|
HS Code |
641625 |
| Chemical Name | (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid |
| Synonyms | DL-4-Bromophenylalanine |
| Molecular Formula | C9H10BrNO2 |
| Molecular Weight | 244.09 |
| Cas Number | 3967-79-5 |
| Appearance | white to off-white powder |
| Melting Point | 220-225°C (decomposition) |
| Solubility | soluble in water, slightly soluble in ethanol |
| Purity | typically ≥98% |
| Storage Conditions | store at 2-8°C, protected from light |
| Chirality | racemic mixture (RS) |
| Smiles | NC(Cc1ccc(Br)cc1)C(=O)O |
As an accredited (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of `(RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid` is supplied in a sealed amber glass bottle with a tamper-evident screw cap. |
| Shipping | Shipping of (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid is conducted in compliance with applicable safety and regulatory standards. The compound is securely packaged in sealed containers to prevent contamination, properly labeled with hazard information, and shipped via certified carriers specializing in chemical transport to ensure safe and timely delivery. |
| Storage | (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid should be stored in a cool, dry, and well-ventilated area, away from light and moisture. Keep the container tightly closed and properly labeled. Avoid exposure to strong oxidizing agents. Recommended storage temperature is typically 2–8°C (refrigerated). Ensure compliance with applicable safety and regulatory guidelines for handling and storage. |
Applications of (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid in Industrial ManufacturingOur capabilities as a direct manufacturer allow us to deliver (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid at consistent quality and technical standards for advanced industrial applications. This specialty intermediate holds an established role in key synthetic pathways across several regulated downstream fields, where customers rely on precisely controlled input, defined compliance, and batch-to-batch reproducibility. The following application scenarios outline how this compound integrates into real-world production chains, addressing compliance, formulation, processing, and end use. 1. Pharmaceutical Active Ingredient Synthesis (API intermediates)This compound functions as a crucial chiral intermediate in the multi-step synthesis of select nonsteroidal anti-inflammatory drugs and CNS-acting pharmaceutical candidates. Its core structure builds key β-amino derivatives required for patented APIs. API manufacturers incorporate the material following rigorous in-process QC, especially for enantiomeric purity, to comply with international submission requirements. It enters the synthetic scheme after initial protection and alkylation reactions, contributing to the target molecule backbone, followed by subsequent steps such as resolution or additional functionalization leading up to the final API crystallization. The technical integration at this stage requires careful stoichiometric control and robust analytical verification. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Custom Peptide SynthesisIndustry leaders in synthetic peptide chemistry employ this compound for site-specific modification in solid-phase peptide assembly, utilizing the β-amino acid motif to alter peptide backbone geometry and introduce functionality not achievable through standard α-amino acid couplings. When integrated into resin-bound peptide elongation strategies, it allows for the creation of bioactive peptide analogs with improved metabolic stability and modulated receptor selectivity. Its use at defined protocol steps demands inspection for residual solvents and heavy metals to align with therapeutic peptide regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Fine Chemical Intermediate for Agrochemical SynthesisProducers of specialty agrochemicals use our material for constructing brominated and amino-functionalized intermediates during synthesis of advanced pesticides and plant growth regulators. The compound’s structure supports regioselective formation of substituted phenylpropanes, which proceed via additional steps—acyclation, chlorination, or oxidative transformation—toward bioactive ingredient assembly. Integration necessitates granular control over residual halide levels and trace contaminants, documented via long-term product stewardship aligned with global agricultural chemical regulations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chiral Analytical Standards and Reference MaterialsOur compound serves analytical laboratories as a critical chiral reference standard for calibration of enantioselective HPLC and capillary electrophoresis systems. QC specialists value the availability of both pure enantiomers and racemic mixtures for method development, system suitability testing, and validation of chiral separation processes in pharmaceutical and chemical production environments. Material supplied for this purpose undergoes extensive batch certification, typically accompanied by COAs specifying optical purity, isotopic labelling (when required), and exact impurity profiles. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive (RS)-Beta-Amino-Beta-(4-Bromophenyl)Propionic Acid prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
Many in the synthetic chemistry field know the challenge of sourcing high-purity beta-amino acids, especially those with halogenated aromatic rings. Over the years, we have dedicated ourselves to advancing the manufacture and refinement of compounds like (RS)-beta-amino-beta-(4-bromophenyl)propionic acid. This compound, which chemists usually recognize by its role in research on new peptide mimetics and pharmaceutical intermediates, requires careful attention at every stage of production. From chiral synthesis routes to final crystallization, the hurdles aren’t purely academic. You want reproducibility, reliable batch-to-batch quality, and competitive pricing delivered by a partner who understands the pressure of tight research deadlines.
