|
HS Code |
513210 |
| Chemical Name | 1-Bromo-3,3-Diphenylpropane |
| Cas Number | 114772-53-5 |
| Molecular Formula | C15H15Br |
| Molecular Weight | 275.19 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 146-148 °C at 18 mmHg |
| Density | 1.256 g/cm³ |
| Refractive Index | 1.586 |
| Smiles | BrCCC(c1ccccc1)c2ccccc2 |
| Inchi | InChI=1S/C15H15Br/c16-11-10-15(12-13-6-2-1-3-7-13)14-8-4-5-9-14/h1-9,15H,10-12H2 |
As an accredited 1-Bromo-3,3-Diphenylpropane factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g net weight, sealed cap, chemical label with hazard symbols, product name, lot number, and handling instructions. |
| Shipping | 1-Bromo-3,3-Diphenylpropane is shipped as a hazardous chemical, typically in tightly sealed containers to prevent leaks and contamination. It should be protected from heat, moisture, and incompatible substances, with clear labeling for safe handling. Shipping must comply with regulations (such as DOT or IATA) for flammable and potentially toxic organic compounds. |
| Storage | **1-Bromo-3,3-Diphenylpropane** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Avoid moisture exposure. Store under inert gas if possible. Clearly label the container and keep it in a secure location designated for hazardous chemicals. |
Applications of 1-Bromo-3,3-Diphenylpropane in Industrial Manufacturing1-Bromo-3,3-Diphenylpropane is a specialized halogenated intermediate produced for critical synthesis in fine chemicals, pharmaceuticals, and advanced specialty polymers. Our manufacturing process ensures high purity and consistent supply for downstream applications that demand stringent quality control and technical support. 1. Pharmaceutical Active Ingredient SynthesisSeveral pharmaceutical companies employ this compound as a crucial building block in the synthesis of antihistamines and CNS-active agents. It serves as an alkylating intermediate, introducing diphenylalkyl chains during active pharmaceutical ingredient (API) assembly, and is often used in routes where selectivity and purity standards are strictly monitored through in-process analytics and traceability. Integration into multi-step batch syntheses permits control over byproduct formation and repeatable scalability. Industry compliance standards
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2. Fine Chemical Intermediates for Agrochemical SynthesisProducers of active pesticides and herbicides utilize this compound to introduce steric protection in multi-aryl agrochemical scaffolds. Its use as an electrophilic agent enables precise functionalization in cross-coupling or carbon-carbon bond-formation steps, offering reliable yield at industrial scale. Strict monitoring of trace halide content is necessary to comply with both national and international regulatory frameworks on agrochemical purity and downstream environmental residue limits during the final product release testing. Industry compliance standards
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3. Specialty Polymer and Resin ModificationManufacturers in the high-performance polymer sector incorporate the compound as a comonomer modifier that imparts hydrophobicity and rigidity to specialty resins, such as polyarylates and engineered plastics. In these systems, careful dosing is essential to preserve polymer chain integrity and achieve targeted mechanical and thermal behavior. Quality control includes gel permeation chromatography (GPC) and FTIR to verify successful incorporation and absence of unreacted halide. Industry compliance standards
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4. Custom Ligand and Organic Electronics Material PreparationResearch and development divisions within the organic electronics and catalysis sector apply this compound for the synthesis of designer ligands and conductive molecules. Its structure enables the construction of large, conjugated frameworks essential for electron mobility and metal-binding performance. This use requires rigorous control of trace impurities, validated by HPLC and GC-MS, and adherence to synthesis protocols outlined in patent and scientific literature. Industry compliance standards
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Every batch of 1-Bromo-3,3-Diphenylpropane to leave our facility reflects what we’ve learned across years of hands-on synthesis and long-term feedback from chemists in the field. When we first started producing this compound, the expectations were simple: reproducibility had to match research demands every single time. Since then, the bar has climbed higher, and our approach has evolved to meet those larger ambitions. Looking at our production lines today, you’ll notice a setup built not only for high purity, but for troubleshooting—the small details that separate trouble-free synthesis from inconsistent results. This compound has earned its place in the real world, not just the theoretical one, by being a steady performer in careful organic transformations, particularly when a reliable secondary alkyl bromide is in demand.
Inside the bottle sits a molecule with a structure familiar to many synthetic chemists: a three-carbon chain, a bromine atom at one end, and two phenyl rings clustered at the center carbon. This gives it the ability to undergo reactions that few related intermediates can match, including those that favor benzylic and alkyl substitution. Over the years, we have listened to university labs and industrial teams alike describe its consistent reactivity in the field. Chemists trying to introduce a diphenylpropyl skeleton into target molecules still turn to this bromide because it saves time they would otherwise lose to ambiguous yields or hard-to-purify side products that can follow less robust leaving groups.
