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Octyl-Beta-D-Glucopyranoside

    • Product Name Octyl-Beta-D-Glucopyranoside
    • Alias OG
    • Einecs 603-061-9
    • 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

    557150

    Cas Number 29836-26-8
    Molecular Formula C14H28O6
    Molecular Weight 292.37 g/mol
    Synonyms n-Octyl beta-D-glucopyranoside, OG, Octylglucoside
    Appearance White powder
    Purity ≥98%
    Solubility In Water 200 g/L (20°C)
    Melting Point 67-70°C
    Storage Temperature 2-8°C
    Usage Non-ionic detergent for protein solubilization

    As an accredited Octyl-Beta-D-Glucopyranoside factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Clear amber glass bottle, secure screw cap, white printed label, contains 25 grams Octyl-Beta-D-Glucopyranoside, chemical information and hazard warnings.
    Shipping Octyl-Beta-D-Glucopyranoside is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packaged according to regulatory standards, typically in amber bottles or HDPE containers. Store and transport at room temperature, away from strong acids and oxidizers. Shipping complies with chemical safety guidelines and labeling requirements.
    Storage Octyl-Beta-D-Glucopyranoside should be stored in a tightly sealed container, protected from light and moisture, at 2-8°C (refrigerator conditions). Keep away from sources of ignition and incompatible materials. Ensure storage in a well-ventilated, dry area, and avoid prolonged exposure to air. Always observe standard laboratory safety practices when handling and storing this chemical.
    Application of Octyl-Beta-D-Glucopyranoside

    Applications of Octyl-Beta-D-Glucopyranoside in Industrial Manufacturing

    Octyl-Beta-D-Glucopyranoside supports specialized requirements in select industrial markets. As the direct manufacturer, we deliver consistent quality tailored for bioprocessing, analytical sample preparation, membrane protein extraction, pharmaceutical formulation, and cell lysis procedures. Below, we present detailed downstream application scenarios, reflecting actual industry standards, process conditions, and finished product categories.

    1. Membrane Protein Extraction for Biopharmaceutical Research

    Research laboratories and manufacturing units in the biopharma sector regularly require efficient, low-denaturing agents for isolating membrane proteins from animal and microbial cells. Our material supports the preparation of pure protein samples for structure/function analysis and therapeutic discovery. Quality control depends heavily on batch consistency, purity levels, and tight regulation of process parameters due to sensitivity of membrane-bound targets.

    Industry compliance standards

    • USP General Chapter <1043> Bioprocessing Equipment
    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211 (finished pharmaceuticals)
    • ISO 13485:2016 (where used with diagnostic product extraction)

    Typical usage ratio

    • 1–4% w/v in extraction buffers for eukaryotic and prokaryotic cell membranes
    • Adjusted depending on protein hydrophobicity and sample load

    Downstream process integration

    • Dissolves directly into hypotonic, isosmotic, or salt-based lysis buffers
    • Added post-homogenization or during immobilization for solubilizing membrane fractions
    • Removed by dialysis or ultrafiltration before downstream chromatography

    Final product types

    • Isolated membrane protein standards
    • Active pharmaceutical ingredient (API) reference materials
    • Monoclonal antibody libraries
    • Membrane transport protein reagents for high-throughput screening

    2. Detergent in Chromatography Sample Preparation

    Analytical laboratories rely on controlled use of non-ionic surfactants for reproducible extraction of complex biological and pharmaceutical samples. Octyl-beta-D-glucopyranoside acts as a mild solubilizer, maintaining native protein conformation and reducing aggregation prior to HPLC, FPLC, or capillary electrophoresis. High batch-to-batch reliability is essential for secure analytical validation.

