Chemistry grows through moments of need and flashes of discovery, and 2,6-Bis(Hydroxymethyl)-P-Cresol serves as a classic example. Lab records from early polymer and resin research in the mid-20th century mention compounds such as this one, often identified through trial and error, before computers and elaborate software could calculate probable molecular behavior. As interest in heat-resistant, impact-modified resins picked up, so did attention to specialty phenols like 2,6-Bis(Hydroxymethyl)-P-Cresol. It belonged to a group that bridge straightforward organic chemistry with the demands of industrial durability, growing out of the desire for structural reliability in plastics and coatings, especially in postwar manufacturing expansions. Seeing older patents and bench notes reveals a pattern—early researchers looked for phenolic compounds that behaved consistently, remained cost-effective, and handled moderately harsh conditions without breaking down, and they found that this compound checked off those boxes long before it gained its now-common applications.
2,6-Bis(Hydroxymethyl)-P-Cresol, better known in labs as a specialty phenolic alcohol, is far more than a simple building block. Chemists identify it by its two hydroxymethyl groups anchored to a cresolic core, with each addition making the molecule more versatile. Ease of modification lets it function as a crosslinker or chain extender across multiple resin backbones. It finds steady use wherever added stability and specific reactivity matter—think in the formulation of durable coatings, composite materials, and adhesives. Its backbone structure carries through into polymers and resins, often lending properties that meet demands for higher performance in heat and chemical environments. Each time I worked with phenolic resins and searched for additives that could improve toughness without offsetting color or other properties, this compound landed high on the candidate list for functional modification.
2,6-Bis(Hydroxymethyl)-P-Cresol appears as an off-white to pale yellow crystalline solid at room temperature. It presents a moderate melting point—typically around 110–115°C—which allows for straightforward melting and mixing in industrial batch reactions. Solubility trends follow expectations for phenolic systems: limited water solubility, but good solubility in polar organic solvents and many alcohols. Its two benzyl alcohol-style functional groups offer convenient points for reaction, particularly esterification or etherification, while the methyl group at the para position keeps reactivity from getting out of control. This set of properties defines why it carries such a niche for manufacturers aiming to tweak performance in specialty polymers. It balances chemical reactivity with a physical form that isn’t dust-prone or hard to handle.
Commercial suppliers describe 2,6-Bis(Hydroxymethyl)-P-Cresol with specifications focusing on purity—usually 98% or greater. Moisture content typically sits well below 1%, a necessity to preserve shelf life and prevent degradation in sensitive catalytic processes. Residual solvents and heavy metal limits receive tight control, as even trace contaminants can spoil entire production batches in high-end resin shops. Product is usually packed in multi-layer paper or plastic-lined drums to minimize exposure to the ambient environment. Labels follow global harmonized system (GHS) standards, laying out hazard pictograms, PPE requirements, and emergency measures for spills or exposure. This level of detail benefits not only large-scale users but also researchers building out bench-scale runs, providing crucial data on minimum handling precautions and product expiry.
Manufacturing of 2,6-Bis(Hydroxymethyl)-P-Cresol favors a condensation sequence using p-cresol as the substrate. Under basic conditions, formaldehyde reacts with the ring positions adjacent to the hydroxyl, yielding the symmetric diol. Companies optimize for yield by holding reaction conditions at slightly elevated temperatures and closely monitoring pH—too much base tilts the product mix toward unwanted tri-substituted byproducts, while insufficient catalyst slows action to impractical rates for industry. Isolation and purification usually combine solvent extraction and recrystallization, steps that ramp up both purity and the price tag. Waste streams feature significant formaldehyde and phenolic residues, so production remains closely regulated and invested in waste minimization through closed-loop recovery and reuse systems. Over years in lab management, I found that scaling up this preparation always demanded more robust emission controls than theory books let on.
As a phenolic compound with accessible -CH2OH groups, 2,6-Bis(Hydroxymethyl)-P-Cresol stands out for the breadth of transformations it allows. Chemists routinely anchor alkyl, acyl, or aryl substituents at these benzylic positions, shifting solubility and reactivity as the application directs. It easily responds to etherification with various alkyl halides, and esterification opens up use in specialty polyester or acrylate resins. In curing systems, chemists use it as a crosslinker in epoxy matrices, taking advantage of the two hydroxymethyl groups which, under acid or base catalysis, react to extend chain length or form bridges. Its phenolic function provides a mild antioxidant character, giving it added utility in protective coating blends. Many synthetic pathways that employ it require fine control over stoichiometry and temperature, as overreaction leads to undesired polymerization, which can send costs up and quality down.
