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2-Amino-4-Hydroxy-1H-Pteridine

    • Product Name 2-Amino-4-Hydroxy-1H-Pteridine
    • Alias Pterin
    • Einecs 204-809-9
    • 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
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    Specifications

    HS Code

    231289

    Chemical Name 2-Amino-4-Hydroxy-1H-Pteridine
    Molecular Formula C6H5N5O
    Molecular Weight 163.14 g/mol
    Cas Number 1742-46-7
    Appearance Off-white to beige crystalline powder
    Melting Point 315-318 °C
    Solubility In Water Slightly soluble
    Pka 7.1 (for the 4-hydroxy group)
    Iupac Name 2-amino-4-oxo-1,4,7,8-tetrahydropteridine
    Smiles C1=NC2=C(N1N=C(N=C2N)N)O
    Storage Conditions Store at room temperature, protected from light and moisture
    Synonyms 2-Amino-4-pteridinone; 2-Amino-4(3H)-pteridinone

    As an accredited 2-Amino-4-Hydroxy-1H-Pteridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Amino-4-Hydroxy-1H-Pteridine is packaged in a 25g amber glass bottle with a secure screw cap and product labeling.
    Shipping 2-Amino-4-Hydroxy-1H-Pteridine is shipped in tightly sealed containers to prevent contamination and moisture exposure. The chemical should be transported in accordance with local and international regulations, with clear labeling. It is recommended to store and ship the compound at room temperature, away from light, incompatible materials, and strong oxidizers.
    Storage 2-Amino-4-Hydroxy-1H-Pteridine should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature. Ensure storage away from strong oxidizing agents and acids. Properly label the container and handle it with appropriate personal protective equipment to minimize exposure and contamination risks.
    Application of 2-Amino-4-Hydroxy-1H-Pteridine

    Applications of 2-Amino-4-Hydroxy-1H-Pteridine in Industrial Manufacturing

    2-Amino-4-Hydroxy-1H-Pteridine serves as a key intermediate in diverse chemical manufacturing processes. Its molecular structure supports various transformation steps, offering specific functional advantages across the pharmaceutical, food, veterinary, diagnostics, and specialty chemicals industries. Below, we detail established downstream applications, highlighting process requirements and compliance at each stage.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antifolate Drugs

    Major pharmaceutical manufacturers rely on this pteridine derivative as a critical precursor in the synthesis of antifolate medications such as methotrexate and related compounds. The material integrates during the core ring assembly and side-chain elaboration phases in multi-step organic syntheses. Each batch must conform to stringent regulatory and trace impurity controls, with particular focus on pteridine-related genotoxins and process stability. Downstream process engineers routinely adjust reagent ratios to maintain yield efficiency as route optimization or scale-up progresses. Final APIs undergo full validation before entering drug product manufacturing for oncology, immunosuppressant, and rheumatoid arthritis indications.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • U.S. Pharmacopeia (USP) Monographs for antifolate compounds
    • EU GMP Part II for intermediates
    • FDA 21 CFR Part 211

    Typical usage ratio

    • Used at 0.12 – 0.23 molar equivalents per target molecule; actual dosage adjusted for reaction yield and purity requirements

    Downstream process integration

    • Enters as a starting heterocycle in core condensation, followed by regioselective functionalization steps

    Final product types

    • Methotrexate API
    • Pemetrexed API
    • Pralatrexate API
    • Pharmaceutical finished dosage forms (tablets, injections)

    2. Vitamin B2 (Riboflavin) Synthesis Intermediate

    The pteridine nucleus is an essential building block for riboflavin production at industrial scale. Food-grade manufacturing facilities introduce the compound early within the multi-step synthesis, where precise control over feedstock input ensures minimal by-product formation and compliance with nutritional additive standards. Feed ratios align closely with the target output volume, adjusting for process efficiency and raw material availability. Downstream, the intermediate undergoes hydrogenation and subsequent deamination prior to full ribitylation. Finished products supply food fortification, dietary supplements, and premix blending operations worldwide.

