|
HS Code |
344268 |
| Iupac Name | 4-(Butan-2-yl)phenol |
| Molecular Formula | C10H14O |
| Molecular Weight | 150.22 g/mol |
| Cas Number | 98-67-9 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 236-237 °C |
| Melting Point | 15-18 °C |
| Density | 0.963 g/cm³ at 20 °C |
| Solubility In Water | Slightly soluble |
| Flash Point | 104 °C |
| Smiles | CC(C)CC1=CC=C(C=C1)O |
| Refractive Index | 1.525 at 20 °C |
As an accredited 4-(Butan-2-Yl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of **4-(Butan-2-yl)phenol** is packaged in a sealed amber glass bottle with a secure screw cap and chemical hazard labeling. |
| Shipping | 4-(Butan-2-yl)phenol is shipped in tightly sealed containers, protected from light and moisture. It is classified as a chemical reagent and should be transported according to local regulations for hazardous materials. Ensure upright positioning, proper labeling, and documentation. Handle with care to prevent leaks or spills during transit. |
| Storage | 4-(Butan-2-yl)phenol should be stored in a tightly sealed container, away from sources of ignition and incompatible materials such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, protected from direct sunlight. Ensure proper labeling and avoid storage near food or beverages. Use appropriate chemical storage cabinets following relevant safety regulations and guidelines. |
Competitive 4-(Butan-2-Yl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Each day in our facility, the team moves with the certainty born from working with real, tangible chemicals—the sort that react how you expect, provided you know what you have in your hands. 4-(Butan-2-yl)phenol has become one of those dependable substances in our operation. This molecule, built around a phenolic core attached to a butan-2-yl side chain, brings forward its own set of use cases and performance profiles.
In the raw chemical business, subtle changes in structure create major differences in utility. Anyone who has worked with phenolic compounds has seen how even a single alteration in the alkyl side chain shifts both solubility and reactivity. What makes the butan-2-yl substitution interesting lies in its precise placement on the phenol ring. Looking at its chemical model—C10H14O for those familiar with chemical shorthand—this material stands out among other substituted phenols both in its physical form and in the way it interacts with other reactants.
Laboratories and manufacturing floors alike demand materials that act predictably under heat, moisture, or pressure. From batch to batch, quality control keeps 4-(butan-2-yl)phenol tightly within specific melting point and purity ranges. Workers on the QA line regularly rely on high-performance liquid chromatography to confirm each drum or container matches specification—no amount of theoretical talk replaces getting the numbers right in practice.
Our own lot records show that even slight deviations in isomeric purity can affect reaction rates further down the process line. In phenolic resin production, for example, the ortho and para substitution patterns affect both the hardness and flexibility of the final resin. What sets 4-(butan-2-yl)phenol apart is its tendency toward a predictable, relatively moderate reactivity, without some of the handling concerns that come with stronger or more volatile derivatives. This plays out directly in less variability during scale-up from lab to production: less time tweaking reactor conditions means more time moving product out the door.
With large-scale chemical manufacturing, safety is never negotiable and any oddity gets flagged. Over the past decade, we’ve seen dozens of batch records with near-zero incidents when proper handling guidelines are followed. Our safety team points out that, compared to lighter alkyl-substituted phenols, the butan-2-yl group helps lower the overall vapor pressure. That means less inhalation risk during transfer and storage. A few years back, we trialed several substitutes with similar aromatic cores; it became clear that the butan-2-yl side chain offered just the right balance of volatility and performance for workers who handle this material every day.
Some of the classic uses stem from the chemical’s phenolic nature. Specialty resin formation stands out as a primary field—taking advantage of its reactive sites to crosslink with formaldehyde or similar agents. In our own workshop, the synthesis of value-added intermediates uses this building block due to its predictable orientation and ease of modification. Scale-up chemists prefer 4-(butan-2-yl)phenol when they need a compromise: manageable costs, relatively straightforward raw material logistics, and compatibility with standard reactor materials.
Our experience shows that this compound resists unwanted side reactions better than some shorter, branched alkylphenols during oxidative processes. In the synthesis of certain agrochemical intermediates, this resistance to autoxidation translates to higher yields and less downtime due to fouled equipment or unexpected pressure surges. You want to see smiles in your maintenance crew? Give them a process that requires less shutdown for line cleaning and less rework due to rogue byproducts.
