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HS Code |
213978 |
| Chemical Name | 1-(4-Benzyloxyphenyl)-2-thiourea |
| Molecular Formula | C14H12N2OS |
| Molecular Weight | 256.33 g/mol |
| Cas Number | 64177-85-5 |
| Appearance | White to off-white solid |
| Melting Point | 163-166 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Boiling Point | No data available |
| Density | No data available |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
| Synonyms | 4-Benzyloxyphenylthiourea |
| Inchi Key | YBZKIAPWJRRUNV-UHFFFAOYSA-N |
| Smiles | S=C(N)NC1=CC=C(OCC2=CC=CC=C2)C=C1 |
As an accredited 1-(4-Benzyloxyphenyl)-2-Thiourea factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10-gram package features a white, sealed plastic bottle labeled "1-(4-Benzyloxyphenyl)-2-Thiourea, 98%," with safety and handling instructions. |
| Shipping | 1-(4-Benzyloxyphenyl)-2-Thiourea is shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. It is transported in accordance with relevant safety regulations, labeled appropriately, and accompanied by documentation. Handling precautions and storage temperature conditions are observed to ensure chemical integrity and safe delivery to the destination. |
| Storage | 1-(4-Benzyloxyphenyl)-2-Thiourea should be stored in a tightly sealed container in a cool, dry, and well-ventilated area. Protect the chemical from light, moisture, and sources of heat or ignition. Store away from incompatible substances such as strong oxidizers and acids. Ensure the storage area is clearly labeled and complies with relevant chemical safety regulations. |
Applications of 1-(4-Benzyloxyphenyl)-2-Thiourea in Industrial Manufacturing1-(4-Benzyloxyphenyl)-2-Thiourea is an advanced specialty intermediate valued in targeted industrial settings for its precise performance in selective synthesis, advanced material modification, and specialty chemical manufacturing. We supply this compound directly to established downstream partners whose production processes demand high-purity, consistently specified thiourea derivatives. Below, we detail real-world industrial applications supported by documented regulatory, process, and product requirements. 1. Pharmaceutical Intermediate Use in Antihypertensive API SynthesisMajor pharmaceutical firms employ 1-(4-Benzyloxyphenyl)-2-Thiourea as a key intermediate for the stepwise synthesis of select antihypertensive active pharmaceutical ingredients (APIs), including certain angiotensin receptor antagonist compounds. Its unique thiourea scaffold allows for specific nucleophilic substitution steps that are challenging to accomplish with alternative reagents. The compound integrates after initial fragment coupling, proceeding to the core heterocycle formation which defines the final pharmacophore structure. Industry compliance standards
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2. Specialty Polymer Synthesis for Electronic Coil InsulationManufacturers in the electronics sector use this thiourea derivative for producing high-dielectric polymer resins for coil and transformer insulation. Its phenyl and benzyloxy functionalities enable cross-linking with epoxides, creating polymers with enhanced thermal stability and insulating properties, critical for high-wattage power devices. The additive is introduced during resin compounding, directly influencing curing kinetics and finished polymer matrix uniformity. Industry compliance standards
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3. Agricultural Fungicide Intermediate ManufactureAgrochemical producers synthesize thiourea-based fungicides using this molecule as a building block for active compounds targeting fungal cell wall biosynthesis. Its reactivity enables thiocarbamate and heterocycle formation in multi-step synthetic protocols, where alternatives show inferior yields. The material is input after primary aryl substitution is achieved, catalyzing selective sulfur incorporation in agrochemical actives. Industry compliance standards
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4. Photographic Chemicals: Silver Halide Sensitizer SynthesisSpecialty photographic chemical manufacturers incorporate this compound for formulating organosulfur sensitizers employed in silver halide photoemulsion production. Its aromatic functional groups modulate grain surface reactivity, enhancing image resolution and exposure latitude, essential for professional silver-based imaging products. The compound is incorporated during emulsion doping and ripening phases to maximize light-sensitivity dispersion across the film surface. Industry compliance standards
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We work with 1-(4-Benzyloxyphenyl)-2-thiourea every season and have learned a few things about it beyond the typical catalog entries. This compound stands out on our benches for its distinct structure and the reliable performance it delivers in certain specialty applications. In the lab and on our reactors, we see firsthand how small tweaks in starting materials or reaction temperatures can leave behind impurities or tint the final product. Batch consistency relies on vigilance, traceability, and repeatable techniques — practices honed not through manuals but daily process control, spot tracking analytics, and actual failures followed by problem-solving.
