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3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid

    • Product Name 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid
    • Alias 3-MIPA
    • Einecs 695-184-9
    • 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

    729780

    Productname 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid
    Casnumber 13192-41-5
    Molecularformula C7H10N2O2
    Molecularweight 154.17
    Appearance White to off-white solid
    Meltingpoint 137-141°C
    Purity Typically ≥98%
    Solubility Soluble in water and polar organic solvents
    Storagecondition Store at room temperature, away from moisture
    Smiles CC1=NC=CN1CCC(=O)O
    Synonyms 2-Methylimidazole-1-propionic acid
    Pka Approx. 4.6 (carboxylic acid group)

    As an accredited 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g package features a white, screw-cap bottle, labeled with the chemical name, CAS number, hazard symbols, and supplier details.
    Shipping 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid is shipped in tightly sealed containers, protected from light and moisture. It is packaged according to chemical safety standards, labeled with hazard information if applicable, and transported via certified carriers, ensuring compliance with local and international chemical shipping regulations to maintain product integrity and safety.
    Storage Store **3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid** in a tightly sealed container, protected from light and moisture, ideally in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Label the container clearly, and ensure storage in a chemical cabinet suitable for organic acids. Follow all standard laboratory chemical storage and safety protocols.
    Application of 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid

    Applications of 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid in Industrial Manufacturing

    As an established manufacturer specializing in high-purity specialty imidazole derivatives, we supply 3-(2-Methyl-Imidazol-1-Yl)-Propionic Acid for advanced chemical production sectors with strictly regulated quality and traceability standards. Our material supports reliable integration into multiple downstream manufacturing scenarios, each governed by strict formulation guidelines and industry compliance requirements.

    1. Epoxy Resin Curing Agents for Electronic Encapsulation

    Electronics manufacturers use this imidazole-based acid as a latent curing agent to enhance crosslinking in epoxy molding compounds and potting systems for sensitive microelectronic assemblies. Its inclusion provides controlled reactivity during pre-gel and post-cure phases, ensuring high dielectric breakdown resistance in final encapsulants. Operators precisely meter the additive into two-part systems to match specific thermal profiles and gel times required in automated component lines.

    Industry compliance standards

    • UL 94 Flammability Rating (V-0 for encapsulants)
    • RoHS Directive 2011/65/EU
    • IEC 61249-2-21 Halogen-free specification for base materials
    • IPC/JEDEC J-STD-033C for moisture/reflow sensitivity

    Typical usage ratio

    • 0.1–0.5% by weight in the epoxy resin formulation, adjusted according to resin type and required latency time

    Downstream process integration

    • Direct blending into part B of two-part epoxy compounds; added before final vacuum mixing; the system is then filled or molded onto PCB assemblies prior to thermal cure (120–150°C).

    Final product types

    • Semiconductor underfills
    • Microchip encapsulation pellets
    • Electronic potting compounds for power modules
    • SMT-compatible adhesives

    2. Pharmaceutical Intermediate for Heterocyclic Drug Synthesis

    The compound serves as a crucial building block in the production of active pharmaceutical ingredients (APIs) containing imidazole rings, notably in antifungal and cardiovascular drug synthesis. API manufacturers incorporate it during key condensation or alkylation steps to construct target heterocycles while controlling impurity levels through validated processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) monographs for intermediate quality
    • European Pharmacopoeia (Ph. Eur.) for API precursors
    • 21 CFR Part 211 (US FDA GMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Stoichiometric amounts as dictated by target molecule synthesis, typically ranging from 1 to 1.2 molar equivalents relative to reactants in the cyclization/condensation step

    Downstream process integration

    • Charged into reactor vessels after primary solvents; reacts during multi-step synthesis for heterocyclic core formation; followed by work-up, purification (usually crystallization), and upstream QC release before API integration.

