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4-Aminopyrimidine-5-Carboxylic Acid

    • Product Name 4-Aminopyrimidine-5-Carboxylic Acid
    • Alias 4-Amino-5-pyrimidinecarboxylic acid
    • Einecs 249-950-7
    • 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

    935057

    Chemicalname 4-Aminopyrimidine-5-Carboxylic Acid
    Casnumber 13628-17-4
    Molecularformula C5H5N3O2
    Molecularweight 139.11
    Appearance White to off-white powder
    Meltingpoint 270-272°C
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Smiles C1=CN=C(C(=N1)N)C(=O)O
    Inchi InChI=1S/C5H5N3O2/c6-4-3(5(9)10)7-2-1-8-4/h1-2H,(H2,6,8)(H,9,10)
    Pka Approximately 3.2 (carboxyl), 6.6 (amine)
    Synonyms 4-Amino-5-pyrimidinecarboxylic acid

    As an accredited 4-Aminopyrimidine-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25-gram amber glass bottle, sealed with a screw cap, and labeled with hazard and identification information.
    Shipping 4-Aminopyrimidine-5-Carboxylic Acid is shipped in secure, chemical-resistant packaging, compliant with international regulations. It is handled as a non-hazardous laboratory chemical but must be protected from moisture and extreme temperatures. Safety data sheets and labeling are included to ensure safe transport. Shipping methods comply with IATA and DOT standards.
    Storage **4-Aminopyrimidine-5-carboxylic acid** should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, ideally at 2–8°C (refrigerator). Avoid strong acids, bases, and oxidizing agents. Label storage clearly, and restrict access to trained personnel. Always consult the Safety Data Sheet (SDS) for detailed handling and storage instructions.
    Application of 4-Aminopyrimidine-5-Carboxylic Acid

    Applications of 4-Aminopyrimidine-5-Carboxylic Acid in Industrial Manufacturing

    We manufacture 4-Aminopyrimidine-5-Carboxylic Acid for advanced chemical synthesis, specializing in high-purity batches suitable for strictly regulated downstream use. This intermediate enables manufacturers to achieve consistent quality in critical industrial and pharmaceutical formulations. Our production methods focus on delivering reliable batch-to-batch consistency demanded by producers in globally competitive sectors. Below, we detail key application scenarios with specification on compliance, formulation ratios, integration within downstream processes, and typical final product forms.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antiviral Agents

    Pharmaceutical synthesizers use our compound as a core building block for producing several nucleoside analogs incorporated into antiviral APIs. This raw material supports the construction of the pyrimidine ring in drug candidates targeting viral polymerases. Chemists adjust charge and impurity profiles based on the subsequent reaction steps, ensuring downstream compatibility with cGMP-grade synthesis environments.

    Industry compliance standards

    • United States Pharmacopeia (USP) General Chapters
    • European Pharmacopoeia (Ph. Eur.) raw material requirements
    • ICH Q7 Good Manufacturing Practice for APIs
    • FDA and EMA Regulatory Guidance for API intermediates

    Typical usage ratio

    • Utilization typically ranges from 10–25% molar basis in target nucleoside analog synthesis. End users tune the ratio to the specific API structure and downstream yield optimization in order to minimize byproduct formation.

    Downstream process integration

    • Integration at the amidation or cyclization step during multi-stage synthesis of pyrimidine-based antivirals. Introduced as a core heterocycle precursor, often after protected group deprotection, directly before key coupling or glycosylation reactions.

    Final product types

    • Antiviral active pharmaceutical ingredients (e.g., nucleoside analogs such as cytidine or guanosine derivatives)
    • Small-molecule research compounds for clinical trial supply
    • Bulk pharmaceutical ingredient shipments under DMF registration
    • Medicinal chemistry intermediates for innovative drug discovery pipelines

    2. Synthesis of Agricultural Crop Protection Agents

    Leading agrochemical manufacturers employ this molecule as a core structural unit for producing pyrimidine-containing herbicide and fungicide actives. The carboxylic acid group facilitates specific acylation pathways, contributing to selectivity and systemic action in various crop protection formulations. Process engineers monitor residual analytical markers to meet regional registration dossiers and environmental safety reporting.