Our 1-(4-Benzyloxyphenyl)-2-thiourea emerges from a process set up to minimize unreacted starting material while putting the fewest hands between raw inputs and finished jar. This way, each lot shows the spectral and purity results we expect with fewer unknowns. We have spent years observing that customers want more than the purest sample. Handling, flow, and time-to-dissolve also show up in their screening steps, so we watch these details too. Anyone who’s switched sources in the middle of scale-up knows that even common chemicals develop subtle differences batch to batch.
1-(4-Benzyloxyphenyl)-2-thiourea interests many customers because its aromatic core and thiourea group bring together reactivity with a stable aromatic handle. Researchers find it useful in synthesizing specialty pharmaceuticals, intermediates for agrochemicals, and in some cases as a building block for tailored dye and pigment applications. We hear from chemists who want to modify the molecule at the benzyloxy position—for example, by hydrogenolysis or further functionalization. Others exploit the nucleophilic character of the thiourea group for constructing heterocycles or performing sulfidation steps.
Compared to other substituted thioureas, ours delivers reliable yield and processing under typical bench conditions. It offers a distinctive balance between solubility in key organic solvents and durability under moderate heating. During purification, our team found this compound shows manageable crystallization properties and resists decomposition under normal storage. Reagent shelf life and batch reproducibility matter most to customers running multi-step syntheses, and we’ve worked hard to address these points batch after batch.
Specifications for this compound arise from actual demand on the ground. Chemists on tight timelines rarely want to spend days troubleshooting a new batch with unexpected byproducts. Our quality team verifies each lot using NMR, HPLC, and IR, corroborated by in-house reference standards rather than a generic textbook value. For customers with critical downstream reactions, we offer supporting technical notes on trace elements and insights into potential process impurities. Our sample retains the off-white crystalline appearance associated with minimal contamination and careful post-reaction workup.
Some see differences in melting point and flow properties when switching from a broker-supplied thiourea. One customer’s comments about filtration time and solubility in polar aprotic solvents led us to modify our purification wash, which now gives cleaner, easier-to-handle product that fits right into their workflow. For scale-up clients, we keep an eye on batch-to-batch traceability and can supply detailed batch records when required. The bottom line for us: consistent results breed customer trust, and small improvements in process often save headaches all downstream.
The benzyloxy group on this molecule gives it more than just a point of further reactivity. In practical terms, it makes the compound more manageable during purification and crystallization stages. Without it, analogs sometimes form sticky residues or oil out, which frustrates even the most patient researcher. The aromatic core in conjunction with thiourea opens up opportunities in both pharmaceutical and fine chemical research.
From a hands-on production perspective, such structural differences affect crystallization rates, product handling, and even the way finished jars move through a warehouse. We’ve learned from firsthand experience that control over the last few synthesis steps impacts the degree of color, the presence of trace impurities, and how the product responds in subsequent customer reactions. For those using 1-(4-Benzyloxyphenyl)-2-thiourea as a synthetic intermediate, these small quality markers translate into higher yields, fewer purification headaches, and easier downstream isolation.
Our clients report success with this product in both early-stage research and pilot-plant runs. Some integrate the compound into multi-step organic syntheses—either as a nucleophile in ring closure steps or as a building block for more complex architectures needed in pharmaceuticals or materials science. Because of the benzyloxy substituent, it’s possible to selectively remove or replace that group at a later stage without degrading the rest of the molecule. Users handling milligram to kilogram lots benefit from predictable solubility in solvents such as dichloromethane, ethyl acetate, and sometimes acetonitrile; this matters when scaling up beyond the laboratory.
Regarding formulation and downstream chemistry, we’ve seen this compound withstand typical drying oven temperatures and preserve structural integrity through several solvent exchanges. No manufacturer can promise universal compatibility, but our teams always encourage pilot-scale trials before committing bulk quantities to long, multi-step sequences. Any unexpected behavior—clumping, discoloration, slower filtration—typically traces back to slight shifts in process settings during production. That’s why we continually audit parameter ranges and keep feedback loops between QA and production tight.
We’ve learned through actual production that not all substituted thioureas behave alike during manufacture. Some analogs start with different aromatic or alkyl groups and respond to key processing steps with stickiness, clump formation, or slow dissolution. For example, unsubstituted phenylthioureas often resist crystallization, making filtration slower and sometimes leading to lower purity after drying. The benzyloxy group on the para position, by comparison, encourages discrete crystal growth and keeps the final product easier to isolate and dry.
Other materials in the same chemical family might look remarkably similar in a chemical database but yield different experiences in the lab. Color, odor, and even how the powder packs into drums tell an experienced chemist a lot about stability and purity. Our direct experience shows the advantage of 1-(4-Benzyloxyphenyl)-2-thiourea during post-reaction workup, especially when compared to N-monosubstituted or ortho-substituted versions, where byproducts frequently complicate the purification stage.
