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HS Code |
715252 |
| Compound Name | 4-Benzylaminocyclohexanone |
| Molecular Formula | C13H17NO |
| Molecular Weight | 203.28 g/mol |
| Cas Number | 802855-66-9 |
| Appearance | White to off-white solid |
| Solubility | Soluble in organic solvents (e.g., ethanol, DMSO) |
| Structure Type | Aminoketone |
| Smiles | C1CCC(CC1)NCc2ccccc2=O |
| Inchi | InChI=1S/C13H17NO/c15-13-7-3-1-2-6-12(13)14-10-11-8-4-5-9-11/h4-5,8-9,12,14H,1-3,6-7,10H2 |
| Storage Conditions | Store in a cool, dry place, away from light |
| Synonyms | 4-(Benzylamino)cyclohexanone |
| Hazards | Handle with appropriate protective equipment; data limited |
As an accredited 4-Benzylaminocyclohexanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical, 4-Benzylaminocyclohexanone, is securely packaged in a sealed 100-gram amber glass bottle with clear hazard labeling. |
| Shipping | 4-Benzylaminocyclohexanone is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with safety and regulatory standards for chemical transport. The product is typically dispatched via ground or air, with appropriate labeling and documentation for handling, storage, and emergency measures during transit. |
| Storage | Store 4-Benzylaminocyclohexanone in a cool, dry, well-ventilated area away from direct sunlight and sources of ignition. Keep the container tightly closed and clearly labeled. Avoid contact with strong oxidizing agents and moisture. Use suitable, chemically resistant containers. Ensure appropriate spill containment measures, and store under conditions recommended on the Safety Data Sheet (SDS). Keep out of reach of unauthorized personnel. |
Applications of 4-Benzylaminocyclohexanone in Industrial Manufacturing4-Benzylaminocyclohexanone serves as a vital intermediate in multiple chemical sectors. Its structural properties allow downstream producers to construct advanced molecules for pharmaceuticals, fine chemicals, and specialty polymers. The following sections outline specific, real-world applications in which this raw material plays an essential part from process to final product. 1. Pharmaceutical Active Intermediate SynthesisIn pharma manufacturing, companies use this substance as a key building block to create central nervous system (CNS) drug precursors. Its reactivity enables selective transformation in amination and reductive alkylation steps. Process engineers tailor the reaction sequence for batch consistency, leveraging cyclohexanone derivatives to build patented small-molecule agents with controlled impurity profiles. Route development teams define its role in GMP-compliant process design and document its lineage within Drug Master Files for regulated product releases. Industry compliance standards
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2. Fine Chemical Building Block for Agrochemical SynthesisManufacturers in the agrochemical sector use this material as an aminoketone core for herbicide and pesticide actives. Its molecular backbone supports the assembly of proprietary protection agents via condensation and alkylation. QC managers monitor batch records to align with zoning and residue-limit regulations. Site engineers adapt solvent, temperature, and pressure parameters for multi-ton scale, balancing conversion with downstream isolations. Industry compliance standards
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3. Intermediate for Specialty Polymer AdditivesSpecialty polymer producers rely on this raw material for modification of resin properties, especially in UV-stable and impact-resistant applications. The ketone-amine structure enables reactive blending in chain-extension or end-capping stages. Product development teams formulate additive packages precisely to meet required migration, mechanical, and regulatory standards. Manufacturing lines employ controlled dosing for batch uniformity, monitored by in-line spectroscopic validation. Industry compliance standards
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4. Research and Development Intermediate in Fine ChemicalsChemical R&D centers deploy this compound for advanced molecule construction, particularly in combinatorial libraries and custom syntheses. Flexible reactivity permits rapid screening of structure–activity relationships, crucial for innovation in biotech and specialty materials. Analytical teams use NMR, HPLC, and GC-MS to ensure purity and reactivity. Each campaign is logged with batch traceability for patent filings and IP management. Industry compliance standards
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Inside our manufacturing halls, new compounds emerge from careful synthesis and close attention to detail. 4-Benzylaminocyclohexanone stands out on the line because this molecule fills a unique gap for those seeking a specific balance between reactivity, selectivity, and structural flexibility. Here we talk about what shapes this product—its properties, the reasons chemists choose it, and the lessons learned over years of production. Our focus remains on clarity and transparency, offering more than catalog descriptions. Instead of reciting lists, we aim to share our lived experience working with and producing this compound every day.
