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4-Bromo-Thiobenzamide

    • Product Name 4-Bromo-Thiobenzamide
    • Alias 4-Bromo-Benzenecarbothioamide
    • Einecs 262-050-9
    • 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

    573275

    Product Name 4-Bromo-Thiobenzamide
    Cas Number 52207-77-3
    Molecular Formula C7H6BrNS
    Molecular Weight 216.10 g/mol
    Appearance Off-white to light brown solid
    Melting Point 132-135°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents like DMSO, DMF
    Storage Conditions Store in a cool, dry place and keep container tightly closed
    Iupac Name 4-bromobenzenecarbothioamide
    Smiles C1=CC(=CC=C1C(=S)N)Br
    Inchi InChI=1S/C7H6BrNS/c8-6-3-1-5(2-4-6)7(9)10/h1-4H,(H2,9,10)
    Synonyms p-Bromo-thiobenzamide

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

    Packing & Storage
    Packing The packaging for 4-Bromo-Thiobenzamide (5 grams) is a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping 4-Bromo-Thiobenzamide is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture exposure. It is transported according to local and international regulations for hazardous materials, ensuring appropriate labeling and documentation. Protective packaging and temperature control may be applied as required to maintain product stability and safety during transit.
    Storage 4-Bromo-Thiobenzamide should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from moisture, heat, and sources of ignition. It should be kept away from incompatible substances such as strong oxidizers. Properly label the container and ensure secondary containment to prevent spills. Use appropriate protective equipment when handling and avoid prolonged exposure.
    Application of 4-Bromo-Thiobenzamide

    Applications of 4-Bromo-Thiobenzamide in Industrial Manufacturing

    As a direct manufacturer of 4-Bromo-Thiobenzamide, we supply this key intermediate specifically processed for industries that demand high-purity, stable chemical building blocks for advanced molecular synthesis. The following application scenarios represent established, regulation-driven uses in downstream productions, each characterized by custom formulation standards, critical integration methods, and defined end-product classes.

    1. Pharmaceutical Intermediate for Thioamide-Linked Heterocycles

    Pharmaceutical companies employ 4-Bromo-Thiobenzamide primarily in the synthesis of thioamide-linked heterocyclic scaffolds, which serve as core molecular structures in drug development pipelines. Research and production facilities utilize its reactivity to introduce thioamide groups into target molecules, particularly for designing kinase inhibitors and anti-inflammatory agents, under strictly monitored cGMP environments to fulfill global regulatory requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II for APIs
    • United States Pharmacopeia (USP) relevant to intermediate handling
    • FDA's 21 CFR Part 210/211 for pharmaceutical production controls

    Typical usage ratio

    • In route-specific syntheses, 4-Bromo-Thiobenzamide typically represents 0.5–2.5 molar equivalents relative to the target compound’s core moiety; actual ratios depend on yield optimization for the heterocycle framework.

    Downstream process integration

    • Introduced during stepwise condensation or cyclization reactions under nitrogen atmosphere to minimize side-product formation, the compound enters after initial aromatic amine derivatization but before final functional-group transformations; batch records require full traceability per cGMP guidelines.

    Final product types

    • API intermediates for kinase inhibitors
    • Experimental anti-inflammatory agents
    • Preclinical lead compounds with thioamide core motifs
    • Heterocycle-based pharmaceutical candidates

    2. Agrochemical Synthesis: Sulfur-Containing Fungicide Intermediates

    In agrochemical manufacturing, the compound serves as a building block for the synthesis of sulfur-containing fungicides and crop protection agents. Process engineers value its functionality in generating thioamide-linked structures, essential for high-performance active substances applied in seed treatment or foliar spray formulations.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 for agrochemical production quality management
    • REACH Registration for chemical intermediates
    • GLP (Good Laboratory Practice) for residue and metabolism studies

    Typical usage ratio

    • Actively integrated at 0.8–3.0% by weight in multi-stage syntheses, with precise dosing automated via inline monitoring; concentration adjusted based on downstream thioamide yield and fungicidal activity data.

    Downstream process integration

    • Added post-halogenation, prior to final sulfonation or oxidative cyclization steps in process reactors; intermediate purity checked at each hold point per batch QC protocols required for crop protection registration dossiers.

