|
HS Code |
156881 |
| Chemical Name | Phenol, 4-Amino-2,3-Difluoro- |
| Molecular Formula | C6H5F2NO |
| Molecular Weight | 145.11 g/mol |
| Cas Number | 151267-03-1 |
| Appearance | Off-white to light brown solid |
| Melting Point | 58-62°C |
| Solubility | Slightly soluble in water |
| Synonyms | 4-Amino-2,3-difluorophenol |
| Smiles | C1=CC(=C(C(=C1F)F)N)O |
| Inchi | InChI=1S/C6H5F2NO/c7-3-1-2-4(9)6(10)5(3)8/h1-2,10H,9H2 |
As an accredited Phenol, 4-Amino-2,3-Difluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Phenol, 4-Amino-2,3-Difluoro- is packaged in a 25-gram sealed amber glass bottle with tamper-evident cap and hazard labeling. |
| Shipping | Phenol, 4-Amino-2,3-Difluoro- should be shipped in tightly sealed containers, protected from light and moisture, and labeled as hazardous material. Transport must comply with relevant regulations (such as DOT, IATA, or IMDG), using appropriate packing materials to prevent leaks or exposure. Handle with care to avoid contamination or spills. |
| Storage | Phenol, 4-Amino-2,3-Difluoro- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as oxidizers and strong acids. Protect from light, moisture, and sources of ignition. Proper labeling and secure shelving are important to prevent accidental release or exposure. Use appropriate personal protective equipment when handling. |
Competitive Phenol, 4-Amino-2,3-Difluoro- prices that fit your budget—flexible terms and customized quotes for every order.
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In the business of advanced chemical manufacturing, product quality starts long before reactors fire up or packaging lines move. Phenol, 4-Amino-2,3-Difluoro- (also referenced in many technical catalogues as 4-amino-2,3-difluorophenol) offers a great example of how thoughtful synthesis, rigorous control, and deep knowledge come together in a finished material ready for the demands of research and production. Bringing this compound to market demands technical know-how and the willingness to continuously improve both the process and the end result.
For chemists and manufacturers, the amino and difluoro substitution on the phenol ring creates a molecule with features prized in fine chemical and pharmaceutical applications. The 4-amino group acts as an active site, lending itself to a range of downstream reactions, while the 2 and 3 positions each bearing a fluorine atom impart properties that can influence metabolic stability and selectivity when used in pharmaceutical research or as a building block for specialty derivatives.
Our typical production runs of Phenol, 4-Amino-2,3-Difluoro- offer material in high purity, with assay values approaching or exceeding 98 percent by HPLC or GC—depending on the application and customer request. We've learned that careful control of the reaction sequence, particularly the fluorination steps, impacts not only purity but also minimizes structural isomer formation. Consistency at this level comes through knowledge accumulated by our process development teams, many of whom have worked with aromatic fluorination and amination for decades.
There is more to this material than purity numbers on a certificate. Our batches present as a pale solid, offering a melting point that typically falls between 95 and 105 degrees Celsius. After drying under reduced pressure, each lot is visually inspected and handled in modest batch sizes to protect from moisture and contamination. Through years of direct feedback, we’ve learned customers value decision points beyond standard specs. Solubility in polar aprotic solvents allows wide latitude for synthetic routes. Trace water content and halogenated impurity levels are checked and maintained well below acceptable industry limits. Our lab samples train the eye for color and clarity, rather than relying solely on instrument output.
Synthetic chemists seek out aromatic amines with defined substitution patterns for the unique reactivity they offer. Our Phenol, 4-Amino-2,3-Difluoro- plays a pivotal part in creating specialty pharmaceuticals, custom ligands, and advanced material intermediates due to the electronically rich and sterically defined ring system. In medicinal chemistry, introducing the difluoro motif helps adjust metabolic properties, resist oxidative breakdown, and open new activity spaces in compound screening. The free phenolic group remains a practical handle for etherification, esterification, or protective group strategies—key steps in combinatorial and library synthesis.
We watch trends in end use directly through collaborative projects: Drug discovery outfits rely on clean, single-lot materials for definitive biological screening. Materials researchers push the phenolic core into specialty dyes, high-performance coatings, and engineered resins. The product’s success often appears in the form of positive feedback, custom requests for modified forms, and repeat orders for scaled-up quantities. These real-world applications keep us invested in maintaining segregation by lot, rapid shelf-life monitoring, and adapting our packing to the often energy-sensitive nature of the compound.
Compared to simple 4-aminophenol or mono-fluorinated analogs, the 2,3-difluoro variant introduces a level of reactivity and selectivity unique to this configuration. The structure resists certain metabolic transformations while staying reactive enough for downstream modifications—a combination that draws attention in early process development and pilot work. Chemists who have tried related ortho- or para-fluorinated phenols often return to this product for cases where they require a balance between chemical flexibility and metabolic resistance in pharmaceutical projects. We don’t just see that preference in data sheets, but in the purchase patterns and candid feedback collected by our field teams.
From the perspective of someone working day-in and day-out with aromatic amines, the 2,3-difluoro arrangement eases purification steps and minimizes co-product formation in certain coupling and derivatization reactions. It's not unusual to see process chemists comparing yields and impurity profiles from a range of building blocks, eventually settling on this difluoro isomer for consistency in larger scale runs. Over the years, our manufacturing staff has documented solvent compatibility nuances and the need for careful storage, both to preserve phenol reactivity and support users working under tight timelines and purity constraints.
