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HS Code |
711569 |
| Cas Number | 103404-87-1 |
| Molecular Formula | C8H17NO3S |
| Molecular Weight | 207.29 |
| Appearance | White crystalline powder |
| Melting Point | 272-275°C (dec.) |
| Solubility In Water | Soluble |
| Pka | 9.1 at 25°C |
| Storage Temperature | Room temperature |
| Synonyms | CHES; N-Cyclohexyl-2-aminoethanesulfonic acid |
| Purity | ≥99% |
As an accredited 2-Cyclohexylaminoethanesulfonic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, sturdy plastic bottle labeled "2-Cyclohexylaminoethanesulfonic Acid, 500g" with hazard symbols, batch number, and tightly sealed screw cap. |
| Shipping | 2-Cyclohexylaminoethanesulfonic Acid is shipped in tightly sealed containers, protected from moisture and extreme temperatures. It is classified as non-hazardous but should be handled with standard precautions. Packages are clearly labeled, cushioned to prevent breakage, and accompanied by a safety data sheet (SDS) in compliance with regulatory requirements for laboratory chemicals. |
| Storage | 2-Cyclohexylaminoethanesulfonic Acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from moisture and incompatible substances such as strong oxidizing agents. Keep the storage area free of direct sunlight and ignition sources. Proper labeling and secondary containment are recommended to prevent accidental spills or contamination. |
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Purity 99%: 2-Cyclohexylaminoethanesulfonic Acid with purity 99% is used in biochemical buffer formulations, where it ensures minimal background interference in enzyme assays. pH Stability 2.0–10.0: 2-Cyclohexylaminoethanesulfonic Acid with pH stability 2.0–10.0 is used in protein purification systems, where it maintains consistent buffering capacity across a wide pH range. Molecular Weight 221.31 g/mol: 2-Cyclohexylaminoethanesulfonic Acid with molecular weight 221.31 g/mol is utilized in electrophoresis protocols, where it provides predictable ionic strength supporting accurate protein separation. Melting Point 270°C (decomposition): 2-Cyclohexylaminoethanesulfonic Acid with melting point 270°C (decomposition) is used in high-temperature biochemical research, where it guarantees buffer integrity under thermal stress. Low UV Absorbance: 2-Cyclohexylaminoethanesulfonic Acid with low UV absorbance is applied in spectrophotometric assays, where it allows precise detection of low-abundance biomolecules. Solubility >80 g/L (water): 2-Cyclohexylaminoethanesulfonic Acid with solubility >80 g/L in water is employed in cell culture media preparation, where it ensures homogeneous buffer distribution for optimal cell growth. Endotoxin Level <0.1 EU/mg: 2-Cyclohexylaminoethanesulfonic Acid with endotoxin level <0.1 EU/mg is selected for pharmaceutical manufacturing, where it reduces pyrogenic risk in injectable drug products. Stability at -20°C: 2-Cyclohexylaminoethanesulfonic Acid with stability at -20°C is used in long-term reagent storage, where it preserves buffer efficacy over extended periods. Particle Size ≤50 µm: 2-Cyclohexylaminoethanesulfonic Acid with particle size ≤50 µm is used in chromatography applications, where it allows rapid dissolution and minimizes filter blockage. Heavy Metals <5 ppm: 2-Cyclohexylaminoethanesulfonic Acid with heavy metals content <5 ppm is used in sensitive analytical methods, where it mitigates contamination-related analytical errors. |
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Walking through any modern lab, you notice shelves full of bottles labeled with names that seem to run together after a while. 2-Cyclohexylaminoethanesulfonic Acid stands out to anyone who has spent time working with biological buffers or running sensitive experiments in biochemistry. Most of us in the biology and chemistry worlds have encountered a frustrating day ruined because the buffer picked for your protocol was a little too unstable in the conditions you needed, or the pH drifted over time. This product has become a go-to for researchers because it brings reliability to the table — a trait that counts for more than a laundry list of features.
2-Cyclohexylaminoethanesulfonic Acid, often abbreviated CHES, is categorized among the zwitterionic buffers. Its chemical properties reveal why it maintains a steady reputation in applications where precise pH control is a must, especially near the alkaline end of the spectrum. Sometimes it's tempting to treat buffers as interchangeable, but one quick look at the structure, with the cyclohexyl ring and sulfonic acid moiety, tells a different story. The pKa lands near 9.3 at 25°C, making it dependable for work in the 8-10 pH range. Some products claim versatility, but struggle to hold pH as temperature or ionic strength shift. CHES has shown over time that its stability keeps experiments honest — a trait you start to appreciate after enough late nights rerunning gels.
