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1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine

    • Product Name 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine
    • Alias HHPP
    • Einecs 212-013-9
    • 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

    364900

    Iupac Name 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine
    Cas Number 506-99-2
    Molecular Formula C6H12N4
    Molecular Weight 140.19 g/mol
    Appearance White solid
    Melting Point 149-151°C
    Boiling Point 282°C at 760 mmHg
    Solubility In Water Soluble
    Density 1.08 g/cm³
    Ec Number 208-060-9
    Pubchem Cid 12683
    Smiles C1CNCCN2C1NCCN2
    Inchi InChI=1S/C6H12N4/c1-3-9-5-7-2-4-10(1)8-6-9/h1-8H2
    Flash Point 125°C
    Refractive Index 1.620

    As an accredited 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque plastic bottle labeled "1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine, 100 grams, for laboratory use only."
    Shipping 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine is shipped in tightly sealed containers under cool, dry conditions, protected from moisture and direct sunlight. All relevant safety regulations and guidelines for chemical handling and transport are followed, including proper labeling and documentation to ensure safe delivery to the destination.
    Storage Store 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-a]pyrimidine in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Ensure proper labeling and keep away from sources of ignition. Store in accordance with local, state, and federal regulations.
    Application of 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine

    Applications of 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine in Industrial Manufacturing

    As a manufacturer specializing in advanced nitrogen-containing heterocycles, we supply 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine for well-established industrial pathways with proven, large-scale commercial deployment. This material’s chemical structure and reactivity profile make it a critical synthetic intermediate in several high-value production channels, where it supports both product performance gains and compliance with international quality systems.

    1. Agrochemical Intermediate Synthesis

    Agrochemical producers utilize this compound as a key building block in the synthesis of select triazine and pyrimidine herbicides. Its integration into the reaction pathway enhances molecular complexity and supports high-yield coupling reactions. Manufacturers optimize dosage based on the specific target molecule, with the compound generally introduced post-amidation via closed reactor processing. End products include advanced pre-emergent herbicides meeting stringent residue limits and crop protection efficacy thresholds for export-regulated markets.

    Industry compliance standards

    • FAO/WHO Maximum Residue Limits (MRLs) for agrochemicals
    • European Union Regulation (EC) No 1107/2009 for plant protection products
    • ISO 9001:2015 certified quality management systems
    • China National Standard GB 2763-2023 for pesticide residues

    Typical usage ratio

    • 5–15% w/w in active ingredient synthesis, with optimization based on final herbicide structure and yield targets

    Downstream process integration

    • Added as cyclization partner at intermediate stage after core ring construction, under anhydrous and inert conditions
    • Reaction proceeds within jacketed glass-lined reactors, often with phase-transfer catalysts

    Final product types

    • Pre-emergent herbicides (e.g., triazine-type granular and liquid formulations)
    • Selective broadleaf weed control agents
    • Herbicide technical grade bulk for formulation houses

    2. Pharmaceutical API Intermediate

    Regional and international pharmaceutical manufacturers source this material as a protected aminal intermediate in the synthesis of anti-viral, anti-tumor, and diuretic active pharmaceutical ingredients (APIs). It functions as a nucleophilic fragment in multi-step syntheses, enabling site-specific nitrogen introduction onto larger molecular scaffolds. Downstream producers calibrate concentrations according to the stoichiometric requirements of their specific API routes, always aligning with validated GMP manufacturing flows.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and Ph. Eur. monographs for APIs and intermediates
    • Chinese Pharmacopoeia (ChP) Edition 2025
    • FDA 21 CFR Part 211 (for pharmaceutical finished product facilities)

    Typical usage ratio

    • 0.8–3.5 molar equivalents, precisely adjusted per target API coupling reaction and expected conversion efficiency

    Downstream process integration

    • Introduced during nitrogen heterocycle assembly, often via refluxed solution in polar aprotic solvents
    • Isolated by crystallization or liquid–liquid extraction, supporting clean downstream API purification

    Final product types

    • Antiviral drug intermediates (purine and pyrimidine analogs)
    • Pyrimidine-based diuretics and cytostatic agents
    • Specialty APIs for export registration dossiers

    3. Corrosion Inhibitor Additive Manufacture

    Industrial producers of water-soluble and oilfield corrosion inhibitor blends employ this compound as a core nitrogenous scaffold to impart strong metal passivation performance in hostile environments. The compound’s cyclic structure facilitates effective chelation and film formation on ferrous surfaces. It enters inhibitor compounding facilities as a batch additive, with dosing finely tuned to local water chemistry or crude processing parameters, ensuring compliance with occupational and environmental norms for downstream use.