    Industry compliance standards

    • FAO/WHO Codex Alimentarius Specification for Food Additives
    • GB 14880-2012 Standard for the Use of Food Additives (China)
    • EU Regulation (EC) No 1333/2008 on food additives
    • FSSC 22000 Food Safety Management System

    Typical usage ratio

    • Typical dosage of 0.18 – 0.22 mol per mol of riboflavin; adjusted based on batch size and conversion efficiency

    Downstream process integration

    • Introduced after formylation of guanidine donors as the key pteridine scaffold; followed by continuous hydrogenation and functional group extension

    Final product types

    • Pure riboflavin (vitamin B2) crystals
    • Food premixes
    • Dietary supplement tablets and capsules
    • Riboflavin feed-grade additives

    3. Diagnostic Reagent and Enzyme Substrate Manufacturing

    Clinical and enzymatic diagnostic reagent manufacturers use the compound as a functional substrate for oxidoreductase enzymes in colorimetric and fluorescence-based assays. It participates in redox cycling necessary for the generation of measurable signal cascades, forming a critical part of in vitro diagnostic (IVD) kit formulations. Quality control checkpoints emphasize purity, absence of interfering fluorophores, and consistency of reactivity. Formulators specify concentration according to enzyme and sensitivity requirements. The processed reagents are distributed to laboratory, hospital, and healthcare testing environments.

    Industry compliance standards

    • ISO 13485 Medical Device Quality Management Systems
    • 21 CFR Part 820 Quality System Regulation for IVD Devices
    • CLSI EP05 and EP17 Guideline for Assay Quality
    • European IVD Regulation (EU) 2017/746

    Typical usage ratio

    • Formulated at 20–90 mg per liter of reagent solution, depending on target enzyme concentration and required assay dynamic range

    Downstream process integration

    • Added to buffer solutions post-purification; often lyophilized together with cofactors or as part of test kit cartridges

    Final product types

    • Colorimetric enzymatic test kits
    • Fluorometric substrate vials
    • Point-of-care diagnostic panels
    • Clinical chemistry analyzer reagents

    4. Veterinary Pharmaceutical Intermediate

    Animal health product manufacturers employ our material as a synthetic intermediate for folate pathway inhibitors used in veterinary medicine. The substance enters multi-step chemical routes, requiring close monitoring for process impurities and batch reproducibility in line with veterinary drug standards. Applications extend to livestock and companion animal therapies, where efficacy and withdrawal periods depend on stringent quality control. Ratio adjustments occur during scale-up for different dosage forms destined for oral or injectable veterinary pharmaceuticals.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practices (for veterinary medicinal products)
    • Ph. Eur. Monographs for veterinary APIs
    • 9 CFR 113 Animal and Plant Health Inspection Service standards
    • GVP Module V (EU) for veterinary medicinal products

    Typical usage ratio

    • Blended at 0.13 – 0.20 molar equivalents relative to target molecule; specific values tuned for species and dosage considerations

    Downstream process integration

    • Introduced post-condensation in pteridine core assembly; further processed by methylation or alkyl addition as required for specific animal application

    Final product types

    • Trimethoprim veterinary API
    • Combination therapeutic products (antibacterials, potentiators)
    • Oral and injectable veterinary drugs
    • Medicated premixes

    5. Specialty Pigment and Dye Intermediate

    Producers in the pigment and specialty dye industry utilize this compound to develop high-performance yellow and green dyes for plastics, synthetic fibers, and security inks. The material supports formation of stable chromophores via further functionalization and metal complexation steps. Usage ratios are calibrated based on color intensity targets and resin compatibility. Regulatory control addresses migration and toxicity limits, particularly for sensitive end uses such as food packaging or children’s products. Finished dye intermediates find application in automotive plastics, consumer textiles, and advanced printing technologies.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemicals)
    • EN 71-3 (Safety of toys: migration of certain elements)
    • REACH Regulation (EC) No 1907/2006
    • ASTM D4236 (Labeling for chronic health hazards)

    Typical usage ratio

    • Applied at 0.08 – 0.16 molar ratio, adjusted to substrate and final chromophore yield

    Downstream process integration

    • Introduced as the pteridine core in condensation and diazotization reactions, then subjected to metallization or sulfonation depending on end-use

