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(R)-2-Aminopent-4-Ynoic Acid

    • Product Name (R)-2-Aminopent-4-Ynoic Acid
    • Alias L-API
    • Einecs 674-419-6
    • 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
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    Specifications

    HS Code

    319095

    Product Name (R)-2-Aminopent-4-ynoic acid
    Cas Number 108345-02-2
    Molecular Formula C5H7NO2
    Molecular Weight 113.11
    Iupac Name (R)-2-aminopent-4-ynoic acid
    Appearance White to off-white solid
    Solubility Soluble in water
    Optical Rotation Specific for (R)-enantiomer, [α]D value available upon request
    Smiles N[C@@H](C#CC)C(=O)O
    Inchi InChI=1S/C5H7NO2/c1-2-3-4(6)5(7)8/h4H,3,6H2,1H3,(H,7,8)/t4-/m1/s1
    Purity Typically >98% (may vary by supplier)
    Storage Conditions Store at -20°C, protected from light and moisture
    Synonyms (R)-Homopropargylglycine

    As an accredited (R)-2-Aminopent-4-Ynoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing (R)-2-Aminopent-4-Ynoic Acid is packaged in a sealed 1-gram amber glass vial with tamper-evident cap and clear labeling.
    Shipping (R)-2-Aminopent-4-ynoic acid is shipped in tightly sealed containers to prevent contamination and moisture exposure. It is transported according to standard chemical safety protocols, often at room temperature, unless otherwise specified. Packaging ensures compliance with regulatory requirements for hazardous materials, ensuring safe and secure delivery to the destination.
    Storage (R)-2-Aminopent-4-ynoic acid should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Store at 2–8°C (refrigerated) in a dry, well-ventilated area. Ensure the storage area is free from sources of ignition. Proper labeling and handling procedures should be observed, following applicable safety and regulatory guidelines.
    Application of (R)-2-Aminopent-4-Ynoic Acid

    Applications of (R)-2-Aminopent-4-Ynoic Acid in Industrial Manufacturing

    (R)-2-Aminopent-4-ynoic acid serves as a specialized intermediate in targeted manufacturing segments where chirality and acetylenic structure play a critical role in molecular functionality. As an original chemical producer, we supply this raw material directly to industries with well-defined advanced downstream processes.

    1. API Synthesis for Anticonvulsant Drug Development

    Pharmaceutical manufacturers integrate (R)-2-aminopent-4-ynoic acid as a chiral building block in the synthesis of next-generation anticonvulsant actives. This application requires strict quality verification and traceability throughout every batch. We ensure enantiomeric excess controls and precise impurity profiling align with the development and commercial API production phases. The material gets introduced after initial scaffold assembly, serving as a cornerstone in the construction of gamma-aminobutyric acid (GABA) analogues.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 211: Current Good Manufacturing Practices for Finished Pharmaceuticals
    • USP and Ph. Eur. monographs for chiral amino acid intermediates
    • European Medicines Agency (EMA) requirements for starting materials

    Typical usage ratio

    • 5–15% of total substrate mass, adjusted for target enantiopurity and downstream coupling efficiency

    Downstream process integration

    • Introduced post-core fragment assembly for chiral center incorporation
    • Employed in amidation or reductive amination reactions creating the pharmacophore backbone
    • Used in high-purity crystallization phases to maximize API yield

    Final product types

    • Anticonvulsant tablets and capsules (Rx)
    • GABA analogues for neurological disorder therapy
    • Investigational new drugs (INDs) in preclinical and clinical phases
    • Bulk API powder for branded and generic formulations

    2. Chiral Ligand Production for Metal-Catalyzed Reactions

    Fine chemical manufacturers apply (R)-2-aminopent-4-ynoic acid to synthesize custom chiral ligands required for enantioselective metal-catalyzed transformations in both crop protection and active pharmaceutical markets. The integration of this intermediate enables complexation with transition metals, supporting high-value asymmetric hydrogenation and allylic amination processes. Batch records document the ligand mass ratio for reproducible catalyst performance.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH (EC) No 1907/2006 Registration for advanced intermediates
    • GMP Part II: Basic Requirements for Medicinal Products

