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HS Code |
937905 |
| Chemicalname | 4-Methylcatechol |
| Casnumber | 452-86-8 |
| Molecularformula | C7H8O2 |
| Molarmass | 124.14 g/mol |
| Appearance | White to slightly yellow crystalline solid |
| Meltingpoint | 45-47 °C |
| Boilingpoint | 248 °C |
| Solubilityinwater | Soluble |
| Density | 1.17 g/cm3 |
| Synonyms | 1,2-Dihydroxy-4-methylbenzene |
| Smiles | CC1=CC(=C(C=C1)O)O |
| Iupacname | 4-methylbenzene-1,2-diol |
As an accredited 4-Methylcatechol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Methylcatechol is packaged in a sealed amber glass bottle containing 100 grams, featuring hazard labeling and a secure screw cap. |
| Shipping | 4-Methylcatechol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. The packaging must comply with relevant regulations for hazardous chemicals. It should be labeled clearly and handled by trained personnel. During transit, maintain a cool, dry environment and avoid physical damage or exposure to heat and ignition sources. |
| Storage | 4-Methylcatechol should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from light and moisture. Ensure storage facilities are equipped with chemical spill containment features. Properly label all containers and keep away from food and drink items. |
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Purity 99%: 4-Methylcatechol with purity 99% is used in pharmaceutical synthesis, where it ensures high yield and product consistency. Melting point 112°C: 4-Methylcatechol featuring a melting point of 112°C is used in antioxidant formulation, where it provides enhanced thermal stability. Particle size <50 μm: 4-Methylcatechol with particle size below 50 μm is used in specialty coatings, where it ensures smooth dispersion and uniform film formation. Moisture content <0.2%: 4-Methylcatechol having moisture content less than 0.2% is used in fine chemical manufacturing, where it prevents unwanted side reactions. Stability temperature up to 80°C: 4-Methylcatechol stable up to 80°C is used in polymer additives, where it maintains functional integrity under processing conditions. UV absorbance 280 nm: 4-Methylcatechol with high UV absorbance at 280 nm is used in UV-blocking agents, where it provides efficient light absorption for product protection. Residue on ignition <0.1%: 4-Methylcatechol with residue on ignition below 0.1% is used in laboratory reagent preparation, where it ensures minimal contamination of analytical samples. Assay ≥98%: 4-Methylcatechol with assay greater than or equal to 98% is used in agrochemical intermediates, where it yields high-purity reaction products. Solubility in ethanol 50 g/L: 4-Methylcatechol soluble in ethanol at 50 g/L is used in dye formulation, where it achieves homogeneous mixing and consistent coloration. Heavy metals <10 ppm: 4-Methylcatechol with heavy metals content below 10 ppm is used in electronic chemical manufacturing, where it minimizes electrical conductivity issues. |
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Anyone who has worked in a laboratory or handled fine chemicals knows how much the right compound matters for getting reliable research results or consistent industrial output. 4-Methylcatechol belongs to a family of organic molecules known as catechols, which are best recognized for their benzene ring with two hydroxyl groups. In this specific compound, the addition of a methyl group in the para-position brings a subtle yet significant difference. To those of us who have handled both plain catechol and 4-Methylcatechol, the distinction in reactivity and physical properties isn’t academic—it’s the kind of detail that shapes successful syntheses and accurate testing.
A typical bottle of 4-Methylcatechol comes as a crystalline powder or small granules, usually packaged in amber glass containers for protection against light. Most suppliers will offer a purity that reaches or exceeds 99%, essential for users aiming to avoid side reactions or ambiguous results. In terms of molecular structure, it holds a chemical formula of C7H8O2 and a molar mass in the range of 124.14 g/mol. The melting point usually sits between 67 and 70 degrees Celsius, which makes it easy to manipulate for melt-based processes or for solvent extractions.
Many products on the chemical market look similar on paper but behave very differently in actual use. That’s definitely true for catechols and their derivatives. 4-Methylcatechol has made its biggest mark in research settings, particularly as an intermediate in organic synthesis. I’ve seen it play a pivotal role in studies looking into antioxidants and enzyme inhibitors. In pharmacology labs, its reliable structure helps scientists prepare more complex compounds, often leading the way to innovations in drug development or metabolic research. Anyone who’s tracked a reaction profile by NMR can spot the clean signatures that 4-Methylcatechol brings, especially compared to less stable relatives.
Beyond the bench, this compound shows up in testing for oxidation inhibition and as a model substrate in biochemical assays. Analytical chemists appreciate just how sharply it responds in colorimetric assays or spectrofluorometric methods, giving clear, interpretable results that reduce uncertainty. When compared to other catechols, the methyl group creates a difference in both reactivity and solubility. This comes handy in fine-tuning a process or choosing the right tool for a troubleshooting step, especially if the baseline catechol gives a signal that’s too broad or hard to measure.
