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10-Bromodecanoic Acid

    • Product Name 10-Bromodecanoic Acid
    • Alias Decanoic acid, 10-bromo-
    • Einecs 212-273-8
    • 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
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    Specifications

    HS Code

    793051

    Product Name 10-Bromodecanoic Acid
    Cas Number 50841-99-9
    Molecular Formula C10H19BrO2
    Molecular Weight 251.16 g/mol
    Appearance White to off-white solid
    Melting Point 41-45°C
    Boiling Point Approximately 340°C at 760 mmHg
    Density 1.345 g/cm3
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C(CCCCCCCCBr)C(=O)O
    Storage Temperature 2-8°C
    Synonyms 10-Bromocapric acid

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

    Packing & Storage
    Packing The 25g package of 10-Bromodecanoic Acid comes in a sealed amber glass bottle with a white screw cap and warning label.
    Shipping 10-Bromodecanoic Acid is shipped in tightly sealed containers to prevent leakage and contamination. It is packed according to hazardous material regulations, typically in glass or HDPE bottles with cushioning material. The package is clearly labeled with relevant hazard warnings, and is handled and transported in compliance with chemical safety standards.
    Storage 10-Bromodecanoic Acid should be stored in a tightly sealed container, away from moisture, direct sunlight, and sources of ignition. Keep it in a cool, dry, and well-ventilated area, preferably in a corrosive-resistant cabinet. Avoid contact with strong oxidizing agents and bases. Properly label the container and handle with appropriate personal protective equipment to ensure safe storage and handling.
    Application of 10-Bromodecanoic Acid

    Applications of 10-Bromodecanoic Acid in Industrial Manufacturing

    As a direct manufacturer of 10-Bromodecanoic Acid, we support downstream processors in specialized sectors that demand consistent quality, strict regulatory compliance, and advanced process integration. 10-Bromodecanoic Acid primarily serves as a functional building block in the synthesis of advanced intermediates, surfactants, and custom chemicals. The following industrial segments represent established, mature adoption scenarios for this material, where its reactivity and molecular structure create specific process advantages.

    1. Pharmaceutical Intermediate Synthesis

    10-Bromodecanoic Acid functions as a halogenated intermediate in the multi-step synthesis of select pharmaceutical active ingredients and specialty APIs requiring long-chain aliphatic structures. Custom synthesis workshops and large-scale API operations use 10-Bromodecanoic Acid to introduce C10 alkyl chains with terminal bromine functionality in targeted molecular frameworks. This intermediate is especially valued when producing lipophilic prodrugs and antiepileptic agents through controlled Grignard, amidation, or esterification reactions, where residue limits, impurity profiles, and batch traceability are critically monitored.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) and European Pharmacopeia (Ph. Eur.) specifications for intermediates
    • FDA 21 CFR Part 211 for quality systems during manufacturing
    • REACH registration and ECHA substance notification

    Typical usage ratio

    • 0.15–0.35 molar equivalent, based on target molecule stoichiometry and degree of substitution; adjusted according to process yield analytics and impurity tolerances.

    Downstream process integration

    • Activation in initial alkyl halide coupling or bromination steps
    • Reactive integration at salt-forming or esterification stages
    • Purification via crystallization or extraction to isolate target intermediates

    Final product types

    • High-purity API intermediates for antiepileptics and nerve-active compounds
    • Lipophilic prodrug building blocks
    • Custom pharmaceutical intermediates for contract manufacturing

    2. Specialty Surfactant Manufacturing

    Downstream surfactant manufacturers incorporate 10-Bromodecanoic Acid as a raw material for synthesizing amphiphilic molecules, where its unique chain length and terminal bromine moiety facilitate controlled grafting, functionalization, or polymerization. This use proves vital in creating nonionic surfactants, specialty cationic surfactants, and antistatic agents for high-value emulsification, dispersal, and wetting systems used in precision coatings, textiles, and electronic cleaning fluids. Batch consistency, trace elemental content, and reactivity index are closely controlled at all stages, ensuring safe use in high-tech applications.

