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Nobiletin

    • Product Name Nobiletin
    • Alias 5,6,7,8,3',4'-Hexamethoxyflavone
    • Einecs 609-663-4
    • 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

    225593

    Chemical Name Nobiletin
    Molecular Formula C21H22O8
    Molecular Weight 402.40 g/mol
    Cas Number 478-01-3
    Appearance Yellow crystalline powder
    Solubility Soluble in DMSO, ethanol, and methanol; insoluble in water
    Melting Point 141-143°C
    Purity ≥98% (HPLC)
    Storage Temperature 2-8°C (refrigerated, protected from light)
    Source Citrus peel (natural flavonoid)
    Synonyms 3′,4′,5,6,7,8-Hexamethoxyflavone
    Iupac Name 2-(3,4-dimethoxyphenyl)-5,6,7,8-tetramethoxychromen-4-one

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

    Packing & Storage
    Packing Nobiletin is packaged in a 1-gram amber glass vial with a secure screw cap, labeled with product details and safety information.
    Shipping Nobiletin is shipped in secure, airtight containers to prevent moisture and light exposure. The packaging usually complies with international regulations for safe transport of chemical substances. Temperature conditions are monitored to ensure product integrity during transit. Proper labeling and documentation, including Safety Data Sheets (SDS), accompany each shipment for regulatory compliance.
    Storage Nobiletin should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. It is typically kept in a tightly sealed container to protect it from moisture and air. For long-term storage, refrigeration at 2–8°C is recommended, and it should be kept away from incompatible substances such as strong oxidizers.
    Application of Nobiletin

    Applications of Nobiletin in Industrial Manufacturing

    Nobiletin, a polymethoxyflavone extracted from citrus peels, features in targeted industrial sectors for its bioactive profile, stability, and functional performance. Below, we detail authentic downstream sectors utilizing nobiletin as a chemical intermediate or functional additive, focusing on precise regulations, integration stages, and main product classes.

    1. Pharmaceutical Ingredient for Cardiovascular Formulations

    Pharmaceutical companies use nobiletin in the formulation of cardiovascular therapy drugs, principally owing to its demonstrated influence on lipid metabolism and anti-inflammatory properties. Manufacturers apply it during the formulation stage, with rigorous adherence to quality and purity to meet regulatory expectations for active pharmaceutical ingredients (APIs). Its integration focuses on controlled dissolution and stability within solid or liquid oral dosage forms. Final pharmaceutical goods often include prescription medicines formulated for dyslipidemia and adjunctive vascular therapies, entering global markets after full compliance verification.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP Monographs (when available), or alternative validated analytical methods
    • Pharmacopeia of the People’s Republic of China (ChP) reference specifications
    • European Pharmacopoeia (Ph. Eur.) testing protocols

    Typical usage ratio

    • Concentration in final formulation: 5 mg–100 mg per dose, depending on product type
    • Adjustments based on pharmacokinetics, solubility, and API load per tablet or capsule
    • Liquid formulations: 0.05%–0.2% w/v
    • Precisely calculated using validated process development studies

    Downstream process integration

    • Enters during API blending with excipients post-standardization and micronization
    • Granulation or direct compression for tablets; suspension blending for liquids
    • Integrated into validated cleanroom filling and packaging
    • Subjected to batch release quality control screens including dissolution and HPLC purity

    Final product types

    • Oral tablets for hypercholesterolemia
    • Soft gel capsules for adjunct cardiovascular support
    • Prescription suspensions with titrated API loads
    • Fixed-dose combination products

    2. Functional Ingredient in Food and Beverage Fortification

    Major food processing entities incorporate nobiletin to engineer functional beverages, dietary supplements, and healthy snacks. Its regulatory status as a bioactive compound in specific regions requires controlled dosing and comprehensive ingredient traceability throughout the batch lifecycle. The addition occurs during premix blending or in the liquid phase for drinks, driven by known stability in acidic and neutral matrices. The focus is on maintaining sensory neutrality and homogeneity, enabling manufacturers to label and market foods enriched with citrus flavonoids for health-oriented consumer segments.

