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HS Code |
178105 |
| Chemical Name | 1-Formylhomopiperazine |
| Molecular Formula | C6H12N2O |
| Molecular Weight | 128.17 g/mol |
| Cas Number | 5978-45-6 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 113-114°C at 20 mmHg |
| Density | 1.075 g/cm³ |
| Solubility | Soluble in water and organic solvents |
| Purity | Typically ≥ 97% |
| Smiles | O=CN1CCCCCN1 |
| Melting Point | -7°C |
| Storage Temperature | 2-8°C |
As an accredited 1-Formylhomopiperazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1-Formylhomopiperazine, 25g, is supplied in a tightly sealed amber glass bottle with a tamper-evident cap and clear labeling. |
| Shipping | 1-Formylhomopiperazine is shipped in tightly sealed containers to prevent moisture and contamination. Packaging complies with chemical safety regulations, ensuring safe transportation. The product is labeled with hazard information and shipped under ambient or recommended temperature conditions. Shipping documentation, including Safety Data Sheets (SDS), accompanies all consignments for proper handling and emergency procedures. |
| Storage | 1-Formylhomopiperazine should be stored in a tightly sealed container, away from direct sunlight and moisture. Keep it in a cool, dry, and well-ventilated area, ideally at a temperature between 2–8°C (refrigerated). Avoid sources of ignition and incompatible substances such as strong oxidizing agents. Ensure appropriate labeling and restrict access to trained personnel only. |
Applications of 1-Formylhomopiperazine in Industrial Manufacturing1-Formylhomopiperazine offers valuable functionality in several advanced chemical manufacturing sectors. Our facility produces this compound under strict quality controls to ensure reliable integration into pharmaceutical intermediates, fine chemical synthesis, polymer modification, and agrochemical actives. Below, we detail verified downstream use cases, process points, end products, and relevant industrial compliance guidelines for each application. 1. Pharmaceutical Intermediate SynthesisManufacturers employ 1-Formylhomopiperazine as a key intermediate for the synthesis of active pharmaceutical ingredients (APIs) and investigational drug candidates. It participates in regioselective N-formylation, affording control over further functionalization of piperazine-based scaffolds during multi-stage API development. Facilities using this intermediate comply with strict traceability and batch-testing procedures, particularly when scaling for direct or indirect use in human therapeutics. Pharmacopoeia monographs, validated impurity profiles, and GMP-compliant documentation are mandatory at all stages. The role of the intermediate affects downstream reactivity, especially across hydrogenation, alkylation, or acylation steps. Final pharmaceutical products comprise small-molecule APIs targeting CNS, cardiovascular, or anti-infective therapies. Industry compliance standards
Typical usage ratio
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2. Fine Chemical Building Blocks for Specialty SynthesisChemical process companies use 1-Formylhomopiperazine as a protected amine reagent for the targeted construction of heterocyclic compounds and specialty building blocks. This material is valued in fine chemical industries requiring selective N-formylation to prepare imidazolium, triazole, or macrocyclic intermediates. Batch records include identity, purity, and residual solvent documentation. Regulatory oversight often comes from internal quality management frameworks instead of government registries, but international distribution partners may request REACH compliance. Process chemists integrate this material during the assembly of complex heterocyclic cores for electronics, catalysts, or specialty ligands. Final goods vary from advanced ligands to light-absorbing units for optoelectronics. Industry compliance standards
Typical usage ratio
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3. Polymer Modification and CrosslinkingProducers of specialty polymers and crosslinked materials employ 1-Formylhomopiperazine as a reactive modifier during the formation of high-performance polymers. Formyl groups serve as temporary protecting moieties or as crosslinking activators for subsequent reaction with isocyanates, epoxides, or acid chlorides. Control of addition rate, mixing sequence, and temperature profiles ensures uniform functionalization across polymer chains. Industrial QC includes FTIR verification and GPC tracking for molecular weight distribution. Final applications favor high-thermal-resistance and specialty engineering plastics, especially in electronics encapsulation and performance coatings. Industry compliance standards
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4. Agrochemical Active Ingredient SynthesisAgrochemical manufacturing facilities utilize 1-Formylhomopiperazine during stepwise construction of novel crop protection molecules. This compound introduces a formyl group at a controlled position, which can be selectively removed or elaborated during further transformations, minimizing side products. Integration occurs after core scaffold assembly and before introduction of functionalized side chains. Producers must comply with regulations governing traceability, downstream effluent controls, and toxicological assessments. End-use products typically include herbicide intermediates, fungicide scaffolds, and insecticidal actives, later formulated into market-ready agrochemical products. Industry compliance standards
Typical usage ratio
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Competitive 1-Formylhomopiperazine prices that fit your budget—flexible terms and customized quotes for every order.
