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HS Code |
173814 |
| Chemical Name | 3-Bromothiophenol |
| Cas Number | 871-24-9 |
| Molecular Formula | C6H5BrS |
| Molecular Weight | 189.08 g/mol |
| Appearance | Light yellow to brown liquid |
| Boiling Point | 225-226 °C |
| Melting Point | 24-27 °C |
| Density | 1.661 g/cm3 |
| Refractive Index | 1.642 |
| Flash Point | 107.5 °C |
| Purity | Typically ≥ 98% |
| Synonyms | 3-Bromobenzenethiol |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=CS1)Br |
| Inchi | InChI=1S/C6H5BrS/c7-5-2-1-3-6(8)4-5/h1-4,8H |
As an accredited 3-Bromothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3-Bromothiophenol, 25g, is supplied in a sealed amber glass bottle with a secure, tamper-evident cap and clear labeling. |
| Shipping | 3-Bromothiophenol is shipped in secure, airtight containers to prevent leakage and exposure. It is classified as a hazardous chemical and must comply with international and local regulations for transport, including appropriate labeling and documentation. The package should be handled with care and stored in a cool, dry place during transit. |
| Storage | 3-Bromothiophenol should be stored in a cool, dry, well-ventilated area away from sources of ignition and incompatible substances such as oxidizing agents. Keep the container tightly closed and protected from light. Use appropriate chemical-resistant containers and store away from moisture and heat. Ensure proper labeling and access control to prevent accidental exposure or spills. |
Applications of 3-Bromothiophenol in Industrial Manufacturing3-Bromothiophenol serves as a key intermediate in several complex downstream chemical manufacturing sectors. As an original producer, we provide consistent quality material supporting nuclear, pharmaceutical, electronic, and agrochemical end-uses. The application details below reflect specific technical pathways and market-driven requirements. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers use 3-Bromothiophenol for the development of key active pharmaceutical ingredients (APIs), especially in oncology and anti-inflammatory drug classes. The compound participates in aromatic substitution reactions to introduce thiol groups, enabling synthesis of aryl thioethers that form APIs or precursors. Its precise reactivity offers high yield and selectivity, and material qualification must match stringent regulatory audits. Scale-up integrates continuous-flow or batch sulfhydrylation with downstream purification, supporting commercial routes to thieno[2,3-d]pyrimidine and related scaffolds. Industry compliance standards
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2. OLED and Organic Semiconductor ManufacturingElectronic component suppliers introduce 3-Bromothiophenol as a key synthetic precursor for the fabrication of conjugated thiophene-based semiconductors in OLED and thin-film transistor applications. The functional group enables step-growth polymerization and cross-coupling to construct high-performance polythiophenes. Stringent control of purity and trace metal content is essential as downstream device performance depends on minimal defect densities and batch reproducibility. Integration frequently occurs in small-molecule toolkit syntheses for developing next-generation display and sensor materials. Industry compliance standards
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3. Agrochemical Active Ingredient SynthesisManufacturers in the agrochemical sector employ 3-Bromothiophenol as a precursor for sulfur-containing pesticides and fungicides. The compound enters synthesis schemes where thiol-functionalized intermediates lead to target actives providing broad-spectrum resistance for crop protection. Material traceability and impurity profile require full documentation as residues must comply with regional limits for agricultural chemicals. Formulators may introduce the raw material directly during early-stage heterocycle formation or as a post-coupling modifier. Industry compliance standards
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4. Advanced Dye and Pigment ProductionDye and pigment manufacturers use 3-Bromothiophenol as a building block for synthesizing sulfur-rich chromophores, particularly for specialty applications like UV-absorbers, photo-stable dyes, and niche textile colorants. Its reactivity supports C–S bond formation critical for aromatic dye molecules exhibiting high photostability and tunable absorption. Downstream quality control focuses on residual halide levels and color consistency. Material selection is process-specific, often linked to the design of performance-driven, high-value pigments. Industry compliance standards
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Manufacturing 3-Bromothiophenol is no routine task, and speaking from years of hands-on experience, we have seen its unique value grow in both scale and scope. Organic chemistry’s progress often rests on subtle improvements, and this compound has enjoyed rising interest across pharmaceuticals, agrochemicals, and advanced material applications. Chemists bring 3-Bromothiophenol (CAS No. 14397-25-2, C6H5BrS) into reaction plans for the reactivity its molecular scaffold offers: an aromatic ring with both bromine and thiol functionalities, combining selectivity with catalytic potential in cross-coupling and functional group transformations.