While publications typically refer to this compound as 2,6-Bis(Hydroxymethyl)-P-Cresol, the marketplace is less formal. Suppliers label it as 2,6-Dimethylol-4-methylphenol, Dimethylol Paracresol, or simply DMPC. In journal articles, names like 2,6-Bis(hydroxymethyl)-4-methylphenol occasionally crop up, reflecting slightly different naming conventions. Regulatory and chemical catalogs tie all these names to common identifier numbers—CAS number 7326-09-6 appears most consistently. Over years of reading MSDS sheets and supplier catalogs, cross-referencing these names saved me from costly ordering errors, particularly when sourcing outside North America.
2,6-Bis(Hydroxymethyl)-P-Cresol carries a hazard profile consistent with other substituted phenols. Skin and eye contact cause moderate irritation, and inhalation of dust should be avoided. Many operations require gloves, goggles, and in some situations, local exhaust ventilation to keep airborne concentrations below occupational limits. Facilities handling bulk amounts install spill containment and eyewash stations, practices born from notorious incidents in resin plants where a single missed procedure led to persistent injuries. Safety Data Sheets mark it with acute oral toxicity and moderate aquatic hazard, and transportation follows the usual procedures for organic chemicals in the phenolic class. Best practices mean training operators on both routine handling and emergency response, as ignoring these steps only leads to avoidable injuries and expensive regulatory fines. Keeping logs of exposure times and incident reports adds not just to workplace safety but also to a culture where people trust the process and each other.
Use of 2,6-Bis(Hydroxymethyl)-P-Cresol stretches across diverse sectors, with each field exploiting its chemical backbone for different reasons. In the plastics industry, it acts as a cross-linker and chain extender in phenolic and epoxy resins, delivering elevated heat stability and mechanical toughness. It helps improve impact resistance and surface durability of molded parts used in automotive interiors and circuit board laminates. Paint and coating manufacturers blend it in to lend scratch and chemical resistance, particularly for industrial and marine applications exposed to harsh settings. In adhesives, it underpins formulations that require a mix of fast cure and high final strength, especially in wood and construction bonds. Lesser-known roles include use in rubber vulcanization accelerators and in specialty intermediates for pharmaceuticals and biocides, often dictated by how companies want to tweak a product’s final test profile.
Innovation teams continue to find new outlets and improved recipes for 2,6-Bis(Hydroxymethyl)-P-Cresol derivatives. Labs design tailored modifications—introducing bulky groups to fine-tune solubility, grafting side chains to boost hydrophobicity, or blocking positions to prevent unwanted side reactions. Work on green synthesis looks for alternative feedstocks and conditions that cut waste, energy use, and hazardous byproducts. R&D also addresses recyclability, as manufacturers push for materials that hold up under repeated melting or shredding, reducing both costs and landfill impact. I often see university and industry partnerships digging into nanocomposites and specialty photopolymers, where this cresol variant forms a backbone for finer property control. In recent years, focus has also shifted to biomimetic applications, exploring molecular designs that mimic naturally occurring cross-linkers but allow synthetic tuning, driven largely by demands for both performance and environmental responsibility.
Studies over the decades show 2,6-Bis(Hydroxymethyl)-P-Cresol as acutely toxic to aquatic life, with moderate risk profiles for mammals at high doses. Long-term animal studies point to low but measurable organ effects at prolonged or high exposures, issues that feed into workplace exposure limits and waste-handling rules. Environmental persistence remains a concern, as the molecule does not break down rapidly in soil or water. Labs use simulated sunlight and microbial exposure to test degradation products, and these investigations often take months to return reliable pointers for safe disposal or treatment. Research also tracks any tendency for bioaccumulation—so far limited but still under close review, particularly in regulatory circles. These findings continuously shape site permits and trade rules for shipping and storage, and remind manufacturers that chemical progress always comes tied to environmental responsibility.
Looking ahead, demand for specialty cross-linkers and stabilizers, especially those that combine reactivity with manageable toxicity, means 2,6-Bis(Hydroxymethyl)-P-Cresol holds a steady role in chemical manufacturing. Its structure still offers room for tweaking, and trends in research favor more sustainable production routes, including chemosynthesis that replaces petroleum feedstocks with bio-based inputs. With end users requiring more transparency on sourcing, lifecycle, and disposal profiles, chemical suppliers explore traceable supply chains and closed-loop systems to keep waste in check. New product categories—high-value 3D printing resins, flexible electronics, medical polymer blends—look to this compound as a safe bet for stability and adaptability. The future will likely demand even tighter control over both practical performance and environmental footprint, and chemists who learn the deep details of how these molecules behave stand well-positioned to guide new generations of safer, more responsible material development.