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Since we started making intermediates for pharmaceutical laboratories and fine chemical industries, our goal has stayed the same: develop and supply compounds that push the limits on efficiency, process safety, and downstream value. Over a decade ago, we added 1-Formylhomopiperazine to our production portfolio. It didn’t take long to realize its synthetic flexibility brings serious advantages for scale-up chemists and researchers grappling with increasingly tough development timelines. In our daily work, we’ve seen the importance of quality and reliability from first concepts through pilot runs and all the way to full orders.
Production of 1-Formylhomopiperazine, with its unique six-membered ring and formyl moiety at the nitrogen, introduces a new dimension into structural design for chemical developers. From a manufacturing viewpoint, achieving the correct purity and minimizing side-products—the sort that complicate downstream chemistry—requires close control from raw material sourcing to finished product testing. Over the years, we’ve honed our process to minimize route-based contamination and ensure low levels of volatile impurities so that clients avoid headache during reactions or purification steps.
Chemical buying teams have a flood of choices. What stands out with 1-Formylhomopiperazine compared to similar secondary amines or even lower homologues is how the extended methylene backbone changes both reactivity and handling characteristics. For example, our own teams have noticed in bench trials that it often participates in cyclizations and N-substitutions that leave ordinary piperazine or morpholine stuck. The extra carbon alters solubility, boosts reactivity in some coupling steps, and still allows for predictable formyl removal in acidic or reductive cleavage settings when needed downstream—qualities that make a big difference when designing synthesis routes for new APIs or protected cores.
Our standard 1-Formylhomopiperazine comes as a pale liquid or low-melting solid, with assay values holding at over 98 % by modern HPLC. As a company running multipurpose synthesis, we get to see how small changes in process—water content, feed rates, or even reagent grade—play out at pilot and commercial scales. If the moisture climbs even by half a percent, downstream purification quickly gets tricky, especially when a client needs a dry, free-flowing intermediate for air-sensitive applications. Years of feedback have guided us towards rigorous in-process control points, using Karl Fischer titration and GC scans tailored to the product’s reactivity profile.
There are quirks, too. 1-Formylhomopiperazine should be stored in tightly sealed containers and remains stable in standard warehouse settings, but over many batches we learned to avoid copper or brass contact surfaces. Trace catalysis from these metals led to minor color formation and subtle breakdown in samples left for months—a lesson drawn from direct experience, with lab logs to prove it. We share such details proactively with development partners to help them cut surprises from their own scale-up efforts.
Pharma process teams and discovery groups might use this intermediate for various purposes, from building substituted piperazines needed in CNS-active leads, to constructing ring-expanded analogs for cardiovascular research, to more established intermediates like protected fragments in anti-infective projects or as building blocks for PEGylation efforts. We have real-world feedback from clients who saw more efficient alkylation or condensation reactions after swapping a shorter amine for 1-Formylhomopiperazine, especially where steric effects or slow nucleophilic steps slowed their runs.