    Final product types

    • Plastic colorants (masterbatches, powders)
    • Synthetic fiber dyes
    • Security and anti-counterfeit printing inks
    • Food contact-safe pigment formulations
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    Certification & Compliance
    More Introduction

    2-Amino-4-Hydroxy-1H-Pteridine: Manufacturing Expertise and Practical Utility

    Real Insights from the Manufacturer’s Perspective

    We have spent decades at the bench and in the reactor halls, refining the craft of producing 2-Amino-4-Hydroxy-1H-Pteridine, a molecule that finds its value not just in theoretical potential but in tangible, delivered performance. Our direct work with this compound makes it clear that the little things — from the moisture of a starting batch to the choice of drying method — ripple through to create big impacts on both the reliability and downstream usability of the product.

    Understanding the Product’s Core

    2-Amino-4-Hydroxy-1H-Pteridine, sometimes recognized in literature by its pteridine structure, walks a unique path thanks to its dual amino and hydroxyl groups resting on a fused pyrimidine-pyrazine ring system. These features give the molecule robust hydrogen bonding behavior and help it engage in reactions needed for key pharmaceutical, biochemical, and diagnostic routes. Years of repeat syntheses reveal recurring quirks in its crystallization and a tendency for strong color — even from trace impurities — that demand vigilance.

    Beyond just making a powder matching the chemical formula, our day-to-day reality involves coaxing the molecule into the intended polymorph, maintaining high assay above 99%, and keeping water content low enough for application chemistry. We monitor color tightly. We watch UV/visible spectra for side products, something that shines a spotlight on both process control and practical experience in the plant. For sensitive applications, we go the extra mile with preparative HPLC, reinforcing the focus on purity for research, pharmaceutical intermediate work, and select specialty diagnostics.

    Model and Batch Consistency

    Our output centers on a base product specification: crystalline 2-Amino-4-Hydroxy-1H-Pteridine, characterized by a bright yellow color and a particle size profile aimed at balancing bulk handling with dispersion in solution. Over the years, small customer feedback — powders packing differently or filters clogging unexpectedly — have shaped our shift toward a more consistent sieve profile, tighter screening, and better storage protocols. These are lessons picked up through direct experience rather than written theory.

    Though many in the field offer “lab” and “industrial” grades by broad definition, our distinction arises from hands-on control over every batch. Each runs through UV/vis, NMR, and HPLC checks; we never send out batch certificates without data from our real syntheses, run on the same lines each time. Repeat clients notice, especially when scale-up challenges come into play — consistency breeds trust, and that relies on the habits of the factory floor more than abstract quality slogans.

    Usage: As Applied, Not Just Listened

    We continually see 2-Amino-4-Hydroxy-1H-Pteridine in action, especially as a precursor for new drug entities and a building block in enzyme assay technologies. It anchors key coupling steps for some folic acid derivatives, showing its real-world worth in both research-grade and pilot factory settings. Insights come back to us not through second-hand distributor channels but from direct collaborations and feedback loops: whether in reactions toward tailored heterocycles, probes for molecular diagnostics, or use in pigment studies, users often run into solubility or stability challenges.

    Tests and tweaks on the shop floor — adjusting pH, rotary evaporation times, or the exact grade of silica during purification — impact whether a researcher struggles or breezes through their synthesis. Some industries lean on it not purely as a building block, but for its ability to absorb and emit at distinct wavelengths, especially after coupling with functional groups that modify its electronic structure. Each batch we make has to support this, so we calibrate our own process steps to deliver predictable, not just nominal, chemical behavior.

    Specifications That Connect to Use

    When we talk about product specification, it means more than a few numbers on a sheet. For example, our 2-Amino-4-Hydroxy-1H-Pteridine typically comes as a free-flowing, fine crystalline powder, bright yellow, free of the dulling grey or brown tints that signal side-reactions or over-oxidation. On a technical note, we run melting point checks — not out of regulatory obligation, but because melting behavior reflects real molecular order and is the direct fingerprint of batch purity. For this compound, a sharp melting point clustered around 290-295°C gives us the confidence to release the batch.

