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L-Propargylglycine HCl

    • Product Name L-Propargylglycine HCl
    • Alias PPG-HCl
    • Einecs 277-371-8
    • 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

    897858

    Product Name L-Propargylglycine HCl
    Cas Number 90777-19-2
    Molecular Formula C5H8ClNO2
    Molecular Weight 149.57 g/mol
    Appearance White to off-white powder
    Solubility Soluble in water
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms L-2-Amino-4-pentynoic acid hydrochloride
    Ph 1 Solution Approximately 4.5-6.5
    Iupac Name (S)-2-amino-4-pentynoic acid hydrochloride
    Canonical Smiles C#CCC(N)C(=O)O.Cl
    Inchi Key MJAFQPWXQCZVHN-UHFFFAOYSA-N

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

    Packing & Storage
    Packing L-Propargylglycine HCl, 1g, packaged in a sealed amber glass vial with a tamper-evident cap and clear labeling.
    Shipping L-Propargylglycine HCl is shipped in tightly sealed containers, protected from moisture and light. It is handled as a non-hazardous chemical but should be stored at controlled room temperature. Appropriate labeling and documentation accompany the shipment to ensure safe transportation and compliance with chemical safety regulations.
    Storage L-Propargylglycine HCl should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry place, preferably at 2–8°C (refrigerator conditions). Avoid exposure to heat and incompatible materials such as strong oxidizers. Follow all relevant safety and handling protocols, and store away from food or incompatible chemicals.
    Application of L-Propargylglycine HCl

    Applications of L-Propargylglycine HCl in Industrial Manufacturing

    L-Propargylglycine HCl, as an alkyne-substituted amino acid, finds focused downstream application in high-value biochemical and pharmaceutical production settings. Our facility maintains strict manufacturing controls to ensure material consistency for regulated verticals. Below, we outline the leading industrial scenarios where L-Propargylglycine HCl is directly incorporated, detailing the compliance standards, formulation ratios, relevant process integration points, and final product types realized by our global industrial clients.

    1. API Intermediates for Cardiovascular and Neurological Therapeutics

    Pharmaceutical manufacturers use L-Propargylglycine HCl as a key intermediate for synthesizing active pharmaceutical ingredients, particularly those that interact with cystathionine γ-lyase pathways relevant to cardiovascular and neuroprotective drug classes. During cGMP API synthesis, customers require traceability and impurity profiling to meet international regulatory submissions, leveraging our supply of precisely characterized lots for validated scale-up.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 FDA Current Good Manufacturing Practice
    • European Pharmacopoeia Monographs compliance for API intermediates
    • WHO GMP certification where required for regulated markets

    Typical usage ratio

    • Processed at 0.2—3.0 molar equivalents relative to target synthetic intermediate; optimized per route and step yield.

    Downstream process integration

    • L-Propargylglycine HCl is introduced at the key condensation or substitution stage during multi-step synthesis of pharmaceuticals such as propargyl-linked drug analogs.

    Final product types

    • Active Pharmaceutical Ingredients (APIs) for antihypertensive, neuroprotective, and cardiometabolic drugs
    • Regulatory-submitted drug substance batches

    2. Research-Grade Chemical Probes for Biomedical Applications

    R&D laboratories, university cores, and contract research organizations source this amino acid derivative to create labeled probes, enzyme inhibitors, and analytical standards essential for studying trans-sulfuration and hydrogen sulfide pathways. Its use underpins peer-reviewed research, requiring batch-level documentation and analytical COAs meeting international research reagent standards.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for chemical synthesis and documentation
    • Fulfills requirements of REACH (EC 1907/2006) for laboratory chemicals in the EU
    • Certificate of Analysis (COA) and traceable lot records per GLP (Good Laboratory Practice) guidelines

    Typical usage ratio

    • Employed at concentrations from 0.05 mM to 5 mM in enzyme inhibition assays or as dictated by assay protocol; precise ratio determined by experiment design.

    Downstream process integration

    • Introduced as a substrate or inhibitor in in vitro assay systems, labeled probe synthesis (e.g., using radioactive/fluorescent tags), or standard curve preparation for HPLC and LC-MS quantitation workflows.

    Final product types

    • Enzymatic assay kits and reagent sets
    • Labeled molecular probes for biomedical research
    • Analytical standards for academic or CRO studies

    3. Specialty Amino Acid Building Block for Peptide Synthesis

    Synthetic peptide manufacturers rely on L-Propargylglycine HCl to introduce alkyne functionalities for click chemistry, post-synthetic conjugation, and site-specific labeling. Its role in custom peptide synthesis demands stringent QC, detailed impurity mapping, and reproducible chiral purity to meet pharma, diagnostic, and preclinical development standards.

