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DL-Homophenylalanine

    • Product Name DL-Homophenylalanine
    • Alias DL-2-Amino-4-phenylbutyric acid
    • Einecs 221-157-8
    • 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

    960044

    Productname DL-Homophenylalanine
    Casnumber 940-37-8
    Molecularformula C10H13NO2
    Molecularweight 179.22
    Appearance White to off-white powder
    Meltingpoint 118-122°C
    Solubility Soluble in water
    Purity Typically ≥98%
    Storagetemperature 2-8°C
    Iupacname 2-Amino-4-phenylbutanoic acid
    Smiles NCC(CC1=CC=CC=C1)C(=O)O

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

    Packing & Storage
    Packing The packaging for DL-Homophenylalanine contains 100 grams, sealed in a white, labeled HDPE bottle with tamper-evident cap.
    Shipping DL-Homophenylalanine is shipped in tightly sealed containers to prevent moisture and contamination. It is transported in compliance with relevant safety regulations, typically in cool, dry conditions. Appropriate labeling and documentation accompany the shipment, ensuring secure handling and delivery. Special care is taken to avoid exposure to extreme temperatures or direct sunlight.
    Storage DL-Homophenylalanine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect from light and moisture. Recommended storage temperature is 2–8°C (refrigerated). Ensure proper labeling and avoid prolonged exposure to air and humidity to maintain chemical stability and purity.
    Application of DL-Homophenylalanine

    Applications of DL-Homophenylalanine in Industrial Manufacturing

    As an original manufacturer, we supply DL-Homophenylalanine to specialized industries worldwide, focusing on applications with established downstream value chains. The following sections detail how our material fits into real-world manufacturing scenarios, referencing industry-specific standards, integration stages, formulation proportions, and ultimate product outputs.

    1. Pharmaceutical Intermediate for Peptide Active Pharmaceutical Ingredient (API) Synthesis

    DL-Homophenylalanine serves as a non-proteinogenic amino acid building block leveraged by pharmaceutical manufacturers for synthesizing complex peptide APIs. Its unique side-chain structure enables the design of enhanced-stability drug candidates, particularly in peptide hormone analogs and targeted peptide conjugates. Incorporated during solid-phase peptide synthesis (SPPS) or solution-phase synthesis, this compound requires rigorous traceability to meet regulatory expectations. Formulators adjust input ratios based on peptide sequence requirements and validation batches, maintaining batch-to-batch consistency under strict GMP oversight.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia (Ph. Eur.) for peptide synthesis substances
    • US Food and Drug Administration (21 CFR Part 211) cGMP regulations for finished pharmaceuticals
    • China Pharmacopoeia ChP

    Typical usage ratio

    • Usually incorporated at 5–15 mol% relative to total amino acids in specific peptide sequences; final proportion determined by peptide design and stepwise assembly strategy.

    Downstream process integration

    • Introduced at the amino acid coupling step during peptide chain elongation in SPPS reactors or solution-phase batch processing; additional purification steps (HPLC, preparative LC) follow incorporation.

    Final product types

    • Injectable peptide APIs (e.g., polypeptide drugs, hormone analogs)
    • Oral peptide formulations
    • Diagnostic peptide reagents
    • Conjugated peptide-drug products

    2. Chiral Synthesis Intermediate for Agrochemical Actives

    Major agrochemical producers use DL-Homophenylalanine as a chiral auxiliary or precursor molecule in the stepwise synthesis of advanced active ingredients targeting plant growth regulation and weed management. Its functional side chain offers opportunities for selective derivatization under asymmetric synthesis protocols, crucial for obtaining agrochemicals with required stereochemistry. The dosage ratio is tailored to the multi-step synthesis yields and downstream derivatization efficiency. Adherence to environmental and chemical safety directives governs its application, especially for products entering regulated markets.

    Industry compliance standards

    • REACH (EC 1907/2006) chemical safety and registration
    • ISO 9001:2015 quality management in chemical manufacturing
    • FAO/WHO Specifications for Agricultural Pesticides
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Ranges from 2–8% w/w as a reactant, depending on the overall molecular yield and scale-up process for the target agrochemical compound.