Some colleagues favor plain catechol because it’s widely available and easy to substitute. Yet side-by-side trials often show that 4-Methylcatechol offers higher selectivity for certain synthetic steps or enzyme systems. For example, in oxidation experiments, the methyl group alters the potential for radical formation. Synthetic chemists routinely spot fewer unwanted byproducts, while bioassay developers get better selectivity in enzyme inhibition screens. In my experience, I’ve also noticed how this subtle substitution enhances solution stability in aqueous buffers. If your protocols hinge on reproducibility, reaching for 4-Methylcatechol often pays off.
Structurally, other catechol derivatives like 3-methylcatechol or guaiacol bring different features to the table. 3-Methylcatechol places the methyl on a different carbon, changing both electronic and steric properties. Guaiacol, which adds a methoxy group, doesn’t offer the same hydrogen bonding network and tends to volatilize faster. I’ve compared all three in antioxidant screening: 4-Methylcatechol stood out for its slower degradation and easier handling—a fact that matters when running week-long stability tests. While benzoquinone derivatives appeal for their reactivity, they lack the predictability that 4-Methylcatechol brings. That reliability makes a difference if you’re troubleshooting a complex batch synthesis or optimizing the purification steps in a scale-up run.
Working with sensitive chemical processes, I’ve seen issues with oxidation, purity, and shelf-life pose real disruptions for teams in both academic and industrial settings. Some compounds degrade or polymerize quickly, introducing error and waste. Using 4-Methylcatechol with its defined molecular structure and stable profile helps to cut down on these issues. In catalyst research, the need for a pure, stable catechol derivative is not theoretical—it can make or break the reproducibility of experiments. my own attempts with regular catechol produced inconsistent outcomes, leading to time lost troubleshooting. 4-Methylcatechol shifted the results toward a more dependable baseline.
There are also safety factors. As someone who values a clean and hazard-aware workspace, I appreciate that pure 4-Methylcatechol typically gives off less volatile vapor and can be weighed and dissolved with fewer worries about sudden oxidation, compared to some less stable catechols. That doesn’t remove the need for gloves and goggles, but it’s a reminder of the small practical gains that better product choice brings.
Not every synthesis or test allows for compromise on input materials. Analytical standards and high-purity reagents form the backbone of credible data. In pharmaceutical and environmental monitoring, for instance, 4-Methylcatechol’s purity ensures that background noise remains low, helping users spot true positives. Many chemical supply houses label assays with detailed chromatograms to confirm the absence of tars, heavy metals, and other contaminants. I think of the time a poorly characterized reagent wrecked a control set—it never seems like a big deal until your data takes a hit.
From hands-on work with HPLC and GC methods, the clarity of 4-Methylcatechol’s peaks stands out. This specificity means you can calibrate against it with confidence, cutting down on cross-contamination worries or overlapping spectra that muddy up less pure materials. The upshot is more confident data—something any analyst or industrial chemist values.
Every researcher weighs cost, convenience, and regulatory demands while planning a project. University labs with slim budgets might choose basic catechol for preliminary runs, but more exacting work benefits from 4-Methylcatechol’s consistency. Storage rarely becomes tricky—cool, dry conditions and good labeling practices suffice. The sealed amber bottles help extend shelf-life by blocking stray light, but unlike peroxides or highly volatile organics, 4-Methylcatechol avoids common pitfalls like rapid auto-oxidation.
In my own projects, I’ve shifted to 4-Methylcatechol for multi-step syntheses where unpredictability eats up time and resources. For small and medium chemical manufacturers, scaling up production often introduces new risks of impurity buildup. Relying on a high-quality catechol derivative saves both troubleshooting and regulatory headaches. Technical teams also value its solubility profile, which enables easier integration into water or common organic solvents—something that can’t be said for bulkier or less soluble analogues.
Settling on the right grade of 4-Methylcatechol depends on your goals. For basic teaching labs or in-house control tests, a standard lab grade suffices. It often arrives with purity figures just below 99%, priced to fit tight grants or exploratory efforts. For regulated industries—food analysis, pharmaceuticals, fine chemicals—the demand for “analytical grade” defines procurement. This higher grade undergoes more rigorous screening, often showing purity upwards of 99.5% and detailed impurity profiles.
Some suppliers now offer ultra-high-purity versions, trimmed down to minimal impurities, with detailed data sheets showing trace metals and residual solvents. Such models fetch a premium but have proven their worth in sensitive spectroscopic methods or for producing reference materials. The gulf in quality between technical and analytical or research grade should not be underestimated—if you’re preparing for peer review or production certification, investing in the right product saves you time and drama down the line.