    Industry compliance standards

    • USP General Chapter <621> Chromatography
    • ISO/IEC 17025 Laboratory Management Standards
    • FDA Guidance for Bioanalytical Method Validation
    • Ph. Eur. 2.2.46 Chromatographic Separation Techniques

    Typical usage ratio

    • 0.5–2% w/v in mobile phases or sample loading buffers
    • Ratio determined by analyte solubility and detection limits required

    Downstream process integration

    • Added to sample buffer post-extraction for proteins and glycoproteins
    • Included at the pre-injection stage for analytical or preparative columns
    • Compatible with filtration and desalting prior to analysis

    Final product types

    • Validated reference protein solutions
    • Pharmaceutical and biosimilar substance quality control panels
    • Certified standards for regulatory filings
    • High-purity analyte preparations for diagnostic assay kits

    3. Cell Lysis Buffer Formulation for Biological Manufacturing

    The material functions as an efficient lysing agent in production-scale extraction of intracellular and periplasmic proteins. Manufacturers of enzymes, recombinant proteins, and microbiological standards prioritize precise blending and minimal batch variation. Surfactant performance during lysis directly influences protein yield and downstream purification success.

    Industry compliance standards

    • WHO TRS 999 – GMP for Biological Products
    • EU EudraLex Volume 4 – GMP for Medicinal Products
    • ISO 9001:2015 Quality Management Systems
    • Relevant OECD Principles of Good Laboratory Practice (GLP) for analytical products

    Typical usage ratio

    • 0.5–3% w/v in cell lysis buffer recipes
    • Adjusted based on cell wall type and intracellular protein concentration

    Downstream process integration

    • Incorporated after mechanical disruption steps (sonication, homogenization)
    • Mixed with buffer components such as tris-HCl, EDTA, and protease inhibitors
    • Compatible with scale-up batch mixing and inline process QC

    Final product types

    • Bulk enzyme concentrates (e.g. DNase, protease, polymerase)
    • Recombinant protein lots for diagnostics
    • Therapeutic protein precursor fractions
    • Cell-free extract standards for in vitro systems

    4. Solubilizing Agent for Vaccine Antigen Production

    Vaccine production lines inactivated or subunit antigens often require nonionic solubilizing agents during antigen isolation and downstream purification. Our product ensures mild dissociation of membrane-bound antigens without drastic conformational changes, supporting immunogenicity retention. Manufacturers demand reliable compliance with pharmacopoeial purity and low endotoxin levels as part of release testing.

    Industry compliance standards

    • European Pharmacopoeia 5.2.3 on Vaccine Production
    • FDA 21 CFR Part 610 – Biological Products: General
    • WHO Guidelines on the Quality, Safety and Efficacy of Vaccines
    • GMP as per ICH Q10 Pharmaceutical Quality System

    Typical usage ratio

    • 0.2–2% w/v in aqueous extraction/perfusion stages
    • Ratio depends on antigen hydrophobicity and process volume

    Downstream process integration

    • Blended after cell culture harvest, before primary clarification
    • Used during antigen release from host membranes or particles
    • Removed by diafiltration prior to final formulation

    Final product types

    • Subunit and conjugate vaccine antigens
    • Virus-like particle intermediates
    • Purified bacterial outer membrane proteins
    • Antigen bulk preparations for final adjuvantation

    5. Solubilizer in Diagnostic Reagent Manufacturing

    Diagnostic kit producers require consistent non-ionic surfactants for reagent formulations in immunoassays, ELISA kits, and automated diagnostic platforms. The material supports sensitive detection of antigen or antibody targets, improving sample dispersion while minimizing background noise in spectrophotometric and immunological workflows.

    Industry compliance standards

    • ISO 13485:2016 for in-vitro diagnostic (IVD) medical devices
    • IVD Directive 98/79/EC (replaced by EU IVDR 2017/746)
    • USP General Chapter <1206> Labeling of IVD Products
    • CLSI Document EP05 for Evaluation of Precision in Clinical Chemistry Measurements

    Typical usage ratio

    • 0.1–1% w/v in pre-mixed buffers and wash solutions
    • Optimized for compatibility with enzyme substrates and chromogenic indicators

    Downstream process integration

    • Added at automated liquid handling or bulk solution preparation stages
    • Key component of ready-to-use kit reagents, including sample diluents
    • Ensures stability during storage and shipping of reagent packs