    Industry compliance standards

    • API RP 682 for mechanical seal system protection fluids
    • REACH Annex XVII and CLP Regulation for inhibitor component use in Europe
    • OSHA 29 CFR 1910.1200 (for safe handling and labeling)
    • Q/SH 020.004 (China Petroleum & Chemical Industry Association technical norms)

    Typical usage ratio

    • 1–7% weight fraction of finished inhibitor concentrate, tuned based on brine and temperature profile

    Downstream process integration

    • Blended post-neutralization into aqueous or oil-soluble phase in stainless-steel reactor trains
    • Optionally reacted further to form quaternized derivatives for enhanced substrate adhesion

    Final product types

    • Pipeline corrosion inhibitor packages for upstream oil production
    • Closed-loop cooling water treatment chemicals
    • Boiler water passivation formulas

    4. Rubber Accelerator Precursor

    Producers serving the rubber and elastomer industry adopt this molecule in the synthesis of select non-thiocarbamate accelerator families. Specifically, it acts as an intermediate ring component that introduces controlled activation potential during vulcanization. Its deployment in compounding facilities focuses on consistent batch quality, with loading formulated to balance cure time and finished goods resilience, verified through bench and production-scale mixing.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in chemical synthesis
    • ASTM D4678-14 for rubber chemical accelerator efficacy
    • EU REACH SVHC compliance (for rubber additives)
    • Japanese Industrial Standards (JIS K 6251-7) for elastomer additives

    Typical usage ratio

    • 2–6% by weight of accelerator pre-blend, modified per elastomer base and vulcanization kinetics

    Downstream process integration

    • Introduced during pre-acceleration stage, blended in ribbon-blender or Banbury mixer with primary accelerator and fillers
    • Subjected to quality testing for activity and residue profile before main compounding

    Final product types

    • Fast-curing rubber accelerators
    • Technical compounds for tire sidewalls
    • Anti-flex cracking industrial elastomers

    5. Specialty Resin Modifier Synthesis

    Producers of functionalized epoxy and phenolic resins introduce this heterocycle in the formation of nitrogen-modified polymer chains. Its application centers on adjusting cross-link density and curability in high-performance coatings for electronics and aerospace uses. The compound enters resin reactors at controlled intervals, its proportion adjusted according to targeted viscosity, glass transition temperature, and downstream regulatory testing for low-emission compliance.

    Industry compliance standards

    • RoHS Directive 2011/65/EU (for electronics coatings)
    • IPC-4101B for high-grade laminate materials
    • UL 94 Flame Retardancy rating for polymers
    • GB/T 22397-2018 low-VOC emission limits for coatings

    Typical usage ratio

    • 0.5–2.8% of total resin mass, varied by final film requirements and process reactivity

    Downstream process integration

    • Metered addition into prepolymer batch during main stage polymerization under vacuum or nitrogen blanket
    • Chain extension or end-capping reaction steps yield polymer with designed functional group density

    Final product types

    • Electronics-grade insulating varnishes
    • High-build coatings for printed circuit boards (PCBs)
    • Advanced flame-retardant laminates
    Free Quote

    Competitive 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    Understanding 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine: Insights From the Manufacturer’s Floor

    Every so often, a molecule comes to occupy a very particular role across fine chemical systems—one of those is 1,3,4,6,7,8-Hexahydro-2H-Pyrimido[1,2-A]Pyrimidine. In our years developing and producing this material, we have seen its purpose shift with the demand for tailored performance in agricultural, pharmaceutical, and specialty chemistry applications. Our days involve more than reactors, columns, and analytics; they also involve daily decisions about quality, purity, and how the smallest process parameter change echoes through our customers’ work. Our experience with this compound can help you see why it stands out from the crowd.

    Building a Reliable Product: From Synthesis to the Drum

    The process behind making 1,3,4,6,7,8-Hexahydro-2H-pyrimido[1,2-a]pyrimidine is neither short nor effortless. Our reaction steps depend on tight control—temperature holds, pH control, and precise dosing. We harvest years of trial runs, not just from bench chemists but from the crew who monitor each batch in production. As the scale climbs, issues like trace by-products, residual solvents, and moisture control stop being theoretical worries and become real obstacles. Getting a clean product means not rushing the vacuum stripping, checking analytical results from each drum, and never assuming last week’s run will guarantee this week’s results.

    Customers usually want this compound in standard crystalline form, not because it’s easiest to transport, but for good reason—crystallinity stores well, and the substance flows easily during downstream use. Typical orders run from 25 kg pails up to several metric tons per year, serving everything from research pilots to continuous plant runs. To us on the production floor, this means both flexibility in batch sizing and a constant attention to reproducibility. We’ve refined a process using a dedicated set of reactors, avoiding cross-contamination and batch-to-batch drift, matching analytical purity targets that suit even the stiffest user specifications.