    Typical usage ratio

    • 0.2–1.5 eq relative to metal center, depending on target ligand architecture

    Downstream process integration

    • Condensation and cyclization steps during ligand scaffold assembly
    • Introduction into batch reactors as the key chiral source before metal salt addition
    • Integrated in ligand recovery processes for catalyst recycling

    Final product types

    • Chiral ligands for homogeneous catalysis
    • Enantioselective palladium, rhodium, and iridium catalysts
    • Custom ligand sets for asymmetric synthesis services
    • Value-added fine chemical intermediates

    3. Peptidomimetic Synthesis in Biotech R&D Programs

    Biotechnology companies source (R)-2-aminopent-4-ynoic acid to introduce conformational constraints in peptide and peptidomimetic synthesis for screening and development platforms. The acetylenic group stabilizes secondary structure motifs and enhances protease resistance in therapeutic leads. Integration into solid-phase peptide synthesis is tightly regimented, ensuring orthogonal protection and stepwise elongation control.

    Industry compliance standards

    • ISO 13485 for medical device R&D components
    • US FDA GLP (Good Laboratory Practice) in biotech research
    • European Pharmacopoeia 10.0 for amino acid derivatives

    Typical usage ratio

    • 1–10 mol% per peptide chain; adjusted for target sequence length and modification density

    Downstream process integration

    • Incoporated during solid-phase synthesis as a protected amino acid derivative
    • Unprotected at late-stage peptide elongation cycles for selective modification
    • Enabled for conjugation to macrocyclic scaffolds enhancing biological activity

    Final product types

    • Peptidomimetic drug candidates
    • Bioactive screening libraries
    • Diagnostic reagents with enhanced metabolic stability
    • Research peptides for protease resistance studies

    4. Functionalized Polymer Precursor for Specialty Materials

    Advanced materials producers use (R)-2-aminopent-4-ynoic acid as a monomeric precursor to generate polymers featuring site-selective alkyne moieties. The resulting functional groups enable post-polymerization modification, such as click chemistry for biomedical coatings and smart material applications. Accurate raw material addition directly affects polymer branching, mechanical properties, and site-specific reactivity.

    Industry compliance standards

    • ISO 9001:2015 for process control in polymer chemistry
    • RoHS Directive 2011/65/EU for electronics-compatible polymers
    • FDA 21 CFR 177 for indirect food additive polymeric materials (when applicable)

    Typical usage ratio

    • 2–12 wt% based on total monomer feed, adaptively set for target polymer density and functionality

    Downstream process integration

    • Copolymerization in solvent or aqueous dispersion systems
    • Addition during controlled radical, RAFT, or ATRP polymerization sequences
    • Facilitates alkyne "click" reactions for melt or solution-phase post-functionalization

    Final product types

    • Biomedical device coatings
    • Conductive polymer films
    • Smart hydrogels for controlled drug delivery
    • Customizable polymer nanomaterials for R&D
    Free Quote

    Competitive (R)-2-Aminopent-4-Ynoic Acid prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

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    Certification & Compliance
    More Introduction

    Meet (R)-2-Aminopent-4-Ynoic Acid: Specialty Amino Acid for Advanced Synthesis

    Understanding (R)-2-Aminopent-4-Ynoic Acid: Our Perspective as the Manufacturer

    The chemical world keeps asking for enantiomerically pure building blocks. In our experience, (R)-2-Aminopent-4-ynoic acid answers this need, providing not just a structural novelty but also critical flexibility for researchers and producers in organic synthesis, medicinal chemistry, and peptide science.

    We’ve been manufacturing specialty amino acids for decades, and among all the molecules we handle, (R)-2-aminopent-4-ynoic acid stands out. It carries the alkyne functional group and chirality on the alpha carbon, which, from a chemist’s point of view, combines options for selective transformations and stereocontrolled outcomes. The CAS number for this product is not just a registration—it signals traceable, reproducible quality lot after lot. Every gram rolling out of our reactors must meet our own standards, set higher than general analytical requirements.

    Model, Specifications, and Consistency of Quality

    For this compound, our standard offering comes as the free amino acid in crystalline form. Typically, purity exceeds 98% by HPLC, measured against authentic standards we keep in-house. Moisture, an overlooked factor in some products, stays well below 1%; precise logs are taken during packaging, and we adjust to customer-specific thresholds if tighter limits are vital.