    Industry compliance standards

    • ISO 9001:2015 Certified Quality Management for chemical manufacturing
    • OECD Guidelines for Testing of Chemicals (Surfactant Biodegradability)
    • REACH Annex XVII (restrictions for industrial surfactants)
    • ASTM D4263 (Water Absorption of Surfactants, if applied to construction)

    Typical usage ratio

    • 1.5–4.0% by weight of surfactant precursor mass, variable according to desired HLB and end-use environment

    Downstream process integration

    • Feeding into bromination or esterification reactors as starting component
    • Functional modification during late-stage polymerization
    • Final neutralization and purification before product bottling

    Final product types

    • Nonionic and cationic surfactants for precision cleaning and degreasing agents
    • Antistatic agents for textile and electronics manufacturing
    • Wetting agents and dispersants used in ink, pigment, or metalworking fluids

    3. Organic Chemical Synthesis for Agrochemical Intermediates

    Agrochemical formulators employ 10-Bromodecanoic Acid in synthesizing custom intermediates for crop protection, specifically to introduce C10 alkyl chains that alter bioavailability or adjust the hydrophobic–hydrophilic balance in active substances. Its role as a coupling reagent or alkylating agent enables precise control over substitution patterns for herbicide, fungicide, or pesticide precursor molecules. Downstream manufacturers focus on process safety, conversion efficiency, and consistency of chain-branched side products.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS) quality standards
    • ISO 17025 Analytical Quality System Requirements
    • EU Regulation (EC) No 1107/2009 on plant protection products
    • REACH Annex II (Safety Data Sheet requirements for intermediates)

    Typical usage ratio

    • 0.9–2.5% wt/wt as a substrate-reactant in multi-step synthesis, adjusted for target selectivity and required yield

    Downstream process integration

    • Stage-wise addition in batch reactors under inert atmosphere
    • Alkyl chain introduction before or after core aromatic substitutions
    • Phase separation and recovery prior to final crystallization or solvent exchange

    Final product types

    • Herbicide and pesticide intermediates with C10-alkylated active groups
    • Fungicide precursors needing specific brominated substitutions
    • Custom molecules for research and pilot-scale plant protection formulations

    4. Functional Monomer and Polymer Additive Production

    The specialty polymer and resin industry adopts 10-Bromodecanoic Acid as a monomer modifier or functional group donor to impart flame retardancy and enhance compatibility in engineering plastics, wire coatings, or high-performance elastomers. The presence of bromine in the decanoic acid backbone provides a reactive site for grafting, co-polymerization, or post-polymer modification, contributing to thermal and fire resistance. Consistent chain length, low contamination, and well-characterized reactivity enable reliable integration into demanding extrusion and compounding operations.

    Industry compliance standards

    • UL 94 Flammability Standards for Plastics Materials
    • EN 45545-2: Fire protection in railway vehicles (if plastics used in transport)
    • ISO 9001:2015 for polymer manufacturing quality assurance
    • REACH Regulation on flame retardant additives

    Typical usage ratio

    • 0.5–1.8% by weight in polymer matrices or as minor monomer during grafting; ratio set by fire resistance targets and mechanical performance requirements

    Downstream process integration

    • Dosing in reactive extrusion systems or pre-polymerization blending
    • Direct addition to compounding batches alongside other functional additives
    • Post-polymerization grafting and surface modification in solvent or melt phase

    Final product types

    • Wire insulation polymers and flame-retardant cable coatings
    • Flame-retardant engineering plastics and elastomers for transportation or electronics
    • Custom copolymers with improved hydrophobic performance

    5. Custom Synthesis for Industrial Biochemistry Reagents

    Biochemical and laboratory reagent producers utilize this material when constructing reference standards, proton donor-rich alkyl bromides for enzyme inhibition research, or hydrophobic templates in specialty assays. Selective introduction of the C10-bromo chain in molecules evaluated for biochemical probe design ensures accurate calibration, process validation, and standardization in regulated laboratory settings. Tight control of purity, trace metals, and residual solvents supports precision in finished reagent characteristics.

