Products

2-Bromobenzoyl Chloride

    • Product Name: 2-Bromobenzoyl Chloride
    • Alias: 2-Bromobenzoyl chloride
    • Einecs: 209-103-6
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications

    HS Code

    448171

    Chemical Name 2-Bromobenzoyl Chloride
    Cas Number 4219-73-4
    Molecular Formula C7H4BrClO
    Molecular Weight 219.46 g/mol
    Appearance Colorless to pale yellow liquid
    Melting Point -2 °C
    Boiling Point 252 °C
    Density 1.6 g/cm³
    Purity Typically ≥98%
    Solubility Reacts with water, soluble in organic solvents
    Refractive Index 1.604
    Smiles C1=CC=CC(=C1C(=O)Cl)Br

    As an accredited 2-Bromobenzoyl Chloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 2-Bromobenzoyl Chloride, 25g, is supplied in a tightly sealed amber glass bottle with a hazard label and safety cap.
    Shipping **Shipping for 2-Bromobenzoyl Chloride**: 2-Bromobenzoyl chloride is shipped in tightly sealed, corrosion-resistant containers to prevent moisture and air exposure. It is classified as a hazardous material and must be transported according to international regulations, with appropriate labeling and documentation, ensuring safe handling and compliance with all chemical shipping standards.
    Storage 2-Bromobenzoyl chloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat sources, and incompatible substances such as strong bases, alcohols, and oxidizers. Protect from light and avoid exposure to atmospheric humidity, as it is moisture sensitive and may decompose, releasing corrosive fumes. Always use appropriate personal protective equipment when handling.
    Application of 2-Bromobenzoyl Chloride

    Applications of 2-Bromobenzoyl Chloride in Industrial Manufacturing

    2-Bromobenzoyl chloride serves as a critical intermediate in multiple specialized sectors, playing a role in processes that demand high precision, strict regulatory adherence, and functional performance in end-use products. As a direct manufacturer, we support customers in regulated and performance-driven industries with consistent material quality and reliable technical support tailored to each downstream application.

    1. Pharmaceutical API Synthesis

    Our material is widely used in the synthesis of active pharmaceutical ingredients that incorporate halogenated benzoyl groups, such as anxiolytics and anti-inflammatory agents. Downstream integration typically leverages the acyl chloride as a key building block in Friedel–Crafts acylation and amidation reactions for custom molecules. Purity and traceability remain paramount, as minor deviations could compromise process yields or final API purity.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (for finished pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) Monographs for chemical intermediates
    • Chinese Pharmacopoeia standards for registration-grade intermediates

    Typical usage ratio

    • Used at 1.0–1.5 molar equivalents relative to substrate nucleophile; exact ratio depends on downstream impurity control and molecular design

    Downstream process integration

    • Introduced during early- or mid-stage API batch synthesis as the acylating agent in acylation/amidation of aromatic compounds or amine-functionalized substrates

    Final product types

    • Active pharmaceutical ingredients for anti-inflammatory, anti-anxiety, and central nervous system medications
    • Regulatory-compliant pharmaceutical intermediates shipped for contract synthesis

    2. Agrochemical Intermediate Manufacturing

    The material finds consistent use as an intermediate in synthetic processes for selected herbicide and fungicide molecules incorporating aromatic bromide moieties. Agricultural chemical manufacturers source it for complex coupling or substitution steps, which require stable halogenated intermediates to meet field application requirements. Trace metal and residual moisture must consistently fall below specified thresholds to avoid batch rejections during scale-up.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH Regulation (EC 1907/2006) registration for intermediates
    • OECD Principles of Good Laboratory Practice (GLP) for agrochemical R&D

    Typical usage ratio

    • Employed at 0.9–1.2 equivalents per reaction step, depending on downstream conversion rates and manufacturing scale; formulation adjustments are made based on yield and process kinetic studies

    Downstream process integration

    • Added as a core building block during aromatic ring functionalization or halogenation phases within industrial-scale multi-step synthesis

    Final product types

    • Finished pesticide active ingredients such as brominated benzoic acid derivatives
    • Protected intermediates used in custom synthesis of fungicides and herbicides

    3. Specialty Organic Pigments and Dyes

    In pigment and dye manufacturing, this intermediate enables the introduction of specific brominated aromatic structures facilitating desired shade, lightfastness, and solubility properties in colorant systems. Dye producers often use it in acylation steps that define the aromatic backbone of pigment dispersions for industrial textile and plastics applications. High-purity, low-halide grades are critical, as off-spec residues can affect chroma and end-use compliance.