    Industry compliance standards

    • GB 2760-2022 China National Food Safety Standard for Use of Food Additives
    • FDA 21 CFR Part 170 – Food Additive Petitions (for US market, only as authorized)
    • European Food Safety Authority (EFSA) Novel Food Regulation (EU) 2015/2283
    • ISO 22000 Food Safety Management System

    Typical usage ratio

    • Functional beverages: 30–80 mg/L (final product concentration)
    • Powdered blends and bars: 50–200 mg/kg depending on product matrix
    • Dietary supplements: up to 300 mg per daily intake, in line with novel food authorizations
    • Adjusted by regional regulation and sensory acceptability trials

    Downstream process integration

    • Added at the vitamin/mineral premix blending stage for powders
    • Dispensed into aqueous phase pre-homogenization in beverage manufacturing
    • Integrated into bar mixes prior to extrusion and cutting
    • Post-mixing stability checks by HPLC analysis and retention testing after pasteurization/UHT

    Final product types

    • Functional fruit juice beverages
    • Granola and functional snack bars
    • Ready-to-drink supplement shots
    • Nutritional powdered drink mixes

    3. Active Additive in Cosmetic/cosmeceutical Formulations

    Cosmetic manufacturers utilize nobiletin for formulation of topical creams, serums, and anti-aging emulsions. Its action as an antioxidant and brightening agent requires strict attention to purity and stability throughout the batch cycle. The active is solubilized and emulsified during the oil or water phase blending steps. Regulatory obligations include full traceability to ingredient origin and declared function per INCI labeling conventions, particularly for products making skin benefit claims in major markets.

    Industry compliance standards

    • EU Regulation (EC) No 1223/2009 on Cosmetic Products
    • FDA 21 CFR Parts 700-740 for cosmetics labeling and ingredient safety
    • ISO 22716 Good Manufacturing Practices for Cosmetics
    • China National Medical Products Administration (NMPA) cosmetic registration, where required

    Typical usage ratio

    • Cream/serum formulations: 0.05%–0.5% by weight
    • Facial masks: 0.1%–0.3% by weight
    • Variation determined by product stability tests and final intended use (leave-on vs rinse-off)
    • Evaluated for dermal irritation and photostability during development

    Downstream process integration

    • Incorporated in emulsification phase as pure substance or standardized premix
    • Dissolved into water or oil phase via controlled temperature mixing
    • Emulsions passed through vacuum homogenizers to ensure particle size and stability
    • In-process QC includes ingredient identity, concentration, and microbe challenge testing

    Final product types

    • Brightening facial creams
    • Anti-aging serums and ampoules
    • Restorative facial mask sheets
    • Specialty lotions for skin tone balancing

    4. Bioactive Additive in Animal Feed Premixes

    Feed manufacturers integrate nobiletin into animal nutrition premixes, targeting poultry and aquaculture segments for its natural antioxidant activity. Compliance focuses on ingredient identity and residue management under regional feed additive rules, with raw material introduced at the vitamin premix or pelletizing stage. Downstream, its addition supports oxidative stability and product shelf life without exceeding allowed maximums in compounded feeds.

    Industry compliance standards

    • Regulation (EC) No 1831/2003 on additives for use in animal nutrition (where authorized)
    • U.S. Association of American Feed Control Officials (AAFCO) guidelines – novel ingredient registration required
    • China Feed Additive Quality Standards (GB/T 29455, as applicable)
    • GMP+ Feed Safety Assurance Scheme

    Typical usage ratio

    • Complete feeds: 50–150 mg/kg in finished feed product
    • Premix stage: 0.02%–0.05% w/w, tailorable by species and formulated diet
    • Adjusted downward for sensitive life stages in aquaculture
    • Factor in documented bioavailability and absence of adverse tissue residues

    Downstream process integration

    • Added to dry vitamin/mineral blends prior to full-scale batching
    • Dispersed during molasses or fat coating processes in pellet mills
    • Homogenized fully before conditioning and extrusion
    • Each lot subjected to third-party ingredient identity and content verification

    Final product types

    • Poultry growth premixes
    • Aquaculture compound feeds
    • Pet food antioxidant blends
    • Laying hen enrichment feeds

