|
HS Code |
679203 |
| Name | 4-N-Propylanisole |
| Cas Number | 838-88-0 |
| Molecular Formula | C10H14O |
| Molecular Weight | 150.22 g/mol |
| Appearance | Colorless liquid |
| Boiling Point | 235-237 °C |
| Melting Point | -31 °C |
| Density | 0.941 g/cm³ at 25 °C |
| Refractive Index | 1.497-1.499 at 20 °C |
| Flash Point | 94 °C |
| Solubility In Water | Insoluble |
| Smiles | CCCNc1ccc(OC)cc1 |
As an accredited 4-N-Propylanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100 mL clear glass bottle with a secure screw cap, labeled "4-N-Propylanisole," hazard symbols, and handling instructions. |
| Shipping | 4-N-Propylanisole should be shipped in tightly sealed containers, clearly labeled, and cushioned to prevent breakage. Protect from physical damage, moisture, and direct sunlight. Transport according to local, state, and international chemical regulations. Ensure compliance with hazardous materials guidelines; typically shipped as a non-hazardous liquid, but verify classification before shipping. |
| Storage | 4-N-Propylanisole should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep it away from incompatible substances such as strong oxidizers. Ensure proper labeling and secondary containment to prevent leaks or spills. Recommended storage temperature is between 2-8°C (refrigerated), but avoid freezing. |
Applications of 4-N-Propylanisole in Industrial ManufacturingAs a specialized manufacturer of fine chemical intermediates, we supply 4-N-Propylanisole for integration into selected advanced downstream processes. The following sectors represent established value-adding uses where our material directly enters customer formulations and manufacturing operations. Each application scenario highlights specific compliance frameworks, precise incorporation points, formulation ratios, and finished product types, reflecting verified practices in actual industry production. 1. Fragrance Ingredient for Cosmetic and Personal Care Products4-N-Propylanisole is widely recognized in fragrance houses and large-scale cosmetic compounding as a character-impact molecule, valued for its sweet, anisic, and slightly floral notes. This compound finds utility in blending medium-to-top note accords for toiletry, fine fragrance, and personal care applications. Quality control teams reference IFRA and cosmetic regulatory matrices to assess batch acceptance and scent performance in target formulations. Industry compliance standards
Typical usage ratio
Downstream process integration
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2. Aroma Intermediate in Flavor Manufacturing for Food ApplicationsMajor food flavor producers utilize 4-N-Propylanisole as an intermediate to engineer sweet spice or herbaceous notes in artificial and nature-identical flavor blends. Its addition takes place at the synthesis or compounding phase, where process control ensures conformity to international food safety protocols. Regulatory oversight covers residue limits and allergen declarations, validated through batch release analytics and documentation trails for each production lot. Industry compliance standards
Typical usage ratio
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3. Pharmaceutical Intermediate in Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers integrate 4-N-Propylanisole as a non-final-step intermediate in the multi-stage synthesis of selected APIs featuring aryl ether motifs. Strict traceability and impurity control apply according to pharmacopeial requirements, with documentation for all sourcing, storage, and in-process verification. Production teams monitor reaction yields and impurity profiles through validated chromatographic methods, underpinning the regulatory submission of the downstream API dossier. Industry compliance standards
Typical usage ratio
Downstream process integration
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4. Fine Chemicals Intermediate for Agrochemical SynthesisAgrochemical manufacturers adopt 4-N-Propylanisole as a feedstock in active substance development, specifically for constructing aryl ether cores in select herbicide and plant growth regulator molecules. Integrated QA/QC programs address material in-spec confirmations from raw material intake to batch release, with environmental and safety documentation supporting process approvals for both pilot and commercial scale. The intermediate enables rigorous process reproducibility essential for data submission under agrochemical registrations. Industry compliance standards
Typical usage ratio
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5. Specialty Chemical Intermediate for Electronic MaterialsChemical producers for the electronics supply chain use 4-N-Propylanisole as a building block when manufacturing customized aromatic compounds employed in photoresist or liquid crystal monomer development. Purity and trace analysis are central throughout process transfer, and all integrating plants operate under stringent materials control to support electronic-grade assurances demanded by downstream device assemblers. Processing teams coordinate material release only after successful qualification for electronic raw material standards. Industry compliance standards
Typical usage ratio
Downstream process integration
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Years of hands-on chemical synthesis reveal a pattern—demand changes, yet the pursuit of reliability and clarity in product identity remains constant. Take, for example, 4-N-Propylanisole, also called 4-Propylanisole or p-Propylanisole. This molecule reflects our commitment to consistency: not just by structure, but by the certainty it offers to chemists and formulators. We put genuine effort into every batch, helped by upstream raw materials that we vet for purity, and by rigorous stepwise reactions that aim to reduce side products. Extraction, washing, and purification steps, honed over trials and pilot runs, form the backbone of our actual manufacturing process. Our familiarity with the molecular nuances lets us vouch for the character and reliability that customers expect.