    Industry compliance standards

    • Standard Methods for the Examination of Water and Wastewater—AATCC for textile dyes
    • Global Organic Textile Standard (GOTS) for textile chemicals
    • ISO 9001:2015 and 14001:2015 for pigment and dye production
    • EU REACH SVHC requirements for pigment components

    Typical usage ratio

    • Added at 1.0 equivalent per aromatic amine or hydroxyl reactant, with slight excess (1.05 equivalents) for high-yield colorant syntheses

    Downstream process integration

    • Dosed directly during aromatic ring acylation or as part of pigment condensation, prior to final hydrolysis or azo coupling steps

    Final product types

    • Organic pigment dispersions for high-performance plastics and coatings
    • Reactive and acid dyes for textile fiber coloration

    4. Liquid Crystal Material Synthesis

    Producers of liquid crystal materials use the compound in forming key mesogen precursors bearing brominated benzoyl segments, which influence the electro-optical properties in display applications. Strict control of residual halide and purity profile remains mandatory to ensure the molecular uniformity required for nematic and smectic phase stability. Upstream monitoring of reaction and post-synthetic purification are major focus areas prior to formulation.

    Industry compliance standards

    • ISO 9001:2015 and ISO 14001:2015 certification for materials manufacturing
    • RoHS (Restriction of Hazardous Substances Directive) for electronic industry usage
    • IEC 61249-2-21 for halogen content in electronic materials
    • JIS C 0950 for display and electronic device chemicals

    Typical usage ratio

    • Dosed at 0.95–1.1 equivalents in mesogen precursor synthesis; the ratio is optimized for structure-retention versus process yield during oligomerization

    Downstream process integration

    • Input as a halogenated acyl unit during first- or second-step condensation in the manufacturing of nematic or discotic liquid crystal building blocks

    Final product types

    • Liquid crystal compounds for LCD and OLED display panels
    • Polymer-stabilized liquid crystal blends

    5. Aroma & Fragrance Ingredient Development

    Fine chemical companies employ this compound for the design of specialty aroma intermediates containing brominated benzoyl groups. Controlled acylation allows for the creation of molecules with defined olfactory profiles or for use as protective groups in complex fragrance ingredient synthesis. Final composition and purity are tuned according to IFRA and allergen regulatory thresholds.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards and Safety Guidelines
    • EU Regulation No 1223/2009 for cosmetic ingredient safety
    • HACCP (Hazard Analysis and Critical Control Points) system for fragrance manufacturing
    • ISO 9001:2015 for flavor and fragrance ingredient processing

    Typical usage ratio

    • Applied at 1.0–1.2 equivalents for aromatic acylation steps within fragrance intermediates synthesis; minor excess may be used to drive full substrate conversion

    Downstream process integration

    • Introduced in initial synthetic routes to acylate aromatic cores during multi-step production of high-purity fragrance ingredients

    Final product types

    • Brominated aromatic intermediates for further modification into fragrance accords
    • Finished minor note components for fine fragrances and specialty aroma products

    Free Quote

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    Certification & Compliance
    More Introduction

    2-Bromobenzoyl Chloride: An Experienced Perspective from the Manufacturer

    Meeting Demand for 2-Bromobenzoyl Chloride

    Over the years, we have seen the demand for 2-Bromobenzoyl Chloride continue to expand among our pharmaceutical, agrochemical, and specialty chemical customers. The model we produce comes with a purity consistently above 98%. Strict quality control, reliable supply, and stable product performance matter most to those who use this compound as a building block in their processes.

