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HS Code |
704275 |
| Chemicalname | 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone |
| Casnumber | 6262-58-6 |
| Molecularformula | C6H2Br4O |
| Molecularweight | 423.70 |
| Appearance | Light yellow to brownish solid |
| Meltingpoint | 162-164°C |
| Boilingpoint | Decomposes before boiling |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Density | 2.81 g/cm³ (calculated) |
| Pubchemcid | 119211 |
| Iupacname | 2,4,4,6-tetrabromocyclohexa-2,5-dien-1-one |
| Synonyms | 2,4,4,6-Tetrabromo-2,5-cyclohexadien-1-one |
| Smiles | O=C1C=CC(Br)=C(Br)C1(Br)Br |
| Inchi | InChI=1S/C6H2Br4O/c7-3-1-2-4(8)6(10,11)5(3)9/h1-2H |
As an accredited 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle sealed with a screw cap, labeled "2,4,4,6-Tetrabromo-2,5-Cyclohexadienone, 25g," with hazard warnings and batch information. |
| Shipping | 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone is shipped as a hazardous chemical, typically in tightly sealed containers to prevent moisture and contamination. Packaging follows UN guidelines for brominated organics, with proper hazard labeling. Transport is via ground or air, in compliance with local, national, and international regulations for toxic and environmentally hazardous substances. |
| Storage | 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of heat or ignition. It should be kept separate from incompatible substances, such as strong oxidizers and reducing agents. Appropriate chemical-resistant secondary containment and clear labeling are recommended to prevent accidental exposure or spills. |
Applications of 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone in Industrial Manufacturing2,4,4,6-Tetrabromo-2,5-Cyclohexadienone serves as a highly specialized brominated intermediate, predominantly supplied to industries focused on advanced flame retardant systems and specialty polymer synthesis. As a direct manufacturer working closely with international processing partners, we ensure consistent purity and reliable supply tailored to the demanding specifications of each target application. Below, find detailed information on its downstream integration in key industrial scenarios from regulatory, formulation, processing, and product perspectives. 1. Flame Retardant Additives for Engineering PlasticsThis material functions as a reactive intermediate in the production of brominated flame retardants, especially those employed in high-performance engineering plastics requiring stringent fire safety compliance. It enters production lines at the monomer or additive stage, reacting or incorporating during resin polymerization to impart long-term flame resistance suitable for electrical and transport components subject to regulatory flammability testing. Industry compliance standards
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2. Brominated Epoxy Resin Synthesis for Printed Circuit BoardsAs a core bromine donor, this compound participates in manufacturing brominated epoxy resins critical for flame retardant laminate substrates used in electronics. It enables producers to formulate resins with high glass transition temperatures and stable fire performance. The chemical is blended into the oligomer synthesis stage, facilitating consistent bromine content across resin batches for multilayer PCB boards. Industry compliance standards
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3. Synthesis of Brominated Polyols for Rigid Polyurethane FoamsThis intermediate acts as a bromine source in the targeted functionalization of polyols used for making rigid, fire-resistant polyurethane foams in thermal insulation and structural sandwich panels. Manufacturers formulate brominated polyols during polyether or polyester polyol production, ensuring uniform halogen distribution and reliable fire performance in building and cold-chain insulation systems. Industry compliance standards
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4. Intermediates for Synthesis of Brominated Specialty DyesCertain specialty dye manufacturers employ this compound as a key building block for creating brominated quinone-type colorants, widely applied in high-temperature plastics and specialty coatings. The material provides controlled bromine introduction into aromatic dye structures during the condensation or oxidative coupling phases, supporting production of heat-stable, low-bleed colorants required by demanding industrial and automotive applications. Industry compliance standards
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Years of hands-on experience in fine chemical synthesis have taught our team to look beyond standard catalog offerings. Chemists need reagents that don’t fall short in performance during mission-critical synthesis. Among the reagents built for reliability, 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone stands apart. Its model, purity profile, and batch-to-batch consistency have each evolved around the stringent standards set by research and industry. Each lot originates in-house, under rigorous scrutiny, because the push in pharmaceutical innovation, advanced dyes, and polymer chemistry leaves little room for raw material surprises.
