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10-Hydroxy-2-Decenoic Acid

    • Product Name 10-Hydroxy-2-Decenoic Acid
    • Alias Queen Bee Acid
    • Einecs 242-893-1
    • 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

    795611

    Cas Number 565-80-0
    Molecular Formula C10H18O3
    Molecular Weight 186.25 g/mol
    Appearance White to pale yellow powder
    Melting Point 75-79°C
    Solubility In Water Slightly soluble
    Purity >98% (typically)
    Odor Mild, characteristic
    Ph Value Neutral (in aqueous solution)
    Storage Temperature 2-8°C (refrigerated)
    Synonyms Queen bee acid, 10-HDA
    Stability Stable under recommended conditions
    Origin Royal jelly (naturally occurring)

    As an accredited 10-Hydroxy-2-Decenoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 10-Hydroxy-2-Decenoic Acid is packaged in a 10g amber glass bottle, tightly sealed with a tamper-evident screw cap.
    Shipping 10-Hydroxy-2-Decenoic Acid is shipped in tightly sealed, chemically resistant containers, protected from light and moisture. The shipment complies with relevant chemical transport regulations, including appropriate labeling and documentation. Depending on the quantity and destination, it may be shipped as a non-hazardous or regulated material by ground or air under controlled temperature conditions.
    Storage 10-Hydroxy-2-Decenoic Acid should be stored in a tightly sealed container, protected from light and moisture, and kept at a temperature of 2–8 °C (refrigerated). Store in a well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and use containment to prevent contamination. Follow standard laboratory safety and storage protocols for chemicals.
    Application of 10-Hydroxy-2-Decenoic Acid

    Applications of 10-Hydroxy-2-Decenoic Acid in Industrial Manufacturing

    As a direct manufacturer of 10-Hydroxy-2-Decenoic Acid, we deliver consistent quality and traceable origin for downstream industrial partners. Please find below the application scenarios documented with regulatory alignment, specification in formulas, typical processing steps in actual manufacturing, and real-world product endpoints.

    1. Nutraceutical Formulations (Royal Jelly Derivatives)

    Dietary supplement producers utilize this compound due to its origin as the distinguishing fatty acid marker of royal jelly. Established nutritional brands incorporate it into capsule and softgel dosage forms to legitimize royal jelly content per international labeling standards, and to authenticate source material for regulatory audits. Formulators balance the inclusion level with reference assays and product positioning, taking into account regulatory status in each target market. Consistency in purity and identity testing (HPLC/GC) is required batch-to-batch for validated claims and compliance.

    Industry compliance standards

    • EU Regulation (EC) No 1924/2006 for nutrition and health claims
    • US FDA Dietary Supplement Health and Education Act (DSHEA)
    • Japanese Food Sanitation Act, Notification No. 370
    • ISO 22000:2018 food safety management

    Typical usage ratio

    • 0.6%–1.7% of total capsule fill; adjustments reflect desired royal jelly activity and regional label requirements

    Downstream process integration

    • Blending in powder form with excipients during dry-mix granulation or direct fill, prior to encapsulation or compression

    Final product types

    • Oral capsules labeled as royal jelly extract
    • Softgels for health food
    • Powder sachets for direct oral consumption

    2. High Purity Cosmetics (Anti-Aging and Skin Repair Creams)

    Leading cosmetic manufacturers include this fatty acid as a bioactive ingredient in high-end rejuvenation products, leveraging its documented effects in peer-reviewed dermatology research. Cosmetic chemists rely on validated purity and stability during emulsification and homogenization processes to ensure shelf life and brand integrity. The material typically enters cream or serum bases under controlled temperature and pH to avoid decomposition or adverse interaction with peptides or botanical extracts.

    Industry compliance standards

    • EU Cosmetics Regulation (EC) No 1223/2009
    • US FDA 21 CFR Part 700–740 for cosmetic products
    • China GB 7916 Cosmetic Safety Technical Standard
    • ISO 22716:2007 GMP for cosmetics

    Typical usage ratio

    • 0.05%–0.4% of formulation weight depending on intended bioactivity and product type

    Downstream process integration

    • Dose addition during cool-down phase of emulsion manufacture, post-emulsification, to maintain integrity; follows full dissolution in appropriate solvents if necessary

    Final product types

    • Dermal repair creams
    • Anti-wrinkle serums
    • Regenerating facial masks

    3. Functional Beverage Additives (Nutrient-Fortified Drinks)

    Producers in the functional beverage sector add this acid into ready-to-drink health beverages as a marker of genuine royal jelly supplementation, commonly for the Asia-Pacific export market. Dosage is tightly controlled under local food additive guidelines, requiring complete solubilization and filtration to avoid sedimentation. Manufacturers closely monitor pH and temperature during blending to minimize loss or alteration of chemical structure before sterile bottling.