    Final product types

    • Imidazole-based antifungal agents (e.g., clotrimazole derivatives)
    • Intermediate alkaloids for cardiovascular APIs
    • Pharmaceutical intermediates for further transformation
    • Custom heterocyclic scaffolds for medicinal chemistry

    3. Corrosion Inhibitor Formulations for Industrial Water Systems

    Process water treatment formulators employ this imidazole derivative as a performance booster in corrosion inhibitor blends for closed-loop and recirculating water systems. It interacts with metal surfaces to form hydrophobic protective films, effectively reducing scaling and oxidation on ferrous and copper alloys even in challenging pH conditions found in industrial chillers or district heating.

    Industry compliance standards

    • ANSI/NSF Standard 60 (Drinking Water Treatment Chemicals—Health Effects)
    • ASTM D1384 (Corrosion Test for Engine Coolants)
    • EU Biocidal Product Regulation (BPR, Regulation (EU) No 528/2012) for formulation safety
    • ISO 9001:2015 (Quality Management for Chemical Additives)

    Typical usage ratio

    • 10–80 ppm in final inhibitor blends, usage fine-tuned during field commissioning and adjusted based on metal content and water chemistry

    Downstream process integration

    • Added during the concentrate preparation stage; system operators dose the blended inhibitor into cooling tower basins or closed loops during scheduled maintenance or start-up protocols.

    Final product types

    • Multi-metal corrosion inhibitor concentrates
    • Chiller protection fluids
    • Boiler scale preventatives
    • Heat exchanger maintenance solutions

    4. Polymer Modifier in High-Performance Engineering Plastics

    Plastic compounders leverage this imidazole-moiety acid as a functional chain extender or reactive modifier, particularly in the production of specialty polyamides and polyesters. It becomes part of the polymer backbone during melt-phase polycondensation, boosting hydrolytic resistance and thermal stability, which are essential for engineered components subject to repeated stress or exposure to harsh chemicals.

    Industry compliance standards

    • REACH Regulation (EC No. 1907/2006) for chemical safety
    • ISO 1874-2 for polyamide molding materials
    • UL Yellow Card (QMFZ2) for flame-retardant plastics
    • RoHS 2011/65/EU for hazardous substance restrictions in electronics housings

    Typical usage ratio

    • 0.3–1.2% by weight in polymer blend; proportion tuned based on target mechanical reinforcement and compatibility with other chain extenders

    Downstream process integration

    • Fed into twin-screw extruders along with primary resin pellets; the compound reacts during melt mixing and remains integrated through pelletizing and base resin QC steps before molding or extrusion.

    Final product types

    • Glass fiber reinforced polyamides (PA6/PA66 blends)
    • Flame-retardant polyester granules
    • Automotive electrical connectors
    • Chemical-resistant pump components

    5. Chelating Agent in Metalworking Fluid Additives

    Producers of cutting and grinding fluids incorporate this carboxy-imidazole as a selective chelating agent to stabilize transition metal ions and enhance anti-wear protection in formulated metalworking additives. It helps inhibit metal salt precipitation and sludge formation in high-load machining operations, improving fluid service life and protecting tooling surfaces during continuous manufacturing runs.

    Industry compliance standards

    • ASTM E2529 (Standard Guide for Testing Water-Based Metalworking Fluids)
    • Germany TRGS 611 (Technical Rules for Hazardous Substances—Metalworking Fluids)
    • OSHA 29 CFR 1910.1200 (Hazard Communication Standard)
    • ISO 6743-13 (Lubricants, Industrial Oils, and Related Products—Family Y: Metalworking Fluids)

    Typical usage ratio

    • 0.05–0.2% by weight in the finished fluid matrix; exact level determined by fluid pH, intended contact metal, and required chelation strength

    Downstream process integration

    • Dispersed into aqueous phase during initial batch blending; followed by pH balancing and microfiltration prior to drum filling or IBC packaging.

    Final product types

    • Soluble oil cutting fluids
    • Semi-synthetic metalworking emulsions
    • High-performance grinding coolants
    • Machine tool lubricants with corrosion control
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