|
HS Code |
513865 |
| Iupac Name | 2-[(E)-(Hydroxyimino)methyl]phenol |
| Cas Number | 556-08-1 |
| Molecular Formula | C7H7NO2 |
| Molecular Weight | 137.14 |
| Appearance | Yellow crystalline powder |
| Melting Point | 160-163°C |
| Solubility In Water | Slightly soluble |
| Density | 1.27 g/cm3 |
| Synonyms | Salicylaldoxime |
| Pka | 10.0 (phenolic OH) |
| Chemical Structure | C1=CC=C(C(=C1)C=NO)O |
| Pubchem Cid | 70793 |
As an accredited 2-[(E)-(Hydroxyimino)Methyl]Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 g of 2-[(E)-(Hydroxyimino)Methyl]Phenol is packaged in a sealed, amber glass bottle with detailed labeling and safety information. |
| Shipping | 2-[(E)-(Hydroxyimino)Methyl]Phenol is shipped in tightly sealed containers, protected from light and moisture. Transportation complies with relevant chemical safety regulations, with appropriate labeling and documentation. Packages are cushioned to prevent breakage and leakage, and handled as a potentially hazardous material. Temperature and ventilation controls are maintained as recommended for chemical stability. |
| Storage | 2-[(E)-(Hydroxyimino)Methyl]Phenol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances like strong oxidizing agents. Protect from moisture and avoid prolonged exposure to air. Use appropriate chemical storage cabinets, label the container clearly, and follow institutional safety protocols for handling and storage. |
Competitive 2-[(E)-(Hydroxyimino)Methyl]Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Inside any chemical plant, day after day, barrels roll through filled with raw potential – that’s where 2-[(E)-(Hydroxyimino)Methyl]Phenol earns its reputation. Years on the production floor have given us a clear view of what makes this product tick and where it shines in real-world applications. This isn’t just another catalog entry or a jumble of numbers and certifications. This is about how we, as those who craft it, make choices batch after batch to keep this compound pure, reliable, and fit for purpose.
Chemists might call it a hydroxyiminomethyl phenol, but in the plant, we’ve seen how its oxime functionality (the =N–OH bit attached to the benzene ring) lets it plug into a range of syntheses that simpler phenols never touch. Over the years, more researchers and technicians have come asking for this specific structure, and there’s a reason: it offers both the reactivity profile of a phenolic hydroxyl and the coordination ability of the oxime group. That translates to a molecule that binds, reacts, and protects in unique ways.
While many aromatic compounds offer either chelating properties or easy downstream modification, the dual functionality here means no compromise between binding strength and further chemical transformation. For those synthesizing pharmaceuticals, chelating ligands, dyes, or other organic intermediates, this difference can cut days off development cycles and reduce missteps in scale-up. Senior staff in synthesis operations often mention how the consistency in melting point, color, and NMR spectrum from our production lots helps spot-check quality in a hurry.
If you come into our operation, you’ll hear plenty about QC columns and run sheets. What makes a batch “model” quality isn’t just about a single magic number. We rely on a range of practices, including regular adjustment of the oximation procedures, choosing which solvents pull the product out purest before recrystallization, and monitoring chromatogram peaks to resolve trace byproducts. Every production round, we reference these physical cues way before the sample ever gets logged into an inventory list. If you’re a formulator or a bench chemist, you can taste the difference when a product lands on your bench with that reliability – faster filtration, cleaner reactions, and less lost time filtering out impurities.
Some requests demand a high-purity grade for research or active pharmaceutical ingredient precursors, where even slight contaminants can throw off downstream results. At other times, a technical grade works just fine for industrial applications like metal chelation or specialty pigment synthesis. Because we’re not simply purchasing another company’s supply, but running each batch in-house, real tuning happens here rather than through a broker’s paperwork.