2,6-Bis(Hydroxymethyl)-P-Cresol rolls up its sleeves in resin manufacturing. Phenolic and epoxy resins benefit from its molecular structure. You see, this compound doesn’t just take up space in the mix; its two hydroxymethyl groups interact with other chemicals to tighten up the polymer network. The end result: resins with greater thermal stability and durability. If you’ve worked in coatings or adhesive labs, you know how heated those cycles can get—both temperature-wise and deadline-wise. A resin that stands tough during production and use keeps things ticking smoothly. That reliability matters for furniture coatings, automotive finishes, and structural adhesives where failure just isn’t an option.
Plastics and rubber manufacturers keep an eye on how materials age. Here, 2,6-Bis(Hydroxymethyl)-P-Cresol steps in as an antioxidant. By slowing down oxidative degradation, it helps products last longer on the shelf and in real use. Whether you’re building weather-resistant cable insulation or medical equipment that faces sterilization, oxidation breaks down ordinary materials over time. This compound helps manufacturers dodge frequent replacements, supporting cost efficiency and reliability. Published studies have highlighted how derivatives like this outperform simpler phenols for resisting polymer breakdown. A single additive can trim costly failures and waste down the line.
In my time collaborating with electronics designers, I’ve noticed how circuit boards, encapsulants, and coatings face serious light and heat challenges. 2,6-Bis(Hydroxymethyl)-P-Cresol finds use in photo-curable resins that harden quickly under UV lamps. That makes it a favorite for companies building touch screens, optical lenses, or thin protective films. Quick cure times help products get to the customer faster without sacrificing performance. For printed circuit boards, both electrical insulation and thermal endurance hold tight, which proved crucial when I saw devices rolling off assembly with near-zero defects following a switch to advanced additives like this.
Researchers in pharmaceutical chemistry keep exploring the structural backbone of 2,6-Bis(Hydroxymethyl)-P-Cresol. Certain derivatives act as intermediates for active drugs. Its chemical reactivity supports the synthesis of agents that require precise molecular modifications. In published works since the 2010s, innovation teams have used its unique arrangement to build inhibitors, anti-bacterial candidates, and other agents. Starting with reliable building blocks speeds up discovery and brings down costs in drug pipelines.
Every advanced additive brings challenges. There’s always pressure to deepen toxicology data and ensure environmental safety. The conversation between product developers and regulators keeps 2,6-Bis(Hydroxymethyl)-P-Cresol under careful review. Strong documentation and transparent sourcing help companies protect both worker health and product safety. Finding ways to engineer more biodegradability or lower toxicity in similar compounds represents an active research push. Lab teams have started taking inspiration from green chemistry principles, testing new routes that cut hazardous byproducts.
Access to high-quality 2,6-Bis(Hydroxymethyl)-P-Cresol supports fields ranging from synthetic polymers to medical innovation. From improved shelf life on plastics, to faster device manufacturing, to creative pharmaceutical research, progress in this compound’s chemistry keeps shaping the products people use every day. Staying aware of both the advantages and the possible trade-offs helps ensure the best outcomes at every step.
Plenty of folks in chemistry circles talk about 2,6-Bis(Hydroxymethyl)-P-Cresol, but the name doesn't exactly roll off the tongue. The structure tells a story before you even get to its job. Take a benzene ring, toss a methyl group on the para-position, then stick hydroxymethyl groups on both the 2 and 6 positions. That layout isn’t random; chemistry’s got a reason behind it.
Its chemical formula comes out as C9H12O3. If you diagram it, you’ll see a six-carbon ring at the center. You find a methyl (-CH3) at the ‘para’ spot, hydroxymethyl (-CH2OH) arms at both 2 and 6 positions. The full IUPAC name is 2,6-bis(hydroxymethyl)-4-methylphenol. Each added group brings new quirks to how it behaves in different conditions.
The way molecules get arranged changes everything. The two hydroxymethyl groups aren’t just accessories for the chemist. They give the molecule the power to build bridges—literally, in the world of plastics and resins. Having multiple reactive spots makes crosslinking possible, which matters when you’re looking for performance in adhesives or coatings. If you’ve worked with resin systems, you know how much those extra reactivity sites can matter for the strength and durability of finished products.
