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HS Code |
173662 |
| Productname | Luteolin-7-O-Neohesperidoside |
| Casnumber | 51829-36-8 |
| Molecularformula | C27H30O15 |
| Molecularweight | 594.52 g/mol |
| Appearance | Yellow powder |
| Solubility | Soluble in methanol and DMSO |
| Purity | ≥98% (HPLC) |
| Meltingpoint | 230-232°C |
| Storagetemperature | 2-8°C |
| Iupacname | 5,7-dihydroxy-2-(4-hydroxyphenyl)-4H-chromen-4-one 7-O-α-L-rhamnopyranosyl-(1→2)-β-D-glucopyranoside |
As an accredited Luteolin-7-O-Neohesperidoside factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Luteolin-7-O-Neohesperidoside, 25mg, is packaged in a sealed amber glass vial with tamper-evident cap and clear labeling. |
| Shipping | Luteolin-7-O-Neohesperidoside is shipped in tightly sealed, inert containers to prevent moisture and light exposure. The outer packaging ensures protection from physical damage during transit. Standard shipping is via express courier, compliant with regulations for non-hazardous chemicals. Temperature-controlled conditions are available upon request to maintain compound stability. |
| Storage | Luteolin-7-O-Neohesperidoside should be stored in a tightly sealed container, protected from light and moisture, at -20°C. Keep it in a dry, well-ventilated place, away from sources of heat and incompatible substances. Avoid repeated freeze-thaw cycles, and handle under inert atmosphere if possible to maintain stability and prevent degradation. Properly label the storage container for laboratory safety. |
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Purity 98%: Luteolin-7-O-Neohesperidoside with purity 98% is used in pharmaceutical formulation, where it ensures consistent anti-inflammatory activity. Molecular Weight 608.5 g/mol: Luteolin-7-O-Neohesperidoside with molecular weight 608.5 g/mol is used in drug delivery systems, where it supports accurate dosing and therapeutic efficacy. Water Solubility 0.2 mg/mL: Luteolin-7-O-Neohesperidoside with water solubility 0.2 mg/mL is used in oral liquid preparations, where it facilitates improved bioavailability. Melting Point 220°C: Luteolin-7-O-Neohesperidoside with a melting point of 220°C is used in heat-stable nutraceutical products, where it maintains compound integrity during processing. Particle Size D90 < 20 μm: Luteolin-7-O-Neohesperidoside with particle size D90 less than 20 μm is used in topical formulations, where it enhances dermal absorption rates. Stability temperature up to 60°C: Luteolin-7-O-Neohesperidoside with stability temperature up to 60°C is used in long-term storage of functional foods, where it preserves biological activity. HPLC Assay ≥99%: Luteolin-7-O-Neohesperidoside with HPLC assay ≥99% is used in analytical research, where it enables highly accurate quantification. Residual Solvent <0.5%: Luteolin-7-O-Neohesperidoside with residual solvent content below 0.5% is used in sensitive therapeutic applications, where it ensures minimal toxicity risk. UV Absorbance λmax 350 nm: Luteolin-7-O-Neohesperidoside with UV absorbance at λmax 350 nm is used in spectrophotometric assays, where it allows reliable compound detection. Microbial Limit <100 CFU/g: Luteolin-7-O-Neohesperidoside with microbial limit less than 100 CFU/g is used in sterile injectable products, where it ensures microbiological safety compliance. |
Competitive Luteolin-7-O-Neohesperidoside prices that fit your budget—flexible terms and customized quotes for every order.
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Luteolin-7-O-Neohesperidoside stands out in our product lineup not just for its technical merits, but for the path it marks in natural product chemistry. Years on the plant floor and long hours spent scaling up extraction and purification have shown that every step counts—right from raw material selection to final packaging. The molecule itself, with its clear yellow crystalline appearance and high purity (≥98% by HPLC in our standard batches), is a familiar sight around our quality control lab. We know almost every batch by how it runs on the chromatogram and how the crystals form in the drying trays.
Unlike intermediaries or resellers, we deal directly with source botanicals and oversee every link in the production chain. Our supply begins with carefully vetted farms, where harvest times, drying methods, and transport conditions contribute to the profile of each lot. By controlling solvent ratios and keeping equipment calibrated, we protect the integrity of the Luteolin-7-O-Neohesperidoside throughout extraction. Colleagues running the blending tanks and filtration columns know that minor temperature swings or solvent impurities can ruin a day's work, so we take special care to double-check every input.
