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Propylamine

    • Product Name Propylamine
    • Alias 1-Propanamine
    • Einecs 200-867-9
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales6@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    582560

    Chemicalname Propylamine
    Molecularformula C3H9N
    Molarmass 59.11 g/mol
    Casnumber 107-10-8
    Appearance Colorless liquid
    Odor Fishy, ammonia-like
    Boilingpoint 48.6 °C
    Meltingpoint -83 °C
    Density 0.720 g/cm3 (at 20°C)
    Solubilityinwater Miscible
    Vaporpressure 400 mmHg (20°C)
    Flashpoint -12 °C (closed cup)
    Refractiveindex 1.388 (20 °C)
    Pka 10.56
    Unnumber 1277

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

    Packing & Storage
    Packing Propylamine is packaged in a 1-liter amber glass bottle with a tightly sealed cap, labeled with hazard warnings and handling instructions.
    Shipping Propylamine is shipped in tightly sealed, corrosion-resistant containers, typically steel drums or cylinders, under a nitrogen blanket. It must be kept away from heat, sparks, or open flames, and stored in a cool, well-ventilated area. The shipping documentation must comply with DOT, IATA, and IMDG regulations for flammable, toxic substances.
    Storage Propylamine should be stored in a cool, well-ventilated area, away from sources of ignition and incompatible materials such as strong oxidizers and acids. Keep the container tightly closed and clearly labeled. Use corrosion-resistant containers and ensure proper grounding and bonding. Protect from sunlight and moisture, and store in accordance with local regulations for flammable and toxic chemicals.
    Application of Propylamine

    Applications of Propylamine in Industrial Manufacturing

    Propylamine serves as a functional intermediate and efficient processing aid in various chemical and industrial sectors. Its reactivity and compatibility with different downstream synthesis pathways make it an established raw material in multiple advanced manufacturing operations. Below, we detail its specific roles, handling practices, and final products within verified industrial segments.

    1. Agrochemical Synthesis: Herbicide Active Ingredients

    Many modern herbicidal APIs rely on short-chain alkylamines in their molecule construction, with propylamine acting as a common aminating agent in the production of selective herbicides. It contributes to the synthesis of amide, carbamate, and triazine functional groups, affecting the crop protection spectrum and environmental behavior of the finished products. Only manufacturers following regional agricultural and chemical standards incorporate propylamine at this stage, where strict traceability and impurity profiles are documented.

    Industry compliance standards

    • EU Regulation (EC) No 1107/2009 for Plant Protection Products
    • U.S. EPA 40 CFR Part 180 Tolerance Reassessment
    • GB 2763-2021 (China Maximum Residue Limits)
    • ISO 9001:2015 Quality Management System (applied to agrochemical synthesis lines)

    Typical usage ratio

    • Between 0.3–1.2 molar equivalents per target intermediate, varying based on the desired selective herbicide structure and batch size

    Downstream process integration

    • Added in the aminolysis or amidation step after base substrate preparation, under controlled temperature and pH to manage reaction selectivity and minimize side product formation

    Final product types

    • Active ingredients for selective broadleaf and grass weed control such as propanil, cyanazine derivatives, and related amide herbicides
    • Processed technical concentrate for crop spraying formulations
    • Pre-blended active ingredient–inert carrier granules

    2. Pharmaceutical Intermediate: Synthesis of Local Anesthetics

    Propylamine plays a definitive role in the synthetic routes for various anesthetic actives, including the formation of substituted amide or amine groups in molecules such as procaine derivatives. Process engineers monitor its addition closely, balancing purity, batch reaction profiles, and regional drug application standards. Its use requires validated protocols within GMP facilities to maintain trace-level consistency from intermediates to finished drug substances.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF (United States Pharmacopeia/National Formulary) monographs for anesthetic intermediates
    • EU EudraLex Volume 4 GMP Guidelines
    • China Pharmacopoeia (2020 Edition, Part II)

    Typical usage ratio

    • 0.2–0.7 molar ratio relative to the main acid chloride or ester precursor, depending on target intermediate and process yield requirements

    Downstream process integration

    • Introduced in the amination or N-alkylation stage, often under anhydrous conditions and monitored for residual starting material and process impurities (<0.1%)

    Final product types

    • Pharmaceutical-grade intermediates for local anesthetics (e.g. procaine, tetracaine analogs)
    • API intermediates for injectable or topical anesthetic formulations
    • Finished local anesthetic drugs exported to regulated markets under DMF (Drug Master File) filing

    3. Rubber Chemical Manufacturing: Vulcanization Accelerators

    Manufacturers use propylamine as a targeted amine source in rubber accelerators, especially in the synthesis of sulfenamide and thiocarbamate class accelerators for high-performance applications. Its inclusion adjusts cure speed and processing safety, with dedicated addition protocols to achieve optimal rubber compound cross-linking and minimize nitrosamine generation.