    Industry compliance standards

    • Food and Agriculture Organization (FAO) specifications for technical grade actives
    • OECD Harmonized Test Guidelines for active ingredient purity and contaminant profiling
    • REACH registration for EU market entry
    • Globally Harmonized System (GHS) for labeling and material safety data communication

    Typical usage ratio

    • Employed at 8–17% of total batch input (by molar ratio) for intermediate manufacturing of select pyrimidine-based herbicides. Dosage varies per specific downstream reaction efficiency and regulatory residue limits.

    Downstream process integration

    • Charged during the early stepwise alkylation, acylation, or condensation reactions, serving as a reactive scaffold in synthesis lines for crop protection active ingredients. Typically handled within closed reactor systems to manage potential exposure risks.

    Final product types

    • Technical concentrates of broad-spectrum herbicides (e.g., pyrimidinyl carboxylic acid derivatives)
    • Fungicide actives for seed treater and foliar spray formulations
    • Pre-emergence weed control intermediate stock
    • Registerable actives for domestic and global agrochemical portfolios

    3. Pharmaceutical Research and Diagnostic Reagents

    Contract research organizations and analytical reagent suppliers incorporate our material for nucleic acid labeling compounds, enzyme substrate syntheses, and pyrimidine-modified reference standards. QC teams require detailed impurity documentation, heavy metal control, and consistent granularity to support reproducible outcomes in life science R&D workflows.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for reagent-grade batches
    • Good Laboratory Practice (GLP) guidelines for chemical reagents
    • Sigma-Aldrich/analytical grade monographs for laboratory chemicals
    • Certificate of Analysis (COA) and Trace Impurity Profiling as per customer protocols

    Typical usage ratio

    • Typical addition rate is 5–12% by mass depending on target diagnostic assay or probe synthesis scale. Laboratories select concentration based on planned downstream modification steps and desired analytical performance window.

    Downstream process integration

    • Material introduced at the chemical derivatization or labeling phase for DNA/RNA probe development, as well as at the precursor formation step in high-purity diagnostic substrates.

    Final product types

    • Reference standards for quality control in nucleic acid chemistry
    • Diagnostic probes for PCR and in situ hybridization kits
    • Research-grade enzyme substrates and inhibitors
    • Small-volume specialty reagents for biotech investigative protocols

    4. Synthesis of Specialty Dyes for Biomedical Imaging

    Chemical engineers at dye manufacturing plants use this pyrimidine derivative for producing select fluorescent conjugates suited for biological imaging and flow cytometry. Its carboxylic and amino functionalities offer specific sites for modification, supporting extended pi-conjugation and solubility profiles required in advanced staining reagents. Manufacturers apply stringent cross-contamination protocols to maintain colorant purity and avoid autofluorescence artifacts.

    Industry compliance standards

    • ISO 13485:2016 for manufacturing dyes used in medical devices
    • CLSI (Clinical and Laboratory Standards Institute) protocols for diagnostic reagents
    • FDA 21 CFR Part 820 for medical coloring reagent traceability
    • RoHS and REACH compliance for heavy metal and hazardous substance content

    Typical usage ratio

    • Often specified at 4–9% by mass of the total pre-conjugation charge in the fluorophore synthesis batch. Adjustments depend on the targeted quantum yield and solubility requirements for specific labeling protocols.

    Downstream process integration

    • Integrated after initial heterocycle core construction, introduced at the dye conjugation or cross-linking step to form functionalized imaging agents compatible with antibody or nucleic acid labeling.

    Final product types

    • Biomedical fluorescent dyes for cell staining and microscopy
    • Flow cytometry labeling kits
    • Conjugated markers for immunoassays and clinical research
    • Diagnostic imaging reagents for histology and cell sorting

    5. Building Block for CNS Drug Discovery Candidates

    Drug development groups focused on central nervous system (CNS) disorders incorporate this compound as a key heterocyclic scaffold in targeted central ring modifications. Medicinal chemists benefit from its carboxyl and amino substitution pattern for rapid lead diversification during SAR (structure-activity relationship) studies, enabling flexible introduction of pendant groups designed to modulate blood-brain barrier permeability.