    The Chemical’s Identity: Structure and Relevance

    2-Bromobenzoyl Chloride, with the molecular formula C7H4BrClO, is a benzoyl chloride substituted with bromine at the ortho position. The presence of both bromine and the acid chloride functional group offers versatility for several kinds of chemical transformations. The chlorine increases reactivity, which makes it easier to introduce the 2-bromobenzoyl motif onto different molecules. This property gets the attention of pharmaceutical and fine-chemical manufacturers aiming for specific substitution patterns not always achievable using plain benzoyl chloride.

    Comparing with Other Benzoyl Chlorides

    Some ask why choose 2-Bromobenzoyl Chloride when alternatives like plain benzoyl chloride or 4-bromobenzoyl chloride are on the market. Direct experience shows that the ortho-bromine position makes a clear difference in reactivity and selectivity. For example, in cross-coupling or Friedel-Crafts reactions, the effect of ortho substitution can steer reactions toward otherwise difficult targets, opening doors not just for pharmaceuticals but also for custom-made materials. Using the correct regioisomer is not a formality; it changes process yields and downstream purification work.

    Every chemist working with these derivatives will notice the reactivity shifts with the bromine placement. The ortho isomer brings electronic and steric factors into play, altering reaction speeds and sometimes improving the final product's properties, like crystallinity or solubility. From years of batch records and customer feedback, the ortho compound's unique attributes have proven indispensable in synthesizing complex intermediates and active compounds. This is why production experience and monitoring isomers at the purity level others often overlook deliver tangible value to the end user.

    Specification Details: What Matters Most

    We control purity above 98%, with moisture and acidic impurities below thresholds that might otherwise interfere with downstream reactions. Our process delivers a white to light beige crystalline powder, stored and shipped in air-tight containers to minimize hydrolysis. Analytical confirmation uses GC, NMR, and titration. Impurity profiles inform every batch, not just at lot release, because we know that even small batch variations can alter reaction success rates for our customers.

    Physical consistency affects chemistry. Fine, uniform crystals pour smoothly and dissolve more readily, so we pay attention to particle size during final packaging. These tiny yet practical details come from decades of tuning our manufacturing steps to suit large-scale and research customers alike. The reason we never just tick purity boxes: successful downstream chemistry is the ultimate validator.

    Uses: Why 2-Bromobenzoyl Chloride Counts

    Our customers use 2-Bromobenzoyl Chloride to build active pharmaceutical ingredients, synthesize agrochemical actives, and create advanced specialty polymers. In pharmaceutical chemistry, the ortho-bromo motif often forms the core of antibacterial, antifungal, or anti-inflammatory compounds. When a process requires halogenated aromatic acid chlorides, this product serves as a trusted intermediate. Its function as an acylation agent—joining with amines or alcohols to make amides and esters—plays a foundational role in these syntheses.

    At the same time, in agrochemical research, many herbicides and insecticides begin with a halobenzoyl chloride scaffold. Agrochemical development cycles get faster and cheaper when intermediates arrive at specified ratios and in reliable containers. Downstream reactions tend to be exothermic; so minimizing unknown impurities isn't a theoretical concern, it reduces product recalls and operator risk.

    Handling and Storage Insights from Daily Practice

    2-Bromobenzoyl Chloride reacts with water, releasing HCl. Moisture exposure is the most common cause for failed batches we hear about from end users. In our own plant, we transfer and pack the material under inert atmosphere. Regular leak checks, worker training, and air monitoring prevent exposure to hydrochloric acid fumes.

    Shipping the compound in steel-lined or high-density polyethylene containers, we see lower rates of hydrolytic decomposition. End users tend to get better performance when storing below 25℃ and resealing containers promptly. We do not cut corners with packaging. A seal left loose can spoil hundreds of kilos of material and disrupt research and production timelines by weeks. The number of technical support calls linked directly to mishandling dwarfs those about batch consistency.

    Critical Differences from Other Halogenated Benzoyl Chlorides

    Seeing the practical impact of ortho-bromination over years of manufacturing, it becomes clear this isomer stands apart from its para or meta-substituted relatives. Reactivity enhancement in coupling reactions, whether by Suzuki, Ullmann, or Buchwald-Hartwig processes, is not speculation. Customers consistently report higher yields when switching to the ortho compound for certain aromatic ring closures and cross-linking jobs. Some pharmaceutical actives with ring systems can only be built practically from this spatial arrangement of bromine.

