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H-D-Phe-NH₂·HCl

    • Product Name H-D-Phe-NH₂·HCl
    • Alias H-D-Phe-NH2·HCl
    • Einecs 254-442-7
    • 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

    593482

    Product Name H-D-Phe-NH2·HCl
    Iupac Name (2S)-2-amino-3-phenylpropanamide hydrochloride
    Molecular Formula C9H13ClN2O
    Molecular Weight 200.67 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Cas Number 180578-17-0
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C
    Smiles N[C@@H](Cc1ccccc1)C(N)=O.Cl

    As an accredited H-D-Phe-NH₂·HCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White HDPE bottle with tamper-evident cap, labeled "H-D-Phe-NH₂·HCl, 5g, research grade, store cool, dessicated."
    Shipping H-D-Phe-NH₂·HCl is shipped in tightly sealed containers, protected from moisture and light. It is typically transported at controlled room temperature, with clear chemical labeling. Documentation includes the Certificate of Analysis and Material Safety Data Sheet (MSDS) for safe handling and regulatory compliance during domestic and international shipping of laboratory reagents.
    Storage H-D-Phe-NH₂·HCl (hydrochloride salt of D-phenylalaninamide) should be stored in a cool, dry place, protected from light and moisture. Keep the container tightly closed and store at 2–8°C (refrigerator) for stability. Avoid exposure to air and extreme temperatures. Store away from incompatible materials such as strong oxidizers. Use appropriate personal protective equipment when handling.
    Application of H-D-Phe-NH₂·HCl

    Applications of H-D-Phe-NH₂·HCl in Industrial Manufacturing

    As a direct manufacturer of H-D-Phe-NH₂·HCl, we supply this advanced chemical intermediate to multiple specialized sectors. Below, we detail its key downstream applications in real industrial manufacturing, with technical insights into compliance, ratio selection, process stages, and resulting end products.

    1. Peptide and Peptidomimetic Drug Synthesis

    Pharmaceutical companies use H-D-Phe-NH₂·HCl as a protected amino acid derivative in solid-phase and solution-phase peptide synthesis. D-Phe units play a critical role in the assembly of synthetic peptides, including therapeutic agents and investigational APIs, especially where chirality and terminal amide groups must be tightly controlled. Chemists integrate this material during stepwise couplings, relying on its high purity to minimize side reactions and maximize yield. Process engineers manage batch or flow synthesis environments to deliver consistent peptide sequences for downstream processing.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) and European Pharmacopoeia (EP) for peptide APIs
    • FDA 21 CFR Part 210/211 for finished pharmaceuticals
    • ISO 9001:2015 Certified Quality Management

    Typical usage ratio

    • 0.2–0.4 molar equivalents per peptide coupling step; adjusted according to peptide chain length and target batch size

    Downstream process integration

    • Added at protected amino acid coupling stage during SPPS or LPPS peptide assembly
    • Deprotected and cleaved after chain elongation

    Final product types

    • Synthetic peptide APIs (antidiabetics, growth hormones, GLP-1 analogs)
    • Bioactive oligopeptides for R&D
    • Peptide-based injectables
    • Vaccines utilizing synthetic peptide antigens

    2. Enzyme Inhibitor and Diagnostic Reagent Manufacturing

    Producers of biochemical reagents employ H-D-Phe-NH₂·HCl as a key intermediate in the assembly of enzyme inhibitors and chromogenic substrates. Its chiral D-phenylalanine moiety is incorporated into molecules used to investigate protease activity, screen pharmaceuticals, or for diagnostic test kits. Analytical labs depend on precision coupling techniques to ensure lot-to-lot consistency and reliable signal responses in enzymatic assays used for clinical, food safety, or research diagnostics.

    Industry compliance standards

    • ISO 13485:2016 for medical devices and diagnostic reagent production
    • OECD Principles of Good Laboratory Practice (GLP)
    • CLSI GP44 for preparation and handling of analyte-specific reagents
    • REACH pre-registration (where applicable within the EU market)

    Typical usage ratio

    • 10–50 mM concentration in inhibitor synthesis; precise formulation adjusted to target enzyme kinetics

    Downstream process integration

    • Integrated during amide bond formation for inhibitor scaffold assembly
    • Introduced as a functional group in chromogenic substrate synthesis

    Final product types

    • Serine and cysteine protease inhibitors (e.g., D-Phe-based benzyloxycarbonyl compounds)
    • Clinical protease activity assay kits
    • Chromogenic and fluorogenic enzyme substrates for microplate assays
    • Specialty biochemical test kits for research

    3. Specialty Chemical Intermediate in Fine Chemical Synthesis

    Manufacturers in fine and specialty chemicals value H-D-Phe-NH₂·HCl as a building block for chiral intermediates and complex heterocyclic compounds. Using its protected amide functionality, process chemists construct enantioselective scaffolds relevant to both pharmaceutical and agrochemical innovation pipelines. The tight control of stereochemistry and purity is critical for compliance with regulatory dossiers and future scale-up studies.