Based on continual in-house verification, our lots run at 98.0% minimum purity by GC, with residual starting materials and impurities limited to levels that analytical teams can readily track. Every run shows a colorless to pale yellow liquid—crystals tend to appear if the bottle spends too long below room temperature, but this doesn’t take away from its response under standard conditions. In past variations, sulfate impurities were the biggest issue for downstream applications, so we integrated chromatographic clean-up and rechecked every lot for halogen balance. Our staff has worked through enough of these purification cycles to spot where phenyl migration tends to kick in, and we account for it before product ever gets close to packaging. For those sensitive to trace metals, we keep an eye on iron and nickel not just in the compound, but throughout the packing process, especially if custom drum options are requested.
Some ask what makes 1-Bromo-3,3-Diphenylpropane different from the more common benzyl bromide or 1-bromo-1,1-diphenylmethane. The answer sits squarely in the backbone. This compound gives two phenyl rings at the gamma carbon, giving it different reactivity in classic nucleophilic substitution and elimination reactions compared to the benzylic and diarylmethyl analogs. You can form carbon-carbon bonds in ways that would otherwise risk rearrangement or loss of selectivity with simpler alkyl bromides. Decades of laboratory and industrial examples support what we hear continually: whether you’re setting up a Grignard apparatus or introducing a unique motif by SN2, you need a side chain that doesn’t behave unpredictably in solution. The physical stability and reactivity profile have made it a staple in the toolbox for both pharma intermediates and custom polymer work.
Applications follow where reproducibility goes. In our observation, most requests come from two sectors. Pharmaceutical chemists request it for its versatility in building blocks leading toward non-steroidal therapeutics and specialty CNS compounds. Our feedback network reports high conversion rates and minimal byproduct formation during alkylation of amines, cyclizations, and in some cases, as the source of a diphenylpropyl radical. Other customers use it in monomer modification, engineering materials with a high degree of steric protection or tuning polymer rigidity where standard alkyl units can’t compete. Manufacturing runs where yield and process reliability are essential show that small variations in bromine content or residual solvents have outsized effects. This led us to double-check all wash cycles and solvent swaps on the last fraction of each run. Minimal errors mean easier downstream purification, whether in kilo lab or pilot plant settings.
Chemistry depends on nuance. Simple alkyl bromides tend to offer predictable SN2 reactivity, but add bulky aromatic groups, and the story changes. For example, 1-bromo-3,3-diphenylpropane brings a steric block at the center carbon, so you avoid certain elimination and rearrangement pitfalls common to smaller, less crowded systems. This translates into smoother, more directed pathway control. Unlike 1-bromo-3-phenylpropane, which can race toward side reactions by virtue of an exposed chain, you get less competition from undesired pathways. Immediate feedback from medicinal teams tells us this reduces late-stage troubleshooting in both route scouting and scale-up. Swapping to 1-bromo-1,1-diphenylmethane changes the entire backbone, removing the spacing critical for some reactions that place a premium on backbone length or flexibility.
In scale-up, another key difference becomes obvious: volatility and handling safety. With our product, flash points and vapor pressures fall in a range that supports safe handling under standard engineering controls. Colleagues with older equipment or non-inert atmospheres have repeatedly asked for a product that won’t off-gas during transfer. This compound keeps that promise better than most benzylic bromides, helping avoid headaches for teams supporting plant safety goals.
Years of supplying kilo-scale and multi-ton orders of 1-Bromo-3,3-Diphenylpropane have shaped our perspective. Real-world users notice stability in long-term storage—batches kept sealed and away from direct light maintain their integrity even after a year. One recurring comment: samples left out during benchwork retain color and solubility, showing little sign of oxidation or decomposition, provided basic lab precautions stay in place. If a bottle sits for a few weeks on the shelf, users see minimal difference in GC purity, and the substance keeps its signature pale color. This reliability matters much more than on-paper numbers when labs face deadlines or need backup stocks in case of supply chain disruptions.
We have fielded plenty of calls from users in the scale-up and pilot plant environment. One challenge mentioned often involves partial crystallization at lower storage temperatures. Instead of pushing blanket instructions, we work through specific cases with each partner: a water bath at mild temperature brings the product back to a pourable liquid state without loss in quality. If the need for weighing or transfer comes up on the production floor, warming and gentle agitation bring solutions without extra steps or surprises.
