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Thionyl Bromide

    • Product Name Thionyl Bromide
    • Alias Sulfurous dibromide
    • Einecs 234-594-8
    • 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
    VTB
    Specifications

    HS Code

    490627

    Chemicalname Thionyl Bromide
    Chemicalformula SOBr2
    Molarmass 223.78 g/mol
    Casnumber 13140-65-5
    Appearance Colorless to pale yellow liquid
    Density 2.523 g/cm³
    Meltingpoint -46.1 °C
    Boilingpoint 39.6 °C
    Solubilityinwater Reacts violently
    Odor Pungent
    Refractiveindex 1.535
    Vaporpressure 160 mmHg (20 °C)

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

    Packing & Storage
    Packing Thionyl Bromide is packaged in a 500 mL amber glass bottle, tightly sealed, and labeled with hazard and handling information.
    Shipping Thionyl Bromide is shipped as a hazardous material in tightly sealed, corrosion-resistant containers. It must be protected from moisture and handled with extreme caution. Transport complies with international regulations for toxic and corrosive substances (UN 1836, Class 6.1, Packing Group I). Proper labeling and documentation are mandatory for safety and compliance.
    Storage Thionyl bromide should be stored in a cool, dry, and well-ventilated area, away from moisture, heat sources, and direct sunlight. Containers must be tightly sealed, made of compatible material such as glass or Teflon, and clearly labeled. Store separately from water, alcohols, bases, and oxidizing agents. Use secondary containment to prevent leaks and ensure proper emergency procedures are in place.
    Application of Thionyl Bromide

    Applications of Thionyl Bromide in Industrial Manufacturing

    Thionyl Bromide supports specialized transformation steps in industrial synthesis pathways, enabling efficient bromination and chlorination reactions. As a manufacturer, we prioritize transparent formulation details and process-specific data to help our clients in the agrochemical, pharmaceutical, specialty intermediates, and advanced materials industries integrate this reagent effectively and compliantly.

    1. Agrochemical Active Ingredient Synthesis

    Global crop protection manufacturers use Thionyl Bromide to introduce bromine atoms into complex organic scaffolds, especially during the final bromination of selective herbicide and fungicide actives. In these sequences, tighter byproduct control is crucial, and the reaction must conform to rigid residual solvent and impurity specifications before field use registration in regional markets.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • EU REACH registration (EC/1907/2006)
    • China National Agrochemical Quality Standards (GB/T 1600 series)
    • EPA 40 CFR Part 180 - Tolerances and Exemptions for Pesticide Chemicals

    Typical usage ratio

    • Reagent quantities: 1.05–1.25 equivalents based on target substrate; precise adjustment to achieve complete conversion while minimizing overbromination and handling excess reagent safely

    Downstream process integration

    • Enters as final-stage halogenation reagent in multi-step batch reactors; requires closed-system charging and active scrubbing of off-gassing, followed by solvent partitioning and vacuum distillation for product isolation

    Final product types

    • Post-emergence herbicide actives (e.g., brominated triazines)
    • Fungicidal azoles and imidazoles
    • Seed treatment agents
    • Intermediate-scale pilot batches for new active registration

    2. Pharmaceutical Intermediate Manufacture

    Thionyl Bromide serves as a selective halogenation agent within the synthesis of advanced pharmaceutical intermediates, where substitution of hydroxyl or amino functional groups by bromine is foundational for active molecule assembly or downstream diversification. Tightly controlled addition and in-process monitoring ensure that final intermediates meet Pharmacopoeia and GMP requirements on residual reagents and genotoxic impurities.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for intermediates (when applicable)
    • US FDA 21 CFR Parts 210/211 (CGMP)
    • Chinese Pharmacopeia ChP Chapter V requirements on genotoxic reagents

    Typical usage ratio

    • Reagent use from 1.1 to 1.3 molar equivalents per functional group; dose variation based on substrate reactivity and impurity threshold limits mandated by finished API quality profiles

    Downstream process integration

    • Added as a fresh solution to cooled reaction mediums, typically under inert nitrogen to maintain product purity; post-reaction, intermediate is isolated after aqueous quench, extraction, and high-vacuum drying

    Final product types

    • Brominated pharmaceutical intermediates for analgesics
    • Generic API precursor blocks (e.g., for antihypertensive and antitumor agents)
    • Advanced intermediates for custom synthesis
    • Regulated reference standards batches

