|
HS Code |
168040 |
| Product Name | DL-Beta-(3-Bromophenyl)Alanine |
| Cas Number | 238747-41-0 |
| Molecular Formula | C9H10BrNO2 |
| Molecular Weight | 244.09 |
| Appearance | White to off-white crystalline powder |
| Solubility | Slightly soluble in water |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8°C |
| Smiles | N[C@@H](Cc1cccc(Br)c1)C(=O)O |
| Iupac Name | 2-Amino-3-(3-bromophenyl)propanoic acid |
| Synonyms | DL-3-Bromophenylalanine |
| Stability | Stable under recommended storage conditions |
As an accredited DL-Beta-(3-Bromophenyl)Alanine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Packaged in a sealed 25g amber glass bottle, labeled "DL-Beta-(3-Bromophenyl)Alanine," with safety symbols and batch information. |
| Shipping | DL-Beta-(3-Bromophenyl)Alanine is shipped in tightly sealed containers, protected from light and moisture, and typically kept at room temperature. Packaging complies with safety regulations for hazardous materials. Appropriate labeling and documentation accompany the shipment to ensure safe handling during transport. Expedited or temperature-controlled shipping may be arranged if required. |
| Storage | DL-Beta-(3-Bromophenyl)Alanine should be stored in a tightly closed container in a cool, dry, and well-ventilated area. Protect it from moisture, direct sunlight, and incompatible materials such as strong oxidizing agents. Keep it at room temperature unless otherwise specified by the supplier, and ensure proper labeling. Store away from sources of ignition and follow standard chemical storage safety protocols. |
Applications of DL-Beta-(3-Bromophenyl)Alanine in Industrial ManufacturingDL-Beta-(3-Bromophenyl)Alanine is a specialty amino acid derivative that finds well-documented application in advanced pharmaceutical synthesis, peptide drug manufacturing, customized biochemical intermediates, agricultural research actives, and analytical reference compound production. As a direct producer with multi-step synthesis capabilities, we supply this intermediate into the following authentic industrial domains, meeting demanding quality and regulatory requirements at each stage. 1. Peptide-Based Drug SynthesisPharmaceutical manufacturers use this amino acid derivative for the production of peptide and peptidomimetic active pharmaceutical ingredients (APIs) targeting central nervous system and oncological therapies. The material’s brominated aromatic side chain enables critical structure-activity modifications that cannot be substituted by generic amino acids. You will find it specifically formulated during solid-phase or solution-phase peptide chain elongation, where precise stereochemical incorporation is required to develop molecules with desired pharmacokinetics and target affinity. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Pharmaceutical Intermediate for Heterocyclic Drug SynthesisThe compound serves as a valuable building block in the multi-step synthesis of heterocyclic drugs, especially for generating brominated benzene derivatives that act as precursors for non-peptidic APIs in CNS and metabolic disorder treatment pipelines. The installed bromo group is directly deployed in Suzuki-Miyaura or Buchwald-Hartwig cross-coupling reactions to access highly substituted aromatic pharmaceutical scaffolds that require strict trace impurity control and reproducible reactivity in GMP batch production. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Biochemical Research and Custom Peptide Library SynthesisContract research organizations and institutional laboratories employ DL-Beta-(3-Bromophenyl)Alanine in combinatorial chemistry projects focused on binding studies, selectivity mapping, and enzymatic probe characterization. Its unique electronic and steric profile makes it essential for constructing peptide libraries in high-throughput screening formats, enabling the exploration of modified binding motifs in receptor-ligand and protein–protein interaction research. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Analytical Reference Material ProductionSpecialty chemical manufacturers and analytical standards suppliers use this compound to prepare certified reference materials (CRMs) and analytical standards necessary for development, validation, and calibration of quantitative methods in pharmaceutical quality control. Its precise molecular fingerprint allows traceable identification and quantification in impurity profiling and stability testing workflows, especially for brominated aromatic residues in regulated drug substances. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive DL-Beta-(3-Bromophenyl)Alanine 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!
In our work, every batch of DL-Beta-(3-Bromophenyl)Alanine begins long before any flask finds its place in the lab. As a team at the manufacturing site, we understand this compound’s critical role for research chemists, pharmaceutical developers, and process engineers. This amino acid derivative often serves as an intermediate for exploring new peptides, small molecule drugs, and fine-tuned catalyst systems that demand precision at the molecular level. We wake up to these challenges every day, committed to consistent, clean output.
Our standard product carries the designation DL-Beta-(3-Bromophenyl)Alanine, without fancy trade names or opaque terms. The “DL” label states what’s inside the drum clearly: a racemic mixture containing both D and L isomers. As synthetic chemists ourselves, we pay constant attention to racemate purity—starting often from chiral sources and validating with each chromatogram. The typical batch appears as a crystalline powder with a white to faintly beige tint. Melting point and solubility measures stay well-documented, and purity by HPLC generally reaches above 98%, a result that takes daily effort in every reactor run and post-processing cycle. Moisture content stays controlled by working in a dry environment, and impurities—brominated or otherwise—get chased down well before bulk filling.
