|
HS Code |
648997 |
| Productname | 5-Bromo-2-(Hydroxymethyl)Phenol |
| Casnumber | 3209-22-1 |
| Molecularformula | C7H7BrO2 |
| Molecularweight | 203.04 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 109-113 °C |
| Boilingpoint | No data available |
| Solubility | Slightly soluble in water |
| Density | No data available |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C=C1Br)CO)O |
| Inchi | InChI=1S/C7H7BrO2/c8-6-1-2-7(10)5(3-6)4-9/h1-3,9-10H,4H2 |
| Synonyms | 5-Bromo-2-hydroxymethylphenol; 5-Bromo-2-(hydroxymethyl)phenol |
| Storagetemperature | 2-8 °C |
| Refractiveindex | No data available |
As an accredited 5-Bromo-2-(Hydroxymethyl)Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5-Bromo-2-(Hydroxymethyl)Phenol, tightly sealed with a screw cap, labeled with safety information. |
| Shipping | 5-Bromo-2-(Hydroxymethyl)Phenol is shipped in secure, airtight containers to prevent contamination and moisture exposure. The package is clearly labeled with appropriate hazard and handling information, compliant with local and international chemical transport regulations. Ensure the material is stored and transported in a cool, dry, and well-ventilated environment. |
| Storage | 5-Bromo-2-(Hydroxymethyl)phenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Protect from moisture, direct sunlight, and sources of ignition. Store at room temperature and handle under appropriate safety conditions, including the use of gloves and eye protection to prevent skin or eye contact. |
Competitive 5-Bromo-2-(Hydroxymethyl)Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Every day in the plant, we watch raw materials transform in our vessels—each detail in process control shaping the character of the molecules we produce. 5-Bromo-2-(Hydroxymethyl)phenol provides a good example of a specialty intermediate that challenges us as manufacturers to maintain both reliability and functionality at scale, especially as downstream users look for consistent purity and reactivity. Each batch tells the story of our own technical diligence, and customers’ expectations only reinforce why this product matters not as a generic chemical, but as a distinct solution in advanced synthesis.
5-Bromo-2-(Hydroxymethyl)phenol carries the molecular formula C7H7BrO2. Whenever our R&D team refines routes, the goal lines up: support end-users where trace impurities or inconsistent appearance would upend their protocols. Quality in this context travels beyond the purity number percentage. Most requests call for material above 98% assay by HPLC. Checking water content, halide impurity profiles, and even the habit of the solid becomes a regular routine. Each specification is a matter of keeping your processes smooth.
We have seen that trace residual solvents from synthetic steps—especially those involving methylation or protection—can cause headaches downstream. To counter this, we validate each batch with a combination of GC-MS and Karl Fischer titration to meet the tightest limits, typically restricting moisture below 0.5%. We also monitor for residual inorganic bromides, working to hold total halide content at minimal levels, since even small shifts in process create major effects in further reactions, especially for those pursuing API intermediates or sensitive coupling reactions.
Output often appears as off-white to light tan crystalline powder. While some may overlook color consistency, we know how changes hint at variations in route or purification. By sticking to a standardized process involving controlled crystallization temperatures and proper solvent recovery, we keep a closer match to the expected appearance, so downstream users don’t need to adjust filtering or recrystallization protocols.
At its core, 5-Bromo-2-(Hydroxymethyl)phenol features a phenol base with both bromine and hydroxymethyl substituents. The twin presence of electron-rich and electron-withdrawing groups unlocks unusual reactivity. Those working in fine chemical, agrochemical, and pharmaceutical development often seek such compounds for selective transformations. For example, the benzyl alcohol functionality at the 2-position opens up scope for etherification and esterification, while the aromatic bromine is a known handle for Suzuki and other cross-coupling reactions. These halogenated aromatics see heavy use as building blocks in syntheses where substitution patterns on the ring impact biological or electronic properties, whether adding functional groups or crafting scaffolds for novel molecules.