Our early process for 1-Bromo-3,3-Diphenylpropane mirrored academic procedures: direct bromination in a basic solvent followed by crude isolation and minimal purification. Over time, the demands of multi-use applications showed us that basic purification won’t always suffice where trace residues disrupt downstream results. Pharmaceutical customers, especially, flagged the sensitivity of later synthetic steps to the presence of minor byproducts. After extending purity controls—adding vacuum distillation, dedicated filtration, and gas-phase analysis—we began seeing fewer customer returns and higher satisfaction on secondary analytical passes.
Packaging feedback has been equally instructive. Laboratories working at bench scale prefer glass with screw caps lined for chemical resistance. For process chemists and material scientists running larger volumes, we reinforced our containers to guard against micro-leaching and ensured mechanical stability during long-haul shipping. These practical steps, grounded in daily use and direct communication, have made proven improvements for our end users.
Chemical manufacturing hands out plenty of claims about purity and reliability. We let lot histories and direct return rates speak for themselves. Analytical teams in our plant check every batch with redundant instrumentation–a walk down our QC hall finds gas chromatographs running side by side with NMR and Karl Fischer titrations. When an outlier crops up, steps go right back to the reactor records. This level of scrutiny stems not from marketing pressure, but because every failed synthesis down the chain means hours—sometimes days—lost for our customers. We know because we have walked production floors, mixing rooms, and analytical labs where small, invisible contaminants cause the most expensive errors.
Labs running parallel synthetic series report that reproducibility outpaces that from alternative sources, especially where secondary alkyl bromides from unregulated vendors bring batch-to-batch shifts in trace residuals. In regulated environments, our consistently low impurity levels passed third-party audits—differences are confirmed by real retention data and mass balance, not best-case guesses. These checks build trust with experienced chemists who want a working compound and not just an impressive label.
The story behind every drum of 1-Bromo-3,3-Diphenylpropane from our plant comes from painstaking improvements and direct, honest feedback loops. We run small campaigns before large-scale batches to validate every run. Chemists needing repeatability get compound that matches assay and appearance—no surprises when downstream yields or purity checks come back. This matters most to demanding customers whose analytical baseline leaves little tolerance for off-specification materials. Recent production campaigns show a near zero incident rate—not from luck, but from hard-won experience and lessons from tough, real-world synthesis where every variable counts.
Every so often, we see a challenge crop up in storage, scale-up, or in a new synthesis context. A recurring issue involves keeping the compound stable during unusually long shipments across climates where container integrity can be threatened. New climate variations, humidity swings, and temperature extremes mean we adapt our logistics to maintain product stability—double-sealing lids, reinforcing pallet buffer zones, and preconditioning containers when required. Customers in extreme climates or with long lead times notice that product resilience means fewer replacements and less downtime. We track every shipment, requesting storage conditions feedback to continue trimming sources of sporadic instability.
We learned early not to treat compound production as separate from the problems facing those who use the material each day. When a pharmaceutical team built a multi-step synthetic route on tight timelines, we worked directly to refine delivery schedules and provide on-the-ground technical details—such as recommended minimum transfer temperatures and fastest ways to restore pourability after cold storage. In applied research, our input sometimes prevents days of lost effort by sharing insights gleaned from earlier batches and tough lessons learned on our own production floor.
Industrial customers using custom packaging or running mechanical transfilling systems appreciate insight on best container options, safest venting routines, and real bench-top transfer solutions. These relationships have shaped not just packaging, but allowed us to keep costs reasonable while holding the line on purity and batch uniformity. We keep learning together, adjusting for new process setups and upcoming projects, giving hands-on insight and simple, practical support.
No one who produces specialty chemicals can stand still. Even time-tested compounds like 1-Bromo-3,3-Diphenylpropane shift with market and application trends. We track developments in green chemistry, solvent substitutions, and downstream regulatory demands with an open mind. Behind each update or change in process is a conversation: is this modification improving real performance, preserving shelf life, or opening new doors for product use? We balance tried-and-tested protocols with incremental improvements that matter in the laboratory and in scale.
Even as we transition some processes to cleaner solvents and higher recovery rates, the central principle remains. Feedback from chemists defines the direction. Application data and honest reporting drive upgrades. We don’t move based on vague trends, but track concrete improvements in output, user experience, and environmental compatibility.
Looking toward the future, our priority with 1-Bromo-3,3-Diphenylpropane stays clear. The compound itself continues to meet changing demands, staying ahead through the reliability customers now take for granted. The original request for a clean, reproducible, and dependable alkyl bromide has expanded, and we measure progress by the real value brought to research, process, and development projects around the world.
Whether for a demanding synthetic project, a high-stakes manufacturing run, or a brand-new research avenue, our focus does not shift. We continue to build up the lessons learned batch by batch, keeping both product quality and customer experience central to every drum and bottle shipped.