|
HS Code |
602264 |
| Chemical Name | 2-Bromothiophenol |
| Cas Number | 645-29-6 |
| Molecular Formula | C6H5BrS |
| Molecular Weight | 189.07 g/mol |
| Appearance | Light yellow to brown liquid or solid |
| Boiling Point | 265 °C |
| Melting Point | 32-35 °C |
| Density | 1.668 g/cm3 |
| Solubility | Insoluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Refractive Index | n20/D 1.676 |
| Flash Point | 120 °C |
| Smiles | C1=CC=C(S1)Br |
As an accredited 2-Bromothiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 2-Bromothiophenol (25g) is a brown glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 2-Bromothiophenol is shipped in tightly sealed, chemical-resistant containers to prevent leaks and exposure. It is classified as a hazardous material and must be handled according to relevant safety and transport regulations, including labeling and documentation. Store and transport in a cool, dry place, away from incompatible substances and direct sunlight. |
| Storage | 2-Bromothiophenol should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect from light and moisture. Use appropriate chemical storage cabinets and ensure containers are clearly labeled. Handle with care, employing suitable personal protective equipment to avoid inhalation and contact with skin. |
Competitive 2-Bromothiophenol prices that fit your budget—flexible terms and customized quotes for every order.
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Manufacturing 2-Bromothiophenol presents unique challenges and opportunities. From the first day we began synthesizing this compound, precision and meticulous attention have shaped our process. Over several production campaigns, our team has handled the volatile nature of thiophenol derivatives, using this experience to refine control methods and boost yield. Every batch originates from carefully sourced raw materials, selected for consistency and purity.
Our product, 2-Bromothiophenol, features a bromine atom attached to the second position of the thiophenol ring. This feature defines its reactivity and value. Chemists often call on this molecule for cross-coupling reactions, especially in pharmaceutical and agrochemical research. It stands out for its reliable performance as a building block where selectivity matters.
Throughout years of production, we have observed that slight changes in the synthetic route transform impurity profiles. Too fast a reaction or an unexpected atmospheric leak introduces contaminants that hinder downstream synthesis. By rigorously controlling every step, from halogenation to distillation, we deliver 2-Bromothiophenol with reproducible specifications.
Each lot of 2-Bromothiophenol leaves our factory as a colorless to pale yellow liquid or solid, depending on storage conditions. The molecular formula, C6H5BrS, reflects its straightforward yet powerful structure. We usually supply it in bulk as a stabilized liquid, with quantity tailored to process requirements. To prevent decomposition or oxidation, our engineers developed a nitrogen-blanketed filling and transfer system. This choice came after a significant loss when early shipments oxidized in transit—an experience that still guides our packaging strategy. Those who work with sulfur-containing aromatics know the distinctive odor, and we advise handling in well-ventilated workspaces.
Laboratory and plant users depend on our published assay values, usually exceeding 98%. Our technical reports detail typical levels of related brominated and debrominated impurities. Routine batches rarely cross the 0.3% impurity threshold because our QC team runs HPLC checks on every drum, without fail. Analytical transparency ensures customers never encounter “surprise” byproducts, allowing them to design reactions with confidence. Transparent specification sheets reflect both our confidence and respect for our partners’ scientific work.
2-Bromothiophenol occupies a unique space among thiophenol derivatives. Simple thiophenol, for instance, lacks the directed reactivity that the ortho-bromine delivers. Over several years, we have fielded requests to supply both 4-bromothiophenol and mixed halogenated variants. The ortho-bromine group in this molecule makes it superior for certain palladium-catalyzed couplings, as we have seen in customer feedback and published research. Other isomers do not match this efficiency for introducing complex aryl groups or alkyl chains. For example, in Suzuki and Sonogashira couplings, unwanted side products occur less often, translating to higher yield and cleaner workups.
We have documented the subtle differences in reactivity between our 2-bromo and 4-bromo products. 2-Bromothiophenol supports regioselective substitutions unavailable from para isomers. Its interaction with transition metal catalysts enables streamlined syntheses—an area many of our bulk buyers value when scaling up for pharmaceutical intermediates. Although each customer’s chemistry is unique, most report higher selectivity and throughput by using the ortho-bromo variant.
From a safety and odor standpoint, thiophenol derivatives share similarities, but bromination at the 2-position slightly alters the volatility and storage requirements. Over time, we switched to drums with improved vapor seals, prompted by lessons from handling both ortho and para isomers.
Process chemists and R&D teams depend on consistency. A more variable product can spell disaster during scaleup, costing time and resources. Having supplied this molecule for countless process runs and laboratory campaigns, we have earned trust with our unwavering focus on batch reproducibility. After facing unexpected outcomes ourselves—such as polymerization or discoloration in stored samples—we found that fine-tuning drying and neutralization steps made significant improvements. Our plant crew now monitors every batch for residual halide and sulfur contamination. Our detailed COAs stem directly from in-house lessons, not abstract compliance requirements.
Older purification approaches often left trace metals or oxidized byproducts, but investment in short-path distillation and vacuum drying eliminated these risks. These upgrades came straight from direct dialog with customers who ran into problems with competitor samples. Through open exchanges and troubleshooting support, we pinpointed process gaps and tailored our production methods for the needs of both research and scaleup campaigns.
