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5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside

    • Product Name 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside
    • Alias X-Gluc
    • Einecs 254-713-8
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    750221

    Product Name 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside
    Synonyms X-Glucoside, X-Glc
    Cas Number 155433-22-6
    Molecular Formula C14H15BrClNO6
    Molecular Weight 424.63 g/mol
    Appearance White to off-white powder
    Solubility Soluble in DMSO and methanol
    Storage Temperature -20°C
    Purity ≥98% (HPLC)
    Usage Chromogenic substrate for beta-glucosidase detection

    As an accredited 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in a 1-gram amber glass vial with screw cap, labeled with chemical name, formula, CAS number, and storage conditions.
    Shipping **Shipping Description:** 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside is shipped at ambient temperature, protected from light and moisture. Packaging is secure to prevent contamination or degradation. No hazardous material classification for transport, but handle as a laboratory chemical. Shipping regulations may vary; check local guidelines for compliance. Suitable for research laboratory use only.
    Storage **5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside** should be stored in a tightly sealed container, protected from light and moisture. Keep at 2–8°C (refrigerator) and in a dry, ventilated area. Avoid exposure to excessive heat or humidity. The container should be clearly labeled, and access restricted to trained personnel. Handle under appropriate safety precautions to prevent contamination and degradation.
    Application of 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside

    Applications of 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside in Industrial Manufacturing

    5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside, often referenced as X-Glucoside, finds critical application across several industrial research and manufacturing sectors. Our expertise as a direct producer ensures full compliance and reliable supply for advanced applications in diagnostics, quality control, and scientific research.

    1. Chromogenic Substrate for Microbial Diagnostics

    In industrial microbiology, this compound functions as a chromogenic substrate for beta-D-glucosidase enzyme activity detection. Diagnostic media producers incorporate it into selective agar blends, allowing rapid identification of bacteria such as E. coli and other coliforms through distinct blue-green colony coloration. Our quality-controlled material integrates directly into high-throughput automated plate pourers and dehydrated media lines, supporting accuracy in regulatory-compliant pathogen detection for food, water, and clinical laboratories.

    Industry compliance standards

    • ISO 9308-1:2014 (Water quality — Detection and enumeration of Escherichia coli and coliform bacteria)
    • U.S. FDA BAM (Bacteriological Analytical Manual, Chapter 4: Enumeration of Escherichia coli and the Coliform Bacteria)
    • European Pharmacopoeia 2.6.13 (Microbiological Control of Non-Sterile Products)
    • EN ISO 11133:2014 (Preparation, production, storage, and performance testing of culture media)

    Typical usage ratio

    • 15–100 mg per liter of completed culture medium, with precise dosage adjusted per test sensitivity and agar composition.

    Downstream process integration

    • Added during aqueous phase blending before autoclaving or sterile filtration.
    • Direct integration into dehydrated base media powder production lines for pre-formulated media blends.
    • Employed in QC release testing to ensure uniform color endpoint in microbial recovery assays.

    Final product types

    • Chromogenic coliform detection agar (e.g., Colorex, Chromocult)
    • Dehydrated media mixes for clinical and environmental laboratories
    • Ready-to-use detection plates for food industry QC
    • Industrial test kit components for water quality labs

    2. Enzyme Activity Assays in Biotechnology Production

    Biotech manufacturers use this substrate for enzymatic screening protocols, primarily to quantify beta-glucosidase activity in enzyme engineering, fermentation monitoring, and microbial strain selection. Its high specificity and clear color endpoint facilitate robust process analytics for enzyme manufacturers engaged in vetting and optimizing beta-glucosidase-expressing microbial cell banks and fermentation batches.

    Industry compliance standards

    • Good Laboratory Practice (GLP) Principles (OECD, FDA 21 CFR Part 58)
    • IUPAC recommendations for enzyme analysis and reporting
    • ISO 17025 (Competence of Testing and Calibration Laboratories)

    Typical usage ratio

    • 0.05–0.5 mM in buffered assay mixtures, modifiable for microplate or tube scale depending on assay detection limits and throughput.

    Downstream process integration

    • Dispensed into standard microplate wells or automated assay vials with test sample preparations.
    • Integrated into robotic liquid handling QC lines for high-throughput batch validation.
    • Batch mixing under controlled pH to ensure substrate stability during test execution.