    From batch to batch, optical rotation tells the story of our stereocontrol during synthesis. (R)-2-aminopent-4-ynoic acid displays a distinct [α]D value, aligned with published enantiopure material. The melting range never drifts beyond a narrow band, signaling an absence of unwanted side products or cross-contamination. It’s not just about ticking boxes, but about making sure any synthetic step that follows—amidation, coupling, protective group installation—proceeds as planned, without unexpected racemization or decomposition.

    Why Chemists Rely on (R)-2-Aminopent-4-Ynoic Acid

    Chemists value three things: purity, reliability, and synthetic potential. This molecule brings all three. The terminal alkyne group at the gamma position opens channels for creative chemistry—think Sonogashira couplings, cycloadditions, or click reactions. Because alkynes can install remotely functionalized tags or create novel scaffolds, (R)-2-aminopent-4-ynoic acid enters projects that can’t proceed with garden-variety amino acids. In all these reactions, a single stereochemistry matters; racemic materials undermine biological or pharmaceutical targets, so our enantioselective synthesis and rigorous chiral analysis assure performance.

    Every year, we see new questions from discovery teams: can they design peptidomimetics that mimic protein surfaces? Will a “noncanonical” amino acid sidestep protease degradation, or introduce an orthogonal handle for site-directed labeling? In-house, we’ve fine-tuned the reactivity profile through purification steps calibrated by mass spectrometry, ensuring that the free acid, not ester contamination or partial salts, defines the product.

    Key Uses: Not Just a Standard Amino Acid

    In medicinal chemistry, (R)-2-aminopent-4-ynoic acid enables rational drug design where introducing an alkyne is more than just a structural flourish; it’s a handle for downstream functionalization or for attachment to bigger, complex moieties. These features are necessary for bioorthogonal labeling, which biochemists exploit to map protein-protein interactions or to create conjugates that retain physiological stability.

    Synthetic peptide chemists also trust this acid to anchor unusual motifs. In solid-phase peptide synthesis, the free amine and carboxylate groups can be quickly modified without interrupting the precious alkyne, as long as the protection strategies are right. We routinely consult on which conditions preserve integrity during Fmoc or Boc cycles. Our technical staff know firsthand the pain of buying a chiral amino acid, only to find its side chain partially hydrogenated or its chiral center partially inverted. We design our process to deliver the pure R-enantiomer, untouched and ready.

    In research and industry, subtle differences matter. If a peptide chain swaps an L- for an R-amino acid, biological function can shift dramatically. Our batches are validated not only with optical rotation but through enantioselective chromatography and comparison to independent, third-party standards. The material supports not just routine synthesis, but method development, SAR studies, and large-scale lead optimization projects.

    Differentiating from Common Amino Acid Building Blocks

    Unlike alanine, serine, or lysine, (R)-2-aminopent-4-ynoic acid introduces a linear, unsaturated backbone that influences both local structure and reactivity. Standard amino acids rarely carry such a precise, removable tag for bioorthogonal chemistry. Incorporating it into peptides or small molecules creates pathways unavailable to other building blocks.

    As the actual producer, we’ve watched researchers periodically attempt to substitute with propargylglycine, or even non-chiral pentynoic acids, only to find the outcome doesn’t match their needs. With (R)-2-aminopent-4-ynoic acid, the chemist secures both the spatial arrangement needed for stereospecific receptors or enzymes and the chemical handles necessary for late-stage diversification or conjugation.

    This specialty acid isn’t the right fit for every application. Price and handling complexity run higher than for standard amino acids. The applications that require such a molecule—precision engineering of biologically active peptides, advanced click chemistry, and next-generation labeling—justify the extra investment. Teams who have attempted their own synthesis tell us of poor yields, chromatographic headaches, and unstable intermediates. Our large-scale manufacturing shortcuts these obstacles through proprietary intermediates, constant monitoring, and careful temperature staging, preserving both yield and enantiomeric excess.

    Practical Handling and Support from the Source

    Anyone who has worked with alkynes knows how unpredictable they can be. We handle raw materials with established precautions, use non-reactive containers, and avoid storing under air or high humidity. Each batch undergoes accelerated stability studies; our results let us guarantee a rational expiration date based on actual degradation—not just guesswork. Shipping teams are briefed not only on regulations but also on chemical reactivity, ensuring your shipment arrives as anticipated.