Over the past decade, our 2-Bromothiophenol has supported diverse innovations. Medicinal chemists routinely request it for early-stage drug discovery where aryl sulfides and thioethers act as key intermediates. In crop protection, the compound shapes the construction of bioactive molecules that improve agricultural yields. We have received clear, positive feedback from API manufacturers regarding its reliability for downstream elaboration—especially where electron-rich thiophenol scaffolds resist typical halogenation.
One major client found that our 2-Bromothiophenol shortened their synthetic sequence by a step, eliminating a costly purification and slashing waste. Extended technical consultation revealed that impurities lower than 1% prevented side reactions, a testimonial we have echoed in documentation. Another customer in the dye industry highlighted that the ortho-bromo configuration led to deeper, more stable dye shades, boosting commercial results. These practical examples reinforce the compound’s place in complex, value-added synthesis.
Every campaign brings new learning. Early in our production history, difficulties in bromination consistency resulted in variable yields and product color. Our technicians experimented with different reagent addition rates and temperature ramps, ultimately establishing a standard that locks yield in the 85-90% range on a routine basis. The most instructive challenges often forced us to adopt new approaches. Controlling moisture content was one such hurdle; a high humidity event in summer caused unexpected hydrolysis, prompting a facility-wide upgrade to environmental control systems.
Sulfur-based aromatics often suffer from characteristic odor and vapor issues. We implemented not just upgraded seals but also new personal protective practices after supplier audits. Our hazard mitigation counts on direct worker feedback. Adoption of closed transfer lines grew directly from an incident at a loading dock—a near miss that convinced us to rethink standard protocols. This hands-on learning changed the everyday safety culture on our shop floor.
No synthetic process runs perfectly without a robust analytical program. We invested early in chromatography and spectroscopy, learning quickly that standard reference samples sometimes missed subtle, run-dependent byproducts. Our analytical lead, drawing from years in thiol chemistry, insisted on developing a library of in-house standards matched to our processes. Years later, this decision paid off; a spike in unknown peaks caught by LC-MS led us to alter a filtration step, tightening batch-to-batch consistency.
Customers rely on clear assurance when ordering specialty chemicals. Each drum of our 2-Bromothiophenol comes with spectral and chromatographic data, drawn directly from our own production—a practice we adopted after a major client’s project stumbled due to misidentified off-spec material from another supplier. We make all data fully traceable, so each batch history can be reviewed if a downstream synthesis hits a snag. These steps align to both internal and industry best practices, developed side by side with the researchers and engineers we serve.
Chemical manufacturing faces growing pressure to cut waste and emissions. As we gained experience, we doubled down on process optimization to conserve raw materials and curb byproduct formation. Our bromination process now reclaims almost all excess bromine, and spent solvent recycling captures over 90% of used materials for reprocessing. Wastewater generated from neutralization is pre-treated before discharge, thanks to in-house upgrades based on early mistakes—once, a batch of untreated aqueous byproduct nearly exceeded permitted sulfur emissions, serving as a major lesson and catalyst for improvement.
Sustainability does not exist in isolation from safety and quality. By integrating green chemistry practices, we found that batch consistency actually increased. Fewer side reactions cut both contamination and environmental impact, a direct benefit for our partners and the surrounding community. Modernizing our infrastructure to focus on resource conservation, not just compliance, has improved morale and made our facility a model for small-scale specialty chemical manufacturing.
Our customers value honest, direct communication grounded in experience. We have supported projects ranging from pilot-scale campaigns to routine bulk supply for several multinational developers. Over the years, we’ve answered urgent requests for technical clarification in the face of failed reactions, sometimes troubleshooting side by side with a client’s team at their facility. Direct support, whether remote or on-site, comes from our hands-on knowledge of the chemistry—years of facing and solving the same obstacles.
Since regulatory and document requirements change across jurisdictions, our compliance officers keep up a dialog with partners to ease import and validation pains. After receiving feedback on documentation delays, we swapped to a digital COA delivery system. Users now receive batch-specific reports before material ever ships. The decision arose from repeated calls with QA managers under tight regulatory deadlines—a reminder that solid manufacturing must also meet operational realities.
We see 2-Bromothiophenol not as a static commodity, but as a product that continues to evolve. Ongoing collaboration with academic and industrial partners keeps us informed about novel applications, such as its use in emerging green catalysis or advanced materials. Several large-scale users are now incorporating the compound in non-traditional contexts, such as high-performance polymers and specialty electronic devices. Our technical team stays ready to work across disciplines, building on a foundation of deep chemical expertise.
Future improvements will likely center on even tighter impurity control and efficiency gains. As automation comes to fine chemical production, we have begun integrating smart sensors to monitor batch progress and flag deviations in real time. These advancements arise from lessons learned—not guided by trends, but by direct experience solving the practical problems that come with producing high-value, reactive molecules.
Manufacturing 2-Bromothiophenol consistently—and responsibly—demands attention to detail at every stage. Our team’s journey reflects the realities of specialty chemical production, shaped by both triumphs and setbacks. Each process tweak, each packaging upgrade, and every delivered batch represent a commitment not just to quality, but to the chemists and engineers counting on the material to deliver reliable, repeatable results. Drawing from years of problem-solving, response to real-world needs, and proactive communication, we continue to shape our approach to this trusted intermediate so customers can focus on what matters: the science and innovation that move industries forward.