    Industry compliance standards

    • China GB 2760 Hygienic Standards for Food Additives
    • Codex Alimentarius Commission standards
    • Japan Ministry of Health, Labour and Welfare Food Additive List
    • FSSC 22000 for beverage industry

    Typical usage ratio

    • 0.01%–0.08% volume per finished drink, calculated based on targeted labeling for royal jelly equivalent content

    Downstream process integration

    • Dispersion into aqueous or isotonic solutions during main batch mixing, immediately before sterilization and bottling

    Final product types

    • Energy and wellness shots containing royal jelly
    • Supplemental honey and herbal fusion drinks
    • Oral liquid vials for tonic applications

    4. Veterinary Feed Supplements (Livestock Fortification)

    Animal nutrition companies use this bioactive to fortify specialty feeds for queen bees, horses, and companion animals, based on scientific studies linking it to improved reproductive and stress resilience metrics. The material must comply with animal feed ingredient listings and support traceability in farm-to-fork quality programs. Feed formulators add the acid at levels that respect species-specific regulatory caps and guarantee homogeneity in premix production, ensuring batch uniformity and efficacy in final feeds.

    Industry compliance standards

    • EU Animal Feed Regulation (EC) No 767/2009
    • AAFCO Ingredient Definitions (US)
    • China GB/T 13078 Quality Standard for Feed Additives
    • GMP+ B2 for feed ingredient safety

    Typical usage ratio

    • 25–120 mg/kg feed weight, adjusted by target species and animal lifecycle stage, always below the regulated daily intake threshold

    Downstream process integration

    • Blending into vitamin-mineral premixes during micronutrient inclusion phase or as a post-extrusion spray on specialty feeds

    Final product types

    • Bee queen rearing feeds
    • Performance horse nutritional supplements
    • Companion animal functional treats

    5. Pharmaceutical Actives (Investigational Dermatology Formulations)

    Contract development and manufacturing organizations (CDMOs) operating within dermatology research manufacture topical formulations incorporating this fatty acid for use in clinical trials targeting inflammatory skin conditions, including atopic dermatitis and delayed wound healing. The raw material must meet ICH Q7 GMP requirements, and every lot passes full analytical testing for residual solvents, heavy metals, and microbial limits. Integration occurs at pilot batch scale first, validated prior to investigational use in Phase I/II studies.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for active pharmaceutical ingredients
    • US Pharmacopeia (USP) <797> for sterile compounding
    • EMA Guideline on Quality of Investigational Medicinal Products
    • Japanese Pharmacopoeia for investigational products

    Typical usage ratio

    • 0.05%–0.3% by weight, protocol-driven and adjusted according to phase-specific clinical trial protocols

    Downstream process integration

    • Solubilization as an active in semi-solid ointment or gel vehicles during compounding; preceding sterile filtration if applicable

    Final product types

    • Topical investigational medicinal products for clinical trials
    • Dermatological gels used under physician supervision
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    Certification & Compliance
    More Introduction

    10-Hydroxy-2-Decenoic Acid: A Manufacturer's Perspective

    Navigating the World of Specialty Fatty Acids

    Experience in direct production has given us a close look at the differences among fatty acids. 10-Hydroxy-2-Decenoic Acid—often referred to as 10-HDA—stands out in our portfolio, not just in composition but also in the specialized role it plays in both formulation and research applications. This compound remains best known as the principal fatty acid found in royal jelly, but its use has moved beyond that natural source and into controlled, scalable industrial processes.

    Our involvement starts long before discussion of market trends or specification sheets. Routine begins in the facility itself—working with batches, checking the clarity of crystallization, and ensuring the purity holds to what research applications demand. Mistakes at this stage echo down the line. 10-HDA demands vigilant temperature and atmosphere control, as any slip can destabilize the molecule and change sample outcomes. Direct manufacturing, in this case, means watching every phase, not only for safety but consistency across lots. Consistency proves to be a major challenge when producing specialty acids, especially one as sensitive as 10-HDA.

    Model and Specifications: What Matters in Reality

    Our standard product comes as a white to off-white crystalline powder with a minimum purity of 98% by HPLC assay. Over the past decade, acid value and melting range have become the most significant markers for clients in the pharma and cosmetic fields. Acid value typically falls between 270 and 310 mg KOH/g, while the melting point stabilizes near 74°C. Water content is kept below 1.0%, and heavy metal limits sit beneath 10 ppm, reflecting the practical challenges in purifying an unsaturated acid without harsh treatments.

    From a chemical structure standpoint, the hydroxyl at the 10th carbon introduces a reactive site that brings out extra solubility in polar solvents and regulates its biological interactions. What sounds like a textbook difference impacts downstream formulation. For example, the hydroxyl group creates extra handles for esterification or custom conjugation, suiting specialized product development. End users in R&D or product development notice subtle but crucial differences in how quickly 10-HDA integrates compared to saturated or straight-chain decenoic acids.

