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HS Code |
843381 |
| Cas Number | 2114-39-8 |
| Molecular Formula | C9H11Br |
| Molecular Weight | 199.09 g/mol |
| Iupac Name | 1-bromo-2-phenylpropane |
| Synonyms | alpha-Bromo-2-phenylpropane |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 105-107°C at 14 mmHg |
| Density | 1.300 g/cm³ at 25°C |
| Refractive Index | 1.5520-1.5560 |
| Flash Point | 79°C (closed cup) |
| Smiles | CC(CBr)c1ccccc1 |
| Solubility | Insoluble in water; soluble in organic solvents |
As an accredited 1-Bromo-2-Phenylpropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 100 mL, with secure screw cap, labeled with chemical name, hazard symbols, lot number, and storage instructions. |
| Shipping | **Shipping Description for 1-Bromo-2-Phenylpropane:** Ships as a hazardous chemical, classified under UN 1993 (Flammable Liquids, N.O.S.). Must be packed in approved containers, clearly labeled, and accompanied by appropriate safety data sheets. Transport follows relevant ADR, IATA, or IMDG regulations. Handle with care to avoid leaks, spills, or exposure during transit. |
| Storage | 1-Bromo-2-Phenylpropane should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Use an appropriate chemical storage cabinet, preferably for organohalides, and clearly label the container. Always follow relevant safety guidelines and local regulations. |
Applications of 1-Bromo-2-Phenylpropane in Industrial ManufacturingWe manufacture 1-Bromo-2-Phenylpropane for advanced chemical synthesis across several high-value downstream industries. Our material integrates seamlessly into specialty manufacturing routes where strict compliance, precise formulation, and process consistency are required. Below are the core application pathways our clients utilize globally. 1. Pharmaceutical Intermediate for Antihistamines Synthesis1-Bromo-2-Phenylpropane plays a critical role in the pharmaceutical sector, particularly as a key intermediate for producing alkylamine-based antihistamine APIs such as pheniramine and chlorphenamine. Downstream pharmaceutical manufacturers use this compound in nucleophilic substitution reactions, often with dimethylamine or other secondary amines, to assemble the core side chain structure of final active pharmaceutical ingredients. Stringent adherence to pharmacopeial purity, process traceability, and batch consistency is essential throughout the value chain, especially for export markets and multinational generics production. Industry compliance standards
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2. Agrochemical Intermediate for Phenethyl-Amine HerbicidesMajor agrochemical companies integrate this compound as a building block in the multi-step synthesis of selective herbicide and plant growth regulator actives containing phenylethylamine structures. The compound enters the pathway during the formation of key amine intermediates, where controlled halogen displacement reactions deliver high selectivity. Process economics benefit from stable yields and manageable byproduct profiles, while compliance focuses on safe handling and traceability for agricultural chemicals. Industry compliance standards
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3. Fine Chemical Synthesis for Chiral Building BlocksResearch and production facilities specializing in asymmetric synthesis employ this compound for creating chiral amines and auxiliaries used in enantioselective reactions. Through controlled nucleophilic substitution and stereoselective transformations, the compound enables access to valuable optically pure intermediates for custom chemical and flavor synthesis, where enantiomeric excess and trace-level impurity control are vital for downstream utility. Industry compliance standards
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4. Specialty Fragrance Compound IntermediateManufacturers in the aroma chemicals domain utilize this raw material in producing synthetic fragrance intermediates and precursors that require phenylpropane skeletons. The compound is inserted in selective alkylation steps under mild conditions to maintain the integrity of aromatic moieties, which are subsequently transformed into aldehydes, alcohols, or ketones with characteristic odor profiles for use in consumer and industrial fragrances. Industry compliance standards
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5. Chemical Intermediate for Dye and Pigment ManufactureProducers of specialty dyes and organic pigments incorporate 1-Bromo-2-Phenylpropane in the stepwise construction of complex chromophores, especially where propyl-substituted aromatic intermediates are needed. The compound undergoes coupling reactions under controlled temperature and solvent conditions to provide efficient aryl extension, with downstream quality assurance focused on color purity, lightfastness, and solvent compatibility for textile and plastics coloration. Industry compliance standards
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Working with chemicals at their point of origin reveals details that rarely make it into textbook overviews or standard technical sheets. 1-Bromo-2-Phenylpropane isn’t simply another substituted aromatic compound; it stands as a workhorse within organic synthesis thanks to its real-world reactivity and straightforward handling properties.
The structure, marked by a bromine substituent on a phenylpropane backbone, gives it some unique behavior. In our production, we focus on tight control over the isomer; the 2-position attachment means that both the phenyl and bromo groups share the propane skeleton, shaping how it reacts in downstream processes. We’ve seen that during alkylation and substitution reactions, this orientation can lead to better selectivity than closely related compounds, simplifying both work-up and purification.