After years spent refining separation techniques, we’ve seen how batch-to-batch reproducibility hinges on trustworthy protocols, not just expensive instrumentation. The specs matter—whether it’s melting point, water content (by KF titration), or UV-Vis absorbance—but hands-on experience sorting out process hiccups matters more. Most published methods never address the swirl in the mixer or the noise in onsite analytical results during stormy weather. Everyone working in production learns that visible color shifts or scent can hint at subtle changes in phytochemical composition long before chromatography backs it up.
Every researcher and developer ordering Luteolin-7-O-Neohesperidoside expects it to perform to spec, but real-world applications highlight why extra diligence pays off. Pharmaceuticals and nutraceuticals rely on known content to guarantee safety and predictable absorption. Cosmetic formulators demand mildness, color stability, and traceability—characteristics that hinge on both purity and low-microbiological load. Analytical standards must match reference values without drift, or projects stall waiting for do-overs. Over the years, customers told us how off-spec supply derailed whole projects or how a single bad run led to weeks of troubleshooting for an experienced formulator. Those lessons stick.
Unlike mixed flavonoid extracts or semi-purified fractions, Luteolin-7-O-Neohesperidoside requires precise verification of content and identity. The natural product industry faces mounting scrutiny regarding adulteration, so every lot includes full NMR trace and HPLC profile, alongside mass spectrum data for customers who submit regulatory dossiers. We’ve found that attention to trace impurity profiling—often skipped in fast-turnaround operations—prevents most regulatory hiccups and customer complaints. It also ensures bioassays produce clear results, supporting reliable claims for antioxidant performance or anti-inflammatory potential.
Many ask about differences between Luteolin-7-O-Neohesperidoside and similar flavonoids—neohesperidin, rutin, Luteolin-7-O-glucoside, to name a few. In our experience, substitution patterns on the sugar moiety and aglycone make a world of difference for both research and application. Luteolin-7-O-Neohesperidoside features a neohesperidose group at the 7-position, which influences solubility in both aqueous and lipid systems, and helps it stand up to pH extremes better than closely related counterparts. In formulators’ hands, this means greater flexibility for developing stable products.
Few flavonoids offer the same balance of antioxidant activity and low bitterness—a factor playing heavily in food and beverage development. Our QC teams routinely compare bitterness panels of neohesperidin dihydrochalcone and Luteolin-7-O-Neohesperidoside, observing significant palate differences even at low concentrations. Researchers also recognize functional group differences impact not just solubility, but also binding affinity in enzyme inhibition studies or anti-inflammatory targeting. Biological models respond differently to sugar-linked and aglycone forms, so clear analytical specification allows developers to match the right molecule to the right use case.
Delivering consistent Luteolin-7-O-Neohesperidoside requires more than meeting a checklist. Direct relationships with raw material suppliers foster transparency in species identification and handling practices. Bioactive content swings according to harvest year, site elevation, and storage conditions, so we monitor marker compounds from the field. Our in-house teams use controlled atmosphere storage and employ lot segregation. Monthly audits and seasonal forecasting protect supply lines from climate or policy disruptions.
Many labs confront trace pesticide, herbicide, or heavy metal residues in plant extracts. Through regular soil and irrigation water monitoring, we work with growers to avoid contamination. After extraction, advanced SPE and activated carbon treatments reduce environmental contaminants to well below regulatory limits. Each final batch receives multi-residue pesticide screening, pyrogen and endotoxin checks, and microbial load tests. For customers with low endotoxin requirements, special aseptic handling lines supply enhanced grade material.
Working closely with academic research teams, we support projects needing milligram-scale reference standards and bulk quantities alike. Small lots destined for mechanistic studies get custom isolation with extended purity checks and a full analytical package—NMR, FTIR, chiral HPLC, and optical rotation. We help troubleshoot problems researchers face with non-standard solvents or co-formulations. In scale-up runs, our batch reactors, filtration, and evaporators handle orders from grams to several hundred kilograms without sacrificing quality. We routinely redeploy process lines to respond to urgent bulk orders, while keeping separate allergen and GMO handling facilities for customers with sensitive regulatory needs.
Several drug discovery groups turn to us for project-specific modifications—deuterated analogs, isotope-labeled trace markers, or rare conjugates. Rather than running long multi-step syntheses externally, we design workarounds using locally sourced precursors whenever possible. Our proximity to analytical teams means problems get flagged early, and method development can adapt to lot-specific quirks. These collaborations help both sides understand how process nuances evolve outside strict laboratory conditions.
