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HS Code |
302090 |
| Chemical Name | 4-Tert-Butyl-2,6-Dinitrophenol |
| Cas Number | 101-63-3 |
| Molecular Formula | C10H12N2O5 |
| Molecular Weight | 240.21 |
| Appearance | Yellow crystalline powder |
| Melting Point | 108-110°C |
| Boiling Point | Decomposes before boiling |
| Solubility In Water | Slightly soluble |
| Density | 1.36 g/cm3 |
| Pubchem Cid | 7642 |
As an accredited 4-Tert-Butyl-2,6-Dinitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g package features a sealed amber glass bottle with a hazard label, displaying the chemical name "4-Tert-Butyl-2,6-Dinitrophenol." |
| Shipping | 4-Tert-Butyl-2,6-Dinitrophenol must be shipped in tightly sealed containers, protected from light, moisture, and heat. Classified as a hazardous material, it requires compliant labeling and appropriate documentation. Transport must follow relevant regulations, such as DOT, IATA, or IMDG, ensuring safe handling to prevent spills, contamination, or exposure during transit. |
| Storage | 4-Tert-Butyl-2,6-Dinitrophenol should be stored in a tightly sealed container, away from light, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area, segregated from incompatible substances such as strong oxidizers, acids, and reducing agents. Properly label the storage container, and ensure access is restricted to trained personnel. |
Applications of 4-Tert-Butyl-2,6-Dinitrophenol in Industrial Manufacturing4-Tert-Butyl-2,6-Dinitrophenol serves as a critical intermediate or processing aid in several specialized chemical production routes. As an original manufacturer, we supply this material to downstream partners who integrate it into precise industrial applications, meeting sector-specific requirements for compliance, performance, and process stability. Below we detail the real-world usage of this raw material in key sectors. 1. Colorant Intermediate for Organic Pigment SynthesisMajor pigment producers utilize this compound for the synthesis of high-performance yellow and orange pigments, particularly for automotive coatings, printing inks, and plastics. Its electron-withdrawing nitro groups help build chromophores with defined absorption spectra, allowing sharp color control after further downstream functionalization via alkali or amine reactions. Throughout formulation, producers monitor purity to minimize off-color shades and processing residues, which could otherwise affect end-use dispersion and hue consistency. Industry compliance standards
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2. Intermediate for Agricultural Herbicide SynthesisAgrochemical manufacturers employ this material as a building block when synthesizing specific dinitrophenolic herbicides. Its chemical structure supports the required electron distribution and steric effects for further functionalization via alkylation and etherification steps. Producers pay close attention to compliance with regulatory toxicological profiles and environmental release limits, checking each batch for residuals to conform with crop safety and application controls set by jurisdictions. Industry compliance standards
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3. Heat Transfer Fluid Stabilizer ComponentChemical plant operators and heat transfer fluid formulators use this compound to stabilize aromatic synthetic fluids against oxidative degradation at elevated temperatures. Its strong electron-withdrawing functional groups help limit chain propagation during high-temperature operation, especially in closed-loop systems for polymer processing, solar plants, and refinery units. Users must break down the optimal ratio relative to base oil and system design, complying with occupational and material safety guidelines for thermal stability and handling. Industry compliance standards
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4. Performance Additive in Polymer ModificationProducers of specialty polymers—particularly those developing high-performance engineering plastics—integrate this material during compounding to tailor light fastness and chemical resistance. The compound’s nitro- and tert-butyl substituents offer controlled polarity and hindered phenol functionality, influencing polymer chain packing and stability under UV exposure or chemical attack. Process controls ensure uniform mixing and proper thermal processing, with sampling and QC benchmarks in place to confirm mechanical and colorimetric specifications on finished goods. Industry compliance standards
Typical usage ratio
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Among the specialty chemicals we produce, 4-Tert-Butyl-2,6-Dinitrophenol deserves particular attention for its multifaceted uses and careful handling. Working with chemicals every day, we have learned that reliability, consistency, and safety guide every step of our process. Our facility specializes in aromatic compounds, and the unique profile of this nitrophenol derivative often provokes questions among chemists and engineers. It’s more than a product on a data sheet; it’s a real material, with quirks and requirements you notice when you put on the coat and goggles and smell the air of the lab. By sharing hands-on experience, we hope to help fellow professionals make informed decisions about sourcing and applying this compound.
The chemical structure of 4-Tert-Butyl-2,6-Dinitrophenol features a tert-butyl group attached to a benzene ring, substituted with two nitro groups. That much gets said in textbooks. But if you have ever measured out this material in a weigh boat with your own hands, the yellow crystalline powder and pronounced odor make a deeper impression. Those who have managed similar phenol derivatives will immediately recognize its handling similarities but also its durability.
