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L-Beta-Homophenylalanine Hydrochloride

    • Product Name L-Beta-Homophenylalanine Hydrochloride
    • Alias H-D-HomoPhe-OH·HCl
    • Einecs 693-031-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    948401

    Productname L-Beta-Homophenylalanine Hydrochloride
    Casnumber 4749-65-9
    Molecularformula C10H14ClNO2
    Molecularweight 215.68 g/mol
    Appearance White to off-white crystalline powder
    Purity ≥98%
    Meltingpoint 210-215°C (dec.)
    Solubility Soluble in water
    Storagetemperature 2-8°C
    Opticalrotation [α]20/D +16.0° (c=1, H2O)
    Synonyms L-β-Homophenylalanine hydrochloride; L-β-Phenyl-beta-alanine hydrochloride
    Iupacname (2S)-2-amino-4-phenylbutanoic acid hydrochloride
    Form Solid

    As an accredited L-Beta-Homophenylalanine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed HDPE bottle labeled “L-Beta-Homophenylalanine Hydrochloride, 25g.” Includes CAS number, purity, handling, and storage instructions.
    Shipping L-Beta-Homophenylalanine Hydrochloride is shipped in tightly sealed, chemical-resistant containers to prevent contamination and moisture absorption. The package is clearly labeled as a laboratory chemical and handled according to all regulatory guidelines for safe transport. Shipping is expedited and temperature-controlled if required to maintain product stability and purity.
    Storage L-Beta-Homophenylalanine Hydrochloride should be stored in a tightly sealed container, protected from light and moisture. Keep at room temperature (15–25°C), in a dry and well-ventilated area away from incompatible substances such as strong oxidizers. Avoid exposure to extreme heat or cold. Proper labeling and secure storage are recommended to ensure stability and prevent contamination.
    Application of L-Beta-Homophenylalanine Hydrochloride

    Applications of L-Beta-Homophenylalanine Hydrochloride in Industrial Manufacturing

    L-Beta-Homophenylalanine Hydrochloride serves as a specialty intermediate in a range of established industrial production chains. As a manufacturer of this compound, we supply material consistently aligned with the technical, regulatory, and operational needs of downstream partners who require stringent compliance and traceability. The following application scenarios present real-world use cases grounded in current industrial practice, emphasizing integration points and process requirements for advanced manufacturing.

    1. Peptide Drug API Synthesis

    Pharmaceutical manufacturers employ L-Beta-Homophenylalanine Hydrochloride as a protected amino acid building block during solid-phase peptide synthesis (SPPS) for the API segment of highly specific therapeutic peptides. The compound's structural features enable precise side-chain modifications where phenylalanine analogues are essential, especially in custom sequence design for metabolic and hormone analog drugs. Downstream partners request well-defined purity and validated traceability documents for DMF submissions and batch release.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) General Chapter <797> and <1078>
    • European Pharmacopoeia (Ph. Eur.) monograph guidance (custom peptide APIs)
    • US FDA Drug Master File (DMF) referencing for raw materials

    Typical usage ratio

    • 0.8–4 mol% per peptide chain, adjusted based on sequence specificity and target substitution
    • Batch ratios determined by target peptide length and modification density

    Downstream process integration

    • Enters Fmoc-SPPS or Boc-SPPS resin coupling step after pre-activation with standard peptide coupling agents
    • Integrated in protected or deprotected forms depending on process flow; monitored for racemization control in QC

    Final product types

    • Custom peptide-based APIs for metabolic, oncological, or hormonal therapeutics
    • Advanced research peptides for clinical pipeline development
    • Peptide intermediates for contract manufacturing organizations (CMOs)

    2. Peptide-Based Diagnostic Reagent Formulation

    Producers of in vitro diagnostic (IVD) test kits use this compound as a non-natural residue during preparation of custom peptide substrates for enzyme immunoassays (ELISA), chemiluminescent immunoassays (CLIA), or biosensor reference peptides. It enables creation of highly selective probe or control sequences that help reduce false signals or improve assay specificity for research, clinical analysis, and point-of-care diagnostics.

