|
HS Code |
547404 |
| Iupac Name | 1-benzyl-4-phenylaminopiperidine |
| Cas Number | 101941-19-9 |
| Molecular Formula | C18H22N2 |
| Molar Mass | 266.38 g/mol |
| Appearance | White to off-white crystalline solid |
| Melting Point | 110-112°C |
| Boiling Point | 420.4°C at 760 mmHg |
| Density | 1.08 g/cm³ |
| Solubility In Water | Slightly soluble |
| Pubchem Cid | 130723 |
| Smiles | C1CN(CCC1N)CC2=CC=CC=C2 |
| Inchi | InChI=1S/C18H22N2/c1-2-6-16(7-3-1)20-15-10-13-19(14-11-15)12-17-8-4-5-9-18-17/h1-9,15,20H,10-14H2 |
As an accredited 4-Anilino-1-Benzylpiperidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Anilino-1-Benzylpiperidine is supplied in a 25g amber glass bottle with a tamper-evident seal and clear labeling. |
| Shipping | 4-Anilino-1-Benzylpiperidine is shipped in secure, chemically resistant containers to prevent leaks or contamination. Packaging complies with local and international regulations for chemical transport. Hazard labeling and documentation are provided. Shipment is handled by licensed carriers, with temperature and handling instructions observed as needed to ensure product stability and safety during transit. |
| Storage | 4-Anilino-1-Benzylpiperidine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible materials such as strong oxidizing agents. Ensure the storage area is secure and access is restricted to authorized personnel. Proper labeling and adherence to local chemical storage regulations are essential for safety. |
Applications of 4-Anilino-1-Benzylpiperidine in Industrial Manufacturing4-Anilino-1-Benzylpiperidine serves as a specialty intermediate across several controlled synthesis sectors. Our facility supports regulatory-compliant supply for strictly limited downstream processes, which are managed by qualified industrial customers. The following segments detail its proven applications under industrial and regulatory conditions. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThis compound acts as a critical building block in multi-step synthetis pathways of select central nervous system drug intermediates, especially within the development of specialized medications in authorized sites. Customers in the pharmaceutical sector require high assay material, supported by validated analytical documentation. Our product integrates during protected stages to ensure traceability and regulatory documentation, with full batch records available for regulatory review and DMF referencing. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Fine Chemical Intermediate for Agrochemical Synthesis4-Anilino-1-Benzylpiperidine participates as a linker molecule in the assembly of certain piperidine-based agrochemical actives, serving customers developing novel crop protection prototypes under local registration. Manufacture requires batch-level traceability, impurity profiling and documented compliance from source to the formulated technical concentrate. We supply product with supporting safety and impurity data for agchem registration filings under recognized frameworks. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Intermediate in Industrial Analytical Standards ProductionThis material serves as a highly specific component in the custom synthesis of analytical reference materials and impurity standards, particularly for laboratories tracking trace contaminants, forensic samples, or when benchmarking controlled substances under a valid research license. Production is managed under restricted protocols, with close monitoring and full traceability from sourcing to custom purification and packaging. Industrial and government labs require precise certification of these tailored molecules. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Reference Compound for Toxicological and Forensic ResearchThe molecule finds documented applications in advanced toxicology research, where industrial and governmental testing organizations synthesize it as a model compound or study matrix for human/animal metabolism and forensic method validation. We support such teams with high-purity material, full batch traceability, and technical documentation, strictly for licensed users in compliance with legal and ethical regulations for hazardous chemicals. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive 4-Anilino-1-Benzylpiperidine 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!
Years of steady practice in organic synthesis have shown us the pulse of research and demand for complex intermediates. 4-Anilino-1-Benzylpiperidine stands out among the toolbox chemicals valued in academic and industrial labs. Its robust framework has earned a solid reputation when fine-tuning the design of advanced functional molecules. We craft batches in-house, controlling every variable from selection of raw materials to downstream purification, so each shipment meets the criteria set by leading chemical research groups—not just our internal benchmarks.
Working hands-on in reaction tanks and pilot lines, we see the daily impact of subtle process choices. The foundation of 4-Anilino-1-Benzylpiperidine lies in the fusion of the benzylpiperidine moiety with an anilino group at the para position. Our technicians monitor color, purity, and moisture content at each step because even small contaminants can derail applications further down the pipeline. We’ve responded to requests from R&D chemists who need lots ranging in scale, from gram samples to controlled bulk manufacturing. Often these clients share feedback about how even minor shifts in crystallinity influence the selectivity in their next-stage reactions—a difference observable only with repeated hands-on use.