    Final product types

    • Enzyme activity screening kits for industrial R&D departments
    • Fermentation monitoring panels
    • Laboratory reference substrates for regulatory documentation
    • Custom enzyme validation panels

    3. Animal Feed Pathogen Testing Panels

    Feed safety labs and animal nutrition product manufacturers deploy chromogenic glucoside substrates for rapid detection of beta-glucosidase-positive contaminants in raw materials and finished feed products. Integration with high-throughput test formats accelerates compliance with veterinary and feed hygiene standards, ensuring end-user safety and batch-to-batch reliability in high-volume production environments.

    Industry compliance standards

    • European Union Regulation (EC) No 183/2005 (Feed hygiene requirements)
    • Association of American Feed Control Officials (AAFCO) - Official Publication
    • ISO 21527 (Microbiology of food and animal feeding stuffs — Enumeration of yeasts and moulds with chromogenic media)

    Typical usage ratio

    • 20–60 mg/L in base test agar or liquid media, determined according to sample matrix complexity and organism load.

    Downstream process integration

    • Incorporated into pre-mixed animal feed screening kits, typically as a dry powder format to ensure stability during shipping and storage.
    • Used during rapid sample prep before pathogen challenge testing and certificate-of-analysis release.
    • Automated blending with other selective chromogens in composite detection panels.

    Final product types

    • Feed pathogen screening cassettes
    • Chromogenic QC test kits for feed manufacturers
    • Veterinary diagnostic assay modules
    • Field test swab kits for livestock production sites

    4. Quality Control Reference Standards for Pharmaceutical Microbiology

    Pharmaceutical QC operations rely on defined substrate media for in-house sterility testing, hygiene verification, and environmental monitoring. Our glucoside integrates into manufacture of reference media, supporting both compendial and in-house validated microbial recovery systems within sterile and cleanroom GMP environments. Users benefit from batch-level traceability and controlled performance attributes for each substrate lot, supporting consistent compliance documentation during regulatory audits.

    Industry compliance standards

    • USP <797> and <1116> Sterile Compounding and Environmental Monitoring Standards
    • European Pharmacopoeia 2.6.12 & 2.6.13 (Sterility and Microbial Count Tests)
    • GMP Annex 1 (Manufacture of Sterile Medicinal Products)
    • JP Pharmacopoeia (Microbiological methods for pharmaceuticals)

    Typical usage ratio

    • 10–40 mg/L for high-sensitivity detection plates, with adjustment for target microorganism and facility-specific validation studies.

    Downstream process integration

    • Weighing and blending under ISO 14644 cleanroom conditions during media preparation.
    • Inline QC checks for uniformity of colorimetric response before batch filling and plate casting.
    • Sterile filtration prior to packaging in ready-to-use and dehydrated product formats.

    Final product types

    • Reference media for cleanroom monitoring
    • GMP-compliant environmental test plates
    • Validated media lots for sterility tests
    • Compendial conformant QC substrate kits for pharmaceutical production
    Free Quote

    Competitive 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside: A Closer Look from the Manufacturer’s Perspective

    Understanding What Sets Our X-Glc Apart

    Years of chemical manufacturing experience shape the way we work with substances like 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside—known throughout research labs as X-Glc. Our connection to this compound traces back to a deep respect for its role in biotechnology and diagnostics. The difference between producing X-Glc yourself and sourcing it elsewhere lies in the way every batch is managed. Chemical manufacturers who follow rigorous, hands-on procedures see things from the inside out, working with raw materials day after day. Our view brings direct knowledge of how purity, consistency, and traceability play out in both quality control and real-world lab results.

    Unlike traders or downstream resellers, manufacturers contend directly with the inevitable reality of variable starting materials, process bottlenecks, and the learning curve that comes with scale-up. Each time we optimize a synthesis, it’s more than just numbers in a data log; it’s a question of how small tweaks in reaction conditions can boost yields without leaving impurities behind. Workers handling X-Glc on the production floor notice subtle color shifts, early signs of degradation, or clumping, often before analytical instruments flag the issue. This level of vigilance doesn’t show up in specs sheets or resellers’ websites, but it matters when researchers rely on substrates with unambiguous performance.