    Further downstream, environmental and safety profiles shift when comparing 2-bromobenzoyl with chloro- or iodo-analogues. Bromine is less reactive than iodine, offering better thermal and storage stability. Compared to chlorine substitutions, bromine installation often assists with selectivity in functional group transformations and, in some cases, allows for easier downstream halogen removal. We have seen more labs move to brominated intermediates to balance regulatory constraints and synthetic ambitions. They seek dependable performance and regulatory documentation, both of which rest on solid production methods.

    Process Reliability: Bridging Lab Scale and Bulk Supply

    Over the past two decades, we have grown from supplying pilot batches to shipping multi-ton lots globally. This transition brought specific lessons. It’s one thing to scale a reaction; it’s another to ensure each drum behaves the same in end-use processes. Unintended trace byproducts, like ortho- and para-isomers or hydrolyzed species, show up in poorly controlled syntheses. These species can spoil reaction runs; a single percent off-standard disrupts chromatography and lowers finished product grades.

    Years of process tweaks make a difference, from the raw bromobenzene selection to in-line water monitoring and temperature-controlled distillation. It’s routine for us to run parallel batch analytics and only ship lots with identical impurity spectra. Customers in patent-protected markets need this, given the analytical scrutiny active intermediates undergo. No trader or small-scale operator can offer such depth of process control, and that is the dividing line between batch failures and high-yield production.

    Regulatory and Compliance Track Record

    Being a bulk manufacturer demands more than just technical know-how. Constant familiarization with REACH, TSCA, and regional chemical regulations affects not only our process documentation but also packaging and waste management. Whether our compound ends up in active pharmaceutical ingredients or in a regulated agricultural product, our audit record helps customers stay ahead of recalls and rejections.

    By maintaining registration files that match real production changes and keeping up transparent supply chain records, we sidestep issues others face when authorities request documentation or conduct site visits. Many customers return for our 2-Bromobenzoyl Chloride because a failed audit with an unregulated supplier costs more than any price discount.

    Supply Stability: Handling Market and Logistics Volatility

    Raw material volatility, such as shortages in high-purity bromobenzene or shipping disruptions from container delays, has become more common. Based on experience, there is no substitute for signed, multi-year offtake agreements with trusted upstream vendors. We have invested in buffer storage and local contract testing labs to minimize customs clearance and release times. In the past, plot delays in one part of the world forced some peers to halt shipments; our buffer policies removed this bottleneck.

    From pandemics to port strikes, lessons learned include building redundancy into everything: double-vendor procurement, local logistics partners, even duplicating critical lab equipment onsite. Sourcing and packaging happen in the same facility, cutting idle time and reducing delivery lead times. Our partners appreciate reduced waiting, and production lines avoid idle downtime.

    Purity Testing and Application-Specific Considerations

    In our in-house lab, verifying the presence and levels of diastereomers is not optional; pharmaceutical clients count on this for IND submissions. For less regulated markets, like specialty polymer synthesis, a small uptick in certain side-products might not affect performance, but we flag and report these anyway. Product consistency—batch to batch—means a lab working up a new synthetic route can plan with confidence.

    Feedback loops from customers, combined with our own sampling records, show that chemists building newer, functionalized aromatic compounds often use 2-Bromobenzoyl Chloride as a stepping stone toward structures that block metabolic oxidation or improve environmental stability in the finished molecule. Lab-to-industry scale-up support makes a difference, especially when switching from one isomer or halogen to another, as reaction kinetics and product isolation sometimes shift unexpectedly.

    Supporting Customers: Lessons from Real Experience

    Direct conversations with process R&D chemists and plant operators shape our improvement cycle. The biggest pain points—unexpected reactivity, incompatible solvents, breakdown from moisture, vial capping issues—get fixed through process adjustments or support documents. We routinely offer technical notes from our own process history, not just generic MSDS sheets, to help users adapt or troubleshoot protocols.