    Industry compliance standards

    • ISO 17034 General requirements for the competence of reference material producers
    • ISO/IEC 17025 Laboratory competence requirements
    • Good Laboratory Practice (GLP) for reagent production
    • REACH Substances for scientific R&D exemption (where applicable)

    Typical usage ratio

    • Variable, typically 0.01–0.2 mmol per assay batch, determined by target assay concentration and intended inhibitory effect

    Downstream process integration

    • Controlled addition to synthesis or analytical calibration stages
    • Post-reaction purification via column chromatography
    • Packaging in micro-scale batches for laboratory distribution

    Final product types

    • Biochemical assay standards for enzyme inhibition studies
    • Specialty laboratory reagents for chemical biology
    • Hydrophobic bromoalkyl templates for analytical reference
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    Competitive 10-Bromodecanoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

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    More Introduction

    10-Bromodecanoic Acid: Practical Value in Synthesis and Industry

    Our Perspective as a Chemical Manufacturer

    Producing 10-Bromodecanoic Acid isn’t as simple as running a batch and bottling up the results. Every step from sourcing raw materials to purifying the final acid means working through a series of technical decisions. Since demand for long-chain bromoacids never slows down, especially from pharmaceutical R&D teams, surfactant makers, and polymer labs, we’ve seen our share of challenges and discoveries with this particular molecule.

    In the plant, consistency matters just as much as accuracy. As a manufacturer, our hands-on experience tells us that controlling every stage—especially bromination—makes the real difference between a reliable product and one prone to unpredictability. Our 10-Bromodecanoic Acid stands out because we commit to starting only with fatty acid stocks containing fewer trace impurities, keeping byproducts to a minimum during bromine introduction. This is more than just a technical detail; the difference shows up downstream, in cleaner reactions and more reliable yields for our customers.

    The Chemistry: A Decanoic Acid with a Distinct Halogenation

    10-Bromodecanoic Acid belongs to a family of long-chain saturated fatty acids that carry a bromine atom on the terminal carbon. The molecule has the familiar structure of capric acid with one atom swapped: a bromine attached to the tenth carbon. In technical terms, its CAS number signals its identity, but what really counts for partners in research or manufacturing is that single, well-placed bromine.

    Our staff pay attention to the reactivity imparted by that bromine. With its strong leaving group ability, reactions based on nucleophilic substitution and elimination gain efficiency. Customers rely on this property for building block uses, especially in industrial and laboratory alkylation and amide coupling reactions. Unlike shorter chain bromoacids, such as 6-bromohexanoic acid, or even longer ones like 12-bromododecanoic acid, the decanoic chain gives the right balance: enough hydrophobic stretch to serve as a surfactant precursor while not too unwieldy for most organic reactions.

    Specifications That Matter in Real Work

    We keep our specifications laser-focused. Purity isn’t negotiable here. As a crude product, even trace levels of unreacted starting acid or overbrominated side-products throw off fine syntheses later on. Quality checks in our facility look for color (white to slightly off-white, but never brown), melting point (just above room temperature, so easy to store but not tricky to weigh), and GC or HPLC purity. Our batches test above 98% on modern chromatography, minimizing contaminants that could trip up complex synthetic work. Each lot also gets analyzed for trace metals and residual halide, both critical in pharmaceutical or advanced surfactant applications.

