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Cholesteryl Oleate

    • Product Name Cholesteryl Oleate
    • Alias Cholesteryl oleyl ether
    • Einecs 212-191-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    619727

    Chemical Name Cholesteryl Oleate
    Molecular Formula C45H78O2
    Cas Number 360-68-9
    Appearance White to pale yellow powder or crystals
    Melting Point 44-45°C
    Solubility Insoluble in water; soluble in organic solvents such as chloroform and ether
    Density 0.95 g/cm³
    Purity Typically ≥98%
    Storage Condition Store at 2-8°C, protect from light and moisture
    Synonyms Cholest-5-en-3-yl (Z)-octadec-9-enoate
    Usage Used in biochemical research and lipid studies
    Origin Ester formed from cholesterol and oleic acid
    Ec Number 206-992-5

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

    Packing & Storage
    Packing Cholesteryl Oleate is supplied in a 5g amber glass vial, tightly sealed, with a tamper-evident cap and clear labeling.
    Shipping Cholesteryl Oleate is typically shipped in tightly sealed containers to prevent contamination and degradation. It should be stored and transported at cool temperatures, away from light and moisture. The packaging must comply with chemical safety regulations, using cushioning to prevent breakage and clear labeling for safe handling during transit.
    Storage Cholesteryl oleate should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry place—typically at 2–8°C (refrigerated conditions). Avoid exposure to air and elevated temperatures, as these can cause degradation. Ensure that the storage area is well-ventilated and that the chemical is kept away from incompatible substances and sources of ignition.
    Application of Cholesteryl Oleate

    Applications of Cholesteryl Oleate in Industrial Manufacturing

    As a specialized manufacturer of cholesteryl oleate, we supply this ester for industries requiring high purity and consistent physical properties. Below we detail established, regulated downstream application areas based on verified industrial demand and technical integration.

    1. Liquid Crystal Displays and Thermotropic Liquid Crystal Materials

    Downstream display manufacturers incorporate cholesteryl oleate in custom cholesteric liquid crystal mixtures to achieve specific color reflection and polarization characteristics. It provides precise control over helical pitch, supports tunable temperature response, and enables stable phase transitions required for temperature indicators, privacy screens, and modern display devices. Integration depends on the physical stability and phase transition temperature, demanding close attention during blend formulation and melt mixing.

    Industry compliance standards

    • RoHS Directive (EU 2015/863)
    • REACH Regulation (EC 1907/2006)
    • EN IEC 61010-1 for materials used in electrical equipment
    • IEC 60950-1 for ICT equipment safety

    Typical usage ratio

    • 10%–40% by weight in the cholesteric liquid crystal blend; precise percentage determined by target helical pitch, operational temperature range, required color reflection, and viscosity needs

    Downstream process integration

    • Direct addition into custom liquid crystal matrix during initial melt blending under inert atmosphere
    • Combined with nematic hosts and co-cholesteryl esters before downstream liquid crystal cell filling
    • Continual QC monitoring for isotropic-cholesteric transition temperature alignment

    Final product types

    • Thermochromic temperature labels and strips
    • Privacy filter films
    • Color-changing film for medical and laboratory applications
    • Specialized digital display panels

    2. Cosmetic Formulation for Lipid-Based Emulsions

    Cosmetic manufacturers use cholesteryl oleate as an active lipid structure modifier in high-value skincare and personal care emulsions. Its molecular structure mimics components of the skin’s natural barrier, making it ideal for barrier creams, moisturizing formulations, and anti-aging products. Formulators blend it into lipid phase systems for enhanced skin feel and occlusive properties, ensuring compliance with ingredient listings for personal care products in regulated markets.

    Industry compliance standards

    • EU Cosmetic Regulation EC 1223/2009
    • United States FDA 21 CFR 700 Subpart B (Cosmetics)
    • ASEAN Cosmetic Directive (ACD)
    • ISO 22716 Cosmetic GMP

    Typical usage ratio

    • 0.2%–2.0% by weight in final formulation; formulation chemists adjust according to skin feel, emulsion stability, and regulatory limits on sterol derivatives

    Downstream process integration

    • Melting into oil phase during manufacturing of water-in-oil (W/O) or oil-in-water (O/W) emulsions
    • Incorporation prior to homogenization and cooling
    • QC verification for physical stability and microstructure