    Young researchers benefit when we share upstream and downstream reaction tips. Knowing how the product handles with various types of bases, which catalysts influence side reactions, or how solvent polarity affects reaction outcomes, can prevent months of trial-and-error. This know-how, built into each batch’s documentation, has shortened project lead times for research clients. For seasoned process chemists, receiving fully controlled analytical data—NMR, GC-MS, HPLC profiles—means they can qualify a batch quickly for plant use.

    Troubleshooting and Common Process Pitfalls

    2-Bromobenzoyl Chloride’s main vulnerabilities arise through unintended hydrolysis and by reaction with nucleophilic solvents. From our incident logs, most downstream waste and yield losses relate directly to improper storage—unsealed drums exposed to humid air, especially in tropical climates. Awareness of these issues motivates us to offer both small and bulk pack sizes, each tightly sealed and inerted.

    In practice, we recommend transferring only the required dose to a glovebox or dry room. Some users still try to sample this reactive acid chloride under atmospheric conditions, leading to hydrochloric acid evolution and crust forming at the drum neck. More failed runs in our customers’ plants stem from careless handling than from any inherent compound instability. Investing in operator training for the acid chloride group in general avoids expensive waste and downtime.

    Environmental and Safety Commitment

    Producers like us have a responsibility beyond batch yields or sales numbers. Our waste gas capture system, in use for years, cuts HCl venting to below local emission limits. Solvent recovery, acid-neutralizing effluent treatment, and real-time emissions monitoring check environmental risks before material ever reaches a drum. Safety standards follow globally recognized practices, and audits keep our team alert.

    By tracking all incoming and outgoing waste streams, we can verify compliance with downstream waste regulations for our clients. This attention to disposal and documentation helps not only in audits but also in long-term community relations. Our neighbors see the value in safe, responsible handling of halogenated intermediates, an area where less diligent suppliers sometimes cut corners.

    Customer Collaboration and Technical Support

    Beyond just supplying drums, our real-world insight comes into play solving issues at customer plants. For instance, when a Japanese pharmaceutical plant suffered low yields, we sent not just COAs but suggested process modifications based on our pilot work, which ended up boosting their reaction efficiency by nearly 15%. Open technical dialogue means customers move faster in their optimization, without hitting roadblocks on analytical problems or impurity troubleshooting.

    For those developing new custom chemicals, we often sign NDAs and help with route scouting using our compound. Our team has even recommended switching from other halogenated benzoyl chlorides to 2-bromo versions where laboratory data indicated clear kinetic or selectivity advantages. These partnerships build long-lasting trust, which is why much of our business now comes from referrals and repeat customers who value expertise over raw price.

    Future Trends in Benzoyl Chloride Derivatives

    Researchers are working on next-generation pharmaceuticals and crop protection molecules where fine control of the halogen pattern on the aromatic ring is required. In many of these synthetic campaigns, 2-Bromobenzoyl Chloride serves as a critical starting point. Fungicide and herbicide R&D efforts, in particular, have begun to demand more refined, high-purity acid chlorides, not only to meet regulatory standards, but also to boost product stability and environmental profiles. Similar trends are seen among polymer researchers who value the predictability and performance tied directly to our production consistency.

    Looking forward, our investment in capacity, automation, and analytical tech should meet growing demand for high-purity aromatic acid chlorides while keeping pace with increasingly strict regulation and new synthetic challenges. Throughout, our record shows that hands-on manufacturing knowledge, transparency, and customer-centric improvements write the story of success for any complex chemical intermediate in today’s competitive markets.

    Conclusion: Manufacturing Matters in 2-Bromobenzoyl Chloride Quality

    A well-made 2-Bromobenzoyl Chloride stands as the difference between a failed and a flawless batch run, a rejected and an approved intermediate, a plant running overtime and a project delivered ahead of schedule. The details—purity, isomer control, documentation, reliability in delivery—come from deep production know-how and daily hands-on management. No sales pitch or specification sheet can cover everything a batch must do in the field. Our history, learning, and technical investment drive us to set benchmarks in this field, building reliable pathways for our customers’ discoveries and products.

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