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HS Code |
820666 |
| Name | DL-2-Aminoadipic Acid |
| Cas Number | 542-32-5 |
| Molecular Formula | C6H11NO4 |
| Molecular Weight | 161.16 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 219-223°C (dec.) |
| Solubility In Water | Soluble |
| Ph | 5.0-6.0 (1% in water) |
| Boiling Point | Decomposes before boiling |
| Purity | Typically ≥98% |
| Synonyms | DL-2-Aminoadipate, DL-alpha-Aminoadipic acid |
| Storage Conditions | Store at 2-8°C |
| Iupac Name | (±)-2-Aminohexanedioic acid |
| Ec Number | 208-807-4 |
As an accredited DL-2-Aminoadipic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | DL-2-Aminoadipic Acid (25g) is packaged in a sealed, labeled amber glass bottle for protection against light and moisture. |
| Shipping | DL-2-Aminoadipic Acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically packaged for transport at ambient temperature, unless specified otherwise. Proper labeling is applied as per regulatory guidelines, ensuring safe handling during shipment. Avoid exposure to excessive heat, humidity, or incompatible substances. |
| Storage | DL-2-Aminoadipic Acid should be stored in a tightly closed container, away from moisture and incompatible substances. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Protect the chemical from direct sunlight and sources of ignition. Proper labeling and secure storage ensure safety and stability during handling and use. |
Applications of DL-2-Aminoadipic Acid in Industrial ManufacturingDL-2-Aminoadipic acid is a specialized intermediate used in several advanced industrial processing chains, supporting the controlled production of downstream pharmaceutical, polymer, and specialty chemical compounds. As a primary manufacturer, we provide high-purity grades for each sector, supporting efficient integration and regulatory compliance at every production stage. 1. Active Pharmaceutical Ingredient (API) SynthesisDL-2-Aminoadipic acid acts as a key precursor in the synthesis of certain rare amino acid-based APIs, including anticonvulsant agents and metabolic disorder modulators. Process chemists use it to construct six-carbon dicarboxylic structures, which are essential in the stepwise assembly of complex pharmaceutical molecules. Each API batch requires traceability of the amino acid source and stringent impurity control throughout hydrogenation and condensation steps to meet global pharmacopoeial requirements. Industry compliance standards
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2. Polymer Engineering for Biodegradable PolyamidesIndustrial polymerization plants incorporate DL-2-Aminoadipic acid in the custom synthesis of biodegradable polyamides, specifically polyamide-6,6 analogues and copolymers designed for controlled environmental breakdown. Its bifunctional character provides a modifiable intermediate for melt polycondensation with diamines, supporting precise molecular weight and mechanical strength tuning to meet technical textile and engineered plastics specifications. Industry compliance standards
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3. Analytical Reagent Production for Amino Acid ProfilingChemical and biotech laboratories utilize this compound as a primary standard in amino acid analysis systems. Manufacturers prepare certified reference materials using DL-2-Aminoadipic acid to support robust calibration of HPLC, GC, and capillary electrophoresis platforms in clinical, pharmaceutical, and food quality control sectors. Purity and trace certification are required for regulated laboratory supply chains. Industry compliance standards
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4. Specialty Chemical Intermediate for Advanced Organic SynthesisDL-2-Aminoadipic acid serves as an intermediate for the synthesis of specialty heterocyclic and chiral compounds, widely used in material science and high-value research chemicals. Its functional groups enable selective protection and deprotection strategies, supporting synthetic pathways toward pyridine and piperidine ring systems. Chemists exploit its reactivity for constructing complex molecular scaffolds in the fine chemicals industry, where batch-to-batch reproducibility and analytical verification are essential. Industry compliance standards
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