Diving into specification sheets or comparing technical data about buffers isn't usually the highlight of the job. I remember the days spent scrolling through supplier catalogs, comparing parameters like solubility, purity, or lot consistency. With 2-Cyclohexylaminoethanesulfonic Acid, the most meaningful specs reveal themselves in use rather than in charts. High-grade CHES typically appears as a white to off-white powder that dissolves readily in water, important if your experiment needs to avoid organic solvents or if you prefer buffers that don't introduce smell or turbidity. In terms of purity, reliable sources deliver CHES with low metal content and minimal UV absorbance — an overlooked detail if you never had your absorbance readings skewed by impurities in your buffer. This matters more to those working with nucleic acids or proteins, where background noise can mask the signal you’re desperate to find.
Another point I’ve encountered: CHES carries a low tendency for biological contamination in storage, compared with some organic buffers that seem to invite colony growth within weeks. Convenience counts. No need to worry about cloudy buffers after a few days at room temperature.
People tend to stick with what works in the lab, and that speaks volumes about any buffer. The most prominent use of 2-Cyclohexylaminoethanesulfonic Acid shows up during protein purification, enzyme assays, or electrophoresis that target alkaline pH environments. I've worked with teams tuning buffer conditions for dehydrogenases, alkaline phosphatases, or DNA-processing enzymes, and CHES earned its place because the margin for pH drift is so slim with these systems. Reliable buffers mean you chase signals, not problems.
Researching with biological samples has taught me that buffer interference creeps up in the subtlest ways. Many commonly used buffers, especially the phosphate-based types, bind to metal ions or react with certain cofactors, messing with your enzymology or binding assays when you least expect it. CHES sidesteps these pitfalls; its zwitterionic nature means weak interaction with most biological molecules and low affinity for cations or metal ions driving catalysis. Many newcomers underestimate that, but repeated experiments reveal that the wrong buffer eats up time, money, and sometimes even enthusiasm for a whole research direction.
There are folks in molecular biology who run bacterial cultures needing controlled pH — not just to avoid cell death but to keep expression levels consistent. CHES gets picked because it doesn't get metabolized by bacteria or eukaryotic cells. Few things frustrate more than discovering the buffer is acting as a secret carbon source for your bugs, skewing growth rates. I've seen entire weeks wasted because of overlooked side reactions like that.
Anyone shopping for buffers runs into an alphabet soup of options — from classic Tris and HEPES to MOPS and Bicine. They all tout pKa values, solubility, and "minimal interference," but the daily reality often differs. CHES distinguishes itself from Tris, for example, by stability at higher temperatures and resistance to reactions with aldehydes and other modifying agents. In some protein labelling protocols, Tris introduces side reactions that compromise your data; CHES steers clear, letting you focus on intended modifications.
MOPS and HEPES, popular for near-neutral pH, can't always pull their weight in more alkaline environments. I once had an issue running DNA gels for longer periods. Buffers like Tris started to show pH drop after a few hours due to CO2 absorption, knocking resolution off just when bands reached the critical separation. CHES runs keep a tighter pH window, keeping gels crisp and experiments reproducible.
From another angle, CHES has a lower absorption at UV wavelengths, especially at 260 nm commonly used for nucleic acid or protein work. If your detection relies on tight signal-to-noise, the assurance you won’t see unwanted absorbance can make the difference between publishing and troubleshooting for another month.
Over the years, industry-wide studies and informal survey data from core facilities continue to show a correlation between standardized buffers and reproducible results. In complex systems biology, big data research, or pharmaceutical assay development, control over variables counts for more than cutting-edge techniques. 2-Cyclohexylaminoethanesulfonic Acid often features in these validated protocols, not because it’s flashy or new, but due to its repeatability. Research published in peer-reviewed journals repeatedly lists CHES among the trusted buffers for cyclic nucleotide assays and membrane studies where other options falter.
Findings from mass spectrometry labs reinforce this theme: amino-based buffers such as Tris give off background ions or react with crosslinkers, muddying data. Chemists who switched to CHES for sample prep report cleaner spectra and lower interference, a claim supported by real output rather than marketing. In protein crystallography, frustratingly small shifts in pH cloud samples or ruin crystal growth. CHES keeps the tray steady throughout the long setups, so you learn to count on the result instead of worrying about whether a buffer ruined the batch.
Lab routine brings enough uncertainty, so anything steady and predictable can change how teams approach experiments. I’ve watched labs carefully manage budgets only to face supply chain hiccups or batch-to-batch variability. Reliable sources of CHES have shown remarkable consistency across lots, which has real value if you’re setting up weekslong experiments or collaborating across sites. Knowing your buffer behaves in one city exactly as it does in another saves both time and trust between partners.