    Industry compliance standards

    • ISO 9001:2015 for quality management throughout chemical synthesis
    • Globally Harmonized System (GHS) for labeling and safety
    • REACH (EC 1907/2006) chemical registration requirements in the EU
    • Responsible Care Program (where adopted)

    Typical usage ratio

    • 5–30% by mol in intermediate step, tailored to target molecule design and scale

    Downstream process integration

    • Charged as a chiral source in reductive amination, amide coupling, or ring closure reactions
    • Purified through preparative chromatography before further derivatization

    Final product types

    • Chiral auxiliaries for subsequent asymmetric syntheses
    • Intermediates for non-peptide pharmaceuticals
    • Specialty heterocycles for catalyst or ligand development
    • Agrochemical lead compounds in preclinical evaluation

    4. Biotechnological Research and Custom Peptide Library Production

    Academic and industrial biotechnology research groups source H-D-Phe-NH₂·HCl for the synthesis of custom peptide libraries and structural probes. Custom peptide sequences require reliable D-amino acid incorporation for structure-activity relationship analysis as well as development of non-natural peptide-based tools. Scientists apply combinatorial chemistry techniques, optimizing reaction conditions to ensure sequence fidelity and enable high-throughput screening applications for fundamental science and drug discovery.

    Industry compliance standards

    • ISO 20387:2018 for biobanking and biological material preparation
    • GLP standards for analytical validation in research
    • Institutional biosafety approval (lab scale)
    • Material Safety Data Sheet (MSDS) documentation for laboratory reagents

    Typical usage ratio

    • 0.1–0.3 molar equivalents per peptide residue, tailored for library diversity and scale

    Downstream process integration

    • Integrated at defined positions during automated peptide synthesizer cycles
    • Applied in split-and-mix or orthogonal sequence diversification protocols

    Final product types

    • High-throughput screening peptide libraries
    • Fluorescently labeled probes with site-specific D-amino acid incorporation
    • Non-natural backbone modified peptides
    • Cell-penetrating or stapled peptide variants

    5. Reference Standard and Analytical Method Development

    Certified reference material suppliers and quality assurance laboratories use H-D-Phe-NH₂·HCl to manufacture peptide and amino acid reference standards. Reference controls are essential for validating HPLC, LC-MS, and bioassay platforms targeting peptides and small molecule therapeutics. Rigorous synthesis and characterized purities allow for consistent calibration and traceability, ensuring compliance with instrument qualification and analytical protocol accreditation in highly regulated environments.

    Industry compliance standards

    • ISO/IEC 17025:2017 for calibration laboratory competence
    • USP General Chapter <11> for reference standards
    • Pharmacopoeial monograph specifications for analytical reagents
    • Good Laboratory Practice (GLP) compliance

    Typical usage ratio

    • Pure standards: 100% for calibration curves
    • Spiking concentrations: 1–100 μg/mL in validation studies, dependent on assay sensitivity

    Downstream process integration

    • Crystallized and quantified before blending into calibration or control solutions
    • Incorporated into instrument qualification and performance verification protocols

    Final product types

    • Certified peptide or amino acid reference materials
    • Calibration blends for mass spectrometry and HPLC
    • Analytical method standardization kits for pharmaceutical QC labs
    • Proficiency testing samples for regulatory submission
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    Certification & Compliance
    More Introduction

    Introducing Our H-D-Phe-NH₂·HCl: Reliability from the Source

    Real Value Starts at the Reactor Bench

    Years of hands-on production have narrowed our focus onto molecules that deliver reliability to pharmaceutical synthesis and peptide research. H-D-Phe-NH₂·HCl is one of those compounds that stands out in our product suite. Our experience with phenylalanine derivatives, starting from the raw starting materials and following through every stage of purification, has brought this product to a place where researchers and process engineers can count on consistent quality.

    What Sets Our H-D-Phe-NH₂·HCl Apart

    There are few shortcuts in the chemical industry, especially when synthesizing key amino acid derivatives used for active pharmaceutical ingredients. H-D-Phe-NH₂·HCl is the hydrochloride salt form of the amide of protected phenylalanine, offering better solubility and handling compared with the free base. We take production seriously—each batch receives extended attention at the purification stage, which reduces side-products, lessens residual solvent traces, and ensures a precise, reproducible amine content every shipment.

    Precision That Begins Far Before Packaging

    Our approach to H-D-Phe-NH₂·HCl starts with raw material selection and verification, using only those phenylalanine lots that meet established purity standards. Our chemists keep a close eye on maintaining stereochemical configuration throughout synthesis. Racemization may seem a minor problem until the final peptide product loses yield or activity. By maintaining low temperatures during the key amidation steps and utilizing gentle acidification, we minimize unwanted byproducts and ensure the L-configuration remains untouched.