    Final product types

    • Commercial ELISA kits
    • Point-of-care rapid diagnostic panels
    • Bulk diluents and wash solution concentrates for hospital labs
    • Clinical chemistry analyzer consumable fluids
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    Certification & Compliance
    More Introduction

    Octyl-Beta-D-Glucopyranoside: The Role of a Versatile Nonionic Surfactant from the Perspective of Its Manufacturer

    Bringing Clarity to Membrane Protein Studies and Beyond

    We pour a lot into crafting Octyl-Beta-D-Glucopyranoside, known to many as OG or OBG. Working as a direct producer, we see firsthand how it transforms research projects and laboratory protocols worldwide. The enthusiasm surrounding this mild, nonionic surfactant comes not just from advertised performance, but real experiences in protein science, biochemistry, and drug formulation. Manufacturing OG in our own facilities has shown us its true value, especially for those who want to keep proteins intact and studies reproducible.

    A Straightforward Approach to Protein Solubilization

    Over years spent refining our synthesis and purification processes, we have learned to avoid cutting corners. OG, with the model name Octyl-Beta-D-Glucopyranoside, starts from specially sourced raw materials and crystallizes beautifully once our controlled process wraps up. The active component’s structure—a glucose head linked to an octyl chain—lets it interact gently with delicate biological molecules. Because our team oversees every batch step by step, the consistency in purity (frequently above 99%) brings an advantage to researchers trying to reproduce experimental conditions.

    A lot of our clients—whether from academic institutes or industrial labs—come to us frustrated with denatured proteins or dirty solubilization. Rather than strip proteins from their natural states, OG slips in and lets extraction happen without chaos. Membrane proteins, especially, tend to resist working in water-based systems; OG dissolves them in aqueous solution while leaving their functional form mostly intact. Years ago, some labs relied on harsher detergents and lost weeks to troubleshooting. Our product helped shift the laboratory mindset toward mild surfactants, and we feel proud every time a researcher gets clear bands in their gels using our powder.

    Key Specifications and Features from Our Manufacturing Experience

    Working daily in bulk chemical production, we keep a sharp eye on each property that matters. Water solubility ranks high—a trait that keeps OG easy to dissolve at ordinary room temperature. The critical micelle concentration (CMC) for our production lots generally falls in the 20-25 mM range, and we maintain a tight grip on moisture content, because even slight deviations can introduce headaches in precise analytical work.

    OG comes to you as a white, crystalline powder—never gritty or lumpy. We don’t ship any batches with questionable particulate matter, and our customers notice. The molecular weight sits consistently at 292.38 g/mol, and our analysis teams regularly confirm low salt residue and a narrow range of carbohydrate by-products. Every jar, bag, or drum delivers measured moisture, low UV absorptivity at 280 nm, and a well-checked melting point around 71-74°C.

    A newly hired chemist once remarked how odd it felt to receive a surfactant “that already acts like it’s in buffer.” A simple truth sits behind that: as direct producers, we can control drying, storage, and handling far better than traders sourcing from unclear pipelines. No batch leaves a shelf without passing through our analytical instrumentation and an internal cross-check, because once this surfactant leaves our site, our name stands behind the data in your publications and technical reports.

    The Advantages in Biochemistry and Cell Biology

    It’s easy for people to talk about OG just as a protein extraction tool, but years in production have shown us how its impact extends deeper. Take the purification of membrane proteins: biochemists often spend months just trying to coax enough target molecule out of bacterial or mammalian cells. Our OG powders give consistent, mild solubilization that keeps membrane-spanning helices preserved, rather than destroyed by harsh ionic detergents.

    Enzyme assays come out cleaner. Transporter proteins maintain function. Even when scientists step out of mammalian systems into bacterial or plant membranes, the mild nature of OG preserves interactions between proteins and lipids. Other detergents—some cheaper and some with flashier names—either fall short in preservation or introduce interference in downstream analytical methods. We’ve spent countless hours talking to our clients: they need reliable extraction, not wild-card chemistry that makes troubleshooting expensive.