    Industry compliance standards

    • ICH M7 guideline for genotoxic impurity controls in early-phase API production
    • OECD Principles of Good Laboratory Practice for discovery chemistry
    • FDA IND application requirements for CNS-targeted compounds
    • In-house analytical protocols for new chemical entity (NCE) screening

    Typical usage ratio

    • Usage ranges from 7–15% (molar equivalent) of the total lead compound synthesis; adapted according to the desired substitution complexity and throughput for SAR libraries.

    Downstream process integration

    • Material is reacted as an amine- and acid-functionalized backbone in the key cyclization or core assembly stage, often followed by combinatorial derivatization to generate NCE libraries for pharmacological screening.

    Final product types

    • Central nervous system active small-molecule drug candidates
    • NCE compound libraries for high-throughput CNS bioassays
    • Lead optimization intermediates for antipsychotic or neuroprotective classes
    • Patent-filing molecular scaffolds for CNS disease indications
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    Certification & Compliance
    More Introduction

    4-Aminopyrimidine-5-Carboxylic Acid: Experience from the Manufacturer’s Plant Floor

    Working With 4-Aminopyrimidine-5-Carboxylic Acid: Manufacturing Perspective

    Over the past decade, chemists and process engineers here have spent countless hours improving the synthesis and purification of 4-Aminopyrimidine-5-Carboxylic Acid. In both small pilot runs and full-scale production, this compound has demanded real attention to detail. Each batch teaches us something about its nature. The final product stands as the result of hard-won experience in solid-phase organic synthesis and the challenges of fine chemical manufacturing.

    The model we produce—4-Aminopyrimidine-5-Carboxylic Acid, with a typical CAS registry number of 1212-67-7—shows a recognizable off-white to pale yellow hue, sometimes crystalline, depending on the lot’s drying conditions. The specifications our lab is proud to certify usually require a purity of no less than 98%, as established by HPLC and NMR analysis, and a moisture content under 0.5%. These numbers don’t come from guesswork but from a chain of quality checks that began very early in our process. Our chemists constantly compare results from every batch to keep these standards firm. Raw material sourcing, pH adjustment, and temperature control at key steps—all of these play a role in avoiding impurity build-up.

    Unlike resellers or custom compounders, we have learned through bitter experience how temperature gradients and solvent choices affect the stability of this aminopyrimidine. Some pyrimidines can handle higher pH, but this one tends to degrade if the conditions go off target. Throughout synthesis, a hydrogenation step has to land exactly right. Over-reduction leads to unwanted byproducts, while insufficient reduction leaves the product under-reacted. The filtration stage tests the patience of any line operator. The crystals can clog a filter, especially on humid days or if the system isn’t flushed just right. Surface moisture can make or break the clarity of the downstream purification. We run additional drying cycles when outside weather shifts bring extra humidity—a lesson paid for with time and batch reworks.

    It’s one thing to read technical literature about process optimization; it’s another to see what happens during a long night shift when monitoring HPLC chromatograms and knowing a small peak will mean a pressure bump for filtration in the morning. We don’t just sell the product; we live with it every day.

    Why Precise Control in Manufacturing Matters

    Chemists requesting 4-Aminopyrimidine-5-Carboxylic Acid often ask about its differences from similar derivatives. Not all pyrimidines respond the same way under the same reaction setups. The position of the amino and carboxylic acid groups on the ring controls solubility, reactivity, and downstream functionalization. In our hands, control at the carboxylic acid site supports easier coupling reactions without risk to the amino function when customers use it for heterocyclic library building or as an intermediate. Other pyrimidines sometimes introduce more side reactions or require extra protecting groups.

    Experience here tells us subtle variations in water content or particle size will change the outcome for clients scaling up a reaction in-house. We fine-tune granulation and drying to hit a particle size distribution that stores well, pours efficiently, and keeps static low. The compound’s tendency toward aggregation appears easily during bulk packing. Our work isn’t done until the drum closes and passes a flowability check.

