|
HS Code |
427441 |
| Cas Number | 87-66-1 |
| Chemical Formula | C6H6O3 |
| Molecular Weight | 126.11 g/mol |
| Iupac Name | benzene-1,2,3-triol |
| Appearance | white to off-white crystalline powder |
| Melting Point | 131-134°C |
| Boiling Point | 309°C |
| Solubility In Water | soluble |
| Density | 1.45 g/cm³ |
| Odor | slightly phenolic |
| Pka | 8.98 |
| Storage Conditions | store in a cool, dry place, away from light |
| Hazard Statements | harmful if swallowed, may cause respiratory irritation |
As an accredited Pyrogallol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pyrogallol is packaged in a 500g amber glass bottle with a tightly sealed cap and a clear hazard labeling for safety. |
| Shipping | Pyrogallol should be shipped in tightly sealed containers, away from light, heat, and sources of ignition. It must be labeled as hazardous: corrosive and toxic. Use compatible packaging and include safety documentation. During transport, ensure compliance with local and international regulations for hazardous materials. Handle with appropriate protective equipment. |
| Storage | Pyrogallol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from heat, light, and sources of ignition. Keep it away from oxidizing agents and incompatible materials. Protect from moisture and air, as pyrogallol can darken and degrade on exposure. Use containers made of glass or compatible chemical-resistant materials to prevent contamination. |
|
Purity 99%: Pyrogallol with a purity of 99% is used in photographic developer formulations, where it enhances image clarity and contrast. Molecular weight 126.11 g/mol: Pyrogallol of molecular weight 126.11 g/mol is applied in oxygen absorption systems, where it increases efficiency in gas analysis. Melting point 132°C: Pyrogallol with a melting point of 132°C is utilized in hair dye production, where it ensures consistent color formation and stability. Particle size <50 µm: Pyrogallol with particle size less than 50 µm is used in analytical reagent preparation, where it enables rapid dissolution and homogeneous reaction profiles. Stability temperature up to 100°C: Pyrogallol stable up to 100°C is implemented in corrosion inhibitor mixtures, where it maintains chemical integrity under elevated thermal conditions. Solubility in water 10 g/100 ml at 20°C: Pyrogallol with a solubility of 10 g/100 ml at 20°C is employed in laboratory redox titrations, where it provides reliable and reproducible results. |
Competitive Pyrogallol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Pyrogallol doesn’t attract much attention outside the labs or factories, but anyone working in analytical chemistry, photography, or specialty manufacturing probably bumps into it sooner or later. This compound, whose chemical formula is C6H6O3, runs under several names—you might hear it called 1,2,3-trihydroxybenzene by those who remember things by their molecular structure, or pyrogallic acid if you leaf through old literature. The white, needle-like crystals catch the eye with their quick browning under air, something the chemistry-curious notice long before they pick up a textbook.
What sets this compound apart isn’t some fanciful application but decades of solid, dependable use. Before digital sensors reigned supreme, pyrogallol helped photographers develop their images. It showed up as a key ingredient in black-and-white developers, giving those old-fashioned prints their depth and nuance. These days, most folks encounter it as a reagent: used to soak up oxygen in gas analysis, pulled into research labs for redox studies, or kept on shelves for the synthesis of dyes and antioxidants. The spectrum of uses might seem niche, but pyrogallol’s role remains vital across these narrow fields.
Experience teaches that not all chemicals with long pedigrees deserve respect, but pyrogallol has earned its reputation. It oxidizes fast in the open air, picking up oxygen molecules and changing color as it goes. For generations of gas technicians, this quality made it the preferred choice for oxygen absorption. It solved practical problems for scientists who wanted accurate gas measurements without an array of expensive machines. Instead of speculation, you could see the results—and you could trust them.
In the dye industry, makers prize pyrogallol for its ability to generate deep hues. Textile workers who blend fabrics or test color stability look at the way it reacts with other chemicals and recognize its reliability. My own experience dabbling in old photographic processes highlighted just how different results can be when using fresh pyrogallol, compared to supposedly improved substitutes. The difference showed up in contrast, tonal range, and fine detail—proof of why some artists stubbornly refuse to switch to digital alternatives.
Most listings give a melting point just above 130°C, with solubility in water and alcohol that lets it mix easily into solutions. Pyrogallol’s breakdown happens faster in alkaline environments, so storage inside sealed, cool, and dark containers makes sense. Not long ago, I talked with a friend who runs gas measures for food storage experiments. They swear by pyrogallol because of its consistency, requiring little calibration. This sets it apart from some enzymatic oxygen scavengers that fluctuate according to batch variability.