    Distinguishing Ourselves from Other Surfactants in the Market

    Some ask us: Why go through the trouble of producing OG instead of something simpler like SDS, Triton X-100, or CHAPS? We’ve produced and supplied those too, and the practice reveals the crucial differences. SDS tears proteins apart, useful if you want denaturation, but a headache if you want function. Triton X-100, now facing scrutiny because of its aromatic structure and environmental persistence, also brings UV absorption that complicates spectroscopy. CHAPS, another nonionic surfactant, works decently for some eukaryotic proteins, but we see plenty of incompatibility with bacterial expression systems and limited use in large-scale purification.

    Compared to those options, OG sticks out for its broad compatibility and minimal background in analytical reads. The UV cut-off makes it nearly invisible at protein detection wavelengths. As direct manufacturers, we avoid the batch variability that sneaks into the supply chain for other detergents. No surprise oddities or byproduct accumulation—customers keep coming back because reproducibility matters to them, and they notice how much cleaner their gels and chromatography traces become.

    Our Responsibility: Delivering Consistency, Minimizing Contaminants

    As manufacturer, we treat attention to detail as both a science and a duty. Our process avoids contamination with heavy metals, because even small amounts disrupt binding assays and enzyme function. We use dedicated reactors for each production line, and our lab regularly runs trace analysis for lead, cadmium, and mercury. Storage rooms never see fluctuating temperatures or humidity, and we employ GMP-trained personnel whose job focuses on cleanhandling and packaging.

    The difference becomes clear to experienced end users. A research group once reached out after switching from imported, poorly stored OG to our carefully stored domestic product. Not only did their extraction yields rise, the downstream NMR spectra grew sharper—fewer unexpected peaks, cleaner baselines, and less background signal. That feedback guides us: every kilo we ship must be something we’d use in our own R&D, not just a bulk raw material sold and forgotten.

    OG in Pharmaceutical Research and Formulation: Beyond Protein Science

    OG’s story does not stop at research. Drug formulators and vaccine developers need surfactants that neither disrupt delicate structures nor introduce toxic residues. OG’s biocompatibility comes from its strictly nonionic and sugar-based structure. Over time, more pharmaceutical partners have started using OG in mixed micelle and liposome formulations. They report that delivering hydrophobic ingredients (like poorly-soluble drugs, peptides, or adjuvants) becomes much easier when using high-purity OG.

    Some delivery systems depend on OG’s ability to form clear, stable micelles at moderate concentrations. As the manufacturer responsible for each batch, we work side by side with formulation teams to optimize for their particular viscosity, clarity, and safety requirements. Our production lines allow for custom lot sizes—everything from small jars for method development to 20-kg drums for process validation. Drug developers, already facing regulatory scrutiny, trust us to avoid cross-contamination, residual solvents, or byproducts.

    The Real-World Impact in Glycobiology and Diagnostic Technologies

    OG surfaces in more niche disciplines, too. Glycobiologists have used our powders in studies parsing out how sugars stick to proteins or play a role in cell signaling. A major challenge in carbohydrate biology is finding a detergent that won’t mask or modify subtle glycan or lectin binding events. Over years of feedback from the field, we have consistently heard how OG rarely interferes with those sensitive pathways. Assay developers building ELISA, biosensor, or lateral flow tests select OG for its mild background and inert nature.

    Diagnostic firms—especially those developing in-vitro products—care deeply about traceability and supplier reliability. It’s not enough to mail a product specification sheet; they want batch-level records, quick turnaround on technical questions, and access to reference materials. Our years in the business, and experience in building direct relationships with laboratory staff, set us apart. They receive not only high-grade material but a technical team that actually understands the impact of a single extra percentage point of purity, or the role of drying in preventing clumping.

    Environmental and Workplace Safety: Considerations from the Manufacturing Side

    With growing concern worldwide about environmental impact, surfactants face much greater scrutiny. OG, thanks to its sugar-derived head and biodegradability, fits the trend toward greener laboratory consumables. Our own manufacturing audits track waste streams, insulin management, and solvent recycling aggressively. We work alongside environmental consultants to minimize discharge and cut down on energy use in each production batch.