Quality in the lab always traces back to the factory floor. We put a premium on purity, typically targeting a finished material that exceeds 98% by GC analysis because trace impurities can feed directly into side reactions, especially at scale. In our experience, even minor contaminants—leftover halides or oxidized byproducts—can drag down yields or complicate separation later, so we run a robust distillation and analytical regimen in every batch. The compound typically appears as a colorless to pale yellow liquid under ambient conditions, reasonably stable in a dry, sealed container away from UV light and moisture. Vapor pressure and density line up within published ranges, supporting predictable handling in most settings.
Even with standard handling, our teams have observed the importance of proper containment and ventilation. The bromine atom brings a certain volatility, and even minor leaks quickly register their sharp odor. Uninterrupted purification sequences and well-sealed drums make a difference for both product and worker safety. On the factory floor, we don’t just talk about material properties—we navigate them daily.
Talking with development chemists and seeing repeated orders come through the plant, it’s crystal clear why 1-Bromo-2-Phenylpropane appears so often on material requests. Its electrophilic character, imparted by the alkyl bromide, opens up a wide door in organic synthesis. We supply to laboratories synthesizing a variety of pharmaceuticals and fragrance intermediates, where the bromine serves as a leaving group in nucleophilic substitutions.
Through years of collaboration with downstream users, we know direct applications include the synthesis of phenylpropanolamines, certain amphetamines, and diarylpropane derivatives. Many researchers come back for this specific bromoalkane rather than its chloro or iodo cousins because its reactivity profile sits nicely in the middle: more reactive than chlorides but easier to control compared to iodides. In heated alkali and polar environments, both laboratory and pilot plant setups see respectable consistency between runs.
Several specialty applications trace back to the unique substitution pattern. During large-scale Grignard or lithium-halogen exchange reactions, we don’t see as much tar formation or side-product build-up as with less well-defined positional isomers. Because regulatory environments keep shifting, especially around precursor chemicals, the sharp identity and traceability of our batches help users clear hurdles more smoothly.
Buyers sometimes ask why not settle for similar compounds or blend in less pure material to cut costs. From long experience, there’s no substitute for using the right bromoarene in synthesis. Even seemingly simple changes in isomer structure lead to knock-on effects in yield, crystallization, and product color. For cosmetic or pharmaceutical work, trace byproducts and inconsistent lots give more headaches than upfront savings can justify.
A direct difference emerges between 1-Bromo-2-Phenylpropane and other options like 1-Bromo-3-Phenylpropane or 1-Bromo-1-Phenylpropane. The placement of the bromo and phenyl groups shifts electronic properties, which shows up in coupling reactions, substitution rates, and the physical behavior of products. Some customers recall days lost when using off-isomer material resulted in puzzle pieces that just didn’t fit in the downstream pathways.
Those new to scale-up quickly discover that certain impurities—like unreacted starting alcohols or over-brominated species—can easily slip through in less careful manufacturing environments. In one particularly challenging example, a project required trace-level detection of byproducts using NMR and GC-MS. Our batches cleared scrutiny, while alternative sources produced little more than generalized brominated “gunk” that refused to move through a crystallizer.
Back in the plant, this isn’t just a molecule on an order sheet. We’ve adapted batch flow to emphasize high conversion of starting phenylpropanol, integrating inline analytical checks so the major byproducts don’t get a toehold. Since bromination can go sideways with even slight temperature or mixing errors, temperature mapping and staged reagent addition stay at the top of our watchlist.
Vacuum distillation rounds off the process. Poorly separated product brings water and higher-boiling impurities that show up as sticky residues or off-colors, and we’ve learned to spot these trouble signs before they leave the plant. A clear fraction, sharp boiling point, and low water content give an unmistakable assurance. This saves users hours of column work and lets projects move ahead without the waiting game for additional rework.
Lab staff and plant operators invest real pride in keeping up quality. We know that cutting corners comes back with a cost, so improvements stick only if they offer robustness day in and day out. Whether it requires tuning the reaction kinetics or tightening packaging seals, these lessons feed directly into the next batch and into the next improvement cycle.
Shipping brominated compounds, especially liquids like this, brings its own set of realities. We avoid steel drums because trace metal catalysis can degrade the material over time. Each container uses fluoropolymer lining or high-density polyethylene, minimizing off-odors and cross-contamination during transit. Repeated field samples confirm that packaging integrity outstrips almost any other variable for shelf-life.
Long-haul shipping across borders demands tight documentation. By maintaining a detailed chain of custody and full batch analytics on hand, regulatory bottlenecks become less of a hurdle for buyers. We’re in regular contact with haulers and local enforcement so missing paperwork or mislabelling doesn’t slow the flow of material.
