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Pyrimidine-2-Carboxylic Acid

    • Product Name Pyrimidine-2-Carboxylic Acid
    • Alias 2-Pyrimidinecarboxylic acid
    • Einecs 629-55-4
    • 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

    572414

    Chemical Name Pyrimidine-2-Carboxylic Acid
    Cas Number 1004-46-6
    Molecular Formula C5H4N2O2
    Molecular Weight 124.10 g/mol
    Appearance White to off-white powder
    Melting Point 204-208 °C
    Solubility Slightly soluble in water
    Boiling Point Decomposes before boiling
    Purity Typically ≥98%
    Pka 2.69 (carboxylic acid group)
    Synonyms 2-Pyrimidinecarboxylic acid; Pyrimidine-2-carboxylate
    Smiles C1=NC(=NC=C1)C(=O)O
    Inchi InChI=1S/C5H4N2O2/c8-5(9)4-2-1-3-6-7-4/h1-3H,(H,8,9)

    As an accredited Pyrimidine-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Pyrimidine-2-Carboxylic Acid, 25g, is supplied in a sealed amber glass bottle with tamper-evident cap and safety labeling.
    Shipping Pyrimidine-2-Carboxylic Acid is shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It is labeled according to relevant safety regulations and accompanied by a Safety Data Sheet (SDS). Transportation follows guidelines for non-hazardous chemicals, ensuring secure packaging and protection from extreme temperatures during transit.
    Storage Pyrimidine-2-Carboxylic Acid should be stored in a tightly sealed container, away from moisture and direct sunlight. Keep it at room temperature, typically between 2°C and 8°C, in a cool, dry, and well-ventilated area. Ensure compatibility with other chemicals and avoid exposure to strong oxidizing agents. Properly label the container and follow relevant safety and handling guidelines.
    Application of Pyrimidine-2-Carboxylic Acid

    Applications of Pyrimidine-2-Carboxylic Acid in Industrial Manufacturing

    Our production of Pyrimidine-2-Carboxylic Acid is dedicated to supporting established and highly regulated industries. Below, we detail its implementation within approved downstream sectors, referencing compliance standards, real-world formulations, process integration steps, and finished product classes according to each specialized application field.

    1. Pharmaceutical Intermediate Synthesis

    Pyrimidine-2-Carboxylic Acid serves as a key intermediate in the multi-step synthesis of several antineoplastic and antiviral active pharmaceutical ingredients (APIs). Its role in constructing heterocyclic scaffolds is critical for creating molecular structures that form the backbone of various patented and generically produced APIs. Process chemists source this material for direct coupling and ring-modification reactions within controlled GMP environments, ensuring both the purity of intermediates and batch-to-batch consistency critical for finished drug substance quality. Our manufacturing control offers traceable batch documentation to support regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for intermediates
    • USFDA 21 CFR Part 210/211 for pharmaceutical manufacturing
    • Chinese Pharmacopoeia (ChP) requirements for intermediates

    Typical usage ratio

    • 5–15% molar equivalent in multistep API synthesis, adjusted based on targeted yield and impurity control strategies. Exact levels depend on the API process route and catalyst system.

    Downstream process integration

    • Charged as a controlled raw material during the initial or mid-stage construction of pyrimidine-containing intermediates through condensation, cyclization, or substitution reactions under inert atmosphere, often involving chlorination or amide coupling steps in reactor vessels equipped with inline analytical QC.

    Final product types

    • Active pharmaceutical ingredients: antineoplastic drugs, targeted antiviral agents, and select CNS compounds containing pyrimidine motifs
    • Registered pharmaceutical intermediates meeting trace impurity thresholds

    2. Agrochemical Active Ingredient Precursor

    Industrial pesticide and herbicide manufacturers incorporate Pyrimidine-2-Carboxylic Acid into multi-stage synthetic schemes to create precursors for pyrimidine-based agrochemicals. The acid group acts as a functional handle for further derivatization, such as esterification and amination, driving the formation of active molecules used in crop protection. Downstream plants depend on standardized material quality to achieve reproducible reaction yields while maintaining residues in accordance with regulatory guidelines for field use and safety evaluation in exported agricultural products.

    Industry compliance standards

    • FAO/WHO specifications for pesticide active ingredients
    • ISO 9001:2015 quality management systems for agrochemical production
    • China National Standards for Pesticide Intermediates (GB/T 3796)
    • EU Regulation (EC) No 1107/2009 for plant protection product ingredients

    Typical usage ratio

    • 8–18% by weight in esterification or amidation precursor steps; exact ratio depends on targeted molecular conversion during batch or semi-continuous processing.