Another practical advantage comes through in blending operations. When working on smaller custom syntheses for pharmaceuticals or antioxidant packages, chemists leverage the subtly raised hydrophobicity from that butan-2-yl group. We’ve seen increased compatibility when blending into both polar and non-polar systems compared to simpler phenols, opening up formulation space for specialty polymers and stabilizers. Some customers have reported reduced migration in finished plastics, thanks to the balance of molecular weight and structure. Such real-world gains don’t show up in the theoretical write-ups yet make all the difference for process engineers and formulators.
The best way to understand the difference between 4-(butan-2-yl)phenol and other phenol derivatives is to look beyond the datasheet. In the plant, you sense it right away during handling and transfer—lower evaporative losses, less pungent odor, and easier blending without the need for elaborate ventilation. We’ve used both tert-butyl and isopropyl-substituted phenols alongside this product, and the distinctions come into play with volatility, purity profiles, and even the shelf life of intermediate batches.
Based on analytical runs from our internal lab, we find that compared to its tert-butyl cousin, 4-(butan-2-yl)phenol yields fewer trace condensation byproducts during hot operations. In practical terms, this means less gum and fewer deposits during distillation or reactor purging. Our production team values this material over the isopropyl variant when targeting tighter reproducibility in phenolic resin hardening rates. Certain additive chemistries depend on this behavior, and getting it wrong can mean rejected lots or additional formulation work outside the reactor.
Not every operation involves large-volume resin synthesis. For those in R&D or fine chemicals, the slightly bulkier side chain allows for a degree of steric hindrance, which can be exploited to guide regioselective reactions. Our colleagues performing nucleophilic substitution have pushed this molecule to create intermediates otherwise difficult to obtain, specifically when seeking to prevent inadvertent ring activation or polymerization. This taps into the broader utility of 4-(butan-2-yl)phenol—a little extra bulk, but not enough to impede solubility in solvents common to the trade.
Industrial settings require steady, repeatable results. Run records from our plant over the past five years show a consistent trend: batches sized from 50 kg up to multi-ton scale have maintained purity ranges above 98 percent, based on optical and chromatographic assays. Any operator who’s chased down troublesome contaminants or uneven reaction rates will recognize the value here. The major technical hurdle remains removal of trace starting material, which usually becomes straightforward with correct temperature profiling during purification.
Routine monitoring flags moisture content as a watch item, especially in humid climates. Our facility staff learned early on that even a minor increase in water content could spark off-coloration or unwanted tar formation under thermal cycling. This is why we monitor bulk storage and shipping conditions closely, running Karl Fischer titrations weekly when ambient conditions fluctuate. These real-world procedures cut back on waste and prevent the downstream complications that cost time, money, and credibility in the supply chain.
We’ve also refined our approach to storage protocols. Early experiences taught us that bulk 4-(butan-2-yl)phenol holds up well under proper sealing, but it benefits from nitrogen blanketing if held for extended periods. We switched to lined containers for larger volume outbound shipments after a few off color incidents years ago. Every plant engineer knows small process tweaks multiply savings over months and years, and in this business, reliability begins well before the truck leaves the dock.
No matter who the end-user is, regulatory compliance drives daily operations. Our internal audits keep detailed logs of purity, absence of certain heavy metals, and compliance with workplace exposure guidelines. For any batch of 4-(butan-2-yl)phenol, we maintain documentation covering source materials, process conditions, and third-party analytical reports. Customers in regulated sectors such as specialty resins or food contact polymers request transparency, and we stand ready to provide that paperwork—experience has shown open records ease clearances and prevent costly delays.
Based on years of practical engagement with authorities and certifying bodies, the process rarely stops at compliance. Stakeholders increasingly ask not just for paperwork but also for traceability of raw materials and proof of sustainable practices. Early adoption of batch-level trace codes, solvent recycling protocols, and reduced-waste distillation lets us hand over audit documentation without scrambling for information. The drive toward cleaner, greener processes has nudged us to continuously update purification steps, solvent neutralization, and atmospheric emission controls. Incremental upgrades such as sealed-system transfers and closed-loop sampling have made a measurable reduction in both operator risk and environmental footprint.