    Final product types

    • Systemic seed-treatment fungicides (granules, powders)
    • Foliar sprayable active ingredient concentrates
    • Blended premix agrochemical intermediates for downstream formulators
    • Sulfur-bridged crop protection agent bases

    3. Specialty Dye Synthesis: Precursor for Sulfur-Modified Azo Dyes

    Manufacturers of high-performance dyes utilize this raw material in select routes where precise sulfur incorporation into aromatic rings is necessary. Its structure facilitates targeted bromination for precursor chains ultimately used in custom azo dye products, primarily for technical textiles with enhanced resistance profiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for harmful substance limits
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001 for textile chemical manufacturing
    • REACH compliance for aromatic and sulfur substances

    Typical usage ratio

    • Generally dosed between 1.2–4.0% by total precursor mass, with actual ratios determined by targeted sulfonic acid group content and color fastness parameters specific to the end-use textile application.

    Downstream process integration

    • Introduced during azo coupling reactions involving aromatic amines, the material enters after diazotization and before acid work-up, permitting controlled sulfur atom transfer onto the molecular backbone, followed by solvent-extraction and filtration for dye purification.

    Final product types

    • Sulfur-containing azo dyes for technical fabrics
    • Textile pigment dispersions with elevated wash-fastness
    • Custom colorant blends for automotive textiles
    • High-performance industrial coatings pigments

    4. Fine Chemical Synthesis for Laboratory Reagents

    Producers of analytical and research-grade reagents deploy this material to synthesize molecular probes, specialty ligands, and reference compounds where the presence of a bromo-thioamide moiety is critical for downstream performance in detection or binding studies. Chemists performing custom syntheses rely on its predictable reactivity and traceable purity for reproducibility in regulated laboratory environments.

    Industry compliance standards

    • ISO 17025 for calibration and testing chemicals
    • ACS Reagent Chemicals Purity Standards
    • Good Laboratory Practice (GLP) protocols for analytical products
    • EU CLP Regulation (EC) No 1272/2008 for chemical labeling and hazard communication

    Typical usage ratio

    • Synthesis batch protocols specify 0.5–2.0 mmol per target reference compound, based on stoichiometric requirements for probe construction; adjustments made for molar yield optimization and impurity minimization.

    Downstream process integration

    • Added at the nucleophilic substitution stage immediately following aromatic ring activation, under controlled temperature and solvent conditions, with sampling after each step for NMR and HPLC verification; finished reagent purified by recrystallization or chromatography before packaging.

    Final product types

    • Research-grade standard reference compounds
    • Specialty ligands for spectroscopic analysis
    • Molecular probes for diagnostic platform R&D
    • Benchmark intermediates for chromatography
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    Certification & Compliance
    More Introduction

    4-Bromo-Thiobenzamide: Product Introduction and Practical Insights from the Manufacturer

    Understanding 4-Bromo-Thiobenzamide from Our Manufacturing Perspective

    For years, our facility has worked closely with research institutions, fine chemical developers, and specialty synthesis teams to meet rising demand for precision reagents. Among our product line, 4-Bromo-Thiobenzamide stands out due to its unique chemical structure and the possibilities it unlocks for advanced molecular synthesis. Manufactured in tightly controlled conditions, this compound offers researchers and formulation experts a practical tool for building complexity and introducing sulfur functionality into aromatic systems, a capability not easily achieved with other similar reagents.

    Product Characteristics: What Makes 4-Bromo-Thiobenzamide Distinct

    Every batch leaves our reactors with a strict adherence to high-purity targets, ensuring consistency in subsequent applications. The molecular formula for 4-Bromo-Thiobenzamide, C7H6BrNS, defines a bromine atom positioned para to the thioamide group, artfully balancing electron-donating and withdrawing influences on the aromatic ring. This precise substitution pattern often dictates reaction outcomes, especially in cases where regioselectivity or fine-tuned reactivity are central to the end-user’s process.

    From our vantage point on the production floor, the most critical quality factors are the control of residual solvents and avoidance of isomeric by-products. Our purification steps include fractional crystallization, solvent selection guided by polarity profiles, and multiple filtration passes. By directly managing each input, our technicians minimize unwanted contaminants that can interfere with delicate ligand or scaffold construction downstream. The final material frequently appears as an off-white to light brown crystalline solid, reflecting minor batch-to-batch variation driven by raw material lots.

