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HS Code |
360783 |
| Product Name | 16-Hydroxyhexadecanoic Acid |
| Cas Number | 506-12-7 |
| Molecular Formula | C16H32O3 |
| Molecular Weight | 272.43 g/mol |
| Iupac Name | 16-hydroxyhexadecanoic acid |
| Synonyms | 16-hydroxy palmitic acid, 16-hydroxyhexadecylic acid |
| Appearance | White to off-white solid |
| Melting Point | 84-87 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents (e.g., ethanol, chloroform) |
| Boiling Point | 443.3 °C at 760 mmHg |
| Density | 0.976 g/cm³ |
| Pubchem Cid | 10464 |
As an accredited 16-Hydroxyhexadecanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 16-Hydroxyhexadecanoic Acid is packaged in a sealed amber glass bottle, containing 5 grams, with a tamper-evident cap. |
| Shipping | 16-Hydroxyhexadecanoic Acid is shipped in tightly sealed, chemically-resistant containers under cool, dry conditions to prevent degradation. Packages comply with local and international regulations for non-hazardous chemicals. Proper labeling, documentation, and cushioning materials ensure safe transport during transit and storage, maintaining product quality and minimizing the risk of contamination or leakage. |
| Storage | 16-Hydroxyhexadecanoic acid should be stored in a tightly sealed container, protected from light and moisture. It is best kept at a cool temperature, ideally in a refrigerator (2–8°C). The storage area should be well-ventilated and free from incompatible materials such as strong oxidizers. Always label containers clearly and handle them using appropriate personal protective equipment to ensure safety. |
Applications of 16-Hydroxyhexadecanoic Acid in Industrial ManufacturingAs a direct manufacturer, we provide 16-Hydroxyhexadecanoic Acid for integration into multiple specialized industrial processes. Our production is tailored to meet the quality, safety, and regulatory standards demanded by each downstream sector. Below are key real-world application scenarios with detailed manufacturing and compliance insight. 1. Biodegradable Polymer ModificationProducers of aliphatic polyesters and copolyesters incorporate 16-Hydroxyhexadecanoic Acid to modify crystallinity and flexibility in biodegradable plastics. The hydroxyl and carboxylic groups participate in polycondensation reactions, serving as chain extenders or soft segments. Adjusting the concentration affects the polymer’s thermal and mechanical properties, essential for bioplastic films, molded containers, and fiber production where controlled degradation and material performance are specified by application and industry sector. Industry compliance standards
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2. Cosmetic Emollient SynthesisCosmetics formulators use the fatty acid as a building block for mild emollient esters, particularly through esterification with glycerol or other polyols. Integration at the synthesis stage enables production of compounds meeting purity and sensory specifications for creams, lotions, and personal care emulsions. The hydroxy functionality contributes to unique skin-feel and controlled spreadability, highly valued in dermatological and premium personal care lines. Industry compliance standards
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3. Lubricant Ester IngredientSynthetic lubricant formulators utilize 16-Hydroxyhexadecanoic Acid as a precursor for biodegradable ester-based lubricants. By esterifying with branched or polyhydric alcohols, they produce base stocks with targeted pour points and viscosity indices suited to metal processing and textile machinery. Its saturated structure offers hydrolytic stability and environmental compatibility for fluids required in sensitive manufacturing environments. Industry compliance standards
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4. Surfactant Intermediate for Mild Cleaning AgentsManufacturers of green surfactants use this fatty acid as a starting material for the synthesis of nonionic and anionic surfactants. Through ethoxylation or sulfonation processes, derivative molecules demonstrate high skin compatibility and controlled foaming. This offers advantages in low-irritation detergents for personal care and household use, where regulatory and allergen-free claims demand precise raw material traceability and batch consistency. Industry compliance standards
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Every batch of 16-hydroxyhexadecanoic acid leaving our reactors represents months of planning, countless QC checks, and decades of honed process control. In the chemical industry, there are no shortcuts, and those who work with specialty fatty acids understand why. Our team has leaned on over twenty years of fatty acid processing, scaling each route to match the needs of research and industry partners who expect reliability at a molecular level.
Those familiar with the long-chain hydroxy acids know just how challenging it is to achieve consistent quality during production. 16-hydroxyhexadecanoic acid, a monohydroxy fatty acid, stands out because it requires tight controls on isomer formation, chain length, and purity. Our model currently features a minimum purity of 98%, which eliminates potential interference from saturated or unsaturated impurities during downstream synthesis or biological studies.
We did not develop our process for 16-hydroxyhexadecanoic acid because the market demanded another indistinct fatty acid. This compound has carved out a niche where others cannot compete. Its presence in suberin, the natural polyester barrier of plant tissue, first caught the attention of polymer researchers and agricultural biochemists. Over the years, synthetic biologists and materials scientists joined that conversation, searching for renewable building blocks with predictable performance.