    Industry compliance standards

    • ISO 13485 Medical Devices—Quality Management Systems
    • Directive 98/79/EC (IVD Medical Device Directive) and IVDR (EU Regulation 2017/746)
    • CLSI (Clinical and Laboratory Standards Institute) sample preparation protocols
    • Self-declaration to RoHS/REACH where biotinylated or labeled substrates are involved

    Typical usage ratio

    • 1–7 mol% of total amino acid content in synthetic peptide substrate, tailored to target enzyme specificity

    Downstream process integration

    • Incorporated at defined cycle(s) in automated or semi-automated peptide synthesizer instrument runs
    • Sequence is cleaved, deprotected, purified, and subsequently conjugated (if required) for platform-specific performance

    Final product types

    • ELISA/CLIA synthetic peptide reagents and calibration standards
    • Peptide-coated biosensor chips for laboratory analyzers
    • Reference or control peptides packaged in validated diagnostic kits

    3. Chiral Intermediate Supply for Pharmaceutical Fine Chemicals

    Chiral synthesis workshops and GMP fine chemical producers use L-Beta-Homophenylalanine Hydrochloride as a specialty intermediate for manufacturing advanced building blocks, particularly where enantiopure non-natural chain extension motifs are needed before downstream phase-transfer catalysis, asymmetric hydrogenation, or chiral auxiliary coupling. This scenario reflects ongoing demand in the supply chains for modern small molecule drug and peptide analogues.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • 21 CFR Part 210/211 (cGMP for Finished Pharmaceuticals)
    • European Medicines Agency (EMA) guidelines for chiral substances
    • Auditable change control for incoming raw materials per ISO 9001:2015

    Typical usage ratio

    • 15–22% by molar ratio as the chiral moiety source within the multi-step synthesis of advanced intermediates
    • Usage intensity calculated based on final enantiomeric purity requirements

    Downstream process integration

    • Activated and introduced during the chiral center formation step, often as the first enantioenriched residue
    • Subsequently modified in functional group transformations prior to target product isolation

    Final product types

    • Chiral building blocks for antidiabetic agents, CNS-active compounds, or investigational drug leads
    • Specialty pharma intermediates for contract research organizations (CROs) or custom synthesis partners

    4. Reference Standards for Analytical Laboratories

    Analytical standards suppliers and pharmaceutical QC labs require high-purity sources of non-proteinogenic amino acids including L-Beta-Homophenylalanine Hydrochloride for calibration, method development, and system suitability testing. The repeatable stereochemistry and well-defined impurity profile make it essential for LC-MS/MS, HPLC, and chiral chromatography reference materials supporting both regulated and research-only applications.

    Industry compliance standards

    • ISO/IEC 17025 Testing and Calibration Laboratories Accreditation
    • USP General Chapter <621> Chromatography
    • FDA Guidance for Industry: Analytical Procedures and Methods Validation for Drugs and Biologics
    • GLP (Good Laboratory Practice) principles as required by end-user industry

    Typical usage ratio

    • Used as reference: 0.1–2 mg/mL in calibration standards, tailored according to instrument sensitivity and method
    • Preparation protocols depend on solvent, matrix, and QC batch validation design

    Downstream process integration

    • Prepared as primary or secondary standard during assay validation and method qualification steps
    • Supplied in sealed ampoules, aliquoted for LC, GC, or capillary electrophoresis systems

    Final product types

    • Chromatographic reference standards for pharmaceutical QC and research
    • System suitability test kits for regulated laboratory workflows
    • Custom reference peptide mixtures supplied to analytical labs
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    Certification & Compliance
    More Introduction

    L-Beta-Homophenylalanine Hydrochloride: An Insider’s Look at Production and Application

    Understanding the Nature of L-Beta-Homophenylalanine Hydrochloride

    Making L-Beta-Homophenylalanine Hydrochloride reaches beyond batch sheets and specifications. Each synthesis line brings its own set of fingerprints. Through years in the reactor halls and QA stations, I have come to appreciate the subtlety of each step. At our facility, the product comes from a careful arrangement of raw materials, where benzyl side chain chemistry plays an outsized role. Unlike basic amino acids or more conventional phenylalanine derivatives, this compound holds its own due to the beta extension and resulting spatial arrangement. We manufacture crystalline hydrochloride salt of L-Beta-Homophenylalanine to ensure water solubility and stable shelf behavior, which makes handling and formulation more straightforward in demanding settings.