Chemists often search for chemical building blocks that help navigate toward target scaffolds quickly. 4-Anilino-1-Benzylpiperidine’s profile enables direct functionalizations of both the aromatic ring and the piperidine core, expanding its versatility across synthetic pathways. We’ve witnessed it employed as a precursor in custom ligand development, polymer chemistry, and heterocycle modification projects. During collaborative projects, teams exploring psychoactive analogs have asked for materials with extremely low heavy metal content or constrained enantiomeric purity. Our dedicated QC line draws from these experiences—we calibrate detection instruments, and reject batches when a single parameter falls out of range.
It’s not just the theoretical molecular structure that matters. The product arrives as off-white to pale yellow solid, with melting points and spectral fingerprints consistent with peer-reviewed references. Handling characteristics such as flow, hygroscopicity, and clumping can trace back to the filtration strategy or solvent system adopted in-house. On more than one occasion, we’ve received questions about the tendency of some competitive samples toward discoloration during storage. Tracking our own observations, fresh sealed product maintains stability for extensive periods, with recommended storage away from heat or moisture swings. Customers gain from these incremental improvements, and so do our lab teams—reduced batch-to-batch variability means greater confidence in mapping new chemical space.
From a synthetic operator’s standpoint, not all piperidine derivatives respond equally to reaction conditions. Blending the benzyl and anilino functions on the same piperidine core delivers useful selectivity and reactivity advantages. For example, compared to a plain piperidine or mono-substituted analog, 4-Anilino-1-Benzylpiperidine can direct site-specific reactivity and help mask or expose reactive handles when constructing more elaborate molecules. A colleague running scale-up routines found this amphiphilic nature crucial when mediating cross-coupling and nucleophilic aromatic substitution in a recent collaboration with a pharmaceutical startup.
Divergence from common alternatives such as 4-Phenylpiperidine lies not only in N-substitution, but in the interplay between the aromatic and piperidine rings, which influences distribution coefficients, basicity, and compatibility with a wide set of coupling agents. 4-Anilino-1-Benzylpiperidine resists certain types of side reactions seen with mono-functional piperidines, based on hands-on trials using both classical and modern catalysis. As a concrete result, researchers have described more straightforward purification regimes, reducing column cycles and waste stream load when using our product as a starting point.
Research is never static. Requests shift—from material qualified for pilot-scale biotransformation to smaller runs for probe development and control incubations. Our team fields inquiries from those scaling new CNS pharmacophore analogs, to those engaged in ligand field tuning for custom metal complexes. We know that researchers working under IP-sensitive environments expect not only purity, but complete batch traceability and accessible documentation. Our digital archive stores run-specific details, logging protocol deviations and analytic records. Several teams have told us that this transparency made the difference in regulatory filings or patent perimeter defense.
Large-scale users leverage our carefully maintained facilities to keep quality consistent across hundreds of kilograms. Small innovative firms contact us for milligram lots, used as reference standards or in combinatorial screening. A specialty polymer chemist recently shared reaction traces showing improved grafting efficiency—attributable to the fine particulate properties gained from adjusted drying protocols tested last quarter in our QA line. We welcome these discussions, often resulting in tighter process controls that further benefit the community of users.
Handling 4-Anilino-1-Benzylpiperidine in wet chemistry or analytical labs brings its own rhythm. Technicians favor its moderate solubility in polar aprotic solvents like acetonitrile, DMSO, and dichloromethane. Solubility trends map cleanly into expected polarity, as measured in our analytical lab using GC and NMR comparison standards. During a recent customer visit, process chemists checked the behavior in both neutral and mildly acidic workups, confirming negligible precipitation and color stability. These user-led verifications echo our experience during product qualification phases. Clear dissolution and compatibility cut out downstream headaches, especially in automated liquid handling or continuous feed systems.
Feedback loops drive many of our technical refinements. A partner pharmaceutical company encountered unexpected byproducts using a competitor’s material with unspecified trace residues. Upon switching to our 4-Anilino-1-Benzylpiperidine, their purification profile sharpened, batch yields increased, and time spent troubleshooting reduced markedly. This switching experience is not unique—other clients have flagged fewer baseline drifts during HPLC assay, obviating costly troubleshooting runs. Quality in, quality out, as our plant team puts it.
We’re frequently pulled into joint process reviews with synthetic chemistry teams. We don’t just supply a barcode—we share pre-shipment COAs, lot files, and sometimes even open raw MS and NMR spectra for group review. These sessions have ranged from technical troubleshooting to co-authoring publications in peer-reviewed journals. More than once, a customer’s experiment on tailored reduction conditions using our compound sparked an internal brainstorm, leading us to trial a new purification resin or drying protocol. Instead of isolated feedback, these conversations feed into practical process iterations—raising the standard for subsequent batches.