    Specifications that Matter: Real-World Considerations

    We analyze each lot using NMR, HPLC, and elemental analysis, not because regulators demand it, but because any deviation in purity (even below the usual 98% benchmark) can cause failed reactions and lost productivity for our loyal users. Melting point ranges are checked with every drum, normally sitting between 110 to 115 degrees Celsius. This isn’t a trivial routine—chemists in custom synthesis operations spot irregularities by matching observed melting points against our data, and quick feedback lets our QC team identify subtle shifts before shipments leave the warehouse.

    Our manufacturing process avoids phosgene-based chemistry, which eliminates a safety risk both on site and in spent waste. We take pride in the fact that each batch receives a COA fully verified by in-house staff who understand the responsibility that comes with supplying fine chemicals to quality-conscious sectors.

    Key Uses of 4-Bromo-Thiobenzamide: Practical Advice from Daily Operations

    Customers typically purchase this compound for two broad applications: as a starting point for medicinal chemistry screening libraries and for the synthesis of heterocyclic compounds bearing both bromide and thioamide groups. The compound’s double-site reactivity supports both nucleophilic substitutions and transition-metal-catalyzed couplings. In pharmaceutical R&D, we supply research-grade material that supports exploration into kinase inhibitors or sulfur-rich intermediates. In materials science, polymer chemists find value in using it as a precursor to conjugated molecules with custom optoelectronic properties.

    One thing we’ve noticed: due to the bromine atom at the para position, cross-coupling reactions, such as Suzuki or Sonogashira, proceed with remarkable efficiency. The thioamide functionality resists unwanted hydrolysis and oxidation under many standard reaction conditions. Users have shared feedback about consistent yields in routes where competing side-reactions caused by more labile sulfur chemistry would compromise output. Stability during handling is another important advantage. We pack the solid in double-layer polyethylene liners inside sealed drums to prevent moisture uptake, a detail that saves time and money for frequent users who don’t have climate-controlled storage environments.

    Comparing 4-Bromo-Thiobenzamide to Similar Aromatic Reagents

    Every manufacturer gets calls for “the closest alternative, but less expensive or easier to store.” We encourage users to compare closely with simple thiobenzamides or other bromo-substituted benzenes, but the presence of both the electron-withdrawing bromine and electron-rich thioamide makes this compound behave differently than either building block alone. Subtle as this point may seem, it shows up in yields, byproduct profiles, and even in the color or crystallinity of intermediates isolated during complex synthetic sequences.

    Bromobenzene itself offers no sulfur chemistry, and straight thiobenzamide derivatives are much less useful for cross-coupling. When someone attempts to substitute with ortho- or meta-brominated versions, purification becomes tougher due to the formation of regioisomers during reactions. We have worked through customer case studies where even a small change in ring substitution had cascade effects on downstream feasibility, from ligand construction to functional monomer synthesis.

    Another point comes from environmental safety: traditional thioamide syntheses sometimes rely on strong acidic conditions or sulfurization with high-pollution reagents. Our process uses less corrosive sulfur donors, a switch made after users in Europe and Japan pressed for lower waste codes and better reproducibility. Years ago we learned these lessons the hard way—poorly controlled sulfur chemistry contaminates downstream catalysts, which not only ruins expensive metal salts but also means extra cleaning costs for every piece of glassware or steel in the pilot plant.

    Meeting Research and Production Needs: Insights from the Field

    Teams that scale from gram to kilogram quantities want assurance that their process can grow with them. Large-batch reproducibility is not just a sales slogan. We have supported pilot runs for clients targeting 2-5 kg of final product per batch, and have witnessed the pitfalls that come with poor scalability—unexpected exotherms, interference from side-reactions, and batch-to-batch variability in assay.

    Stable supply depends on raw materials—not only in purity, but predictable freight and customs clearance. Brominated chemicals are sometimes flagged for special handling in many countries. Our shipping department works directly with regulatory teams to ensure rapid clearance and unrestricted flow, a lesson learned from several nearly-missed delivery deadlines that almost cost our customers precious development time.

    Handling and Storage: Manufacturer’s Best Practices

    4-Bromo-Thiobenzamide holds up well in standard laboratory storage over at least six months without appreciable degradation in purity. For users working in high humidity regions, we advise storing drums in sealed secondary containers and minimizing time spent open to air. In some cases, buyers ask about repacking large volumes for multi-site distribution. Our technical staff have managed transfers by weighing under nitrogen and vacuum-packing small aliquots, which saved one pharmaceutical partner weeks of requalification work by avoiding the need to resubmit every lot for new analytical testing.

