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2,4-Diamino-6-(Hydroxymethyl)Pteridine

    • Product Name 2,4-Diamino-6-(Hydroxymethyl)Pteridine
    • Alias pterin-6-ylmethanol
    • Einecs 204-731-1
    • 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

    572519

    Chemical Name 2,4-Diamino-6-(Hydroxymethyl)Pteridine
    Molecular Formula C7H8N6O
    Molecular Weight 192.18 g/mol
    Cas Number 2215-77-2
    Appearance White to off-white solid
    Melting Point Above 300°C (decomposes)
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protect from light
    Synonyms 6-(Hydroxymethyl)pteridine-2,4-diamine
    Iupac Name 2,4-diamino-6-(hydroxymethyl)pteridine
    Smiles NC1=NC(N)=C2NC=NC(CO)=C2N1

    As an accredited 2,4-Diamino-6-(Hydroxymethyl)Pteridine 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 sealed amber glass bottle containing 10 grams, labeled with chemical name, formula, hazard symbols, and storage instructions.
    Shipping 2,4-Diamino-6-(Hydroxymethyl)Pteridine is typically shipped in tightly sealed, chemical-resistant containers to prevent moisture and contamination. It should be transported at room temperature in accordance with standard regulations for non-hazardous laboratory chemicals, with accompanying safety data sheets (SDS). Avoid exposure to extreme temperatures, direct sunlight, and incompatible substances during transit.
    Storage 2,4-Diamino-6-(hydroxymethyl)pteridine should be stored in a tightly closed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Avoid exposure to heat or direct sunlight. Store away from incompatible substances, such as strong oxidizers. Clearly label the container, and ensure access is restricted to trained personnel following standard laboratory safety protocols.
    Application of 2,4-Diamino-6-(Hydroxymethyl)Pteridine

    Applications of 2,4-Diamino-6-(Hydroxymethyl)Pteridine in Industrial Manufacturing

    2,4-Diamino-6-(Hydroxymethyl)Pteridine serves as a key intermediate in multiple regulated downstream manufacturing chains, meeting precise standards for life sciences, diagnostics, and specialty chemical production. Our technical stewardship and direct engagement with customer plants enable consistent, specification-driven performance in practical process environments.

    1. Pharmaceutical Synthesis: Antibacterial and Antiprotozoal Agents

    Our material acts as a critical intermediate for synthesizing selective diaminopteridine-based active pharmaceutical ingredients (APIs), especially those developed for folate pathway inhibition in antibacterial and antiprotozoal drug categories. GMP producers incorporate the compound in condensation and cyclization steps, enabling accurate pteridine ring formation with controlled purities aligned to final API pharmacopoeia requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • USP-NF specifications for pharmaceutical intermediates
    • 21 CFR Part 211 (United States FDA)
    • European Pharmacopoeia authenticated reference standards

    Typical usage ratio

    • 0.98–1.03 molar equivalents relative to sulfonamide or relevant substrate, adjusted during process validation based on yield and impurity profile.

    Downstream process integration

    • Introduced after recrystallization in the early synthetic stage.
    • Mixed with sulfonamide derivatives for condensation reaction under inert conditions.
    • Integrated into purification stream before API isolation.

    Final product types

    • Sulfamethoxazole API
    • Pyrimethamine API
    • Related pteridine-based antimicrobial raw materials

    2. Veterinary Medicine Active Ingredient Production

    Veterinary pharmaceutical manufacturers source this pteridine derivative to build APIs targeting coccidiosis and protozoal infections in livestock. Its high assay and low impurity level support compliance with VICH guidelines and veterinary pharmacopeia monographs during the batch-controlled synthesis of feed additives and medicated premixes.

    Industry compliance standards

    • VICH GL3 Good Manufacturing Practice
    • Pharmacopoeia of the People's Republic of China (Veterinary, Part IV)
    • European Feed Additives Register (1831/2003 EC)

    Typical usage ratio

    • 1.00–1.05 equivalents molar basis in key condensation steps; adjusted based on premix load for optimal feed-grade API content.

    Downstream process integration

    • Charged directly into the initial reactor with other pteridine cycle components.
    • Purified before granulation or blending with carrier for feed premix application.
    • Subject to additional QC to meet low-residual impurity thresholds.

