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4-Bromophenyl Isothiocyanate

    • Product Name 4-Bromophenyl Isothiocyanate
    • Alias 4-Bromophenyl isothiocyanate
    • Einecs 249-681-8
    • 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

    304827

    Chemical Name 4-Bromophenyl Isothiocyanate
    Synonyms 1-Isothiocyanato-4-bromobenzene
    Molecular Formula C7H4BrNS
    Molecular Weight 214.08 g/mol
    Cas Number 3419-98-3
    Appearance Light yellow to brown solid
    Melting Point 62-64 °C
    Boiling Point 285 °C
    Density 1.68 g/cm³
    Solubility Insoluble in water; soluble in organic solvents
    Storage Conditions Store in a cool, dry, well-ventilated place
    Purity Typically ≥ 97%

    As an accredited 4-Bromophenyl Isothiocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 4-Bromophenyl Isothiocyanate; features hazard labels, screw cap, and product information label.
    Shipping 4-Bromophenyl Isothiocyanate is shipped in tightly sealed containers, protected from moisture and light. It is classified as a hazardous material, requiring compliant packaging and clear labeling. Transport should comply with relevant regulations (such as DOT, IATA, IMDG), ensuring safety and preventing leaks or contamination during handling and shipping.
    Storage 4-Bromophenyl Isothiocyanate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area. Keep it away from sources of moisture, heat, and incompatible substances such as strong acids, bases, and oxidizers. Store under inert atmosphere if possible, and protect from light. Always follow appropriate safety protocols and label containers clearly to avoid accidental misuse or exposure.
    Application of 4-Bromophenyl Isothiocyanate

    Applications of 4-Bromophenyl Isothiocyanate in Industrial Manufacturing

    4-Bromophenyl Isothiocyanate serves as a critical intermediate in advanced chemical synthesis. Our manufacturing partners use this compound throughout specialized downstream sectors, each requiring precise handling, accurate formulation ratios, and strict regulatory adherence from initial processing to finished end products.

    1. Pharmaceutical Intermediate Synthesis

    Major pharmaceutical manufacturers rely on this compound for constructing isothiocyanate-functionalized building blocks, especially in targeted oncology and CNS research pipelines. Formulators introduce it during heterocycle assembly, allowing the attachment of brominated aromatic motifs essential in kinase inhibitor and receptor ligand scaffolds, following multi-step GMP syntheses that demand phase-appropriate documentation and validated analytical protocols.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directives (EudraLex, Vol 4)
    • Pharmacopoeial monographs (USP <467>, Ph. Eur. 2.4.24 Isothiocyanates)
    • FDA 21 CFR Part 211 requirements for process control and impurity profiling

    Typical usage ratio

    • 1.0–2.5 molar equivalents relative to nucleophilic amine or thiol functional groups, depending on target molecule complexity and desired purity

    Downstream process integration

    • Enters at Stage II or III for direct amine isothiocyanation, followed by purification (chromatography or crystallization), and analytical release testing for residual isothiocyanate content

    Final product types

    • Small molecule kinase inhibitors
    • Brominated sulfonylureas for diabetes therapy R&D
    • CNS-active pyrazolyl derivatives
    • Antibacterial β-lactam conjugates

    2. Agrochemical Active Ingredient Synthesis

    Leading crop protection firms apply this compound in the thiocarbamoylation of aromatic amines to design selective herbicides and insecticide intermediates. The aryl-bromine group provides reliable points of late-stage functionalization, supporting downstream derivatization steps under controlled environmental compliance protocols. Batch sizes scale accordingly, with precise stoichiometry maintained to guarantee field performance and regulatory acceptance.