This compound’s molecular configuration creates a balance between reactivity and stability, making it popular in specialized synthesis pathways. Other dinitrophenols with different alkyl groups—say, the methyl or ethyl-substituted types—do not always provide the same physical robustness or desired melting point. If you operate a batch reactor or manage fine tuning in organic synthesis, you will spot the difference quickly in yield and separation stages.
On our plant floor, precision begins with raw materials and carries through filtration, washing, drying, and finally the quality control lab. After drying, the final product emerges as a strongly colored powder. Visual inspection usually matches spectroscopic data. Reassurance comes not from paperwork, but from repeatedly observing reliable melting points, and from HPLC results that match expectations batch after batch. Purity targets often reach above 98%, but this takes more than a checklist; it takes watchful eyes in the purification room.
Granule size can make or break your downstream process. In our setup, we learned that the optimal crystal size emerges not from just one filtration setting, but from a controlled drying curve and carefully adjusted solvent composition. When granules become too fine, static builds; too coarse, and you lose surface contact in blends. Anyone working with dinitrophenols in coatings or as precursors for specialty polymers appreciates the difference that hands-on tweaking delivers.
Scaling from pilot batches to ton-level runs changes every parameter. We’ve seen too many “small-scale-only” successes that collapse when transferred to larger vessels. In our early years, temperature gradients at scale shifted the color and purity profile unexpectedly. Direct temperature sensors, experienced operators, and extensive process tracing keep that in check now. Each vessel’s personality—the way it heats, the way it cools, even how crystals settle—affects final product.
During actual runs, the presence of the tert-butyl group demands careful attention to oxidation conditions, since side reactions compete more aggressively under suboptimal conditions. Over time, adjusting agitation speeds and solvent ratios made the difference between occasionally off-spec and predictably good results. Most lab data sheets don’t mention these “personality traits,” but for routine large-batch users, these subtleties often define whether a run succeeds or needs reworking.
People come looking for 4-Tert-Butyl-2,6-Dinitrophenol for its role as an intermediate in the synthesis of specialty resins, dyes, and sometimes agricultural compounds. In the find-tuning of resins, for example, users report improved thermal stability when they integrate this dinitrophenol compared to unsubstituted variants. The tert-butyl group increases the molecule’s bulk, which translates to greater steric hindrance, an asset for those seeking oxidative stability in final products. Paint formulators often call on this grade specifically where color consistency and heat endurance matter.
Fine chemical synthesis shops, particularly those focused on custom organic molecules, note that the specific substitution pattern saves steps in multi-stage processes. In our experience, companies who regularly synthesize azo dyes or undertake complex organic modifications find that using the same base stock each quarter makes their work far more predictable. Some printers and pigment producers have shared stories where switching to this compound cut production time by reducing unwanted byproduct formation—and the headaches that often follow.
Anyone familiar with nitrophenol derivatives treats them with respect. We ensure rigor in protective equipment use and process ventilation. Static build-up becomes an issue during dry handling, especially if humidity drops. Years ago, we installed anti-static flooring and dedicated powder containment hoods after workers noted a faint taste after long shifts. Weekly safety talks emphasize not just PPE, but also the importance of small practical decisions—like double-checking gloves or how to remove a powder filter bag.
For shipping, the danger lies not just in the chemistry but in the packaging and environment. We tested multiple options for liners and barrels before landing on our current lineup, which balances chemical resistance, ease of access, and proper venting. We never rely on “the usual” if there’s a better way, knowing that complacency breeds errors.
Colleagues sometimes ask why this compound stands out when several dinitrophenol analogs exist. The main difference appears in downstream applications. The tert-butyl branch gives this molecule a unique blend of melting point, solubility, and vapor pressure. If you compare this variant to methyl or isopropyl-substituted dinitrophenols, you quickly find solubility differences in organic versus polar solvents. For users running continuous systems, that means less downtime for cleaning and reduced risk of blockages.
Heating studies show that 4-Tert-Butyl-2,6-Dinitrophenol sometimes endures higher operational temperatures without decomposing as quickly as lower-alkyl analogs. That feature matters where color or function must hold under heat or sunlight, such as in outdoor coatings or advanced polymers. Over several years, after many production runs, we’ve observed that resins prepared using this compound experience fewer incidents of yellowing or post-cure discoloration—a claim supported by feedback from repeat clients.