    Final product types

    • Trimethoprim-based feed additive premix
    • Soluble vet-formulated oral powders
    • Injectable antiparasitic veterinary drugs

    3. Clinical Diagnostic Kit Formulation

    Producers of in vitro diagnostic (IVD) kits and reagents utilize the compound for enzyme assay substrate synthesis, particularly in quantitative folate and microbial growth testing. Controlled particle size and traceability documentation enable batch consistency crucial for CE-IVD and FDA-cleared kit assembly lines.

    Industry compliance standards

    • ISO 13485 Medical Devices Quality Management
    • 21 CFR Part 820 (FDA QSR for IVD manufacturers)
    • CE marking under Regulation (EU) 2017/746 (IVDR)

    Typical usage ratio

    • 2.0–5.0 mg per test well reagent, standardized at 0.1%–0.5% w/v in bulk substrate solution depending on target sensitivity and test type.

    Downstream process integration

    • Added during liquid substrate or indicator reagent compounding.
    • Filtered and sterilized before kit filling to ensure assay stability.
    • Referenced at batch release as a critical raw for downstream shelf-life monitoring.

    Final product types

    • Automated microbiological folate test kits
    • Clinical enzyme substrate IVD panels
    • Point-of-care folate blood level diagnostic cassettes

    4. Research-Grade Biochemical Reagent Preparation

    Research chemical manufacturers use the material to synthesize pteridine derivatives assessed in academic and commercial laboratories for enzyme inhibition and cell culture growth studies. Purity grades above 99.5% and defined heavy metal controls allow research institutions to meet procurement and audit requirements. Documentation includes full trace analytics for grant compliance.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation for Analytical Testing
    • ACS Reagent Grade quality controls
    • REACH Regulation (EC) No 1907/2006 submission for laboratory chemicals

    Typical usage ratio

    • 10–50 µmol/L in in vitro assay setups; preparative reactions apply 0.5–1.5 equivalents depending on screening protocol.

    Downstream process integration

    • Dissolved in analytical-grade solvents as the initial experimental substrate.
    • Purified by preparative HPLC for downstream test compound generation.
    • Tracked via lab inventory systems to maintain batch traceability in published work.

    Final product types

    • Screening pteridine analog standards
    • Cell culture folate metabolic inhibitors
    • Custom research substrates for biochemical pathway studies

    5. Specialty Dye and Pigment Intermediate Manufacturing

    Dye and pigment producers incorporate our raw material as a pteridine scaffold in the synthesis of light-stable specialty yellow-green pigments used in security printing and functional coatings. Strict control over transition metal traces and isomeric content support compliance with product registries for export into regulated commercial print applications.

    Industry compliance standards

    • EN 71-3:2019 Safety of Toys (Migration of Certain Elements) for pigment safety
    • EU Regulation (EC) No 1907/2006 for dyes and pigments (REACH)
    • ISO 9001 certified production systems for specialty chemicals

    Typical usage ratio

    • 5–12% by mass in pigment condensation reactions, adjusted for target chroma and light stability in final application.

    Downstream process integration

    • Charged during initial pigment condensation reaction step.
    • Purified and milled before dispersion in binder systems.
    • Undergoes additional screening for color fastness and migration control before shipment.

    Final product types

    • Security and anti-counterfeit printing inks
    • Specialty fluorescent pigment dispersions
    • Functional coatings for industrial substrates
    Free Quote

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    Certification & Compliance
    More Introduction

    Understanding 2,4-Diamino-6-(Hydroxymethyl)Pteridine: A Manufacturer’s Perspective

    Meet 2,4-Diamino-6-(Hydroxymethyl)Pteridine

    As a chemical manufacturer, we see each intermediate in our plant as a unique challenge. 2,4-Diamino-6-(Hydroxymethyl)Pteridine stands out among specialty pteridine derivatives for its consistent performance in synthesis routes demanding both purity and reactivity. For chemists engaged in the life sciences, especially those concerned with folate biochemistry or custom API development, this compound often becomes a linchpin. Its molecular model, featuring a hydroxymethyl group at the 6-position, gives it distinctive reactivity compared to plain 2,4-diaminopteridines.

    Model Characteristics and Physical Properties

    Our production lines push for clarity and reproducibility in every batch. The molecule offers a pteridine core with diamino groups at positions 2 and 4, alongside a hydroxymethyl handle at position 6. The off-white to pale yellow crystalline appearance tells an experienced technician about the minimal contamination during crystallization. Batches finish up with a solubility profile distinct from closely related analogs, not just in water, but also under varying pH conditions. We make sure the end product achieves high assay values—something we routinely track via HPLC and NMR. Our spectroscopic data have helped research customers confirm structure, especially where tight specifications on end-use are involved.

