|
HS Code |
328261 |
| Chemical Name | Benzyl hydantoin |
| Cas Number | 535-47-3 |
| Molecular Formula | C10H10N2O2 |
| Molecular Weight | 190.20 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 132-136°C |
| Boiling Point | 424.2°C at 760 mmHg |
| Solubility In Water | Slightly soluble |
| Density | 1.29 g/cm3 |
| Flash Point | 210.4°C |
| Smiles | O=C1NC(=O)N(Cc2ccccc2)C1 |
| Pubchem Cid | 11989 |
As an accredited Benzyl Hydantoin factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White crystalline powder sealed in a 100g amber glass bottle, labeled "Benzyl Hydantoin," with hazard and handling instructions. |
| Shipping | Benzyl Hydantoin should be shipped in tightly sealed containers, protected from moisture and light. Store and transport at room temperature, in compliance with local and international chemical transport regulations. Ensure proper labeling, documentation, and handling precautions to avoid spills or exposure. Not classified as hazardous for transportation under most guidelines. |
| Storage | Benzyl Hydantoin should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. It should be kept in a cool, dry, and well-ventilated area, ideally at room temperature. Avoid exposure to sources of ignition and incompatible substances such as strong oxidizing agents. Always label the container clearly and follow relevant safety and handling guidelines. |
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Purity 99%: Benzyl Hydantoin with purity 99% is used in pharmaceutical syntheses, where it ensures high yield and minimal impurity formation. Melting point 125°C: Benzyl Hydantoin with a melting point of 125°C is used in agrochemical intermediates, where it provides consistent thermal stability during formulation. Particle size <50 microns: Benzyl Hydantoin with particle size less than 50 microns is used in fine chemical manufacturing, where it enhances reaction kinetics and uniform dispersion. Stability temperature 150°C: Benzyl Hydantoin with stability temperature up to 150°C is used in polymer additives, where it maintains performance integrity under processing conditions. Moisture content <0.5%: Benzyl Hydantoin with moisture content less than 0.5% is used in specialty resin synthesis, where it reduces hydrolysis risk and improves product shelf life. Molecular weight 190 g/mol: Benzyl Hydantoin with molecular weight 190 g/mol is used in biochemical research, where it supports reproducible assay performance and standardization. Viscosity grade low: Benzyl Hydantoin with low viscosity grade is used in coating formulations, where it enables smooth blending and uniform surface application. Assay 98% HPLC: Benzyl Hydantoin with 98% assay by HPLC is used in medicinal chemistry, where it provides accurate dosing and reliable pharmacological profiling. |
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Benzyl Hydantoin has become a familiar name for chemists and industry professionals who value consistency and practical performance over gimmicks. The model most recognized in labs and manufacturing facilities is the unsubstituted 5-benzyl derivative, a white crystalline compound with a subtle, almost chalky scent. Just by glancing at the pile on a glass dish, you’ll notice a solid granule that doesn’t clump or cake under normal conditions. The chemical formula—C10H10N2O2—sets it apart from ordinary hydantoin compounds, marking a step ahead from the base hydantoin structure by attaching a benzyl group to the fifth carbon of the ring core.
Practical experience with Benzyl Hydantoin tells a story of versatility. It doesn’t claim to change the world overnight, but it has helped many projects run smoother, from pharmaceutical synthesis to specialty chemical production. After spending years with crowded storerooms, I’ve seen why companies gravitate toward this compound: it behaves predictably under pressure, heat, or exposure to common solvents such as ethanol or acetone. In the business of scaling up reactions or refining product lines, surprises in reactivity can mean lost time and wasted money—something this compound sidesteps gracefully.
Looking closer, the structure of Benzyl Hydantoin opens doors to a handful of reactions. The hydantoin ring provides two nitrogen atoms with a keen ability to participate in ring-opening reactions, and that makes the compound adaptable in synthesis. The benzyl group increases the molecule’s stability against hydrolysis, especially when compared to methyl or ethyl-substituted hydantoins. It gives the compound a handy balance of stability and reactivity that chemists appreciate when they’re working on new intermediates or APIs.
Research into the molecule’s physical properties backs up the anecdotal experience. Melting at around 130°C, it resists low humidity and does not deliquesce under normal lab conditions. This creates an edge in storage and shipping—two trouble spots where less robust compounds break down, sometimes causing contamination or even product recalls.