    Industry compliance standards

    • FAO & WHO Technical Specifications for Plant Protection Products
    • REACH Annex VII-VIII Registration (EC 1907/2006)
    • OECD Guidelines for the Testing of Chemicals
    • ISO 9001:2015 Certified Quality Systems

    Typical usage ratio

    • 0.9–1.3 equivalents per aromatic amine core, with minor variation for optimizing yield or minimizing unreacted isothiocyanate residues

    Downstream process integration

    • Introduced directly before cyclization or oxidation in API (active ingredient) formation; residual monitoring performed during solvent exchange and washing steps

    Final product types

    • Selective pre-emergence herbicide intermediates
    • Pyrazole-based insecticide platforms
    • Aromatic carbamate fungicides
    • Field trial seed treatment molecules

    3. Development of Specialty Polymers for Material Science

    Advanced materials research teams use this compound in aryl isothiocyanate functionalization of specialty polymers. Reacting under controlled solvent and temperature conditions, 4-Bromophenyl Isothiocyanate introduces UV-responsive or flame-retardant groups at specific backbone positions, tailored for niche electronics insulation or precision optics matrices while achieving consistent repeatability and required migration limits set by industrial standards.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) regarding restricted substances
    • UL 94 flammability standard for plastics
    • IEC 61249-2-21 for halogen content in base materials
    • ASTM D4066 for labeling and identification of plastics

    Typical usage ratio

    • 2–7% by weight in polymerization feed, with adjustments based on desired grafting density and target mechanical properties

    Downstream process integration

    • Fed into continuous stirred tank reactors post-monomer addition; inline IR and NMR used to verify functional group conversion before extrusion or casting

    Final product types

    • UV-resistant circuit board coatings
    • Halogenated flame-retardant engineering plastics
    • Photo-patternable resins for microfabrication
    • Precision optic matrix polymers

    4. Fine Chemical Synthesis for Analytical and Diagnostic Reagents

    Chemical producers specializing in laboratory diagnostics utilize this compound in assembling custom aryl isothiocyanate tags for protein and peptide labeling reagents. Manufacturers establish tight batch traceability and employ high-purity grades to ensure minimal background in downstream LC-MS and immunoassay protocols. Synthesis under cleanroom or controlled environment prevents contamination and preserves labeling efficiency.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for Medical Devices
    • EN ISO 10993-18:2020 for chemical characterization of medical devices
    • Good Laboratory Practice (GLP, OECD Principle)
    • Custom QC protocols for analytical reagent grade chemicals

    Typical usage ratio

    • 2–5 molar equivalents relative to amine or thiol groups in protein substrates, calculated to achieve high labeling efficiency with minimal unreacted compound

    Downstream process integration

    • Added to buffered protein/peptide solutions during conjugation phase; excess removed by ultrafiltration or chromatography; QC release includes HPLC purity and MS-based identity confirmation

    Final product types

    • LC-MS peptide labeling kits
    • Fluorescent or biotin isothiocyanate probes
    • Immunoassay derivatization reagents
    • Custom isothiocyanate-tagged standard references

    5. Active Agent Synthesis for Liquid Crystal Displays

    Producers in the liquid crystal and display sector incorporate this raw material during side-chain modification of mesogenic cores. The inclusion supports electro-optical tuning and thermal stability patching, offering downstream integrators reliable transition temperatures and compatible processing for advanced TFT-LCD and OLED display matrices. Strict purity and trace-level contaminant controls form an essential part of our deliveries to this sector.

    Industry compliance standards

    • IEC 60747 for semiconductor device materials
    • Japan Electronic Information Technology Association (JEITA) LCD Material Standards
    • ISO 9001:2015 Quality Assurance for Electronic Components
    • In-house SOPs for trace contaminant limits

    Typical usage ratio

    • 0.5–1.8 equivalents per mesogenic building block, adjusted according to electro-optic performance targets and viscosity control during product formulation

    Downstream process integration

    • Used in precursor functionalization prior to oligomerization or polymer alignment processes; purity optimized to prevent display haze and aging artifacts

    Final product types

    • High-transmittance liquid crystal mixtures
    • Temperature-stable TFT display media
    • Specialty alignment layers for OLEDs
    • Advanced switching and modulation agents

    6. Synthesis of S-aryl Thiourea Catalysts for Organic Process Catalysis

    Catalyst manufacturers deploy this compound for synthesizing S-aryl thioureas, which act as key ligands in asymmetric catalysis. Typically, chemists introduce it during nucleophilic substitution on sulfur or nitrogen centers, followed by complexation with transition metals. This route enables control over stereoselectivity for downstream pharmaceutical and fine chemical transformations, supported by batch records and strict material compatibility reviews.