I’ve spent time in research labs watching quality depend on these little details. A batch with a slightly different functional group distribution changes not only the viscosity but how tough or water-resistant the end result gets. It's a lesson I picked up the hard way—thinking you can swap out a similar phenol, only for the resin to fail pull tests. Some lessons stick, especially those that involve expensive product recalls.
People use 2,6-Bis(Hydroxymethyl)-P-Cresol in more than just one narrow field. In the production of modified phenolic resins, its crosslinking ability makes it a prime choice. It also gets attention in the world of stabilizers for plastics and even specialty coatings, where the resistance to heat and chemicals becomes critical. These aren’t theoretical needs—industries that run hot, like electronics manufacturing, see the value every day.
Beyond industry, the basic structure pops up in academic settings too. Masters students and PhDs like to bring up its footprint in organic synthesis, not only for teaching, but for developing custom molecules with specific binding properties. The placement of each group could determine interactions with metals or enzymes. Once again, structure sits at the core.
Despite its usefulness, production isn’t without roadblocks. Access to reliable, high-purity 2,6-Bis(Hydroxymethyl)-P-Cresol sometimes gets tricky, especially when manufacturers cut corners and leave impurities behind. Those leftovers can block desired reactions or even prompt unexpected side effects in finished goods.
Improving synthesis routes and pushing for tighter quality control inside the plant makes a major difference. Partnering with trusted suppliers helps, but testing every new batch became common practice after one too many headaches. Greater transparency in sourcing and a stronger focus on purity set the foundation for consistent results, not just theories.
Education keeps making an impact. Younger chemists, armed with better tools and a clear understanding of structure-function relationships, catch potential pitfalls earlier in development. This knowledge, paired with steadily improving tech, holds promise for better and safer uses of not just this molecule, but others like it.
2,6-Bis(Hydroxymethyl)-P-Cresol pops up in the world of industrial chemistry, often used to tweak polymers or plastics, and sometimes in the making of specific resins or as a stabilizer. Most folks outside research or chemical engineering probably never handle it directly, but it plays an invisible role behind the scenes in everyday products.
There’s a lot of confusion around whether this substance poses a real hazard. Let’s lay out what actually matters: toxicity depends on how much of the material a person absorbs, inhales, or ingests, not just whether the compound has a scary name. According to available studies, 2,6-Bis(Hydroxymethyl)-P-Cresol can cause irritation to the skin, eyes, and respiratory system, especially in powder form. There’s lab data showing that high exposure might mess with animal organs, particularly the liver and kidneys, when animals receive big doses over time. Nothing out there suggests casual, short-term contact is likely to lead to severe health effects, yet chemical companies always call for protective gear — gloves, goggles, masks — during handling. Most of these safety precautions come from good old-fashioned caution rather than clear evidence of disaster looming behind every spill.
The EPA and the European Chemicals Agency both give this chemical close attention. They push for clear labeling and risk assessments before workers deal with any significant quantities. One big reason: substances with phenolic groups sometimes cause harm after long exposure, especially if inhaled as dust or vapor over several years. No one likes rolling the dice when it comes to health at the job. My own time in a small-scale manufacturing shop taught me that it’s easy to shrug off chemical hazards until someone develops dermatitis or asthma out of the blue. Seeing a trusted coworker sidelined by what started as an innocent powder made me believe in being proactive about these potential risks, not just checking off boxes for regulations' sake.
Polymer and chemical factories use ventilation, closed processes, and basic personal protection to minimize exposure. Emergency showers and eyewash stations reduce the harms of accidental splashes. Workers get yearly health checks, which can catch problems before they balloon. Companies also review Safety Data Sheets and swap extra-hazardous substances out for safer ones as science evolves. Specific handling rules limit how much airborne dust or vapor hangs around, backed up by real workplace measurements.
Modern chemistry brings new materials with every decade, some helpful, some needing strict management. 2,6-Bis(Hydroxymethyl)-P-Cresol fits into the middle ground — not innocuous like table salt, but not as terrifying as some legacy toxins. Factories respect the risks by treating this chemical with proper controls, clarity about what it can and can’t do, plus a healthy respect born of experience. That’s the only way to keep scientific progress rolling without new generations inheriting old mistakes.
