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HS Code |
577239 |
| Name | Bromophenol Red |
| Cas Number | 34725-61-6 |
| Chemical Formula | C19H10Br4O5S |
| Molecular Weight | 669.97 g/mol |
| Appearance | Red to violet powder |
| Solubility In Water | Slightly soluble |
| Melting Point | 279 °C (decomposes) |
| Ph Indicator Range | 5.2 - 6.8 |
| Color Change | Yellow to purple |
| Maximum Absorbance Wavelength | 443 nm |
| Storage Conditions | Store at room temperature, away from light |
| Synonyms | BPR, Tetrabromophenolsulfonphthalein |
As an accredited Bromophenol Red factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Bromophenol Red, 25g, is supplied in a sealed amber glass bottle with a secure screw cap and clear identification label. |
| Shipping | Bromophenol Red is shipped in tightly sealed containers, protected from moisture and light. Packages are labeled according to chemical safety regulations. Standard shipping is by ground or air, compliant with local and international transport guidelines. Handling requires gloves and eye protection, and shipping documents include the material safety data sheet (MSDS) for reference. |
| Storage | Bromophenol Red should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances like strong oxidizers. Protect it from moisture, direct sunlight, and excessive heat. Ensure proper labeling and avoid physical damage to the container. Store at room temperature and follow all applicable safety guidelines for chemical storage. |
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pH indicator: Bromophenol Red pH indicator (pKa 5.1) is used in laboratory titrations, where accurate endpoint detection is achieved through distinct color change. Purity 98%: Bromophenol Red, with purity 98%, is used in clinical diagnostic assays, where high assay sensitivity and reliability are ensured. Molecular weight 670.98 g/mol: Bromophenol Red with molecular weight 670.98 g/mol is used in electrophoresis gels, where consistent migration patterns and dye mobility are maintained. Melting point 273°C: Bromophenol Red with melting point 273°C is used in high-temperature biochemical tests, where thermal stability prevents decomposition. Salt-free grade: Bromophenol Red salt-free grade is used in protein quantification protocols, where minimized ionic strength avoids sample interference. Particle size ≤20 μm: Bromophenol Red with particle size ≤20 μm is used in microplate-based assays, where rapid dissolution and homogenous distribution are achieved. Absorbance maximum 443 nm: Bromophenol Red with absorbance maximum 443 nm is used in spectrophotometric measurements, where precise quantification by absorbance wavelength is ensured. Stability pH range 3.0–8.0: Bromophenol Red with stability in pH range 3.0–8.0 is used in buffer system monitoring, where consistent indicator response over a wide pH range is provided. Aqueous solubility 3 g/L: Bromophenol Red with aqueous solubility 3 g/L is used in liquid assays, where uniform reagent preparation and complete dissolution are accomplished. Trace metal content <10 ppm: Bromophenol Red with trace metal content <10 ppm is used in enzyme activity assays, where low contamination prevents enzyme inhibition. |
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Every laboratory relies on trusted indicators to measure and observe subtle shifts in chemical environments. Bromophenol Red stands out for anyone who tracks pH changes—either in research, routine medical analyses, or classroom teaching. Known for reliable color shifts and a clear transition range, Bromophenol Red grabs attention because it delivers results without demanding specialized equipment or intricate prep. In my own college days, sitting at the bench stained with splashes of indicator solutions, I always reached for Bromophenol Red when titrations called for quick, unmistakable shifts. Its straightforward working range gives students a visual cue for learning, and that carries through to more complex analytical laboratories later on.
Bromophenol Red is often found under the CAS number 115-39-9. In most settings, the product comes as a fine, orange powder. Some suppliers offer high-purity grades—upwards of 98% purity—which makes sense when results must be accurate down to the smallest variables. Most labs prepare a stock solution by dissolving a few milligrams of the powder in distilled water or, occasionally, in a buffer suited for the experiment at hand. Students grab a bottle labeled at 0.04% weight volume for experiments, while researchers may require custom concentrations for trace analyses. Clear labeling and batch traceability have become the norm across reputable lab supply companies, giving users added confidence in every measurement.
Bromophenol Red clearly earns its place as a staple in analytical chemistry. With a transition range around pH 5.2 to 6.8, the color shifts from yellow under acidic conditions to purple-red as the solution turns more alkaline. I remember my own initial frustration as a student confusing similar indicators, mixing up methyl orange and bromocresol purple, then realizing that Bromophenol Red’s colors stood out clearly even to a tired eye at the end of a long lab session. It’s used as a pH indicator in titrations, but extends into more creative territory. For instance, clinical chemistry uses this dye as a reagent to detect albumin in urine samples—offering insights into kidney function or early disease. In biological research, some protocols incorporate Bromophenol Red as a tracking dye, helping scientists visualize sample migration in techniques like gel electrophoresis. These everyday applications remind us that even the simplest tools have a quiet but critical influence across disciplines.