    Industry compliance standards

    • ISO 17025:2017 for calibration and testing of catalyst materials
    • GHS/CLP labeling compliance for laboratory and pilot-scale production
    • REACH Substance Registration relevant to catalyst precursors
    • Technical Data Review in process validation protocols

    Typical usage ratio

    • 1.0 equivalent per thiourea or amine functional group; specific ratio alters based on desired ligand density and application in target catalysis

    Downstream process integration

    • Reacted with precursor amines or thiols at controlled temperature and pH; final complexes purified and tested for catalytic activity and metal content

    Final product types

    • Chiral thiourea-based organocatalysts
    • Transition-metal coordination complexes
    • Batch-scale asymmetric synthesis agents
    • Research-grade catalytic process tools
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    Certification & Compliance
    More Introduction

    4-Bromophenyl Isothiocyanate: Direct from the Production Floor

    An Introduction Rooted in Experience

    At our plant, every batch of 4-Bromophenyl Isothiocyanate runs through stainless reactors under the careful watch of technicians who know the subtle cues that separate a clean, consistent product from a batch plagued by side reactions. We built our current process on years of trial, steady refinement, and the plain fact that even a small impurity can throw off a downstream reaction in anyone's lab. This is not a product that can be pushed without respect for the chemistry and applications that demand high purity.

    Understanding the Product: Structure, Identity, and Form

    4-Bromophenyl Isothiocyanate stands out among isothiocyanates for its distinctive aromatic profile—driven in large part by the presence of a para-positioned bromine substituent. Our output, labeled by its batch and date, emerges in the pale-yellow crystalline form expected by professionals who need visual confirmation of a legitimate product. The compound’s molecular weight and melting point help confirm its identity for any chemist running simple QC before moving on to more sensitive analysis.

    What Experience Teaches About Isothiocyanate Production

    Anyone who’s spent days scrubbing glassware after a sticky, sulfur-laden run knows why tightening process controls matters. Hydrogen sulfide off-gassing, exothermic spikes, and even the subtle fluctuations in pH during aqueous work-up stage all leave a mark if ignored. We’ve learned to watch for fine variations in agitator speed, material feed rates, and temperature ramps to minimize unwanted by-products—especially the formation of troublesome bis-thiocyanates.

    Strict in-house chromatography calibrations keep us honest about what’s really leaving the post-recrystallization tanks. By sticking with proven methods, such as selective extraction and drying procedures, we consistently narrow down side contaminants even when minor, unexpected shifts in our starting brominated anilines try to sneak in. That’s how we maintain the high-purity lots customers expect.

    Model, Presentation, and Handling

    We ship 4-Bromophenyl Isothiocyanate in sealed glass containers layered with inert gas. Before filling, we run each container through a dedicated vacuum line so that trace moisture can’t degrade the isothiocyanate functional group. The product, typically denoted as Model-4BPI-alpha in our facility, leaves room for traceability and discussion: each model reflects a slight shift based on upstream feedstock and purification throughput.

    Shelf-life concerns come straight from real-world lab observations. Overexposure of isothiocyanates to air, especially humid environments, leads to hydrolysis and a gradual decline in reactivity. Those who’ve watched old stocks lose their potency appreciate the benefit of fresh, well-packaged material delivered in compact, manageable lots suited for immediate use.

    Intended Uses: Chemical Toolbox in Action

    In pharmaceutical and agrochemical industries, 4-Bromophenyl Isothiocyanate acts as a reliable intermediate in the synthesis of biologically active molecules. Medicinal chemists draw on it when assembling complex heterocycles or introducing functional groups onto aromatic systems. We’ve worked alongside researchers optimizing routes for kinase inhibitors and crop-protection agents, where minor variations in purity sometimes mean the difference between a successful multi-step synthesis and repeated, frustrating failures.