    Downstream process integration

    • Fed into the initial reactor sequence for ester or amide synthesis, followed by halogenation or ring-modification reactions; handled under closed-system to withstand temperature, pressure, and catalytic environments typical for modern agrochemical pre-formulation lines.

    Final product types

    • Pyrimidine-based herbicides and insecticides (e.g., selective post-emergence herbicides)
    • Registered intermediates for branded and generic crop protection formulations

    3. Dye and Pigment Intermediate Development

    Specialty dye and colorant producers utilize Pyrimidine-2-Carboxylic Acid to introduce nitrogen heterocycle cores into advanced pigment molecules. Its carboxyl functionality supports coupling reactions with various amines and alcohols, producing azo and metal-complex dyes with improved solubility and colorfastness for technical fabrics and printing inks. In this sector, the precursor’s batch purity and precise specification grading are essential for controlling shade uniformity and performance in end-use substrates subjected to industrial service conditions.

    Industry compliance standards

    • OEKO-TEX Standard 100 for dyes in textiles
    • REACH Regulation (EC) No 1907/2006 for pigments and dye intermediates
    • ISO 13321 for particle sizing in pigmentation
    • ZDHC Manufacturing Restricted Substances List (MRSL) compliance

    Typical usage ratio

    • 3–12% as a coupling component by total input mass in diazotization or condensation reactions; proportion adapted for the desired shade depth and chromatic intensity of the target pigment.

    Downstream process integration

    • Reacted with substituted anilines or phenols in aqueous or mixed-phase reactors; incorporated prior to downstream purification, granulation, or microencapsulation required for stable pigment dispersion in aqueous or solvent-based media.

    Final product types

    • Technical dyes for digital and textile printing
    • Organic pigments for coatings, plastics, and specialty inks

    4. Specialty Chemical Building Block for Electronic Materials

    The electronics and functional materials industry incorporates Pyrimidine-2-Carboxylic Acid into the synthesis of advanced organic materials used in semiconductors, organic light-emitting diodes (OLEDs), and liquid crystal components. High-specification material purity and trace-metal control ensure that formulations achieve electronic-grade dielectric properties and thermal stability, crucial for reliable device performance. Chemical engineers qualify sources to support reproducibility in microelectronic manufacturing lines and downstream coating and photolithographic processes.

    Industry compliance standards

    • SEMI C91 specification for electronic chemical purity
    • IPC-4101/40 & IPC-4552A for materials used in printed circuit board processing
    • RoHS Directive (2011/65/EU) for restricted substances in electronics applications
    • ISO 9001:2015 for electronic chemical production traceability

    Typical usage ratio

    • 1–6% within functional monomer or oligomer synthetic routes; optimized based on required conductivity or light absorption parameter in the electronic device’s end-use environment.

    Downstream process integration

    • Introduced during early formulation stages as a heteroaromatic scaffold, further functionalized through palladium-catalyzed cross-coupling or amidation, and then purified to the sub-ppm impurity level prior to casting, deposition, or spin-coating of thin layers for semiconductor fabrication.

    Final product types

    • Organic semiconductors for thin-film transistors
    • Functionalized liquid crystals for display technologies
    • Precursor solutions for next-generation OLED materials
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    Certification & Compliance
    More Introduction

    Pyrimidine-2-Carboxylic Acid: Trust in Precision Synthesis

    A Chemical Crafted for Technological Demands

    Working daily at the reactor line, my hands guide the synthesis step by step, right through to the final package. Pyrimidine-2-carboxylic acid (CAS 4594-46-3) didn’t just become another number on our product list; it reflects decades of incremental improvements and careful control. Over the years, our engineering approach zeroes in on repeatable quality, because this molecule’s role in critical synthesis never allows for shortcuts.

    This compound forms the backbone of several modern research programs. Its pyrimidine core, with the carboxylic acid at the two-position, brings an edge for derivatives that other compounds struggle to mirror. Molecule developers and med-chem groups gravitate toward this acid, not for historical inertia, but because traceable quality makes the difference in long synthetic sequences. Our batches pass through multiple HPLC and GC layers to verify purity above 99%, aiming to stop downstream complications before they can start. The odorless and off-white nature points to minimal contamination, which customers have counted on for more than ten years.