Scaling up this compound from gram to multi-kilogram lots challenged even our seasoned chemists at first. Fluorinated aromatics often bring with them not just routine hazards, but also unique waste streams and equipment compatibility puzzles. Considerations around worker safety, venting, and byproduct management become even more important in larger runs. We invested in corrosion-resistant glass-lined reactors and upgraded air handling to improve both safety and product quality. Ongoing training of our operators, and the deliberate pace of batch monitoring, has kept output tightly controlled—avoiding the costly failures that can come when reactivity outruns experience.
When quality deviations occur, the response is never just a paperwork fix. Our supervisors sit down with production logs, analyze points of contamination or yield loss, and review changes that worked (or failed) in previous campaigns. That willingness to examine each cycle down to unit operations—wash protocols, filtration conditions, trace residual solvent checks—builds a knowledge base that gets handed down between staff and through our training. We see this iterative learning process reflected not only in customer satisfaction but in more robust procedures and steadily improving product specifications year on year.
Handling halogenated aromatics means direct responsibility for careful waste management and minimization of environmental footprint. Every production run produces not just product but also solvent streams and byproducts containing fluorine. Regulations around waste disposal don’t just guide our actions—they force creative thinking about solvent recovery, thermal treatment of residues, and reduction at source. Sometimes a minor improvement—shifting a distillation cutpoint or adjusting aqueous workup—yields measurable gains in environmental performance and cost. Our technical teams submit each new process revision for internal review, with monthly audits of hazardous waste output documented and tracked.
We know that sustainability is not just a marketing word paraded in annual reports. Operators working on the line bring forward practical ideas for drum reuse, cleaned solvent recycling, or in some cases, the ability to repurpose waste streams within adjacent product campaigns. Our process engineers have piloted alternatives in extraction solvents and energy sources, and they routinely query raw material suppliers about responsible sourcing and transport. The goal: less waste leaving the plant, lower risk to the men and women making the product, and the ability for customers downstream to trust that regulatory compliance goes deeper than printed declarations.
Direct communication with research customers and production users shapes much of our ongoing development. No specification is static—feedback about handling, storage life, odor, or batch-to-batch variability powers the small improvements that matter most under real conditions. Our technical support listens when a research group needs smaller pack sizes to reduce material loss, or when a contract API manufacturer asks for tighter limits on organic impurities ahead of a submission. We track all non-conformance reports to identify emerging issues, and quarterly meetings between production and technical marketing ensure these insights lead to improvements, rather than excuses.
We've found that the best answers come from close collaboration, not distance. Laboratory scale users want clear, reliable spectra and analytical details. Process engineers care about filtration kinetics, byproduct volatility, and cost predictability more than catalog copywriting or elaborate brochures. We respond with real data—QC profiles, actual trace impurity chromatograms, and on-request discussions about reaction conditions that match those faced by our customers. The willingness to share operational know-how means fewer surprises, less pilot plant downtime, and faster qualification of Phenol, 4-Amino-2,3-Difluoro- into new projects.
The regulatory world rarely stands still around specialty arylamines and halogenated phenols. Changes in listings, use restrictions, and raw material approvals drive continual review. Our compliance teams monitor regulatory listings not only across our domestic markets but in Europe, Japan, and emerging Asian countries. As requirements become more nuanced—new REACH restrictions, added GHS labeling details, or the demand for traceability in every precursor—the only way to stay ahead is proactive data collection, timely risk assessment, and regular process refreshes to keep the supply chain clean.
Sometimes, the greatest value to a customer is simple access to batch-level MSDS updates, full trace impurity profiles, or answers about major-minor isomer content collected from the plant floor the week before. The responsibility rests with us to maintain fast turnaround when customers confront regulatory deadlines or move toward more formal pharmaceutical qualification. By keeping an open channel between regulatory affairs, plant QC, and the needs voiced by researchers, we catch issues before they snowball into shipment holds or product re-qualification. That builds trust, and it keeps the wheels turning for both sides of the transaction.
Every challenge encountered during the production and support of Phenol, 4-Amino-2,3-Difluoro- brings an opportunity for learning and refinement. Problems never solve themselves—solutions depend on hands-on troubleshooting and the accumulated understanding that only comes from repeated experience. Our operators have improved cleaning and recharging cycles to remove subtle contamination that used to complicate downstream purification. Minor adjustments in crystallization technique, developed through repeated small-scale side-by-sides, now lock in the consistent batch morphology that eases filtration and packing.
Process teams keep detailed logs that capture both successes and failures, avoiding the trap of “black box” manufacturing where problems get swept under the rug. Cross-training in analytical chemistry and technical operations deepens team capacity to spot issues before they reach the customer. Regular process reviews—sometimes prompted by a tricky batch or a new impurity spike—draw in stakeholders from every level, not just management. This culture of shared improvement bleeds into product quality, customer support, and even the morale of staff who know their hands and brains make a daily difference to the finished goods.
What elevates Phenol, 4-Amino-2,3-Difluoro- beyond a dot on a chemical inventory sheet connects back to the real-world demands of the people who use it. For a discovery scientist tweaking drug candidates or a production chemist optimizing a polymerization feed, every shipment carries not just a formula but the investment of a team determined to meet unpredictable needs. No company can anticipate every application, but it is our job to respond quickly and honestly, admitting failures, celebrating successes, and improving the supply chain cycle by cycle.
We bring our own insights, gained through handling, analysis, and production scale-up, to every discussion about this compound. This means more direct answers, fewer frustrations for the user, and a level of transparency rarely seen outside the world of direct manufacturer-customer partnerships. Ultimately, the physical product delivers the promise—but it is the depth of experience, the hands-on correction of mistakes, and the constant refinement that shape not just Phenol, 4-Amino-2,3-Difluoro-, but the relationship that grows with every batch produced and every challenge overcome together.