    Industry compliance standards

    • ASTM D4678 for Rubber Compounding Materials
    • ISO 9001:2015 for process and batch traceability
    • EU REACH Regulation for registration and use acceptance
    • DIN EN ISO 14001 Environmental Management (waste stream controls)

    Typical usage ratio

    • 0.5–1.8% by weight of the final accelerator composition, tailored based on rubber matrix and required cure profile

    Downstream process integration

    • Charged during the synthesis of primary accelerator, following in situ reaction with thiol-containing or carbon disulfide precursors before addition to rubber masterbatch blend

    Final product types

    • Vulcanization accelerators for synthetic and natural rubber
    • Rubber compound masterbatches for tire, hose, and belt manufacturing
    • Finished molded rubber goods with defined cure kinetics

    4. Corrosion Inhibitor Formulation: Oilfield Operations

    Oil and gas field chemical suppliers incorporate propylamine to synthesize amine-based corrosion inhibitors, especially for applications in acidizing, water injection, and gas gathering systems. Its primary use involves quaternization reactions, producing tailored amphiphilic molecules that form protective layers on ferrous metal surfaces under high salinity and variable temperature conditions typical in upstream operations.

    Industry compliance standards

    • NACE MR0175/ISO 15156 for oilfield equipment protection
    • API RP 14J guidelines for chemical usage offshore
    • REACH registration for downstream chemical use in the EU
    • Industry-specific MSDS documentation as required by OSHA Hazard Communication Standard

    Typical usage ratio

    • 3–15% by weight in concentrated corrosion inhibitor packages, adjusted according to brine composition and water/condensate ratio

    Downstream process integration

    • Reacted during batch production of amine quats or imidazolines, with subsequent blending into water- or oil-soluble concentrates formulated on-site or at chemical service hubs

    Final product types

    • Pipeline and wellbore corrosion inhibitor concentrates
    • Ready-to-dose oilfield additive blends for continuous injection
    • Packaged chemical sets for oilfield service companies and E&P operators

    5. Dye and Pigment Intermediate Processing: Azo Dye Synthesis

    In the colorant manufacturing sector, propylamine acts as a nucleophilic agent for producing propyl-substituted diazo compounds, shaping color properties and lightfastness in specific azo dye product lines. This step requires careful feed control to maintain narrow color specification ranges and minimize off-tone byproducts. Relevant only to facilities meeting international textile and environmental safety requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile chemical safety)
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL compliance
    • EU REACH Annex XVII for azo dyes
    • ISO 9001 for quality-controlled pigment production

    Typical usage ratio

    • 0.1–0.25 molar equivalent per diazonium salt, fine-tuned according to chromophore structure and batch scale

    Downstream process integration

    • Alkylamine is introduced at the diazotization coupling step in aqueous or solvent systems, with real-time monitoring of color development and by-product formation

    Final product types

    • Propylated azo dyes for textile, paper, and ink applications
    • Dispersible colorants for synthetic fiber spinning
    • Stable pigment concentrates for high-performance coatings

    6. Flotation Agents for Mining: Collector Synthesis

    Chemical suppliers to the minerals processing industry use propylamine as a key building block for cationic collector compounds. These agents improve selectivity and efficiency in the separation of quartz and silicate from valuable ores. Its integration focuses on hydrophobic modification in collector molecules, customized to the physical conditions and mineralogy of each ore body.

    Industry compliance standards

    • ISO 14001 Environmental Management for chemical handling at mine sites
    • Chinese Mining Chemical Standards GB/T 50754-2012
    • MSHA (U.S. Mine Safety and Health Administration) chemical registration
    • SDS documentation per GHS requirements

    Typical usage ratio

    • 5–12% by weight in collector concentrate formulations, optimized by mineral test work and slurry composition

    Downstream process integration

    • Undergoes alkylation and amination reactions during collector synthesis, followed by stabilization and dilution to customer-defined strength for direct use in flotation circuits

    Final product types

    • Collector amines for feldspar and iron ore separation
    • Cationic flotation agents for quartz removal
    • Finished collector solutions for direct pump dosing in flotation cells
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