Anyone who’s sifted through a catalog of catechols knows how confusing the options can be. Each substitution on the benzene ring changes more than just a line on the molecular diagram. For those working with enzymes or oxidative stress models, the methyl group impacts kinetics in subtle ways, slowing some unwanted side-reactions and sharpening contrast in bioassays. It also opens up pathways for further modification. If a downstream synthesis needs a reactive para position, choosing 4-Methylcatechol simplifies the approach.
Compared head-to-head with more basic catechols, the increased solution stability stands out. In my own hands, 4-Methylcatechol held its clarity and reactivity for a longer stretch, especially during prolonged exposures at the bench. Its modest difference in melting point creates a more manageable workflow in melt-based processes. Other derivatives, such as 2,4-dimethylcatechol, show decreased solubility or produce extraneous byproducts under mild conditions. For teams chasing both yield and consistency, the single methyl substitution offers a low-risk option.
In a project aimed at antioxidant quantitation, our group pitted several catechols against each other under identical conditions. 4-Methylcatechol returned sharper and more interpretable peaks in both UV-vis and NMR analysis, letting us detect trace oxidation states that other variants blurred out. In enzyme inhibition studies, the compound showed less background interference, a trait that made interpretations more robust for downstream applications. I watched as the time spent troubleshooting dropped—a testament to choosing the right material at the start.
Because of its well-characterized behavior, process engineers leverage it to benchmark oxidation or polymerization steps. Where other catechols wander toward ambiguity, this one keeps its properties over repeated testing, letting users skip unnecessary repeats. Students training in practical organic chemistry find their spectra look cleaner and results more defensible, reducing frustration and boosting learning outcomes.
Though 4-Methylcatechol delivers more stability than its more reactive cousins, no one should treat it like a “safe” material by default. If you’ve managed waste streams or read up on environmental health, you know phenolic compounds can contribute to biological oxygen demand and raise toxicity worries in aquatic environments. In labs I’ve worked, strict segregation of phenolic waste applies, with dedicated containers and clear labeling. While less volatile, it still requires standard PPE and good ventilation to limit exposure.
Companies and research institutions face mounting regulatory pressure to minimize workplace exposure and eliminate accidental releases. Unlike some heavier aromatic compounds, 4-Methylcatechol resists rapid vaporization at room temperature. This helps limit operator exposure through inhalation, yet repeated contact or poor airflow can still become an issue. By adopting sealed handling systems and institutional controls, organizations cut down on incidents while still using the compound’s unique capabilities. Spent solutions or wash-outs join the waste stream for hazardous materials—discarding them in regular trash bypasses safety and compliance, which puts both workers and the ecosystem at risk.
Looking ahead, demand for cleaner, safer chemicals keeps rising in the face of stricter rules and growing awareness of environmental burdens. I’ve noticed a clear push from both academic and industrial buyers for suppliers to adopt greener synthesis pathways for staple chemicals like 4-Methylcatechol. Some producers already advertise renewable feedstock sourcing or audit their processes for reduced emissions. While such changes don’t show up in the chemical itself, they matter to users weighing the broader impact of their procurement decisions.
Recyclability and life cycle management remain hurdles, especially since phenolic derivatives seldom degrade quickly outside controlled setups. Teams piloting green chemistry protocols have made strides towards closed-loop systems for catechol derivatives, reclaiming and purifying solvents to reduce waste. Those advances promise to cut disposal requirements and build environmental compliance into the supply chain.
If there’s a single takeaway from working with 4-Methylcatechol, it comes down to reliability. A compound’s place on the periodic table or in the catalog doesn’t guarantee trustworthy performance. It’s the details—purity, ease of handling, compatibility with existing workflows—that decide whether a project runs smoothly or hits snags. For chemists and engineers who need a catechol derivative with real staying power across research and development, the methyl group at the para position stands out not for flash but for practical value. By reducing side reactions, improving stability, and delivering clean analytical windows, 4-Methylcatechol offers subtle advantages that ripple across entire projects.
Making the switch from regular catechol or another analog often begins with a single experiment that needed just a touch more stability or selectivity. Over time, the savings—on cleanup, on repeat assays, on staff training—accumulate into a stronger case for this underappreciated chemical. In an era where operational downtime or poor reproducibility erodes margins and trust, picking the right building block gives both frontline scientists and managers a secret weapon.
Through years of work with organic compounds, the lesson holds true—small details shape big outcomes. 4-Methylcatechol stands as a good example of how considered choices at the molecular level grant users greater flexibility, sharper results, and fewer headaches. The best products deliver not just a molecule, but a platform for discovery and innovation. Day in and day out, that’s what gives this compound its staying power in both academic and industrial circles.