    Most outside observers recognize the name and ask about its performance against ordinary phenylalanine or alpha-variations. I often answer by putting the focus on chiral stability and downstream reactivity. Our product offers a consistent L-configuration, produced through stereoselective routes, and every kilogram must pass strict checks for optical purity. This attention in synthetic control pays off for anyone scaling up production in peptide synthesis or looking to ensure consistency across batches of complex pharmaceuticals.

    Specifications That Matter in Day-to-Day Operations

    Specifications on paper mean little unless they connect to real fabrication and lab uses. Our usual batch presents as a white to off-white crystalline powder, and it brings a molecular weight in line with theoretical values for C10H14ClNO2. Moisture content is tightly capped, which prevents degradation or caking during storage. During packing, we take great care to avoid cross-contact with other amino compounds, as the presence of even minute impurities—be they structural isomers or similar halide salts—complicates further processes and reduces customer yield. Purity, as measured by HPLC, consistently surpasses 99%, since peptide researchers and pharmaceutical formulators do not tolerate less.

    As someone who deals with customer feedback directly, I have seen how quickly small changes in raw material or process temperature show up in NMR or MS testing. We respond to this not with slogans but by running extended verification protocols, catching trace enantiomeric contamination or residual solvents long before bulk consignments leave the warehouse. Such tight windows are necessary: downstream processes like solid-phase peptide synthesis punish any deviation, leading to unpredictable purities or failed bonds.

    Usage Beyond the Literature: Practical Applications

    Industry veterans know that L-Beta-Homophenylalanine Hydrochloride turns up in places where ordinary amino acid units fall short. On the pharma side, it takes part in building biologically active peptides, especially those that prize extra backbone length or require altered side-chain orientation for receptor targeting. This subtle difference in carbon architecture translates to differences in binding affinity, metabolic stability, and resistance to enzymatic cleavage—issues straight out of pharmacology meetings but rarely discussed in trade catalogs.

    Researchers rely on the hydrochloride form for its enhanced solubility and predictable dissolution rate in aqueous solvents. Since our batches use controlled crystallization and low-temperature drying, the resulting powder dissolves smoothly, without grittiness or excess foaming. Development teams in peptide therapeutics often add our product at critical steps: when trying to introduce flexibility or mimic extended conformations in peptide scaffolds. The beta extension increases the conformational space available to peptide backbones, leading to new possibilities in molecular design.

    Besides pharmaceutical synthesis, we have seen uptake in academic peptide R&D, where researchers substitute in this amino acid to test novel backbone structures. It serves as a valuable intermediate or building block during the manufacture of unnatural peptides, molecular probes, and other bioactive agents intended to probe enzymatic or receptor functions. Every time our product ships out for a new project, it feels rewarding to know that novel protein mimetics or metabolic pathway studies trace back to these reactors and purification lines.

    Production Integrity from Start to Finish

    True product value starts with the supply chain and doesn’t stop when the drum or bottle lands on a customer’s bench. At our manufacturing site, each input batch receives careful tracking from reception through final inspection. There’s a temptation in this field to focus on cost-cutting or minimal processing—yet experience shows that any drift in precursor purity or even reactor cleanliness gives rise to impurity profiles that haunt later steps.

    Our process begins using controlled fermentation to produce the chiral precursor, followed by chemical transformation under inert atmosphere. Each intermediate salt or free-base form gets sampled and analyzed before proceeding. Temperature, pH, mixing rates—every step has trained eyes and hands monitoring them. In the final hydrochloride formation and crystallization, process engineers run slow-cool protocols, minimizing occluded solvent and potential salt byproducts. As a practitioner responsible for both yield and reliability, I work closely with QA to calibrate detectors and verify that specifications don’t just meet but exceed standards needed for GMP-compliant pharmaceutical work.