    3. Production of Organic Bromide Intermediates for Fine Chemicals

    Specialty organic chemical producers employ Thionyl Bromide in dedicated lines converting hydroxy- or amino-functionalized aromatics into aryl bromides. These intermediates feed further into dye, pigment, and polymer industries demanding precise halogenation with narrow impurity profiles. Closed system operation and continual on-line analysis restrict worker exposure and control emission levels according to chemical manufacturing regulations.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for chemical process development
    • ISO 9001:2015 for process quality management
    • EU Industrial Emissions Directive 2010/75/EU
    • China GB 18597-2001 for hazardous waste storage and treatment

    Typical usage ratio

    • 1.0–1.2 equivalents per substrate batch; proportion adjusted by substrate purity and intended downstream reactivity requirement shaded by customer specification

    Downstream process integration

    • Introduced as a neat reagent in jacketed reactors with controlled dosing, followed by vacuum or steam stripping and subsequent integration with in-line washing stations

    Final product types

    • Bromophenol and bromobenzene derivatives for pigment and dye synthesis
    • Monobrominated and dibrominated alkanes for flame retardants
    • Specialty polymer additives
    • Custom halogenated building blocks for export

    4. Specialty Catalyst and Ligand Preparation

    High-purity Thionyl Bromide is selected for bromination reactions during the synthesis of specialty ligands and catalysts designed for metal-organic frameworks and homogeneous catalysis. These applications demand ultra-low metal and organic impurity content and strict batch traceability under advanced materials workflows, typically operated under non-aqueous and inert conditions.

    Industry compliance standards

    • ISO 17025 accredited analytical methods for catalyst components
    • Electronic batch record requirements for advanced materials manufacturers
    • REACH Art. 33 (communication on substances in articles)
    • RoHS restriction on heavy metals (for electronic catalyst applications)

    Typical usage ratio

    • Ranges from 1.05 to 1.20 equivalents against selected substrate moiety; mathematic optimization based on ligand yield and purity KPIs as defined by catalyst end-use category

    Downstream process integration

    • Reagent charged by metered pumps to glovebox-sealed reactors; end of process includes solvent removal under reduced pressure and direct transfer to high-purity crystallization steps

    Final product types

    • Brominated phosphine and NHC ligands for catalysis
    • Metal-organic framework precursor blocks
    • Homogeneous and heterogeneous catalyst intermediates for electronics production
    • Research-grade specialty chemicals
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    Certification & Compliance
    More Introduction

    Introducing Thionyl Bromide: A Perspective from Chemical Manufacturing

    What We Know about Thionyl Bromide in Production

    In the world of inorganic chemical manufacture, thionyl bromide isn’t a headline-grabber, but those who use it quickly learn the value of precision handling and reliability from their supplier. In our facility, every decision around thionyl bromide reflects decades of familiarity with halide chemistry and the daily grind of what it really takes to move challenging chemicals from lab concept to practical supply. The chemistry behind thionyl bromide (SOBr2) fascinates from a process standpoint, but what keeps operators on their toes and managers up at night is quite simply its reactivity.

    Our production uses a batch process, where we combine pure thionyl chloride with high-grade hydrogen bromide, keeping a watchful eye on temperature and pressure in lined reactors—not just to get the desired yield, but to avoid runaway reactions. Hydrobromic acid and thionyl chloride combine to form thionyl bromide and HCl gas. Continuous monitoring for moisture and strict protocols against contamination make sure each lot stays on spec. When people discuss models or grades, we keep it straight: chemical purity typically ranges between 98%–99%, with water content verified below 0.5%. Most users rely on a colorless to faintly yellow liquid, with assay and free bromine content key markers for anyone downstream.

    Why Thionyl Bromide Matters

    In our shop, thionyl bromide serves specialized corners of the chemical world. Production lines using this compound aren’t running at the scale of commodity chlorides or acetates, but the impact stretches far. Clients ask for thionyl bromide by name when they need to introduce the S(O) group and double bromination reactivity in one motion. We ship this chemical for users in pharmaceutical research, advanced material synthesis, and specialty reagent preparation. It’s not just about the molecule itself; it’s the chemistry it unlocks.

    One area regular clients bring up is upstream synthesis of acyl bromides and organobromine intermediates. Standard brominating agents sometimes fall short where thionyl bromide shines: a compact reaction profile, relatively lower excess reagent requirements, and cleaner separation of byproducts. Thionyl bromide doesn’t just toss out bromine atoms. It reacts vigorously with alcohols, carboxylic acids, or primary amides, pushing toward corresponding bromides and producing sulfur dioxide and hydrogen chloride gas as the main byproducts—quite manageable with standard scrubbers. Comparing this to phosphorus tribromide, for example, thionyl bromide enables some acylation or conversion reactions at lower temperatures, cutting down thermal stress on sensitive compounds.