    Why Purity Translates Into Results

    5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside acts as a chromogenic substrate for beta-glucosidase enzymes. In short, it reveals enzyme activity through color. Take one look at a row of plates using differently sourced X-Glc and the impact of off-grade material jumps out at you. Smearing, faint zones, unexpected background colors—all these stem from impurities or slight changes in the manufacturing pathway. Our team has learned over years that buyers who want to stretch reagent budgets by using cheaper grades spend more time troubleshooting than saving money. A difference of mere micrograms in contaminant levels can undermine selectivity; split batches that aren’t monitored rigorously can yield unpredictable performance, which bounces back on the original producer.

    From the manufacturing bench, controlling these processes means ensuring batch consistency from lot to lot. Since X-Glc tends to degrade when exposed to moisture or high temperatures, environmental controls become a frontline defense. As a manufacturer, you notice that color changes during storage indicate hydroxylation or halogen displacement at the indole ring. Regulating trace water levels during crystallization has become second nature. Storage systems must shield from humidity, and each packaging run incorporates tight vacuum sealing. This vigilance reduces the risk that researchers waste time chasing false positives, shadow colors, or product breakdown.

    Specifications That Matter in Practice

    Not all specifications carry equal weight on the production line or at the bench. X-Glc is mostly encountered as a pale to bright blue powder, depending on trace impurity levels and the lot’s exposure to air. Particle size distribution, mostly overlooked by non-manufacturers, directly affects solubility and plate background appearance. Smaller particles dissolve more readily, producing cleaner plates; larger aggregates can leave undissolved residue, distracting from assay results. Material with a controlled, narrow particle size distribution saves both technician efforts and helps avoid costly repeat experiments.

    We keep water content below specific micro-percentage levels using Karl Fischer titration on every finished batch. Moisture content isn’t just academic—it determines shelf life, along with how quickly the powder forms lumps or degrades during storage. Our experience tells us that paying attention to residual solvent profile is equally important. X-Glc synthesized through traditional indole acylation or Vilsmeier-Haack pathways carries the risk of trace solvents or unintended by-products such as 3-haloindoles. Detecting and controlling these requires robust chromatography and routine NMR scans. We never rely solely on the purity stated by precursor suppliers. Full traceability from each batch remains integral—otherwise, it remains impossible to troubleshoot problems that manifest in end-user applications.

    Direct Insights Into Usage: Beyond the Obvious

    Working with X-Glc reveals a story that goes past the chemistry. In microbiology and molecular cloning, this substrate helps researchers spot colonies expressing beta-glucosidase: a blue color marks the positive picks. It enables rapid screening in environmental and food safety testing. The predictability of color development isn’t guaranteed, we’ve learned, without careful attention to storage, handling, and substrate layering. Too much substrate on agar plates can cause toxicity; too little leaves plates washed out. Our technical support finds that even advanced labs sometimes over-concentrate X-Glc, chasing brighter stripes but hitting enzyme inhibition instead.

    One direct improvement we introduced years ago was tighter granulation controls, prompting more predictable dosing by customers. We also found that packaging in light-resistant, hermetically sealed containers cuts spoilage rates. These might sound like small details, but as actual manufacturers, the customer feedback loop comes directly; if a run shows poor signal intensity or throws unexpected false positives, we can crosscheck tracking details on package batches and react quickly.

    How Batch-to-Batch Traceability Addresses Lab Headaches

    In real-world laboratory work, even skilled researchers encounter issues due to chemical variability between lots. We’ve seen even slight fluctuations in composition translate into months of troubleshooting, which is frustrating for both researchers and those of us who produce their materials. Documenting every step of manufacture, right down to which reactor batch supplied which jar, transforms troubleshooting from guesswork to traceable science. Customers approach us with questions ranging from “Why is there a faint green edge to my plates this time?” to “Has the bottling line changed last month?” Documented traceability allows for rapid investigation.

    As manufacturers, we recognize how bugs in the process—say, a temporary shift in humidity during drying, or a new filter material—can produce subtle but significant changes. Where traders and middlemen may respond with generic apologies, we dig into batch logs, isolate the variable, and directly adjust protocols. A single feedback call can instigate shifts to tighter environmental controls or an additional washing cycle.

