|
HS Code |
679383 |
| Iupac Name | 1-(4-Fluorobenzyl)-1,4-diazepane |
| Molecular Formula | C12H17FN2 |
| Molecular Weight | 208.28 g/mol |
| Cas Number | 40932-60-7 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 285-287°C (estimated) |
| Solubility | Soluble in organic solvents (e.g., DMSO, ethanol) |
| Purity | Typically ≥98% (for reference standard) |
| Smiles | FC1=CC=C(CN2CNCCCN2)C=C1 |
| Inchi | InChI=1S/C12H17FN2/c13-11-3-5-12(6-4-11)10-15-8-1-2-9-14-7-10/h3-6,10,14-15H,1-2,7-9H2 |
As an accredited 1-(4-Fluorobenzyl)-1,4-Diazepane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 1-(4-Fluorobenzyl)-1,4-Diazepane, sealed with a tamper-evident cap and labeled for research use. |
| Shipping | 1-(4-Fluorobenzyl)-1,4-Diazepane is shipped in secure, airtight containers to prevent contamination and exposure. Packaging complies with chemical safety regulations, and all relevant documentation, including SDS, accompanies the shipment. Transport is arranged via authorized carriers, ensuring compliance with regional and international hazardous material shipping guidelines. Temperature and handling instructions are followed as required. |
| Storage | 1-(4-Fluorobenzyl)-1,4-diazepane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible materials (such as strong oxidizers). Ensure the storage area is clearly labeled and access is restricted to trained personnel. Keep the chemical at room temperature and avoid exposure to moisture or extreme temperatures. |
Applications of 1-(4-Fluorobenzyl)-1,4-Diazepane in Industrial Manufacturing1-(4-Fluorobenzyl)-1,4-Diazepane serves as a key intermediate in specialty chemical synthesis, meeting diverse performance and regulatory demands across multiple high-value industrial sectors. As a direct producer with integrated quality management, we ensure batch-to-batch consistency and traceable supply for mission-critical downstream processes. 1. Pharmaceutical Intermediate for CNS-Active Molecule SynthesisThis compound is widely used as a core intermediate in the synthesis of active pharmaceutical ingredients targeting central nervous system (CNS) disorders. API manufacturers introduce it during the main ring-building or side-chain functionalization stage, leveraging its unique diazepane scaffold and fluorinated aromatic group for enhanced receptor binding in novel NCEs intended for anti-anxiety, anticonvulsant, or nootropic segments. Sourcing from qualified factories is critical to meet the strict impurity control and documentation required in regulated GMP API manufacture. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Building Block for Specialty Agrochemical SynthesisMajor crop protection research groups and contract synthesis houses introduce this entity as a functionalized intermediate in the design and optimization of fluorinated pesticide or fungicide candidates. Its diazepane motif provides rigidity and the para-fluorobenzyl group enables selective tuning for target pest proteins. Large-scale production in this segment emphasizes cost efficiency, reproducible purity, and clear process documentation for legal registration dossiers. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Intermediate for Custom Synthesis in Fine Chemical R&DChemical research institutes and contract development organizations depend on this structure for complex molecule assembly, combinatorial chemistry projects, and customized fine chemical solutions. Its two-point functionalization, plus the tuneable fluorinated aromatic group, provide scaffold diversity in discovery-scale syntheses for sectors where molecular novelty, purity, and documentation are mandatory. Orders typically require production flexibility and full documentation to support downstream analytics or patent packages. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Precursor in Functional Polymer SynthesisPolymer chemistry groups employ this diazepane derivative as a precursor to functional monomers used in specialty polymer engineering. The structural motif introduces defined molecular geometry and the fluorinated benzyl sidechain imparts enhanced thermal stability, hydrophobicity, or chemical resistance to the polymer backbone. Controlled reactivity and high purity ensure reproducibility in downstream vinyl, epoxy, or polyamide syntheses targeting advanced performance materials. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 1-(4-Fluorobenzyl)-1,4-Diazepane 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
Flexible payment, competitive price, premium service - Inquire now!
Inside our plant, the process of synthesizing 1-(4-Fluorobenzyl)-1,4-diazepane has evolved through decades of chemical engineering experience. Our facility uses high-purity starting materials and carefully controlled reaction conditions. Our team monitors temperature, reaction time, and purification steps with attention to every batch, always aiming for consistent quality. Drawing on years spent troubleshooting production challenges, we have learned which variables require extra vigilance, especially during the introduction of the 4-Fluorobenzyl group. This step demands accurate reagent measurement and disciplined handling to secure a clean, stable product. We do not rely on guesswork. Each stage of synthesis receives careful documentation, owing to lessons learned from years of minimizing contamination and protecting final yield. The product emerging from this process reflects the kind of reliability that research chemists and industrial formulators expect from direct manufacturers.