    Final product types

    • Premium moisturizing creams and lotions
    • Barrier repair balms
    • Facial anti-aging treatments
    • Dermocosmetic products for sensitive skin

    3. Pharmaceutical Delivery Systems and Lipid Nanoparticles

    Drug delivery formulation specialists utilize cholesteryl oleate to construct stable lipid nanoparticle systems such as solid lipid nanoparticles (SLN) and nanostructured lipid carriers (NLCs). Its inclusion offers control over particle structure, drug encapsulation efficiency, and controlled release behavior. Manufacturers must optimize loading ratios relative to active pharmaceutical ingredient (API), surfactant levels, and matrix stabilizers, with strict adherence to pharmacopoeial standards for excipients used in injectables and topical drug delivery systems.

    Industry compliance standards

    • US Pharmacopeia (USP) / National Formulary (NF) standards
    • European Pharmacopoeia (Ph. Eur.) monographs
    • Good Manufacturing Practice (GMP) under ICH Q7
    • 21 CFR Part 210/211 for finished pharmaceuticals

    Typical usage ratio

    • 5%–20% by weight of total lipid matrix for SLN/NLC systems; loading customized per drug compatibility, target release profile, and particle size distribution

    Downstream process integration

    • Solubilization in lipid melt during nanoparticle pre-emulsion step
    • Emulsification with surfactants and co-lipids under high shear
    • Rapid dispersion and solidification during cooling; followed by filtration and sterile processing

    Final product types

    • Nano-encapsulated injectable drug formulations
    • Topical dermatological treatments
    • Ophthalmic lipid nanoparticles
    • Oral drug delivery microcapsules

    4. Analytical Standards and Biochemistry Research Reagents

    Diagnostic reagent and reference material producers employ cholesteryl oleate as a lipid control analyte in clinical chemistry and biochemical research kits. Its defined chemical structure supports calibration and validation of enzymatic or chromatographic assays measuring cholesterol esters, and plays a key role in in vitro standardization studies. Raw material integrity and traceability must be documented according to global laboratory practice standards.

    Industry compliance standards

    • ISO 17034:2016 (General requirements for reference material producers)
    • ISO/IEC 17025 (Laboratory competence)
    • US CLIA (Clinical Laboratory Improvement Amendments)
    • GLP (Good Laboratory Practice) standards

    Typical usage ratio

    • Defined by calibration protocol; often 0.01–0.2 mmol/L in final reference matrix for enzymatic cholesterol assay controls

    Downstream process integration

    • Dissolution into organic phase for preparation of lyophilized or liquid control materials
    • Dispersion in serum simulants before analytical kit filling
    • Fine adjustment of content for traceable, lot-specific documentation

    Final product types

    • Reference control solutions for cholesterol ester analysis
    • Calibrators and standards for enzymatic test kits
    • Biochemical assay reagents
    • Research-use-only (RUO) controls

    5. Nutritional Lipid Ingredient in Infant Formula Research

    Research-driven infant nutrition product developers integrate cholesteryl oleate in pilot studies to simulate the sterol ester fraction found in human milk fat. This approach allows detailed assessment of absorption, bioavailability, and structural influence in experimental formula matrices. Integration demands pharmaceutical grade purity and strict absence of animal-derived contaminants to comply with food safety regulations.

    Industry compliance standards

    • Codex Alimentarius Standard 72-1981 (Infant Formula)
    • EU Regulation 2016/127 (Infant Formula Composition)
    • China GB 10765-2021 (Infant Formula National Food Safety Standard)
    • HACCP and ISO 22000 Food Safety Management

    Typical usage ratio

    • 0.01%–0.2% of total fat phase in research and pilot formulations; ratio determined by targeted mimicry of human milk sterol profile

    Downstream process integration

    • Co-melt with other triglycerides and phospholipids before homogenization
    • Dispersal in pre-emulsified fat phase for laboratory-scale formula production
    • Documentation of identity, purity, and allergen status for product safety reviews

    Final product types

    • Human milk fat analog research formulae
    • Experimental infant formula prototypes
    • Specialty clinical nutrition powders (developmental stage)
    • Scientific study samples for feeding trials

    6. Ophthalmic Ointment Base Manufacturing

    Sterile ophthalmic ointment compounders select cholesteryl oleate as a structuring agent within non-aqueous, anhydrous ointment bases. Its unique viscosity and melting profile contribute to sustained ocular lubrication and controlled drug release profiles. Regulations require pharmaceutical purity and low peroxide content to ensure patient safety in finished ophthalmic preparations.