Every so often, supply hiccups force us to lean on inventory built by forecasting customer needs ahead of schedule. Hurricanes, infrastructure disruptions, or sudden spikes in demand for related downstream drugs all ripple up the supply chain. Direct contact with users helps us stay ahead and avoid delays that tie up R&D or finished product release on the client’s side.
A product isn’t just measured on arrival—it’s measured by the way it performs in the chemist’s hands. We pay close attention to the needs of those working at gram or tonnage scale, tailoring our process so key product characteristics remain consistent from batch to batch.
Periodic sampling throughout the reaction and post-purification stages weeds out off-spec material early. Some of the yardsticks we live by: clarity of liquid, minimum light absorbance, and absence of residual acid or base. For some customers, material must be crystal clear even in thin films; colorless product often signals a tighter impurity profile and smoother downstream isolation.
Our teams invest time in ongoing method development, from improved GC methods to better internal standards. As more sophisticated analytical tools become available, our lab integrates them to raise the bar on detection limits and reduce batch-to-batch variance. A missing signal or unexpected background peak is an opportunity for process adjustment, not just a headache for users.
Behind every pack of material sits a network of plant operators, technicians, and drivers committed to responsible practice. We ensure all staff have protective equipment up to and including full-face shields and solvent-resistant gloves. Regular ventilation checks and spill drills keep incidents to a minimum.
Over the years, waste minimization has climbed in priority. The bromination step always creates a risk for mixed organic streams, and we’ve redirected waste flows to certified handlers able to recover and recycle solvents where possible. Not every supplier invests in this level of compliance, but stewardship in the workplace carries forward to customer sites and local communities.
Most manufacturers know that true product value only emerges downstream. Some clients request micro-scale samples for analytical method validation before moving up to production tons. We encourage these pilot projects, fielding direct feedback from end-users who test how the material behaves in their unique setups. Adjustments—from finer filtration to tighter batch records—often emerge through these back-and-forth exchanges.
In periods where regulatory lists shift and controls on phenylalkylamines tighten, customers appreciate rapid notification and lot traceability. We build those needs into our operations, retaining full certificate data for years so customers can reference back to lots shipped well in the past.
Collaborative pilot projects sometimes drive process tweaks before full-scale launch—such as solvent swaps, extra drying, or even packaging variations—which can only be achieved through close two-way communication. Each adjustment reflects the realities of both chemical manufacturing and end-use requirements: a balance between high yield, regulatory safety, and cost containment.
Competitors sometimes market cheaper or off-isomer material under similar-sounding names, but experience shapes what arrives in the drum. Picking up the phone to troubleshoot problems with users often uncovers material made by shortcutting purification or skipping in-process controls. These short-term savings turn to loss when downstream issues pile up.
We’ve stepped in on projects where previous material clouded unexpectedly or underwent slow side reactions during storage. Each report of a failed reaction feeds documentation and guides incremental improvements. The tradition of custodianship runs strong because in-house troubles feed straight into the plant’s priority list.
From the shop floor to the final user, reliability outweighs marginal cost savings. Customers conducting long, multi-step synthesis projects realize too late that product instability or byproduct build-up aren’t abstract risks. It takes repeat collaboration and a direct pipeline between production and application to foster long-term trust.
Chemistry doesn’t stand still. Every year brings changes in the end-user landscape—new synthetic techniques, evolving pharmaceutical targets, and smarter methods for personal care and performance materials. Our advantage as direct manufacturers comes from building improvements right into each process revision based on feedback from those synthesizing on the other end of the pipeline.
Recent upgrades include the introduction of finer in-line drying units, steadily reducing water content and improving reaction consistency in water-sensitive steps. We’ve also explored alternative brominating agents to lower the footprint of organobromide waste. Pilot trials, conducted with full customer input, open up routes to even higher selectivity and material safety.
Consumer and worker safety regulations, particularly in the EU and North America, drive us to adopt improved containment, data tracking, and even batch-level serialization, so every drum tells its story from source to application. Each year, we introduce process enhancements and roll them out transparently, letting direct users qualify new lots for their own protocols.
Many in the industry treat specialty bromides as commodity chemicals with little story beyond the drum label. From our vantage point as hands-on manufacturers, each molecule of 1-Bromo-2-Phenylpropane embodies the history of careful process control, regulatory adaptation, and a thousand unrecorded tweaks emerging from years of working directly with the compound. The value for our partners lies not only in consistent physicochemical properties but in the readiness and attitude to build improvements based on those who trust our product in their daily work.
End-use diversity means production always stays a step ahead—balancing practical scale-up, evolving analytical standards, and changing regulatory tides. By marrying technical know-how with credibility earned through transparent supply practices and rapid response, we stand ready to support the next phase of developments, whether in pharmaceuticals, materials science, or other value-added fields. 1-Bromo-2-Phenylpropane, in the hands of those who know, is more than just a reagent: it’s a demonstration of chemical manufacturing knowledge, reliability, and partnership made tangible.