    5. Natural Intermediate in Specialty Chemical Synthesis

    The specialty chemicals sector employs nobiletin as an intermediate for constructing advanced bioactive molecules and enzyme inhibitors, relevant for fine chemical and research industries. Entry to the process typically occurs at the synthesis or derivatization step, monitored for contaminant profile and trace solvents. Documentation must demonstrate batch reproducibility and impurity control, with downstream producers applying purification, crystallization, and analysis steps aligned with chemical industry best practices.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for process documentation
    • REACH (Regulation (EC) No 1907/2006) substance registration, evaluation, authorization
    • GHS (Globally Harmonized System) Safety Data Sheet preparation
    • UN Transport of Dangerous Goods standards for bulk intermediate shipments

    Typical usage ratio

    • Intermediate input: 3%–10% molar ratio depending on target molecule complexity
    • Gram/kg scale for small molecule synthesis projects
    • Batch scale-up parameters based on pilot reaction yield and efficiency
    • Adjusted for desired product purity and carbon efficiency

    Downstream process integration

    • Charged at synthetic reactor loading
    • Subjected to catalytic or enzymatic reaction for downstream derivatization
    • Intermediate isolated via solvent extraction and column purification
    • Batch samples processed through NMR and LC-MS for identity confirmation

    Final product types

    • Reference standard chemicals
    • Pharmacological lead compounds
    • Biochemical probes for research
    • Synthesized enzyme inhibitors
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    Certification & Compliance
    More Introduction

    Nobiletin: A Closer Look From the Manufacturer’s Floor

    What Nobiletin Means for Modern Formulators

    Every batch tells its own story. Manufacturing Nobiletin starts with hand-selecting citrus peels, a process focused on both purity and consistency. We don't just talk about the science—our chemists know what it means to scale up from research to full production, making sure every drum or vial holds the same promise as it did in the lab years ago. For projects ranging from advanced nutritional blends to topical applications in cosmetics, the day-to-day realities in production shape both the quality and character of this flavonoid. Years spent with extraction columns and crystallization tanks have shown us that getting the right compound isn’t about following checklists—it’s about experience, timing, and responding to what you see and measure in real time.

    Form, Function, and Model

    In-house, we prepare Nobiletin in a refined crystalline powder, targeting a purity above 98%. Our standard model, NOB-98, reflects that threshold and gives researchers, food technologists, and product formulation teams a predictable compound for new development. The particle size falls generally into a fine mesh—easy to disperse, thorough in solubility tests, and stable for both short- and long-term storage. The characteristic light-yellow color comes from rigorous purification, not shortcuts. Before it leaves our floor, each lot undergoes HPLC verification for identity and residual solvent checks. Manufacturing these details into the product costs more time and labor, but we’ve learned that a shortcut at this stage means trouble down the road for both us and the next person handling our material.

    Why Specification Details Matter Beyond a Certificate

    Specifications aren’t just numbers for paperwork—they mean each chemist or buyer knows what actually comes in the drum. Purity for Nobiletin isn’t an abstract marketing claim; it is a result of exacting extractions and multiple crystallizations. Our batches regularly show an assay above 98%, often closer to 99%. Moisture control comes after we found early on that even small differences—a percentage point here or there—could cause cake formation during shipping, or release unwanted aromatic notes when opening a container. Not every manufacturer makes those adjustments, but repeated feedback from formulators and process engineers told us exactly what they ran into mixing other brands: clumping, inconsistent dispersibility, or even off-odors from overlooked impurities. Over time, we reworked our drying stage to consistently bring loss-on-drying well below 2%.

    Ash and residual solvent levels are kept extremely low, because every clean synthesis step from our end means fewer headaches down the line for customers concerned about food safety or cosmetic compliance. We routinely run GC, HPLC, and ICP-MS screenings even when it slows our process; those extra hours at our QA bench pay off in clean, fast-moving downstream manufacturing for clients.

    Field-Tested Applications: Not Just Raw Numbers

    Customers tell us the real story once our Nobiletin leaves the plant. Nutritional supplement developers use it as an antioxidant and anti-inflammatory ingredient. In those applications, stability during formulation becomes critical—small impurities or high moisture from cheaper production runs can tank shelf-life or cause color changes during high-temperature blending. Some feedback led us to modify the way we dry and store product at the plant, transitioning from bulk bags to sealed steel-lined drums, especially for large lots headed overseas.

