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HS Code |
440999 |
| Name | 2-Benzyloxyaniline |
| Cas Number | 1637-39-4 |
| Molecular Formula | C13H13NO |
| Molar Mass | 199.25 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 61-64 °C |
| Boiling Point | 360.6 °C at 760 mmHg |
| Density | 1.17 g/cm³ |
| Solubility In Water | Slightly soluble |
| Smiles | c1ccc(cc1)COc2ccccc2N |
| Inchi | InChI=1S/C13H13NO/c14-12-7-4-5-11(10-12)15-9-13-8-2-1-3-6-13/h1-8,10H,9,14H2 |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, protected from light |
As an accredited 2-Benzyloxyaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g 2-Benzyloxyaniline is packaged in a sealed, amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | 2-Benzyloxyaniline is shipped in tightly sealed containers compliant with chemical safety regulations. It should be protected from moisture, heat, and direct sunlight. Packages are clearly labeled with hazard information and handled by authorized carriers following all relevant transportation guidelines for hazardous chemicals. Shipping documentation includes safety data sheets (SDS) and handling instructions. |
| Storage | 2-Benzyloxyaniline should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible materials such as strong oxidizing agents. Protect from light and moisture, and ensure proper labeling. Follow all relevant safety and regulatory guidelines for handling and storage to avoid contamination or hazardous reactions. |
Applications of 2-Benzyloxyaniline in Industrial Manufacturing2-Benzyloxyaniline functions as a key intermediate in diverse chemical value chains. Our proprietary synthesis ensures strict batch consistency, supporting advanced formulations and custom process needs among leading industrial sectors. The following segments reflect its best-established, compliant downstream uses. 1. Synthesis of Active Pharmaceutical Ingredient IntermediatesPharmaceutical manufacturers incorporate this compound during multi-step API production, especially for the preparation of complex aromatic intermediates. Aminobenzyloxy structures support selective functionalization reactions, such as amide formation and cyclization steps. Process engineers adjust charge ratios to optimize conversion and minimize impurities in regulated GMP environments; elevated temperature stages often use this material in a pre-coupling or acylation step. Output quality receives routine verification through HPLC and NMR compared to pharmacopeial standards. Industry compliance standards
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2. Specialty Dye and Pigment ManufacturingProducers of high-performance organic dyes employ 2-benzyloxyaniline for azo coupling and as a protected amine in chromophore synthesis. It serves as a nucleophile in diazotization and subsequent coupling reactions, supporting controlled molecular modification. Purity and reactivity profiles influence final color attributes and reproducibility in volume production. Process QC includes thin-layer and column chromatography coupled with UV-Vis spectral analysis to track intermediate conversion. Industry compliance standards
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3. Fine Chemical Intermediate for Agrochemical SynthesisAgrochemical formulators draw on 2-benzyloxyaniline as a precursor for synthesizing active crop protection agents, especially in aromatic heterocycle assembly. It participates in nucleophilic aromatic substitution and condensation with esters or chlorinated derivatives to form key fungicide and herbicide backbones. Reaction scalability and impurity suppression are critical, as regulatory authorities monitor residuals and transformation byproducts in end-use formulations. Continuous synthesis lines integrate in-line GC-MS for real-time monitoring. Industry compliance standards
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4. Polymer Additive and Crosslinker ManufactureSpecialty resin producers utilize 2-benzyloxyaniline as a reactive modifier during synthesis of thermoset and engineering plastic materials. Amine moieties, protected by benzyloxy substitution, allow controlled introduction during polymer backbone formation, especially in epoxy and polyimide systems. This increases flexibility during curing and modifies final mechanical properties. QC labs use quantitative NMR and FTIR to certify incorporation and residual content meets industry and client acceptance limits. Industry compliance standards
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At our chemical plant, every batch of 2-benzyloxyaniline represents the result of decades working hands-on with aniline derivatives. Our chemists still remember the first kilo we made; much has changed, yet the backbone of production—meticulous quality control and respect for every step—remains unchanged. Each day, workers on the shop floor and in the lab focus on providing this fine organic intermediate to customers without compromise.
2-benzyloxyaniline, C13H13NO, distinguishes itself with its purity and performance in both research and commercial synthesis. This compound carries a benzyl-protected hydroxy group on the aniline ring's ortho position. We produce it regularly, following strict protocols, as a white to light beige crystalline powder with higher purity grades available according to demand. Chemists familiar with aromatic amines know its clean reaction profile and stable bench behavior, so trusted by users in industries that cannot allow a mistake.
We run the synthesis at scale using carefully sourced benzyl chloride and o-aminophenol, tracking every variable from batch to batch. Each run sees close monitoring by technicians who know the process in depth—down to the way the crystals look under the microscope and the aroma of the filtered product. Every kilogram comes through purification steps that remove potential colored or resinous impurities. This hands-on familiarity has taught us how small changes affect melting point, solubility, and even how the compound behaves in downstream reactions.