    Synthesis Insights and Technical Merit

    Unlike more common diamino pteridines, the presence of the hydroxymethyl functional group influences both synthetic versatility and downstream processing. Our team sees this difference every time purification steps produce higher yields and cleaner filtrate. More specifically, the extra substitution at the 6-position allows for smooth modification in the hands of downstream chemists, such as derivatization or coupling reactions relevant for antifolate or enzyme inhibitor development.

    Our technical team often fields requests from process chemists curious about scalability. The extra group on the ring backbone doesn’t just tweak reactivity in flask-scale experiments, it carries through to pilot runs. Feedback from scale-up lines shows that temperature-sensitive steps handle better thanks to improved solubility and less by-product formation.

    Applications That Stress Consistency

    Pharmaceutical teams ask for this product due to its importance in complex folate antagonist syntheses. Academic groups, particularly those studying enzyme mechanisms in microbiology or pursuing cellular pathophysiology models, find value in the structure’s role as a scaffold. We listen to feedback from both sides—industrial customers monitoring impurity profiles downstream, and university labs focused on reproducibility. Both stress that a reliable supply of high-grade 2,4-diamino-6-(hydroxymethyl)pteridine can make the difference between a lengthy troubleshooting process or a straightforward experimental run.

    Years of meeting regulatory and research standards push us to refine handling from raw inputs to final packaging. Unlike high-volume commodity chemicals, this molecule draws attention to trace contaminants and minor variations between lots. That’s why we work closely with our sourcing team to ensure only select starting materials make their way into the reactors. After all, volatile impurity carryover can mean failed QCs at the very end of a long synthesis pathway.

    Comparing to Other Pteridine Compounds

    Many buyers start with standard 2,4-diaminopteridine, trying to economize on up-front costs. Through technical support calls, our staff hears about bottlenecks later in the process; sometimes reactivity lags, or an extra protecting group step becomes unavoidable. The hydroxymethyl mod gives users a more direct route to target molecules where precise substitution is needed, shaving hours off a project or sidestepping challenging conditions that less-forgiving analogs demand.

    Researchers who have switched to this compound cite reduced amounts of by-products and cleaner final products—meaning less downstream processing or purification headaches. In contrast, pteridine analogs lacking the hydroxymethyl substituent often fall short in multi-step syntheses, with side reactions eating into material yield or introducing impurities tough to purge completely.

    Addressing Process Challenges Head-On

    Manufacturing a specialty intermediate like this one comes with its own learning curve. It doesn’t clock in as a bulk commodity where slight process fluctuations go unnoticed. Every step—from reagent addition to crystallization temperature—demands careful oversight. Efforts to optimize waste minimization and streamline process water usage find practical implementation at each campaign.

    At times, even minor adjustments to stirring speed or pH during final work-up shift the appearance or stability of the final solid. Our QA team works in tandem with production to flag inconsistencies right away, using continuous data logging and feedback loops between lab and plant. Shared goals between departments keep the process robust and output predictable, a necessity when downstream R&D programs depend on reliable material.

    Quality and Analytical Verification

    No matter the end use, confirmation of both identity and purity keeps customers coming back. Our experience guides the use of multidimensional HPLC runs alongside elemental analysis and spectroscopic fingerprinting. We have learned the fine points of resolving pteridine peak clusters and determining the best wavelength settings for consistent integration.

    We pay close attention to stability data under normal storage conditions—sampling in intervals, checking for color shift or formation of unknown degradants. This diligence finds roots in early days of troubleshooting, where on rare occasions, a poorly capped batch would show degradation, resulting in off-spec supply or loss of valuable product. These experiences shape current storage and packaging practices, with desiccation and light protection forming standard operating procedures.

    Listening to User Experience: Academic and Industry Voices

    End-users’ feedback shapes every manufacturing cycle. Large pharmaceutical customers report time savings on route selection, notably when attaching folate analogs or preparing key intermediates under CGMP. Their comments motivate us to keep every documentation trail clean and every internal process auditable by external parties.

    Meanwhile, academic teams, often with tighter budgets and different priorities, emphasize batch-to-batch consistency. Some use the compound in enzymology, tracking substrate-channeling or reading out kinetic parameters in a range of buffers. Others probe for cellular uptake, where small impurities can mean noisy backgrounds and confounding data, especially in fluorescence-based assays.

