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HS Code |
703822 |
| Product Name | 1-Benzoylpiperidine-4-Carboxylic Acid |
| Cas Number | 74181-51-2 |
| Molecular Formula | C13H15NO3 |
| Molecular Weight | 233.26 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 129-133°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Purity | Typically ≥98% |
| Chemical Structure | Benzoyl group at nitrogen, carboxylic acid at 4-position of piperidine ring |
| Synonyms | 1-Benzoyl-4-piperidinecarboxylic acid |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Smiles | C1CN(CCC1C(=O)O)C(=O)C2=CC=CC=C2 |
| Inchikey | CEAZBKURLNBYAR-UHFFFAOYSA-N |
As an accredited 1-Benzoylpiperidine-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The product is supplied in a 25g amber glass bottle, sealed with a screw cap, and labeled "1-Benzoylpiperidine-4-Carboxylic Acid." |
| Shipping | 1-Benzoylpiperidine-4-carboxylic acid is shipped in compliance with all relevant chemical safety regulations. The product is securely packaged in sealed containers to prevent leaks or contamination, clearly labeled, and accompanied by a Safety Data Sheet (SDS). Shipments are handled by certified carriers and tracked to ensure safe, timely delivery. |
| Storage | Store 1-Benzoylpiperidine-4-carboxylic acid in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances (such as strong oxidizing agents). Keep the container tightly closed when not in use. Avoid exposure to moisture. Ensure proper labeling and use secondary containment to prevent accidental spillage or contamination. Follow standard laboratory safety protocols during handling and storage. |
Applications of 1-Benzoylpiperidine-4-Carboxylic Acid in Industrial ManufacturingAs an established producer of 1-Benzoylpiperidine-4-Carboxylic Acid, we supply this intermediate to multiple industrial sectors that demand strict quality, traceability, and consistent performance. The following sections detail recognized applications in core industrial fields, specifying formulation protocols, compliance frameworks, manufacturing stages, and resultant end products. 1. Active Pharmaceutical Ingredient (API) Intermediate SynthesisThe pharmaceutical sector utilizes this compound as a key intermediate in synthesizing multiple APIs, particularly those within the neuropharmacology and psychiatric medicine segments. Our product supports primary amidation and condensation reactions in GMP-compliant API lines. Customizable purity grades address batch-to-batch consistency and regulatory requirements for scale-up and new chemical entity development. Industry compliance standards
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2. Agrochemical Synthesis and Crop Protection FormulationsDownstream agrochemical manufacturers formulate crop protection agents, including specific herbicide and fungicide actives, via piperidine route intermediates. The material’s reactivity allows production of protected functional groups necessary for selectivity and stability in controlled-release crop formulations. Industry compliance standards
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3. Specialty Polymer Modifier and Crosslinker ManufacturingManufacturers of advanced polymer materials employ this compound as a controlled crosslinking agent or chain terminator in the synthesis of high-performance resins. Its structure enables functional group modifications that influence polymer branching, solubility, and mechanical properties in adhesives, coatings, and molded end-use goods. Industry compliance standards
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4. Chemical Research Reagent and Reference Compound SupplyLeading research labs and specialty fine chemical producers order this compound for use as a characterization reference standard, reaction precursor, and in route scouting for novel heterocycle and benzamide derivative synthesis. Its defined structure assists with method validation, stereochemical analysis, and high-purity compound comparisons in applied R&D environments. Industry compliance standards
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On the production floor, the journey from raw feedstock chemicals to a finished molecule like 1-Benzoylpiperidine-4-Carboxylic Acid involves more than just following a recipe. Each batch gives us new cues, every test speaks about subtle differences, and every lot experiencing scale-up shows something new in the process. This compound, with the CAS number 1197-01-9, brings together the benzoyl group and the piperidine structure, making it important in several medicinal chemistry projects.
Many in the pharmaceutical and fine chemical sectors look for advanced intermediates that offer versatility but also reliability under a variety of process conditions. 1-Benzoylpiperidine-4-Carboxylic Acid plays a key role for teams pursuing piperidine-based structures. In practical terms, its unique ring system supports the synthesis of complex heterocyclic drug scaffolds, setting it apart from simpler straight-chain or monocyclic carboxylic acids. In our line, we see demand from both specialized drug development programs as well as academic research groups exploring piperidine derivatives.
The material customarily arrives in fine white to off-white crystalline forms, sometimes with faint variations caused by different crystallization and drying cycles. Our team regularly checks for purity exceeding 98% by HPLC, as this level directly impacts downstream reactivity and ease of purification for formulators. The molecular weight stands at 233.26 g/mol, important for stoichiometry in multistep synthesis. Water content and solvent residues get tight attention in our lab – not simply to tick boxes but because variations in these figures often lead to unpredictable reactivity, which can derail sensitive reactions.