    Material scientists take advantage of its reactivity during conjugation chemistry, especially in the development of specialty polymers or surface modification of nanomaterials. Our experience handling both milligram and kilogram scaleups helps clients who start with exploratory studies and move into pilot runs: the product’s batch-to-batch repeatability means fewer surprises during late-stage development.

    Comparing to Other Isothiocyanates and Substituted Anilines

    Talks with clients and internal R&D chemists often center on why brominated versions like this one get the nod over simple phenyl isothiocyanates. The answer sits in the balance between steric hindrance and electronic effects brought in by the para-bromine—a key edge in regioselective transformations and fine-tuning biological properties downstream. From a production standpoint, crystalline separation differs from the rapid oiling-out behavior seen with more volatile, unsubstituted isothiocyanates.

    Handling safety improves over more reactive alkyl isothiocyanates, which off-gas aggressively and call for fume hoods working overtime. The aromatic system stabilizes the molecule, providing a longer practical window for manipulation at the bench. Chromatographic purification runs cleaner, less prone to tailing, because the bromine influences polarity and facilitates detection.

    Practical Differences: Beyond the Data Sheet

    Real differences show up not just in the numbers but in the workflow. Pure phenyl isothiocyanate generates headaches in poorly vented labs, while the 4-bromo version proves easier to handle, stowing with less risk of evaporation loss. Laboratories frustrated with the mess of isothiocyanate polymerization and byproduct formation appreciate a solid product that holds form throughout routine manipulations.

    Our process technicians point out that even minor process tweaks—like the timing of base addition or the decision to use continuous rather than batch extraction—subtly influence the ease of downstream purification. Consistent feedback shaped our purification protocol, where we prioritize vigorous, multi-stage washing and mechanical drying to eliminate residual amines and sulfur-based impurities. The large-scale reactors remain tuned for each run, matching solvent ratios not just to comply with written SOPs but in response to the accumulated observational wisdom in our teams.

    Quality Considerations: Consistency through Every Batch

    Experienced chemists no longer trust certificates alone. They run quick-thin layer chromatography plates or check melting points, expecting suppliers to match performance with what’s delivered on paper. Our commitment is to provide transparent batch histories and rapid response to any out-of-spec findings. Product batches that don’t meet our internal standards get rejected outright rather than passed down the chain—a discipline learned from years watching how minor slippage in quality multiplies headaches for complex synthesis.

    We keep spare reference samples from every batch, ready for rerun analysis or further method validation, preserving full traceability. Our approach mirrors simple honesty: let the product speak for itself at the bench, not just in the paperwork.

    The Market and Application Landscape

    Surges in demand for brominated isothiocyanates trace directly to real-world application trends. A jump in pharmaceutical lead optimization programs means more hands reaching for versatile intermediates that tolerate harsh conditions and enable straightforward functionalization. The material also reflects broader shifts toward greener, more atom-economical transformations, as regulatory pressure encourages leaving out hazardous heavy-metals and excessive reagents.

    Process chemists favor this intermediate as it steps easily into palladium-catalyzed cross-couplings, giving new routes to heterocycles once considered difficult and low-yielding. Research groups focusing on SAR (structure-activity relationship) studies come back repeatedly because they know what they’re getting in each shipment—consistency that lets them focus on the chemistry, not batch troubleshooting.

    Handling Hazards, Mitigation, and Real-World Practices

    Chronic exposure to even aromatic isothiocyanates can irritate skin and lungs. Our process lines run closed wherever possible, with air-scrubbing systems catching vented vapors. Training means more than box-checking—every operator understands routes of exposure and keeps spill kits, neutralizing bases, and absorbents within reach of every processing area. The urgency here doesn’t come from safety memos; it stems from real-world incidents where a slow response cost valuable product and time.