Solubility in water runs average, but you’ll notice improvement in polar organic solvents, which comes in handy during purification or formulation steps. It’s these subtle but real advantages—borne out by empirical testing and day-to-day practice—that build trust over years, not just product cycles.
The pharmaceutical sector remains a major user. As early as the 1970s, Benzyl Hydantoin caught attention as a stable intermediate in the synthesis of anti-epileptic drugs. More recently, some research mentions its potential role in forming optically pure amino acids, critical for custom peptide production. In both settings, I’ve seen that the compound’s resistance to uncontrolled side reactions means fewer failed batches, saving anxiety in QA labs.
Beyond medicine, Benzyl Hydantoin enters the realm of specialty chemicals. Industrial plants find value in its role as a building block for resins and high-performance polymers. In everyday practice, this often means equipment that lasts longer: fewer fouling deposits, less breakdown during heat cycling, and easier cleaning. While benzylated derivatives cost more than simple hydantoins, the lower downtime and higher product yield often balance out the extra expenditure.
Choosing Benzyl Hydantoin can feel like opting for a pair of sturdy work boots instead of flashy sneakers. Consistency, grit, and day-after-day reliability count for more than short bursts of promise. In manufacturing, this translates to fewer headaches chasing down the source of impurities, or dealing with inconsistent product weights and textures. Anyone who has watched a production line grind to a halt over a stuck pump knows the value hidden in a reliable granular compound.
Since the product brings in a pure benzyl group, those working in synthetic organic chemistry benefit from its clear, stable reactivity profile. There’s no sifting through extraneous byproducts or wrestling with color changes that can complicate downstream analysis. Often, those saved hours add up across years, helping push a process from the test bench to full-scale output.
Back in the storeroom, Benzyl Hydantoin stores cleanly in sealed containers, and does not require exotic handling or expensive containment. I've seen bulk drums survive long cross-country hauls, with product integrity steady and little sign of breakdown, even after months in less-than-ideal warehouse corners.
Comparison with other hydantoin derivatives gives more depth to Benzyl Hydantoin’s reputation. Take methyl or ethyl hydantoins as examples. They show a higher tendency toward hydrolysis, which can turn a sealed sample into a pasty mess—an annoying risk for any engineer or lab technician. Aromatic substitutions like phenyl hydantoin offer stability, but they often lack the fine-tuned balance of reactivity and selectivity seen with the benzyl group.
Brominated and chlorinated hydantoins, well known for their use as biocides in water treatment, find homes in pools and hot tubs, but pose different hazard profiles and need tighter environmental controls. These don’t fit pharmaceutical use where purity, predictable byproduct formation, and low toxicity are vital. Benzyl Hydantoin’s clean breakdown, stability, and safer storage draw a sharp distinction here.
Many modern production managers have shifted to Benzyl Hydantoin to avoid compliance headaches. The compound’s byproducts rarely trigger the same regulatory red flags associated with halogenated hydantoins. This lightens the compliance workload, letting teams focus on improvement instead of endless rule-checking.
Scaling up Benzyl Hydantoin production has its quirks, but it needn’t overwhelm a decently equipped facility. The main challenge arrives from the precision needed at the condensation step—something seasoned chemists recognize as a pivotal stage. NMR and IR analyses confirm batch-to-batch consistency, a crucial factor if a manufacturer promises reliable supply for medical or fine chemical use.
Those formula tweaks—whether for wet granules, powder, or compacted blocks—depend on end-use specifics. For oral pharmaceutical intermediates, micronization amps up bioavailability. In polymer resin production, slightly coarser crystals work best, keeping the melt flow predictable. The lack of strong odor or taste in the finished material gives it an edge in these uses, as it does not interfere with flavor or scent in sensitive formulations.
I remember a pilot plant run for an epoxy resin project. Swapping in Benzyl Hydantoin lowered the rate of side product formation by more than a third, cutting waste and nozzle clogging. The formula flexed to accommodate a higher solids load without gumming up, pushing productivity above targets.
Modern users expect not just performance but a sustainable supply chain. Benzyl Hydantoin producers have responded, moving toward greener synthesis protocols and phasing out harmful catalysts where possible. Lifecycle assessments, published by research groups, highlight lowered solvent waste and energy use for most commercial processes.
