|
HS Code |
369698 |
| Chemical Name | 3-(Sec-Butyl)phenol |
| Cas Number | 123-39-7 |
| Molecular Formula | C10H14O |
| Molecular Weight | 150.22 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 241-243 °C |
| Density | 0.967 g/cm3 |
| Flash Point | 106 °C |
| Refractive Index | 1.513 |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry, well-ventilated area away from sources of ignition |
| Synonyms | 3-(1-Methylpropyl)phenol, m-sec-Butylphenol |
| Smiles | CC(C)Cc1cccc(O)c1 |
As an accredited 3-(Sec-Butyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3-(Sec-Butyl)Phenol, sealed with a screw cap and labeled with hazard information. |
| Shipping | 3-(Sec-Butyl)phenol should be shipped in tightly sealed containers, compliant with chemical transport regulations. Keep away from heat, sparks, and incompatibles such as oxidizing agents. Use appropriate hazard labeling (flammable, irritant). Ensure secure packaging to prevent leaks. Transport should follow applicable local and international guidelines for chemical substances. |
| Storage | 3-(Sec-Butyl)phenol should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it in a tightly closed container, separated from strong oxidizers, acids, and bases. Prevent moisture and avoid prolonged exposure to air. Ensure proper labeling and compliance with chemical storage regulations to prevent leaks, spills, or contamination. |
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Chemists in the manufacturing space recognize the unique value 3-(Sec-Butyl)Phenol brings to the table. This compound, known by its CAS number 99-72-9, introduces a secondary butyl group at the meta position on phenol’s aromatic ring. From a production standpoint, this alteration reshapes both the molecule’s reactivity and its market value. Over years of working with phenolic intermediates, we have seen small changes in structure alter the downstream chemistry dramatically.
3-(Sec-Butyl)Phenol does more than just add another isomer to the batch. The secondary butyl group reshapes its boiling point, modulates solubility in various organic solvents, and yields distinct reactivity in bulky-substituted phenol reactions. Chemists select this molecule where they seek a blend of steric hindrance and electron-donating effects, not just for the sake of chemical moderation, but for the distinct endpoints these properties afford in finished goods.
Our facility produces 3-(Sec-Butyl)Phenol through refined alkylation routes, drawing on years of process optimization. We maintain purity levels above 99% GC, minimizing typical byproducts such as para- or ortho-sec-butyl isomers and other alkylphenolic residues. Color often sits below 20 APHA at shipment, and water content consistently remains less than 0.1%. The molecular weight calculates out to 150.22 g/mol, a detail that matters when you’re running precise stoichiometric additions. We keep melting and boiling point data on hand from regular QC runs: this phenol variant melts near 12°C and boils near 238°C. Such reliability in physical parameters means better consistency both in your lab trials and on the scale-up line.
Our experience tells us that any deviation in trace impurity profile affects downstream applications, especially where polymerization catalysts or resin finishes are concerned. Close control in batch distillation, vacuum stripping, and purification stages defines every shipment. Feedback from partners in adhesives, resin synthesis, and specialty intermediates underscores the criticality of these tight controls.
Down on the production floor, where high-purity phenolic intermediates become the backbone of adhesives, resins, and surfactants, 3-(Sec-Butyl)Phenol earns its reputation. In phenolic resin production, the secondary butyl group brings moderate steric protection while still participating actively in condensation reactions. Unlike straight-chain butyl substituents or tertiary isomers, its balance avoids runaway viscosity shifts during resin cure.
We see this compound show up where adhesive formulators demand controlled open times and consistent thermal stability profiles. In surfactant production, its hydrophobic tail strikes a balance between too-rapid phase separation (as seen in higher alkyl groups) and excessive water miscibility (common in shorter chains). The primary effect customers report is greater control in tuning the hydrophobic-lipophilic balance of specialty surfactant lines.
Our technical teams engage regularly with research users developing specialty antioxidants and UV absorbers. The electronic effects of the secondary butyl group at the meta position offer more than just a molecular tweak—these effects support greater resistance to oxidative breakdown and photoyellowing, resulting in end products that serve high-value coatings, plastics, and specialty ink markets.