Supplying 4-(butan-2-yl)phenol goes beyond round-the-clock reactors and GC-FID graphs. Securing the base phenol is just one link in a longer chain that runs from chemical feedstocks to finished fine chemicals. In our market, shifts in hydrocarbon feedstock prices or shipping delays ripple quickly to the plant floor. Nobody needs surprises during high-demand cycles. Our experience integrating local raw materials and forecasting process times has preempted more than one supply crunch, especially during regional port slowdowns or unexpected price swings in basic aromatics.
What sets manufacturers apart is the willingness to reroute materials, work with alternative suppliers up to our QC standards, and communicate honestly with downstream users. We learned hard lessons during force majeure situations, but these helped shape our current policies: always hold safety stock of key intermediates, maintain running supplier audits, and keep cross-trained staff to flex production schedules as needed.
For custom requests or urgent shipments, our process team works directly with buyers to reconfigure batch sizes, adapt purity targets, or adjust packaging. It’s never about just selling a drum—it’s about understanding exactly how that lot will fit into someone else's downstream process, where a single off-spec component can ruin a week’s worth of work. Our teams keep close to process trends and real-world case histories; that’s how patterns are recognized and adjustments made ahead of time, not after.
Even the most stable chemical has its operational challenges. We have encountered stalling in downstream reactions due to trace oxidized aromatic byproducts, often surfacing in older storage lots or batches exposed to high ambient temperatures. To combat this, we've layered in additional routine testing for peroxide content and colorimetric indices. Process tweaks, like altered distillation cut points, are deployed on-the-fly based on operator experience and QC data—there’s no substitute for seasoned plant hands who can smell or see the difference before instrumentation even kicks in.
Another challenge lies in meeting unique customer formulations. Specialty resin manufacturers may require a degree of para-isomer enrichment, demanding tighter control in synthesis routes and downstream separation steps. Our lab techs have adapted small-batch fractional recrystallization and custom distillation setups to deliver on such one-off specs, keeping detailed run records so those procedures scale effectively when larger quantities are required in future runs. Flexibility on the floor matters as much as planning in the meeting room.
Often, feedback from downstream users provides the insight needed for process improvement. When resin manufacturers reported issues with tack or cure times, we re-examined trace impurity profiles using updated GC-MS methods. Adjustments followed: tweaks in temperature gradients, solvent ratios, and storage conditions. Sometimes, it isn’t high-tech fixes that bring the best results, but simple re-training in material handling—for example, instituting a new drum venting protocol to cut down on moisture intrusion.
Day in and day out, no process holds up without a crew that understands the practical realities behind the chemistry. After spending years working with 4-(butan-2-yl)phenol, our operators and engineers know the specific “feel” of the material: how solids should flow, what a clean transfer looks like, the subtle difference in scent that hints at a change in purity. There are textbook answers, and then there is the reality of catching small process deviations before they cascade. That repeatable, practiced attention is what drives high-quality output batch after batch.
Continuous improvement meetings aren’t just corporate exercises—they draw upon tens of thousands of operating hours, where each shift log or deviation record gets reviewed to extract better ways to prevent cross-contamination, optimize temperature profiles, or lighten the workload for the packaging crews. Some of our best process innovations have come from a single operator flagging an unusual reaction rate or requesting a trial of a new transfer hose. In the practical world, those firsthand experiences guide both product quality and workplace safety.
Many of our longtime clients began with conventional resin synthesis and have since shifted toward more complex polymer and additive needs. Marker trends indicate rising demand for tailored, functional intermediates that build upon the dependable performance profile of 4-(butan-2-yl)phenol. Our R&D group has ongoing programs using this molecule as a springboard for new classes of UV stabilizers, polymer flow agents, and customized antioxidant blends.
The substance continues to prove itself as a flexible platform, responsive to process tweaks and adaptation for next-generation products. The same molecule that once filled reactive resin markets now finds a home in more advanced coatings and high-performance polymers. We see a future where 4-(butan-2-yl)phenol serves as the basis for even more specialized products, drawing on collaborative research, novel catalyst systems, and advanced purification technologies.
As chemical manufacturing keeps pace with tighter regulations and greater environmental demands, we expect to see materials like this play a larger role in greener, safer, and more efficient processes. Our commitment, grounded in hands-on operational knowledge, remains unwavering: supply quality, innovate sensibly, and keep the realities of end-users at the core of every ton shipped.