On the compliance side, Benzyl Hydantoin rarely features on restricted substance lists. This matters to medical device companies focused on RoHS and REACH rules, where ambiguous chemical status can derail a product launch. With Benzyl Hydantoin, the paperwork clears faster, letting developers focus on bringing products to market instead of scrambling for last-minute alternatives. That said, waste must still be managed sensibly—no shortcut makes up for careless disposal practices.
In my own experience, audits involving Benzyl Hydantoin inventory wrap up quicker. Inspectors recognize the compound and know it doesn’t demand extensive hazard controls. The relatively benign breakdown products make life simpler for downstream recyclers as well.
Much of Benzyl Hydantoin’s value shows up in the small details of daily handling. Unlike some specialty chemicals which demand desiccators or inert gas blankets from the moment a drum opens, Benzyl Hydantoin fares well in common ambient warehouses. Laboratory users can scoop out portions without panic over runaway humidity or airborne dust events.
Workers report few, if any, irritation risks from inhalation or skin contact, assuming typical chemical hygiene routines. Material Safety Data Sheets point out the need to avoid deliberate ingestion or protracted exposure, but these precautions don’t go far beyond normal industrial practice. In larger settings, spill containment isn’t complicated by excessive dust or fume release, minimizing risk of workplace incidents.
Switching manufacturing inputs rarely goes without friction. Introducing Benzyl Hydantoin can spark concerns over compatibility, sourcing, and cost. For teams who’ve invested years tuning a line to work with the quirks of a different hydantoin variant, even subtle molecular changes spin out new SOPs. Missteps at the interface with downstream processes—be it a subtle shift in crystallinity or an unexpected tweak to dissolution time—can trigger hiccups at scale.
Most issues, though, correct themselves quickly. Early collaboration between quality control and process engineers often smooths out implementation. Batchwise trials, running side by side with legacy inputs, reveal whether minor process changes are needed. Some teams build in a buffer period for troubleshooting, letting routine problems emerge before formal signoff. This hands-on approach, learned from long nights debugging blends on shop floors, works better than endless paperwork or theoretical modeling alone.
Cost concerns often surface in budgeting sessions. Upfront, Benzyl Hydantoin sometimes looks like the pricier pick. Tracking yield, raw material waste, and cleaning time over six months often points to net savings. The real wins hide in reduced batch failures, less downtime for cleaning, and smoother audits. Trusted suppliers invest in open communication and provide full traceability: I’ve seen how this builds peace of mind, especially when dealing with high-stakes medical or consumer product rolls.
Looking at the research pipeline, Benzyl Hydantoin stands to see even broader use. I read through recent journal articles describing its role in custom peptide synthesis—a rising interest as biotech firms design next-generation therapeutics. Researchers also see untapped potential as a scaffold for enzymatic modifications, which could produce greener synthetic routes to rare amino acids or fine chemicals.
Regulatory shifts nudge research toward more benign alternatives for common plastic additives and flame retardants. Here, derivatives like Benzyl Hydantoin may soon step into applications from wire insulation to electronics, possibly trimming the field’s reliance on less sustainable brominated compounds. For anyone following chemical policy developments over the past decade, smart adaptation to these rules promises a safer, more durable product landscape, where compounds like Benzyl Hydantoin play an increasingly central role.
Benzyl Hydantoin isn’t flashy—it doesn’t show up as a flagship product in glossy marketing brochures or dominate splashy trade show booths. Its standing grows from a quiet, steady reputation among practitioners who value showing up every day with dependable, straightforward tools. Even though alternative compounds crowd the market, those who have handled Benzyl Hydantoin firsthand understand the confidence that comes from seeing batch after batch come out as expected, with minimal fuss.
A lot of the future for Benzyl Hydantoin will depend on how industries keep pushing for both performance and reduced environmental impact. Its proven track record, manageable hazard profile, and ease of storage and handling give it an edge over riskier or less consistent options. As I look back over the piles of field notes, lab reports, and shipping logs collected through years of firsthand experience, one pattern holds true: the work gets easier when the materials just do their job, day in and day out. For me—and for many colleagues—Benzyl Hydantoin has quietly earned its place on that short list of reliable chemical building blocks that quietly support modern science and manufacturing.