    Consistent Output for R&D and Scale-Up

    Each season, we collaborate closely with lab teams who come straight to source, not through layers of sales brokers. Direct dialogue helps nail down if a gram, kilogram, or larger quantity best fits their project window. It’s common for discovery chemistry groups to request small lots of pyrimidine-2-carboxylic acid for first-run screens, while pharmaceutical pilot plants seek bulk orders when scale-up hits. As demands shift from milligrams to tens of kilos, granular attention to drying, storage, and shipping becomes crucial. We built our logistics to shield material from moisture and cross-contamination, since these variables are known triggers for unwanted side reactions.

    Not every synthetic challenge asks the same from raw material. For some, trace levels of transition metals or residual solvents stall progress much later along the pipeline. Over the years, our analytical lab invested in more sensitive detection, constantly lowering impurity specs. We’ve seen too many research blocks caused by a supplier’s lenient standards; so we focus on tighter controls, ensuring confidence at every downstream stage. Pyrimidine-2-carboxylic acid is not only used to build nucleic acid analogs and specialty ligands, but sits at the crossroads of dye chemistry, crop protection, and even uncatalogued biochemistry tools. Each customer draws out new uses and sometimes pushes for improvements over last year’s process.

    Pyrimidine Structure Opens Unique Pathways

    Compared to more common heterocyclic acids, such as pyridine-3-carboxylic acid or the widely used benzoic acid, the pyrimidine scaffold brings a set of electronic properties all its own. The ring nitrogen configuration in pyrimidines affects how substituents react, setting it apart from simple benzene derivatives. Pyrimidine-2-carboxylic acid, specifically, allows selective modification on neighboring positions, encouraging robust structure-activity studies. The carboxyl group at position two, rather than at three-four or five-six, drives different binding orientations in metallorganic assemblies or peptide mimetics. Chemists with experience in nucleic acid analogs often seek this reagent, since it better matches native base-pairing motifs when compared to related acids.

    Our pilot batches confirmed long ago that no two pyrimidine acids behave identically under peptide coupling or halogenation. Pyrimidine-4-carboxylic acid shares the ring but not the same acidity or solubility profile, shifting product isolation. The 2-carboxylic acid variant stands out for forming stable intermediates during amidation and esterification—this sometimes shortens protocols by a step or two. From what we’ve documented, headaches start multiplying when generic carboxylic acids introduce side reactions or fail to cleanly salt out.

    Optimizing Processes for End-Users

    We take pride in tweaking synthesis routes according to real-world feedback. Over years of on-site partnership, several clients reported trouble with non-homogeneous batches from other makers—issues ranging from dark color impurities to water content that tipped past 0.5%. At our facility, rigorous stepwise crystallization narrows the particle size and boosts shelf stability. By avoiding high-temperature decolorization, molecular integrity remains intact, leading to better downstream output for API precursors or agroscience actives.

    We track each batch back to raw intermediates and solvent sources, flagging and logging even minor deviations. This traceability remains essential for teams who submit regulatory filings on novel drugs or chemical entities. We welcome site audits and open technical dialogue rather than waiting for complaints. Many research chemists who work with us say that visible, granular process notes make their scale-up transitions easier—no mystery workarounds needed.

    Pharmaceutical groups rely on our product’s reproducible melting point and spectral signature, confirmed by NMR and FTIR each quarter. Maintaining this specification isn’t a paper exercise. Some years ago, one batch flagged abnormally by a diligent QC manager led us to discover a slightly altered solvent profile from an upstream supplier. That transparency, shared immediately with our customers, prevented a cascade of wasted reactions and built what now stands as standard practice in our quality system.

    Tackling Supply Chain and Regulatory Challenges

    Demand for pyrimidine-2-carboxylic acid often spikes unexpectedly—especially when perfluorinated building blocks or selective kinase inhibitors trend in literature. Our production planning grew more sophisticated, with standing agreements to keep core raw materials in secure inventory. We work with global regulators and process engineers to ensure every outgoing lot satisfies local and international requirements. Documentation always travels with the shipment, and we run additional test cycles for customers prepping IND applications.

    Occasionally, price pressure from generic manufacturers drives speculation about sourcing cheap pyrimidine-2-carboxylic acid. The learning here is that sub-optimal manufacturing quickly translates into inconsistent results down the line. Several clients who chased cheaper supply found their yields dropping, and their purity profiles showing unexpected byproduct signatures. Our sales and R&D teams collect real-world case studies on how “invisible value”—in stable supply, regulatory support, or batch reproducibility—often outweighs short-lived savings.