Some producers ask why choose the sec-butyl isomer over more familiar n-butyl or tert-butyl substitutions. Over the years, our chemists have run countless bench and pilot plant comparisons. The distinction comes down to both reactivity and performance.
n-Butylphenol, for instance, offers high reactivity in alkylation and etherification recipes, but tends toward lower thermal stability in resins. Customers producing molded phenolic parts note softening or flow issues at elevated cure temperatures when n-butyl variants dominate. On the other hand, tert-butylphenol’s larger group steers reactions away from certain pathways entirely—sometimes what you need, sometimes not.
In practice, 3-(Sec-Butyl)Phenol gives resin producers an optimal midpoint: a workable melt flow without the hazardous volatility profile of lighter analogues, and a reactivity profile that neither lags nor races ahead uncontrollably during crosslinking. End-use evaluations consistently show mechanical properties—especially dimensional stability and creep resistance—edge slightly ahead when the secondary butyl isomer fills the meta position.
In surfactant and specialty chemical synthesis, the balance of hydrophobic/lipophilic character adjusts with many variables, but the sec-butyl structure delivers sought-after performance in both solubilization power and low-temperature stability. Customers in agrochemical and oilfield service formulations cite better dissolution and improved shelf life.
Years ago, much of the alkylphenol market overlooked isomer-specific sourcing. Now, industries—driven by higher performance standards and regulatory scrutiny—demand tighter tolerances in both product and process. Our experience shows that better selectivity in the alkylation process, coupled with advanced liquid-phase separations, yields purer 3-(Sec-Butyl)Phenol and reduces waste streams. This environmental and regulatory pressure isn’t just theory for us. Real process improvements over the past decade have lowered distillation energy usage and cut byproduct volumes.
With more global attention on environmental fate, we regularly evaluate biodegradation data, partition coefficients, and aquatic toxicity for each batch. Unlike longer-chain or more sterically hindered phenols, the secondary butyl arrangement at the meta position impacts surfactant breakdown rates and environmental emissions. By focusing on batch traceability, we support downstream users with clear documentation for compliance reporting.
Moving away from legacy phenolic intermediates often means a recalibration of process controls and a bank of new application trials. Our technical support works closely with partners as they design-in sec-butylphenol for next-generation adhesives, coatings, and bespoke polymer lines. We routinely provide small-scale samples, application insights based on real-world feedback, and analytical support. This open exchange—between chemist and manufacturer—pushes both product design and process efficiency ahead.
Stewardship goes beyond purity and reactivity. Industry veterans recall a time when chemical safety guidelines lagged actual handling requirements. From decades on the plant floor, we know accidents rarely stem from exotic hazards and more often come from complacency in routine transfers, storage, and blending. 3-(Sec-Butyl)Phenol, like its relatives, has a strong phenolic odor and presents skin and eye irritation risks. Where possible, we’ve moved packaging formats toward sealed drum and IBC options, aiming to minimize headspace vapor and prevent worker exposure.
Closed loading, vapor recovery systems, and real-time monitoring form the backbone of our modern logistic chains. Training practical awareness—from line operator to process engineer—is a non-negotiable part of the routine. Most spill response and mitigation protocols build from simple but disciplined engineering controls, supported by on-hand neutralizing and containment materials. Customers adopting these measures report fewer lost-time incidents and improved on-site retention, especially as process chemistry moves toward higher throughput and automation.
Disposal and environmental control play into the daily and long-term value of any industrial intermediate. For 3-(Sec-Butyl)Phenol, most users incorporate distillation residue recycle streams into resin and polymerization byproducts, reducing both cost and waste output. The linear and circular integration of these byproducts relies on careful documentation—tracking precisely which streams remain within spec and which move to controlled offsite treatment. Mature supply chains require transparency in waste allocation: batch numbers trace through each process, and waste manifests tie back to supplier and site.
The push-pull between specialty chemical innovation and evolving regulatory frameworks shapes every aspect of 3-(Sec-Butyl)Phenol manufacturing. Over years of navigating REACH, TSCA, and evolving national policies, we’ve learned that regulatory adaptation starts long before any substance listing changes. Each time authorities adjust guidance on alkylphenol emissions or end-use scenarios, downstream industries react with new protocols and performance requirements. Our team consults regularly with industry working groups, contributing data from real production scenarios to inform regulatory bodies and customer compliance officers.