Some peers in analytical chemistry mention subtle batch differences as a source of concern, particularly for trace analysis. I’ve handled pyrogallol crystals from different sources, and, indeed, some batches seem dustier or browner right out of the bottle. Generally, the material sourced from established chemical suppliers looks bright and clean, lasting longer in storage. These details feed directly into scientific work; a subpar batch can spoil a run, so careful selection matters more than glancing at a list of specs.
Pyrogallol doesn’t clock overtime in a home kitchen, but it slides naturally into routine industrial and research settings. In metallurgy, techs might rely on its quick reaction to oxygen for testing gas purity during welding. Skip over to environmental labs: here, pyrogallol runs as a color developer, revealing trace metals or oxidizing pollutants during water sample testing. Art restorers mix it—carefully—into solutions for cleaning metal artifacts, stripping sulfide stains without harming the underlying patina. As odd as it sounds, even hair dye formulas (especially in the past) occasionally made use of pyrogallol’s staining abilities, though this fell out of favor for safety reasons.
I’ve spent hours trying to measure dissolved oxygen in sealed systems. Modern probes and meters often require recalibration, new membranes, or a trip back to the manufacturer. If you’re chasing a simple, quick check, pyrogallol offers a direct, visual read. The color shift from clear to brown means fewer steps and a lower chance of user error. It’s a tangible difference—the kind that makes small-budget field research possible and supports teaching demonstrations where equipment costs become a stumbling block.
Many newer products claim to replace pyrogallol’s functions while improving on its drawbacks. Some enzymatic oxygen absorbers avoid the toxicity issues and mess of handling strong chemicals, but they’re often less robust in mixed-gas environments or break down when stored outside recommended temperature ranges. Electrochemical devices for oxygen measurement offer speed and accuracy, yet their upfront costs and maintenance can strain budgets. Pyrogallol, by contrast, survives on shelves for months, answers only to basic storage habits, and lands at a lower price.
Colleagues in the chemical analysis trade laud the clarity and reliability of the “wet” classical approach—especially when confirmation matters more than speed. I’ve heard complaints about digital sensors drifting off calibration just at the worst time, and about replacements being expensive or impossible to source in remote areas. Pyrogallol doesn’t answer every call; it doesn’t measure nitrogen or carbon dioxide, and its toxicity means keeping protocols in place to prevent accidents. Still, it remains a workhorse: not elegant, but delivering what’s needed in chemistry teaching labs, small factories, or one-off experiments where every dollar counts.
Any chemical with a long safety profile also brings baggage. Pyrogallol shouldn’t come near your skin or eyes, and inhalation presents risks—facts hammered home during lab training sessions and in every chemical hygiene plan. Accidental spills discolor tabletops and skin almost instantly, so veteran users keep gloves handy. Issues with toxicity led to stricter controls and gradual removal from some consumer-facing products, such as hair dyes.
Waste handling looms large in any discussion of classic reagents. Pyrogallol oxidizes fast, but the breakdown products contribute to environmental load if dumped carelessly. Waste streams containing pyrogallol generally go through incineration or special chemical treatment. This process, though not unique, marks a point against bulk industrial use where safer alternatives make sense. Awareness of these limits matters, especially as regulations tighten and chemical purchasing decisions reflect not just cost but sustainability. Some labs turn to new reagents, not because of price or convenience but to comply with evolving disposal requirements.
My early lab days involved plenty of experiments measuring oxygen in sealed glass tubes. Pyrogallol made the job straightforward. Mix the crystals in a little sodium hydroxide, inject the solution, and watch the gas volume drop as the reaction soaks up the available oxygen. Errors crept in only when using stale or improperly stored pyrogallol. Moisture and oxygen in air chew through stored pyrogallol, so savvy users portion it out, seal the rest in the dark, and avoid opening large containers unless absolutely necessary.
Labeling remains essential. Spilled crystals turn brown fast, blending with wood benches or old lab tile, making them hard to spot. Lapses in handling can lead to stains that survive years, a lesson learned in one of my first independent projects. Compared to enzyme-based alternatives, pyrogallol’s rapid, unmistakable color change offers reassurance; at the same time, proper air movement and PPE stay non-negotiable. In situations where students handle it, adult supervision and pre-measured doses limit risk.