In the hands of an experienced researcher, Bromophenol Red adapts to a range of sample types. Solutions with faint yellow hues signal a buffered acidity, while deeper purple-red hints at neutralization. What sets this compound apart is its sharp transition, reducing the room for guesswork when precise readings matter. I recall labs where pH adjustment had to be pinpoint accurate, with no time to double-check under a spectrophotometer. Bromophenol Red provides that clarity—no complicated calibration curves, just an honest color change visible to the naked eye. That’s practical science for both newcomers and professionals on a tight schedule.
The world of pH indicators includes classics like phenolphthalein, methyl red, and bromothymol blue. They all have distinct pH transition ranges and color shifts. What puts Bromophenol Red in its own category is the sweet spot of its transition zone. It fills the gap between broad-range indicators that blur subtle distinctions and narrower-range dyes that miss gentle shifts. For instance, phenolphthalein spikes from colorless to pink near pH 8.2 to 10, which suits strong base titrations but misses the point in mildly acidic solutions. Methyl orange runs from red to yellow around pH 3.1 to 4.4, ideal for quick reads at lower pH but unhelpful around neutral conditions. Bromophenol Red covers that middle range, lighting up the transition zone that often goes unmonitored in fast-paced or teaching labs.
In practice, switching indicators can confuse or even ruin a critical titration. I recall an incident where a colleague handed me a mislabeled bottle—intending bromothymol blue, but giving Bromophenol Red instead. The resulting color shift caused the endpoint to appear earlier than expected. We realized only after reviewing the charts and repeating the test. That experience showed me just how much these differences matter. Each indicator’s unique chemistry, not just the color palette, shapes the outcomes in subtle ways. By sticking with Bromophenol Red for mid-range acid-base reactions, results stay reproducible across different settings. This consistency supports accurate teaching demonstrations, clinical testing, and protocol-driven research without the risk of ambiguous endpoints.
Bromophenol Red owes much of its dependable reputation to consistent performance and solid documentation. Reliable sources recommend storing the powder in tightly sealed containers, away from light and moisture, to prevent degradation. In my experience, most routine labs keep indicators on labeled, dust-free shelves right next to titrant bottles. Accidental spills aren’t a disaster—Bromophenol Red does stain clothes and skin with a brief orange tint, but it washes out. Its safety profile offers an assurance many other dyes lack. No known severe toxicity appears in common lab settings, so even students in crowded labs work confidently with it. That being said, good glove use and careful pipetting remain good practice. Trusted suppliers provide detailed documentation, including Certificates of Analysis and safety data sheets, which help users verify lot-to-lot consistency.
The dye’s photostability means stored solutions remain stable for reasonable periods, reducing the likelihood of drift or unexpected results due to compound breakdown. Keeping familiar dyes in routine circulation cuts back on preparation risks—no need for constant recalibration or elaborate validation for each fresh batch—and encourages safer, more consistent handling habits.
Lab safety now extends to environmental thinking. Many old dyes, including some heavy-metal-based indicators, raise alarms about waste disposal. Bromophenol Red carries a lower risk profile. After its role in titration or tracking, solution remnants go into regular aqueous waste streams but still require basic protocols—no dumping into sinks without neutralization. In larger laboratory networks, colorimetric waste accumulates through the semester, sparking conversations about green chemistry and improving waste minimization. Although Bromophenol Red breaks down more easily than dyes containing lead or mercury, it’s still synthetic and doesn’t belong in open water systems. By using only as much as necessary, modern labs can help shrink the environmental impact.
In educational settings, students often create excess indicator waste through overuse or accidental spillage. Instructors set clear guidelines for minimal-dose usage and safe waste segregation. From my teaching experience, emphasizing the importance of using small indicator volumes—often just a single drop or two per test—dramatically reduced waste while training better lab habits for advanced coursework and professional life.
In recent years, laboratory suppliers have faced supply chain hiccups, affecting even basic chemicals. What’s reassuring about Bromophenol Red is its chemical simplicity and stable production. Large-scale manufacturers synthesize the compound regularly, so no major shortages or inflation spikes shake its market price. In research institutions I’ve worked with, purchasing teams inspect lot documentation for expiration dates and purity specifications, but rarely face backorder delays or complicated import paperwork. Reliable access supports everything from introductory chemistry lessons to serology labs screening patient samples.
Quality control remains top-of-mind for anyone sourcing reagents. Reputable brands back up their products with analytical testing—users look for full transparency regarding testing methods, purity tests, and, in some contexts, absence of hazardous contaminants or residues. This openness aligns with trusted laboratory practice and meets rising standards in research reproducibility and downstream applications. For example, consistent lot-to-lot purity allows scientists to compare results across different labs or replicate experiments years later without revalidating every aspect of their protocol.
