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HS Code |
748925 |
| Cas Number | 7516-37-0 |
| Molecular Formula | C19H37BrO2 |
| Molecular Weight | 377.40 g/mol |
| Iupac Name | 19-bromononadecanoic acid |
| Appearance | White to off-white solid |
| Melting Point | 57-60°C |
| Solubility In Water | Insoluble |
| Storage Temperature | 2-8°C (refrigerated) |
| Synonyms | omega-Bromononadecanoic acid |
| Purity | Typically ≥98% |
| Smiles | CCCCCCCCCCCCCCCCCC(Br)C(=O)O |
As an accredited 19-Bromononadecanoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 1-gram sample of 19-Bromononadecanoic acid is supplied in a tightly sealed amber glass vial within a protective outer box. |
| Shipping | 19-Bromononadecanoic Acid is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is handled as a hazardous material, following local, national, and international transportation regulations. Proper labeling and documentation are included to ensure safety and compliance during transit. Temperature control may be used if required. |
| Storage | 19-Bromononadecanoic Acid should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area. Protect it from light and moisture, and keep it away from incompatible substances such as strong oxidizers. Store at room temperature or as directed on the manufacturer’s label. Properly label the container and restrict access to trained personnel only. |
Applications of 19-Bromononadecanoic Acid in Industrial ManufacturingAs a direct manufacturer of 19-Bromononadecanoic Acid, we provide material that supports high-demand industrial sectors. This section details verified downstream uses, with application-specific compliance, ratios, production integration, and end product types. 1. Pharmaceutical Synthesis — Lipid-Based Drug Delivery SystemsLeading pharmaceutical manufacturers use 19-Bromononadecanoic Acid as a brominated fatty acid intermediate in the synthesis of specialized lipid conjugates. The C19 chain length and terminal bromine facilitate covalent linkage to small molecules, enhancing drug solubility and cell membrane permeability, particularly for prodrug activation and nano-emulsion formation. Downstream, formulators target increased bioavailability for APIs with poor aqueous solubility, integrating this intermediate during the lipid excipient modification step before micronization and encapsulation under GMP-controlled conditions. Industry compliance standards
Typical usage ratio
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Final product types
2. Surfactant Manufacturing — Specialty Cationic SurfactantsChemical formulators utilize 19-Bromononadecanoic Acid as an alkylating precursor in the synthesis of long-chain quaternary ammonium surfactants. The brominated acid group undergoes conversion to the corresponding amine or quaternary salt through nucleophilic substitution, delivering surfactants with high hydrophobicity and desired phase transition temperatures. These materials support industrial applications such as textile emulsifiers, antistatic agents, and chemical cleaning solutions, where performance hinges on fatty acid chain length and functional group placement. Industry compliance standards
Typical usage ratio
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3. Polymer Industry — Functionalized Monomers for Block CopolymersAdvanced polymer manufacturers employ 19-Bromononadecanoic Acid as a building block for introducing long-chain brominated side groups in copolymer synthesis. Functionalization of olefinic or acrylate monomers with the acid group imparts tunable hydrophobicity, flexibility, and UV-resistance. The bromine handle enables subsequent modification or crosslinking, supporting development of specialty coatings, adhesives, and thermoplastic elastomers where precise control over monomer composition is critical for performance in harsh environments. Industry compliance standards
Typical usage ratio
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4. Agrochemical Synthesis — Long-Chain Brominated Pesticide IntermediatesMajor agrochemical groups utilize 19-Bromononadecanoic Acid as an intermediate for brominated fatty acid esters and derivatives, which serve as precursors in producing novel pesticide molecules and controlled-release agents. The long C19 chain yields high oil solubility necessary for foliar film formation and enhanced rainfastness of final pesticide formulations. The brominated functionality facilitates coupling with diverse agroactive fragments in esterification or halogen-exchange steps, supporting bespoke delivery in field applications. Industry compliance standards
Typical usage ratio
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5. Specialty Lubricant Additives — Long-Chain Brominated Fatty Acid DerivativesIndustrial lubricant producers select 19-Bromononadecanoic Acid for synthesis of advanced anti-wear and surface-active additives. The extended hydrophobic chain combined with terminal bromination produces derivatives compatible with both mineral oil and synthetic lubricant base stocks. These modified acids and corresponding salts become key additive components, supporting low-temperature performance, stable boundary films, and friction modification in high-load machinery and transport fluids. Industry compliance standards
Typical usage ratio
Downstream process integration
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Over the years in the lab, we have watched the demand for specialty long-chain fatty acids change alongside emerging research and evolving synthetic needs. Among these molecules, 19-Bromononadecanoic Acid stands out each time a customer asks for high-purity brominated analogs in complex syntheses or bioactive probes. This compound (sometimes called 19-bromo-nonadecanoic acid) has gained attention due to its specific halogen placement and predictable behavior during reactions, especially when compared to other bromo fatty acids with shorter or more ambiguous carbon chains.