Analytical testing accompanies each batch. Thin-layer chromatography, gas chromatography-mass spectrometry, and melting point analysis give us quick assurance that the material meets strict specifications. Residual solvents and byproducts get flagged at trace levels. We invest time and money in traceability because a missed impurity at our end can turn a customer's reaction crosstown into a failure. No customer needs to ask us about batch-to-batch consistency—QC is a habit, not a policy.
Most clients request 99% or better purity for 2-benzyloxyaniline, but over the years, we've also supplied lower and custom grades for special applications. Some need the free-flowing powder for packing into automated reagent feeders; others request it pre-packed under inert atmosphere due to sensitivity to oxidative discoloration on storage. The melting point, usually in the 68-72°C range, and solubility in standard polar organic solvents influence applications and shipping conditions, so we pay attention to those outright. Detailed Certificates of Analysis follow every batch, recording moisture, appearance, and residual byproducts.
Every manufacturing run gets documented for internal traceability. Logistic staff label each drum with precise lot codes, and every product sits in sealed, tamper-evident packaging. These practicalities make the difference when customers audit our plant or send their own samplers for side-by-side analysis. We've learned that great attention to proper labeling, container closure integrity, and neat paperwork—not merely in-lab purity claims—helps our customers meet regulatory demands downstream.
2-benzyloxyaniline serves as a reliable intermediate for making specialty dyes, agrochemicals, and advanced pharmaceuticals. In our experience, few compounds offer such dependable reactivity for complex coupling and protection-deprotection schemes in aromatic systems. Multiple pharmaceutical projects have succeeded when our product replaced less reliable imports. Synthetic chemists in R&D praise the compound's role as a building block for dye precursors, kinase inhibitors, and advanced materials.
For those in colorant manufacturing, this molecule acts as a crucial node in the synthesis of azo and heterocyclic dyes, offering high color yield and good fastness. It helps clients formulate dyes that withstand sunlight and washing cycles—a key demand for textile and ink industries. Pharmaceutical chemists use its benzyl group as a temporary protecting group, removed cleanly in final steps without unwanted side reactions or contamination, thanks partially to how we control trace metals and halide byproducts during our process.
We've worked closely with start-ups scaling up novel compounds where every step relies on intermediates like this one. Our consistent product lets them focus on innovation, not supply chain hiccups. Their feedback rounds out our manufacturing approach—lessons we use to make tweaks in both quality and availability. Our technical team always watches for trends in downstream uses. Right now, we see growing interest from researchers developing new classes of fluorescent probes, as the ortho-benzyloxy substitution brings unique optical properties after further functionalization.
Customers often ask what sets 2-benzyloxyaniline apart from similar aniline derivatives like 4-benzyloxyaniline or 2-methoxyaniline. Chemically, the ortho position of the benzyloxy group in our product impacts its electronic and steric properties, driving differences in subsequent reactions and the overall stability of derived compounds. We see how even subtle changes in substitution patterns backfire in sensitive reactions: a customer once tried swapping for a para-substituted version and reported major drop-offs in yield.
Unlike 2-methoxyaniline, which trades the benzyloxy group for a methoxy, 2-benzyloxyaniline offers a removable protecting group that adds bulk, increasing selectivity in protection strategies. This matters when complex molecules need selective functionalization without overreacting or scrambling. Our experience shows that certain dyes turn out far brighter and more stable when built from the ortho-benzyloxy rather than methoxy intermediates. This is more than theory—years of hands-on results back it up.
From a handling standpoint, our compound also outshines related products in its solid state stability and shelf life, provided proper packaging. The bulk and aromatic character of the benzyloxy group guard against unwanted side reactions that sometimes plague less hindered analogues. Over the years, we’ve seen that oxidation—common in storage for many aniline-type molecules—progresses slowly with our 2-benzyloxyaniline, saving clients from color changes or losses in active content before use.
Since we oversee every step from raw material selection to final delivery, we recognize the anxiety customers face sourcing critical intermediates. Our approach keeps supply lines robust through local sourcing networks and global contacts we’ve cultivated over decades. This attention to procurement keeps us running when others face shortages or price swings in benzyl chloride or aniline base stocks.
Our own warehouse team keeps enough inventory throughout the year to buffer seasonal swings. At the busiest times, the team works late, careful to avoid any mislabeling or cross-contamination risks. In the past few years, chemical regulations have grown stricter worldwide. We have never viewed compliance as a box-ticking exercise—our regulatory team checks every newly sourced raw material and every waste stream. Our history with audits by customers and global agencies covers every inch of our operation, which boosts end-user confidence.
