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HS Code |
991198 |
| Chemical Name | 1,3-Propylenediamine |
| Synonyms | Trimethylenediamine |
| Molecular Formula | C3H10N2 |
| Molar Mass | 74.12 g/mol |
| Cas Number | 109-76-2 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 140-141 °C |
| Melting Point | -12 °C |
| Density | 0.89 g/cm³ at 20 °C |
| Solubility In Water | Miscible |
| Flash Point | 46 °C |
| Vapor Pressure | 6 mm Hg at 25 °C |
As an accredited 1,3-Propylenediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,3-Propylenediamine is packaged in a 500 mL amber glass bottle with a secure screw cap and hazard labeling. |
| Shipping | 1,3-Propylenediamine is shipped as a hazardous chemical, typically in tightly sealed, corrosion-resistant containers such as drums or tanks. It should be transported under cool, well-ventilated conditions, with proper labeling according to regulations. Handle with care to prevent leaks and exposure, and follow all applicable transportation and safety guidelines. |
| Storage | 1,3-Propylenediamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as acids and oxidizing agents. Avoid exposure to moisture, direct sunlight, and excessive heat. Clearly label the container, and ensure appropriate chemical safety measures and personal protective equipment are available for handling. |
Applications of 1,3-Propylenediamine in Industrial Manufacturing1,3-Propylenediamine, as a direct manufacturer, supports a range of critical downstream processes in the chemical and polymer industries. Below, we detail prominent industrial sectors and specific use cases, addressing regulatory compliance, correct formulation ratios, integration steps, and downstream product outcomes. All information reflects direct manufacturing usage, not third-party trading. 1. Epoxy Resin Curing AgentsThe chemical structure of 1,3-Propylenediamine provides ideal nucleophilicity and reactivity for use as a chain extender and curing agent in epoxy resin systems, especially in high-performance industrial coatings and composite manufacturing. End-users in marine coatings, aerospace-grade laminates, and electronics encapsulation select this diamine to enable precise control over cross-linking density, thermal stability, and mechanical resilience. Resin formulators must maintain compliance with industrial standards and manage viscosity and gel time via controlled amine-epoxy stoichiometry, ensuring consistent quality across automated or manual application environments. Industry compliance standards
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2. Polyamide and Polyurea SynthesisProducers of specialty engineering plastics and thermoplastic elastomers use 1,3-Propylenediamine as a critical monomer for linear and branched polyamide chains. Its molecular characteristics deliver intermediate flexibility in the polymer backbone, enabling formulation of fibers, films, and extrusion-grade granules. In polyurea formation, the diamine reacts rapidly with isocyanates in two-component spray and casting systems, controlling hardness and elongation properties for coated textiles and pipeline linings. Precise amine isocyanate index management ensures reproducibility and standard-compliant performance. Industry compliance standards
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3. Corrosion Inhibitor FormulationsIndustrial water treatment and hydrocarbon processing facilities incorporate this diamine into multi-component corrosion inhibitor packages, maximizing protection for mild steel, copper alloys, and process pipelines under neutral to weakly alkaline conditions. Its ability to adsorb at the metal-solution interface, interrupting electrochemical corrosion pathways, depends on strict concentration management and compatibility with biocides, defoamers, and oxygen scavengers as required by system design and operational standards. Industry compliance standards
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4. Textile Fiber ModificationManufacturers of specialty synthetic fibers exploit the unique reactivity of 1,3-Propylenediamine in modifying polyamide chains for differential dye affinity, antistatic behavior, and enhanced softness. Inserted into spinning dopes or post-polymerization modification baths, the diamine can generate functional end groups, boosting processability and dye take-up. Careful balance in dosing and reaction control ensures compliance with global textile chemical safety and ecological impact standards, while maintaining high spinning and weaving yields. Industry compliance standards
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5. Chelating Agent ProductionDownstream synthesis of chelating agents utilizes 1,3-Propylenediamine as a bifunctional precursor in the manufacture of aminopolycarboxylate ligands. These compounds face critical usage in water softening, metal separation, and detergent formulations, requiring defined purity and minimal trace metals to avoid interference in end-use processes. Manufacturing must align with global chemical handling and food safety requirements when producing for the detergent or water additive markets. Industry compliance standards
Typical usage ratio
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