    Cosmetic formulators often come to us after running into trouble with other suppliers. Too much insoluble matter leads to cloudy gels or discolored creams, something even trace contamination can trigger. Our team’s familiarity with fine particulate filtration, a lesson learned after early batches from other lines failed suspension tests, has shaped how we filter and dry every new lot.

    In animal health and advanced research, Nobiletin proves valuable as a tool compound for signaling pathway investigations or metabolic studies. Researchers in those fields need strict confirmation of isomeric purity and trace contaminants—one extra cooling or evaporation stage at our site keeps those factors optimal. Without these controls, final readouts in a lab could shift—a risk the scientific teams depend on us to help eliminate.

    Some manufacturers accept lower yields in pursuit of price; our approach puts more labor on the team but keeps the value in the drum, not in the waste bin. We have learned that these decisions ripple through the entire supply chain: less rework, more trust, fewer late-night phone calls about failed trials. Lab techs and scale-up managers want to move quickly; our job is to prevent their headaches, not create new ones.

    Comparing Nobiletin With Other Citrus Flavonoids

    On paper, a number of citrus-derived flavonoids look similar. Naringenin, hesperidin, tangeretin, and sinensetin often appear in the same reference texts or research abstracts. But in practice, structural differences bring out distinct solubility, stability, and bioactivity. Nobiletin’s methoxyl groups change its polarity and make it more fat-soluble than many counterparts; hands-on, we also see bigger challenges in initial extraction and later purification.

    A less experienced facility might struggle separating Nobiletin from similar flavones, ending up with a mix that passes a rough TLC screen but fails in either taste or in downstream performance. Years ago, a batch we received from an outside source—run as a process comparison—fell far below our standards. Tailings showed tangeretin presence, clouding up in organic solvents and creating residuals in food simulants. Since then, we have refined our proprietary methods to consistently achieve mono-component purity. Our protocols target Nobiletin as a clear single peak on HPLC, with other methylated flavonoids below 0.5%—a margin many others treat as ‘trace acceptable.’

    Those differences play out across industries. In dietary supplement production, customers trying to promote cognitive support or cardiovascular benefits expect data and strong, credible sourcing. Nobiletin’s unique structure has been investigated for neuroprotective, anti-inflammatory, and lipid-modulating effects. Supplement brands trust our material when performance data relies on chemical uniformity, not just plant source. On the bench, repeatable animal study results back up our efforts.

    Compared with hesperidin, often touted for its own cardiovascular benefits, Nobiletin offers greater lipophilicity, changing absorption rates and compound activity. Cosmetic chemists working with us often note less oxidative discoloration from our processed Nobiletin than from cheaper flavonoids prepared with fewer refining steps. That means less risk of product returns from shelf-storage failures or end-user complaints.

    Production Barriers and Hands-on Solutions

    Manufacturing plant-derived compounds means adapting to the realities of nature. Weather, soil, and variety all shape the chemical profile of the starting material in each citrus peel shipment. Over the years, we have built partnerships directly with citrus growers, selecting for breed and agricultural practice instead of sheer price-per-kilogram. Harvest timing and post-harvest handling also impact the proportions of nobiletin and related flavones. Early efforts at batch-to-batch consistency forced us to develop our own assessment protocols—UV-Vis and LC-MS screens at intake, not at the tail end.

    Extraction presents its own set of daily challenges. Citrus peels harbor oils, waxes, pigments, and other phenolics. We developed multi-stage solvent extraction techniques, including pH adjustment and pressure filtration, to avoid dragging along unwanted side-components. On tough days, the plant team puts in extra shifts to tweak extraction parameters after real-time HPLC checks reveal drift in yield or co-extracted impurities.

    Scaling up from pilot to full plant calls for more than just bigger tanks. At every stage, environmental controls make a difference—humidity control prevents the sticky clumping that once halted production for hours at a time. Temperature stability in crystallization helps maintain color, and prevents the slight caramelization that plagued earlier, lower-budget operations.

    Waste management cannot stay an afterthought. Our facility captures and neutralizes spent solvents, recycling much of the ethanol used and treating waste solutions to keep downstream discharge clean. Cleaner production doesn’t just check a regulatory box—it reduces costs and improves community relations in our manufacturing region. Years of investment in these upgrades have returned value both in terms of customer safety profiles and internal trust among the staff handling solvents each day.

