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HS Code |
502182 |
| Chemical Name | 2-Benzylcyclohexanone |
| Molecular Formula | C13H16O |
| Molecular Weight | 188.27 g/mol |
| Cas Number | 16613-47-7 |
| Appearance | White to off-white crystalline solid |
| Boiling Point | 332.1 °C at 760 mmHg |
| Melting Point | 44-47 °C |
| Density | 1.06 g/cm³ |
| Refractive Index | 1.550 |
| Purity | Typically ≥98% |
| Solubility | Insoluble in water; soluble in organic solvents |
| Smiles | O=C1CCCCC1CC2=CC=CC=C2 |
As an accredited 2-Benzylcyclohexanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Benzylcyclohexanone, 25g: Supplied in a sealed, amber glass bottle with a tamper-evident cap and clear hazard labeling. |
| Shipping | 2-Benzylcyclohexanone is shipped in sealed, chemical-resistant containers to ensure safety and stability during transit. It is handled according to standard chemical regulations, protected from moisture, heat, and direct sunlight. Proper labeling and documentation accompany each shipment. Transportation complies with international regulations for non-hazardous organic chemicals. |
| Storage | 2-Benzylcyclohexanone should be stored in a cool, dry, and well-ventilated area, away from sources of heat, ignition, and moisture. Keep the container tightly closed and clearly labeled. Store away from incompatible substances such as strong oxidizing agents. Protect from direct sunlight. Use appropriate chemical storage cabinets and ensure spill containment measures are in place to prevent environmental contamination. |
Applications of 2-Benzylcyclohexanone in Industrial Manufacturing2-Benzylcyclohexanone is a specialty intermediate widely used across several industrial sectors, predominantly for its value as a keybuilding block in advanced synthesis pathways. As a direct manufacturer, we focus on supporting downstream partners in fine chemicals, pharmaceuticals, flavors & fragrances, and polymer additive segments. The following application scenarios outline typical industry adoption, compliance requirements, process roles, and expected finished goods. 1. Pharmaceutical Intermediate for CNS Active CompoundsPharmaceutical API manufacturers use 2-Benzylcyclohexanone as a critical intermediate in the synthesis of select central nervous system (CNS) agents. The raw material enters multi-step synthetic procedures, typically serving as a scaffold for further functionalization and cyclization reactions. Control over impurity profile and isomer ratio is essential, as downstream processing may include hydrogenation, alkylation, or acylation steps relevant to the target API. Production requires full compliance with stringent pharmaceutical industry regulations and rigorous documentation from the starting material onward. Industry compliance standards
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2. Precursor in Fragrance Ingredient ManufacturingIn the flavors and fragrances industry, processors deploy 2-Benzylcyclohexanone during synthesis of musky and amber-like aromatic compounds. Its unique cyclohexanone structure enables condensation or cyclization reactions that yield high-value fragrance bases, particularly those used in luxury perfumery and fine aroma compositions. Facilities handling such transformations must meet global IFRA standards and maintain strict process hygiene to avoid contamination with non-permissible byproducts. Industry compliance standards
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3. Intermediate for Agrochemical Active Ingredient SynthesisSelective pesticide and herbicide manufacturers utilize 2-Benzylcyclohexanone as a custom intermediate during the assembly of complex cycloalkyl-based agrochemical actives. The keto group’s reactivity supports regioselective alkylation and further ring functionalization, important for tailoring biological activity profiles. Compliance with agrochemical traceability and toxicity regulations is mandatory, and typical QC includes batch assay, impurity mapping, and documentation for export markets. Industry compliance standards
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4. Modifier in High-Performance Polymer Additive ManufacturingSpecialty polymer compounders may integrate 2-Benzylcyclohexanone as a chain-modifying or end-capping agent to improve plasticizer properties, UV stability, or mechanical flexibility in engineered materials. The unique benzylated cyclohexanone backbone can enhance compatibility and functional group availability in select thermoplastic and thermoset systems. Compliance with downstream sectors, including electronics and automotive, requires adherence to materials safety standards and robust documentation of additive migration and leachability testing. Industry compliance standards
Typical usage ratio
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From years spent in chemical process development, I’ve found that 2-Benzylcyclohexanone distinguishes itself in a tightly competitive field. This compound, produced through selective alkylation and hydrogenation routes, presents a clean cyclohexanone core substituted at the second position with a benzyl group. Our typical product grade sits at 98% minimum purity, supported by GC and NMR testing at each batch. As chemists, we know the devil is in the details—so exacting quality and reliable lot-to-lot consistency always come first on our plant floor.