    Production cycles take careful planning, because thionyl bromide decomposes in moist air, generating HBr and sulfinyl-containing byproducts. This isn’t a trivial inconvenience. The need for dry air, dedicated lined containers, and reliable seals influences packaging and shipping decisions from start to finish. Years ago, we saw users ordering by the drum for routine conversions, but these days, the shift has gone toward smaller package sizes—whether winchesters or ampoules—sometimes pressurized under inert gas, because waste, safety, and cost tracking have become paramount for end users.

    What Sets Thionyl Bromide Apart in Use

    Experienced chemists know there’s no “universal” brominating agent. In our plant, we keep side-by-side specifications for thionyl bromide alongside phosphorus tribromide (PBr3), hydrobromic acid, or even elemental bromine. Thionyl bromide is not ideal for introducing a lone bromine atom into an aromatic ring; that’s classic elemental bromine territory, often with a Lewis acid catalyst. Instead, where thionyl bromide excels is the conversion of carboxylic acids to acyl bromides— a key precursor step in many pharmaceutical syntheses— or transforming alcohols to alkyl bromides with selectivity and efficiency. For those familiar with thionyl chloride (SOCl2), the comparison is immediate. Thionyl chloride disproportionately dominates for everyday transformations, particularly in tertiary or non-sensitive substrates, but thionyl bromide broadens the toolkit for those targeting downstream modifications that demand the bromide leaving group.

    One reason clients turn to thionyl bromide instead of phosphorus tribromide boils down to byproducts and waste management. Phosphorus tribromide produces phosphorous acid, setting up issues for neutralization and disposal in volume operations. Sulfur dioxide and hydrogen chloride produced from thionyl bromide can be handled with more established scrubbing systems in many plants, fitting cleanly into bulk chemical workflows. At scale, plant managers look for reagents that work within existing abatement, not ones that force massive infrastructure changes.

    On-Site Realities

    There’s a difference between reading about a reagent and watching it move through a chemical plant. Thionyl bromide never becomes “routine.” Our operators don full-body PPE to load, transfer, and unload. Accurate batch registration and environmental monitoring are not just checkboxes, but a daily defense against moisture ingress. I watched a seasoned technician spot a trace leak in a drum valve—not with high-tech sensors, but with a good nose and years of practice—prompting immediate containment.

    Plants handling thionyl bromide must harden pipelines and valves with corrosion-resistant linings to stand up to potential formation of HBr. Storage tanks sit under dry inert gas. Every valve gets checked against leaks. The complexity isn’t only about the chemical itself, it’s about the chain of procedures you build to keep every movement safe.

    We track every lot with full traceability. This grows critical for pharmaceutical manufacturers—regulators expect clear records of every drum, every transfer, every disposal ticket. In the early days, we tracked on paper. Now, electronic systems flag even minor deviations. Lost paperwork is more than a nuisance; it’s a regulatory headache, so adopting rock-solid digital tracking systems separates a true manufacturer from a slapdash operator.

    Supply Risks and Reliability

    Supply of thionyl bromide doesn’t just depend on the raw materials. Our experience through global disruptions showed raw thionyl chloride supply could zigzag either from geopolitical issues or shifts in global bromine production. Even a minor kink in the hydrogen bromide line demands backup sources and preplanned inventory. In years where mineral brine output dipped, we saw price spikes ripple up, with smaller buyers scrambling for reliable pipeline. Chemical manufacturing isn’t for the faint of heart; it rewards those who plan for long game supply relationships, not those who chase spot bargains.

    Clients trusting us with thionyl bromide demands realize this. Repeat business comes not just from price, but from consistent quality and honest reporting. They value full COA transparency, batch sample retention, and direct technical assistance if specifications drift off. More than once, we’ve caught minor impurities and traced them back to a vendor source, swapped out feeds, and retested the lot—to ensure a batch never leaves until it fits not just our spec, but the end user’s needs downstream.

    Safe Handling and Environmental Stewardship

    Working with thionyl bromide is never just about the chemistry; it’s about responsible stewardship. Our protocols require sealed drums, storage in dry, isolated sections, and routine inspections for pressure fluctuations. Packing lines avoid soft-seal materials—many commodity gasket materials break down rapidly under even trace HBr exposure. For transport, DOT and IMDG limits shape everything from container choice to paperwork. Regular drills keep emergency teams sharp, because a pinhole leak of SOBr2 can create a localized hazard in seconds.

