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HS Code |
988548 |
| Chemical Name | 2,6-Dihydroxybenzoic Acid |
| Synonyms | γ-Resorcylic acid |
| Cas Number | 303-07-1 |
| Molecular Formula | C7H6O4 |
| Molecular Weight | 154.12 g/mol |
| Appearance | White to off-white crystalline powder |
| Purity | ≥99% |
| Melting Point | 253-257 °C |
| Solubility In Water | Slightly soluble |
| Storage Temperature | Room temperature |
| Density | 1.698 g/cm³ |
| Pubchem Cid | 8377 |
| Inchi Key | PXJSFQKZADWTKB-UHFFFAOYSA-N |
As an accredited 2,6-Dihydroxybenzoic Acid (≥99%) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2,6-Dihydroxybenzoic Acid (≥99%) is packaged in a sealed 100g amber glass bottle with tamper-evident cap and labeling. |
| Shipping | 2,6-Dihydroxybenzoic Acid (≥99%) is shipped in secure, airtight containers to prevent contamination and moisture absorption. The packaging complies with safety regulations for laboratory chemicals, and material safety data sheets (MSDS) accompany each shipment. Transport is conducted via standard ground or air freight, depending on customer location and urgency. |
| Storage | 2,6-Dihydroxybenzoic Acid (≥99%) should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from light and moisture. Store at room temperature, ideally between 15–25°C (59–77°F). Ensure proper labeling, and keep away from sources of ignition and direct sunlight. |
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Purity: 2,6-Dihydroxybenzoic Acid (≥99%) is used in pharmaceutical synthesis, where high purity ensures reproducible active ingredient production. Melting Point: 2,6-Dihydroxybenzoic Acid (≥99%) is used in analytical standards, where a precise melting point enhances method calibration accuracy. Molecular Weight: 2,6-Dihydroxybenzoic Acid (≥99%) is used in peptide synthesis, where defined molecular weight facilitates reliable product characterization. Solubility: 2,6-Dihydroxybenzoic Acid (≥99%) is used in biochemical assays, where excellent solubility promotes homogeneous reaction mixtures. Stability: 2,6-Dihydroxybenzoic Acid (≥99%) is used in reference material preparation, where high chemical stability supports long-term sample integrity. Physical Form: 2,6-Dihydroxybenzoic Acid (≥99%) is used in materials science research, where consistent crystalline powder form allows uniform dispersion in composites. |
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Few compounds earn a place in the supply cabinets of serious labs the way 2,6-Dihydroxybenzoic Acid does. Many call it by another name, like γ-resorcylic acid, but the real importance lies in what this chemical brings to the table. At ≥99% purity, this batch isn’t just for ticking boxes—it’s made for precision. Each bottle gives researchers, analysts, and chemists peace of mind in projects that leave little room for error.
Trying to analyze delicate samples or synthesize accurate products with anything but high-purity chemicals leaves results open to guesswork. Low-grade reagents might seem cost-effective at first, but there’s an invisible price. I’ve seen corners cut with cheaper grade acids, only to waste hours troubleshooting unexplained signals and re-running tests. With 2,6-Dihydroxybenzoic Acid at this purity level, labs keep those headaches out of the workflow. Unwanted byproducts just don’t get in the way, and that single variable gives a solid foundation for meaningful data.
Manufacturers label some batches as “for research use only,” and while that sounds limiting, it also lets labs trust that what’s inside meets research-grade standards. The white crystalline solid (CAS: 608-19-1), with a molecular formula of C7H6O4 and a molecular weight of 154.12, melts in the range of about 205-209°C—a simple but powerful marker for confirming identity. Bulk shipments and small packs both offer the ≥99% designation, which signals uncompromising product for downstream use, whether in routine UPLC-ESI-MS screening or more complex peptide mass fingerprinting.
Talking about 2,6-Dihydroxybenzoic Acid in abstract chemical terms overlooks the stories unfolding at lab benches. MALDI-TOF mass spectrometry, for example, leans on this acid as a matrix, picking it over others because minimal impurities mean clearer, cleaner spectra. Colleagues who’ve settled for lower purity variants ended up chasing peak distortions, while those who stick to ≥99% enjoy streamlined work and crisp results. The bottom line isn’t just protocol—it's about producing findings that stand up to scrutiny.