(DL)-beta-amino-beta-(4-bromophenyl)propionic acid (CAS 172632-44-5) is produced in our plant at varying lot sizes, most often between 500g and several-kilogram batches, depending on project or program demand. This product showcases a commitment to strict control of both optical and chemical purity. Our team relies on repeated chiral chromatography and NMR confirmation as standard practice, backed by decades of know-how training chemists to detect even minor side impurities or epimerization events. Raw starting materials for each batch undergo full analytical verification, since minute differences in precursor quality can influence reaction efficiency or the final crystalline phase.
Some manufacturers look only at yield and cost. We have found that focusing so narrowly often drives up hidden waste—unwanted isomers, trace bromide contaminants, and problematic agglomeration during drying. Our workflow adapts to minimize these issues through modest changes: using high-purity base reagents and monitoring bromination levels by GC-MS analysis in-line, for example. The downstream effect? Fewer batch reworks, more predictable product characteristics, and critically reduced risk to downstream pharmaceutical purification steps. With a history of custom synthesis contracts for pharmaceutical research and academic collaborators, we listen closely to the chemists who build upon our materials. Their feedback has shaped the surface finish and flow properties of our final acid product—details traders and distributors often miss.
Beta-amino acids like this one serve as building blocks in non-proteinogenic peptide synthesis, chiral ligand development, and even as test substrates for enzyme engineering. Our process for (RS)-beta-amino-beta-(4-bromophenyl)propionic acid never loses sight of the danger in over-granulated or uneven particle size, which can slow reactivity or complicate downstream process steps. We mill each batch under controlled conditions, collect particle size distribution data in real time, and only accept lots with established midpoint and range measures. Instead of leaving research chemists to chance, we provide a product that weighs, dissolves, and reacts as published literature predicts.
Our team learned early not to rely on a single analytical technique when certifying purity. NMR, HPLC, and mass spectrometry—combined with rigorous Karl Fischer moisture analysis—give a more complete picture of each lot. Some customers request HPLC chiral purity greater than 98%. This target didn’t arrive as a marketing pitch; it resulted from real-world troubleshooting with large peptide synthesis runs, where even a 1% impurity can affect process reproducibility. Our work involves continuous checkbacks to established syntheses and peer-reviewed data, not just certificate paperwork.
Many laboratory reagents move through complicated supply chains, picking up byproducts and ambiguities at each handoff. Here, every kilogram shipped receives batch documentation generated by the same staff who ran synthesis, quality checked by chemists who understand the risks of brominated impurities or incomplete resolution. This direct connection between manufacturer and customer reduces shipment delays and allows for faster troubleshooting if questions arise during research scale-up.
Bromophenyl-based beta-amino acids present a special challenge: bromine derivatives leave a much wider window for trace-level tox analysis compared to simple non-halogenated acids. As a direct manufacturer, we run every batch through updated heavy metal and halogen testing, keeping record sets that can be shared in case of regulatory queries or unexpected assay results. When colleagues down the chain encounter anomalies, we can track the specific dates, synthesis routes, and purification steps involved—transparency that third parties simply can’t offer.
From molecular formula to melting point, the details hidden in a product’s spec sheet only tell part of the story. Let’s take specific optical rotation as an example. Some suppliers offer racemic or enantiopure forms of beta-amino acids but will not specify whether they have tested actual activity. We discontinued that practice, choosing instead to measure actual activity on every production lot, and sharing data well beyond simple minimums. These measurements have been cross-verified against published standards in journals focused on amino acid chemistry.
Specifications matter most where deviation causes real-world pain. Moisture content above 0.3% can lead to localized caking in automated synthesisers. Acid content outside a narrow range causes pH drift, affecting coupling efficiency in peptide assembly. It takes years of repeated synthesis and hands-on troubleshooting to recognize when a minor variation on paper means a major interruption in practice. Our chemists revisit published application notes, react these beta-amino acids in actual targets, and tune specifications to avoid problems before they occur, not after a return request.
Many beta-amino acids fail to reach researchers in pure, shelf-stable form. Some lose clarity or color due to light or oxidation during shipment or storage. By refining in low-light conditions and storing under controlled atmosphere, our process preserves white to off-white appearance and sharp melting point, meeting both internal and published monograph standards. Each lot is packaged immediately after drying in moisture-impervious liners and sealed containers, backed by tracked temperature loggers for large shipments.
Some users report difficulty in dissolving related beta-amino acids, a problem traced back to residual inorganic salts or unreacted starting brominated benzenes. We avoid the need for excess rinsing in downstream reactions by cleaning intermediates at every stage, not just after final isolation. When introducing this product to our own pilot research labs, we scrutinize not just infrared and HPLC profiles, but the ability to reconstitute to the required molar concentration in standard buffers. Real feedback from our own bench chemists provides the best early-warning system to catch issues that might only emerge during actual use, not on a spec sheet.