Producing 1-(4-Fluorobenzyl)-1,4-diazepane in our own facility gives us an up-close view of the compound’s character. The 1,4-diazepane backbone brings flexibility and reactivity, while the 4-fluorobenzyl substitution offers subtle benefits in stability and targeting. The result carries a clear, faintly aromatic odor, signaling that the synthesis went as planned and no residuals linger. Our technical team can spot subpar material before it leaves the production hall, and our on-site quality assurance matches samples against analytic fingerprints from gas chromatography and NMR spectrometry.
Many researchers and product developers reach out to us for a reason: direct manufacturers have more control over batch consistency, traceability, and response to process feedback. No herbal-flavored marketing language can replace real-world know-how. Once our team shipped a batch to a pilot plant only to hear rapid feedback about a possible impurity. Because the entire chain was in our hands, we traced it back in hours, not weeks, and fixed the process or replaced the shipment with minimal delay for our customer. That is a level of responsiveness seldom experienced with intermediaries or brokers trading from unknown sources.
Different applications ask for different specifications. We routinely tune our process for small batches with higher purity, as well as larger-scale runs where throughput and cost matter just as much as cleanliness. For those seeking pharmaceutical-grade 1-(4-Fluorobenzyl)-1,4-diazepane, our lines deliver a product free from organic solvents, with limited water and impurity traces. For early-stage research, we know speed and flexibility often count more, so we ship quickly for confirmed research customers who need to trial new synthetic routes or compare fluorinated and non-fluorinated analogs.
Our material typically comes as a white to off-white crystalline solid, confirming that residual color bodies have been purged in purification. Melting point and chromatographic purity always form part of our outgoing inspection. In our field, we watch for slight deviations: a lower melting point than expected hints at remnant byproducts, an off-color may indicate incomplete washing. Over the years, our lab techs have built up a clear, shared sense for what top material looks and smells like. Clients who work hands-on with our product send clear feedback about solubility, filterability, and processing ease. We use that feedback to drive every improvement.
Every manufacturer dreads surprises on the customer’s end. We listen closely to the ways 1-(4-Fluorobenzyl)-1,4-diazepane finds a place in broader formulations and synthesis plans. Customers in pharmaceutical research often explore this building block when designing new CNS-active agents. The presence of the 4-fluorobenzyl group offers a balance between metabolic stability and activity, often proving superior to non-fluorinated peers for lead optimization. Formulators working on specialty polymers and ligands value this molecule for its reactivity and its ability to introduce a stable, electron-rich aromatic moiety into their structures.
Direct feedback loops shape our process every year. One research house reported clogging during scale-up reactions because an earlier vendor’s crude material contained persistent traces of chloride. Once we learned about this challenge, we tightened our isolation process and documented the difference in their subsequent runs: improved clearances, faster reaction times, fewer unwanted byproducts. The real lessons come from these customer collaborations, not from abstract datasheets.
Working as the direct producer puts us in a position to see not just specs on paper, but the lived differences between similar compounds or alternative sources. 1-(4-Fluorobenzyl)-1,4-diazepane holds advantages beyond its chemical curiosity. Compared to traditional diazepane derivatives, the fluorobenzyl group changes the metabolic fate and physical properties of finished products. In medicinal chemistry, this often translates to better CNS penetration, measured half-lives, and controlled activity. Materials scientists can tune hydrophobicity and interaction profiles with carriers or catalysts better using our molecule than with simple benzylated analogs.
Those who have tested industry-sourced material from traders or bulk suppliers share familiar stories with us. Variable purity, uncertain batch records, inconsistent physical appearance—these factors don’t just annoy QC managers, they disrupt entire timelines and cost thousands in lost time or reruns. Our factory approach means customers get continuity between lots, clear documentation for regulatory review, and a direct line for technical consultation when a formulation or process change requires a tweak in input quality.
We also set ourselves apart from products sourced through indirect channels in how we trace and minimize byproducts or synthetic residues. In many cases, trading houses can’t offer meaningful answers on remaining halides, residual solvents, or batch-to-batch differences. Our laboratory profiles every run, storing spectroscopic records for years. If an end user requests a historical COA or analysis report, we pull it from our database, not from an overseas aggregator or generic catalog available to anyone with a login. This dedication supports researchers preparing patent filings, regulatory submissions, or journal publications who must answer to auditors armed with demanding review checklists.