Over the years, customers approach us with more than just a CAS number; they want bonds they can trust in both structure and supply chain. Our own teams have checked and run propyl group introductions on aromatic rings, ensuring position-specific substitution for a clean para isomer. The satisfaction comes through when repeated analyses remind us that a little attention to controlling temperatures and solvent ratios decisively reduces ortho and meta by-products. For those familiar with crude mixtures, a product whose spectrum clears up at the right signals solves many headaches downstream. In this way, we focus daily on making the difference tangible.
This molecule falls within the anisole derivatives, distinguished by its three-carbon propyl chain attached to the aromatic ring’s number-4 position. From once having to extract, distill, or purchase irregular product from unpredictable sources, we realized the importance of relevant physicochemical criteria. Our procedure yields material that shows a clear, colorless liquid at room temperature, which, for many, matters as cloudiness or yellowness in the drum slows down production QC and causes downgrades. Years ago, it wasn’t uncommon to see slightly colored product due to oxidation or trace iron from careless transfers. We went through rounds of upgrades to our handling: inert gas blanketing, seamless piping, and less exposure to air at fill—to keep reported color levels low even after storage.
In purity, talking in numbers alone rarely gives the full story. We employ gas chromatography and NMR for every batch, not just as a regulatory checkpoint but as part of our learning process. Small peaks that hint at positional isomers or lingering starting materials catch our chemists’ eyes. Not every anisole derivative supplier does this. That’s a split between a simple trader, who might not track what each impurity means for your next synthesis step, and a manufacturer who knows batches can’t all be averaged away—variability multiplies in scaled-up reactions. We can trace each drum's story, from drum serial to which reactor it came from, how long it cooled, and which filters we swapped mid-run. That knowledge travels down the pipe in every shipment.
Old project notes from our R&D teams tell a clear story—aromatic ether molecules like this remain popular for very directed applications, and our output has regularly served the demands of clients who need consistency in every bottle. The para-orientation, confirmed by our internal NMR panels, gives it subtle reactivity that makes a difference, especially in industries synthesizing advanced agrochemicals, specialty pheromones, or certain perfumery intermediates. We’ve seen order patterns that reflect ongoing work in olfactory science—formulators blending this substance to test with their own panels before going larger scale.
Unexpectedly, the shift toward more customized molecules over the last decade has meant that standardization has become more precious. Some buyers, seeing a generic label, ask if small impurities or traces of metals may alter catalyst-driven steps. Our approach to manufacturing—the internal pressure to rerun or repolish batches if purity feels in doubt—sprung from fielding these calls directly. We know that what’s written on paper sometimes looks similar, but actual performance in a multistep synthesis can expose weaknesses. Having run synthetic sequences ourselves, we’re picky; and we support customers troubleshooting sticky methylations or challenging Grignard reactions, often involving our 4-N-Propylanisole as a reactant or solvent.
Today, the product finds itself in stockrooms worldwide, feeding into bigger syntheses, being tested in formulations, and explored by research labs. Some choose it because the para-propyl group resists certain undesirable side reactions. We’ve found that this resistance offers customers leeway in reaction conditions, saving waste and time spent chasing unwanted intermediates. That’s an advantage traders rarely understand—but for us, watching the actual reaction flask, it’s clear that the structure spells fewer problems later on.
We take pride in describing what sets our delivery apart—not just a simple product outflow, but a process with deliberate choices. We source our anisole feedstock from producers we visit and audit ourselves, not from anonymous upstream brokers. Our synthesis route moves through Friedel–Crafts alkylation, using carefully metered propylating agents. Handling exotherms and purging by-products stand as critical tasks for our operators, many of whom have been in our plant before our latest automation lines. The cleaning-in-place steps between runs have grown slowly more rigorous, resisting the easy way of running “mixed product” campaigns that introduce new contaminants.
Our team has learned tough lessons in what gives batches long-term shelf stability. Years spent tracking customer complaints taught us how even trace moisture or air ingress causes degradation days or weeks later, particularly under summer heat. So we made sure to use nitrogen-blanketed reactors and finish every fill with a pressure cap. Not every supplier takes this step, but for us, it prevents reruns—an obvious win if you see product not lose clarity after it lands in your warehouse. By investing in equipment and habits that address the root causes of instability, we deliver fewer surprises to our partners.
We maintain lot records that run through details—when each run started, which operator sampled for analysis, and which shipping container every batch entered. We do this not to meet regulations, but because tracing allows us to double-check when irregularities pop up, whether reported by freight services or a customer’s QA team. Years of sharing this log with customers show they appreciate the hands-on engagement and know they’re getting the real material—not a relabeled or adulterated drum pieced together by a middleman.
