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HS Code |
943321 |
| Iupac Name | 3-(3-Bromophenyl)prop-2-yn-1-ol |
| Molecular Formula | C9H7BrO |
| Molecular Weight | 211.06 g/mol |
| Cas Number | 55855-44-0 |
| Appearance | White to off-white solid |
| Melting Point | 69-72°C |
| Purity | Typically >98% |
| Synonyms | 3-(m-Bromophenyl)propargyl alcohol |
| Smiles | C(#CC1=CC(=CC=C1)Br)CO |
| Inchi | InChI=1S/C9H7BrO/c10-9-4-1-3-8(7-9)5-2-6-11/h1,3-4,7,11H,6H2 |
| Solubility | Soluble in organic solvents (e.g., DMSO, dichloromethane) |
| Storage Conditions | Store at 2-8°C, in a dry, well-sealed container |
As an accredited 3-(3-Bromophenyl)Prop-2-Yn-1-Ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25 grams, tightly sealed with a screw cap and tamper-evident seal, labeled with product details and hazard warnings. |
| Shipping | 3-(3-Bromophenyl)prop-2-yn-1-ol is shipped in tightly sealed containers, protected from light and moisture. It is typically packed as a hazardous chemical, according to applicable regulations. Shipping is carried out via certified couriers, ensuring proper labeling, documentation, and adherence to temperature and handling requirements to maintain product stability and safety during transport. |
| Storage | 3-(3-Bromophenyl)prop-2-yn-1-ol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area. Protect it from direct sunlight, moisture, and sources of ignition. Store separately from strong oxidizing agents, acids, and bases. Handle under an inert atmosphere if necessary, and ensure proper laboratory labeling in accordance with chemical safety guidelines. |
Applications of 3-(3-Bromophenyl)Prop-2-Yn-1-Ol in Industrial Manufacturing3-(3-Bromophenyl)prop-2-yn-1-ol plays a critical role as a synthetic intermediate in a variety of specialized industrial sectors. Used primarily by manufacturers of pharmaceuticals, agrochemicals, specialty polymers, advanced materials, and liquid crystal intermediates, it supports the development of high-value compounds where functional group transformation and brominated aromatic frameworks are required. Below are detailed downstream application scenarios specifying its role, relevant compliance, formulation details, and integration within finished product manufacturing. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ this compound for constructing complex active pharmaceutical ingredient (API) scaffolds, particularly where the introduction of an aromatic bromine and a terminal alkyne enhances pharmacological profiles. Chemical synthesis teams utilize it in coupling reactions, Sonogashira reactions, and for specific functionalization of aromatic rings during API building block production. In QC-controlled environments, batch records log its use at precise stoichiometric ratios as a designated intermediate under cGMP supervision. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingAgrochemical manufacturers integrate the raw material during heterocyclic compound synthesis, particularly for brominated alkyne-pyridine or alkyne-benzene derivatives. In proprietary pesticide and herbicide R&D lines, research chemists value its functional groups for further derivatization such as click chemistry and for the generation of high-activity scaffolds. Production records demonstrate controlled ratios to avoid excess unreacted alkyne under GHS hazard management post-synthesis. Industry compliance standards
Typical usage ratio
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3. Advanced Materials and Specialty PolymersProducers of advanced polymers utilize the compound as a functional monomer precursor to introduce bromoalkyne side chains or cross-linked moieties. Its use in polyaddition or polycondensation allows downstream manufacturers to impart precise electronic and adhesion properties to specialty films, optoelectronic materials, and high refractive index coatings. Technical documentation highlights batch-to-batch consistency to control incorporation rates for final performance parameters. Industry compliance standards
Typical usage ratio
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4. Liquid Crystal Intermediate ProductionLiquid crystal component manufacturers deploy the bromoalkyne intermediate in the synthesis of aromatic core units with rigid linear or nonlinear structures. The material supports Suzuki–Miyaura and Sonogashira cross-coupling reactions to create precise mesogenic units, tuning refractive and dielectric properties for LCD and OLED display applications. Quality groups document sourcing traceability and purity profiles to meet display grade requirements. Industry compliance standards
Typical usage ratio
Downstream process integration
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The organic synthesis landscape keeps changing as new molecules and building blocks come to the market. 3-(3-Bromophenyl)prop-2-yn-1-ol stands out for anyone working in the synthesis of advanced intermediates or exploring specialty chemicals, including pharmaceuticals or agrochemicals. In our labs, this material does not just serve as an entry on an order form—it is a reliable partner in multi-step sequences, particularly when tight control over functional groups is required. As direct manufacturers, we have watched requests for this compound grow in both volume and sophistication, especially as researchers seek highly substituted aromatic systems or aim for more selective transformations.
Our 3-(3-Bromophenyl)prop-2-yn-1-ol is produced under consistent reaction conditions, emphasizing core principles that experienced chemists appreciate—purity, transparency in documentation, and performance in downstream use. Routinely, we manufacture and supply material with a minimum purity of 98% by GC, a melting point in line with literature expectations, and a guaranteed low level of volatile impurities. Trace metal contamination remains tightly controlled, as palladium and copper-catalyzed reactions are integral in many syntheses using this building block, and trace contaminants often complicate later steps.