It may sound like all benzoic acids do the same job, but separating this one from the pack reveals more than a few differences. 2,6-Dihydroxybenzoic Acid sets itself apart with a dihydroxy arrangement that opens specific chemical pathways, especially for ionization in MALDI techniques. Others, like 3,5-dihydroxybenzoic acid, don’t provide the same selectivity, often complicating analyses. In antioxidant assays, the placement of hydroxyl groups on the molecule noticeably shifts outcomes. This version, at ≥99% purity, steps into that niche, where purity means the difference between a result you can trust and one you’re forced to question.
There’s more to chemistry than glassware and numbers. Trust starts with the source material. I’ve relied on ≥99% 2,6-Dihydroxybenzoic Acid not because it checks a box, but because it keeps projects moving undisturbed by mystery contamination. Reproducibility gets mentioned a lot, but nothing replaces seeing months’ worth of assays line up cleanly without nagging doubts caused by suspect chemicals. Few things grind progress as harshly as impure starting materials, and nothing builds confidence like opening a new bottle and knowing every scoop measures up the same as the last.
What’s powerful about 2,6-Dihydroxybenzoic Acid isn’t just how it shows up on a shelf, but where it goes next. In my experience, this compound shows up in proteomics every time someone wants to profile proteins with clarity in biochemical samples. Its role as a matrix in MALDI-TOF MS unlocks peptide and polymer analysis for many academic and pharmaceutical projects. Some even leverage it for antioxidant activity studies or as a benchmark additive in specialty coatings where its predictability means fewer unwanted surprises in formula stability.
In a world where deadlines and grant renewals hang on reliable data, impurities cost more than time. One project I joined relied on a lower grade matrix acid, leading us down weeks of troubleshooting false peaks and possible contamination. After a switch to ≥99% 2,6-Dihydroxybenzoic Acid, the issue disappeared, confirming that even minor deviations in source material can magnify in high-stakes applications. Chasing cost savings sometimes leads only to longer hours and wasted funding, which isn’t a lesson I’m eager to repeat.
Comparing 2,6-Dihydroxybenzoic Acid to something like sinapinic acid or α-cyano-4-hydroxycinnamic acid helps show where each shines. Matrices in MALDI mass spectrometry work by gently transferring energy from the laser pulse to the analyte molecules, allowing softly ionized species to enter the gas phase. The unique placement of the hydroxy groups on this molecule mediates energy transfer in ways competing acids struggle to match. Lower purity options don’t bring the same reliability to unknown sample analysis or reproducibility across experiments. That’s a strength you remember the first time a crowded mass spectrum sorts itself out.
With experience comes respect for chemical stability. 2,6-Dihydroxybenzoic Acid holds up under cool, dry, and dark conditions—away from the reach of moisture and direct sunlight. Laboratories focused on repeatable results keep half-used bottles tightly sealed, sometimes flushing with dry nitrogen after use if really chasing analytical-grade performance. Thermal cycling or careless handling introduces breakdown products, which create new problems that could have been avoided. Proper care pays off in the long run, keeping every test and synthesis step as precise as the last.
Quality reagents back more than a single experiment—they quietly support the credibility of published data and the trust granted by funding agencies and the public. As science moves toward open data, reproducibility, and rigorous peer review, sourcing high-purity chemicals like 2,6-Dihydroxybenzoic Acid matters at every stage. No lab gets a second reputation with reviewers. Data clouded by contamination or unexplained outliers can sideline a promising thesis or slow regulatory approvals for new therapies. That’s not just a chemist’s headache; it’s about honoring the greater mission of scientific discovery.
Instruments keep getting better, pushing for sharper resolution and lower detection limits. Mass spectrometry has seen this trend most clearly—modern machines routinely resolve analytes at sub-part-per-billion levels. As these machines demand more of their consumables, reagents like 2,6-Dihydroxybenzoic Acid can’t lag behind. Researchers moving into fields like glycomics or advanced polymer science expect background signals to fade away, showcasing their targets without interference. Low-purity supplies not only muddy results, but undermine confidence in state-of-the-art equipment. Choosing the right grade signals a commitment to staying ahead.