Contract manufacturers working on advanced intermediates often look for a clean slate: low color, narrow impurity profile, and consistent physical form lot to lot. Long before the market moved in that direction, we reworked our crystallization and distillation techniques so that researchers could weigh and blend reaction charges without dealing with sticky, hygroscopic residues. Small issues—like crystal size changes or cold-flowing liquids—can bottleneck sampling and downstream handling. Our operators, some with twenty years operating glass-lined vessels, know this first-hand. It becomes clear that keeping batch temperatures controlled very closely eliminates out-of-spec forms or unpredictable melting ranges.
It’s tempting in chemistry to see functionalized piperazines and secondary amines as interchangeable. On paper, a direct substitution seems logical—swap a ring, swap a substituent, and expect the same results. We see the reality when a process falters or a researcher calls with questions about unpredictable reactivity. In large parts of medicinal chemistry, standard piperazine derivatives have dominated scaffolds, but 1-Formylhomopiperazine’s longer ring introduces new reactivity, both at the nitrogen and across the backbone carbons. Our team observed that certain alkylating agents react faster and with cleaner profiles; others, especially weakly activating acyl groups, need milder conditions to avoid decomposition.
Those differences might sound subtle, yet they can make or break tight deadlines. We helped a mid-size pharma client troubleshoot after a campaign failed with shorter-ring intermediates. Their key coupling stalled due to side reactions only mitigated after switching to our 1-Formylhomopiperazine, which delivered exceptional selectivity and eliminated the need for extra purification runs. Our records show they increased yield, slashed process time, and hit project milestones that had slipped for months.
Compared to straightforward diamines, the formyl group also adds value for protection strategies. Direct N-formylation of homopiperazine using our preferred methods produces a stable intermediate—resistant to ambient hydrolysis, yet de-protectable under customizable acidic or catalytic hydrogenation conditions. Teams looking to protect against overreaction during multi-step synthesis appreciate how it lets them advance to late-stage elaborations without rework due to premature deprotection. In short, the structure lets chemists decide where the chemistry happens, not the compound.
Manufacturing 1-Formylhomopiperazine at consistent quality, batch after batch, requires more than a synthesis protocol. Upstream, we rigorously vet every supplier for precursor homopiperazine and test for residual metals and trace non-volatiles. We learned the hard way that early batches can hide issues invisible to typical surface tests—color changes, off-odors, subtle pH drift in solution. These may not wreck a bench procedure, but they scale up fast under production conditions.
Every year, we invest in improving process analytical support. Advanced spectroscopy, trace impurity mapping, automated gravimetric assays—these aren’t buzzwords. They shape the timing and reliability of your orders, especially if your project has tight deadlines. If you need custom options—such as specific water content, defined impurity limits, or adaptations for regulatory filings—we keep technical support at hand, not in a distant office. We’ve shipped customized variants for global clinical projects where batch traceability, analytical documentation, and approval cycles have to align perfectly. There’s simply no substitute for experience gained from supporting real-world supply chains.
Industries talk a lot about sustainable chemistry, but for us it’s a matter of responsibility on the plant floor. Our process relies on closed-system charging and dedicated scrubbers for emission reduction, both driven by lessons learned on site, not hoped-for goals. Every run, our staff double-checks that formyl intermediates don’t build up in waste streams or onsite storage. We monitor exotherms, vent flows, and loadings based on actual operator feedback. Shifting from manual to semi-automated controls cut time and improved operator safety without compromising cost structure.
We worked alongside logistics planners to trim packaging waste for this product. After a handful of spills from secondary amine leaks in legacy containers, our teams engineered double-seal drums rated for long-haul shipment—details that came from freight data, not catalog pages. Downstream, we help clients design safer transfer or blending steps, offering guidance grounded in actual plant hazards and transport records.
The market for protected amines keeps shifting, and regulatory expectations tighten every year. Our role as actual producers—not just marketers or agents—forces us to anticipate documentation needs as well as batch reproducibility. Each batch undergoes third-party analysis where appropriate, with sample archiving so that regulatory authorities, from the US to the EU, can audit or check documentation as needed.