    By partnering with research teams both onsite and at end-user facilities, we learn where practical improvements can be made, from switching personal protective equipment standards to adopting packed-column ventilation on smaller pilot reactors. We regularly consult occupation health experts to keep our standards in line with the latest recommendations, adapting protocols every time we see a credible practice that further cuts down exposure risk.

    Supply Chain Insights: From Raw Materials to Final Packaging

    Any delay in receiving high-purity 4-bromoaniline ripples through our schedule. To hedge against quality drops and market hiccups, we split sourcing among vetted partners and build in regular in-coming checks. We don’t just inspect for assay: each drum undergoes side-by-side assessment against historical samples, catching subtle color or odor drifts that tell us something shifted upstream. These lessons, learned through years of inconsistent supply, drive us to keep buffer stock and tight communication with our resin and solvent vendors.

    At the packing station, technicians take pride in hand-inspecting every vessel before shipping. Labels matching batch traceability codes, secondary containment in sturdy cartons, and rigid standards for shipment splits deliver peace of mind for recipients. We accept only shipping partners with a proven record for temperature and shock control, especially for international deliveries.

    What Sets Us Apart: Confidence in Practical Application

    Direct manufacturer involvement brings benefits no spreadsheet or catalog can substitute. We work shoulder-to-shoulder with researchers scaling bench discoveries to the pilot plant, tracking every hiccup and breakthrough in real time. Our staff, from chemical engineers maintaining reaction systems to packaging crews clamping the last case, know that consistency matters as much as paperwork. This real-world grounding, married to advanced production controls, means the 4-Bromophenyl Isothiocyanate we ship today stands up to rigorous use tomorrow.

    Every query—whether from a major pharmaceutical lab or a university team running new probe molecules—gets the attention borne from understanding how real deadlines, not sales targets, drive progress. We pick up lessons from every discussion and build them into our production and logistics approach.

    Challenges and Learning from Industry Trends

    Supply chain agility faces constant pressure from shifting regulations on hazardous materials and environmental performance. We watch updates on international transport rules, carbonate-free solvent mandates, and new limits on waste effluent. Adaptation means redesigning extraction protocols, testing biodegradable solvents, and reworking purification steps to align with future compliance demands. This ongoing investment in process change protects not just our staff and neighbors, but our clients’ own regulatory positions, keeping everyone a few steps ahead.

    We’ve adopted digital tracking for every container, integrating it directly with our inventory and fulfillment systems. If a client reports an odd analytical result, we trace back instantly to root out possible sources—be it a slip in raw material quality or a need for process calibration. This visibility ensures customers never face the black-box frustration of unaccountable third-party trading.

    Supporting Research and Development

    By working closely with research groups, we often hear about new coupling strategies or reaction cascades that put 4-Bromophenyl Isothiocyanate at the heart of emerging synthetic ventures. Meeting these requests sometimes means tweaking our purification approach or scaling up with tailored timelines. We listen for specific needs: minimal residue, defined particle size, special packing formats, and rapid despatch for time-critical discoveries.

    We field questions that run beyond shipping and purity, including solvent compatibility and long-term storage behavior. These interactions highlight the practical knowledge our teams carry, earned over years of hands-on troubleshooting. Clients come back when they know they’re heard—and when their suggestions get folded into the next production run.

    Concluding Insights: The Manufacturer’s Perspective

    On any given day, tanks bubble and columns run at full tilt to keep pace with project timelines. Maintaining direct control over the entire process means we don’t dodge responsibility or cut corners. We build everything on a foundation of respect for the people trusting what comes out of our loading dock, blending operational discipline with a willingness to listen.

    In the hands of research scientists, medicinal chemists, or industrial teams exploring greener syntheses, 4-Bromophenyl Isothiocyanate from our own production lines represents more than just a commodity—it’s a tool fine-tuned by continuous feedback. Years of accumulated observations, daily process optimizations, and a steady refusal to compromise on quality blend together in every lot. Whatever the application, we make sure each batch starts from genuine understanding and lands on the workbench ready for ambitious chemistry.