine our procedures. One medical device manufacturer moved toward us after extracting their own material from third-party sources repeatedly, only to face lower-than-expected performance metrics. Their project timeline improved once they saw batch-to-batch consistency and lost less material cleaning up after avoidable contaminants.

    In agricultural R&D, teams adapting this molecule for agrochemical discovery have specific solubility targets and tolerance for trace solvents. Small changes in water content or trace mineral presence matter. Our crew controls for trace metal content, not because of regulatory compliance, but because customers running sensitive proprietary processes have flagged occasional issues with “clean room” suppliers. Direct feedback and trust between bench chemists and manufacturing get better results with less paperwork and fewer surprises down the line.

    Manufacturing Know-How—A Day-to-Day Perspective

    Every production lot teaches us more about subtle shifts in sourcing and process control. Equipment investment matters, but talent in our operating team makes a bigger difference. New hires spend their first few weeks shadowing experienced crew, learning to anticipate trickier steps: how temperature curves drift with larger-scale batch sizes, where filtration can break down, or when to intervene to guarantee full conversion.

    Lab testing tells one part of the story, but process consistency across months takes a deeper kind of know-how. Our team carries a mental watch list for lot deviations—pressure inconsistencies, solvent recovery oddities, humidity swings in seasonal shipments. We track all this to head off problems before the product ever leaves our dock.

    Shipping also teaches discipline. Products with the “right” certificate can still degrade in transit. We have learned how to shield this material from light or moisture, based directly on field failures or cold-chain missteps that caused headaches downstream for loyal customers.

    The Value of Source Transparency

    In a field crowded by paperwork and endless “manufactured for/by” documentation, suppliers who actually make what they sell earn loyalty beyond just a contract. We take calls directly from technical teams and build relationships not only with procurement, but with the chemists who set up their HPLC. This approach has brought us long-term relationships that survive pricing cycles and evolving regulatory pressures.

    Global compliance has risen in importance. Our facilities and documentation meet all core expectations for controlled chemical processing, but our value comes from helping customers pass their own audits. Auditors from three continents have walked our lines and asked hard questions. Our batch records and chain of custody practices stand up to real inspection, not just box-ticking. We learn from every engagement and adopt best practices that translate to better support and quality assurance.

    Support That Extends Beyond the Shipping Dock

    Labs working on tight schedules have real problems when a batch delays or a technical issue throws off a milestone. What separates manufacturers from traders is the ability to spot batch anomalies before shipment, offer real-time technical notes, and track usage feedback for future improvement.

    For one customer, we reran a fresh batch overnight after discovering micro-residue during routine re-testing. We have sent extra spectral analysis, walked through solubility adjustments for users trying a new application, and provided archive samples years after first delivery if regulatory authorities called for it. These experiences taught our crew the responsibilities that come with claiming “actual manufacturer” on every certificate and shipment.

    Long-Term Impact and Solutions to Typical Production Pain Points

    Scaling up N-(5-Amino-2-Methylphenyl)-4-(3-Pyridyl)-2-Pyrimidineamine has always required careful resource balancing. Plant downtime, raw material fluctuations, and even weather patterns—all influence how efficiently a batch can reach the customer. Over time, smarter inventory and supply chain communication has stabilized our capacity. When precursor supplies tighten in global trade disruptions, our team switches to verified alternative routes and double-checks cross-reactivity.

    Unexpected batch failures have their root cause in either overlooked raw material changes or unforeseen reactor problems. After learning that lesson early in our setup years, we put in place tighter incoming inspection standards, operator-driven monitoring, and regular equipment recalibration. Engineers on our crew don’t just tick off completed checklists; they escalate anything out of the ordinary, saving time and headaches in the next step of synthetic work.

    Industry-wide, pushes for greener chemistry and less waste have driven us to improve solvent recycling, energy use efficiency, and raw material sourcing. We have partnered with raw materials producers for better traceability and stricter testing. These steps reduced batch rejection rates, kept down both direct and system-wide costs, and minimized delays for our customers, especially those running time-sensitive research.

    Our production philosophy is simple: learn from customer feedback and every failed batch. Experience counts for more than jargon. Each year brings new performance demands, and our crew adapts, taking pride in reducing the noise and keeping chemistry moving forward.

    What Makes the Difference for the Real End User

    Chemists and project leads focusing on results appreciate suppliers that do more than resell. We build value by delivering reliability, open communication, and steady improvement based on direct, documented experience. Data sheets, safety files, and compliance paperwork meet requirements, but the key is always reproducibility at bench scale and in full process runs.

    Without hands-on knowledge in actual reaction environments, it's all too easy to miss variability in performance between seemingly identical batches. By handling the molecule from raw input to finished package, we catch and correct these issues at the source.

    The experience gained in real plant and lab environments gives us insight that no virtual catalog or drop-ship supplier can compete with. Over the years, our product hasn’t just helped research succeed—it has changed expectations about partnering with a genuine manufacturer, not just a voice on the phone.

    In a world where every delay can cost a research day and every overlooked impurity can erode trial results, better sourcing isn’t just about molecules—it’s about backing up our partners in the lab, every day, with results they can count on, from a crew who knows the chemistry by heart.