At its core, 4-Benzylaminocyclohexanone features a cyclohexanone backbone with a benzylamino substitution at the 4-position—a distinctly different structure compared to simple cyclohexanones or classical aminocyclohexanones. Minor structural tweaks can lead to major differences in how a molecule behaves. The presence of the benzyl group introduces both steric and electronic changes; this tailors the compound for projects that demand either increased selectivity in synthesis or a different profile in downstream reactions. As those in organic synthesis know, fine-tuning can lead to improved yields or reduced by-products, which helps cut both costs and waste.
Working with this product daily means constantly observing subtle but important differences in how it behaves during storage, transport, and reaction planning. Chemists often point out that even slight substitutions on cyclic ketones change their reactivity profile. For example, 4-Benzylaminocyclohexanone resists certain nucleophilic attacks compared to an unsubstituted cyclohexanone or its methyl analogues. The benzylamino group not only adds rigidity, it also forms opportunities for selective transformations, especially during reductive aminations or condensation reactions.
Years of feedback from our customers, many of whom work in pharmaceutical research or advanced materials, highlight why 4-Benzylaminocyclohexanone remains a staple in their protocols. One recurring theme is reliability: Chemists trust that each batch brings uniformity in melting point and chromatographic purity, minimizing the need for additional purification steps. Our production teams track every parameter from solvent ratios to crystallization conditions to keep impurities away, as even trace contaminants may disrupt sensitive syntheses.
Several large-scale projects employed 4-Benzylaminocyclohexanone when other aminocyclohexanones caused inconsistent yields or failed to provide the right intermediate for their process. This isn’t an isolated experience; similar feedback appears in both medicinal chemistry and polymer development. Synthetic chemists often value the fine balance between reactivity and stability, especially in pilot runs for drug candidates or custom materials. Where other cyclic ketones produce unwanted by-products, this compound offers cleaner, more predictable profiles.
On paper, it might seem practical to swap 4-Benzylaminocyclohexanone for other cyclohexanone derivatives, like 4-aminocyclohexanone or the analogous methylaminocyclohexanone. In the plant, real-world results diverge from bench-top assumptions. 4-Benzylaminocyclohexanone’s bulkier benzyl group provides distinct selectivity in certain condensation reactions, especially where steric effects steer the reaction pathway. For example, in reductive aminations aimed at producing specific analogues for pharmaceutical leads, the difference between a benzylamino and methylamino group shapes both the speed and outcome of the reaction.
During pilot batch scaling, differences in substrate volatility, solubility, and even minor impurities shift both the reaction profile and purification requirements. Our own teams have run side-by-side comparisons between the benzyl, methyl, and unsubstituted versions in similar conditions. The benzyl derivative often produced higher isolated yields with simpler workups, especially when using polar aprotic solvents. Downstream, this translated to more consistent crystallization and easier handling, which matters in full-scale production where waste and solvent usage become critical economy points.
Daily handling teaches us limits and best practices. 4-Benzylaminocyclohexanone offers robust thermal stability compared to several other aminocyclohexanone analogues. This means it tolerates elevated temperatures in some reaction setups, useful during multi-step synthesis or post-reaction purifications. In storage, the solid remains free-flowing and resists caking under ambient conditions with standard humidity controls. In contrast, some related molecules clump easily or require frequent rework to maintain usability in automated dispensing systems.