Those of us at the production line see clearly that pharmaceutical innovation leans heavily on uninterrupted supply. DL-Beta-(3-Bromophenyl)Alanine often forms the skeleton of larger structures, whether in chiral auxiliaries, peptidomimetics, or as a starting point for halogenated pharmacophores. Scientists count on reliability. Our shop runs multi-step synthesis with in-process controls—not every lab tolerates trace solvent, so we focus on high-vacuum drying, routine GC analysis, and rigorous cleaning between runs. Chemical smell, color, and texture tell us as much as any analytical report. Equipment cleaning logs serve us as a shield against cross-contamination and keep residual bromide and unrelated amino analogues out of the material.
Manufacturers face the reality that global procurement looks for competitive cost but rarely rewards hidden shortcuts. We buy raw phenylalanine from vetted partners who disclose every upstream solvent and catalyst. Supply chain integrity matters because robust, reproducible synthesis supports product claims in the field and avoids headaches in regulatory filings. On-site, chemists wear more than gloves—they wear responsibility to ensure no byproduct carries through the process. Our internal batch records track time, temperature, and reagent lot numbers for every vessel change.
DL-Beta-(3-Bromophenyl)Alanine shows its strengths best as a versatile building block—its beta-positioned bromine opens more options than unsubstituted phenylalanine or ortho/para-substituted analogues. Electrophilic aromatic substitution, Suzuki coupling, and nucleophilic aromatic substitution run more smoothly and provide synthetic flexibility. In many labs, this lets researchers modify peptides post-assembly, add tracers, or experiment on a lead series with safer halogen swaps. We’ve seen the molecule become a platform for radiolabel introduction, or a point of attachment in D-amino-acid chimeric peptides. Having both D and L forms mixed simplifies screening early in discovery.
Comparing to standard phenylalanine or even para-bromo derivatives, the meta-bromo position changes both reactivity and physical behavior. During custom synthesis projects, chemists prefer this regioisomer due to distinctive steric and electronic effects in peptide backbones. By producing the beta-(3-bromophenyl) variant, we help project teams reduce synthesis steps and gain structure-activity insights that would otherwise take longer to unlock.
Laboratories and pilot plants handle this material in multi-gram to commercial scales, using it in peptide synthesis, targeted pharmaceuticals, and building block inventories for custom libraries. Researchers exploring brominated tyrosine analogues or halogen-rich drug scaffolds often contact us about batch-to-batch consistency. Our plant has supplied DL-Beta-(3-Bromophenyl)Alanine for both solid-phase and solution-phase peptide assembly. Over the years, we have retooled our process as users have shifted from simple methyl ester intermediates to more complex protecting group strategies—each adjustment guided by user feedback and published data.
Sometimes, small impurities in a fine chemical don’t impact high-throughput screening—analytical instrumentation picks out minor contaminants without confusion. Drug discovery, peptide sequencing, and radiolabeling research demand more. Sample purity translates to adaptability: one project leader once described how a poorly resolved isomer nearly derailed their lead series investigation. After switching to our material, they avoided unnecessary purification and kept timelines. These stories echo across customer feedback, and, as a manufacturer, we use that real-world experience to fine-tune process parameters.
Neither regulatory tightening nor market shifts stand still in the specialty chemicals world. End-users raise questions about trace metal residues, phthalate contamination, or cross-reactive halogen sources. A few years ago, our team invested in expanded in-process testing, using both automated HPLC and inductively-coupled plasma analysis. This adds hours to our workflow, but also keeps our certification process smooth—especially for partners preparing for FDA or EMA submissions. Frequently, we run side-by-side method validations with formulation scientists, directly comparing our feedstock performance against historical lots.
Logistics pose their own evidence of a changing landscape. Fluctuating import duties, pressure on cold chain shipment, and documentation for customs compliance each pull our attention daily. Countries treat halogenated amino acids differently under import regulations. We prepare compliance documents for every order, but real-time traceability for every kilo means barkeeping at the drum level—the same vigilance we would want from our own suppliers. Organic traces and stability in long-term storage move us to upgrade container materials, switching from standard PE drums to specialized liners that prevent water ingress and reduce static buildup.
Environmental scrutiny falls on chlorinated and brominated intermediates more each year. Our manufacturing process produces some waste containing residual bromide and organic solvent, a reality every producer faces. We operate on a closed-loop principle: off-gas scrubbers and liquid-phase neutralization help minimize emissions. Used mother liquors undergo solvent recovery and selective phase separation, not disposal. These adaptations didn’t come from regulation alone—they reflect the values of our technical staff, many of whom started in academic labs that drilled sustainable chemistry long before it became industry standard.