From the outside, it looks like only top university or pharmaceutical labs might need lab-grade purity on this scale, but the reality is different. Small teaching colleges and regional diagnostic centers run experiments that affect local policy and even public health standards. These groups often hit budget limits harder and can be tempted by bargain options. Experience shows that cutting corners here often costs more in downtime, repeat orders, and strained faculty-student trust. Adding meaning to basic experiments with top-tier chemicals bridges the gap between textbook learning and discovery. Students and new researchers end up building habits of rigor that last throughout their careers.
On paper, the price premium for ≥99% 2,6-Dihydroxybenzoic Acid looks steep, especially against mixed-quality competitors. The hidden savings unfold later. Time spent troubleshooting, repeating suspect runs, and accounting for spikes and drifts eats into productivity and morale. I’ve worked with principal investigators who swear by tracking total cost per result, not just cost per gram. Their numbers add up: stable, high-purity reagents let postdocs focus on data analysis, manuscript writing, and new experiments, rather than spending weekends in the lab chasing potential contamination from last week’s batch of acids.
Cleaner chemistry means fewer headaches in compliance and disposal, too. Higher purity reagents, with minimal side products, cut down on hazardous waste output. Many funders, especially in Europe and North America, now ask how labs work to minimize environmental impact, and chemicals like this help keep waste streams simple and safer to handle. Good bottle management further lowers the environmental load, as consistent performance keeps expired stock and redos to a minimum. Saving on waste disposal fees and paperwork isn’t glamorous, but it’s real progress toward more responsible science.
Sourcing high-purity 2,6-Dihydroxybenzoic Acid can still trip up smaller teams. Local suppliers often run out during peak cycles, such as before grant deadlines or thesis season. Large distributors keep inventories moving, but that sometimes means months-old stock. One solution involves building relationships directly with trusted suppliers or establishing recurring orders that match project timelines. Purchasing consortia, where groups of labs coordinate bulk buys, lets even small teams secure top-grade material at prices that don’t bust the annual budget. Diligence in receipt inspection and quick QC checks help spot issues before work begins.
There’s always the risk of counterfeit or misrepresented chemicals finding their way to market—purity labels alone don’t always tell the whole story. Labs protect themselves by demanding up-to-date certificates of analysis and running their own batch checks. Melting point checks and rapid TLC or LC-MS screening only need a fraction of a gram but can flag problems before protocols go off track. Peer networks also help share trusted sources and expose sellers who don’t live up to their claims. After a few misadventures with mixed-output chemicals, those extra steps start feeling less like overkill and more like standard practice.
People don’t use 2,6-Dihydroxybenzoic Acid in a vacuum—it shows up in environmental studies, plant metabolomics, pharmaceutical testing, and material sciences. Anywhere trace-level detection matters, precision matters more. I’ve watched collaborations between academic groups and biotech startups stall because a single reagent batch didn’t live up to its stated grade. High expectations for purity and batch consistency let cross-disciplinary teams blend skill sets without getting bogged down in unexpected chemistry.
Science never stands still. The baseline for “acceptable” purity creeps up each year. What passed for good enough five years ago now strains to meet today’s expectations. Having ≥99% 2,6-Dihydroxybenzoic Acid available lets labs pivot to new methods and keep pace with cutting-edge protocols. The value comes not just from purity alone, but from the momentum it gives to individual researchers and team projects alike. Labs that invest early reap the rewards in data reliability, higher publication rates, and stronger grant proposals.
Modern labs keep digital inventories, logging every chemical entering and leaving. Being able to trace each use of 2,6-Dihydroxybenzoic Acid to a specific lot number ensures confidence in revisiting old data, updating methods, or troubleshooting unexpected results. The best suppliers make access to digital COAs seamless, which suits the need for transparency in collaborative work. This kind of recordkeeping does more than tick regulatory boxes—it keeps teams accountable and supports clean science when big questions or audits arise.
The lessons from years in the lab point in one direction: shortcuts in reagent quality undermine the effort and intelligence invested in every research project. 2,6-Dihydroxybenzoic Acid (≥99%) doesn’t just meet a threshold; it raises the bar. From cutting clear paths through mass spectrometry analysis to tightening the reliability of every result in applied chemistry, this compound saves time, protects hard-won insights, and builds the foundation for discovery. By focusing on substances that serve the highest scientific standards, today’s labs strengthen their work and deepen the reservoir of knowledge future researchers can trust.