    Water content cannot be left to rough estimation, as even a percentage point too much alters reactivity, stirs up clumping, and interferes in critical coupling reactions. As a result, Karl Fischer titration is embedded in our batch release routine, and not just as an afterthought. We keep typical moisture content below 0.5% w/w, as verified by repeated in-house controls. UV/visible spectra show us if pteridine or related chromophores are present as by-products, especially relevant for processes involving photoreactivity. These are not add-ons, but established checkpoints rooted in years of field feedback when projects either succeed or bog down over what seemed like “small” impurities.

    Differences from Seemingly Similar Molecules

    With so many structural relatives in the pteridine class — like 2,4-diaminopteridine, or tetrahydropteridines — selecting and making the right one is not trivial. 2-Amino-4-Hydroxy-1H-Pteridine distinguishes itself by its reactivity: the unique arrangement of its amino and hydroxyl groups changes the way it couples and the stability of its intermediates. Mechanistically, this means that amidine formation, nucleophilic attack, or even salt creation behave in ways that can surprise an unwary chemist who expects parallel reactions to those of other, superficially similar, pteridines.

    We have learned, often through direct troubleshooting with bench chemists and from hard-earned plant-scale lessons, that the purity of 2-Amino-4-Hydroxy-1H-Pteridine plays an outsize role in catalyst studies and in pharmaceutical API pathways compared with the more forgiving nature of certain pteridine analogues. Even a few parts per thousand stray isomers flip the reaction or ruin spectral clarity, most tangled with the electronic properties of the pteridine core. Our experience proves that controlling the synthesis, not just starting from catalogue-grade raw materials, delivers performance in demanding downstream chemistry.

    Some customers once used 2,4-diaminopteridine as a default substitute, only to report lower yields or inconsistent results in enzyme selectivity and colorimetric assays. Through collaborative troubleshooting, we showed that the electron distribution and protonation pattern of the hydroxy/amino version made all the difference in both reactivity and detection sensitivity. This has guided our approach to process purification, choosing specific organic solvents and controlled atmospheres to prevent tautomer shifts and oxidative degradation.

    Direct Manufacturing Experience Shapes the Product

    From a manufacturing floor perspective, every batch presents its own personality. Synthetic routes demand real-time decisions: should the reaction run under argon, or is nitrogen enough? Should the intermediate be filtered hot or cold, given shifts in product solubility? Too many manufacturers lose control over these decisions, outsourcing the process or skimping on quality for volume. Working at the origin of synthesis means we see, day by day, how unanticipated changes in ambient humidity, glassware cleaning, or even batch operator experience push shifts in final product quality.

    Consistency is never abstract; it traces back to the technician’s practiced stirring, the supervisor’s demand for an extra recrystallization, and the operator understanding the sound of a well-behaved rotary evaporator. Years of watching how even minute contamination alters 2-Amino-4-Hydroxy-1H-Pteridine’s quality goes into every release batch. These are hands-on judgments that cannot be replaced with automated checklists — they come from lived manufacturing experience.

    Addressing Problems with the Compound’s Stability and Handling

    The stability of 2-Amino-4-Hydroxy-1H-Pteridine is a real-world concern, and from the factory side, we have tackled a share of packaging and logistics questions. Exposure to air and moisture can slowly tarnish the vivid yellow color, driving oxidation or encouraging slow breakdown. Standard packaging simply does not suffice for long-term storage. To handle this, we now use airtight, light-blocking containers, backfilled with dry inert gas; this minor factory expense saves headaches both for us and for clients who might otherwise lose batches to slow degradation.

    Powdered pteridines are dust-prone, so special care in our filling lines, with enclosed systems and static controls, cuts cross-batch contamination. Customers often overlook storage — keeping the compound cool, dry, and shielded from light extends its working life. This comes straight from our accumulated evidence: shelf tests and real returns teach us more than any textbook. Extending the practical shelf life means adjusting drying and avoiding unnecessary contact with plastics or rubber seals that can leach additives into sensitive reagents.