Another point worth addressing involves sensitivity to oxygen and light. Benzyl-substituted compounds sometimes display greater resistance to air oxidation than alkyl analogues, and experience supports this. Over months of warehouse storage, we noticed lower peroxide formation, requiring less frequent checks. This reliability stretches from our tanks to your benches. Tracing each drum back to the synthesis lot, we flag any batch that fails strict light and air stability checks, which keeps surprises out of the customer lab.
Specifications go beyond paper numbers. They influence real-world workflow costs, product safety, and regulatory compliance. Our routine in production involves calibrating every step to hold the melting point within a narrow range (with typical values observed during QC), monitoring residual solvents far below accepted thresholds, and logging every anomaly flagged by infrared and HPLC analysis. Years of process tweaks—like switching to higher-purity starting acids or optimizing hydrogenation catalysts—reduced batch-to-batch variation and improved overall reproducibility.
This commitment shows up in internal statistics: we track variance in key parameters (melting point, assay, moisture) and have reduced out-of-spec batches to less than 0.5% per quarter. These aren’t just numbers for auditors; every deviation that slips through could mean hours lost in our customer’s lab, so we close the loop before shipping. Using digital traceability from batch records to barcoding in the warehouse, we solve most specification issues at the source.
Making 4-Benzylaminocyclohexanone on a commercial scale leads us to focus on green chemistry principles. The benzylation reaction carried challenges that stimulated us to develop lower-waste approaches. Through years of tweaks, we reduced by-product formation by moving to cleaner benzylamines and by using phase-transfer catalysts that cut down on excess reactant needs. Such process innovation led to a measurable decline in wastewater loading and solvent loss.
In daily practice, our teams recycle solvents wherever possible and neutralize any hazardous streams before disposal. Routine choice of high-recovery distillation setups and closed-system transfers slashes fugitive emissions. The cumulative effect—safer operations, lower environmental footprint, happier neighbors—results from making responsible choices in every shift rather than vague promises or one-off improvements.
Users select 4-Benzylaminocyclohexanone for a spectrum of reasons, and over the years, patterns emerged. In pharmaceutical R&D, this compound acts as a critical intermediate for certain analgesics and central nervous system agents, where its unique substitution pattern enables selective building of functionalized ring systems. Working closely with formulators, we observed how the product’s purity and low color level became essential for downstream transformations, particularly for reactions sensitive to trace aldehydes or amines.
Some chemical engineers use it for specialty coatings and polymers. Here, the functional flexibility of the benzylamino group offers routes to cross-linked materials with performance characteristics unattainable using simpler cyclohexanone cores. In such cases, manufactured batches must not just pass chemical purity standards; workability in the plant, dusting tendencies, and ease of dissolution or mixing directly affect throughput on the line. Seasoned operators look for microcrystalline powders that are free of clump-formers, based on daily experience measuring and transferring kilograms at a time.
Feedback also comes from labs pushing into custom syntheses. Synthetic teams exploit the benzyl group as a removable protecting group, enabling stepwise elaboration of cyclohexanones with high regioselectivity. The ability to deprotect under mild hydrogenation conditions—without harming other functional groups—gives researchers room for creativity. Several clients commented on smoother hydrogenation with the benzyl derivative, encountering fewer over-reduction problems compared to alternative protecting strategies.
Routine does not mean standing still; each production run lets us spot opportunities to improve. For 4-Benzylaminocyclohexanone, switching to greener oxidants and tailoring purification to reduce mother liquor discharge led to better overall yield and less environmental footprint. Years ago, we ran amid a batch that threatened to foam over due to an unexpected exotherm during benzylamine addition—an experience that spurred both better real-time temperature monitoring and more robust reaction control.
As the market changed and regulatory expectations rose, we moved from manual crystallization setups to fully automated flow reactors. Not only did these changes improve throughput and uniformity, but real-time sampling and feedback controls nearly eliminated off-spec crystallizations, curbing rework and wasted material. Automation also freed operators from tedious batch checks, letting them focus on process improvements and safety checks instead.