    Industry compliance standards

    • ISO 13485:2016 for medical device/diagnostic component manufacturing
    • USP/NF for excipient quality where relevant
    • Documentation standards aligning with ISO 9001 and customer-specific QC requirements

    Typical usage ratio

    • Incorporated at 1 equivalent per desired peptide residue position; typically 1–5% w/w in solid-phase synthesis based on peptide length.

    Downstream process integration

    • Integrated into peptide chains during solid-phase Fmoc or Boc synthesis, facilitating bio-orthogonal conjugation chemistry or probe development in downstream protocols.

    Final product types

    • Click-conjugated peptides used in diagnostics and bioconjugates
    • Site-specifically modified research peptides
    • Peptide building blocks for preclinical compound libraries

    4. Cell Culture Media Additive for Specialized Biomedical Research

    Producers of advanced cell culture media include this compound at precise, trace-levels as a metabolic modulator for studies involving sulfur amino acid pathways or tailored cell line engineering. Customers require assurance of low endotoxin, pharmaceutical-grade purity, and batch homogeneity to avoid impacting sensitive cell assays.

    Industry compliance standards

    • ISO 13485:2016 for cell culture media components in the diagnostics sector
    • USP <1043> Ancillary Materials for Cell, Gene, and Tissue-Engineered Products
    • Ph. Eur. 5.2.12 requirements on media additives for cell culture

    Typical usage ratio

    • Typically supplemented at 10–100 μM final concentration in custom media formulations, adjusted based on cell type and experimental protocol.

    Downstream process integration

    • Added to sterile-filtered media prior to cell seeding or introduced as a pulse during experimental protocol for pathway modulation screening.

    Final product types

    • Custom-formulated cell culture media for biomedical research use
    • Specialized media for stem cell, neuronal, or microbial cell studies
    • Screening kits for pharmaceutical R&D workflows
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    Certification & Compliance
    More Introduction

    L-Propargylglycine HCl: A Manufacturer’s Perspective on Reliable Amino Acid Solutions

    Introducing L-Propargylglycine HCl

    Working every day in this industry, we see firsthand the challenges presented by specialty amino acids. L-Propargylglycine HCl comes up in critical research and pharmaceutical synthesis projects—no surprise, considering its unique structure and practical roles. Our team approaches this compound as more than just another item in the product catalog. L-Propargylglycine HCl offers predictable purity and performance that chemists have come to rely on. This molecule, with the formula C5H7NO2·HCl, shows up in synthetic pathways where typical glycine derivatives fall short. We have produced this compound for years and know its true worth not only from a chemical standpoint but from the many troubleshooting discussions and application feedback shared by customers at the bench.

    Consistent Quality Backed by Direct Manufacturing

    Turning raw materials into high-purity L-Propargylglycine HCl requires careful handling at each step. Quality starts on the plant floor—where our controlled environment tracks every reaction, from solvent charging to purification and drying. Continuous in-process analytics check for unwanted byproducts or batch inconsistencies. Final batches meet tight purity specifications, and the product leaves our facility sealed after passing both HPLC and NMR analysis. We routinely see purity levels at or above 98%, which helps eliminate headaches down the line in applications where a single percent of impurity can cause experimental setbacks.

    Details Influence Applications

    End-users often remark on the material’s performance in bioactive molecule synthesis and enzyme inhibition studies. Some glycine analogs offer limited reactivity, but once you introduce the propargyl group, it dramatically changes substrate utility in click chemistry, cyclization, and alkynyl-based tagging. Our L-Propargylglycine HCl consistently supports copper-catalyzed azide-alkyne cycloaddition reactions, giving researchers more predictable yields and cleaner separations. Moisture control remains key—clumping or discoloration points to mishandling, which our process engineers address with robust drying cycles and rapid-packout. Each batch features a white to off-white crystalline appearance, making it easy for researchers to spot material that meets expectation.

    No Substitute in Key Research Domains

    We’ve seen the landscape of glycine derivatives expand, but none fully replicates what the propargyl moiety provides. For those designing inhibitors targeting specific PLP-dependent enzymes, or tracing chemical pathways by stable-labeling, L-Propargylglycine HCl continues to be the tool of choice. Throughout the years, we’ve fielded requests for substitutions—sometimes alpha-alkynyl analogs, sometimes other protected amino acids. Chemists report back a common theme: the alternatives rarely match both reactivity and biological selectivity. One customer documented how substituting L-Propargylglycine HCl with N-propargylglycine slowed down a late-stage click reaction, adding hours to their purification times. These real-world outcomes drive our dedication to keeping the product consistent and free of process drift batch after batch.