    In parallel, workplace safety officers in research facilities note OG’s low skin irritation profile and low inhalation hazard. Bulk container handling benefits from the crystalline nature of our powder—little dust, little mess, few spills. Training teams at client sites rarely report incidents linked to OG, and our own staff uses the same product for internal pilot work, so we treat the question of worker exposure seriously.

    Challenges in Manufacturing and Future Directions for OG Production

    As raw material costs and customer expectations rise, we face new hurdles. Sourcing pure octanol and glucose without pesticide or synthetic impurity traces has proved challenging. Crop quality, shipping delays, and even global economic shifts can nudge prices in ways that challenge both predictability and fairness to customers. Over time, we have responded by building a network of vetted suppliers and investing in real-time analytics on incoming feedstocks.

    Even chemical production carries its own learning curve: maintaining batch purity at scale, reducing carbon footprint, and hitting ever-trickier analytical benchmarks as detection methods advance. We once prided ourselves on reaching 99% OG—now clients ask for beyond 99.5%, and some for custom lots measured by specific HPLC or mass spectrometry standards. For some, the focus is trace sodium; for others, it's about organic solvent residues. Our facilities adapt, bringing in new columns, using Lyophilization instead of forced air-drying, and maintaining careful documentation for every run. We share these insights not as marketing, but as honest reflections of what it takes to keep pace with high-level laboratories and regulated manufacturers.

    Real Partnerships with Customers: Beyond the Transaction

    After decades in chemical production, we see the difference between selling and helping. Many of our long-term clients call us for troubleshooting, not for bulk pricing alone. We listen to process engineers dial in extraction methods, researchers who’ve lost controls to inconsistent surfactants, and new lab managers looking to pass audits. Real partnership builds around transparency—not hiding process notes, offering open-door batch record checks, and admitting when a run doesn’t meet expectations so remediation starts quickly.

    Our technicians step in to explain pH drift, or why one OG lot clumped a bit under humid conditions while the previous one stayed free-flowing. This feedback loop between producer and user forms the backbone of products that earn trust over years, not just invoices. Each order that goes out reflects not a single production line, but a collective of process engineers, analytical chemists, and quality auditors who see their work in the hands of scientists worldwide.

    Developing the Next Generation of Surfactants: Feedback Informs Innovation

    Innovation follows demand and suggestion. Researchers ask for new functionalized variants—alkyl chains of different lengths, custom labeling for fluorescence, or improved compatibility with mass spectrometry. Pharmaceutical clients need surfactants that clear rapidly from the body and meet intricate toxicology requirements. Our R&D team, informed by years spent on OG itself, looks for routes that avoid excessive solvents, or leverage enzyme catalysis to minimize waste. The current push? Reducing microparticle carryover, and producing mixed surfactant compositions that hit precise CMC or micelle size targets.

    As environmental rules tighten, we collaborate with academic partners on ways to streamline wastewater processing. Some methods are now piloting on our shop floor: in-situ resin scavenging, catalyst recycling, and monitoring glycerol levels in mother liquor. Each improvement finds its way back into our literature, so longtime users can see for themselves how supply chain adjustments or process tweaks affect their finished product.

    A Commitment Backed By Field Experience

    What sets a manufacturer apart at the end of the day? It’s not just purity numbers or cost per kilo, though we never ignore those. From regular conversations with lab scientists and formulation engineers, we know OG stands out for reproducibility, batch-to-batch reliability, and a manufacturing process built to respect the needs of real-world research. By keeping every critical step in-house—from reagent sourcing to post-production quality checks—our company stays nimble and open to direct, decisive feedback.

    Researchers use OG to reveal the shape and function of proteins, assemble diagnostic kits, deliver new medicines, or track how carbohydrates interact in living systems. Our commitment means every bottle arriving at their bench has survived a journey of careful design, chemical rigor, and personal investment. What matters here is more than just selling a commodity chemical—it’s ensuring that every vial, jar, or sack follows a story of knowledge, discipline, and respect for the scientists who rely on our work every day.