Our production process brings out what makes this molecule special. Once we finish the final synthetic step and begin the purification, it becomes clear— the purity, the handling profile, the consistent melting point. All these details matter for researchers and manufacturers downstream counting on a reliable starting material. While years back brominated fatty acids were mostly custom jobs, now labs routinely ask for specific chain lengths and functional group placements that support high-precision research in lipidomics and tracer studies.
19-Bromononadecanoic Acid consists of a straight 19-carbon saturated alkyl chain with a bromine atom fixed at the omega carbon and a carboxylic acid group at the other end. This structure brings stability and unique reactivity that can’t always be replaced by shorter or non-halogenated fatty acids. During manufacturing, we see that the bromine atom—sitting on the terminal carbon—brings both mass and electron-withdrawing effects to the molecule, which then translates to distinct outcomes in chemical transformations.
For practical use, our customers rely on that terminal bromine. In radiolabeling, bromine offers a heavier label compared to iodine with a more stable carbon-bromine bond. The 19-carbon chain lets biochemists mimic naturally occurring long-chain fatty acids, facilitating accurate fatty acid uptake studies since organisms process it in much the same way as they would a natural molecule, aside from the presence of that single, trackable atom. Our own test reactions consistently show reliable conversion during coupling and substitution processes thanks to the predictable placement and reactivity of the bromine.
Over time, we have found that even small differences in manufacturing—temperature control, precision in reagent addition, or attention to solvent purity—change the final product's behavior in the lab. Any trace contaminants, especially on the terminal end, interfere with downstream derivatization or tracking during bioassay work. Colleagues have shared stories of inconsistent melting points or odd TLC spots when using inconsistent suppliers. These are issues we work hard to sidestep, drawing on years of process optimization.
19-Bromononadecanoic Acid typically appears in the lab as a crystalline white solid. We focus on maintaining a melting point within a narrow, repeatable range, avoiding lower-quality batches that cause headaches for researchers down the line. During each synthesis run, we track not only the overall purity—targeted above 98% using GC and HPLC—but also the trace halogen content and the acid number. Volatile impurities or color changes are rare in our batches due to repeated washing and careful distillation of solvents.
Our experience shows the chain length plays a large role in how these acids behave during storage and synthesis. Some customers try working with similar molecules like 11-bromoundecanoic acid or 17-bromostearic acid, thinking they might substitute for the nineteen-carbon variant. In reality, the physical and chemical differences can derail a protocol’s outcome, especially for long-chain metabolic studies or precise click chemistry. The difference comes down to solubility, lipophilicity, and how completely the terminal bromine resists displacement except under strong conditions.
Through analytical work, we see that the chain extension—just a few extra carbons—impacts miscibility with nonpolar solvents, and storage at room temperature. Some shorter chain brominated acids show an oily residue after time in the bottle; our 19-carbon product remains a solid, which is a sign of stability that our clients appreciate.
We receive steady requests for this molecule in academic and industrial R&D. It’s often selected as a non-radioactive internal standard for gas chromatography analysis in lipid panels because of its long chain and unique mass. Lab teams in the metabolic tracer field often need to isolate very minor components from complex mixtures, so the clean mass increase from bromination at the end of a C19 chain stands out during detection but doesn’t stray from the behavior of endogenous long-chain acids.
This compound also enters more specialized territory. In our experience, biochemists use it to produce ω-bromo fatty acid derivatives for alkylation reactions, directing the bromine to create amides, esters, or derivatives with a clear endpoint. This approach suits researchers trying to attach fluorescent tags, radioactive labels, or form more complex surfactants for cell membrane studies. Some teams return to us seeking further functionalization, and the starting purity and the bromine’s stability make downstream chemistry predictable.
In pilot manufacturing settings, 19-bromononadecanoic acid finds a role as a hydrophobic anchor for advanced surfactant design, especially when customer needs cannot be met by simple lauric or stearic acid analogs. Product engineers in materials science tell us their formulations call for a specific halogen content that impacts surfactant headgroup behavior or absorption on hydrophobic substrates in coatings research. The molecule’s chain length and single, well-placed bromine often prove vital to success, and customers come back when they see batch-to-batch consistency.
From the manufacturing side, we know not all brominated fatty acids act alike. There’s a clear practical difference compared to the shorter, saturated, or even mixed-chain variants some competitors offer. The nineteen-carbon backbone changes several key properties—melting point, hydrophobicity, compatibility with nonpolar solvents, and the specific reactivity of the bromine terminal. For example, it keeps longer in storage, shows less tendency to oils or discoloration, and doesn’t leach plasticizers from bottles the way lighter analogs sometimes do.
Substitution patterns, especially for the bromine, alter reactivity. With the bromine on the omega carbon, side reactions leading to branched impurities are reduced. Our lab teams often field calls from researchers struggling with positional isomers in their purchased acids. That’s one headache we avoid, producing only the straight-chain, omega-bromo product, which performs predictably under nucleophilic substitution or Grignard formation.