    How We Support Precision in Research and Synthesis

    Every production run starts with a fresh lot of precursor amines, and our operators review the entire batch record before charging reactors. We minimize cross-contamination by strict scheduling and closed transfer systems. Where some suppliers might rely on third-party repackers or bulk intermediates shipped half a globe away, we control every transfer from raw material acceptance to the final packed drum or bottle. Stable packaging—using certified HDPE bottles with double-layer seals—prevents atmospheric moisture and environmental ingress that can degrade sensitive functional groups.

    Feedback loops matter. Our technical staff listens to reports from chemists deploying propargylglycine in labeling and conjugation experiments. If a customer encounters solubility drops or notices a change in melting point, we pull reference material from our retains library and reevaluate our drying and storage methods. Over the years, adaptation to these insights has led us to modify shelf-life studies and tweak desiccant specifications for lots headed to more humid regions.

    Contrasts That Count: L-Propargylglycine HCl Versus Other Amino Acid Inputs

    Within our own walls, we test and compare related glycine derivatives alongside L-Propargylglycine HCl. Adding the propargyl group fundamentally shifts reactivity compared to standard glycine hydrochloride or N-methylglycine salts. The triple bond unlocks new pathways in click chemistry—allowing for rapid, catalyst-guided connections that aren’t feasible with plain secondary or primary amine groups. Tweaks to crystal size and surface area can also affect dissolution times and line-clearance protocols in automated synthesis platforms. By running comparative NMR and dissolution studies, we find that L-Propargylglycine HCl loads rapidly and evenly into aqueous or polar organic solvents, a step up from bulkier or more hydrophobic derivatives.

    Researchers ask about differences between the HCl salt and the free base forms. Our own experiments and customer feedback confirm that the hydrochloride salt brings better stability, longer shelf life, and reduced oxidation risk. Stability studies show that unpackaged free L-Propargylglycine degrades faster in humid storage, leading to inconsistent starting materials. These subtle but significant differences rarely feature in product brochures, yet they change real outcomes in scale-up reactions or peptide syntheses. Chemists engaging in bioconjugation—where every functional group counts—get consistently higher conversions by sticking with the well-characterized hydrochloride salt.

    Empowering Laboratories and Industry

    The growth of click chemistry, bioconjugate chemistry, and custom peptide design continues to drive demand for difficult-to-synthesize, highly reactive amino acids. Instrumentation advances—such as automated flow peptide synthesizers or micro-scale combinatorial platforms—require starting materials that respond predictably to programmed conditions. L-Propargylglycine HCl fits into these workflows by maintaining batch-to-batch consistency and avoiding the common pitfalls of batch drift or variable solubility. Our own labs have supported industry clients working at both gram and multi-kilogram scale, providing technical insight when scaling up from R&D benchwork to pilot plant runs.

    Regulatory landscapes change. The pharmaceutical sector demands traceability, full certificates of analysis, and supply chain transparency. Our direct manufacturing process, with full in-house documentation and historical batch data, supports these requirements. Feedback from API and process chemists has spurred us to implement even tighter in-process controls, so analytical results reflect the real-world conditions researchers see. Downstream, that confidence in material quality speeds regulatory submission and reduces time spent troubleshooting synthesis bottlenecks.

    Customer Cases: On the Bench and in Production

    Customers have brought our L-Propargylglycine HCl into projects ranging from basic science to full-scale pharmaceutical intermediate synthesis. One academic team shared the story of developing novel enzyme inhibitors: their results depended heavily on the reagent’s lot-to-lot repeatability. Small differences in purity or moisture radically altered kinetic data, introducing avoidable error. By supplying well-documented, homogenous lots, our product helped them minimize repeat runs. In another case, a peptide synthesis group working at commercial scale pointed out that a subtle change in particle size distribution caused valve clogging in their semi-automated peptide synthesizer. Drawing from in-plant experience, we adjusted our drying and milling process, restoring reliable flow and solution clarity. These experiences help us tune future production and ensure we keep up with evolving needs in research, diagnostics, and therapeutics.

    Understanding the Markets and Applications

    The pharmaceutical, biotechnology, and chemical synthesis industries seek out L-Propargylglycine HCl for its adaptability. In their hands, it becomes a tool for making enzyme inhibitors and for exploring metabolic pathways that standard glycine derivatives can’t access. Our synthesis partners often report that, without the alkynyl group, they hit dead ends or need extra steps to construct the required bonds or labels. Some groups apply L-Propargylglycine HCl as a building block in developing next-generation antibody-drug conjugates, where selectivity and clean reaction profiles matter more than ever. Reaction run logs that reach us show better reproducibility and cleaner endpoints, important for regulatory filings and IP protection.