Not every brominating agent can deliver the same performance under the pressure of scale, or the sensitivity of complex functional group chemistry. From the project failures we’ve witnessed during our earlier years—most often triggered by off-spec halogenation agents—our team sharpened focus on uniform crystallinity, purity, and shelf-life. 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone, offered predominantly in white to off-white crystalline form, reflects these lessons. We verify melting range and bromine content at multiple stages. By synthesizing under strictly controlled thermal and atmospheric conditions, our chemists keep unwanted byproducts under the detection limit.
Success often hinges on minutiae. Over the years, variation in melting point, the flatness of the UV absorption curve, and traces of polybrominated contaminants have spelled trouble. In response, monitoring remains hands-on—our chemists routinely cross-check infrared spectra and HPLC profiles before any batch release. Such direct oversight reassures those who rely on us for reproducible reactivity in Knoevenagel condensations, halogenations, or routes to brominated aromatics. There’s no substitution for having a sample made to the same standard as one’s published routes, run after run.
Colleagues in pharmaceuticals, agrochemistry, and electronic materials often highlight the difference between products sourced from primary manufacturers and material from the open market. In our operation, raw stock undergoes double-checks for traces of potentially catalytically active metals, halogenated phenols, and ionic bromide prior to formulation. Looking back, early feedback from polymer additive developers showed how improper reagent profiles led to color instability or chain scission. That experience turned our attention to removing even faint organobromide residues, often missed by standard titration.
When a customer scales from grams in the lab to multi-kilo lots, the expectations shift. Slight changes in solvent participation, impurity carry-through, or even particle morphology have triggered unexpected delays more than once. By maintaining in-house granular control from reaction to isolation and drying, we’ve avoided the most common pitfalls. The current manufacturing process eliminates key risks such as incomplete ring bromination, batch oxidation, or aberrant moisture uptake—factors directly at odds with stable handling and practical shelf life.
Our long years supporting custom synthesis operations show few brominating materials handle electron-rich systems as gently as 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone. Many customers came to us carrying frustration from overbromination or inconsistent halogen source uptake. This cyclohexadienone derivative, with its particular substitution pattern, acts as a controlled bromine donor in cases where molecular bromine or NBS gives unpredictable results—especially with heterocycles or unsaturated aromatics. Clear selectivity and migration speed, as proven by GC-MS in pilot plants, have become a trademark for those developing organobromides, specialty flame retardants, or unique pigments which rely on high-purity intermediates.
In dye chemistry, we’ve seen firsthand how sensitive intermediates react poorly to the slightest trace of extraneous halides or protic solvents. Our product supports sustained color stability and improved solubility, an edge for formulators who’ve struggled to tame batch-to-batch variability. The experience speaks loudest with manufacturers of pharmaceutical building blocks. Medicinal chemistry has shifted toward heavier halogen incorporation, driven by structure-activity relationships and patent protection pressure. Ready access to a reliable source of 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone shortens preclinical development, as teams spend less time resolving inconsistencies from impurities or fluctuating reactivity.
Classical bromination with molecular bromine, though cheap and reactive, brings persistent hazards: corrosive fumes, handling risk, and widespread byproducts. Years back, lab teams reported high waste treatment costs and inconsistent yields. Alternatives like N-bromosuccinimide (NBS) or the more recent phase-transfer bromine sources help, but each comes with its own drawbacks—faster decomposition, chalky dust formation, or uncontrolled side-product formation under acid or base conditions.
Our journey underscores how 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone holds up where traditional brominators lag. Process engineers note lower volatility hazards, more gentle release of bromine in alkylation or aromatic substitution, and ease of incorporation into automated process lines. Importantly, selectivity and shelf-stable form cut down on both routine troubleshooting and unexpected plant shutdowns. In high-value applications—like creating new pharmacophores or engineering advanced flame-retardant monomers—failure because of raw material instability simply isn’t an option.