Over time we have heard directly how formulation chemists appreciate minimal side products in this intermediate, because so much material ends up transformed in a single further step. Even minor isomeric or colored byproducts can end up traced into the final APIs or disrupt purification, especially for regulators looking for impurity tracking. We have worked closely with several partners who move on to produce higher phenolic ethers and bioactive compounds from our 5-Bromo-2-(Hydroxymethyl)phenol. At higher volumes, the physical properties—flowability, tendency to cake, filtration ease—have shaped our own approach to packaging and handling. The right particle size distribution, achieved by careful control at the drying and micronization stage, can speed up handling without excessive dust, reducing loss and simplifying weighing and charge-in on customer lines.
Another common request concerns solubility and compatibility with various solvents. We track patterns: this compound shows moderate solubility in organics like methanol, ethanol, or acetone, while remaining sparingly soluble in water. This lets downstream users set up parallel reactions or crystallizations, and shuttle intermediates through multi-step syntheses without worrying about unwanted precipitation or losses during extraction.
No discussion from a producer’s perspective ignores safety and regulatory scrutiny. When working with halogenated phenols, proper handling is central—both on our shop floor and for our customers. Our operating experience drove us to upgrade local exhaust systems and implement redundant monitoring for residual brominated organics, reducing both worker exposure risks and cross-contamination with non-halogenated product lines. Each lot’s full raw data archive is available for audit, building downstream trust for those tracking every input toward regulated APIs or advanced material applications.
Traceability starts long before the product ships. We document starting material sources, maintain on-site analytical records, and perform stability tests shedding light on both shelf life and shipping behavior. Our own shipping department treats packaging as more than a regulatory checkbox—inner PE liners, desiccant capsules, and UN-compliant outer drums protect product quality through storage and transit. More than once, feedback from partners has prompted us to adjust liner thickness or drum type, as we learn firsthand how product can settle, compact, or even discolor after weeks en route. These real-world user reports drive incremental improvements, not just for compliance, but for practical reliability.
With dozens of brominated phenols on the market, experienced buyers and end-users care about subtle points. Compared to analogues such as 2-bromo-5-hydroxybenzyl alcohol or 5-chloro-2-(hydroxymethyl)phenol, a difference in halogen placement and functional group orientation often spells altered reactivity. Our process selects for the 5-bromo orientation, giving a product that performs reliably in electrophilic substitution without excess unreacted starting material or positional isomers that scramble downstream chemistry. We set batch production up to minimize dimer and oligomer formation that can frustrate those working under catalytic protocols or high-dilution conditions.
Customer chemists have mentioned that with competitor samples, issues can arise from color instability or microimpurities, leading to extra purification steps and even revalidation in customer labs. Paying attention to storage recommendations and shelf life helps, but so does running extra stress tests on temperature and humidity effects at the production site. That way, by the time the product lands in customer facilities, both purity and reactivity profiles match original COA claims without the surprises of discolored, clumped, or decomposed product.
Direct dialogue—real questions from those using our product under scale-up or pilot conditions—have pointed out challenges that rarely come to light in standard product briefs. For instance, some customers flag that certain polymorphic forms dissolve faster or slower than expected, impacting how material performs in continuous processes. Others note that subtle shifts in melting point, outside stated ranges, can suggest batch drift or thermal instability before any analytical issue shows up. After running our own process adjustments and batch comparison studies, we’ve built a tighter feedback loop: not just passively relying on analytical readings, but taking time to see how our material behaves in actual customer environments.
Growing pressure for responsible production pushes us to look closely at waste, emissions, and process efficiency—not only for our own sustainability metrics but for downstream users needing “greener” supply chain inputs. The bromination step—often a major environmental and safety hazard in older syntheses—has moved in our plant toward closed-system operation with recovery and recycling of excess reagents and solvents. Thermal oxidizers and active carbon scrubbers further cut halogenated byproduct release, and we monitor effluent for both organic load and trace bromine levels.
On resource use, process intensification has trimmed both water and energy demand per output kilo, freeing capacity for flexible scheduling and reducing overall cost burden. Rather than wait for top-down mandates, our technical and production teams meet to discuss near-miss or efficiency stories—how to get better yield, cleaner mother liquors, or less packaging waste, translating “small wins” on the shop floor to real operational improvements.
We’ve also seen a market push for documentation around “green chemistry” attributes. Regular audits of our process—tracking renewable solvent content, bromine recovery rates, overall atom economy—feed directly into sustainability reports required by pharmaceutical and agrotech clients. By highlighting improvements achieved in actual production, we hope to shorten compliance cycles for those aiming for eco-labels or more robust supplier audits.