As beta-amino acid analogs gain use in medicinal chemistry and material science, researchers push these molecules through increasingly diverse reactions: metal-catalyzed couplings, asymmetric hydrogenation, and combinatorial screening. Each expansion brings up new demand for reactivity and purity, sometimes in unpredictable ways. Our plant brings together synthetic and analytical chemists to discuss feedback from every industry segment—academic, pharma, diagnostics—so that recurring problems become catalysts for process improvements. Unlike traders who only see a finished product, we stay involved when unexpected side reactions arise, often running small-batch reproductions to investigate anomalies in real time.
Another benefit of direct manufacturing is flexibility with customization. If a collaborator’s process needs a specific hydrate or salt form, our team can modify the workup and packaging accordingly. This close communication leads to high overall product consistency, where both small and large scale projects receive material with the same rigorous documentation, and adjustments to particle or form are available without long lead times or questionable sourcing. Many customers have reported smoother scale-up and fewer wasted runs compared with material from non-integrated supply chains.
Over time, regulatory requirements in the chemical and life sciences space have grown tighter. A deep understanding of GHS classification and local transport laws impacts our lot formulation, documentation, and packaging processes. This approach goes beyond simple compliance. We train all technicians and handlers in real-world chemical risks, not relying on superficial documentation. For beta-amino-beta-(4-bromophenyl)propionic acid, controlling dust levels, secondary containment, and documented storage temp ranges means you receive a material as stable and safe as possible.
Direct engagement with regulatory updates helps us catch small details that, if overlooked, can lead to future shipment or import headaches. We keep robust audit trails for every batch, and repeat ourselves often on paperwork details that prevent confusion for labs preparing for FDA or EMA submissions. At the plant, records go back many years, down to the level of precursor lot and assigned technician. Chemists should not have to act as detectives for issues that already occurred—keeping the line straight from raw input to finished output saves everyone time and effort.
Anyone working with substituted beta-amino acids has seen it: crystals that suddenly shift form, loss of color purity after exposure, or surprising gaps in documentation. These pitfalls nearly always stem from a lack of direct involvement in process and post-processing. We devote resources to constant controls, routine checks, and updating procedures based on real-world user feedback. Instead of focusing only on yield maximization, we chase fewer batch failures and easier user experiences. The result is a compound that not only matches published standards on paper, but survives the realities of shipping, storage, and varied applications—an element that sometimes gets forgotten by those only thinking in terms of volume and margin.
Each innovation we introduce—new controls on bromine addition, extra rounds of fine milling, double-checks on moisture, or custom packaging cuts—comes from repeated direct experience, including setbacks. In our history, every misstep led to tighter controls and better products. The stakes are real when a customer’s result depends on every milligram, whether in basic research or advanced manufacturing.
Our (RS)-beta-amino-beta-(4-bromophenyl)propionic acid doesn’t resemble standard racemic or enantiopure analogs in minor ways. The bromine atom introduces both chemical reactivity and potential analytical complexity that requires more careful synthesis and testing methods. Over time, our experience shows that not all suppliers reach the same level of attentiveness. We have witnessed firsthand the effect of poorly controlled bromination leading to persistent impurities, or unstable isomeric mixtures that leave researchers with unusable material.
Some competing products arrive under-labeled, lacking information on test method or purity grade. In contrast, our shipments always include not just a short COA, but full spectra on request, detailed test standards, and cross-references to relevant literature. The approach our team takes starts with hands-on technical experience, not simply reading off a catalog. Our direct connection to R&D can clarify questions about molecular structure, stability, and side-chain reactivity, giving end users security in applications from peptide library construction to early pharmaceutical screening.
Innovation in synthetic chemistry keeps moving, often in unpredictable directions. For every new method or catalyst, new needs arise for substrates with lower impurity profiles, consistent melting points, or improved shelf stability. We keep in constant contact with collaborators, using their real feedback to guide batch adjustments and process improvements. Some of the most important changes in our manufacturing came because a researcher shared their final application, letting us tune the product better for both immediate and future use.
As a result, our focus stays on keeping pure, reliable, well-characterized beta-amino acids flowing from our plant to the lab, batch after batch. Trust is built when chemists receive material that matches expectation every time, and when they know the team they’re working with has enough technical insight to actually understand their process. Our work isn’t complete until the material is running smoothly in applications ranging from classic solid-phase peptide synthesis to new small-molecule catalyst cycles.
Years in chemical manufacturing teach lessons that can’t be found in catalogs or data sheets. Each new batch of (RS)-beta-amino-beta-(4-bromophenyl)propionic acid reaffirms the value of hands-on problem-solving, direct control of every aspect from synthesis through delivery, and unbroken communication between plant and researcher. The small differences—tightly specified analytical checks, timely updates after every regulatory change, direct feedback loops, and willingness to customize batch properties—combine to deliver a product seldom matched by generic or brokered supply chains.
As research and discovery in life and material sciences grow, these kinds of direct, technically informed partnerships only become more important. The focus on details, from optical purity to moisture level and packaging, comes from working alongside the scientists who use our products every day. This is how we define real quality and real value—through attention, effort, and long-term collaboration.