    Waste treatment is another ongoing theme. The conversion processes on-site produce offgassed SO2 and HCl; both are neutralized through well-maintained scrubbers connecting to either sulfur cycle recovery or neutralization beds. On a regional level, our emission checks go hand-in-hand with local air and water standards, and we train all personnel to handle accidental releases or residue neutralization without waiting for outside help. The value of thionyl bromide comes only when the environmental costs are managed, not simply exported to the next link in the chain.

    Differences from Related Products

    Thionyl bromide or SOBr2 draws strongest comparison to thionyl chloride (SOCl2) and phosphorus tribromide (PBr3). From a manufacturing perspective, thionyl bromide is more demanding in storage. It’s less stable, more likely to degrade if even a trace of water enters storage tanks. Thionyl chloride can sit comfortably longer, and is easier to transport at ambient storage, so it remains the first go-to in bulk acylation and chlorination steps.

    As for phosphorus tribromide, controls on phosphorus procurement and downstream residue disposal make it a trickier fit for some plants—particularly where regulations tighten around heavy element waste. Thionyl bromide provides a workaround, especially in advanced materials and fine chemical labs set up for scrubbing and recycling sulfur oxides. Another comparative difference arises in the reactivity profile: whereas PBr3 can be harsher on labile substrates and produces a more complex mixture of byproducts, thionyl bromide produces two main gaseous side streams, making both capture and environmental management more straightforward—for those with the right infrastructure.

    Price-wise, thionyl chloride still sits cheaper thanks to larger global demand and mature production technology. Thionyl bromide’s market remains small: dedicated to educated buyers willing to pay for a compound that delivers specific technical benefits in niche downstream reactions. For those converting sensitive starting materials, minor price premiums often get repaid by higher yields, faster workups, and clearer downstream isolation.

    The Future for Thionyl Bromide Operators and Users

    Every year, something new shakes up the specialty reagent world—more stringent laws, updates to transport codes, or even a new academic method catching fire that sends buyers scrambling for uncommon halides. We don’t expect thionyl bromide to ever displace larger players like thionyl chloride, but we see its niche cemented by need for selectivity and unique byproduct handling.

    Feedback loops matter: we listen to clients not just at order, but after each run—an odd impurity in an NMR readout, an unusual color shift, a question about a drum valve spec. Eleven times out of ten, it’s not about the textbook chemistry, but about dealing with the realities of rust filters, dry room fails, or handling errors. Pros in this industry share details, not to split hairs, but because we all want reliability day after day. This communication drives constant small upgrades in our protocols and, sometimes, in the design of the product packaging itself.

    We’ve seen growth not only from academic labs but from emerging tech companies pushing organobromine building blocks into new OLED displays, advanced polymers, and next-generation batteries. Old application manuals sometimes lag far behind what’s happening at the workbench. It’s not unusual for a customer with a good idea to redefine the limits of yield, speed, or purity possible from a classic tool.

    As the global market matures, questions around supply chain transparency, ESG reporting, and safety will only grow more pointed. Reputable manufacturers get ahead of these changes, sharing data on impurity profiles, batch traceability, energy usage, and emissions right down to the barcode. For thionyl bromide, with its toxicity and reactivity, this isn’t window dressing but the core of what separates a trusted supplier from a risk.

    Moving Forward with Experience

    Working with thionyl bromide requires a blend of rigor learned from years in heavy industry, precision in process control, and active curiosity to adapt as needs shift. Our shop continues to maintain direct technical support for users with demanding protocols, and we invest in staff who know the rhythms of this product from decades on the floor. Whether it’s fielding a late-night panic call about a leaky valve or troubleshooting a puzzling impurity, the foundation of trust comes from the long hours spent making sure every tank, every analysis, and every seal earns its mark.

    The evolution of thionyl bromide usage keeps us on our toes, pushing for better technical solutions in containment, analytics, and collaborative R&D. Production looks more digital, regulations demand ever-tighter records, and markets weave closer as industries globalize. But production experience still matters, and buyers in the know seek out manufacturers who carry their scars as well as their successes, and who don’t shy away from hands-on support beyond the delivery dock. For those seeking a partner in thionyl bromide who understands both its chemical temperament and the industrial realities behind every bottle, shared experience becomes the real value every time.