Working on a broad product line of aromatic ethers, we see the small differences between isomers and alkyl substituents add up in handling and application. While ortho- or meta-substituted anisoles may have similar reactivity on paper, our trials show that separation steps, crystallization rates, and even boiling behavior in reactors shift in practice. Our para-propyl product offers a single, dominant isomer; we confirm this not just because analytical rules say so, but because certain formulation labs have reported that even slight changes in substitution position led to shifts in their end-product scent or efficacy.
From direct experience, we observed that some users new to anisole chemistry underestimate the importance of subtle structural shifts. For example, the ortho-propyl variant, with its substituent sitting closer to the methoxy group, can create steric challenges in downstream functionalization—something our in-house synthesis chemists noticed during trial batch campaigns. Extra isolation steps, or more aggressive purification, were needed, slowing throughput and risking yield loss. Customers who moved to para-substitution once pointed out that their purification times dropped, and overall process predictability improved—a small shift in position on the ring, with concrete impact on real operations.
The length and branching of the alkyl side chain also matter more than is apparent at a glance. Our plant has processed a spectrum of alkyl anisoles, from methyl to propyl to even longer chains. We noticed the three-carbon propyl group at the para position balances volatility and solubility properties, allowing easier handling than with longer chains, which get oily and sluggish, yet offering better application potential than the simple methyl analogs. For custom applications in fragrance or advanced material intermediate synthesis, clients report less filtering, faster blending, and more repeatable finished properties compared to lesser-optimized alternatives.
In our production workflows, safety is not a document but a practice. Operators wear full PPE handling each stage—from raw material charging to final drumming. We have invested in inline leak monitors on loading arms and added vapor recovery systems; a few solvent-rich batches years ago taught us that worker comfort and local air quality warrant ongoing attention. While not strictly a “hazardous” substance in every jurisdiction, we treat 4-N-Propylanisole as a responsible manufacturer should: clear SOPs, dedicated storage, and robust record logs for every moved drum.
We strongly recommend that handlers at customer sites mirror the care we show. Direct observations in our facility show the difference—with proper ventilation, spill containment at loading, and quick-seal closures, issues turn rare. In regions with hotter climates, we have run studies to see how container exposure character alters product lifespan, and now many of our clients follow our advice to use inert gas padding for drums in outdoor storage. Lessons like this get shared not to sell a product, but to close gaps in the chain and keep product quality in line from drum to lab bench.
Every major product launch or process improvement in our plant stems from real stories. Some customers want to scale up custom syntheses where every side reaction costs time and money; others look for reliable supply chains that stretch through uncertain shipping environments. Working side by side with both types, our role doesn’t end at the factory gate.
Technical teams from downstream users regularly contact our plant, sending spectra, reporting sensitivities, or flagging unusual results. We’re able to respond promptly since our teams sit feet away from where the drums are filled, not in a remote trading office without hands-on context. This proximity lets us gather new data, hold internal reviews, and sometimes go back to the synthesis bench to replicate, tweak, or suggest theoretical changes. In many cases, issues traced to minor impurities and residual solvents led us to tweak drying protocols or add another filter press—small changes for us, big ones for a downstream AgChem or fine fragrance synthesis.
On export logistics, we partner with freight specialists who keep containers clean, schedule direct routes, and keep cycles short. This comes from the lessons learned: in the early days, we noticed that indirect or consolidated shipments led to more temperature swings and more dunnage damage. Working closely with the shipping floor, we instituted a process of quick customs clearance prep, limiting container idle times at ports and avoiding unnecessary repacking at warehouse hubs. Fewer transit anomalies translate into lower risk for our clients and a direct tie between what rolls off our line and what arrives in your warehouse.
As regulations surrounding aromatic intermediates grow tighter, we approach compliance not as a box to tick but as an honor code. Our compliance staff train directly with synthesis chemists, reviewing material traceability, batch logs, and GHS documentation—essential practices for tightening material stewardship across our industry. This partnership between manufacturing and compliance shortens the feedback cycle: when standards change, we shift sourcing, update protocols, and share these updates in real language—not boilerplate—so that clients know precisely what changes, and why.
Looking forward, we invest continuously in both greener process chemistry and real-world data capture. A recent investment in more robust catalyst recovery dovetails with our goal to lower chemical and energy use per ton produced. Our team pilots small, reusable reaction vessels—built to check for kinetic and yield differences between traditional and newer approaches. We share these outcomes with industrial partners, supporting vetted process tweaks for those seeking more efficient, lower-impact production.
In a field where trust rarely grows overnight, we know that the little details—like shipping a technical whitepaper with each new lot, or admitting outright when something didn’t work—matter more than perfect words on a webpage. Our stance is shaped by decades on the production floor, where every product, including 4-N-Propylanisole, emerges not just from a reaction pot but from enduring collaboration with those who use it most.