    During storage and transport, we move the product in sealed, moisture-controlled containers. Routine checks in our in-house stability chambers reveal even minor trends in discoloration or caking—so we improve each batch year after year. Over the long haul, these investments shine through in customer lab results and repeat orders.

    Comparing L-Beta-Homophenylalanine Hydrochloride to Its Peers

    This compound draws questions from experienced chemists focused on distinguishing among similar-looking molecules. The structural deviation—a beta extension compared to standard alpha-phenylalanine—comes through in its properties. In practical peptide synthesis, this extra methylene unit changes both the backbone configuration and the way the molecule interacts with other reagents. Our process ensures that the finished hydrochloride form stays stable on the shelf and performs without surprises under reaction conditions, which matters to those running complex, multi-day reaction schemes.

    Against alpha-phenylalanine hydrochloride, L-Beta-Homophenylalanine Hydrochloride delivers different steric and electronic effects when incorporated into growing peptide chains. This proves essential in applications requiring more flexibility or hydrophobic character in the peptide sequence. As a manufacturer directly involved with technical service inquiries, I can say few things frustrate researchers more than finding subtle impurities from less careful producers—issues like overlapping HPLC peaks or unexpected rotameric mixtures. Our material brings peace of mind and higher downstream yield for those with demanding purification and sequencing steps.

    We get regular requests to compare alternative suppliers, and some end-users even send in their own samples for parallel testing. Batch after batch, our L-Beta-Homophenylalanine Hydrochloride has shown tighter impurity windows, more consistent moisture levels, and smoother dissolution compared to several international brands. Part of this strength comes from vertical integration—we source, process, and verify every critical input, skipping the pitfalls of resell-heavy networks.

    Factual Learnings from Manufacturing Challenges

    No plant or process line runs flawlessly in this business, and years of work with L-Beta-Homophenylalanine Hydrochloride teach plenty about what sets reliable product apart. The common pain points include nuisance levels of side-product, occasional racemization under harsh hydrolysis, and slow filtration or wash performance during salt formation. Early years brought plenty of trial and error—with filtration aids, solvent swaps, and temperature programming—before landing on the current protocol.

    On a few occasions, batches suffered cosmetic changes or slightly lower yields due to poor recrystallization control. Through these scars we refined plant SOPs and reinforced in-line checks, so the current product lines rarely see old problems repeat. As a responsible manufacturer, rework means more than paperwork—it means risking customer trust and stalling vital research. So every adjustment in the plant goes through validation batches before scaling up again.

    Customers tell us they notice the differences in lot-to-lot consistency and spectrum fit. Our approach brings analytical chemists to the table during production—running real-time NMR, HPLC, GC-MS, and even low-level NOE studies—so functional groups and stereochemistry line up per the controllable process envelope. Plant surprises happen, but preparation, expertise, and hands-on troubleshooting keep problems rare and short-lived.

    Market Demands and Customer Concerns

    Demand for L-Beta-Homophenylalanine Hydrochloride comes from two broad directions: pharmaceutical intermediates (with an emphasis on regulated process controls) and research chemical markets where flexibility, small batch sizes, and customization matter. We hear concerns about cross-contamination, shelf stability, and document traceability. Our internal batch record system tracks every movement, and we provide supporting analytical data for each lot that leaves our facility. Open communication with technical teams at leading pharmaceutical firms lets us anticipate changing purity standards or new documentation needs.

    Every inquiry about packaging choices, moisture sensitivity, or re-certification leads to conversation with our QC and R&D teams. Raw feedback, instead of marketing focus groups, determines new process controls or sometimes improved packaging. In one example, a recurring customer from an API startup flagged glass ampoule static leading to trace caking; our packaging team responded within a month by testing antistatic liners and improving seals to lock in product mobility.

    Besides core regulatory requests, recurring customers ask about additional ion profile reporting, enantiomeric purity confirmation, and tailored documentation for international shipments. We routinely respond with rapid-turnaround documentation and cross-reference results with external labs to confirm accuracy.