In our production facilities, we have worked with a variety of bromo- and thiol-containing aromatics. 3-Bromothiophenol has created a place for itself thanks to the versatility the para-substitution offers. The bromine atom at the third position sets up chemists for efficient halogen-lithium exchange, Suzuki-Miyaura, and Stille coupling, while the thiol group allows for selective alkylation, click-type reactions, and novel ligand synthesis. Whereas other bromo-thiophenols might create limitations in substitution patterns or steric hindrance, the meta orientation here opens routes not possible with ortho- or para- isomers.
Across the years, research teams have returned to this compound when they need precise reactivity. Drug discovery projects favor its handle for conjugation, as the thiol can anchor small molecules to larger frameworks or metallic surfaces. Material scientists working in thin films or optoelectronics rely on the fine-tuned properties given by the bromine group, which can be elaborated or displaced under mild conditions. We have watched the growth in demand from customers developing sensors, as thiol groups form strong bonds with gold surfaces, stabilizing self-assembled monolayers.
We do not view 3-Bromothiophenol as a commodity. Each batch draws from quality starting materials and optimized conditions, as contaminants can interfere with downstream chemistry. Control over oxygen and moisture contents matters when the product is meant for air- or water-sensitive transformations. Here, painstaking distillation and on-site GC/MS monitoring remove uncertainty—because customers need reproducible purity, not just attractive numbers on a specification sheet.
Throughout our process development work, we found that side reactions often cloud the product with difficult-to-remove byproducts. By taking samples during reaction and distillation at critical stages, and by tailoring purification strategies to the chemical’s tendency for oxidation, our team delivers a product with minimized sulfurous impurities. These small details have an outsized effect on reaction outcomes, especially for large-scale users or projects that require strict validation.
Specifications are not just paperwork for our team; they represent a shut door on costly reruns and failed syntheses. We aim for a product concentration above 99 percent (by GC), with peroxide and oxidized sulfur below detection. Residual solvents, where present, do not reach levels that inhibit palladium catalysts often used in cross-coupling. Arguably, lab-scale users may not always notice subtle differences—until a pilot batch or kilo-scale run produces glitches linked to a problematic impurity or latent degradation.
We choose to offer 3-Bromothiophenol in moisture-tight, amber glass bottles, ranging from small 25-gram packages up to larger bulk quantities. Experience taught us that permeable plastic bottles often let in trace moisture or air, causing unwanted oxidation and color change. Years of shipments to research labs and process plants have reinforced how packaging influences shelf-life and practical usability.
In our direct conversations with process chemists and R&D managers, the range of applications always stands out. One biotech group harnessed the thiol group for site-specific protein labeling, granting selectivity unattainable with broader-spectrum nucleophiles. Electronics clients used it as a linker molecule, taking advantage of the robust Au-S bond for nanoscale wiring and conductive surface coatings.
We’ve received feedback from several pharmaceutical partners highlighting how the para-bromine position on the aromatic ring empowers controlled functionalization that avoids meta- and ortho- side products often seen with alternative bromo-thiophenol isomers. This selectivity simplifies purification downstream, reducing waste and costs in multi-step syntheses. Another team, working on new photoresponsive dyes for display technologies, utilized the dual reactivity of both the aromatic bromide and the thiol group for stepwise modification, innovating molecular architectures that push device efficiencies.
Looking at 2- and 4-bromothiophenol analogues, as well as halide or methyl-substituted thiophenols, clear practical differences emerge in the lab. The position of the bromine dictates which carbon centers are available for further transformation, a factor that shapes entire synthetic strategies. Many institutions seeking substitution at a specific site on the aromatic ring quickly see why 3-Bromothiophenol outperforms one-size-fits-all thiophenols. The meta-bromo configuration creates unique possibilities for selective ortho-lithiation, meta-selective catalysis, and coupling reactions that avoid unwanted competition with the sulfur.
We often hear requests to compare 3-Bromothiophenol with 3-Bromoanisole or 3-Bromophenol. Unlike methoxy or hydroxy groups, the thiol adds strong nucleophilicity and allows for thioether formation, but comes with the challenge of oxidation sensitivity. Managing storage and handling of 3-Bromothiophenol is not trivial, but our protocols minimize spoilage and ensure product consistency for demanding synthetic work.