    Attempts to store enantiomerically pure amino acids without proper sealing quickly lead to color changes or decreased solubility. For this acid, we recommend storage under inert gas and away from light. Each package leaves our warehouse sealed, with batch details and analysis reports tailored to customer requirements. Our technical service helps troubleshoot unexpected behaviors, from solubility quirks to reaction recipe advice. Our bench chemists speak directly with customers, skipping go-between bureaucracy and cutting delays on real problems.

    Quality Assurance: Real Lessons from Manufacturing

    Some firms chase volume by cutting purification steps or outsourcing critical chiral separations. We’ve learned from experience that every shortcut found in the supply chain erodes trust for chemists at the bench. Our own SOPs specify on-site synthesis, continuous monitoring by TLC, NMR, and HPLC, and certification from both in-house and outside labs. These protocols aren’t bureaucratic hurdles—they arose from actual, observed problems early in our production history.

    We manage waste, temperature, and reagent quality with our own technicians, not remote partners. Inventory is calibrated to anticipate both small custom orders and industry-scale demand surges. When regulatory or pharmacopoeial standards update, our documentation adapts, supporting full traceability from starting reactants to packaged product. Our warehouse logs temperature, humidity, and light exposure to flag any deviation that might threaten material integrity.

    Chiral purity often drops off at the end of the process if steps aren’t booked tightly. Our technical staff rotates weekly to review analysis and cross-check chiral purity—not just in pre-shipment checks, but before every critical diversion to packaging. That discipline evolved from hard experience: early on, missing even one TLC spot allowed contamination that forced weeks or months of reprocessing. Today’s customers benefit from all the hard-won lessons built into every jar.

    Regulatory and Safety Feedback from the Lab

    As a direct manufacturer, we register new submissions for compliance in all jurisdictions served. Our safety and environmental guides reflect findings from our own operations and customer reports. We incorporate new lessons into our safety sheets as soon as our own scientists or clients observe features not captured by older literature—solubility shifts, peculiar reactivity in downstream reactions, or volatility increases under certain solvent systems.

    For export and domestic shipments, our compliance paperwork accompanies every shipment, customized for destination as regulations demand. Laboratories that have special needs—pharmaceutical, veterinary, or research—can request supporting analytical or risk data from us, not just off-the-shelf bureaucracy. Our safety teams regularly revalidate literature data against our own observations, giving timely updates if packaging or transport recommendations shift.

    Feedback from Researchers and Repetitive Use Cases

    The most valuable insights come from labs returning to us for their next order. Many clients share that their first experience with (R)-2-aminopent-4-ynoic acid forced them to change their protection group strategies or solvent systems. What sets repeat buyers apart is how quickly they integrate its advantages into new projects—smaller tags, more robust bonds, or unique crosslinking not achievable by classical amino acids. From GMP pilot plants to university projects, this material powers workflows that aim beyond catalogue chemistry.

    We get research requests from those aiming to build unnatural peptides that resist enzyme action, or small-molecule bioconjugates that demand delicate, residue-specific labeling. Most feedback circles around two topics: reaction yield and product purity. Reports of consistent, clean coupling—rise alongside comments on clear NMR and MS spectra. Difficulties, when reported, usually relate not to the product’s flaws but to reaction planning or handling errors. For these, our technical consulting helps bridge knowledge gaps without the wait or templated replies common from intermediaries.

    From time to time, labs share surprising uses: the acid’s alkyne has triggered new thinking in materials science, acting as a pivot point in designer polymers or ligands not documented in textbooks. This back-and-forth with customers enables us to improve synthesis, develop purification protocols, and suggest new research pathways.

    Facing Challenges in Scale-Up and Custom Requests

    Large-scale production of chiral amino acids is full of pitfalls invisible at small scale. Protecting the alkyne during certain synthetic steps, controlling temperature gradients, and employing non-racemic catalysts all stretch the limits of standard manufacturing. We designed our reactors for exact temperature, pressure, and agitation, automating cleaning to prevent any trace of cross-product contamination.