    Supporting Downstream Synthesis and Customer Success

    A chemical’s value lies not in its existence but in how reliably it performs in the hands of those who need it. Our guiding principle as manufacturers is to engage continually with direct application — whether supporting a scientist synthesizing folate analogs, a diagnostics developer fine-tuning a colorimetric assay, or a researcher creating new fluorescent probes. This product owes its edge not just to bench purity, but to the sum of incremental improvements and process adjustments made in response to customer-specific feedback.

    Direct clients often share outlier results or unexpected synthesis failures. More often than not, we trace problems to subtle changes in product crystallinity or the buildup of low-level colored byproducts. Introducing extra filtration steps, multiple crystallizations, or switching up the point of intermediate quenching can make all the difference. These interventions come from our observations, not abstract regulatory frameworks. Our batch records preserve these insights, feeding back improvements to each production run.

    Hands-on work with the compound has taught us to watch for minute differences that only surface in the lab: how temperature ramps affect binding partners or how solvent residue triggers unwanted side reactions. At times, we’ve had to reformulate drying protocols just to anticipate shifts in end-user assay performance or yield. This customized attention stems from the mindset of a manufacturer who has a direct stake in practical outcome, not just shipping a product and walking away.

    Quality Control Rooted in Practice

    No shortcut replaces real batch-to-batch analysis and the discipline of re-verifying our in-house reference standards against global libraries. Each production cycle begins with reagent validation and ends in review meetings, dissecting not only the yields and purity data but also costly missteps and surprise outcomes.

    Repeated feedback cycles with industry partners have underscored the distinction between retail- or trader-supplied material — often re-bagged or repackaged redundantly — and genuine, origin-manufactured 2-Amino-4-Hydroxy-1H-Pteridine. Inconsistent reprocessing, unknown shipping conditions, and overlooked batch histories can all turn a nominally “pure” powder into an unreliable input. Our recordkeeping, which travels with every dispatched lot, gives researchers and process chemists a bridge to manufacturing insight. No impersonal data sheet can substitute for that.

    Environmental and Safety Considerations: Practical Day-to-Day Realities

    From the inside of production, attention to health, safety, and environmental issues becomes second nature, not a matter of ticking boxes. The synthesis and downstream handling of pteridine compounds can release fine dust and trace nitrogen-containing emissions, which we control through closed filtration and scrubbed exhaust systems. Waste minimization and solvent recovery factor into every production batch, guided by observed yields and solvent stability, not just compliance to outside standards.

    Every shift teaches new lessons — a clog in the dust filter, a technician noting an unusual odor, or infrared sensors capturing a spike in light absorption. Such observations drive our continual upgrades to containment and cleaning procedures. Familiarity with the frontlines of chemical production teaches us not to trust even the smallest overlooked residue; that vigilance is what guarantees batch safety both for the workers and for client laboratories.

    Collaboration and Long-Term Improvement

    Industry progress often comes from steady dialogue with users. Direct exchanges with researchers — over email, late-night phone calls, or factory visits — have driven process tweaks and even major overhauls. Our improvements to the 2-Amino-4-Hydroxy-1H-Pteridine process would never have come about from staying behind the plant gates. The best innovations came from problem-solved setbacks, incremental data collected through failed reactions, and constant attention to detail.

    Those who work at the intersection of scale-up chemistry and real-world applications recognize where minor variations amplify into bottlenecks or create opportunities. Through tough product launches and corrective batch recalls alike, we recognize the pivotal role the manufacturer must play in listening, adapting, and sustaining quality. We anchor new modifications in reality, bringing safety, reliability, and practical transparency to every batch.

    A Product Forged by Experience, Delivered with Accountability

    When we produce 2-Amino-4-Hydroxy-1H-Pteridine, customers receive much more than a simple chemical. They benefit from years spent tuning reaction times, tweaking drying cycles, and building up a documentation system that reflects each real-world batch outcome. With every lot, our plant teams deliver their hands-on knowledge, staying involved until the compound moves successfully from package to process.

    Every customer’s challenge or surprise result sparks a new round of internal review and often, a modification or upgrade in our own methods. This ongoing cycle — grounded in direct experience — is the backbone of our product’s steady reliability, and the reason our partners keep coming back, project after project.