    Downstream process integration

    • Added during the chiral resolution or initial coupling stage in multi-step synthesis reactors, with subsequent transformations yielding the bioactive compound; used in intermediate purification and pilot-scale validation steps.

    Final product types

    • Herbicide actives with specific stereochemistry
    • Plant growth regulator active ingredients
    • Synthetic pathway intermediates forwarded for formulation
    • Technical-grade active materials supplied to agrochemical formulators

    3. Raw Material in Nutraceutical and Dietary Supplement Peptide Manufacturing

    DL-Homophenylalanine is selected by functional food and nutraceutical manufacturers for producing specialty bioactive peptides embedded in dietary supplements. It enables fortification of peptides with non-standard amino acids, enhancing bioavailability and supporting custom formulations for sports nutrition and metabolic support. Inclusion levels are dictated by product registration limits and the peptide’s intended nutritional claims. The material enters the solution-phase or enzymatic hydrolysis process, and its use must conform to regulations relevant to food-grade materials production and labeling.

    Industry compliance standards

    • US FDA 21 CFR Part 111 (Dietary Supplement GMPs)
    • EU Regulation (EC) No 852/2004 on Food Hygiene
    • ISO 22000:2018 Food Safety Management
    • China’s GB 14880-2012 on Food Nutrient Fortification Substances

    Typical usage ratio

    • 0.1–0.8% by weight of the peptide blend, calculated based on active ingredient content and conforming to safety assessment outcomes.

    Downstream process integration

    • Mixed into amino acid feed solution prior to enzymatic hydrolysis or during direct peptide synthesis; followed by spray drying or filtration to yield consumable peptides.

    Final product types

    • Bottled bioactive peptide supplements (capsule or powder)
    • Functional beverage peptide fortifiers
    • Sports nutrition peptide-enriched formulas
    • Peptide tablet and lozenge products

    4. Advanced Fine Chemical Synthesis for Flavor and Fragrance Intermediates

    Fragrance and flavor ingredient manufacturers incorporate DL-Homophenylalanine as a precursor for synthesizing rare aromatic compounds and chiral building blocks used in flavoring agents and perfumery accords. Its molecular framework allows for targeted transformation into specialty aldehydes and alcohols via controlled reduction and cyclization, essential for complex aroma formulations. Use ratios in fine chemical formulation depend on target yield specifications and downstream distillation or refinement steps. Producers must observe relevant IFRA codes and local chemical safety legislation.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Regulation (EC) No 1334/2008 on Flavourings
    • IFRA/IOFI Labelling Manual
    • REACH registration for aromatic intermediates

    Typical usage ratio

    • Input at 0.5–2% as process intermediate, optimized based on byproduct minimization and reaction conversion rate assessments.

    Downstream process integration

    • Charged into reaction vessels for reductive amination or cyclization, forming essential fragrance notes or flavor precursor molecules; proceeds to molecular distillation and compositional blending stages.

    Final product types

    • Synthetic aroma chemicals for fine fragrances
    • Flavoring bases for beverages and confectionery
    • Fragrance intermediates for detergent and personal care aromas
    • High-purity chiral alcohols used in luxury perfumery
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    Competitive DL-Homophenylalanine prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    Introducing DL-Homophenylalanine: Precision Synthesis from the Chemical Manufacturer’s Bench

    DL-Homophenylalanine: A Closer Look

    DL-Homophenylalanine sits on the shelf in nearly every synthetic amino acid section across our plant. We have shaped our production lines through decades of hands-on batch synthesis to meet consistent demands from teams working in research, pharmaceuticals, and fine chemicals. Our specific model, typically recognized as DL-2-Amino-4-phenylbutyric acid, carries the chemical formula C10H13NO2, a molecular weight of 179.22 g/mol, and mixes both D- and L-isomers in equal measure. Each batch reflects our attention to purity and low-moisture handling, which have a daily impact on reactions and yields for end users.