Scaling up production of 3-Bromothiophenol is not a simple multiplier of lab-scale chemistry. Challenges in exotherm control, hazardous intermediate management, and phase separation become central concerns. Early in our manufacturing experience, we encountered batch failures linked to trace metal impurities catalyzing sulfur oxidation. By introducing chelation steps and process monitoring at pre-defined hold points, we cut defect rates significantly. Near-miss contamination incidents forced us to reassess not just chemistry, but plant layout and staff training.
Among the most frustrating problems faced in the past was incomplete removal of dibrominated thioethers, which formed during over-bromination at higher reaction temperatures. These contaminants resist standard purification, so we invested in fractional distillation setups with in-line purity checks, ensuring product fit for both fine chemical synthesis and more stringent semiconductor material uses. Each production cycle is audited for adherence to process safety and environmental stewardship, as our reputation is closely tied to product integrity.
A drum or bottle alone does not solve chemistry’s challenges. Over time, we shaped our support team to field technical questions on storage life, compatibility with varied solvents, and optimal handling practices. By sharing real-world experiences—such as the risk of storage above room temperature triggering slow color changes or peroxide development—we arm customers for success. Our technical team works with users to troubleshoot synthetic routes, recommend compatible reagents, and prevent costly troubleshooting at the plant scale.
Some clients navigate challenging purification protocols where the thiol group complicates silica-based chromatography or triggers column fouling. Having solved these issues in our own plant, we provide practical advice: from scavenger resins for trace peroxide removal to nitrogen-blanketed transfer systems. In the realm of large-scale operations, minimizing batch-to-batch variability becomes more valuable than incremental cost savings, and our experience enables customized solutions for such cases.
No manufacturer can afford complacency about workplace or environmental safety, especially with sulfur-containing aromatics. Early investments in fume collection, closed-loop containment, and operator training have paid dividends not just in compliance, but in the trust received from industrial partners. Where government regulations on air emissions or waste sulfur handling apply, our production and disposal protocols comply with strictest standards. We invested in solvent recovery and emission scrubbing units, knowing that the cost of short-term savings would never justify reputational damage or health risk to staff and neighbors.
We routinely update safety data and internal risk assessments, reflecting emerging research and process learnings. Our commitment extends to packaging recycling initiatives and safe on-site neutralization, keeping waste streams in check. Several years back, a process audit prompted the switch from disposable to reusable intermediate bulk containers for bulk shipments, with both environmental and logistical payoffs.
Reflecting on the continual feedback from researchers and process engineers, innovation in 3-Bromothiophenol production stands as an ongoing effort, not a finished chapter. Synthetic chemists push for new derivatives and variants, which spurs us to adapt plant processes and expand QC techniques. Demands for higher-purity and lower-residual metal levels have driven adoption of advanced filtration and analysis—including ICP-MS for parts-per-billion impurity tracking that was once seen as excessive for a building block chemical.
Our interest in 3-Bromothiophenol extends beyond transaction. Partnerships with customers investigating new pharmaceutical scaffolds or functional materials have shaped both scale and technical capabilities. Recent collaborations include cooperative work on validating greener synthetic routes, with reduced reliance on halogenated solvents and more sustainable raw material sourcing. Our development chemists welcome opportunities to tailor production protocols for unique project needs, such as delivering greater enantiomeric purity for asymmetric synthesis, even when the core molecule itself is not chiral.
Making and selling 3-Bromothiophenol is a partnership rather than a transaction. Every kilogram connects us to the next generation of medical treatments, electronics, or greener technologies. Years of experience grounded us in the details that matter: regular in-process verification, transparent documentation, and a refusal to compromise on the small process changes that safeguard quality. Our lines remain open to feedback from any client, whether a global manufacturer or a university lab running a lone flask.
The journey from raw material sourcing to shipment spans more than chemistry: it includes worker training, waste management, and supply chain transparency. Our teams do not separate process improvements from product responsibility, and every batch tracks back to a constant search for incremental excellence. This philosophy has steered us through both routine business and periods of sudden demand upswings, helping customers navigate supply chain troubles with confidence.
The most rewarding part of manufacturing 3-Bromothiophenol is the knowledge that every order serves as a springboard for discovery. From small startups to global leaders, users continually surprise us with novel transformations and unanticipated applications. We see this building block not as an end, but as a starting point for chemical creativity. Demand for tailored starting materials will only increase, and our foundry stands ready to answer with equal parts experience, precision, and care.