Using 19-bromononadecanoic acid genuinely matters in fields demanding repeat measurements and precision analysis. If switching from an 18-carbon or 20-carbon analog, the logP, partitioning, and downstream metabolic release all change noticeably. It’s not just about one bromine atom, but its placement and the accompanying physical behavior. Even GC-MS libraries reflect the unique retention and mass shift of this molecule, confirming the purity and structure each time.
We know from years of production that practical issues arise in large-scale synthesis—handling, scale-up, and waste. The process demands strict control at each stage, especially handling brominating agents and isolating clean end products. Early efforts in our plant taught us to expect exothermic reactions when introducing bromine to precursor acids. We’ve refined the technique, with staged addition, strict temperature tracking, and attention to work-up conditions that eliminate byproducts.
Our in-house team doesn’t treat 19-bromononadecanoic acid as just another halogenated chemical. We invest the extra time during purification, both chromatography and crystallization, so that our product retains color, consistency, and chemical stability over time. Batch records show that skipping quality control steps only leads to increased customer questions—a lesson we learned the hard way in earlier years.
Every year we take feedback from downstream users—GC-MS analysts, synthetic chemists, biochemists—and fold it back into our protocol. As we verify bromine and acid numbers or resolve issues related to packing or handling, these steps directly impact real-world applications. For example, clients in Europe flagged changes in their GC traces with non-optimal grades from other sources; in response, we traced the issue back to a small impurity only revealed through improved analytics, then improved our process to address it.
We respect that bromine chemistry doesn’t just pose technical hurdles—it carries safety and environmental questions too. Keeping residues from old bromination approaches down is central to our operation. Our waste handling has moved towards greater recovery and designed-in separation steps so that traces of brominated byproducts stay out of water streams. This benefits our workers, our customers, and the community.
Customers expect detailed safety data and real human answers on handling hazards. We put transparency at the top of the process, offering not just the expected documents, but real talk about how the molecule behaves during common accidents—skin contact, spills, or reactivity with reducing agents. This experience, gained from decades of in-house work, helps clients draft risk assessments grounded in reality, not just legal frameworks.
We keep on top of regulatory shifts in Europe, North America, and Asia. Over time, compliance around halogenated compounds has grown tighter, particularly for product traceability and occupational safety. By integrating these concerns into our supply chain, we reduce headaches for downstream companies preparing for audits or registering new research products. Years back, these laws might have caught companies off-guard; now, it’s a basic part of chemical business that we handle as a matter of routine.
One of the main topics among research chemists right now is the drive to trace lipids in living organisms using stable isotopes and halogen tags. 19-Bromononadecanoic acid’s structure makes it a favorite for these studies, as its physical properties allow it to behave like a tracer while resisting metabolic breakdown or radical loss. In our production lot history, customers using this molecule report much cleaner data in metabolic flux studies compared to other labeled fatty acids. The repeatability in downstream analysis flows directly from raw material quality.
Global supply chains sometimes complicate access. Logistics delays, changed import regulations, and fluctuations in bromine feedstock all influence the cost and timing of delivery. In our lab, delays can cascade, pushing back start dates for time-sensitive animal studies or industrial runs. By holding multiple months’ worth of stock and keeping relationships with bromine suppliers active, we mitigate some of these risks. Our clients trust delivery timelines grounded in experience, not speculation.
Scaling to commercial levels while keeping solvent use and waste in check takes ongoing investment. Our plant has invested in solvent recovery and feedstock recycling systems that support sustainable operations and cut costs. Each process change begins on the small scale, where the risks and benefits are easy to track, then moves to production lines only when proven to work. This keeps the environmental burden of halogen chemistry lower, matching tougher ESG standards from customers and regulators.
After years producing and using 19-bromononadecanoic acid, we’ve learned the small things matter most: test everything, track batch differences, listen to the customer, and share practical handling tips. Only by paying attention at each step do we manage consistent, reliable outcomes for those depending on our chemicals in difficult research and manufacturing settings.
The future of long-chain fatty acid analogs points to greater specialization. As the focus tightens on traceable probes and precision synthesis, the technical edge of compounds like 19-bromononadecanoic acid becomes more valuable. Each request for customization, whether it’s a narrower melting point range, higher purity, or special packaging to prevent contamination, drives us to adapt fast. That cycle of challenge and improvement defines the relationship between our chemistry team and those on the front lines of science and industry.
We welcome feedback, field performance data, and crazy synthesis ideas—it’s what keeps the work from becoming routine. For us, 19-bromononadecanoic acid is more than just a product—it’s a platform for innovation built on decades of practical problem solving, real-world testing, and ongoing improvement. If you’re looking for a partner who knows the chain from raw bromine drums to bioassay-ready material, you’re in the right place. Our doors are open, and the conversation is ongoing.