    Environmental Considerations in Production

    As a manufacturer rooted in the chemical industry’s reality, we face mandates to limit the environmental load. The process behind 2,4-diamino-6-(hydroxymethyl)pteridine succeeds best with targeted solvent recycling and reaction path management that sidesteps highly toxic intermediates or explosive solvent combinations. Our engineers devote time to minimizing volatile waste as much as practical by integrating recovery units and closed-loop systems, reducing exposure risks for the operational crew, and cutting down vent-stack output.

    We've seen regulatory expectations ramp up year by year. We track wastewater with precision, seeking to meet evolving benchmarks on heavy metals, organic content, and bioburden. By coordinating upgrades before inspections, we turn compliance into part of the workflow—not an outside imposition, but a badge of quality for responsible chemical stewardship.

    Worker Safety and Production Health

    Those who have handled pteridine intermediates know the importance of chemical hygiene. Every operator in our plant follows protocols centered on respiratory and skin protection, not only out of necessity but out of respect for long-term workplace health. Periodic training sessions reinforce emergency handling for spills. Years on the line have taught us that even low-toxicity compounds require vigilance to avoid cumulative exposure or cross-contamination.

    Supervisors invest time in reviewing near-miss incidents and reevaluating PPE guidelines. These checks and balances draw from real-life lessons—each minor event translates into a reminder to double-check goggle seals and ventilation settings on lab-scale reactors. This practical risk management culture ultimately finds its way into every drum and bottle we prepare for shipment, ensuring our responsibility doesn’t end at the loading dock.

    Shipping Concerns and Global Reach

    Delivering sensitive compounds worldwide isn’t just a matter of putting a label on a container. This molecule, although stable when kept dry and cool, fares poorly in shipments exposed to excess heat or fluctuating humidity. We engage directly with carriers and logistics providers, emphasizing controlled environments and short dwell times at transfer points. Traceability remains a top concern; complete shipping documentation aligns with our own batch tracking systems, ensuring that a customer in a distant lab receives exactly what they expect.

    Experience reveals that remote deliveries occasionally challenge this process. Customs delays, extreme weather, or mishandling en route can turn a routine shipment into a customer service issue. Our shipping coordinators now build contingencies and backup notifications into each order, offering advanced notice and corrective shipments if issues develop.

    Supporting Problem-Solving for the End User

    Much of our engagement with customers extends beyond a single transaction. Technical support doesn’t just resolve complaints—it closes the loop between manufacturing reality and experimental ambition. Teams working with advanced synthesis strategies sometimes approach us with specialized requests, needing variant forms or custom packaging. Our technical partners deliver feasibility studies and sample options where possible, built upon firsthand production knowledge rather than sales scripts.

    Not all questions revolve around the compound’s chemistry. Many times, requests pertain to certificate details, origin of raw materials, or long-term storage recommendations—especially important for long-running experiments or programs dependent on extended material stability. We cheerfully provide these details, drawing from our quality archives and decades of operational notes.

    Sustaining Continuous Improvement

    If there is one certainty in specialty manufacturing, it’s the need to evolve. Customer input, regulatory trends, and internal audits all shape the next chemistries and improvements we pursue. Adjustments to reaction efficiency, solvent management, and even automation get reviewed as each campaign wraps up. Our R&D group pushes the envelope, balancing the theoretical wish lists of synthesis chemists with the practical constraints of safe, predictable, large-scale output.

    Process improvement has never been about one breakthrough. Small, incremental upgrades, such as fine-tuned agitation cycles or newly sourced raw materials, often outpace dramatic changes in impact over the long term. Regular exchange with industrial peers—through consortiums or supply chain audits—keeps us honest about how we benchmark performance and manage risk.

    Fostering Trust in Scientific Supply Chains

    Trust builds slowly in chemical manufacturing. We know every customer counts on more than paperwork to judge quality; they rely on our reputation as a steady provider. Our track record comes from a commitment to transparency, an open door on production issues, and fast corrective action when a rare glitch occurs. Much of this stems from hands-on manufacturing: seeing the plant, knowing the batch, troubleshooting missteps on the floor. This realism shapes our interactions and keeps us grounded in the science and practicalities of large-scale production.

    2,4-Diamino-6-(Hydroxymethyl)Pteridine remains a specialty product—no two campaigns run quite the same way, and no set of user requirements follows a simple standard. Through honesty about our processes and a willingness to share both successes and setbacks, we continue to supply a chemical valued not just for its structure but for the reliability behind its manufacture. This approach creates lasting partnerships with our clients, and in the world of specialty chemicals, that trust represents the best endorsement of all.