Collaborating with equipment makers allowed us to custom-fit our reactors and drying systems to this molecule’s nuances, avoiding bottlenecks and scaling challenges. Sourcing molecules like benzylamine remains a supply chain challenge, especially with tightening global trade, so we continuously evaluated multiple suppliers and audited their processes for consistency and compliance.
Years of real-world logistics taught us how to package and transport 4-Benzylaminocyclohexanone for peak shelf life and minimum headaches. Chemically, it fares well in sealed, UV-blocked containers, holding up during warm summers or even unexpected cold snaps. Experience shows that layered packaging—using both moisture-barrier liners and rigid drums—keeps humidity-induced caking at bay. This isn’t theory; early on, we learned the hard way that single-layer packaging allowed subtle hydrolysis in coastal storage, which led to off-odors and extra filtration work.
Whether shipments move overland or sit in storage for weeks, real test comes during receiving at our customers’ sites. Based on historical claims, adopting desiccant inserts and regular seal checks reduced transportation losses by well over 90%. For bulk users with automated dispensing, our teams designed and validated packaging gauges allowing direct drum-to-tank transfer, which lowered spills and operator handling time.
Sourcing chemicals as a buyer often means wrestling with unpredictable lead times and variable batch quality. As a manufacturer, years of experience taught us the value of clear communication and transparency—no one benefits from guesswork or surprise delays. By investing in larger buffer inventories and redundant supply routes, we can promise steadier deliveries, even as global logistics face ongoing turmoil from weather, geopolitics, or freight disruptions. We act quickly on any deviation from schedule, updating customers immediately, rather than waiting for a simple tracking number to reflect reality.
This two-way relationship with end users paid dividends. Engineers and chemists trust our documentation because it reflects actual plant practice—not just what looks good on paper. They know each batch links directly back to our in-house synthesis and quality control. Allowing audits and even real-world process consultations strengthened these ties. For custom jobs, our process chemists consult on formulation and application, sharing both what worked and what stumbled during scale-ups, leading to fewer surprises in client applications.
Close ties with the community of users mean the learning never stops. Notes from pilot plant visits and follow-up calls reveal where real problems and opportunities lie. For 4-Benzylaminocyclohexanone, the feedback loop led to incremental but meaningful changes—shifting drying temperatures or extending QA checks on melting point and color yielded fewer batch rejects and smoother downstream syntheses at client sites.
User feedback often flagged subtle points no spec sheet would catch. For example, some polymer chemists noticed minor discoloration at scale even when analytical purity looked perfect. When questioned, we traced the issue to trace levels of benzylamine dimer that snuck through the final purification step. Adjusting the scrubber configuration fixed the problem, preventing off-color batches from reaching the user.
Taken as a whole, these experiences reinforce that manufacturing isn’t just about meeting numbers—it’s about understanding application context, the realities of plant operations, and the many ways a molecule fits into larger projects. The more we learn from chemists and operators at client sites, the better we make the product and the smoother the transition from our factory floors to the final user’s process.
Looking ahead, regulatory scrutiny grows tighter each year, pushing for stricter controls on residual solvents, trace contaminants, and documentation of sourcing. These pressures only underscore the importance of in-house process knowledge and relentless process improvement. Our current projects focus on both optimizing the energy footprint and further minimizing process waste, targeting both the direct process and supporting utilities.
Clients ask for more customized forms and packaging, including micronized powders or specific blends to meet their downstream processing requirements. These requests challenge our teams to push further on innovation, piloting alternative drying and sizing setups to preserve both purity and ease of handling. Each new request serves as both a challenge and an opportunity to fine-tune our offering.
As industry standards shift and market needs evolve, our teams remain ready to adapt. Communication and openness, coupled with hands-on manufacturing expertise, keep us at the forefront—delivering not only the chemistry but the reliability and partnership our users expect.