Consistently producing high-quality 1-(4-Fluorobenzyl)-1,4-diazepane doesn’t come without challenges. Early in our manufacturing experience, we ran into bottlenecks during scale-up. Small lab glassware tolerated local temperature spikes, but as batch sizes increased, even slight hotspots skewed reaction kinetics and, at times, resulted in unexpected side products. We invested in automated jacketed reactor systems with real-time temperature data logging. Over a series of fifteen batches, we tracked the delta between target and achieved conversion rates, adjusting stirring speeds and reagent addition profiles. Only by iteratively adjusting our approach, drawing upon real performance data and bench chemist experience, could we smooth out those inconsistencies.
Safety remains a daily focus. While 1,4-diazepane derivatives pose relatively low acute hazards, the introduction of the fluorobenzyl group requires careful management of fluorinated intermediates. Any escape of gaseous byproducts or uncontrolled heating can visit a world of trouble on a processing team. Our safety protocols sprang from actual incidents—a minor pressure increase in a flexible exhaust line once tripped sensors and reminded us where our limits lay. Experience sharpened our response plans, introducing redundant monitoring and regular staff drills. Every shift covers both targeted safety lessons and open conversation about near-misses to grow beyond basic compliance.
Waste management and sustainability take center stage, too. Industry-wide, regulatory requirements around halogenated waste streams get more demanding every year. Our plant pursues on-site solvent recycling wherever possible, recovering a large share of our reaction media and passing the rest to licensed offsite handlers. Keeping a close eye on the entire production lifecycle, we track and minimize halogen release and solvent loss. Customers who buy directly from us often ask about these efforts, knowing that their own sustainability initiatives increasingly weigh supplier practices in procurement decisions. We field these inquiries seriously and release thorough, audit-quality breakdowns of our waste streams and recycling ratios.
The success and reliability of 1-(4-Fluorobenzyl)-1,4-diazepane production in our facility has opened pathways for downstream derivatives. Over the last few years, requests for selectively substituted variants and related ring systems have grown. Because our staff understands the parent molecule’s chemistry, we can respond nimbly to R&D queries about possible analogs and new synthetic strategies. Some partners in medicinal chemistry circles work closely with us to brainstorm route changes that shave steps or simplify purifications—a source of joint pride that can only come from direct, trusting relationships.
Manufacturing advances never stand still. Our technical team invests in improved reaction monitoring, new purification media, and advanced analytics on a rolling basis. This year, our plant initiated a pilot project for in-line NMR to streamline batch decisions, heading off issues before they develop. The margin for error shrinks as demand for purity grows, so our pace of internal process improvement matches the pressure to deliver ever cleaner, more reliable product. We bring both seasoned legacy staff and younger chemists together—one group sometimes teaching the other hard-learned lessons about plant controls, another group pushing for adoption of fresh green chemistry ideas.
We also participate actively in industry consortia sharing updates on regulatory, safety, and environmental advances. By sharing anonymized information or aggregate data, we both help to lift category-wide standards and benchmark our operation. Questions about traceability, impurities, and lifecycle management do not end in the QC lab—they form part of an industry-wide conversation. Our product, and our approach, reflect a strong sense of responsibility for both user safety and broader chemical stewardship.
The ultimate proof of a manufacturer’s value rests not just in purity certificates but in how real customers use the product. Over the years, we have received feedback from across the globe: lab groups excited by a clean new synthetic route, pharmaceutical innovators reporting faster route-to-candidate times, chemical engineering teams proud of successful scale-up campaigns after working through sample trials with us. One medicinal chemistry team shared data showing that switching to our lot cut their number of failed catalysis steps in half. We think about that win every time a technician checks reactor seals for the hundredth time on a long shift.
Frustration with inconsistent or anonymous suppliers motivated many repeat buyers to bring their custom projects to us as well. When customers call with requests for custom packaging, tight impurity profiles, or technical documentation for regulatory bodies, they know they get answers from the individuals who synthesized, purified, and tested the material. The supply line shrinks, the conversation gets more focused, and peer-to-peer trust deepens. That trust lets us push chemistries further, brainstorm new approaches, and improve efficiency together.
Every kilogram of 1-(4-Fluorobenzyl)-1,4-diazepane that leaves our plant represents a mix of chemical precision, human attention, and learning from earlier successes and missteps. The work does not finish with hitting a purity mark. It continues in hands-on conversations with users, in plant team meetings about next quarter’s batch plans, and in careful responses to a field’s changing technical and ethical standards.
Our team understands that supplying a specialty chemical means combining science and responsibility, listening to real-world needs, and earning trust with every delivery. Researchers, developers, and formulators have choices. Ours continues to be shaped by experience, pride in workmanship, and a shared belief that doing things right—every batch, every day—will always matter. That is how we define and stand behind our 1-(4-Fluorobenzyl)-1,4-diazepane.