In-house manufacturing gives more than traceability—it grants rapid diagnosis and correction. Over the decades, off-the-shelf brokers routinely introduced batch variables, leading to non-homogeneous samples or unexplained yellowing. Here, we initiate every synthesis with raw materials purchased against verifiable incoming standards. Automated and manual testing protocols at key checkpoints, especially during bromination and final drying, guarantee customers the same experience from pilot scale through full production.
Beyond the laboratory, the realities of transport, storage, and handling demand careful packaging. Dehumidified environments and inert gas backfills stop hydrolysis and caking—a nod to many hours spent salvaging compromised drums after international transit. We’ve designed packaging to withstand long-term warehouse layovers and rapid transfers to glovebox environments without drop-off in reactivity. Feedback from end users, especially those producing kilogram quantities of organics for regulatory approval, confirm that packaging integrity is as vital as the material itself.
Experience dealing with multinational compliance gave us key insight—consistency in documentation, impurity dossiers, and long-term test results often trumps any savings from quick purchase. In pharmaceutical and electronics supply chains, regulatory scrutiny falls now not only on product content, but also on cross-contamination and trace environmental release. Each batch of our 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone arrives with full analytical documentation, including trace element and halogen residuals often ignored by resellers or brokers. Efforts to surpass guideline minimums—covering both typical USP/ICH reporting and more stringent local expectations—have won us repeat business from the world’s most demanding sectors.
We directly support formulation development and investigative troubleshooting. More than once, teams developing new flame-retardant plastics sought root causes for unanticipated coloration or polymer backbone breakdown. By cross-analyzing suspect samples against our in-house reference spectra, we helped several partners regain process control. Further, familiarity with regulatory frameworks helps end users anticipate and document compliance for final product registration.
During the early years, missteps with temperature control or subpar final drying highlighted how even minor lapses could degrade product quality over time. Accumulated learning translated to new protocols. Chemists in our facility review each purification and drying stage, checking for loss of active bromine. This end-to-end accountability takes more effort but shields customers from failed reactions and waste at scale. We’ve seen time and again how missing these steps in the pursuit of quick output brands a manufacturer unreliable—a reputation hard to recover from.
Greater transparency has emerged as a crucial industry trend. Customers ask for real answers about provenance, not generic assurances. By taking queries on particular synthetic routes or shelf-life problems seriously—instead of deflecting with catalog statements—we stand apart from traders and intermediaries. Our R&D group engages directly, whether the challenge lies in developing new solid forms or shifting to greener solvent recovery.
Those who’ve run side-by-side trials with 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone from multiple sources report stark differences. Samples from upstream producers, uncontrolled batch reactors, or simple repackaging operations typically show broad melting range and random color fluctuations. These markers signal impurity. Downstream process teams pay the price in extra purification, off-spec final products, and lost time troubleshooting. Our commitment focuses on minimizing those pain points, started by putting experienced chemists—rather than batch operators—at each control point along the line.
This attention to detail outweighs headline purity numbers advertised by resellers. Selectivity in the field, mid-point reactivity for late-stage intermediate synthesis, and reliable hazard identification suit bench scientists and plant operators equally. We have resolved real-world customer issues by isolating specific trace side-products, redesigning packaging to weather temperature swings, and even collaborating on waste minimization for environmentally sensitive operations.
Our history as chemical manufacturers drives every decision in producing 2,4,4,6-Tetrabromo-2,5-Cyclohexadienone, from the first weighed gram to the final drum. Customers share feedback directly, raising points often overlooked by generic sources. Seasoned process chemists, R&D project leads, and plant managers alike trust that batch information, handling recommendations, and analytical details reach them unfiltered and complete. We have no incentive to shortcut specifications, misrepresent origin, or play catch-up with critical root-cause investigations.
We’ve learned the hard way there’s no trade-off—dependable performance springs from hands-on oversight at every production step. Customers in industries governed by regulation, cost efficiency, and manufacturing speed deserve better than vague provenance or unpredictable results. As always, we invite dialogue on any process, application challenge, or idea for improvement. In our view, the standards our customers expect match the standards we insist upon ourselves. That shared foundation guides everything we do.