    Industry compliance standards

    • United States Pharmacopeia (USP) Chapter <795> (Pharmaceutical Compounding – Nonsterile Preparations)
    • EU GMP EudraLex Volume 4, Annex 1 (Sterile medicinal products)
    • 21 CFR Part 200 (Ophthalmic Drug Products)
    • Ph. Eur. 5.0 General Monograph for Excipient Purity

    Typical usage ratio

    • 1%–7% by weight in ophthalmic ointments; determined by required hardness, spreadability, and compatibility with active agents

    Downstream process integration

    • Fusion into paraffin or white petrolatum at controlled temperatures under aseptic conditions
    • Homogenization with active drugs during ointment compounding
    • Post-production testing for sterility and physicochemical properties

    Final product types

    • Sterile eye ointments for dry eye relief
    • Lubricant ophthalmic ointments
    • Medicated ointments for ocular surface diseases
    • Veterinary ophthalmic balms
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    Certification & Compliance
    More Introduction

    Cholesteryl Oleate: Reliability and Performance from an Experienced Manufacturer

    Understanding the Value of Cholesteryl Oleate

    Working in chemical manufacturing all these years, we see firsthand how cholesteryl oleate shapes performance and stability in a wide range of products. After countless production cycles and continuous quality trials, we know this ester intimately—not just its chemical code or CAS number, but its character and real-world behavior from order to application. Our experience in producing cholesteryl oleate makes us acutely aware of the specific needs formulators face every day, especially where dependable sourcing and consistency truly matter.

    What Sets Our Cholesteryl Oleate Apart

    Year after year, chemists approach us looking for a material that doesn’t just meet generic specifications. In making cholesteryl oleate, we pay attention to purity, color, and handling—details that often get overlooked until they become a headache in scale-up or downstream processing. Our technical grade product, under model designation CO-9005, holds a purity above 98%. We focus our process on a narrow melting point range, usually between 38°C and 42°C, which makes scaling from the bench to production less of a juggling act for our customers. From the start, we've put time into refining our crystallization steps and solvent controls because stability problems in the field often trace back to overlooked corners in upstream manufacturing.

    Applications That Trust Cholesteryl Oleate

    Cholesteryl oleate remains vital in cosmetic and skincare research, where it serves as a building block for emulsion structures and delivers a skin-feel that synthetic alternatives haven’t matched. In my own meetings with R&D specialists, many want the natural lipid aesthetics, especially as trends move toward more biocompatible and sustainable formulas. In our batches, the low residual solvents and neutral odor draw praise from labs aiming for consistent sensory properties in creams and lotions.
    Pharmaceutical developers focus on its ability to mimic biological lipid behavior. This ester often acts as both excipient and functional ingredient in lipid-based delivery systems, with reliability tied closely to manufacturing reproducibility. Even a minor drift in fatty acid composition leaves a fingerprint on the drug release—something most buyers won’t even notice until a formulation goes out of spec months down the line. Our strict feedstock traceability and quality audits stem from facing these issues early in our own process development.

    Real Differences: More Than a Commodity

    Comparing cholesteryl oleate to other esters—like cholesteryl stearate or cholesteryl linoleate—we see different physical properties and formulation results. Oleate’s lower melting point gives softer texture and easier spread in topical applications, while stearate stays firmer at room temperature. This has big impact for formulating lipsticks, soft solids, and even controlled-release capsules. Cleaning up fouling or phase separation in trials comes down to picking the right structure for the desired feel and processing window. We draw these distinctions in everyday technical calls, not just from catalog descriptions.

    Beyond other cholesterol esters, comparing directly with plant-derived or petrochemical analogs reveals subtleties. Plant esters, for example, may seem interchangeable on paper, but customers tell us about silicone incompatibility, haze formation, and reduced consumer appeal because the texture or appearance isn't quite right. The solution often lies in knowing how our cholesteryl oleate performs in that specific recipe, sometimes even reformulating to blend the benefits. Our technical team documents lot-specific feedback so we can guide these adjustments for both pilot-scale and commercial batches.