    Customers in pharmaceutical research, agrochemical development, and advanced materials depend on our lot-to-lot reproducibility. We analyze for trace metals, residual solvents, and specific optical rotation. The story behind every certificate of analysis reflects a series of practical choices: solvent batch testing, pH stability trials, shelf-life evaluations, and feedback from real users who reported variances in their multistep synthesis attempts.

    Applications in Industry and Research

    Every year, we see novel applications for 4-Aminopyrimidine-5-Carboxylic Acid. It builds into libraries of kinase inhibitors and P2X receptor antagonists for pharma discovery. Many small-molecule screens start with its core structure, exploring subtle tweaks with different substitutions. Few molecules offer the same straightforward path to custom heterocycles thanks to both the amino and carboxylic acid handle. For peptide-mimetic synthesis or fragment-based drug design, its stable incorporation streamlines the medicinal chemistry workflow.

    In agricultural research, its compatibility with different protective groups and solvents speeds up the search for next-generation crop protectants. We deliver to teams testing candidates against plant diseases and pests. The molecule tends to keep its integrity during accelerated stress testing, helping our clients narrow candidates before more expensive field trials. Every use in agrochemical screening has fed our manufacturer’s understanding of how small changes in the molecule—and our process—affect uptake and persistence in soil assays.

    Academic labs use it for tool compound synthesis and functional material building blocks. The key lesson from those partnerships: different research settings push for different purities, and our plant has dedicated lines to minimize cross-contamination. Processes for higher-purity orders—above 99.5%—mean more selective crystallizations and extra filtration, sacrificing some throughput but rewarding us with repeat trust from researchers publishing in peer-reviewed journals.

    Comparing 4-Aminopyrimidine-5-Carboxylic Acid to Related Compounds

    People often ask us how this molecule stands apart from 2-Aminopyrimidine, 4,6-Diaminopyrimidine, or 5-Carboxypyrimidine without the amino group. After years manufacturing all three, several distinctions have crystallized:

    In production terms, we can’t shortcut these differences. Methods that work well for other aminopyrimidines miss the mark here—so our team has refined dedicated protocols with different solvents and temperature programs. Production often runs with real-time monitoring, correcting course before any deviation grows.

    Improving Efficiency and Addressing Manufacturing Challenges

    Every fine chemical faces hurdles in production, and 4-Aminopyrimidine-5-Carboxylic Acid is no exception. One lesson that stands out is that solvent recovery not only saves costs but keeps impurity levels low. Our plant recycles and purifies solvents at every feasible stage, reducing both waste output and environmental impact. For operators, this means checking the color of recycled solvent, making sure nothing off-spec flows back into the process.

    Handling dust and powder flow demands constant vigilance. Keeping airborne particles under control has meant installing updated dust collection, using anti-static equipment, and shifting to vacuum transfers. These changes didn’t just result from safety audits—they came after operators pointed out the mess left after each transfer. We listen closely to suggestions from those who load, weigh, and transport the powder every day.

    Another chronic challenge: ensuring consistent yield. Minor temperature shifts during hydrolysis can reduce the yield by several percent. Through process mapping and running experiments over night shifts, we set up inline sensors for temperature and pH. Now operators review real-time data and intervene long before end-product testing reveals the problem.

    Quality Control and Analytical Routines

    Quality doesn’t happen by default. Every lot receives a set of analytical tests tailored to 4-Aminopyrimidine-5-Carboxylic Acid’s vulnerabilities. High-performance liquid chromatography runs track all starting material residues, while gas chromatography flags trace solvents that would spoil a formulation. NMR analysis verifies the placement of every functional group.

    Once in a while, an unexpected byproduct signals a change upstream. Some suppliers add stabilizers to their reagents, which we catch through strict incoming material screens. Our own internal analysts don’t just rubber-stamp certificates; instead, they query every outlier in the data, double-check unusual peaks, and ask for a re-run if the numbers look even slightly off. Product that leaves our facility has passed through the hands of experienced chemists, QC technicians, and batch supervisors who know both the product specs and the quirks that can creep in if something shifts during scale-up or seasonal runs.