    The Evolution of Production: Learning from Experience

    Early on, we produced X-Glc using conventional methods—batchwise halogenation and standard glucosylations. Over time, new process chemistries and automation technologies reduced impurity loads, saved operational costs, and improved worker safety. Our staff picked up right away that minimizing open transfers means fewer opportunities for hygroscopic materials like X-Glc to pick up atmospheric water. Batch yields climbed by a few percentage points, but more importantly, we saw product variability shrink. That is, customers began reporting more consistent color reactions and fewer returns.

    We also learned that it’s not only about the final synthetic step; upstream vendor controls matter too. Sourcing the highest quality 4-chloro-5-bromo-indole decreased background colors and random plate noise. Establishing tighter checks on the glucosyl chloride, ensuring the absence of trace acid or unreacted sugar, further reduced decomposition down the distribution chain. Our ability to test and qualify each new lot highlighted problems that went unnoticed under third-party purchasing models. Years of refining both the chemical sourcing and process flow carved out a level of reliability that downstream packagers and traders struggle to match.

    Why X-Glc Isn’t Interchangeable With Other Substrates

    Researchers familiar with chromogenic substrates often compare X-Glc to its relatives, such as X-Gal (used with beta-galactosidase) or magenta-glucoside derivatives. While they may seem interchangeable if you stare at a list in a catalog, experience at the bench—and at the process tank—proves otherwise. X-Glc activates a specific set of enzymes, producing a single, distinct blue product. Substitutes trigger different color profiles, have varying sensitivities, or worse, introduce undesired reactivity in mixed assays. We routinely field questions from users wondering why a red or purple tint has crept into their plates after switching from one source to another; many times, the answer lies in subtle differences in side product content or residual metals.

    Our technical group frequently tests incoming comparator samples from labs struggling with inconsistent results after switching to off-brand or generic material. An X-Glc run from our plant, tested side-by-side against a lower-purity variant, regularly shows sharper borders, lower background noise, and consistent blue intensity. These details cannot be extracted from spec sheets alone. The interaction between synthetic pathway choice and product stability is something gained only from experience running kilo-scale batches, not from repackaging drums of anonymous powder.

    Managing Shelf Life and Degradation: Lessons Learned

    One of the first lessons our warehouse teams absorbed about X-Glc was the critical importance of moisture and light exposure. We’ve cut down on return rates and field complaints by developing new packaging protocols—dark, airtight vials, batch-stamped and triple-checked for leaks. Light exposure doesn’t just fade the color over time; it also accelerates molecular breakdown, leading to erratic substrate performance. Only direct experience with multi-batch storage failures and analytical data over years forced us to take these extra steps.

    From the chemical production perspective, monitoring degradation kinetics informs best storage practices. X-Glc stores best at lower temperatures, in dry, dark conditions, away from acids and strong oxidizers. Our labs track color and product integrity at defined intervals, building a firm basis for shelf life recommendations. Failure at this step impacts not just the product but also research timelines and costly project delays. As originator, the responsibility to catch early signs of spoilage and alert customers falls squarely on us.

    Supporting Research, Not Just Supplying Reagents

    Manufacturers don’t just make compounds; they support scientific discovery. Our customer-facing chemists consult directly with clients to optimize assays using X-Glc. That means fielding questions about buffer compatibility, recommended concentrations, even troubleshooting unusual plate results. Over the years, advice we contributed—such as preferring phosphate over acetate buffers to reduce spontaneous hydrolysis—helped researchers get clearer results. Our hands-on insight comes from troubleshooting failed runs using our own product, providing practical solutions, and then seeing these tips pay off in our customers’ data.

    Unlike resellers, we’re also accountable for what happens downstream. Regulatory teams review product handling and disposal methods; every change in formulation or process must be logged for end-user safety and compliance. Many cutting-edge researchers depend on subtle assay tweaks; producing and supporting X-Glc calls for far more than simply following a recipe. The most effective solutions to tough plating issues—such as persistent background haze or zone growth—come from blending production-side insights with customer experiences.

    Responding to Changing Industry Demands

    Year by year, the needs of the research and industrial community evolve. New automation platforms, higher-throughput screening, and environmental sustainability requirements all exert subtle pressures on substrate manufacturing. In response to increasing demand for smaller-scale, specialty-packaged X-Glc lots, we reengineered our filling line for versatile order sizes. Automation made our output more reliable without compromising lot-level tracking or rapid order turnaround. We heard from biotech startups pushing into novel enzymatic assays that required tighter substrate tolerances than the market provided, so we invested in new in-line analytics to consistently deliver on these needs.