From our vantage point, the most interesting stories come from how customers use our 5-Bromo-2-(Hydroxymethyl)phenol to unlock new chemistry or unblock process bottlenecks. Over the years, we’ve supplied both kilo-labs and commercial-scale operations across sectors. In one case, a customer transitioned from phosgene-based synthesis to a milder, single-pot etherification protocol, enabled by our consistent intermediate. In another, a research team leveraging our product managed regioselective Suzuki coupling under mild conditions, opening access to rare aryl-alkyl scaffolds for preclinical trials. Each success feeds back—adding pressure to maintain and tighten quality, since at-scale process hiccups quickly force recalibration.
Technical questions never stay “on paper”: reaction yield drops, unpredictable exotherm, or new reactivity trends show up in customer facilities and labs. Our technical support and analytical teams take these reports seriously, running parallel tests with retained samples to check for off-spec drift, contamination, or unexpected degradation. This open loop reinforces each new order; long-term partners appreciate that our approach to problems is “hands-on” rather than supply-and-forget.
Moving specialty chemicals from the factory to the end user sometimes seems simple, but practical hurdles pile up. During hotter months, even “thermally stable” materials have shown unexpected caking or color shift if stored under poor conditions. To solve these problems, we’ve upgraded transport modes and storage guidance, using thermal insulation liners, GPS-logged containers, and third-party warehouse audits for major shipments. Our logistics team tracks and communicates ETA in real time, coordinating with receiving departments to plan for controlled-temperature offloading or segmented storage if needed.
From a handling perspective, the hygroscopic nature of 5-Bromo-2-(Hydroxymethyl)phenol means exposure to even minimal ambient humidity may impact apparent assay. We include both quantitative test frequency and subjective inspection (appearance, free-flowing property, odor checks) on load-out and inbound logistics. This emphasis on observable, practical handling factors helps customer QC labs verify product status on receipt, and check against internal standards. Feedback from these steps often traces back, prompting minor but cumulative improvements on our end.
As a producer, our perspective is shaped by more than just codes or lab data—it’s defined by real communication with customers. One batch flagged for off-odor, another for high insoluble particulate in a coupled synth: each report sends us back to our plants and process engineers. We share not only batch records, but also open troubleshooting notes, suggestions for purification tweaks, and ideas for handling under less-than-ideal conditions. The result so far has been shorter lead times for routine orders, proactive planning for custom specs, and an expanding set of test protocols grounded in both analytical and field feedback.
Collaboration goes both ways. Several major clients have welcomed site visits, letting our formulators observe performance not just in isolation but inside multi-ton reactors, with the tough realities of scale at play. Our chemists pick up on the details sometimes lost in translation—how a slight yellowing at one stage dings the next, or how particle size from our mill affects dispersion in their feedlines. Such firsthand insight directs real improvements, giving new life to “old” molecules by crafting products that answer more than just the minimum assay.
Shifting regulatory frameworks, rising purity expectations, and growing demand for tailored building blocks all shape our approach to producing 5-Bromo-2-(Hydroxymethyl)phenol. It’s not enough to simply match a standard anymore; instead, we dig deeper into feedback, track new requirements, and invest in plant upgrades that deliver safe, consistent, traceable product. Every challenge, whether caking in transit, slow dissolution, or troublesome color variance, teaches us something new about both the compound and the context in which it’s used.
By treating our work not as the finish line, but as a flexible process shaped by real-world users, we support long-term partners and new entrants alike. The journey to producing 5-Bromo-2-(Hydroxymethyl)phenol without compromise goes hand-in-hand with sustainable practices, transparency in documentation, and active collaboration. This mindset extends beyond commodity supply to true specialty collaboration in the downstream synthetic world.
For any company or research group deeply invested in building new molecules from robust, reliable starting points, our commitment stands: each lot sent out reflects lessons learned, problems solved, and an open channel for future improvement. As demand for advanced functional ingredients continues to rise, we keep finding new ways to enhance—and not just maintain—the value delivered by each shipment of 5-Bromo-2-(Hydroxymethyl)phenol.