In-house, our analysts know that 1-Benzoylpiperidine-4-Carboxylic Acid can, if overlooked, carry through traces of residual benzoyl chloride or piperidine byproducts. Addressing these is not a formality; small traces have led customers to return products in the past, especially those running catalytic coupling or amidation reactions. Through rotary-evaporation controls and extended vacuum drying, we reduce these residuals to levels not easily measurable by standard methods.
The compound’s bulk density, typically ranging between 0.45 and 0.55 g/cm3 in our product, doesn’t just matter for packaging. It plays a role in automated dispensing systems in advanced pilot plants. Variations in compactness can jam some feeders – something we worked hard to troubleshoot with both our engineering team and several customers. Out of such collaborations, we adjusted milling conditions and particle size distribution, supporting smoother, more continuous synthesis operations on the user end.
Real-world work flows rarely go according to textbook predictability. In the laboratory, 1-Benzoylpiperidine-4-Carboxylic Acid provides a platform for a broad range of C–N and C–C bond-forming reactions. Our customers regularly link this intermediate into morpholinone and other fused heterocycle targets. The benefit comes from its compatibility with coupling reagents used in peptide and oligonucleotide synthesis, accommodating both aggressive and mild reaction protocols.
As part of a dynamic process stream, the carboxylic acid function helps introduce variety into final products through amidation or esterification. For companies working on central nervous system drugs, the piperidine core delivers a specific conformational rigidity. Chemists often share with us how switching to this compound from open-chain analogues or even simple piperidines resulted in much greater final conversion rates and fewer side-products during hydrogenation and acylation stages.
One team using the compound for β-lactam antibiotic intermediate synthesis described better yields versus tetrahydropyridine acids. In that lab, higher product purity meant a reduction in overall purification steps, helping slash costs for a multi-kilo campaign. When molecules handle cleanly in scale-up, everything from reactor fouling to product isolation gets simpler – and we see that difference clearly between 1-Benzoylpiperidine-4-Carboxylic Acid and competitors using less rigorously controlled materials.
No two shipments leave our plant in quite the same way. Trucks, climate, and even humidity in the warehouse each make their mark. Over the years, we learned that improper storage leads to hydrolysis of the acid, forming benzoic acid and piperidine byproducts at detectable levels—even sealed drums sometimes see surges in these trace impurities. We added desiccant packs and adjusted container liners to manage this risk. Our regular sampling at three-month intervals checks whether storage impacts solubility or melting point, both of which indicate subtle breakdown or contamination.
A few years ago, we worked with one partner addressing batch inconsistency between summer and winter productions. The cause turned out to be not the process temperature per se, but the rate at which patent solvents evaporated in final crystallization, which changed the crystal habit. These physical but not immediately obvious changes led to differences in downstream processing—in one case, poor filtration rates and in another, greater dust generation during transfer. Fixing these issues required talking directly with customers’ production chemists, sharing batches across seasons, and tweaking protocol rather than just sticking to a dry product spec.
Analytical integrity matters as much as chemical purity. While common analytical tools such as HPLC and NMR remain gold standards, we often run GC-MS and FT-IR as well to cross-check trace contaminants and fingerprint crystal forms. Focus on multidimensional quality control grew out of customer audits where missing subtle solvent spikes, for instance, led to project setbacks or regulatory pushback at the user end. We maintain detailed batch histories, linking back not only yield or initial purity but documenting process upsets and operator notes that have, more than once, prevented a repeat of obscure failures across product lines.
In the spectrum of piperidine carboxylic acids, 1-Benzoylpiperidine-4-Carboxylic Acid stands apart from 1-benzyl and 1-phenyl analogues. The benzoyl group, compared to a simple benzyl, serves as a stronger electron-withdrawing function, which can shift reactivity in couplings and hydrogenations. In-house benchmarking experiments have shown that during reductive amination, the benzoyl derivative often provides greater selectivity and less overreaction than more electron-rich analogues. This means less labor in downstream purification and higher confidence in batch consistency, especially where medicinal chemists chase strict impurity profiles.
Handling properties differ, too. Where plain piperidine acids can form oils or low-melting solids, our benzoyl-piperidine acid delivers a robust solid, rarely presenting caking or liquefaction under standard packing and storage. This makes things far simpler for automated dosing in manufacturing – less downtime from blockages, fewer operator interventions.
In the controversial arena of chiral intermediates, this compound comes as a racemic mixture unless specified. We've observed a steady interest over time in resolving the enantiomers using chiral HPLC and asymmetric crystallization techniques. While the carboxylic group offers functional handles for derivatization, the benzoyl group’s steric and electronic properties can restrict routes for direct enantioselective modification. Half our development time in this area has focused on helping partners either resolve the racemate in-house or selectively functionalize before resolution steps.