    Our facility handles custom order sizes, but each scale jump brings its own growing pains. Sometimes, fine-tuning a batch for a unique customer requires weeks of pilot runs, scrutiny over stereoselective catalysts, and even supply chain audits for starting reagents. We have committed R&D to optimizing each critical transition, especially chiral resolution. Our chemists and engineers meet regularly, analyze sample data from both failed and successful runs, and tweak protocols before any shipment of commercial lots.

    Supply chain reliability matters just as much as technical mastery. In years of production, we’ve had to replace vendors of raw materials whose inconsistencies, while not obvious at first, compromised overall product quality. Only through hands-on evaluation and strict vendor audits do we guarantee a stable, high-quality supply, regardless of order size or frequency.

    Environmental Responsibility During Manufacturing

    Every kilogram of specialty amino acid generated produces waste—and minimizing this impact sits high on our agenda. In our own plant, we recover solvents, neutralize hazardous byproducts, and recycle unused reagents wherever possible. Waste minimization is not just a compliance issue but a sign of care for the chemists who use our products, as well as the environments where residual material might ultimately end up.

    Process engineers have introduced second-generation purification steps that capture valuable byproducts for use in allied syntheses. This culture of reuse and smart disposal grew out of necessity: early disposal challenges prompted a complete review of our waste streams, and today, no batch leaves the plant without passing internal environmental audit.

    For (R)-2-aminopent-4-ynoic acid, managing the residue and mother liquor from purification is particularly tricky. We constructed in-house scrubbers designed for the unique mix of organic and aqueous phase wastes, capturing volatile organic compounds and routing them for certified disposal. Regular monitoring and review by third-party environmental consultants confirm that we’re hitting our own targets for waste reduction.

    The Value of Direct Manufacturer Support

    In this field, chemists can buy amino acids from any number of channels, but years of experience have shown that buying directly from the manufacturer provides more than just a product—it offers accountability, adaptability, and authentic technical support. Customers turning to us gain direct dialogue with the people who actually developed and manufactured the batch, receiving faster answers to questions about product structure, batch variability, or even creative synthetic options.

    We see first-hand the limitations of third-party distribution: delayed questions, incomplete documentation, and frustratingly slow troubleshooting. Our approach values transparency and technical rigor, never handing off problems to middlemen or relying exclusively on standard data sheets. In practice, this saves research teams both time and budget, especially for deadlines that don’t allow back-and-forth through multiple channels.

    We also work closely with clients on regulatory submissions, supporting filings or internal reviews with authentic, primary-source data. Customization of batch characteristics, documentation, and support services is not simply a matter of ticking boxes: it’s a fast, frictionless process for us thanks to our tightly integrated production and QC systems.

    Continuous Improvement and Looking Ahead

    Technical innovation never stands still. We conduct ongoing R&D into synthesis and purification, always seeking to make our process safer, cleaner, and more robust. Each time a new challenge emerges—sharper purity requirements, unusual specifications for coupling chemistry, or demands for incredibly tight chiral control—we answer with new protocols tested under real production conditions.

    Much of what sets our (R)-2-aminopent-4-ynoic acid apart comes from incremental improvement—feedback loops between bench, plant, and technician. Every improvement comes from documented success or a learned lesson from failed attempts. Our team reviews analytical data monthly, addresses customer feedback in workflow adjustments, and never assumes a process is finished just because it passes basic QA.

    Looking forward, we plan to add more real-time monitoring to our production process, leveraging automation that integrates batch data directly into QC dashboards, lowering data transfer delays and catching emerging issues. Input from our customers will continue shaping these changes, building confidence in the product and streamlining how research teams incorporate it into ever more ambitious projects.

    Summary: More Than Just an Amino Acid, A Strategic Tool

    From the hands of chemists to the bench, (R)-2-aminopent-4-ynoic acid acts as a key enabler for cutting-edge research and synthesis. By controlling every element of its manufacture, from raw materials and reactor parameters to QC analytics and documentation, we provide a product that does more than serve as another chemical—it becomes a strategic research partner. As science evolves, specialty chemicals like this one continue to play an outsized role, and our responsibility as manufacturers is to keep pace, to innovate responsibly, and to support our clients with transparency and expertise born on the factory floor.