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HS Code |
196224 |
| Cas Number | 4478-71-5 |
| Molecular Formula | C5H9NO2 |
| Molar Mass | 115.13 g/mol |
| Iupac Name | (S)-2-amino-4-pentenoic acid |
| Synonyms | L-2-Amino-4-pentenoic acid, (S)-Allylglycine |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 224-226 °C (dec.) |
| Purity | Typically ≥98% |
| Storage Temperature | 2-8 °C |
| Ph 1 In Water | 4.0 - 6.0 |
| Optical Rotation | [α]D20 +7° to +9° (c=2, H2O) |
As an accredited L-Allylglycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | L-Allylglycine is packaged in a sealed amber glass bottle containing 25 grams, labeled with product details, hazard symbols, and handling instructions. |
| Shipping | L-Allylglycine is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packed securely and labeled according to chemical safety regulations. The package includes the proper hazard identification and transportation documentation, and is typically shipped via ground or air transport, depending on the destination and customer requirements. |
| Storage | L-Allylglycine should be stored in a tightly sealed container, protected from light and moisture, in a cool, dry place—ideally at 2-8°C (refrigerated). Ensure the storage area is well-ventilated and clearly labeled. Keep away from incompatible substances such as strong oxidizers. Follow standard laboratory safety protocols to minimize the risk of contamination or degradation. |
Applications of L-Allylglycine in Industrial ManufacturingL-Allylglycine serves as a specialty amino acid intermediate in advanced industrial sectors where precise control of chiral purity and reactivity impacts the quality and compliance profile of value-added processes. Below are key downstream applications where this material enables differentiated manufacturing outcomes. 1. Active Pharmaceutical Ingredient (API) Synthesis for AnticonvulsantsPharmaceutical manufacturers use L-Allylglycine as a building block in the targeted synthesis of anticonvulsant APIs, exploiting its unique side chain to introduce functional groups and molecular chirality essential for pharmacological activity. Throughout API production, quality teams monitor for residual amino acid content and chiral excess, ensuring batch-to-batch repeatability in the final drug substance. Industry compliance standards
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2. Peptidomimetic Compound ManufacturingChemical producers utilize L-Allylglycine as a monomer for constructing peptidomimetics, tailoring molecular frameworks to mimic the biological activity of natural peptides while increasing structural stability and resistance to enzymatic degradation. This enables discovery and upscale of drug-like molecules with defined sequence control. Industry compliance standards
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3. Fine Chemical Intermediate for Agrochemical SynthesisSpecialty agrochemical producers leverage L-Allylglycine as an intermediate to introduce amino functionalities during the development of selective herbicide and fungicide actives. Its allyl group supports downstream derivatization strategies, expanding the range of crop protection molecules designed for improved bioavailability and environmental persistence. Industry compliance standards
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4. Research-Grade Reagent for Enzyme Inhibitor ScreeningL-Allylglycine is implemented by biochemical laboratories as a prototype substrate or regulator in enzyme inhibition studies, especially in screening programs targeting aminotransferase and protease mechanisms. Its molecular features enable investigation into enzyme kinetics, guiding advanced screening and lead development projects. Industry compliance standards
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5. Precursor in Synthesis of Functionalized PolyamidesAdvanced polymer research and specialty materials companies adopt L-Allylglycine as a functional monomer to incorporate controlled amino and allyl side chains into polyamide backbones, modulating chain flexibility and enabling chemical post-modification. This supports the development of novel engineering plastics and films with application-tuned surface reactivity. Industry compliance standards
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6. Chiral Auxiliary for Asymmetric Synthesis in Fine Chemical ResearchChemical research groups and custom synthesis manufacturers use L-Allylglycine as a chiral auxiliary, exploiting its configuration to direct stereocontrolled transformations in the preparation of fine chemical intermediates. This approach permits reproducible access to defined enantiomers valuable in downstream development of specialty molecules. Industry compliance standards
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