Chemists working on organic synthesis find pyrogallol a steadfast building block. Those three hydroxyl groups grant diverse pathways to more complex molecules, including antioxidants, dyes, and even certain pharmaceuticals. Research teams redesign classic syntheses where cost or availability of raw materials limits progress. Pyrogallol’s price point and reliable performance keep it in the mix for inventors looking for old tools to solve new problems.
Several environmental monitoring techniques rely on pyrogallol for its sensitivity to oxygen. Microbiologists who need anaerobic chambers can rig custom gas-scavenging setups without fancy machines, using pyrogallol solutions in jars or containers. Subtle shifts in color provide not just a result but clues about contamination or leaks. This hands-on feedback loop suits small labs, field researchers, and teachers training the next batch of scientists. Modern gadgetry often asks for trust in electronics; pyrogallol’s reaction tells its story plainly.
Alternative oxygen scavengers, such as sodium dithionite or ascorbic acid derivatives, struggle to deliver the same resilience under mixed gas conditions. Some lose activity when faced with atmospheric moisture, while others provoke side reactions that cloud results. For dye synthesis, competitors might win on price but falter in producing deep, stable hues without long curing times or extra finishing steps. Pyrogallol’s strength, drawn from its simple yet effective structure, brings predictability to both chemical reactions and final product quality.
I’ve watched dye technologists compare batches of wool and silk after different treatments. Pyrogallol-based solutions offer color penetration and reproducibility that newer, “greener” alternatives sometimes chase without reaching. In analytical chemistry, classic volumetric tests run with far less drift in control samples when pyrogallol steps in compared to aldehyde-based systems. This might not impress on paper, but in a busy commercial setting, where rework or recall hurts, the difference grows obvious.
No story about a time-tested chemical can ignore progress, and pyrogallol stands at a crossroads. Pushes for safer, easier-to-dispose-of reagents guide many labs away from older substances. Sometimes, substitutes work well; sometimes, only the original will do. The cost to switch can include retraining, new waste treatment systems, or unexpected failures. Digital oxygen sensors promise clean, repeatable data—and deliver it under most circumstances—but not every system welcomes their installation or upkeep. Training budgets and equipment schedules influence decisions as much as published studies do.
In education, teachers favor chemicals that illustrate concepts plainly, without complex instructions. Pyrogallol’s simplicity suits that need, while its safety profile demands respect and lessons in careful handling. This hands-on experience matters more than any digital simulation or pre-packaged kit. Watching a solution change before your eyes beats reading about it, embedding chemical understanding in memory.
Experienced users improve safety by keeping pyrogallol away from moisture and storing it in tinted bottles. Labs train students and staff to use PPE and to neutralize spills quickly. Some universities set up shared stocks, reducing overall inventory and limiting exposure risk. In industry, batch testing and quality checks screen out off-color pyrogallol, ensuring consistent results downstream. Waste minimization techniques—smaller scale reactions, shorter storage times, and better process controls—lighten the environmental load.
Research into greener oxygen scavengers and color developers continues. Teams study bio-based molecules, rare-earth catalysts, and even custom-designed enzymes. While some replacements work for select applications, few span as wide a field as pyrogallol. Its low raw cost, visual color changes, and comfortable handling (when rules are followed) ensure it won’t vanish soon. For now, the task lies in teaching best practices—handling, storage, and disposal—instead of dropping the compound altogether. Real change happens step-by-step, with users learning from mistakes and building on the lessons passed down from mentors, textbooks, or direct trial and error.
Pulling back from the fine technical points, pyrogallol marks a point of connection between industrial chemistry, scientific history, and hands-on education. Its role in photography ties it to cultural memory, linking hobbyists, artists, and scientists in a shared tradition. Chemical suppliers keep it on the shelf, knowing the demand stays steady, if not spectacular. Universities put it on training syllabi, thanks to its mix of practical value and accessibility. Each field—analytical chemistry, dye-making, water testing—pulls a different thread through pyrogallol’s story, making it more than just one more name in a catalog.
Few chemicals linger for generations in practical use without reason. Pyrogallol’s longevity reflects qualities valued by humans: simplicity, clarity, and reliability. Storing a jar in the cupboard, I’m reminded that real progress comes from combining the trustworthy tools of yesterday with the promises of tomorrow. Pyrogallol supports experiments, creative projects, and careful manufacturing—all because it offers tangible, consistent performance across settings. It makes chemistry direct; it turns theory into action, and experience into knowledge. The responsibility, now, lies with users and educators to apply that knowledge wisely—respecting the risks, maximizing the benefits, and shaping the next wave of innovations in the chemical world.