2,6-Bis(Hydroxymethyl)-P-Cresol comes up in a wide range of chemical and industrial uses, including as a stabilizer or intermediate. Its white crystalline form can look harmless, but the real concern lies in what happens if storage or handling goes wrong. I’ve seen lab mishaps from carelessness with basic chemicals, so being practical about how we store and move things like this can help avoid real problems.
This substance can irritate if it touches skin or eyes. If inhaled, you can expect coughing or throat irritation. Extended exposure or large spills in closed spaces can be even more problematic, as inhaling fine powders or dust clouds shouldn't be taken lightly. It might sound technical, but reading the Safety Data Sheet (SDS) gives a better grasp of its health risks. Sometimes people think small quantities need less care, but anyone who has struggled with a chemical-induced rash or eye sting can tell you that’s not something you want to repeat.
Room temperature storage away from direct sunlight works best for 2,6-Bis(Hydroxymethyl)-P-Cresol. This keeps the material stable. I would never tuck it away on a high shelf near a window, especially if the area gets stuffy during summer. Store it in tightly closed containers, never open bags left folded over. Moisture can clump powders or change their potency, sometimes even start weird chemical reactions. Using desiccators or silica gel packs goes a long way if you're in a place with high humidity. Even in a small lab closet, ventilation matters. If vapors build up inside enclosures, that's asking for trouble. A basic chemical cabinet with a vent or at least a space near an extractor fan gets the job done.
Few are eager to suit up for every chemical, but gloves, safety goggles, and a lab coat save time in the long run—fewer medical runs, and no ruined clothes. Nitrile gloves hold up well, and if powder spills, skip the urge to sweep with your bare hands. Keep chemical splash goggles handy, not just reading glasses. It’s easy to wipe powder away with a napkin, but that just spreads things around and risks it getting on skin or inhaled later. A quick hand wash after use makes a real difference. The extra steps feel unnecessary, until your skin itches for days or you get an eye burn to the cornea.
We’ve all seen the temptation to tip leftover chemicals down the drain, but that isn't safe for mixes like these. Designate a waste container, label it, and use secondary containment. If a spill happens, wipe with damp towels and toss everything in a proper disposal bag. Sweeping up powders can launch dust into the air. And always check local disposal rules; city waste workers don’t appreciate surprises in the trash. After cleaning up, go through and double-check that all lids are tight and the area’s been aired out. Taking that extra minute can stop a lot of future headaches—chemical smells travel fast, and so do accidents if containers leak.
The safest labs I’ve worked in had clear, simple steps posted and didn’t leave anything to guesswork. Check containers every few weeks for leaks or labels peeling off. Let newcomers handle small amounts under experienced eyes. Even seasoned people make mistakes when rushed. Reliable, practical routines pay off, and anyone who’s dealt with emergency decontamination would say it beats cleaning up avoidable messes. Safety with chemicals like 2,6-Bis(Hydroxymethyl)-P-Cresol doesn't take fancy equipment—just consistent, reasoned habits and the right respect for what’s on the shelf.
Cracking open a technical data sheet for 2,6-Bis(Hydroxymethyl)-p-cresol—sometimes called BMP or BHMPC—usually kicks up a cloud of numbers and jargon. But anyone with a hand in coatings, adhesives, or polymer work knows how tiny details can send a batch into the weeds. Forget the label-fluff and get right to the nitty gritty: what’s inside, what makes it good, and why specification sheets matter more than price quotes.
Most chemical suppliers send out this stuff in high purity, usually above 99%. Hitting that number isn’t marketing. Things like trace metals, water, or unreacted toluene can twist reactions, shift curing times, or plain spoil a day. I’ve seen what happens when minor impurities creep in—think failed polymer chains, off-color batches, and plenty of blame to go around. Getting a solid 99% or higher on the assay means more than dodging headaches. It keeps things predictable in the barrel, on the scale, and during production.
BMP is a white powder, sometimes a bit lumpy or free-flowing, easy enough to spot if something’s off. Moisture shows up in nearly every certificate of analysis, typically stated below 0.5%. Too much water—and the whole lot can clump, spoil, or throw off formulators using sensitive resins or curing agents.
Lead, iron, or copper all show up in trace analysis, even if they sit below 10 parts per million (ppm). Producers usually keep lead below 1 ppm, iron around 5 ppm, and copper even lower. No one likes chasing down funky side-reactions, and metal contamination can fuel a mess in polymer chemistry or when antioxidants get finicky.