Clients asked us to prepare forms of 1-Formylhomopiperazine tailored for registration batches, reference standards, or custom impurity profiles. Since we see firsthand how these requests shape production, we maintain electronic production histories and stability data, ready to share for any development or regulatory file. Such records help project chemists align their filings or troubleshooting steps with up-to-date product data, saving time and avoiding unexpected responses from authorities. We don’t view traceability as a cost, but as a foundation for partnership and mutual trust.
Current interest in green chemistry also led us to re-examine the formylation step for 1-Formylhomopiperazine. Traditional processes employed hazardous reagents or hard-to-handle solvents. By optimizing for lower-toxicity reagents, solvent recycling, and operator protection, we support the shift to safer, more sustainable supply chains without sacrificing cost control. This focus flows straight from our conversations with safety officers and environmental officials during site visits.
No matter how advanced the intermediate, chemistry remains a collaborative field. We have sat across the table with process engineers solving late-stage development snags, analysts troubleshooting variability, and procurement leads trying to align cost and delivery windows. Every successful delivery is rooted in direct communication, from raw material arrivals to finished lots. We believe lasting value is built not just from the product itself, but from the relationships behind each order.
Working with innovators in pharmaceuticals and other fine chemical arenas, we see how the small details—like consistent melting ranges, low-odor profiles, and tight analyte windows—determine confidence and repeat business. Whenever a client brings process feedback, even on seemingly minor batch differences, we fold those lessons into our next campaign. Over years of feedback loops, our real stability data and in-process records keep reducing error rates, rework, and delays for all partners.
Beyond its classic applications in medicinal chemistry and protected intermediates, 1-Formylhomopiperazine increasingly finds use as a building block in specialty polymers, complex surfactant design, or as a test component in analytical method development. Academic research groups pursuing novel catalysts or enzyme mimetics have turned to this structure for its tunable reactivity and consistent response under various test conditions. Thanks to stable supply and technical transparency, our product serves R&D labs needing both consistent results and rapid sample support.
For established manufacturers, the expanding use of 1-Formylhomopiperazine represents a chance to raise the bar on production discipline. Each successful new application builds on decades of refining plant practices and improving the rapport between producer and end-user. By building adaptability into our production process—from lot size adjustments to rapid-response analytical backup—clients benefit from a steady, collaborative approach.
The chemistry of 1-Formylhomopiperazine, with its unique structure and specific reactivity, rarely leaves room for short-cuts. While there’s growing global competition to offer intermediates at rock-bottom prices, we’ve learned that price alone tells only part of the story. Batch failures, product recalls, or regulatory rework costs quickly outstrip any initial savings. Production expertise, rigor in analytical support, and traceable documentation mark the difference between reliable supply and project risk.
In high-stakes projects, our partners have come to rely on the consistency and technical backup that only a true manufacturer can provide. Teams in pharma, biotech, and fine chem know this through their own experience: when their timelines slip or data go missing, it pays to have a supplier who understands technical requirements and responds directly, without phone tag or delays.
Supplying 1-Formylhomopiperazine is more than a transaction. We treat it as an evolving collaboration with scientists, engineers, and procurement specialists working on ambitious new products. Production knowledge matters as much as technical grade. Every shipment carries the legacy of batch logs, purification records, and decades refining both process and support systems.
In practice, we see every day that lifting quality logic from decades of reactor time creates tangible advantages: less downtime, safer batches, and far fewer headaches for downstream chemists. Our staff stays on the ground, managing factory issues, giving technical feedback, and updating protocols with each new campaign. We shape our support based on hands-on work, not out-of-date datasheets.
We remain committed to supporting our partners with the facts and experience needed to achieve success in demanding applications, new product launches, and tough process challenges. For all our customers in R&D or manufacturing, 1-Formylhomopiperazine isn’t just a reagent; it’s a product shaped by real knowledge, tested by years in the field, and supported by a team that stands behind every lot.