In research and development reviews, we’ve partnered with academic groups aiming to replace stoichiometric halogenation steps with catalytic or biocatalytic alternatives. Such methods aren’t mature enough for every order, but we see evidence in pilot-scale runs that future synthesis could trim energy and raw input needs. One ongoing project uses electrochemical bromination on a flow basis, a technology that could cut both waste and hazard in the years ahead. While that research continues, we update our batch records to document every deviation and keep external auditors informed—openness with our process advantages and flaws builds lasting trust.
In the world of fine chemicals, subtle differences turn into costly mistakes or breakthrough opportunities. Standard phenylalanine analogues—whether ring-unsubstituted, para-brominated, or D/L segregated—show distinct solubility, melting, and reactivity profiles compared to DL-Beta-(3-Bromophenyl)Alanine. We hear from formulation chemists that the meta-bromo group enables better incorporation into secondary structure probes, fluorogenic assays, and halogen bonding screens. The compounded effect of beta-substitution and meta-bromination reveals itself downstream; a change here leads to altered pharmacokinetic and stability profiles in the final compounds.
Beyond chemical differences, our manufacturing experience separates DL-Beta-(3-Bromophenyl)Alanine from mass-market offerings. Some firms ship product containing variable water content, or skip rigorous chiral purity checks, betting on user-side purification to fix unrefined goods. We run each lot through dual HPLC and NMR, confirming identity and racemate equivalence. As a producer, responsibility does not end after the drum leaves our hands. We engage directly if any customer detects an off-profile batch, and are prepared to run stability or impurity analysis alongside them. This is not just a supply chain—it’s an ongoing technical partnership, forged from the reality that every product quality slip costs users time and trust.
Our sourcing team depends on face-to-face meetings with material suppliers, whether in raw phenylalanine, protected intermediates, or specialty reagents. Every new lot brings a new analysis file. We never trust a paper certificate alone; in-house verification makes up the bedrock of our incoming QA workflow. Purity, water content, and trace solvent levels often reveal more about a producer than polished catalogs. Once material clears inspection, our production chemists monitor every stage from bromination through chromatographic purification and final packaging.
Several years ago, an unexpected drop in purity from a solvent vendor nearly forced a major production halt. We responded by tripling supplier audits and installing real-time impurity detection at drum filling. These upgrades cost us a few weeks and a few thousand dollars, but our repeat customers now benefit from fewer “out-of-spec” headaches. To us, manufacturing quality remains not just a regulatory checkbox, but a reflection of our technical values.
Listening to the research and production communities, we absorb direct and unfiltered user feedback. Stories matter: like the bioprocess developer who reported a single contaminant spike derailing complex enzyme screens, or the contract research firm that switched suppliers after repeated batch failures from inconsistent material. In most cases, we adjust our cleaning procedures, swap auxiliary reagents, or invest in another level of analytical coverage. Directly engaging with customers, our technical staff understand firsthand the implications for time, data integrity, and ultimately, product development.
User demand for flexible scale and packaging grows each year. By keeping in-house blending and filling, we address requests ranging from multi-gram research samples to multi-kilogram production runs. Researchers often start with small exploratory batches, later requesting kilogram lots for scale-up or production. Custom pack sizes and blending protocols mean more hands-on effort in the factory, but our experience shows that responsiveness outweighs the simplicity of a single fixed-size SKU.
We’ve learned that adjusting particle size, re-granulating for custom reactors, and switching filling containers solves logistical challenges for formulation or robotic sampling. This “on the ground” learning doesn’t get captured in glossy marketing slides—it happens through trial, correction, and collaboration with users in the field.
Each year presents a mix of opportunity and unresolved challenge. The popularity of DL-Beta-(3-Bromophenyl)Alanine in emerging drug pipeline projects, high-throughput peptide synthesis, and new cross-coupling strategies continues to grow. Our commitment as a manufacturer centers on direct technical communication, robust internal controls, and investment in cleaner, smarter synthesis processes. We pledge to keep revisiting our own assumptions as the field evolves. We draw lessons from our peers, from user community experience, and from every batch we process—not just to maintain today's standards, but to set new benchmarks for reliability, sustainability, and transparency in specialty amino acid production.
As manufacturing chemists, we know the journey from raw aromatic building block to finished pharmaceutical, probe, or material starts with choices made in our own plant. The trust extended to us by scientists, developers, and engineers is sustained through care, attentiveness, and openness about the challenges and trade-offs of modern chemical manufacturing. DL-Beta-(3-Bromophenyl)Alanine represents both the progress and the complexity of this journey. We keep building better products—listening, learning, and adapting with every collaboration and every kilogram delivered.