    What Sets This Compound Apart

    Some clients ask if there’s a practical difference between 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine and simple cyclic ureas or substituted triazines. Long experience tells us the differences are real. Structurally, the compound puts together two fused pyrimidine rings in a hexahydro conformation. This unlocked scaffold supports a unique profile of chemical reactivity. Lab results and large-scale synthesis both reveal how the strong nucleophilicity and basicity manifest when the molecule is used as either an intermediate or an end-use component.

    For example, one common use is in specialty pesticide intermediates. Unlike linear diamines or simple amines, the ring system delivers higher stability under many formulation pressures. We often see research customers exploring its reactivity for custom catalysts or as a ligand—applications where non-cyclic alternatives would struggle with hydrolysis or lack persistence in solution. Manufacturers who work with us often note improved downstream yields because the purity and consistency of our product avoid introducing side-products into complex syntheses. These benefits don’t show up in a certificate of analysis but make all the difference in a pilot or manufacturing line.

    The Value of Consistency and Process Know-How

    Reliable supply draws more interest now than it used to. Over the years, we’ve seen plenty of stories where a minor process change at a supplier ruins a customer’s batch or forces new validation cycles. Keeping parameters steady isn’t just about copying a recipe—it’s about seeing how little upsets, like a filter running slow or a solvent tank running low, might stray final quality.

    Several users, especially in regulated industries, raise questions about reproducibility. Our operational teams work out how to prevent contamination, making sure drum cleaning meets tough internal standards, and adjusting drying cycles based on weather and humidity. Every time we shift from a lab-scale run to a 1,000-liter batch, our operators, not just supervisors, watch for shifts in melting point, color, or fine particulate formation.

    Over the past decade, we’ve improved our drying and handling procedures with concrete, on-the-floor feedback. Too rapid a vacuum pull led to caking; too slow, and solvent residues crept up. These are observations gathered from handling tons of material, not just from reading textbooks. We know the cost of skipping steps: a customer notices increased impurities or asks for samples from a different drum.

    Insights Into Applications: What Our Customers Create

    We see the biggest draw in industries aiming for robust, specialty performance. Researchers in agrochemical synthesis prize the molecule for forming stable, high-yield intermediates. Several pharma teams mention using it in routes to build ring-fused actives or as a masking group for more reactive amines. The ring system creates hydrogen-bonding patterns and electronic effects simple monoamines can’t match. As a manufacturing team, we observe how each end-user cares about the trace footprint of side-products and how easy it is to handle bulk deliveries.

    On the catalytic front, some laboratories push the molecule in exploratory projects—especially as a ligand or base in transition metal chemistry. In those settings, our clients need a product free from trace sulfur, chloride, and water, all of which we deal with at the process control level. Some customers tried substituting basic heterocycles but often came back, reporting that only 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine delivered their required reactivity and shelf stability.

    How Purity and Handling Shape Real-World Results

    It’s easy to treat chemical purity as an abstract threshold, but in the plant, it’s concrete. Products with just a fraction more residual starting material or moisture invite caking, color change, or poor solubility in downstream solvents. Over the years, we noticed orders from regions with high humidity preferred custom drum liners, while pharma plants consistently requested zero-residue packaging and explicit GC and HPLC trace analysis before shipment. For these users, an off-spec batch doesn’t just mean a rejected lot—it might mean halting a campaign and missing a market window.

    Our response comes directly from the shop floor: maintaining sealed transfer lines, frequent on-site calibrations of analytical tools, and thorough operator training to reduce batch-to-batch variation. Repetition and discipline matter more than chasing new gadgets. While some labs might tolerate one-off spec bumps, global manufacturers count on repeatability. You won’t find this written in a glossy brochure, but our workers know the impact of letting a small shortcut slip by. Tracking process variables—moisture, residual solvent, purity, and bulk density—helps us keep repeat clients satisfied without surprises.

    Avoiding Issues Seen With Other Compounds

    Some clients try to run processes using more accessible analogues—cyclic ureas or unsubstituted amines—only to find shorter shelf lives, lower reactivity, or difficulty forming consistent solutions. Over time, we’ve compiled feedback on why these analogues fall short. Simple amines lack the extra ring strain and electron distribution that give 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine an edge in forming robust complexes or durable intermediates. Colleagues in materials chemistry report better crystal formation and improved shelf stability compared to open-chain alternatives.

    Other frequent issues include unexpected yellowing or increased viscosity, especially in bulk storage. We found this links back to trace oxygen ingress or incomplete de-gassing at filling. Those lessons shaped our routines: every operator learns to work with oxygen meters and nitrogen flushes from their first weeks on the job. Maintaining color stability, particle size, and solubility means regular in-process checks, not just at shipping but as the drums move across the warehouse floor. These routines pay back with lower rejection rates and less hassle for our customers’ logistics teams.