Melting point justifies double-checking for anyone running at scale. BMP slides into a melt between 110°C and 114°C. Variations here can mean leftovers from incomplete reactions or the presence of isomers. Not something to gloss over—especially when jobs are on the line.
You’ll see “chemical grade,” “reagent grade,” or even “polymer grade” slapped on paperwork, but labels alone don’t speak for what sits inside the bag. I’ve sourced material from small batch suppliers and heavyweights in China, the US, and Germany. Prices shift, specs usually align, and the best suppliers deliver documentation to back up their claims. Good ones offer COAs, traceability, and sometimes a quick phone chat if there’s a hiccup.
Problems sneak in when the urge to cut costs overrides quality checks. It pays to put every new drum or batch through in-house testing—there’s no glory in saving pennies only to spend thousands fixing botched product. Moisture, melting point, and TLC checks cost small money but offer peace of mind. I tell every processing tech: don’t trust the sticker, trust the method.
BMP’s market isn’t just fine chemicals anymore. Phones, paints, wire coatings and even medical plastics depend on consistency and reliability. As regulations bear down on heavy metals and batch contamination, companies chasing the bottom dollar eventually lose. The best path I’ve found: vet the paperwork, test the product, and build relationships with suppliers who pick up the phone—before and after the deal.
It’s tempting to treat specialty chemicals as commodities, but every time the paperwork gets sidestepped, risk creeps up. BMP has every sign of a “simple” molecule on paper, yet a missed impurity or a stray bit of water can slow, stall, or spoil an entire line. Ask for the full assay, challenge the specs, and check every metric—each detail is a shield against tomorrow’s trouble.
| Names | |
| Preferred IUPAC name | 2,6-bis(hydroxymethyl)-4-methylphenol |
| Other names |
2,6-Dihydroxymethyl-4-methylphenol 2,6-Bis(hydroxymethyl)-4-methylphenol BRN 0980945 p-Cresol, 2,6-bis(hydroxymethyl)- Phenol, 2,6-bis(hydroxymethyl)-4-methyl- |
| Pronunciation | /tuː sɪks bɪs haɪˌdrɒksɪˈmɛθɪl piː ˈkrɛsɒl/ |
| Identifiers | |
| CAS Number | 14742-43-5 |
| Beilstein Reference | 113871 |
| ChEBI | CHEBI:28210 |
| ChEMBL | CHEMBL489867 |
| ChemSpider | 16253 |
| DrugBank | DB03813 |
| ECHA InfoCard | 03b6a5e6-4cfb-4549-8f0b-10c0e6f5bbbf |
| EC Number | 204-623-0 |
| Gmelin Reference | 92503 |
| KEGG | C06505 |
| MeSH | D065573 |
| PubChem CID | 72819 |
| RTECS number | SZ8575000 |
| UNII | D8J2A06A91 |
| Properties | |
| Chemical formula | C9H12O3 |
| Molar mass | 182.20 g/mol |
| Appearance | White to off-white crystalline powder |
| Odor | Odorless |
| Density | 1.22 g/cm³ |
| Solubility in water | slightly soluble |
| log P | 0.79 |
| Vapor pressure | 1.42E-7 mmHg @ 25°C |
| Acidity (pKa) | 8.6 |
| Basicity (pKb) | 13.7 |
| Magnetic susceptibility (χ) | -62.0·10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.595 |
| Viscosity | 1500 - 2500 mPa.s (25°C) |
| Dipole moment | 3.13 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 211.5 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -710.6 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -5530 kJ/mol |
| Pharmacology | |
| ATC code | D08AE04 |
| Hazards | |
| Main hazards | Harmful if swallowed. Causes serious eye irritation. Causes skin irritation. |
| GHS labelling | GHS07, GHS09 |
| Pictograms | GHS07,GHS09 |
| Signal word | Warning |
| Hazard statements | H315, H319, H335 |
| Precautionary statements | Precautionary statements: P261, P280, P305+P351+P338, P337+P313 |
| NFPA 704 (fire diamond) | 1-1-0 |
| Flash point | 163°C |
| Lethal dose or concentration | LD50 oral rat 3070 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral, rat: 2100 mg/kg |
| PEL (Permissible) | Not established |
| REL (Recommended) | 100 mg/L |
| Related compounds | |
| Related compounds |
2,4-Bis(hydroxymethyl)-6-methylphenol 2,4,6-Tris(hydroxymethyl)phenol 2,6-Dimethylphenol 4-Methylphenol 2,6-Dihydroxymethylphenol |