    No Substitute for Direct Production Experience

    Long before high-throughput purification techniques, isolating 10-HDA proved hit-or-miss when using enzymatic or classical extraction from bee products. The instability of unsaturated acids meant rapid oxidation. Quality swings were common. As direct manufacturers, we initiated a shift towards fermentation or total synthesis routes. These controlled processes now form the backbone of our 10-HDA line. They allow tighter control over impurities—such as geometric isomers or saturated homologs—which rarely show up for end customers purchasing only from resellers, as those teams lack process control over upstream variables like oxygen migration or temperature spikes.

    Comparing our 10-HDA to commonly available fatty acids unearths substantial differences in actual use. Saturated decenoic acids, such as decanoic acid or capric acid, offer basic hydrophobicity and act as emollients or excipients. By contrast, 10-HDA supports bioactivity research, owing to the hydroxyl and the position-specific double bond. These structural tweaks do not only change melting profiles or solubility; they pivot the molecule from a base ingredient to a tool for new product research. The side-chain hydroxyl sharpens functional group diversity, which customers in the pharmaceutical, cosmetic, and even nutraceutical fields appreciate.

    Practical Uses: Insights from Real Production and Application

    Our clients apply 10-HDA largely in three sectors: biomedical research, cosmetics, and nutraceuticals. Each of these fields places unique demands on the product. For biomedical investigators studying lipid signaling, trace metal impurities or odd-chain byproducts can skew the entire experiment. As a producer, we learned early on that any inconsistency in ferrous or copper contamination inside process equipment left stubborn background signals in cell assays and mass spectrometry. Avoiding these pitfalls took active monitoring with ICP-MS and optimized equipment to reduce unintended catalytic action. These lessons did not come from literature; they arrived after getting back chromatograms that looked nothing like expected, despite passing basic purity measures.

    For customers formulating skincare products, physical texture and solubility pose their main concerns. This acid, with its unsaturated nature, combines softness with a crisp melting point—delivering a distinctive sensory feeling compared to traditional fatty acids like stearic acid. In creams or serums, the hydroxyl group encourages better emulsification. Over time, we noticed that when our product contained even a trace more water, emulsion stability dropped. It is a small operational detail, but it divides mediocre creams from those that glide onto skin.

    Nutraceutical firms have always chased higher bioactive content in their formulations, looking especially for natural origin claims. The challenge emerges because natural-sourced royal jelly cannot meet the scaling or purity expectations needed for mass-market stable capsules. This drove a broader movement towards fermentation or synthetic approaches—whereby the main objective has become reliably producing food-grade, tested, and standardized powder. Our repeated efforts at keeping pesticide or bee-derived allergens below quantifiable limits paid off in client order retention and reputation management, which is impossible to safeguard through mere distribution.

    Why 10-HDA Outshines Common Fatty Acids in Sensitive Applications

    Many new users arrive with the misconception that 10-HDA acts similarly to other medium-chain fatty acids in all settings. The lived reality inside a formulation lab tells another story. The double bond at carbon 2 and the terminal hydroxyl grant this molecule rapid reactivity in biochemical settings. In anti-inflammatory studies, it behaves in ways that plain decanoic acid cannot: triggering specific gene expression or modulating enzyme targets. This fact draws continuous research interest from universities and startups alike, with peer-reviewed studies validating its cellular impact.

    Cosmetic chemists moved to 10-HDA after finding that conventional fatty acids lacked the same feel or oxidizing resistance when blended with actives. The key learning from our consistent feedback loop is that minor process shifts—be it storage humidity or recrystallization solvent—leave fingerprints in viscosity, melting behavior, and shelf life. These nuances become important for durable, high-performing applications like facial serums or encapsulated oil blends.

    Troubleshooting Quality and Purity: The Real Day-to-Day

    Crafting a product as delicate as 10-HDA invites continual re-examination of process standards. For us, keeping up with evolving analytics is not a set-and-forget operation. Customers expect batch-to-batch reliability; drift in purity translates into practical headaches—poor solubility, slow reactions, false positives in analytics. We set up redundant quality checks at each phase, including HPLC, GC-MS, and NMR runs, as a way of staying ahead of unwanted isomer formation or cross-contamination. Direct feedback from formulation failures inspired incremental improvements to storage, handling, and packaging systems. The cost of every returned batch or unexpected performance issue outweighed any marginal expense on analytics.

    The issue of heavy metals crops up too often with suppliers lacking internal process control. 10-HDA behaves as a mild chelator at times, making it susceptible to picking up trace contaminants from plant piping, glassware, or even atmospheric deposition during drying. We run below 10 ppm for lead, cadmium, and arsenic, using regular independent verification. Not all third parties hold this line, as we've seen in customer complaints about off-coloration or poor melting profiles in comparative samples. This aspect, often invisible to end-users, comes sharply into focus the moment an assay shows unexplained toxicity or a color shift in final formulations.