Our packaging team faces constant requests about shelf life and optimal storage. Based on in-house and real-time stability data, we recommend storing Luteolin-7-O-Neohesperidoside at 2–8°C in airtight, light-protective containers. Standard amber glass or aluminum foil pouches work well unless higher humidity presents a risk, in which case desiccants come into play. Some customers running field sites without climate control opt for double-bagged PET and lined drums with nitrogen flush, which wards off both moisture and oxidation.
We draw from thousands of feedback points. Customers using the product in high-throughput screening complained about batch-to-batch variations in solubility, so we adjusted drying protocols and checked particle size distribution post-grinding. Cosmetic producers found old packaging led to trace yellowing; we pivoted to opaque laminate and switched to inert filling. The dialogue continues openly—sometimes we advise against over-engineering controls, when simpler solutions solve real issues faster.
Navigating compliance—be it GMP, ISO, or ICH guidance—demands rigor and documentation. Our in-house team keeps up to date with evolving monographs, pharmacopeial requirements, and new MAAs that reference Luteolin-7-O-Neohesperidoside data. Regulatory teams in pharma and nutrition often ask for expanded impurity profiles or customized documentation. We invest in standardized reference spectra, digital audit trails for every analytical step, and periodic proficiency testing using external controls. These systems cut down on customer submission delays and ensure that data packages meet scrutiny from the toughest regulators.
Keeping up with new detection methods means regularly swapping in updated LC-MS protocols, qNMR, and metabolomic profiling panels. European and North American customers require extra attention to residual solvent and allergen statements, while Asian manufacturers look for alternate documentation with more detail on plant origin. Having an experienced technical support group pays off. They can clarify isomer interferences, discuss matrix effects, and track down root causes of off-odors or visual deviations no matter which part of the QC chain flagged them.
Manufacturing plant-derived products carries a responsibility for stewardship. Harvesting, extraction, and purification generate organic solvent waste, spent biomass, and packaging waste. Drawing on operational audits, we systematically recover and recycle ethanol, limit hazardous reagents, and ship recovered waste to certified disposal partners. Biomass not suited for downstream valorization gets composted or sent for biogas generation. Where local regulations allow, we partner with adjacent industries to upcycle by-products into animal feed or fertilizer.
Employees regularly contribute environmental and safety audit suggestions. We track environmental KPIs—air emissions, water use per kilo, and accident-free days—visible to everyone from the board office to the warehouse floor. Fair wages, transparent contracts, and safe working conditions are not optional; they are the lifeblood of a stable supply operation. When regional weather threatens harvest, we maintain open lines with growers, sharing risk and costs.
Production lines, even running on years of experience and data, still face hiccups. Unusual rainfall can weaken plant material, reducing yield. Equipment breakdowns risk cross-contamination or unplanned downtime. During the global pandemic, logistics slowdowns forced a rethink of raw material warehousing and buffer stock strategy. Instead of relying only on courier updates, site staff began working with local farmers on short, direct supply chains and invested in process redundancies—spare pumps, backup power, and cross-trained crews.
Multiple checks at raw material receiving—identity, potency, contaminants, and even quick on-site TLC plates—catch most issues before they escalate. Open lines with logistics teams and downstream customers prevent surprises on delivery schedules. When specific batches cluster near out-of-spec limits due to atypical weather, we offer early notification and alternatives rather than shipping questionable lots. Sometimes, stepped analytical workups reveal an unexpected new impurity. Collaboration between QC and R&D teams leads to method tweaks, or ultimately, refining and reprocessing, all communicated to end users.
Every person who has labored in manufacturing knows the sense of pride in achieving a clean batch, smooth workflow, and satisfied customer. As end markets for molecules like Luteolin-7-O-Neohesperidoside grow and diversify, we shift from strict compliance to problem-solving partnerships. Process improvements, investment in people, and incremental gains in environmental performance are not bonus initiatives but necessary parts of sustainable supply. Learning from failures, sharing data with partners, and drawing from every complaint or returned drum shapes how we keep tightening our systems.
Real quality comes from corporate memory, daily vigilance, and meaningful engagement on the ground. No product advances in isolation; advances come from dogged attention to detail at every step from seedling to site delivery. Our teams—operators, analysts, lab managers, and warehouse crews—work together to deliver on every promise behind every lot shipped. In the end, producing Luteolin-7-O-Neohesperidoside gives not only a benchmark for purity and potency, but a lens on how real dedication transforms a quality chemical into a trusted tool for science and society.