    Producers face chemistry’s rough edges. We see it in moisture drift over seasons, in how packaging makes all the difference in shelf-life, and in real-world storage conditions. Purity isn’t just a number to us—it translates into downstream results. We operate under the realities of large-scale synthesis, balancing between cost-effectiveness and advanced purification stages. Every lot we produce for DL-Homophenylalanine pushes us to minimize byproduct carryover and contamination, which might only be measured in parts per million but can wreck painstaking lab work for our customers.

    Decades of Dealing with Real-World Manufacturing

    In the world of manufacturing, repeatability can be a daily challenge. Operators wrestle with temperature variations or small differences in solvent grade between shipments. Those headaches are familiar in our plant, and DL-Homophenylalanine suffers from no fewer risks than other amino acids. Unexpected precipitates, stubborn solids during crystallization, even the slight brown tint that sometimes appears from air exposure—these are the nuts and bolts that influence every kilo we send out the door.

    Other products may have a naturally glossy reputation; L-Phenylalanine and D-Phenylalanine, for instance, have clear clinical and nutritional stories because of their biological relevance. DL-Homophenylalanine carves out a more specialized place. It does not figure as a natural amino acid in proteins, but it delivers reactivity for synthetic peptide building and as a precursor for custom organic frameworks, chiral intermediates, or even as a scaffold in drug discovery work.

    Our process begins with careful selection and inspection of starting benzyl compounds and pure L- and D-forms of phenyllactic intermediates. The practical realities of industry-standard synthesis, including careful control of reductive amination conditions, separation of hydrophobic co-products, and labor-intensive filtration, form the heart of our routine. Glitches in these steps show up fast as cloudiness or poor crystallinity. Troubleshooting these problems is never academic; they impact shipping schedules and, in turn, laboratory test runs for the scientists who depend on us.

    Specifications Anchored in Performance

    Labs and R&D teams order DL-Homophenylalanine by specification. Purity is the standout metric, routinely pushed beyond 99% through careful crystallization and vacuum drying in our facility. Early runs decades ago struggled with trace contaminants—residual solvents, unconverted benzyl derivatives, or racemization byproducts. Today, systematic HPLC analysis checks each lot for unwanted side products well below 0.5%. Melting point ranges remain tight, and optically inactive (racemic) character ensures predictable solubility and reactivity regardless of downstream stereochemistry.

    Our technical team learned to keep free amino and carboxyl ends intact, with minimized residual chloride or sulfate from purification. Each adjustment, from slow solvent drops during precipitation to additional filtration of micro-crystals, improved recovery while keeping moisture below 0.2%. Analysts test for heavy metals and validate batch homogeneity, for a material that grinds into a non-hygroscopic white powder, easily handled in research rooms or pilot plants.

    Using DL-Homophenylalanine: From the Factory to the Workbench

    Organic synthesis teams lean on DL-Homophenylalanine for its flexibility. The additional methylene group compared to regular phenylalanine changes its utility—it helps in building extended peptide backbones, custom ligands, or as an unnatural building block in peptidomimetic design. Medicinal chemists have used our material to probe receptor selectivity, alter peptide half-life, and investigate drug metabolism. Some use it to generate analogs in SAR (structure-activity relationship) studies, using the extra carbon as a spacer to block or enhance interactions in biological systems.

    We also see DL-Homophenylalanine in crop science applications and material research, where scientists value its ability to introduce rigidity or distance between functional groups. End users tell us that the solid, particulate format of our product dissolves smoothly in aqueous base and is compatible with typical peptide-coupling protocols without foaming or generating sticky residues. As a manufacturer, this feedback shapes every process change we make to grinding, particle size control, or packaging atmospheres.

    Comparing DL- and L- Forms: Why Go for the Mixed Isomer?

    The difference between DL-Homophenylalanine and its optically pure L- or D- variants seems subtle but has practical impact. Labs synthesizing peptides for biological testing will often seek the L-form for direct biological mimicry—cells “recognize” the right-handed version. But in drug development, or catalytic and material science, both isomers or their racemic mixture can provide broader activity, or enable new structure types when chirality isn’t the first concern.

    We keep DL-Homophenylalanine as a standard offering because the racemic model—both D and L produced together—offers a stable, cost-efficient option that integrates readily into chemical development plans. Separating the isomers means extra equipment, more column runs, and naturally, higher pricing. Not every research direction justifies that outlay. For those working on broad screening or needing bulk quantities, the racemic type balances price and usability—qualities we stress to procurement partners from years of talking shop with their chemists.