Our acid, also known as 16-hydroxy palmitic acid, plays a direct part in several focused industries. Its main value shows up during synthesis of plant cuticular wax analogs, as well as in studies investigating the hydrophobic barriers in roots and tubers. Cosmetic formulators and pharmaceutical researchers request hydroxyhexadecanoic acids for their unique emollient properties, which combine the long fatty chain’s occlusivity with mild reactivity at the terminal hydroxyl. These dual features allow specialists to design formulations that lock in moisture while controlling release rates.
Manufacturing this acid in-house teaches the importance of proper feedstock and purification. Crude tallows and plant oils rarely contain neat 16-hydroxyhexadecanoic acid. Our technicians learned to watch for side-reactions, which tend to creep in if the hydrotreatment step drifts out of tolerance. We source precursors with careful documentation. By focusing on batch consistency, our 16-hydroxyhexadecanoic acid avoids the “browning” phenomenon and off-odors that can crop up during peroxide-prone oxidations.
Our current specifications include a low peroxide value, water content below 0.25%, and clear crystalline form. Melting point recordings should remain inside a tight window, which simplifies quality control and offers confidence to formulators. Each lot is GC- and NMR-verified before release. Having raw spectral data at hand gives scientists on the other end peace of mind—they know the acid’s structure hasn’t been compromised by excessive heating or trace metal catalysis.
On paper, many fatty acids look similar. In practice, their subtle differences show up in the beaker. 16-hydroxyhexadecanoic acid’s most valuable feature comes from the secondary hydroxyl. This hydroxyl at the far end sets it apart from palmitic acid, stearic acid, and other more common chain members. This allows our acid to act as an anchor for covalent bonding, not just passive mixing.
Our team has tested this property many times. In biopolymer applications, the additional -OH enables chemical crosslinking—an advantage not found in simple saturated fatty acids. Because of this reactivity, formulators working on plant-inspired coatings, amphiphilic blends, or slow-release systems choose this acid to add mechanical strength or modulate hydrophobicity. We have seen how too much branching, too many unsaturations, or contamination with isomers throws off the repeatability of those finished materials. That is why we focus on the single-chain, linear hydroxyhexadecanoic configuration.
In cosmetics and dermatology research, products that use regular palmitic acid or stearic acid tend to sit on the surface or offer only temporary benefits. By introducing 16-hydroxyhexadecanoic acid, those designing barrier creams or bioactive lipid carriers report an increase in the cream’s ability to spread and hold moisture. Our own collaborative tests suggest it improves occlusivity, allowing for finer emulsions and less greasy residue. That small change in molecular structure translates to a practical improvement, one we have validated under repeatable lab conditions.
Supply chain confidence means more to our customers than marketing jargon. In a specialty segment like hydroxy fatty acids, even slight variances matter. We provide full COA documentation for 16-hydroxyhexadecanoic acid shipments, including impurity profiles and spectral analysis. Shipping teams monitor storage closely, using nitrogen purging and cool packing during transit for sensitive lots.
Researchers in plant biochemistry often ask about trace byproducts—such as 9,10-epoxyhexadecanoic or 16-oxohexadecanoic acid—that can co-elute with the hydroxy compound. Our QC department uses internal standards monitored by GC-FID and LC-MS/MS to ensure target molecule integrity. Many years ago, after feedback from a university client, we invested in better column technology and stricter water removal protocols. As a result, customers rarely encounter issues associated with unwanted side products.
Those aiming for analytical reproducibility—as in complex mixture mapping, metabolic flux studies, or lipidomic surveys—depend on the batch-to-batch consistency our in-house process delivers. Our facility keeps sample archives for two years, allowing researchers to trace anomalies and match profiles long after their initial purchase. Maintaining this transparency does not just serve immediate needs; it strengthens the relationship between us and the research community.
Scaling up hydroxy acid production deals out its fair share of challenges. During the early years, our batch yields ran low, mostly owing to emulsion issues and low selectivity in the hydroxylation step. Process engineers adjusted temperature curves and reaction times, shifting from direct chemical oxidation to more selective biotransformations. By blending biological catalysis with conventional purification, our unit now turns out product with higher selectivity and lower waste.
A common misconception holds that all hydroxy fatty acids behave the same way during scale-up. More than one plant tried to use the same protocol for 10-hydroxystearic acid or ricinoleic acid, only to find 16-hydroxyhexadecanoic acid doesn’t respond to the same pressure and pH profiles. Recognizing these differences alone preserves final product integrity and cost control.
Handling the acid as a solid or in solution—often in toluene, hexane, or methanol—brings practical downstream considerations. In our facility, we reserve dedicated glass-lined reactors to avoid any polymeric build-up from hydroxyl group reactions. Operators receive specialized training, particularly during recrystallization, to keep the acid within specification. That care pays off; signs of residual paraffin or unsaponifiable matter have not appeared in years.
Many requests for 16-hydroxyhexadecanoic acid come from researchers breaking new ground in biomaterials. Polymer teams have experimented with direct esterification, using the terminal -OH to build polyesters with variable flexibility. Others, in the realm of controlled-release fertilizers, incorporate the acid as a matrix component to help nutrients leach gradually into soil. Feedback from the field has driven incremental changes in our process—these users notice even a half-degree drop in melting point or a slight increase in color.