Another ongoing problem in experimental chemistry surrounds contaminants. Trace metals or residual organics in some buffers interact with metal-requiring enzymes or add noise to analytical reads. Out of the products compared, CHES — especially in research and molecular biology grades — provides confidence through visible batch analyses and supplier transparency, which backs up its reputation for purity. That kind of accountability is something regulatory agencies, journal editors, and research funders increasingly demand.
Choosing your buffer is rarely just about chemistry. The cost, preparation labor, shelf stability, impact on downstream processing, and even the disposal profile matter. 2-Cyclohexylaminoethanesulfonic Acid wins loyalty from those who have made the mistake of picking cheaper, less stable buffers only to lose the savings to troubleshooting or wasted materials. Its lower tendency towards microbial growth means fewer headaches managing contamination risks and less frequent buffer replacement, which impacts both cost and cleanup logistics.
CHES also simplifies workflows for teams interested in regulatory compliance or environmental safety. Some common buffers release toxic byproducts during autoclaving or become hazardous on mixing with lab disinfectants. Labs using CHES have reported fewer accident incidents and easier training for new staff. If you work at the intersection of science and safety, this can mean slimmer incident reports and happier safety officers.
Research keeps progressing into more sensitive, multi-step protocols, particularly in fields like genomics, proteomics, and drug discovery. Buffers that avoid interfering reactions and minimize batch variability represent more than a convenience — they allow researchers to tackle complex questions with fewer variables. 2-Cyclohexylaminoethanesulfonic Acid often gets a reputation as a specialized, niche buffer, but reality keeps bringing it back into broader relevance. The expansion of high-throughput screening, alongside stricter reproducibility standards from journals and funding agencies, has made selecting the right buffer matter to more people than ever.
This shift also forces both suppliers and end-users to demand more transparency. Researchers are pushing for more analytical data on sources, contaminant profiles, and lot verification. As a result, CHES now often comes with certificates of analysis for each batch and open communication around quality control processes. I’ve watched colleagues switch suppliers or alter workflows based solely on the confidence they build from such transparency — a reflection of where science is heading.
If you spend time reading scientific literature or attending conferences, the issue of reproducibility always comes up. Investigators report chasing failed protocols or contradictory results, often because of minor changes in reagents like buffers. Consistently, 2-Cyclohexylaminoethanesulfonic Acid features in published protocols for experiments where small changes in pH can upend months of work. Teams who rely on this buffer see fewer retractions and greater trust in their methods. Tracking back through the evidence, it’s clear that the choice of buffer is not just an afterthought; it underpins the entire experimental system.
Most labs could do more to optimize their buffer selections. Anyone starting with new workflows benefits from small-scale pilot runs using CHES alongside other candidates. In my experience, letting data drive decisions, not just habits or supplier promotions, leads to fewer regrets. Cataloging results from different buffers strengthens protocol resilience and provides documented justification to skeptics or auditors.
Training for new lab members often skips the importance of buffer properties, focusing instead on protocol steps and equipment. Including targeted discussions about why CHES works, and its specific advantages and limits, has improved outcomes — especially for those designing novel enzyme reactions or planning multiplex assays.
Another workable solution lies in collaboration. Some research groups establish shared buying programs or exchanges for specialty reagents like CHES, reducing overall costs and strengthening collective bargaining for higher-quality products. This model has led to more predictable supply chains and stronger connections across research centers, ultimately benefiting everyone’s science.
Even with its reputation, some barriers exist to wider adoption of CHES. Accessibility at smaller institutions or in developing regions remains uneven, often because procurement policies favor generic reagents that miss out on the subtleties built into more specialized products. Broader outreach by suppliers, as well as more transparent educational resources about buffer properties, can narrow this gap.
Creating open-access databases of buffer properties and real-world feedback facilitates smarter decisions, allowing labs to learn from the experiences of others rather than repeating common mistakes. Peer-to-peer knowledge transfer remains one of the most powerful tools for pushing good science forward. In conversations at conferences and workshops, practitioners sharing buffer stories and troubleshooting strategies solve more problems than isolated technical sheets ever could.
Not every solution in science comes from revolutionary technology. Sometimes, the power to drive progress comes from incremental improvements — like consistently picking buffers that keep experiments moving and results reliable. 2-Cyclohexylaminoethanesulfonic Acid, with its unique chemistry and history of trust in the field, stands as an example. The next wave of discoveries in biology, chemistry, and medicine will depend on details often overlooked, and buffer choice sits among them. Drawing from years spent troubleshooting experiments and mentoring new researchers, I’d argue that investing in the right reagents is not a luxury; it’s the backbone of lasting scientific achievement.