    Pharmaceutical teams sometimes start broad, running screens with the racemic material, then zero in with purified enantiomers once they discover which isomer drives activity. Our process allows us to scale output in either direction, adjusting crystallization conditions to favor enantiomeric enrichment or stay with the racemic baseline. This manufacturing agility took years to perfect and pays off when customers call wanting both options, fast.

    Industry Reality: From Milligram Vials to Bulk Production

    Every kilogram of DL-Homophenylalanine we produce brings its own story. Some orders leave our docks in sub-gram glass vials, bound for high-throughput discovery labs pushing the edges of chemical genetics. Others move in sturdy polyethylene drums for pilot plant synthesis in pharma or agricultural R&D. We never lose sight of the variability in client demands; our own QC teams double up on environmental monitoring and enclosure integrity so no lot leaves with unwanted moisture or exposure to volatile impurities.

    We’ve seen shifts in usage patterns over the last decade. Early customer requests came almost exclusively from pharma discovery groups. As peptide therapeutics and bioactive compound programs spread beyond the biggest companies, universities and specialty startups began to feature in direct consultations with us. We learned to balance small-lot flexibility with the brute-force reliability expected by large buyers who can’t tolerate line downtime from inconsistent raw materials.

    Handling and logistics play an outsized role for DL-Homophenylalanine compared with more common amino acids. Temperature shifts during long-haul transit can affect powder behavior, even the integrity of vacuum seals. Our staff responded by working with local freight partners, improving insulation and packaging, and running accelerated stability studies. The payoff comes from lower returns and fewer late-night troubleshooting calls from frustrated end users, whose only priority is starting their experiment on time and finishing it with clear results.

    Beyond the Factory Gate: Working With End Users

    No batch is complete until it works in practice for the customer. Our technical support lines handle questions not just about paperwork and certificates, but on-the-ground issues: why a particular lot might clump, how best to dissolve a stubborn sample, what solvent sequence will deliver the cleanest product in a custom peptide synthesis. Our own staff return time and again to field test feedback, calibrating everything from batch stir times to drying atmospheres on the strength of what real researchers report back from their benches.

    End users value technical depth—experienced operators expect not just a specification sheet, but experienced troubleshooting from our chemists. We keep a full panel of in-house data: HPLC traces, melting points, water content trends. These results steer our own process changes and form the basis for regular customer updates. Such detailed engagement secures trust, built one successful batch at a time rather than through flashy presentations or generic promises.

    Customers facing formulation bottlenecks or irregular yields from DL-Homophenylalanine know there is a direct line to our team. We have adjusted batch particle size, drying time, and even container choice to address issues in specific use cases, whether it involves automated dosing robots or manual benchwork. Out in the field, practical experience matters as much as formal training. Our development chemists often rely on lessons from past mishaps—minor spills, sticking clumps, or surprising reactivity in side reactions—more than abstract theory.

    Why Consistency and Integrity Matter in Today’s Supply Chain

    Quality in chemical manufacturing cannot get by on numbers alone. The supply chain world reacts sharply to shifts in regulation, raw material prices, and logistical headaches that might seem remote in the laboratory but become urgent when a process grinds to a halt. For DL-Homophenylalanine, consistency means every order matches those before it—not just in purity, but also in feel, solubility, and processing ease. Customers remember the bad batches, the shipment that arrived with caked or inefficient product. We work to make those stories rare, even as the world of supply shifts beneath our feet.

    Tracking each drum, from raw material inbounds to finished good release, forms the backbone of our quality assurance process. Production staff log environmental readings, note every raw material test, and detail changes between production runs. If anything interrupts the flow—say, an unexpected impurity spike or a shift in color—those notes feed directly into root cause reviews. We learn fast in manufacturing; small signals, caught early, steer big decisions affecting the reliability our customers count on.