Supply chain dynamics also evolve. Disruption in raw material sourcing—for example, refinery maintenance cycles or logistics bottlenecks—translates directly into lead time and inventory pressure. We maintain buffer stock not as a luxury, but as a necessity, aligning purchase cycles with forecast risk, rather than just-in-time procurement. Partnering directly with end users helps us anticipate formulation surges or seasonal demand, reducing the friction of last-minute order changes. Through these relationships, we help to bridge the supply chain gaps that can force premature product reformulation.
Scaling bench-level innovation to full-scale plant runs always uncovers new challenges. With 3-(Sec-Butyl)Phenol, limitations in alkylation selectivity have traditionally resulted in variable impurity profiles, especially as batch sizes move beyond pilot plant gallons. Investing in continuous-flow alkylation technology, supported by real-time analytics, has allowed production teams to catch process drift earlier and produce tighter lots. By leveraging near-infrared and chromatography QA tools, the risk of off-spec delivery drops sharply—a lesson driven home after watching customers troubleshoot off-standard raw material loads over the years.
Waste minimization remains a major technical challenge, especially when downstream partners demand cradle-to-grave traceability on every molecule. Internal reclamation—re-distilling offcuts, re-purposing out-of-spec product rather than burning it, and blending into compatible resin streams—goes beyond cost-cutting. It serves customer mandates for greener footprints and supports our own goals for resource maximization.
Another lesson: real-time customer support solves issues faster than paperwork or post-hoc investigations. Our technical team maintains an accessible log of successful and failed application trials, providing it to customers at onboarding. This lived knowledge, refined in direct collaboration, saves time and reduces downtime for all parties.
Stories from the application floor stick with us. Polymer developers working to toughen thermoset adhesives documented a consistent 5-8°C bump in glass transition temperature after switching from p-butylphenol to 3-(Sec-Butyl)Phenol. Lab notes and finished goods data confirmed this, and a switch to sec-butyl meta-phenol produced fewer process upsets during scale-up, cutting unplanned batch reworks by nearly a third.
In surfactant shops developing high-performance emulsifiers for oilfield stimulation, reports highlighted better shelf stability and cold weather transportability when the meta-sec-butyl configuration entered the mix. Where other alkylphenol isomers formed gels or separated at low temperature, sec-butyl systems flowed freely and re-blended without extensive reprocessing.
Adhesive customers share similar feedbacks—polyurethane prepolymer productivity climbed after switching to sec-butyl meta-phenol intermediates, notably due to reduced side reactions and easier clean-up at the mixing head. The machinery downtime savings and product consistency added up to measurable bottom-line improvement—real numbers, not marketing projections.
The flavor and fragrance world sometimes experiments at the outer edge of phenolic chemistry, seeking unique character from novel isomers. Here, secondary butyl at meta brings a mild, woody aromatic profile that rounds off more aggressive base notes. It won’t replace cresols or traditional phenolic elements in every formula, but in select blends it unlocks new sensory results.
In the context of electronics and automotive component manufacturing, partners evaluate sec-butyl meta-phenol for its dielectric properties and chemical resistance. Early results present promising resilience during aggressive solvent cleaning regimes, hinting at larger potential for integration in printed circuit board lacquers and protective coatings.
Even in agricultural chemistry, the ability to tailor active ingredient solubility through sec-butyl modified phenolics renews formulation options where frothing, settling, or environmental dissipation once limited performance.
No single manufacturer carries all the answers, but decades in the field teach the importance of direct communication and hands-on technical service. Our product development approach welcomes direct, honest discussion with process engineers, formulation chemists, and QC managers at every stage. From first order to ongoing supply, the goal stays the same: reliability and openness. Facing formulation shifts, evolving regulations, or new product launches, practical knowledge transfer makes the difference between mere compliance and real-world success with 3-(Sec-Butyl)Phenol.
Our investment in plant-level analytics, advanced process controls, and end-user support has grown from these relationships. Every application challenge, every shipping bottleneck, and every regulatory hurdle shapes these improvements. In our experience, customers return again and again not just for material supply, but for the confidence that comes from working with a dedicated manufacturer who listens, learns, and adapts.