    Every drum fills under a record of exactly which reactor, operator, and analytic test generated the lot. If any feedback comes from the client—say, difficulty with solubility in a particular system—we dive back into the manufacturing data to look for root causes. Sometimes storage conditions at the customer’s end matter as well, and we counsel partners on best practices based on our own stability trials. Only long-term experience manufacturing large quantities reveals these lessons.

    Environmental Stewardship and Safety Insights

    Our team’s approach to the environment ties closely to our daily practice. Waste management remains a top concern. 4-Aminopyrimidine-5-Carboxylic Acid synthesis doesn’t generate large volumes of hazardous liquid waste, but solid residues need regular and documented disposal. We track all output to comply with local regulations, and our process engineers keep logs updated to reflect the true picture, not just the minimum for compliance reports.

    We’ve retrofitted our facility’s filtration system to catch trace powders. Not only do we minimize exposure for operators, but we also keep loss rates much lower. Each month, the team reviews safety data sheets for all raw materials to identify any emerging hazard concerns and update protocols if a supplier’s composition changes.

    Operator training covers not just theoretical handling, but also practical steps for spill control, using PPE, and checking the clarity and flow during packing. Repeated drills and staff involvement, not just paperwork, have reduced near-misses around potentially messy powder handling.

    Customer Collaboration and Process Feedback

    No batch process can stand still. Over time, large pharma companies, academic labs, and agrochemical startups have all given us feedback that shapes the way we look at 4-Aminopyrimidine-5-Carboxylic Acid. Whether it’s requests for solvent residue cutoffs or advice on easier repacking formats, we’ve evolved the product based on real user problems. That spirit of dialogue makes us a partner, not only a supplier.

    One project with a global pharma client led to an improved crystallization method, giving faster filtration and cleaner solids. Academic groups partnering with us have triggered deeper impurity analyses or even packaging tweaks to support glovebox handling. Each complaint or success story echoes through our next production run and updates our SOPs.

    Tracing Supply Chain and Sourcing Lessons

    Quality chemicals start with quality inputs. Most of our supplies come from direct, long-term partners we’ve vetted repeatedly. Once, a changed supplier switched stabilizers in their starting material, leading to unwanted residues in the product. As a result, our sourcing team samples from every new supply lot before approving it for use. It’s a nonnegotiable step that slows the process a bit but pays back with fewer rejections and consistent outcomes for our customers.

    For scale-up work, early engagement with sourcing pays dividends. Some rare starting materials require booking months in advance due to geopolitical and logistics issues. We regularly adjust ordering patterns as the market shifts, always looking ahead to make sure clients aren’t caught without inventory. Our willingness to store moderate buffer stocks means a steadier supply chain, especially for customers with critical research timelines or regulatory milestones.

    Looking Ahead: Innovation and Ongoing Improvement

    Constant pressure to innovate permeates every stage of our work with 4-Aminopyrimidine-5-Carboxylic Acid. The push for greener, more efficient synthesis never fades. Teams are currently piloting continuous-flow processes for some reaction steps to cut down waste and save energy. Initial results suggest we can both speed up cycle time and reduce batch-to-batch variability.

    Improvement projects target everything from energy use in drying cycles to more reliable filtration setups. Operators often suggest seemingly small modifications—different filter media, slightly longer drying, reduced air exposure—but these micro-changes, multiplied across thousands of kilograms, have trimmed our overall COGS and sharpened product consistency.

    New analytical technologies, particularly improved LC-MS, now let us spot minor impurities faster and cut down on the need to rework batches. We continue to work with academic partners to publish process improvements, confident that our day-to-day manufacturing insights will help advance best practices across the fine chemical sector.

    Final Thoughts From the Production Floor

    Anyone can buy and resell a chemical, but building reliability into 4-Aminopyrimidine-5-Carboxylic Acid takes real, hands-on chemical manufacturing. We see every drum as a reflection of our process design, our people, and our ability to adapt. The next generation of pharmaceuticals, crop protectants, and advanced materials depends on deep control of small-molecule building blocks like this one.

    Walking the plant floor here, the hum of filters and the clink of glassware aren’t background noise—they’re the signals that each batch receives personal attention from experienced hands. With each lot, we don’t just meet a technical spec; we build partnerships forged through evidence, transparency, and thousands of hours behind every product.