    Feedback Loops: Listening to Customers, Improving the Process

    The learning curve in this business never flattens out. Over the years, we adopted small but crucial changes after customer visits and audit results. Sometimes, buyers flagged surface issues—clumped product, inconsistent lot labels, or slow sample responses. Walking clients through the plant, they spot something as simple as a new hose connection or a packaging method that aligns with their own factory workflow. There’s no paperwork as valuable as seeing a customer’s process in action and hearing exactly where failures cost them time or yield.

    On these tours, we answer questions about how we segregate batches, what sample retention protocols we follow, and how often we train staff on critical points like nitrogen purges and line cleaning. Feedback from their side directly influences our next improvement—upgraded drum liners, better humidity management, routine double-checks before final labeling. Our workflow thrives when it learns from plant-floor, not just office-level, insights.

    Transparent Communication—Not Just Sales Pitches

    Transparency matters more today, as inward supply chains run tighter. Calls don’t just come from purchasing managers, but also from QC analysts and R&D chemists, directly invested in how our production cycles mesh with their project timelines. The toughest questions usually revolve around impurity profile, shelf life, and how we can ramp up volume without diluting quality.

    We remain open about grade differences too—for clients needing higher-purity or special handling, we share not just the numbers but the concrete steps: validated drying rooms, dedicated filling lines, or analytical traces mapped against their own reference standards. This kind of mutual visibility promotes lasting partnerships and sets the bar higher for internal training and documentation. Instead of relying on templated claims, we point out real adjustments, tracking raw material sources and timing batch releases to match just-in-time deliveries.

    Supply Chain Headaches and How We Curb Them

    Long experience in specialty chemicals teaches hard lessons about logistics. Delayed raw materials, inconsistent drum supply, or hitches at ports—all these cut through plans. We built flexibility into our storage and loading systems, supporting orders that swing between small-lot R&D demand and ton-scale production. Our team monitors raw stock not just for cost, but for upstream reliability, keeping backup suppliers vetted and rotating through trial deliveries.

    For overseas clients, packing standards can differ. Some want vacuum-sealed liners; others prefer reusable drums. Regional differences in transport humidity or heat stress prompt us to re-evaluate not just our containers, but our in-process control and documentation. Each client’s delivery requirement forces us to rethink how to minimize risk and incident, from securing containers against sea shocks to monitoring for condensation or shifting bulk inside drums. We continue tweaking our routines based on shipping reports and customer claims, aiming for a shipment record we can stand behind.

    Comparing to the Market—What We See, What We Hear

    On the supply side, markets sometimes offer competing products at lower prices or with faster promises. Years of feedback confirm that moving to off-brand or underprocessed alternatives often means more repair than anticipated: increased off-spec batches or regulatory headaches for clients who trace every impurity. For production runs where purity, shelf life, and reactivity matter, less rigorous sources quickly show their limits.

    We have watched competitors claim easier synthesis or simpler storage, but real-world trials bring back the same core insight—getting the process right pays off more than slashing initial costs. Tight purity specs and reliable batches matter more than headline numbers. To many research and manufacturing partners, our edge comes from a blend of technical acumen, steady QA routines, and the willingness to throw time and people at problems until they’re solved.

    Future Directions: What We’re Watching

    Chemical manufacturing stays in flux: new environmental controls, cleaner chemistries, and pressure to deliver ever-tighter spec compounds (all while trimming carbon footprint and cost). Our focus tracks not just the rules on paper, but the day-to-day shifts in the field. As regulatory pressures intensify, we adapt with process audits, carbon accounting, and solvent recovery upgrades.

    Recent research, especially in custom synthesis for pharma and new material areas, points to growing need for ring-fused, nitrogen-rich heterocycles like 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine. What changes on our end is the tighter control of impurity profiles, moisture management, and data-driven parameter checks on every lot. Our investment follows those trends—automated QC, analytics that link each batch to both input and process steps, and ongoing staff education to prevent small errors from snowballing.

    Straight Talk From the Manufacturing Lines

    In making 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]pyrimidine, the realities of chemical production go far beyond molecules and reaction vessels. Reproducibility, reliability, and practical partnership drive returns for everyone involved. We watch the details because customers’ work hinges on every drum being just as intended. Partnering with users, listening to their plant-floor headaches, and sharing real-world lessons shapes both our process and their results. The ultimate advantage comes not from paperwork or slogans, but from grounded daily work—knowing the pitfalls, circling back to correct them, and refusing to accept “almost right” as good enough.