    Unopened containers typically see minimal clumping. If a drum sits sealed but unused for more than one year, we recommend a quick check of melting point before committing it to critical routes. From time to time we get requests for smaller packaging formats, such as 100 g vials with foam fill. While this adds cost, real-world experience shows it helps smaller labs avoid cross-contamination, especially those that lack full bench-scale cleaning capabilities.

    Typical End-User Feedback: What Chemists Tell Us

    Surveys and one-on-one conversations with formulation groups reinforce a few basic points. Chemists value the combination of high assay and low residual solvent content, noting that our material dissolves cleanly in chlorinated and non-chlorinated media. Formulators working with late-stage intermediates appreciate the absence of colored impurities, as these can complicate HPLC monitoring.

    More than one medicinal chemistry group has commented that using our product shortened project timelines by cutting weeks off purification steps compared to suppliers who drag their feet on in-process analytics. Moreover, when chromatography is necessary, the clear-cut melting point and consistent HPLC profiles make for straightforward fraction picking. These operational details matter because they translate directly into more molecules, faster structure confirmation, and easier compliance for internal audits.

    Quality Assurance from the Manufacturer’s View: Practical Steps We Take

    The chemical sector runs on trust, and that trust builds on repeatable outcomes. Our QA team runs side-by-side analytical tracks for every drum, keeping an archive of spectral and chromatographic fingerprints. Over the years, we found customers rely not only on a printed certificate, but also on direct staff-to-staff contact when troubleshooting. This transparency helped one client identify a minor contaminant whose only clue was a faint baseline uptick on a third-party GC trace, which we tracked back to an old drum-head gasket in our filling line.

    We upgraded seals and retrained our packaging crew as a direct result. Our willingness to invite auditors in, and to share potassium bromide IR data and proton NMR original files, sets a practical standard. While a few users request custom purity grades (or alternate salt forms), the vast majority find our default production profile matches their workflow with little or no modification.

    Environmental Responsibility and Waste Minimization: On-the-Ground Actions

    No producer can ignore the disposal and environmental impact of sulfur and bromine intermediates. In the early days, off-gassing from reaction vessels caused headaches (sometimes literally) and led us to redesign vent scrubbing systems with active carbon and caustic traps, which now cut emissions far below local and international guidelines. Solvent recycling is standard, and spent mother liquors are reprocessed for bromine recovery, which reduces both raw material demand and hazardous waste. Partnering with water treatment firms allowed us to recover clean rinse water, further closing the loop and lightening the regulatory reporting load.

    This approach—rooted in hands-on experience—translates into a safer workplace and a smaller carbon footprint. We avoid single-use plastics in bulk transport wherever possible, using returnable drums for high-volume customers and sturdy liners that withstand multiple filling cycles. Many clients have adopted similar measures in their own labs, reflecting a shared commitment to responsible chemical management.

    Troubleshooting Tips: From Our Lab Bench to Yours

    Even with an established quality control program, occasional challenges arise. Dusting and static cling sometimes hamper precise weighing, especially on dry winter days. Our warehouse team pre-cools samples in a humidity-controlled chamber ahead of packing. Some users report slight color changes following long-term storage, typically due to trace oxidation, but this effect does not affect assay or performance based on our accelerated stability studies.

    Cross-contamination worries, a frequent topic at industry roundtables, seldom come up among our customers. We maintain dedicated lines for bromo- and thioamide work, and train operators to double-check batch codes and undertake line-clearing verification before each production run. If out-of-spec material does appear, immediate root cause analysis and open communication keep disruptions short and confidence high.

    Forward Outlook: What’s Next for 4-Bromo-Thiobenzamide Production

    On the horizon, regulatory shifts in both North America and the EU may affect shipment permit requirements, especially as researchers employ more boron-coupling technology requiring high-purity aryl bromides. We monitor these changes constantly, ready to tweak packaging or supply chain arrangements to ensure smooth delivery. Our R&D is also testing routes to generate 4-Bromo-Thiobenzamide using greener chemistry—alternative solvents, flow-reactor syntheses, and improved workup steps. Small pilot lots from these processes consistently meet market need, and we share preliminary results with several innovation-focused chemical firms.

    As manufacturers, we stay grounded in the core values of reliability, transparency, and continuous feedback. Our engagement with both small labs and major producers keeps us attuned to rising technical standards and evolving user expectations. With each shipment, our focus stays fixed on that blend of science and trust—supplying the right chemical, in the right way, for world-class research and manufacturing outcomes.