    Batch Consistency Informed by Years on the Floor

    It’s rare to talk about batch-to-batch consistency without referencing PAT tools and Lean methodologies. We view these as starting points, not endpoints. In the production of H-D-Phe-NH₂·HCl, we run every batch through both automated in-line checks and manual verification. There’s no overreliance on theoretical results here—chromatograms are compared, moisture content is quantified, and the solid’s color and texture are checked by seasoned technicians who’ve worked hundreds of runs. If a lot doesn’t meet our standards, it doesn’t leave the site.

    Meeting the Needs of Medicinal Chemistry and Peptide Manufacturing

    In daily use, H-D-Phe-NH₂·HCl provides clear benefits to laboratories prepping short peptides, peptidomimetic drug candidates, or diagnostic reagents. Synthetic chemists like a reliable amino acid amide which dissolves cleanly and reacts predictably. Our hydrochloride form avoids the handling risks and irritant dusts of the free amine, allowing for a safer preparation space. The structure enables rapid peptide bond formation, thanks to the preserved amino protection and clean reactive group.

    Specifications That Handle Real-World Demands

    Our standard lots feature high chemical purity and a tightly controlled water content, verified by Karl Fischer analysis and further reflected in sharp melting point ranges during QC. The solid powder flows freely and is suitable for scale-up, whether researchers order small flask quantities or larger container shipments for contract manufacturing. We store and ship H-D-Phe-NH₂·HCl with attention to humidity and temperature, as the amide and hydrochloride salt both attract ambient moisture if left unprotected.

    Reduction of Impurity Profiles—A Commitment, Not a Slogan

    We have always treated impurities not as inconveniences, but as research-stopping obstacles. The main impurities in H-D-Phe-NH₂·HCl stem from over-acidification, incomplete amination, and occasional trace byproducts from precursor amino acid lots. Using analytical HPLC and mass spectrometry, our QC team spots impurities below 0.5 percent, giving customers confidence that peaks won’t emerge from nowhere in their chromatography runs.

    Feedback Shapes Forward Progress

    Direct and often critical feedback from our longstanding pharmaceutical partners has shaped how we process, store, and release this compound. No marketing team could have predicted how batch uniformity helps with late-stage process development or the degree to which moisture stability supports reproducible solid-phase peptide syntheses. We keep open lines of communication with chemists who use this compound in everything from automated peptide synthesizers to specialty probe development.

    Safety Contemplated from the Factory Floor

    Raw experience working alongside operators handling the amide under varying shop floor conditions taught us about practical safety. Even crystalline products release fine dusts. We provide packaging with static control and moisture barrier protections—not only to meet regulatory requirements but to ensure employees, both ours and downstream, have safer material to work with. Our product labels go beyond basic naming to feature synthesis batch numbers and real-world shelf lives tracked from the day of manufacture.

    Direct Comparisons with Other Amino Acid Amides

    A question we often hear is how H-D-Phe-NH₂·HCl stacks up against protected phenylalanine derivatives like esters or free amides. Chloride salt forms generally win for ease of handling and solubility in polar solvents. Free base forms sometimes cake or clump, especially after months on a shelf in variable climates. Esters serve their own purpose but fall short when a direct amide introduction is needed without additional protection group removal. We target the hydrochloride salt to match high throughput synthetic protocols while still permitting manual bench techniques.

    Applications Beyond the Obvious

    The main area for H-D-Phe-NH₂·HCl lies in peptide synthesis, especially where custom peptide libraries or sequence optimization are required. Recently, demand from the diagnostics and agricultural peptide sector has grown. Our customers have found new preparations for this building block in metabolic pathway probes and enzyme inhibitor screens, taking advantage of the reliable L-form preservation. Because this compound forms clean bonds and rapidly incorporates during automated cycles, it suits both academic research and high-throughput industry.

    Supporting Quality in Life Sciences

    We trace every lot of H-D-Phe-NH₂·HCl back to its raw materials and reagents—no mixed-source origins or unclear chain of custody. Pharmacopeial compliance may remain a moving target, but our production methods stay ahead of the latest standards. We keep impurity and organic solvent residues below established limits for API-intermediate manufacturing, publishing results with every certificate of analysis so researchers and procurement teams know what arrives.

    Production Workflow Informed by Years of Trial and Error

    Producing an amino acid derivative like H-D-Phe-NH₂·HCl is no theoretical exercise. Real production involves hands burning from slips with acid, hundreds of washes to isolate the pure product, and hard-won understanding of how drying temperature swings harm a batch. Our process engineers adjusted agitation speeds, swapped filter materials, and streamlined post-synthetic workup for years to find what works best. It comes down to controlled sequence: dissolve, aminate, isolate, purify, dry, and pack—guided by real feedback, not hypothetical models.