    Lessons Learned from Decades of Production

    Each batch of cholesteryl oleate we pour carries layers of experience—sometimes lessons learned after discovering a raw material’s batch variability, or the time a key filter breached and clogged downstream lines. Early on, we discovered that small changes in temperature control or vacuum settings skewed melting point and color, resulting in complaints from cosmetic producers. Over the years, we installed continuous online monitoring and reusable recycling steps to manage trace byproducts and avoid process upsets—even if upstream suppliers altered their specs without notice. We take notes from every deviation—if a drum arrives off-color, we test it in-house, adjust parameters, and feed what we learn right back into daily procedures. This loop runs through our entire operation, not as a regulatory checkbox, but because customers call us out as soon as product inconsistency creates rework or cost creep on their end.

    Traceability gets a lot of attention from auditors, but our motivation runs deeper than passing paperwork. If a clinical trial product fails, back-tracing a batch to a specific test point saves everyone time and money, and upholds our reputation. That’s why we keep lot samples long after shipment, always tracking their physical and chemical fingerprints. We’ve seen urgent queries from buyers racing the clock for a formulation deadline, asking for molecular weight verification, or low-level impurity profiles. Because our team handles these tests in-house, we don’t leave partners stranded waiting for third-party results, especially under tight project timelines.

    Supporting Research & Development

    Many of our long-term relationships began with sharing technical advice, sometimes even before signing a supply agreement. Our team collaborates with research groups and pilot plants from the concept stage, not just shipping off a product sheet and walking away. Adjusting melting curves for unusual processing temperatures, providing compatibility trial lots, or even creating custom-sized shipments to reconcile budget with new experimental needs—these steps build trust. University labs and startup innovators often face hurdles with materials that behave unpredictably in formulation. Because we’ve solved process kinks internally, we point out options that sidestep common pitfalls, from solubility snags to avoiding phase separation at scale.

    Our internal R&D often validates how cholesteryl oleate impacts product shelf life, sensory attributes, and performance in multi-phase gels. We continuously gather feedback from partners, running stability tests under a wide band of temperature and humidity conditions, sharing real data rather than theory. This constant back-and-forth gives customers clear results before making production commitments. Our input isn’t a sales pitch—it’s grounded in cycles of scale-up testing, so R&D teams spend less time debugging and more time innovating.

    Environmental Responsibility in Practice

    In the chemical world, sustainability claims sometimes float around without substance. Our plant doesn’t just rely on buzzwords. We invested in closed-loop solvent recovery and reprocess side cuts to minimize waste and support responsible discharge. Our cholesteryl oleate line follows these same practices—not out of obligation, but from watching competitors lose certifications or face supply chain disruptions over compliance issues. By aligning our filtration and distillation with the latest best practices, we offer a product that lets downstream manufacturers clear tight regulatory scrutiny, especially in personal care and pharmaceutical applications. Third-party audits and certifications matter, and we back documentation with real process records from every campaign.

    With rising interest in “green chemistry,” we spend time reviewing raw material sources, prioritizing renewable inputs, and minimizing the use of high-emission solvents. Overhauling long-entrenched plant infrastructure isn’t easy. In the early 2010s, we converted from batch-based to semi-continuous systems, which cut energy use and brought more predictable batch qualities. These investments paid off as climate reporting tightened and multinationals adjusted their procurement standards. Having skin in the game, we actively contribute to industry discussions and sustainability forums—sharing not only success, but also setbacks and workarounds that other supply partners can draw on.

    Addressing Challenges and Finding Solutions

    Producing cholesteryl oleate teaches a manufacturer humility. Unexpected raw material delays, regulatory tweaks, and spikes in demand all force rapid adaptation. Sometimes even straightforward improvements—like switching to a new grade of solvent—reveal unforeseen side reactions that jeopardize a batch. We tackle these by holding open debriefs after every quality issue, involving frontline technicians who spot and flag trends well before sales teams notice order problems.
    On the customer side, issues such as storage stability and compatibility can cost time and money if missed during product launches. We address those concerns by maintaining flexible shipment schedules, adding technical bulletins on best handling practices, and sharing real-world experiences of what worked or failed in storage at different locations. When a batch displays unexpected characteristics, the answer often lies not only in the data sheet, but in honest conversations and data sharing across the entire supply chain. Collaborative problem-solving rarely follows a roadmap, but trust gets built one resolved problem at a time.