    Learning from Customer Needs and Industry Trends

    We have watched the profile of 10-HDA change as awareness grows around the world. Originally, buyers wanted only small lots for lab-scale research. With advances in topical delivery, demand shifted to cosmetic firms seeking clinical benefits. Food and supplement manufacturers have since joined, requiring strict documentation and audited traceability. For these buyers, non-GMO production, allergen statements, and supplier audit trail carry as much weight as the product itself. We invested in data tracking, lot documentation, and digital batch records as part of this transition. These protocols did not appear to us from a regulatory standpoint alone; they resulted from live audits, site visits, and customer-driven requests for ever-greater assurance of safety and provenance.

    Working directly in synthesis rather than distribution gives a different outlook on traceability. Customers often ask for full transparency—not only for purity, but also for environmental impact. Major downstream users want to know how solvents are recovered, whether waste is minimized, and what steps reduce energy use. We found solutions through reusing process water, recovering solvents, and carefully choosing between batch versus continuous process setups. This kind of practical stewardship extends beyond compliance; it answers real user expectations about how sustainable chemistry can be practiced, even for specialty products like 10-HDA.

    Addressing Process Limitations and Future Improvements

    No process is perfect, and even with tight control, bottlenecks show up in scale-up. For our formulation runs above 100 kilograms, crystallization time increases, and solvent recovery balances shift. Instead of doubling reactor size, we use parallel runs and staggered purification trains to keep output consistent. These adjustments, suggested by frontline technicians rather than distant consultants, have kept us on schedule with large inventory turnover demands.

    Stability remains a weak point common to unsaturated acids. Bulk storage brings challenges—especially with long-term exposure to light or oxygen. To limit peroxide and byproduct formation, we use minimal headspace packaging, vacuum purging, and inert gas shielding. Routine checks flag batches with even slight odor or appearance deviations, preventing off-quality shipments. From experience, customers rarely forgive visual changes, even if purity reads above specification.

    Raw materials sourcing represents another hurdle, especially for sustainable input streams. Many intermediates required for effective 10-HDA synthesis share origins with agricultural byproducts. Fluctuations in global supply—be it from droughts, export disruptions, or regulatory shifts—make long-range planning more involved. Access to stable feedstocks, verified for absence of pesticide residues and allergens, leads to closer relationships with vetted upstream producers. Over time, this approach outperforms generic buying and ensures cleaner raw input, which translates to measurable improvements in finished 10-HDA.

    Why Buyers Rely on Manufacturer-Direct Sourcing

    Having spent years fielding performance feedback, we understand why most downstream innovators prefer sourcing 10-HDA directly from us. Every intermediate, every finished batch, tells a story of its production environment—who handled it, what environmental controls were in place, which variables shifted during crystallization, and how it was packed. Reseller samples cannot answer these questions with the same authority or guarantee re-order consistency. Buyers in pharmaceuticals and advanced cosmetics want reliable partners who can offer immediate technical troubleshooting, provide custom batch documentation, and tailor the product to fast-evolving protocols.

    We also make a priority of sharing technical updates. When the latest assay methods or regulatory reviews suggest tighter controls or new impurity thresholds, our on-site teams adapt the protocol and communicate the change. No outside distributor maintains this hands-on approach. Real improvements—easy open packaging, simplified batch certificates, rapid sampling—emerged directly from conversations with formulation chemists and QC leads, often far from the sales floor.

    There is a tangible difference between distributor relabeling and direct manufacturer engagement. We see proof in returns: fewer rejected lots, quicker fulfillment, and more repeat business when clients trust us to innovate alongside them. That’s earned through transparency and the real willingness to solve practical problems in real time.

    Looking Forward: Real-World Potential and New Insights

    Years of continuous production taught us that delivering outstanding 10-HDA isn’t only about chemistry. The molecule inspires curiosity and pushes research into new directions, from novel cell health interventions to unique topical skincare. Each time a customer uncovers a new use case, we tune into their application. Knowledge travels both directions. We learn just as much from packaging teams who want a better shelf-life profile as from medical researchers probing new biological pathways.

    As 10-HDA adoption grows around the globe, we remain focused on the fine points—be that eliminating trace residuals, improving handling protocols, or searching for lower-impact synthetic methodologies. By listening to those working hands-on in labs and factories, and sharing what’s proven to work, we ensure every kilogram released meets the real expectations of today’s demanding projects.

    Working as a direct manufacturer of 10-Hydroxy-2-Decenoic Acid means holding our process and product to a standard defined by the real-world needs of research, formulation, and end use. Every improvement, every quality run, and every satisfied project represents not just chemistry done right, but chemistry done with care for those driving innovation forward.