We rarely discuss purity as an abstract number. Instead, batches show their quality in how they behave afterwards. Color consistency signals minimal trace impurities. Solid-state stability in storage ensures longer shelf life. Melting point variation tells us immediately if something diverted from spec, so we can hold the line before it goes any further. In our own plant, nobody likes an unexpected surprise mid-process; these physical details affect both our loading procedures and the confidence of every dispatcher sending material across the country.
Our longest-tenured technicians spend time sniffing out not just analytical data but the less formal indicators of a solid run, too. Minimal dusting, consistent flow through hoppers, and a lack of caking in the drums are markers other sectors overlook, but obsessing over these differences adds up to real efficiency shifts in end-user operations.
It’s easy to tell a story about a molecule’s theoretical use – reality sometimes has a mind of its own. For years, we saw this compound in specialty pharmaceutical synthesis, especially those steps involving selective transformations of the oxime group to amines or amidoximes. Laboratories valued predictable yields and few side products, and our own engineers spent months perfecting crystallization methods to minimize mother liquor waste.
Things didn’t stop there. As more synthetic chemists began exploring stable ligands for transition metal complexes, requests for 2-[(E)-(Hydroxyimino)Methyl]Phenol increased for applications in catalysis, separations, and even battery technology. Direct feedback from those process developers pointed out that other sources often carried traces of aldehyde or over-oxidized materials, which severely affected enzyme assays and bio-catalysis runs. Resolving these issues meant adjusting our washing protocols and sometimes choosing costlier but cleaner solvents – decisions you feel in the plant’s bottom line, not just in brochures.
We also watched pigment chemists put this molecule to use as a key intermediate for azo dye precursors. There’s a direct impact here: the shade, brightness, and lightfastness all respond to how pure and structurally perfect the compound is going in. The teams formulating high-value inks and coatings cared as much about trace metals and dustiness as they did about over-ambitious certificate numbers.
Take a bag of standard hydroxybenzaldehyde and line it up next to our material. Despite similar scaffolds, adding the oxime function brings a new world of application. While you might turn to simple phenols for antioxidant chemistry or basic resin synthesis, this compound steps forward as a foundational starting point for ligand formation, chiral catalysts, and selective protective group strategies.
Every project coordinator we’ve talked to mentions that the range of downstream reactions benefits from that extra handle on the molecule. Whether that’s for forming Schiff base ligands, or using the oxime for mask-and-unmask strategies in fine chemical synthesis, the gap in utility is clear to those who spend hours optimizing on the bench.
Our own R&D group, collaborating with both industrial and academic partners, found gains in using this molecule as an intermediate for anti-cancer agents and as a reagent in trace metal analysis protocols. Over the past decade, we’ve documented cleaner conversions and fewer process shutdowns than we ever saw with non-oxime-substituted phenols, especially under the harder scale-up conditions of real-world manufacturing.
Living with a product day-in and day-out means we see firsthand how even small tweaks in process impact outcomes for customers. Feedback often points to the overall “feel” of a batch – how it pours, how it dissolves, if it gunks up equipment unexpectedly. We respect that because in our own blending rooms, time lost is real productivity lost.
To prevent disruptions, we keep the levers close: hands-on involvement in purification steps, strict temperature control during both oximation and subsequent crystallization, and attention to packaging integrity. If a customer in a pharmaceutical lab flags a problem, our techs can pull corresponding shift records within hours, not days. Troubleshooting happens at the source, not through a phone chain with intermediaries.
Over the years, staying this close to every stage of manufacture, and holding material for internal evaluation when needed, has allowed us to catch drifting impurity patterns before they reach the market. Any long-time user will notice fewer inexplicable side reactions, higher overall throughput, and less rework once raw material is dialed in to this degree.
Chemistry doesn’t sit still. As green chemistry pushes forward, we’ve spent considerable time swapping older solvents for those with lower toxicity, and optimizing waste streams for recovery instead of sending them to disposal. This wasn’t about marketing – it came from wanting the same things every worker in this field wants: safer conditions, less environmental headache, and improvements that actually lower total cost of ownership.