Our partners sometimes compare the use of 1-Benzoylpiperidine-4-Carboxylic Acid against simple linear amino acids or non-aromatic ring acids. Success typically comes when projects demand not only physical stability but also distinct chemoselectivity in linkages, something less predictable with open-chain or non-benzoyl piperidine analogues. For high-barrier API intermediates where trace reactivity can make or break a batch, this product tends to win because it balances reactivity and manageability better than most in its field.
Scale brings new surprises at every turn. On the kilo lab bench, handling a few hundred grams may seem simple. At a five-hundred-kilogram scale, subtle problems grow large—dust formation, static buildup, and changes in bulk handling can slow down entire production lines. In scaling up, our crew runs stress tests for both product quality and pack-out integrity. This testing picked up unexpected static charge accumulation in a certain lot, which caused wall-sticking in automated feed hoppers. Additional antistatic packaging and a change in particle size distribution for that batch addressed what could have derailed days of operation at a partner facility.
Repeated feedback points strongly to one thing: users value reliability in behavior during reaction setup and clean-up. We run internal process validations after every three batches, not because a certifier tells us to, but because broken runs cost our own team time and reputation as much as our customers. Every single deviation in product, whether a color change or a minor slip in melting range, gets traced and recorded alongside detailed operator logs. These records get shared with repeat customers, helping them plan scale-up chemistries with fewer unknowns.
Transport logistics have turned up new priorities for our logistics crew. Over several large-scale export orders, we discovered that certain humidity spikes in trans-ocean transport caused micro-clumping, impacting ease of use even for end users accustomed to working up slurries. Modified liner materials and coordinated shipment with desiccant insertion meant the last several export lots arrived free-flowing and dry, saving our partners both time and rework.
Waste handling grows pivotal in specialty chemicals. Through a detailed lifecycle assessment prompted by a project with a sustainable pharma startup, we mapped the major environmental hotspots for 1-Benzoylpiperidine-4-Carboxylic Acid. Key impacts arose not just from the synthesis itself but also solvent management and cleaning operations. Process optimization—pointing to solvent swaps and enhanced workup protocols—reduced our per-batch solvent waste by about 12%.
On the waste treatment side, we invested in distillation columns that allow us to recover and recycle a substantial fraction of used solvents. Results go beyond compliance; they take direct cost out of the process by reducing virgin solvent purchasing.
Some regulations for this intermediate remain in flux, especially as downstream users develop novel APIs. We keep engaged with regulatory updates and industry groups, as more compliance requirements inevitably pass from the lab bench into plant Reality. Product stewardship isn’t about ticking a box; having technical staff ready to interpret new requirements and preemptively adjust our process means fewer disruptions for collaborators down the line.
Each negotiated order and every technical consultation weave us closer to the projects shaping new medicines. We see how academic teams and small biotech startups push 1-Benzoylpiperidine-4-Carboxylic Acid into untested synthetic routes. Often these users ask for tweaks—an alternative salt form, or a specific particle size for rapid dissolution trials. Rather than placating them with generic stock, we make pilot batches, run comparative analytics, and support process tweaks to help them hit the reactivity window or API profile they aim for.
One memorable collaboration involved a research group pursuing novel antipsychotic scaffolds. They struggled with poor solubility and uneven conversion in coupling stages. A joint effort tracking particle size distributions and solvent compatibility led to a custom-milled lot, which lifted their conversion rates by more than ten percent and cut project time by over a month. These kinds of partnerships rarely appear on a technical data sheet, but they drive the real differentiation people experience when choosing between commodity and truly manufacturer-supported compounds.
In the years since we scaled up production, the real learning grew in those shared results, operator notes, and hands-on tweaks. It’s these adjustments—born of direct feedback and ongoing dialog with formulation chemists and pilot plant operators—that make the product worth returning to for high-spec research and industrial needs.
One truth shines across all our experience: trust in specialty intermediates grows through real consistency under changing pressures. Sometimes the biggest test comes not from a published spec or a sales pitch but from the compound performing again and again in unpredictable real-life lab and plant settings. For our crew, 1-Benzoylpiperidine-4-Carboxylic Acid stands as an example of the difference between just meeting the standard and exceeding it through every step of production, testing, packaging, and support.
We know the molecule by more than its registry number. We recognize the smell of a just-purified batch and the feel of its crystals between gloved fingers. We chart its quirks, chase its deviations, and learn with every fresh synthesis campaign. In offering this product, we share more than a chemical; we participate with our partners in the intricate, demanding world of modern synthetic chemistry.
As the industry shifts, so does what is expected for performance, traceability, and true reliability. What shaped our approach, and what still shapes it, springs from experience, ongoing curiosity, and the shared challenge of achieving something better than yesterday’s best run.