Formulators in cosmetics—antiperspirants, lotions, and balms—appreciate how our acid brings both structure and skin tolerance. Results from collaborative patch tests point to low irritation levels. At the same time, the acid helps prevent water loss without feeling heavy, a benefit the industry values highly. Unlike many synthetic emollients, our process neither introduces nor concentrates microplastic byproducts, which appeals to brands eyeing sustainability claims.
Industrial clients experimenting with high-barrier films or biocomposite coatings value the ability to functionalize the hydroxy terminus. Modified 16-hydroxyhexadecanoic acid participates in epoxide and ester chemistries, opening up routes to attach various functional groups. Our plant maintains isolate lines to work with these clients directly. Custom orders sometimes call for alternative counter-ions or solvent-free delivery, and since we control the process from reaction through packaging, we can respond quickly.
Several fatty acids populate the same landscape as 16-hydroxyhexadecanoic acid, but our years of side-by-side production reveal why subtle variances have such a big impact in the lab or plant. Palmitic acid, despite sharing a backbone, brings no hydroxyl reactivity and cannot take part in the same crosslinking steps. 9,10-dihydroxystearic acid presents both an increased polarity and different melting range, which can render it unsuitable for wax-type product development.
Ricinoleic acid, renowned in industrial lubricants and plastics, features an internal cis-double bond and a hydroxyl on the C12 position, marking it as less stable under heat or oxidative stress. Our acid, lacking such unsaturation, remains robust through multiple thermal or UV cycles, which enables broader compatibility with manufacturing methods. The straight C16 chain, plus terminal hydroxyl, gives it a perfect balance between solubility in alcohols and stability in alkanes. This matchup explains its value in both waterborne and oil-based systems.
In early pilot projects, some clients tried substituting lauric or oleic acids in polyester synthesis, only to report major shifts in hardness, flexibility, and solvent resistance. Real-world data pointed back to 16-hydroxyhexadecanoic acid as the small but decisive ingredient for optimal polymer structure or cream stability. Our technical experts review these findings along with the scientific literature, confirming with batch-specific documentation so clients see for themselves what structure-function means for their applications.
Few things matter more in chemistry than knowing who made your reagent and how it was handled at every step. By owning our production, not buying from outside traders, our quality team can follow each batch from the raw material intake through every reactor, filter, and drying line. If something veers from specification, an experienced eye catches it early, and we isolate the affected material without delay.
This hands-on method remains our answer to batch variability—a problem in the hydroxy acid business for decades. Drug development teams, food additive researchers, and coatings chemists call us because they’ve been burned by inconsistent material from traders who cannot trace origin or process. Having a transparent, single-source origin lets us guarantee traceable, repeatable quality every time.
Our facility’s in-situ monitoring regime, including FTIR and HPLC, keeps each run on course. Operators and lab staff continuously review purity and consistency. Finished lots undergo more than one type of analysis, including detailed impurity mapping that goes beyond basic chromatographic purity. This way, our product takes the guesswork out of scale-up or final testing in customer labs.
No successful project happens in a vacuum. For those working in formulation, scaling new materials, or troubleshooting unique applications, our open-door policy for technical queries means issues are addressed early. Every month brings fresh use cases. From start-up coatings developers to major biopolymer companies, our technical staff discuss molecule behavior, solubility quirks, and reactivity concerns openly—not hiding behind generic documentation or disclaimers.
Some industrial clients need 16-hydroxyhexadecanoic acid in bulk, others request analytical-scale packs. By controlling all stages, from procurement to processing to custom packing, meeting those needs becomes practical. In the rare instances where a batch calls for deviation from standard, our process engineers and QC chemists adapt the workflow to fit. Feedback flows both ways, and several improvements over the last ten years came from user insights and applied feedback loops.
Those creating bio-sourced or environmentally conscious products track high standards on more than just purity; they look to the entire chain. Our operation sources precursor oils with sustainability in mind, and our closed-loop water and solvent systems reduce environmental impact. Effluents exit treatment lines within accepted environmental norms, which reflects the broader commitment of our staff to responsible industrial citizenship.
For end-users, particularly those supplying cosmetics or cosmeceuticals, regulatory traceability matters. Every output batch comes supported by documentation on trace solvents, heavy metals, and allergen content. Knowing this, partners investing in certification or regulatory submissions can move with confidence through approval stages, backed by data, not only assurances.
Our journey manufacturing 16-hydroxyhexadecanoic acid delivers daily lessons in precision, patience, and practical application. Each lot represents the combined wisdom of decades in specialty chemical production and collaboration with users breaking new ground from the lab bench to the factory floor. As product standards and applications evolve, our focus on hands-on manufacturing, open data, and flexibility anchors our ongoing commitment to those who trust our acid for their projects. By listening, solving, and delivering from our own reactors, not someone else’s catalog, we build results one batch at a time.