Conversations with users sometimes reveal new uses we hadn’t predicted during initial product development. Specialty adhesive producers, for instance, have mapped out reaction routes that save hours and solvents by starting with tert-butyl-dinitrophenol. In rubber compounding projects, trial blends using this molecule consistently demonstrated more predictable performance during curing. This real-world feedback inspires us to continually re-examine our process for quality, safety, and efficiency enhancements.
It’s easy to check off purity and solubility on a quality report. The more important feedback often happens over the phone late in the day, while someone describes troubleshooting a process flow or fixing line fouling. We record every such conversation—anonymous or otherwise—and feed those lessons into the next batch. It has improved the uniformity and predictability of our shipments in ways that excel spreadsheets never would have predicted.
We run each lot through a battery of in-house checks before boxing it up. GC-MS results, melting points, assay purities—these numbers matter, but consistency matters more. If a product line creates dust or agglomerates more readily, it shows up in the mixing room. Seasonal humidity changes have previously caught us off-guard, triggering us to tweak storage protocols mid-shift.
In early production years, an unexpected UV absorbance deviation led us to find a minor batch contamination that standard testing would have missed. It showed us nothing replaces careful observation, not even robotic analytics. Since then, both automated and manual review have become expected parts of our release process. Employees know to flag anything “off” long before management or customers experience trouble.
Some buyers require shipment in the hottest months, others in ice-cold winter. Over time, we identified optimal packaging to protect stability across real-world storage conditions. Our teams monitor sample bags for caking and sublimation risks, maintaining a balance between over-engineering and practical usability. Many stability stories start after the sale, when end users call with storage questions after three months in a non-climate controlled warehouse. Because the tert-butyl group resists hydrolysis better than some alkyl analogs, our shipments consistently arrive with little change from their lab-fresh state.
We keep updated with regulatory shifts for all aromatic nitro compounds. Tracking requirements for transportation, use, and disposal is not just about compliance; it’s about public safety and reputation. Increasing attention on environmental persistence drives us to minimize organics in process streams and invest in better trapping systems for off-gassing and filtrate cleaning.
Shifts in compliance rules, from local (national hazardous material designations) to international standards, can change overnight. That reality prompts us to review new shipments, destination regulations, and any downstream uses our customers report. Our technical team cross-references each compound’s use case with the latest chemical control updates to support smooth customs and audit outcomes. The reality is that a batch’s journey doesn’t end at our dock door.
As buyers adjust to stricter requirements, we have adapted by optimizing our reaction media and solvent recycling. Byproducts go through dedicated scrubbing and neutralization steps—a priority not only for meeting emission standards but also for building neighborhood trust. On more than one occasion, visitor tours have triggered process optimizations after discussing operator experiences and waste-handling improvements face to face.
Researchers increasingly want better documentation of trace residues, supporting the trend toward ultra-pure applications in electronics and advanced manufacturing. We’ve invested in upgrading our spectrometers and reinforcing in-line monitoring so that we match or exceed what high-end users now demand given the tighter end-use requirements. This means sharing detailed spectra and extra analysis upon request—as experience shows, proactive transparency reduces confusion and builds longer relationships.
Every batch run feels different in subtle ways. We learned early to tweak filtration sequences to avoid powder clumping in the final pack-out step. Some clients required alternate crystal size distributions, leading us through multiple campaign runs with minor adjustments. Most people in the field would agree: talking through application specifics with end users before a sale almost always saves troubleshooting down the line. Serious buyers share a project’s intended operating conditions, and we take those hints into account, refining the next batch’s drying schedule or rethinking packaging closure systems.
The blend of technical controls and human observation plays out every day—the faster a team notices a subtle color shift or unexpected settling rate, the less likely issues reach the end user. Where product deviates from expectations, personalized follow-up and technical troubleshooting—sometimes over video chat—resolve problems faster than endless threads of paperwork ever could. Years of seeing returns and complaints on our floor taught us that most mishandling or non-conformance starts with out-of-date communication at either end of the supply chain.
Making 4-Tert-Butyl-2,6-Dinitrophenol combines discipline, technical focus, and respect for the material’s quirks. No two production years are the same. The learning curve still surprises us, especially when process changes reveal new challenges or edge cases previously hidden by luck or limited data. That’s why we maintain direct lines of communication with clients and suppliers and share every new insight with our operating teams.
We recognize the responsibility of controlling every detail, from precursor quality to final shipment. Continuous improvement is more than a slogan. Whether the focus is on finer control of granulation, better analytical precision, or taking in customer feedback to shape next-year protocols, producing this compound is equal parts chemistry, observation, and adaptation. Most days, reliability means double-checking what you thought was already right. Every month brings new insights, new users, and new stories that, in the end, shape the way we approach chemistry for the next season’s batches.