    Quality and Traceability in Every Batch

    Traceability and consistent quality do not come from chance. Behind each drum, an employee records production data, monitors solvent recycling loops, and maintains line cleaning schedules. Our philosophy recognizes that trace impurities do not simply vanish—they must be tracked, measured, and, when possible, eliminated. By tying every package to a unique production record, we can assess customer feedback all the way back to raw material lot and reactor number. This depth is not industry-standard; many companies lose control across intermediaries or out-of-house sourcing.

    Repeated audits and mock recalls test our actual response times and reporting. We believe customers should see exactly what they’re getting, and have full transparency if questions ever arise. By learning from manufacturing events—equipment wear, vendor supply changes, even local humidity swings—we know how quickly downstream customers experience the effects of any change.

    Adaptation and Progress in Synthesis Methods

    Each year brings new analytical tools and insight into crystallography or process kinetics. Our manufacturing team regularly reviews progress in asymmetric synthesis and purification, incorporating best practices as they become established in peer-reviewed science. Early plant iterations depended on less precise temperature gradients and longer reaction times. Now, in-situ monitoring and digital control bring more precise conversions, reducing waste and unwanted side products. Peptide innovators seek out suppliers who manifest this adaptability, keeping pace with new analytical demands instead of lagging behind.

    We have worked with multiple academic groups to trial new catalytic systems and optimize reagent costs—sometimes successfully, sometimes running into fresh hurdles. These partnerships generate lessons that filter directly into our plant training materials and process validation runs. We view our role as more than just a material provider—the manufacturer’s perspective means seeing every customer’s challenge as a prompt to improve production, not just to ship out what’s easy or standard.

    Customer Experience and Ongoing Support

    Engaging daily with researchers and pharmaceutical developers, I see the direct impact of a reliably manufactured L-Beta-Homophenylalanine Hydrochloride. Because our team works closely with users, we catch early issues before they escalate—be it unusual HPLC backgrounds, changes in color, or feedback about packaging. One memorable exchange involved a university group trying a new ligation protocol; after troubleshooting, we realized a subtle batch-to-batch pH drift in their lab was interacting with our material’s minor counter-ion content. Through open dialogue and rapid sample reruns, their team got the data needed, and we used this incident to further tune our own in-line monitoring.

    Ongoing support goes past the point of sale. Our technical service team keeps close ties with regular buyers, providing guidance, batch documentation, and even custom splits for those conducting method development. Because we control the entire process from raw inputs forward, adapting labeling, batch documentation, or package size requires only an internal review. We pride ourselves on offering more than a disconnected drop-ship experience; our users rely on real answers from those who actually design, produce, and verify every shipment.

    Looking Ahead: Future Directions

    The fields using L-Beta-Homophenylalanine Hydrochloride keep evolving, especially as next-generation peptide drugs, protein mimics, and bioconjugates gain attention. The plain reality: new applications bring harder standards and tighter process windows. Being rooted in manufacturing, our team thrives on that challenge. Continuous investment in reactor scale digitalization, inline sensors, and purification automation lets us match the industry’s push toward higher purity and batch size variability.

    We regularly meet with partnering labs and formulation teams searching for unique amino acid analogs. Their requirements change, so our production does too—testing new salt forms, stabilizers, or crystallization methods. Our expertise grows through shared problem-solving with customers, not generic solutions or copy-paste documentation. By building traceable, responsive manufacturing lines, we empower the next wave of researchers aiming for breakthroughs that depend on reliable access to highly pure building blocks like L-Beta-Homophenylalanine Hydrochloride.

    As someone who’s spent years monitoring, adjusting, and delivering successful product lines, I recognize the value of hard-won reliability and the trust that comes with it. Each kilogram shipped reflects the human experience behind manufacturing—a cycle of subtle adjustments, fast troubleshooting, and real-world engagement with the chemistry community. We look forward to further advances, knowing our team stands ready to support each new challenge with the experience only direct manufacturer engagement can provide.