    The Value of Manufacturer Experience

    Our experience as an original producer means we see the full picture. Every lot originates from careful material sourcing and process verification. Problems don’t get outsourced—they’re solved internally by people who know the products and understand what chemists expect from a specialty compound supply. We’ve built our production philosophy on anticipating and responding to those unseen needs: how often does the customer need single-use packaging for moisture-sensitive storage, or what fill weights best suit high-throughput screening? Even details like jar material and tamper-evident labeling stem directly from user input. These touches grow out of years on both sides of the supply chain—making it, testing it, and walking through troubleshooting with partners.

    Direct feedback has prompted alterations and upgrades. At one stage, repeated concerns about caking during transit led us to install new airtight packaging lines and desiccant-integrated shipping cartons. After we released these upgrades, reports of degraded or clumpy samples dropped sharply. Researchers gained confidence in weighing and dissolving their materials, cutting down sample prep errors and reruns. This ongoing process of feedback and improvement shows why the manufacturing perspective adds a layer of reliability beyond standardized data sheets.

    Supporting Advancing Science

    Science moves quickly. New discoveries in bioorthogonal labeling, click chemistry, or enzyme mechanism studies often lead to revised purity or sterility requirements in starting materials. Our manufacturing adjustments keep up with this progress. Processes that worked five years ago might lag behind current needs for mass spectrometry compatibility or automation-readiness, so we keep R&D staff engaged with both chemical literature and emerging application notes. By running pilot-scale syntheses in parallel with production, we learn how the compound performs outside the textbook, reinforcing the knowledge that can’t be found in off-the-shelf reference guides.

    The growing demand for scalable and reliable specialty chemicals raises questions about supply chain security and transparency. In response, we have developed full-chain traceability systems. Each lot of L-Propargylglycine HCl features a unique identifier that customers can reference for audits or regulatory submission. As researchers seek out robust data for reproducibility and method transfer, this connection between the maker and the end user becomes indispensable.

    Comparisons That Matter for Decision-Makers

    The market sees a flood of amino acid derivatives, but real-world performance and reliability keep driving repeat requests for L-Propargylglycine HCl from our lines. I’ve seen teams switch vendors and run into sudden process failures—solubility drops out, or an unknown spectral impurity slips by. Unpacking why helps us strengthen our own controls. Years ago, a partner switched to bulk packs from a generic source to cut costs, only to find the material unmanageable in dusty, high-throughput environments. After returning to our process, they noted a steady decline in downtime and cleaning costs, which matters in high-paced sample turnaround. The lesson holds: not all sources are interchangeable, especially when downstream syntheses or QA standards raise the bar.

    The HCl salt form in particular offers more than just longer shelf life. Its improved handling characteristics make it easier for automated lab systems to measure and dispense, reducing the drifts that delay high-throughput screening projects. Each time we tighten our micronization and packing protocols, those savings show up in fewer user complaints, steadier reaction yields, and repeat orders from scientists who value consistency over novelty.

    Industry Trends and Our Response

    Research and application trends now tilt toward more complex molecules and asymmetric synthesis, placing pressure on supply partners to offer robust, reliable intermediates. L-Propargylglycine HCl sits at the crossroads of traditional amino acid chemistry and innovative click chemistry approaches. Customers now ask not just for a high-purity molecule but for documentation supporting residual solvent levels, specific polymorphic forms, and even spectral analysis from advanced platforms like 600 MHz NMR. Our process evolves in response, and we don’t hesitate to implement process changes that improve customer outcomes—even if it means redesigning a key purification stage or approving extra QC checkpoints.

    A new generation of chemical and pharmaceutical professionals, raised on digital information flows, relies on quick access to specification data and lot-to-lot analytics. In-house software development ties every production, testing, and packaging phase into a traceable structure, so technical requests don’t linger unanswered. Periodic reviews of these systems, based on both internal audits and external customer feedback, have helped us pinpoint and reduce data-entry errors or analysis bottlenecks that could otherwise disrupt the high standards our end-users expect.

    Looking Forward: Supporting Chemistry Without Compromise

    We know that chemists, biologists, and engineers select reagents and intermediates based not only on upfront cost, but on the reliability and confidence gained through every stage of research or development. High-impact experiments depend on repeatable material quality; results matter day to day, not just on paper. Our approach to L-Propargylglycine HCl production aims to deliver that security through transparency, adaptive manufacturing, and open communication.

    Chemistry doesn’t stand still. Every synthesis project, stability trial, and new application raises another question about how specialty amino acids perform when it really counts. As producers, we work hard to set a standard, driven by the problems and opportunities real researchers face. The lessons, challenges, and successes we pick up along the way cycle back into each gram of L-Propargylglycine HCl we ship out. That’s the real value of relying on a direct manufacturer—each lot represents experience, adaptability, and commitment you can trust at every stage of your process.