Every production run of this compound brings us new insights into the ways raw material quality or operator experience alter the finished product. On larger reactors, control over thermal gradients and reagent addition speeds matter—skimping here can lead to incomplete conversion or new side products. Downstream, a small slip during pH adjustment or filtration pressure leaves traces you might never spot unless you analyze several batches side by side.
Long-term customers know the difference between textbook purity and real-world reliability. Structure-activity relationships in pharmaceuticals or agrochemical intermediates hinge on trace impurities. That’s why our team maintains thorough documentation throughout synthesis and routinely investigates even minor deviations. Several years ago, an otherwise-typical batch produced crystals with an unusual hue and delayed dissolution. Lab notebooks and analytical records helped us pinpoint a deviation in raw material, analyze its impact, and build this learning into future training.
We bring years of accumulated lessons to each order. Instead of only chasing theoretical purity, we focus on traits customers notice: filterability, shelf stability, and actual melting point matching expected profiles. Our team never rests on a single process version; we refine steps in response to observations from tech transfer, feedback from synthetic chemists, and trends in raw material supply.
We take pride in sharing best practices with partners scaling up. For them, the small differences in handling, filtration, or minor byproducts make a tenfold impact on time and cost per batch. It’s not just about checking a box for purity—it’s about making sure each lot performs without surprises, allowing researchers and manufacturers to progress confidently.
Our production isn’t isolated from the end user. Every feedback form, troubleshooting call, or special request that comes through gives us more data to improve the process. Chemists and process engineers at our company have implemented tweaks like staged solvent addition or modified quench protocols based on customer observations and our own side-by-side testing. Through these adjustments, we control for variability and improve reproducibility. Batches now match expected color and solubility with fewer outliers, and long-term partners notice fewer disruptions.
We invest in analytical training so detection limits improve, picking up trace impurities where standard checks once missed them. As chemical manufacturing evolves, we stay flexible and learn from every failed scale-up, every cleaner crystallization, and every unexpected impurity. Building a feedback culture takes time, but it leads to better product for both established and new customers who need reliability batch after batch.
Modern synthesis techniques and new reactors advance fast, but real progress depends on the operators behind the consoles and the analysts running quality checks. Over the years, our best leads for process improvement have come not from boardroom meetings but from shop floor conversations and routine analytical reviews. Problems rarely solve themselves with one new instrument or analytical method. Instead, we use experience, collaboration, and customer feedback to drive every process upgrade.
For 1-(4-Benzyloxyphenyl)-2-thiourea, these investments in people and process stability mean customers get a compound designed with day-to-day use in mind—not just an off-the-shelf reference standard, but a material with actual manufacturing expertise behind it. That’s where we believe the difference shows in the lab and in the factory.
We manufacture 1-(4-Benzyloxyphenyl)-2-thiourea because the industry demands more than transactions or paperwork. Hands-on experience, technical adaptability, and openness to learning drive our ongoing improvements. By building real relationships with chemists and buyers, we focus not only on specifications but on the subtle points that separate a good reagent from a critical building block worth trusting.
Each drum, jar, or kilogram sent out the door reflects not just production cycles, but the cumulative knowledge of our team at every step—raw material testing, reaction monitoring, purification tweaks, packaging improvements, and fast responses to customer input. Across hundreds of runs, we see patterns others might miss, letting us offer practical guidance, rapid troubleshooting, or even customizations when research or process scale-up calls for a tailored approach.
No manufacturer excels alone. Many of our best process adjustments came from customers who took time to share real-world data, unexpected results, or operational preferences. We’ve hosted site visits, bench-scale demonstrations, and even on-the-fly troubleshooting to work alongside partners who care about both quality and reliability. Through every step, we see the value of honest conversations over transactional exchanges. Chemists at the bench and engineers at the control panel become part of the solution, not just buyers or specs in a database.
Manufacturing 1-(4-Benzyloxyphenyl)-2-thiourea keeps us learning. Our best work comes from being ready to adapt, listening to the needs of those at the sharp end of synthesis, and never underestimating the value of a fresh perspective—whether from a new customer or a veteran in our own lab. We’ll keep striving for new ways to combine technical rigor with hands-on practicality, knowing that our place in the value chain is earned batch by batch, shipment by shipment.
High-quality chemical production doesn’t happen by accident or only by following static procedures. Our ongoing work with 1-(4-Benzyloxyphenyl)-2-thiourea shows that even subtle variations in process or sourcing can change the experience for labs and plants all over the world. We approach each order with the responsibility of making every kilogram as reliable as the last—never sacrificing commitment for convenience. In our experience, supporting innovation and scientific progress means striving for excellence, not only in purity, but in accountability, adaptability, and collaboration with the global chemical community.