    Facility Investments and Responsible Chemistry

    Over more than two decades on this site, we’ve seen expectations shift. Clients who once asked only for technical grade now push for lower residual solvents or targeted isomer control. We rebuilt our purification suite, adding more automated chromatography and dedicated glass-lined reactors. These changes sharply reduced worker exposure and minimized cross-contamination between products. Any waste generated is held for external treatment, monitored per local regulations. External auditing and regular training keep every technician up to pace with evolving HSE norms.

    The story isn’t just about the finished acid itself. Downstream users rely on our documentation supporting hazard, environmental footprint, and disposal methods. We encourage open discussion if a customer faces unusual local regulations or end-user concerns. Meeting high standards starts on the plant floor—minimizing releases, digitizing batch records, and opening any record for scrutiny from regulators or strategic partners. It’s not simply about ticking a compliance box, but about protecting employees, communities, and our shared reputation as reliable chemical manufacturers.

    Direct Support for Process Chemists

    Lab users sometimes call right from the workbench—questions about solubility, stability in nonaqueous media, compatibility with coupling reagents, or shelf life when stored under nitrogen. Having real-world trial data at hand, we respond quickly, often supplying not just the product but tips learned during pilot studies. Years of troubleshooting alongside customers taught us that successful chemistry isn’t only about reagents but the whole workflow—from order planning to safe product retrieval.

    We do not hold back intellectual property that could help a research partner, so process improvements learned in-house are passed along directly. Whether the challenge involves filtering off crystalline salts, overcoming slow dissolution in DMSO, or fine-tuning chiral separations, our in-house teams log and share every practical detail that can save hours or weeks for collaborators.

    Because real laboratory work rarely fits into the boxes of standard operation, we support special requests—be it a differently micronized batch for rapid suspension, or a consultation for in situ derivative formation. It’s not rare for a returning customer to request an alteration based on their own pilot findings. Years of back-and-forth have fine-tuned our flexibility, making the path from pure acid to finished analog much smoother.

    Cross-Disciplinary Applications Raise New Challenges

    A material with a simple formula and name often grows into new disciplines. Our pyrimidine-2-carboxylic acid’s reach stretches from medicinal chemistry to materials science. In the last decade, nanomaterials groups have explored it as a ligand or as a scaffold in supramolecular arrays. Crop science firms ask about its selective toxicity and environmental breakdown, wanting reliable degradation patterns not just raw numbers.

    As new uses emerge, unexpected compatibilities or difficulties show up. Not every customer needs the same particle size, density, or residual water content. What the electronics developers want doesn’t always sync with expectations in a GLP bio-lab. The reality is, no specification survives unchanged for long if science keeps moving forward. Over the years, we’ve adapted by building in feedback loops: immediate tech support, on-site troubleshooting, fast documentation updates for each new project scope.

    Materials scientists using pyrimidine-2-carboxylic acid for functionalized polymers report different requirements than those designing new nucleosides or bioconjugates. Our role as manufacturer becomes one of partnership—modifying process steps, flagging purity profiles, and revisiting data as research venues broaden. Direct links between our technical staff and their end-user counterparts keep improvements focused on real bottlenecks, not just theoretical wishes.

    Looking Forward: Reliable Building Blocks in a Rapid World

    Sourcing chemical building blocks used to revolve around price alone. Now, as supply chains tighten and breakthrough discoveries demand higher confidence, the manufacturer’s role grows central. Pyrimidine-2-carboxylic acid isn’t just one of many products rolling off the line. Behind each shipment stands a network of process specialists, analytical chemists, and technical partners dedicated to flushing out hidden risks and keeping every lot on spec.

    Every quality manager or research chemist who calls us knows the conversation goes further than “does this pass Q.C. this quarter?” We strive to think ahead—anticipating changes in end-market regulation, or early-stage research shifts that call for tighter chiral control or new grade definitions. Immediate service matters, but so does planning for unforeseen demand or regulatory shifts.

    The path from starting material to finished innovation runs smoother with clear and consistent supply. Direct sourcing, technical transparency, and a culture that encourages real discussion beat out arm’s-length brokering every time. Customers find not just a chemical, but a working relationship worth investing in repeatedly.

    For pyrimidine-2-carboxylic acid, and every derivative made in our reactors, the underlying message remains: real innovation comes out of craftsmanship, openness to change, and partnerships built on hard evidence, not just a page in a catalog. Every year raises new hurdles in synthesis and supply, yet with teamwork between manufacturer and end user, solutions come faster—and the next wave of tools and therapies stands on a more solid foundation.