    While technical sheets often toss out the phrase “meets or exceeds industry standards,” our view is different. We keep communication open with end users. Their test reactions and feedback shape our actual process, not just the spec sheet. This sometimes means adjusting distillation conditions or washing steps between lots, to block out ambiguity and ensure downstream applications stay robust. It’s a two-way street; some customers want higher-purity grades for sensitive pharmaceutical applications, and others prefer cost-efficient synthetic grades for non-critical surfactant projects. We talk through these use cases directly, instead of hiding behind generalities.

    Practical Usage in Chemical Synthesis

    The ring of bromine on the end of the carbon chain opens doors for introducing further modifications. Customers often ask about the value of 10-Bromodecanoic Acid over its unbrominated cousin or even fluorinated derivatives. Here, direct experience shows its worth as an intermediate for synthesizing omega-bromoalkanoyl derivatives, which eventually find their way into biomolecule tagging, lipid research, and even as starting materials for functional polymers. The C10 chain length offers a midpoint—flexible enough for a variety of solubilization schemes but robust enough to avoid volatility and instability that can plague shorter chains.

    Some research teams pick this acid specifically for making specialized surfactants. Ethoxylation and amidation routes use the omega-bromo functionality to build amphiphilic molecules, targeting detergent, cosmetic, and pharmaceutical formulations. Compared to non-halogenated decanoic acid, the brominated version forms a much more potent reactive intermediate, allowing follow-up coupling under milder conditions or with a wider reagent choice.

    In our years of fielding questions and lab trials, one pattern stays constant: users see more reliable reactivity with our 10-Bromodecanoic Acid versus suppliers who skip on purification steps. This isn’t a matter of luck—it traces directly to our approach around batch consistency, clarity in documentation, and open technical support for in-process troubleshooting. A pharmaceutical chemist doesn’t want a batch-to-batch shift when making a tagged fatty acid probe; a surfactant developer can’t afford downtime if unreacted acid slows up their mixing line.

    A Manufacturer’s View on Differences with Other Products

    Having produced a range of bromoacids, our team gets weekly questions about differences with similar products. On paper, similarities abound between 10-bromodecanoic acid and its analogues, but small differences have outsized impact. Longer chains such as 12-bromododecanoic or shorter like 8-bromooctanoic aren’t always simple substitutes. The chain length determines solubility in polar and nonpolar solvents, final surface activity in surfactant blends, and ease of purification after coupling steps. Our customers point out these nuances in performance—sometimes confirmed by trial runs in their labs, sometimes flagged only after scale-up reveals a solubility or stability challenge.

    A common question: does it make sense to swap capric acid (decanoic acid) for the brominated analogue? If the end use involves further coupling or nucleophilic substitution, especially on the omega position, the answer is usually yes. Bromination delivers a distinct advantage for post-functionalization. Yet, with halogenation comes higher cost and necessary attention to safe handling procedures. Our production team’s perspective comes down to risk management: we’ve invested in proper ventilation, smart waste disposal for halogenated byproducts, and regularly review safety protocols—not because regulations demand it, but because real-world hazards can balloon at the factory scale.

    Compared to other halogenated derivatives like 10-chlorodecanoic or 10-iododecanoic acid, the bromine variant offers a strong compromise. Iodinated chains are pricier and often suffer from poor stability. Chlorinated chains are lower reactivity—serviceable for some tasks, but often requiring harsher reaction conditions, which isn’t ideal for complex substrates. Decanoic bromide provides the functional punch most common downstream reactions ask for, and it sits at a cost-to-benefit balance we see more pharmaceutical and materials chemists relying on.

    Genuine Manufacturing Challenges and Solutions

    Every batch of 10-Bromodecanoic Acid we’ve made over the years turned up fresh insights. Achieving selective bromination at the omega position means marrying robust chemistry with industrial-scale practicality. Early on, inconsistent batches showed up as odd color or odor in test samples. Our solution wasn’t just better raw material prep. It meant refining reagent ratios, adjusting temperatures, and extending washing steps to knock out traces of overbromination or unwanted halides.