Feedback from customers shapes a better product for all. Once, a research group flagged a faint yellowing in a shipment destined for high-purity synthesis. They sent detailed photos and spectra. We tracked the batch internally to the source drum and tweaked final filtration parameters. The next run emerged colorless throughout. This openness—honest error tracking and full record-keeping—forms a real partnership; we see our clients benefit, the plant improves, and the cycle repeats.
Our process for making 2-benzyloxyaniline borrows both from legacy chemistry and recent advances. In past decades, purification relied on repeated crystallization and careful draining to yield a clean product. Increasing throughput brought opportunities for continuous extraction and modern filtration, but every upgrade needs careful vetting to avoid compromising specs. Last year, we upgraded solvent recovery, cutting emissions while delivering a cleaner product—a challenge worth the weeks spent in pilot testing.
Handling hazardous reagents obliges us to maintain both physical protection and incident response plans, updated by training drills and real-world feedback. There have been rare occasions where byproduct build-up forced an unplanned production stop. Our plant crews engage daily in practical risk reduction—double-checking reagents, cleaning workups, logging reactor inspections—to keep every run safe. These realities rarely show up in glossy marketing brochures, but in the trade, safety and reliability stand hand in hand.
Environmental controls affect every part of our process. From solvent selection to emissions scrubbing and waste acid recovery, our factory budget far more time and resources for environmental compliance than most outsiders realize. Years back, a local inspector challenged our vent stack emissions calculations, prompting a full system overhaul. Today, data loggers track emissions monthly, and wastewater leaves our plant only after tight treatment and double checks, documented for both records and peace of mind.
As the manufacturer, we hold responsibility for supplying a safe, reliable product. That philosophy extends beyond our gates—all labeling, documentation, and MSDS preparation reflect our knowledge of where and how 2-benzyloxyaniline is used. Clients receive not just a drum or bottle, but full traceability and guidance based on our own shop floor experience. We advise on preferred storage—dry, dark, and cool, humidity below 60%—to minimize risks of self-heating and oxidation. These recommendations come from our own real-world losses, not just literature.
Packaging evolved through years of feedback. We shipped early quantities in thin poly bags nested inside cardboard; occasional complaints of product clumping in humid environments nudged us to develop multilayer, vapor-barrier liners and heat-sealed, tamper-evident closures. Now, long shipping routes pose fewer headaches for our overseas customers, and no residue leaps out on opening. Still, every receiving chemist should transfer and close the product promptly. Problems always surface when materials sit out too long, so a bit of speed and care after arrival ensures best results downstream.
We watch first-hand as more customers push beyond standard uses. Some recent consignees work on OLED materials, peptide modifications, or novel light-absorbing compounds. The feedback loops between our factory and end-users sharpen our methods and allow for custom runs or process tweaks on quick turnaround. Academic researchers contact our lab seeking help with purification beyond standard grades; industrial innovators call us in for troubleshooting when unexpected side products crop up, tracing them down to subtle issues in the starting material substitution.
Cost control ranks high among concerns, especially as energy and feedstock prices rise. We work with clients to design minimum-waste, batch-optimized shipments. Some request drums under nitrogen for longer storage; a few demand split-lot sampling and staged delivery. These needs challenge us to stay nimble and humble. Each request brings new insights—sometimes the solution is as simple as an extra day in drying, or as complex as redrafting a batch protocol to eliminate a recurring byproduct noted in a downstream reaction.
What seems a minor intermediate to outsiders can make or break a production line, research campaign, or even an entire product launch. We understand this intimately. Our team—many of whom spent whole careers with us—recognize their handiwork in every bottle reaching a distant research lab or production site. Errors matter, and wins count not in sales volume but in problem-free shipments and calls of thanks from clients who finally cracked a stubborn synthesis.
We hear stories from end users measuring the last grams conserved for a tricky reaction after shipments delayed by storms. Others share their scaling success after switching from a less reliable or less pure supplier. Not every story ends well, but the role a stable, high-quality intermediate like 2-benzyloxyaniline plays proves essential. Old hands in the trade know that behind every clean HPLC trace lies months—often years—of patient manufacturing improvements and a commitment not to cut corners. We remain dedicated to supporting those who work in the lab or plant, crafting new molecules, processes, and products that lead the industry forward.
The work behind every shipment of 2-benzyloxyaniline extends beyond synthetic pathways and analytical results. It encompasses trust, transparency, and an ongoing dialogue with end-users, regulators, and our team. As manufacturers, we recognize the responsibility of supporting innovation and advancing quality standards that keep downstream processes running smoothly. Future success relies on continuing this partnership—delivering on our promises, listening closely to those on the front lines of chemistry, and never ceasing to improve.