    User-Driven Process Adjustments—No Ivory Towers

    Nothing beats practical feedback from frequent users of H-D-Phe-NH₂·HCl. We’ve received calls on solubility quirks in automated platforms and questions about slurry density in large volume applications. Each production cycle spurs us to adjust washing protocols or look for subtle off-odors, which though minor, signal an impurity to address. This ongoing loop with contract manufacturers and bench-level scientists shapes our process as much as any standard operating procedure.

    Everyday Handling and Storage Practices

    Even seasoned chemists can underestimate the impact of humidity fluctuations on amino acid salts like H-D-Phe-NH₂·HCl. Moisture affects everything from accurate weighing to solution clarity. We fill and seal product in controlled rooms with desiccation as a priority. Our warehouse teams keep stocks away from heat sources, sunlight, and even shared storage with volatile solvents, minimizing cross-contamination risk and supporting long shelf lives.

    Offering Smart Solutions for Scaling Up

    Production line experience tells us that scaling up odd-lot amino acid derivatives triggers new challenges. We designed our workflow to produce both kilogram- and gram-scale lots with identical starting materials and purification steps. No shortcuts—every run gets parameters dialed in from the lab, then verified at pilot scale. On customer request, we supply tailored documentation on synthesis route, residual solvent profile, and batch stability, helping regulatory filings proceed smoothly.

    Why Source From the Actual Manufacturer

    In the lab and in procurement, there’s a world of difference between compounds sourced direct from the reactor versus passed down layers of resellers. We know exactly how and when each lot of H-D-Phe-NH₂·HCl was produced. There’s no mystery regarding product age, transportation conditions, or handling. We can answer technical questions on origin, enantiomeric purity, synthetic pathway, and long-term stability, because the same team synthesized, tested, and packed this compound before sending it on.

    Stewardship in the Face of Regulation

    Even for catalog research chemicals, regulatory demands grow stronger every year. Our experience with regular audits, environmental controls, and continual upgrades means no unpleasant surprises down the road. We document compliance for REACH, RoHS, and ICH guidelines where relevant. Our cleaning protocols and operator training extend beyond the paperwork—they form part of our shop floor routines.

    Minimizing Waste, Maximizing Usability

    Wasted product on a batch isn’t just a cost to us. In-process loss means energy, solvents, and time all went for nothing. We have trained our teams in targeted isolation, stepwise washings, and efficient drying to trim down yield losses and deliver usable material through every stage. Our products reflect years of learning from yield setbacks and process fine-tuning.

    Learning in Partnership

    We view every order as the beginning of another round of improvement, not as the conclusion of our work. Customers introduce new automation systems, request tighter impurity limits or offer insight into improved process efficiency. Our regular communication feeds improvements back into our daily operating procedures. Where a new analytical method enhances impurity detection, we add it to our QC checklist. This method of production by adaption and direct feedback ensures that H-D-Phe-NH₂·HCl keeps pace with scientific advances.

    Delivering Peace of Mind to the Laboratory and Production Plant

    What matters day in and day out is knowing that the compound sent out actually matches the compound ordered. We invest in traceability, frequent retraining, and direct involvement from senior process chemists in each shipment. For our customers, this level of assurance on every order translates to research progress without delays. Whether a batch is for an urgent R&D drive or a regular supply shipment to a formulation plant, our processes stay transparent and our standards stay high.

    Commitment to Dependable Supply

    Ambitious research projects and fast-moving product launches require suppliers that can stick to timelines. Our manufacturing group maintains backup production capacity and system redundancy. When orders for H-D-Phe-NH₂·HCl spike—owing to a new biomedical breakthrough or seasonal demand changes—our planning and reserves avoid disruption. Our logistics staff work hand-in-hand with production to ship on time, cutting out excuses and last-minute surprises.

    What Makes an Efficient Building Block

    Not all amino acid amide salts behave the same. We’ve reviewed process feedback from hundreds of applications, identifying which properties matter most in real world use. Our H-D-Phe-NH₂·HCl’s batch-to-batch reproducibility and solubility have reduced setbacks in coupling reactions and short synthesis cycles. Chemistry teams find they can dial in conditions and get consistent results—it’s this reliability that’s been earned through years of hands-on production.

    No Overpromise, Just Delivery

    Much of the chemical supply world promises broad application and theoretical performance. As people who get our hands wet on batch days, we’ve learned to only guarantee what has stood up to real world scrutiny. Our H-D-Phe-NH₂·HCl reflects this commitment—a building block that shows up as expected, meets the details on its certificate, and supports the relentless challenges of modern organic synthesis. Everything else is just sales talk.