Every chemistry student learns the ropes by experimenting with indicator dyes. The clarity of Bromophenol Red’s transition makes it a favorite of educators teaching titration, buffer preparation, or basic pH measurement. Students see an immediate shift in color and gain intuitive understanding of acid-base balances. Experienced instructors craft lessons around visible chemical change, reinforcing theory with real reactions. The approachable nature of Bromophenol Red supports inclusive pedagogy, giving students from diverse backgrounds or visual abilities a better chance at recognizing test outcomes. No expensive sensors or high-end glassware get in the way of learning.
In my own teaching, I noticed that students remember experiments with engaging color transitions long after more abstract math lessons fade. Instructors can time lessons on weak acids and bases precisely to align with Bromophenol Red’s pH range, reinforcing theory with practice. Beyond classic titration, creative lesson plans use the dye in test strips or microplate formats, making introductory lessons memorable and preparing students for more advanced hands-on work. Teachers choose Bromophenol Red not only because it works, but because its reliability helps spark curiosity that persists beyond the classroom.
Contemporary research stretches even traditional compounds like Bromophenol Red into new roles. Biochemists sometimes use this dye as a loading control in polyacrylamide gel electrophoresis, where it helps track the progress of proteins or nucleic acids during separation. I’ve watched colleagues rely on its dependable migration pattern as a visual confirmation that gel runs are proceeding as expected, then snap digital images to document variability or unexpected results. Analytical chemists may further exploit Bromophenol Red’s reactivity for colorimetric assays, designing tests that change color in response to specific biochemical interactions. In both cases, speed and visual clarity override the need for expensive digital sensors.
Materials science also finds creative uses for Bromophenol Red. Thin films or hydrogels embedded with this dye reveal pH fluctuations in sensors designed for environmental monitoring or smart wound dressings. By incorporating sensitive colorimetric indicators, researchers gather continuous feedback without bulky instruments. These emerging uses extend Bromophenol Red’s value beyond basic wet chemistry, connecting classic chemistry with modern innovation in health and environmental technology.
Despite a strong track record, Bromophenol Red isn’t a fit for every scenario. Its pH transition may be too narrow or misplaced for titrations outside the 5.2 to 6.8 range. In such cases, researchers and students consult charts comparing indicator profiles, then pair alternatives like bromothymol blue or phenol red to specific needs. Some users working in color-sensitive fields have noted that Bromophenol Red’s color shift—yellow to purple-red—can be tricky under dim or colored ambient lighting. Teachers and lab designers overcome this obstacle by installing adequate white-light sources and encouraging colorblind-friendly teaching protocols, which often include reference cards or digital color apps.
Bromophenol Red, like most organic indicators, can degrade if left exposed to strong light or air. Although less prone to breakdown than some dyes, open bottles or dusty containers can invite contamination or spoilage. Best practice involves using tightly sealed, properly labeled vials, as well as periodic replacement from fresh stock. Batch testing and standardized use protocols further guarantee sample integrity. In some of the institutions where I’ve worked, routine shelf-life reviews and careful inventory checks help maintain quality and avoid the stress of sudden unexpected indicator failure during critical experiments.
Environmental advocates push for greener alternatives across chemistry, including in indicator selection. Researchers continue to investigate plant-based or biodegradable dyes for some applications, gradually reducing reliance on synthetic compounds. Bromophenol Red’s relatively low toxicity keeps it in favor, yet as green chemistry evolves, labs may pivot toward indicators with even less environmental impact. Institutions balancing educational tradition and ecological goals will continue to monitor advances, updating best practices whenever feasible.
Relying on trustworthy suppliers plays a key role in getting the most out of Bromophenol Red. Laboratories commit to transparent sourcing, scrutinizing each batch’s supporting documents, and choosing partners with a strong record for safety and consistency. I’ve worked in lab contexts where open communication between purchasing teams and vendors improved both pricing and quality—sometimes negotiating batch-specific certificates or direct access to technical support staff answering questions about compatibility with downstream applications. Open access to certificates of analysis, third-party purity tests, and long-term supplier relationships build confidence across both educational and professional research institutions.
Knowledge-sharing helps grow a more informed community of practice. Senior staff mentor newcomers on the specific quirks of each product, pass on stories of both successful and failed color transitions, and maintain a collective record of supplier dependability. This human aspect of scientific practice relies on building culture and habits, not just standardized protocols, and Bromophenol Red carries with it a history of trusted use.
From hands-on lesson plans to advanced research, Bromophenol Red serves as a trusted visual communicator in the lab. Its color shifts land right where many common acid-base reactions take place, offering critical endpoints with eye-level clarity. Reliable production and a strong safety profile contribute to peace of mind, while transparent quality control allows professionals and educators to lean on its performance year after year. Young students and seasoned researchers alike recognize its value. New environmental priorities will likely shift indicator usage little by little, but Bromophenol Red’s proven usefulness and long tradition offer a foundation upon which tomorrow’s innovations build. The more we understand the strengths and limits of even the humblest reagents, the better our science and teaching can become.