    New regulations on consumer product safety and labeling mean that both upstream and downstream partners look for ever-more detailed impurity profiles, source documentation, and allergen status. We stay proactive in updating these records and don’t shy away from technical scrutiny. Many of our clients learned the hard way that finding quality cholesteryl oleate isn’t just about the molecule itself, but also about everything that comes with it—the responsiveness, transparency, and willingness to adapt as regulations or consumer expectations shift.

    The Long Road to Reliable Quality

    For a specialty chemical like cholesteryl oleate, shortcuts in production nearly always backfire. Throughout our history, we’ve learned that skipping a polishing step to save a few hours or marginally increasing throughput only leads to complaint returns, shelf instability, or unplanned downtime during critical orders. As a result, we embraced lean manufacturing principles and continuous improvement. Our team undergoes cross-training so anyone can intervene when deviations begin—whether that’s troubleshooting a reactor vibration or fine-tuning a temperature ramp to avoid crystallization issues.

    We believe that real-world feedback—success stories and daily frustrations alike—drives steady improvement. We regularly schedule meetings with product developers, procurement teams, and end-users. This interaction gives us unfiltered insight into how our cholesteryl oleate really performs on their lines, not just how it looks coming off our finishing mill. Those conversations feed directly into training, equipment upgrades, and pilot-scale trials, keeping us aligned with what matters most to the people and projects depending on our product’s performance.

    Beyond the Molecule: Service as a Differentiator

    Our history in producing cholesteryl oleate has taught us that reliability involves more than keeping to specs. We stake our reputation on support and responsiveness throughout the purchasing and R&D process. Customers reach out not just for the product, but for insight on best practices in storage, formulation suggestions, or to troubleshoot an issue no off-the-shelf guideline ever predicted. We keep open communication lines and make experienced staff available to share lessons from past projects.
    That commitment also means being honest about what we can and can’t deliver, whether it's unusual volume requests, specialty packaging, or blending with companion ingredients at the plant. We prefer finding solutions together, even if it takes a little extra time, testing, or adaptation. Our honest discussions about trade-offs, lead times, or substitution strategies help everyone move forward faster—because surprises and finger-pointing drain resources and erode goodwill.

    Remaining Agile in a Shifting Market

    Trends in end-use markets keep evolving. More natural and “clean label” cosmetics, personalized medicine, and specialty encapsulation push demand for cholesteryl oleate in new forms and at new quality thresholds. Our adaptability in production lets us pivot as markets shift—from tightening heavy metal specifications for pharma partners, to building trace non-GMO documentation for clean beauty brands, to helping food ingredient customers comply with emerging labeling standards.

    Collaboration with supply chain partners, both upstream and downstream, builds resilience. We maintain relationships with vetted raw materials providers and invest in vertical integration where possible. As disruptions—natural disasters, logistics breakdowns, or regulatory changes—affect sourcing, we respond by sharing information and prioritizing risk mitigation strategies. Critical planning, buffer stocks, and honest status updates help our customers anticipate and adjust, avoiding downtime and lost market share.

    Focusing on the Customer Experience

    Every shipment of cholesteryl oleate carries the weight of our team’s reputation. Our plant operators, QC analysts, and support staff know the challenges faced at each link in the chain. Supporting not just purchasing, but efficient, safe, and reliable application means putting ourselves in the shoes of formulators, lab managers, and production leads who depend on timely, consistent supply.

    We stand by our record of delivering batches that hold true to their analysis and handle as required for final product assembly. On the rare occasion an issue arises, we’re candid about root cause, correction, and impact. This openness has brought many customers back for repeat business, moving beyond transactional relationships to true partnerships that span multiple projects and market cycles.

    Quality is a Journey, Not a Checklist

    Each step in making cholesteryl oleate reflects a mindset rooted in continual improvement. Beyond paperwork and industry certifications, manufacturers in our sector share an unspoken commitment to get things right—even as specifications, market demands, and scientific understanding keep evolving. For us, the privilege of being trusted with supply into regulated, high-value applications brings a responsibility that can’t be fulfilled through shortcuts or hollow claims.

    From careful process monitoring, open technical collaboration, investment in better systems, and genuine responsiveness to customer needs, we’re reminded daily that our product’s true value goes beyond the molecule itself. As new applications for cholesteryl oleate emerge and standards rise, our dedication keeps us focused on delivering the performance and support our customers rely on, shipment after shipment.