    Green chemistry has entered the conversation, too. As manufacturers, we know reducing solvent waste and improving energy efficiency isn’t just about meeting regulations; it also makes economic and scientific sense. Solvent recovery systems on our glucosylation reactors slash both emissions and material costs, with these savings channeled back into broader quality improvements. Each process innovation undergoes real-world validation, making sure that performance in the customer’s hands matches our analytical certification.

    Collaboration Anchored in Experience

    Our strongest contributions occur at the junction of manufacturing know-how and laboratory science. Researchers facing unexplained background staining or ambiguous color shifts receive direct, experience-grounded support from people who've engineered, synthesized, and QC’d the product from start to finish. These conversations form a feedback system that makes X-Glc from our facility more adaptable—and more dependable—compared to anonymous, repackaged lots circulated via middlemen. Fielding technical queries about X-Glc, our chemists draw not just on published literature but on a long history of hands-on troubleshooting, root-cause analyses, and collaborative problem-solving.

    Working directly with users, we’ve built a living library of best practices. Temperature logs, buffer recipes, substrate layer thicknesses, and plating times all feed into our guidance, shaped by continual real-world learning. This feedback travels back up the chain, helping us spot persistent issues faster than data sheets alone reveal. We adjust production runs, packaging, or QC focus as the needs of the community evolve, keeping X-Glc performance relevant to today’s techniques as well as tomorrow’s innovations.

    Comparing X-Glc to Alternative Substrates: A Manufacturer's Point of View

    The push to use alternative colorimetric substrates remains strong, particularly as research budgets tighten or new enzymes appear. Yet, after decades spent producing, modifying, and supporting substrate platforms, we know that simple substitution rarely yields equivalent assay performance. Magenta or yellow analogs deliver unique color outcomes, but rarely match the sensitivity, selectivity, or plate contrast that genuine X-Glc offers for beta-glucosidase. Process-originated byproducts—such as nitro- or additional halogenated indoles—distinguish different substrates in more than color alone; these intruders can change toxicity or even subtly interfere with growth patterns in microbial assays. We frequently run cross-comparisons upon request and, more often than not, researchers revert to X-Glc after pilot tests with alternatives highlight error margins bigger than the expected cost savings.

    As raw material suppliers change, so does the available product profile, forcing manufacturers to adjust protocols or revalidate inputs. In some cases, shortages of key intermediates have driven us to develop parallel sourcing or even pilot green chemistry routes to insulate both ourselves and our customers. These investments aren’t obvious until you’re peeling back layers in a thoroughly documented manufacturing pipeline, but they translate into more robust supply and more predictable product output.

    Sustainability and Future Improvement

    Like all responsible manufacturers, we recognize that sustainable operations strengthen both our business and the scientific work of our clients. We continually evaluate how solvent and material selection, waste treatment, energy usage, and encapsulation technology affect the integrity and safety of our X-Glc. Implementing newer, less polluting reagents for halogenation steps has required process retooling and careful transition, all under tight analytical scrutiny. The payoff comes through higher process yields, cleaner product profiles, and lower downstream environmental loads.

    Ongoing investments in training for our technical and manufacturing staff remain critical. A skilled operator’s intuition often flags developing trends faster than automated monitors can. These insights ensure that future batches of X-Glc remain as reliable as today’s, strengthening the trust scientists place in our products year after year. Sharing best practices, internally and with the research community, drives continuous improvement from the production bench through to bench-top experiment.

    Pride in the Work: Direct Manufacturer Value

    Day-to-day life inside a chemical manufacturing operation means tackling more than just technical puzzles; each run of X-Glc embodies the experience, vigilance, and direct responsibility of everyone involved. We see where differences in process, storage, and even shipping conditions create meaningful impacts downstream. Supporting scientists demands more than simply filling orders; it calls for firm control over every step, open dialogue with users, and an unwavering commitment to high standards. Only by working side-by-side with those developing new protocols and products can we continually elevate the performance, safety, and reliability of 5-Bromo-4-Chloro-3-Indolyl-Beta-D-Glucoside.