Customers today want traceability, and in direct manufacturing, that’s not a problem. Barcodes trace each drum to individual operator logs and batch runs. Analysts can tie impurity data or downstream problems directly to the shift it was made. These records make regulatory audits straightforward, but they also make improvement cycles much faster. Recommendations from the floor or science group get tested and logged as formal process updates – a feedback system that eventually reflects in the consistency of the supplied product.
Our work doesn’t come from whiteboards alone. Some of our staff have two decades behind the tanks, remembering the time before rigorous in-house HPLC could be run on every batch. Our upgrades in the past years include more frequent spot-testing, improved drum handling to keep particulate levels down, and automation steps that reduce mix-up risk between phenolic intermediates.
As downstream industries push for lower impurity levels and more transparent supply chains, we have the tools to adjust without bottlenecks. Product consistently arrives with the same shade, melt behavior, and solubility characteristics year after year, because our operators have the authority to tweak, pause, or quarantine batches that don’t make the grade. If a partner needs a custom particle size or wants extra spectral data, we’re accustomed to running those analyses directly rather than passing requests through countless hands.
Not every product leaves the facility destined for headline applications or major pharma launches. Some become routine reagents in smaller plants, teaching labs, or pilot lines. These users need the same level of attention to physical and chemical integrity. Through real conversations, we’ve adapted packaging, batch sizes, and even labeling so each user knows not just what they’re getting, but why each batch behaves as it does.
We often hear that the most valuable difference isn’t only in claims but in delivering a product that responds consistently over months, not just one shipment. Trust builds with each new order where performance matches the last, and that’s only possible with control at the manufacturing level.
Competitors may offer technical or high-purity grades, but they often resell rather than create, which means every hiccup becomes a communication marathon. By making every kilogram ourselves, we keep eyes on at each finish line. Standard phenols still serve their purpose for many basic oxidation reactions or polymer uses, but our customers needing that oxime edge find themselves solving challenges other suppliers couldn’t address.
Some alternative intermediates feature similar skeletons but lack the same dual reactivity, so chemists need workarounds that slow development or scale-up. Others come in with attractive specs but fall down on storage, leading to caking or loss of functionality after a few weeks on the shelf. We’ve tackled these hurdles by tightening up both synthesis cleanliness and moisture-control practices, lessons learned from customers’ own process setbacks.
Anyone with boots on the ground knows that “purity” isn’t just an NMR spectrum. It’s about whether the batch survives transit, stores without degradation, and enters downstream processes without gumming up filters or skewing critical control points. The scalabilty test is real – products that work in a 1-gram ampoule often disappoint at 100 kilos if they aren’t engineered with robustness in mind.
This is where repeated investment in both people and equipment pays off. Automated filtration, closed-system solvent transfers, and in-process testing make today’s material better than might have been possible even five years ago. Prompt internal communication plus rapid troubleshooting helps catch small issues before they spiral, making each batch slightly more user-friendly than the last.
Ultimately, the true measure of value comes not from a spreadsheet, but from a frank exchange with the chemist, the operator, or the process engineer at the other end: Did the product support their work, keep downtime in check, and help deliver the end results needed? For those who use 2-[(E)-(Hydroxyimino)Methyl]Phenol where its dual functions have no real substitute, these benefits become clear over time.
The market keeps shifting. Regulations evolve, science pushes boundaries, and end-uses sometimes surprise even the design teams. Here, we stay connected – to both our own production lines and the many users who push this molecule furthest. Over time, improvements add up, whether in how a product handles during transfer, lasts on the shelf, or plays its part in more complex syntheses.
What often keeps loyal partners returning is this cycle of honesty, responsiveness, and direct responsibility for every shipment. It isn’t an abstract commitment, but a lived experience from one chemical plant to process bench and back again. That, more than charts and certificates, is what has given 2-[(E)-(Hydroxyimino)Methyl]Phenol its steady place in ever more demanding labs and factories. We look forward to sharing the benefits of that cumulative knowledge with anyone who sees, as we do, that chemical manufacturing is about getting the details right, every time.