Each transfer of 4-Anilino-1-Benzylpiperidine to clients comes with a record file showing analytical confirmation against in-house and external standards. Academic labs ask for details on residual solvents; contract research organizations want full chain-of-custody logs. Our batch books catalog starting inputs, yield data, analytic cut points, and deviations, keeping compliance alignments with ICH, USP, and relevant local controls. This documentation is not just paperwork—it grows out of direct audit experiences, program qualification checks, and the lessons learned from failed shipments over decades in chemical production.
In real cases, our technical auditors guided partners through updates after regulatory site visits, helping them respond quickly with clear source and characterization details. Instead of surface fixes, our compliance team believes in robust internal training, documented process traceability, and periodic review of change control protocols. Such routines anchor customer trust, streamlining not only research supply chains, but also process scale-up to GMP lines if and when that step becomes necessary.
It’s tempting to assume every chemical input behaves predictably. In practice, feedback from the end user makes a difference. Examples from real-world implementation highlighted the importance of defined batch homogeneity and standardized micronization. Several discovery chemists commented on how our particle sizing cut down on agglomeration, allowing reliable metering in high-throughput screens.
An industrial client’s automated addition valve clogged when tested with a generic competitor’s lot. Under side-by-side testing with our material, flow metering ran smoothly for a weeklong process run. In such ways, product attributes born from upstream process control can provide cost and time returns far beyond the bottle price. Our plant focus on fine crystallization and filtration consistently delivers on these fronts, as confirmed by customer-run process validations.
Our roots remain in batch synthesis, but frequent troubleshooting with partners shapes new directions. Customers developing next-generation pharmaceuticals, performance polymers, or advanced materials often approach us directly for guidance on adapting 4-Anilino-1-Benzylpiperidine into more convoluted synthesis regimes. Our technical staff share insights gleaned from hundreds of production runs—experience that books and literature reviews rarely capture. Solutions sometimes emerge in off-hand discussions over chromatograms or after-hours emails, often leading to minor—but important—adjustments in delivery forms or packing to fit glove-box workflows.
During an international conference, a project lead described unexpectedly strong selectivity gains in late-stage modifications when working with our sample compared to a benchmark lot. The difference traced to a process tweak in purification and drying, introduced months earlier at the request of a medicinal chemistry group. These stories underline how manufacturer insight directly influences project outcome.
On paper, 4-Anilino-1-Benzylpiperidine serves as an intermediate in complex molecule synthesis. In laboratory life, its traits make it a lynchpin for scaffold assembly, signaling molecule prototyping, or late-stage functional group installations. Material produced under tight controls routinely produces sharper LCMS and NMR signatures, as noted by quality control chemists running side-by-side verifications after supplier switchovers.
Unlike commodity substitutes, our product shines in applications requiring low color-forming impurities and high batch-to-batch reproducibility. This reliability fuels its use in pharmacological screens, specialty dye precursor projects, and the design of advanced resin linkers. The subtle balance between aromatic and amine content delivers options for both nucleophilic and electrophilic modifications, a fact R&D staff leverage when time lines are short and route scouting is underway.
Investing in chemical manufacturing infrastructure means more than running reactors. Our teams organize real-time tracking of order timelines, in-process data, and batch release confirmations. These routines matter during seasonal scale-ups, holidays, and changing market dynamics. Clients depending on timely shipments for grant milestones or commercial launches benefit directly from the continuity our process brings.
Several repeat buyers in academic and bioscience research point to the confidence our supply brings, cutting downtime between experiments and reducing back-order risk. We ship with direct lot documentation—not generic COAs pulled from years-old files. This commitment combines the lessons of seasoned production teams and continuous systems refinement, all aimed at serving the chemists who rely on our building blocks.
Our focus on 4-Anilino-1-Benzylpiperidine stems from both intrinsic demand and years of dialogue with those seeking to solve complex synthetic puzzles. Quality claims ring hollow unless tested in the field—this shortfall has shaped our process and communication priorities from the earliest batch. Every anecdote from a user struggling through a tough purification, every test run with findings on side reactions or unusual solvent interactions, gets folded into both manufacturing and customer support practice.
It’s this practical, iterative improvement—born from listening as much as making—that separates a manufacturer’s supply from shelf-stocked commodities. For labs, startups, and established players alike, the difference between “available” and “reliable” can spell the outcome of the year’s major project. Our team understands these stakes, and has adapted not out of necessity, but out of shared purpose with the scientific community.