    Quality Practices That Go Beyond the Label

    Delivering on promised specifications depends on more than laboratory numbers; hands-on product testing at every stage comes standard. In-process samples head straight from the drying house to QA benches for multiple verifications. Staff use multi-wavelength UV-Vis, GC analysis for trace contaminants, and repeated moisture readings on each lot. Routine staff training on batch documentation prevents errors in labeling and storage, which reduces the risk of misshipment or downstream complaints.

    Some lessons come the hard way. We learned early that even the strongest certificate claims mean little without visible, repeatable results in real-world applications. Industry feedback from contract manufacturers running our Nobiletin in tableting or encapsulation processes has guided minor but vital improvements: tweaks in grind size, changes in drum liners, modifications to outer packaging based on field reports from hot, humid ports. Since then, returns and complaints have dropped to near zero.

    Our technical support remains a direct line to the production floor, not a distant call center. When researchers or process managers contact us about a perceived issue, a member of our lab or QA team can troubleshoot in real time, often replicating the process and offering workable tweaks or confirming performance. This partnership-based approach reflects hard-earned trust on both sides of the shipping dock.

    Growing Demand and Global Logistics

    Markets for Nobiletin have expanded, drawing interest from functional food companies in North America, supplement manufacturers in Europe, and cosmetic developers in East Asia. This growth presents challenges for scaling production without sacrificing quality. Experience shows that not all logistic partners handle delicate goods the same way. We reinforce shipments with moisture barriers and temperature-controlled pallets, a small investment compared to the cost of a single damaged lot after trans-oceanic shipping.

    Supply chain disruptions, from adverse weather in citrus-growing regions to shipping hold-ups, can threaten both continuity and consistency. Years spent walking the fields with growers have paid off in upright relationships; early warnings and diversified sourcing keep production moving. For our own operation, doubling up on inventory for critical compounds proved prudent as global events reminded everyone of transportation limits.

    Regulatory hurdles continue to shift as new regions apply different limits on solvent residues, microbial content, or trace allergens. We track updates with our own regulatory expert, and adjust processes to fit without waiting for non-compliance notices. These moves protect customers working under FDA, EFSA, or NMPA rules, giving them fewer regulatory headaches at their end.

    Responsible Manufacturing: Environmental and Ethical Commitments

    Every process that extracts bioactives from agricultural inputs comes with responsibility. Waste water, spent solvents, and vegetable residues can burden local ecosystems. Years of investment in solvent recovery, emission controls, and clean energy sourcing reflect a commitment to environmental safety—and a practical business sense. Reducing solvent use and improving recovery not only reduce our overhead, they make long-term operation possible in increasingly regulated jurisdictions.

    We source peels only from growers with sustainable crop practices, which helps both traceability and community relations. Our teams regularly audit supplier fields for pesticide control and labor standards, because our own standards don’t stop at the factory gate. A reliable product starts with reliable partners—whether that means working with independent farmers or co-ops in citrus-rich provinces.

    We design our manufacturing schedule around the harvest cycle, minimizing waste and encouraging multiple uses for by-products—from animal feed to bioenergy conversion. These choices reflect years of learning what makes not only a better Nobiletin, but a better outcome for our workers, the local community, and buyers.

    Meeting Market Demands With Practical Experience

    Buyers and researchers can count on more than a technical description. Every process, from extraction through to shipment, draws on decades of incremental improvement. The nuances learned from working directly with extraction technicians, research chemists, and corporate customers shape both our short-term and long-term production plans. Our Nobiletin stands out because it brings together hands-on production skill, investment in quality tools, and feedback-driven evolution.

    Developers of functional supplements and advanced cosmeceuticals demand transparency. To help them move through both formulation and regulatory approval, we support batch-specific documentation, hands-on technical guidance, and practical recommendations based on years of experience. An open feedback loop turns field complaints into process improvements; every suggestion shapes future production runs.

    As interest in Nobiletin grows across the health, cosmetic, and research sectors, product purity, batch consistency, and secure logistics will continue to drive decision making. Working from direct manufacturing experience, we hold our production team to measurable, visible standards—and share those lessons with every partner looking to harness the potential of this unique citrus-derived compound.