Product lots pass regular characterization using NMR, GC-MS, and HPLC. From experience, subtle differences in quality—sometimes difficult to ascertain without direct comparison—can make or break success in micro-scale to pilot-scale runs. We work closely with analytical chemists to ensure transparency and reproducibility, as we recognize just how sensitive many modern synthetic routes are to impurities.
Laboratory teams and scale-up engineers find 3-(3-Bromophenyl)prop-2-yn-1-ol useful primarily as a functionalized aromatic alkyne. The presence of a bromine atom ortho to the propargylic alcohol gives synthetic chemists a versatile handle for further elaboration. Coupling this with the alkyne functionality lets process teams pursue Sonogashira, Buchwald-Hartwig, or other modern cross-coupling strategies with confidence. In advanced stages of many syntheses, this building block provides access to heterocycles, substituted phenylacetylenes, and more complex bicyclic motifs.
As an example, research teams across pharmaceutical R&D projects have turned to this molecule during late-stage intermediate synthesis. Its carefully positioned functional groups offer more than modular assembly: downstream transformations—such as incorporation into kinase inhibitors or anti-inflammatory drug cores—often depend on exacting substitution patterns only accessible with precisely defined intermediates like 3-(3-Bromophenyl)prop-2-yn-1-ol. Scale-up chemists appreciate that its melting profile and solubility characteristics allow clean work-up and straightforward purification, even as processes transition from gram to multi-kilogram batches.
Academic and industrial collaborators sometimes reach out to us for technical input on reaction optimization. From our vantage point as manufacturers, we’ve seen the common stumbling blocks. Solubility issues, exothermicity in coupling steps, and moisture sensitivity during storage can create hurdles. Years of feedback from process teams allow us to adjust handling protocols, recommend robust solvent systems, and document shipping conditions that help researchers get consistent results from the first vial to the hundredth.
Many chemists weigh alternative propargylic or bromophenyl compounds, hoping to address specific challenges in synthesis planning. 3-(3-Bromophenyl)prop-2-yn-1-ol occupies a unique position because it brings both an activated alkyne and a bromine atom positioned for downstream functionalization. Directly related compounds like 3-(4-bromophenyl)prop-2-yn-1-ol or 3-phenylprop-2-yn-1-ol offer their own advantages, for example, via substituent electronic effects or steric profiles, but they don’t match the reactivity or selectivity demanded in some advanced routes.
From the point of view of reaction designers, a meta-bromo substituent can open up regioselective C-H activation pathways or provide custom electronic tuning when building up more complex scaffolds. Reports in the recent literature highlight the increased demand for functionalized alkynes with challenging substitution where ortho or meta orientation of halogens confer extra value in fine-tuning reaction outcomes. The practical upshot is an expanding market for such specialized building blocks, and manufacturers like us must invest heavily in both process development and rigorous analytical verification because the academic and industrial community insists on more than just an “off-the-shelf” intermediate. Each batch, every new scale-up, is a learning opportunity and an evolution in what quality really means on the bench and in the plant.
Producing 3-(3-Bromophenyl)prop-2-yn-1-ol on any kind of serious scale is not a sideline task. Sourcing quality starting materials, managing reaction exotherm, and ensuring consistent activation during halogenation steps all matter. As upstream producers, we’re on the line not only for consistent chemical identity but also for removing colored byproducts and minimizing odorous impurities, both of which can indicate side reactions or incomplete work-ups.
Technical staff work through batch records, scale-up reports, and cell sheets with practical concerns in mind—how to ensure the propargylic alcohol doesn’t over-oxidize, how to keep the terminal alkyne clean and free from copper or palladium residues. Material from small pilot vessels frequently sees sample requests from clients, which we encourage; direct feedback tightens our specification ranges and helps build trust. Some of our long-term relationships with process chemists began over an off-spec batch that, after a root-cause analysis, led to improvements in both our analytical pipeline and production SOPs spanning our alkyne product line. That kind of feedback loop sharpens every run.
Researchers who order material straight from manufacturers often mention just how many trial runs and failed reactions arise from inconsistent quality. By handling the entire production, we tackle issues upstream rather than patching over problems in warehousing or reselling. We keep detailed run-to-run logs, which translate to faster troubleshooting when customers have technical queries. It’s not just a matter of pride—close tracking lets us pinpoint if a drying step drifted out of spec or if a new lot of bromobenzene gave an unexpected impurity profile.
Over the years, our teams have documented variations caused by environmental conditions: ambient temperature swings, vessel coating breakdown, or inconsistent agitation all create subtle—yet significant—changes in the outcome. In a recent multi-ton campaign, researchers hit a snag during a late-stage annulation. Our team reviewed the entire batch history, flagged a minuscule shift in distillation cut-points, and worked directly with the process chemists to resolve the matter. Sharing data from our quality control efforts not only resolved the bottleneck but also helped the research team fine-tune their strategy for future scales, reducing both cost and time.