Historically, 2-Benzylcyclohexanone shows up most often in research chemistry, especially where structure-activity relationships demand a bulky, aromatic cyclohexanone derivative. In our process, batch controls pay close attention to water and chlorinated solvent traces since sensitive reactions down the line tend to falter in the presence of these contaminants. I remember a project where a customer’s scale-up hit a yield wall traced back to a sub-ppm solvent impurity; solving it required several process tweaks, high-vacuum distillation, and patience during endpoint monitoring.
Most buyers originally approach cyclohexanone or cyclohexanone derivatives expecting rather broad chemical behavior, but the benzyl substitution at the 2-position changes both the reactivity profile and practical handling. Standard cyclohexanone, as used in nylon manufacture or as a solvent, reacts rapidly at the alpha-positions, and can undergo both electrophilic and nucleophilic substitutions with ease. With the benzyl group occupying the ring, the molecule’s electronic properties shift. We observe resistance to oxidation compared to unsubstituted analogs and a distinct selectivity in alkylation and condensation reactions. More than once we’ve received feedback from R&D teams noting that pathways viable for cyclohexanone either stall or result in unexpected side products with the 2-benzyl analog. Our job, as a production team, becomes less about making just another ketone and more about delivering material that meets the nuanced demands of structure-based project pipelines.
There’s also a marked difference between 2-Benzylcyclohexanone and benzylacetone or 4-benzylcyclohexanone. Placement on the ring impacts biotransformation, especially where enzymatic reductions or oxidations are in play. The 2-benzyl compound often resists enzymatic cleavage at the benzylic position, which can spell success or failure in medicinal chemistry optimization. From pilot to kilo scale, we routinely confirm the precise ortho-substitution using reference NMR spectra and mass spectrometry fragmentation. This prevents misassignments, which used to haunt earlier efforts with off-the-shelf material from third-party vendors. We handle verification in-house, training our QC team to spot the subtle differences in proton coupling patterns and splitting ratios.
Our customers often come from R&D departments of pharmaceutical and specialty chemical companies, chasing leads on new catalytic transformations or potential drug candidates. 2-Benzylcyclohexanone forms a starting point for building advanced chiral ligands or key intermediates in neuroactive compound synthesis. You’ll find it tested in reduction reactions, where stereochemistry at the ring can dictate the success of a project. Its resistance to base-catalyzed ring opening makes it more robust than comparable cyclic ketones. At our facility, any production campaign for this molecule involves careful dosing of reagents and temperature ramping profiles—overheating or insufficient agitation leads to colored impurities, which act as coordination poisons in downstream reactions.
Scale isn’t always straightforward. Several of our customers run both 100 g syntheses for discovery work and 20 kg campaigns for clinical trial material. Even as the base synthesis route remains constant, the work-up must change. Filtration media, solvent choice, and time under vacuum all influence not just product purity, but also how much active catalyst or residual inorganic base rides through to the final product. Our team has developed isolation protocols that allow crude product to be held without significant oxidation—an issue for less stable derivatives but manageable for 2-Benzylcyclohexanone thanks to our proprietary antioxidant system, which we blend in post-reaction and then scrub in the final purification.
On the production floor, operator safety and regulatory compliance cannot be afterthoughts. 2-Benzylcyclohexanone, with its low vapor pressure and mild, aromatic odor, behaves less aggressively than volatile ketones. The compound’s flash point and thermal stability give us some margin during distillation and solvent stripping, but repeated observation and monitoring remain essential. We’ve seen that even modest exposure over long cleanups can cause skin dryness and minor irritation, so our policy includes robust PPE, dedicated transfer pumps, and closed-loop nitrogen blanketing during bulk handling.
Spill management for this compound is more straightforward than with most cresols or chloroketones. We use clay-based adsorption, followed by containment and solvent mop-up for small releases. The solid tends toward pale yellow crystals at room temperature, rarely forming problematically viscous residues in plant drains. Disposal channels are predictable thanks to a well-documented degradation route in oxidative incineration.
Transparency in sourcing supports compliance and customer confidence. We never blend, cut, or rework product streams from external suppliers into our batches, which eliminates the risk of trace contaminants. Each batch carries legacy documentation showing every step, including exact lot numbers of upstream precursors, solvent grades, and the approved techniques for intermediate workup. Auditors have commented positively on our sample retention protocol, where retained vials from every shift run are available for up to five years post-manufacture, supporting back-tracking and root cause analysis in case of downstream issues.
Issuing a certificate of analysis doesn’t stop with checkboxes; our QC chemists record secondary data—chromatographic baseline purity, residual solvents, and even trace metals so procurement and regulatory teams are kept in the loop. Sometimes these details call attention to small adjustments or process improvements. For instance, a single outlier in water content from a raw material forced us to tweak drying times, which ultimately led to consistently better product.