    On a plant floor, even tiny amounts of side-products can linger. Some resins in purification columns can retain both brominated and non-brominated fats, slowing throughput. We reassessed our chromatography techniques, replacing old resin types with modern phase media, which gave better separation for these long-chain molecules. In months with supply chain pressure—say, bromine shortages or inconsistent decanoic acid shipments—our quality department doubles down on incoming inspection. Versatile sourcing and a strong logistics team become as valuable as the right lab skills.

    Handling brominated fatty acids generates its own set of safety and waste disposal puzzles. Plant operators work with local authorities to make sure halogenated effluent gets neutralized and destroyed before any water discharge. Fume hoods and scrubbing towers line our process rooms. Fielding these overhead costs is just part of the real cost of doing business; these steps keep people and the environment safe, and they make sure our product never gets flagged for residual contamination.

    Supporting New Applications in Research and Industry

    Years of feedback from labs and factories give us a pretty direct sense of where 10-Bromodecanoic Acid fits best and where customers sometimes push it too far. The molecule doesn’t outpace all competitors, but when it fits, it fits well. Bioactive lipids, radiolabeling precursors, and controlled-reaction intermediates each call for slightly different forms of the acid: different crystallinity, dryness, or solvent delivery. Our manufacturing line isn’t static—we build in flexibility so our batches can be tweaked to suit exactly these scenarios.

    One university lab reached out for help working up an animal-model diet for metabolic tracing, using our acid. They needed assurance of near-total purity, neutral taste, and firm reporting on trace impurities. This led us to develop a cold filtration step, stripping off any volatile or non-standard side products more efficiently. Other clients test our products in high-temperature polymerizations, where thermal stability and lack of catalytic impurities count for more than appearance.

    Several research programs use our bromoacid as a linker or tagging agent in proteomics or lipidomics projects. In these settings, the reagent’s function is to introduce a “handle” for later chemical manipulations—whether fluorescence, biotin tagging, or isotope labeling. Only the right degree of purity and the right chain length will work for these tightly controlled experiments. In each case where something goes off-spec—traces of color, odd odor, measurable ash content—our technical support works one-on-one, reviewing batch reports and walking through solutions.

    Quality and Trust: Long-Term Lessons

    In our field, talk about quality only matters if it matches reality. Return customers base their decisions on consistency, not just price. A patchwork of inconsistent supply or corner-cutting on purification ruins relationships faster than a missed delivery date. That lesson shapes how we work, and our systems favor transparency. All QC data stays available for review, and traceability links each bottle back to lot-level details. Inside our own lab, running parallel sample analyses—swapping different solvent systems, running duplicate TLC—serves as one last check that nothing will surprise the user.

    Some buyers want the cheapest bromoacid possible—and our field experience confirms price pressure never disappears entirely. But after trialing a cheaper source, disappointed customers often circle back. Poor performance downstream, clumping solids, or batch instability catch up fast in major projects. We’ve seen supply chains tighten in tough market years. Still, the most discerning customers keep valuing documented, verifiable quality over short-term savings.

    Key Takeaways from Daily Production

    The technical feel of 10-Bromodecanoic Acid goes far beyond what a simple data sheet can tell you. Every decision at the plant or lab bench ends up reflected in the small details—whether that’s a slightly better melting profile, higher yield in a partner’s coupling reaction, or fewer headaches at scale-up. For us, success hinges on a cycle: listening when users flag problems, rolling improvements back into our batch process, and offering real-time data to anyone who requests it. If scientists don’t get reliable, actionable performance from our reagent, we hear about it fast—and we make sure the next lot solves it.

    As research in lipid chemistry, advanced materials, and specialized surfactants grows, the role of 10-Bromodecanoic Acid promises to expand. The most successful applications come from an ongoing, transparent collaboration between maker and user, not a faceless supply chain. With each batch, our team’s experience grows—pushing us to refine, adapt, and keep the product as dependable and versatile as modern industry demands.