Deep knowledge of the target molecule’s chemistry lets us anticipate issues at every stage. Purification plays a big role. Some intermediates escape early detection until they show up as stubborn peaks during HPLC. In regular production schedules, our teams adjust chromatographic methods seasonally, often updating mobile phase composition or detector settings as required. Analysts catch small anomalies before they become big problems during scale-up, and synthetic chemists get a product that behaves as literature and protocol predict.
For demanding clients running custom transformations, we frequently provide detailed spectral libraries—including several NMR nuclei and comparison spectra from both reference-grade and real production batches. These extra steps, though time-consuming, save researchers countless hours in method validation or troubleshooting. The extra transparency also means regulators and internal QA teams have less heavy lifting to do, an advantage increasingly valued as compliance requirements expand in regulated industries.
Stability under real-world shipping and storage conditions cannot be treated as an afterthought. We choose packaging designed to minimize moisture pickup and protect sensitive functional groups against light and oxidation. Feedback from customers who operate in humid or high-temperature zones has led us to tweak our protocols, delivering improved product performance in challenging environments. We run stability testing as a matter of course, loading samples into accelerated aging chambers for weeks at a time.
Sustainability is a key part of how we approach chemical manufacturing. We recover and recycle as much solvent as possible, monitor waste streams, and regularly review our reagent choices. Cleaner operations upstream benefit both our workers and downstream users. In the past five years, we’ve moved to adopt more green chemistry practices, focusing on reducing halogenated waste and maximizing the use of renewable feedstocks wherever available. It’s not only about staying competitive; sustainable approaches produce real savings over time and answer the growing inquiries we get from forward-thinking customers.
Long-standing partners provide new perspectives on how 3-(3-bromophenyl)prop-2-yn-1-ol stands up to repeated use in process development and full-scale manufacture. We value constant feedback on yield, reproducibility, and impurity carry-over. Process reliability depends on what happens not just in the flask but all the way through downstream work-up and final product isolation. As synthetic strategies have grown more ambitious, users have become more attuned to even slight material inconsistencies. By responding rapidly to questions about trace byproducts, alternative lots, or custom purity requirements, we help keep projects on track.
Some clients rely on this compound for route scouting, while others run continuous campaigns toward advanced APIs or novel functional materials. Each application brings fresh insight. For example, academic groups working on transition-metal-catalyzed cyclizations have shown us how tiny adjustments to the propargylic moiety’s purity lead to sharper separation profiles or improved functional group tolerance in multi-step schemes.
The accelerated pace of custom molecule development creates consistent demand for reliable precursors. 3-(3-Bromophenyl)prop-2-yn-1-ol continues to serve a strategic role in the assembly of bioactive scaffolds and engineered materials. Unlike commodity-grade reagents, this building block rewards deliberate process control and targeted analytical methods. We often work side-by-side with contract research organizations and fine chemical partners as they tweak synthetic plans or scale campaigns beyond initial feasibility.
From our perspective, chemical manufacturing should be as much about collaboration as about output. Teams at the bench frequently push the boundaries of known chemistry, requiring new adaptations or customized specifications. Our commitment centers on more than timely delivery; it’s about applying direct experiences to help project stakeholders avoid common pitfalls and make progress wherever they are in their discovery pipeline.
Looking back on hundreds of production campaigns, we find direct manufacturing knowledge offers the most value—it lets us give more practical advice and troubleshoot in real time instead of relying on generic guidance or distant hearsay. This level of engagement helps both established companies and agile startups accelerate R&D aims and move toward commercial launches.
On a more day-to-day level, the hands-on expertise of our technical staff means researchers can reach out for nuanced advice—what solvent choices play best with the compound in their specific method, what purification strategies have been effective, and what to expect in downstream hydrolysis or cross-coupling. This is more than customer service; our chemists understand the chemistry, and that makes all the difference in a time-sensitive setting.
Accountability remains a touchstone for our operation. Unlike companies that broker off-the-shelf intermediates, we have a direct line to every production run, raw material batch, and analytical result. Documentation is robust, and we keep a meticulous archive of spectral data, stability records, and manufacturing deviations as a foundation for continuous improvement. When researchers need to trace an anomaly, our records provide not just a paper trail, but a practical roadmap to resolution.
We have learned over the years that simple claims of quality are not enough—detailed, auditable records and direct responsiveness demonstrate ongoing responsibility to both researchers and regulatory stakeholders. As scrutiny around chemical provenance and supply chain integrity grows, the ability to offer complete transparency positions us to support both routine research use and highly regulated programs with equal confidence.
3-(3-Bromophenyl)prop-2-yn-1-ol deserves its growing role among synthetic building blocks, offering both reactivity and selectivity for next-generation discoveries. Our experience as direct manufacturers gives us a front-row seat to the steady evolution of chemical synthesis, providing solutions in real time and addressing challenges with real-world data. Chemists engaged in challenging, multi-step sequences can count on a partner who understands not only specifications, but the detail and discipline that advanced chemistry demands. If your research or production aims push the envelope, you need suppliers with both the perspective and the commitment to keep pace.