Modern specialty chemical production faces hard scrutiny over both environmental burden and waste generation. We’ve engineered our 2-Benzylcyclohexanone process in response to this. Our plant cut halogenated solvent use by nearly 90% over the last three years. Hydrogenation now employs a closed manifold, eliminating atmospheric release, and every campaign finishes with recovered and purified process solvents, reducing both waste and operational costs. Filtration residues, once a mixture of spent catalyst and organic fines, are now separated, washed, and characterized in our in-house lab before external disposal or reclaim.
A successful campaign is measured not just in kilograms shipped, but in kilograms not discharged as waste. Our batch records show reductions in process water per kilogram of product and steady improvement in organic recovery rates. The drive to lower our energy profile has resulted in more heat integration, with waste-heat from one reactor feeding pre-warming loops for the next. These gains are incremental, but they add up to measurable sustainability improvements over time.
The sticker price of 2-Benzylcyclohexanone reflects more than just the sum cost of starting materials or the time on reactor. Routine QA/QC, segregation of raw material feeds, daily plant calibration, and investment in in-house method validation are all built into the product cost for a good reason. Early experience showed that cost-cutting in these areas solves little and risks a batch recall, which helps no one in the long run.
Comparisons with third-party traders often ignore the deeper process control and embedded risk management we conduct on-site. Substitutes sourced through distributors, especially generic grades, don’t match our batch-to-batch spec in surface-active impurity content. Over several years and projects, customers who tried outside sources typically returned to us for supply dependability. Whether for a two-liter round-bottom or plant-scale run, the importance of honest, traceable, and batch-specific technical support ranks above mere price tags in this industry.
Manufacturing 2-Benzylcyclohexanone does not end at drum shipment. Most synthetic chemists using this material need direct lines to the manufacturer for troubleshooting or ROH analysis. Our technical team spends as much time fielding complex questions about reactivity or alternative workups as we do with day-to-day logistical support. More than once, a customer sent over NMR and IR scans of failed test reactions, leading to on-the-fly adjustment recommendations that brought projects back on track.
Direct manufacturing gives us an edge. We control variable step temperatures, distillation profiles, and reaction monitoring with in-factory oversight. Daily, our staff logs temperature deviations, pressure anomalies, and feed rate fluctuations—reviewing outliers and making process adjustments before a deviation ever reaches the final tank. If a client requests non-standard lots, such as D-labeled or deuterated analogs, we already have the infrastructure and R&D methods validated to support it.
In chemical manufacturing, the learning never ends. Even established production routes surprise us. A shift supervisor once caught a barely detectable solvent carryover that would have polluted a pilot batch intended for scale-up synthesis. The lesson led to a procedural audit and the installation of redundant drying columns on the feed line. Failures are logged, reviewed, and drive our continuous improvement program—rarely is a problem isolated; process risk reduction cycles repeat across campaigns. Our story with 2-Benzylcyclohexanone is full of such cases.
Customers sometimes come with strict project deadlines and tight scheduling windows; small disruptions can cause a chain reaction of missed timelines. We plan double-batch reserves for these cases, holding extra stock as a buffer. A philosophy of transparent communication with our clients, including early warnings about scheduling or supply issues, ensures alignment and mitigates unpleasant surprises.
Research into new synthetic applications often leads to requests for higher-purity lots, special packaging, or absence of certain trace elements. Our plant responded recently to a spike in interest from neuroscience-focused startups developing new central nervous system (CNS) agents. They needed extra assurance that residual nickel from hydrogenation would remain under 5 ppm. In revising our process, we trialed three filtration approaches, ultimately settling on a dual-bed column that dropped metal traces to undetectable levels—even by ICP-MS.
Industry trends don’t follow static playbooks, so flexibility counts, both in synthesis design and interaction with clients. Repeat feedback cycles allow us to retool downstream processing, add customized analytics, and trace impurity profiles beyond standard specs. This adaptability brings added costs, but it also reinforces our reputation among companies who prize certainty over simple cost-savings.
Manufacturing 2-Benzylcyclohexanone is more than producing a chemical—it’s a practice grounded in daily attention to process, an ongoing conversation with clients, and a sustained attempt to push technical standards higher each year. Production means showing up every day, watching numbers, cross-checking results, and acting on what experience teaches in the high-stakes game of specialty chemical manufacture. Strong, ongoing relationships between buyers and ground-floor producers help untangle difficulties when they arise, allowing projects to continue instead of stalling at the material supply stage.
Problems will keep cropping up as regulatory and performance expectations evolve, and as new chemistry reshapes demand for building blocks like 2-Benzylcyclohexanone. Our job is to respond, anticipate, and keep lines open with those who rely on our material. Only through this kind of openness and technical depth can a specialty chemical truly support both discovery work and scalable production over the long haul.