    Building trust also involves transparency about setbacks. If a lot runs late due to equipment downtime, or a shipment needs retesting, customers hear it from us directly. We know their production lines depend on ours—and a missed deadline could topple their own launch schedules. Such transparency helps both sides adjust and plan: if someone in procurement knows of a hiccup on our end morning-of, they can shift internal priorities before costs snowball. For us, a working relationship built on honesty always trumps a one-off rush order delivered with apologies.

    Differences from Other Amino Acid Compounds

    DL-Homophenylalanine stands apart from standard proteinogenic amino acids like glycine, alanine, or phenylalanine, not only in its structure—having that extended methylene chain beyond the phenyl ring—but in where and why it's used. Standard amino acids fit straight into nutritional and bioregulatory cycles, with universal assay procedures and market pressures that drive cost down and volume up. Those compounds show up by the ton in animal feeds, food enhancement, or basic clinical nutrition, where pricing and bulk throughput rule decision-making.

    Our product plays in a narrower lane. Custom syntheses depend on that extra carbon. In peptide mimics and pharmaceutical discovery, this extended backbone grants medicinal chemists more latitude to shift activity, retool metabolic stability, or design receptor probes that avoid some enzyme breakdown pathways. Some of our regular buyers use it purely as a chiral pool starting point—building from the racemic blend to dial in selective reactions and separate enantiomers only when necessary.

    Handling, stability, and intended use set DL-Homophenylalanine apart in our process flows. Regular amino acids pack into their standard drums, with workflows set almost in stone. Our experience managing special purity demands, closer environmental controls, and smaller, more frequent batch scheduling pays off for the science teams pushing past routine reactions into genuinely novel chemistry.

    Feedback from the Field: Ground-Level Solutions

    Years of troubleshooting and feedback cycles sharpened how we make and package DL-Homophenylalanine. Our clients suggested tamper-evident seals after one case of powder exposure during long summer transits. Another research group documented more stable solubility curves from batches filtered with new membrane grades. Sometimes, even the minor tweak—switching jar liner materials or shifting a batch between production lines—halves the time it takes to go from drum to finished compound in our customers’ own synthesis.

    We learned rapidly that what seems minor in the plant—say, a single extra step of air drying, or swapping to a nitrogen blanket—could restore shelf life by months or resolve a sticking point for an entire drug screen. These changes never show up in glossy spec sheets, but we keep notes and train new techs by walking them through not just what works, but why it works, based on lived experience and direct user feedback.

    On-site support shapes our strategies, too. Our senior chemists travel to see customers’ own set-ups, learning the subtle differences between bench-top solubilization and industrial-scale tank dissolution. Sometimes, a new peptide coupling method requires different grind or moisture profiles. Sometimes, handling practices upstream change downstream yields by only a few percent but make all the difference in launch timelines. We take these lessons seriously, closing the loop between our production floor and real-world application.

    Navigating the Road Ahead

    Sustaining excellence in DL-Homophenylalanine production isn’t a routine job for us. We adjust processes in response to market shifts—new regulatory rules, altered transportation lanes, or advances in synthetic chemistry that change preferred specifications. Chemical manufacturing remains unpredictable, but our experience anchors us in reality. Every question a customer brings, every complaint or request for modification, gets weighed against our manufacturing limits and logistical capacity for fast adaptation. In today’s climate, agility matters as much as tradition.

    Teams in academic, biotechnological, and pharmaceutical labs keep discovering fresh uses for DL-Homophenylalanine. As we listen to their stories and adapt our workflow, the product finds new relevance—whether as a bridge to smarter peptide-based drug designs, or in material science frontiers. Maintaining high and stable purity, keeping lots free from batch-to-batch drift, and offering flexibility in lot size or delivery timing all come from lessons won through hands-on troubleshooting and relationship-building, not just technical jargon on a data sheet.

    Summary

    DL-Homophenylalanine’s value does not rest only in its chemical structure, but in the experience and consistency behind every batch that leaves our floor. From the production chemist at the pump frame to the technical team answering field calls, our experience shapes a product that meets real scientific challenges. Whether for routine screening runs or demanding, high-stakes pharmaceutical campaigns, reliability wins trust and repeat business. We continue to adapt, listen, and act to keep DL-Homophenylalanine not just available, but at a level of quality backed by our work and expertise, every step of the way.