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1H-Imidazole-4-Carbaldehyde

    • Product Name 1H-Imidazole-4-Carbaldehyde
    • Alias Imidazole-4-carboxaldehyde
    • Einecs 629-616-9
    • 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
    VTB
    Specifications

    HS Code

    978509

    Productname 1H-Imidazole-4-Carbaldehyde
    Casnumber 3034-41-1
    Molecularformula C4H4N2O
    Molecularweight 96.09
    Appearance White to off-white solid
    Meltingpoint 153-157°C
    Solubility Soluble in water, ethanol, and DMSO
    Purity Typically ≥98%
    Iupacname 1H-imidazole-4-carbaldehyde
    Smiles C1=CN=CN1C=O
    Inchi InChI=1S/C4H4N2O/c7-3-4-1-5-2-6-4/h1-3H,(H,5,6)
    Storagetemperature 2-8°C
    Synonyms Imidazole-4-carboxaldehyde

    As an accredited 1H-Imidazole-4-Carbaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a 25g amber glass bottle with a secure screw cap and a clear hazard label displaying safety information.
    Shipping **Shipping Description for 1H-Imidazole-4-Carbaldehyde:** This chemical should be shipped in tightly sealed containers under cool, dry conditions. It is recommended to use appropriate hazard labeling, with protection from moisture and incompatible substances. Handle as a laboratory chemical, ensuring compliance with local, national, and international transport regulations (such as DOT, IATA, or IMDG).
    Storage 1H-Imidazole-4-carbaldehyde should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. The storage temperature should ideally be at room temperature (15-25°C). Proper labeling and safety precautions should be observed to prevent accidental exposure or spillage.
    Application of 1H-Imidazole-4-Carbaldehyde

    Applications of 1H-Imidazole-4-Carbaldehyde in Industrial Manufacturing

    1H-Imidazole-4-carbaldehyde finds essential use in highly specialized sectors within the fine chemical and pharmaceutical industries. As a manufacturer with hands-on plant integration, we directly support operations requiring exacting synthesis, strict compliance, and reproducible performance. Below are the principal real-world applications, organized by sector, each with process-critical standards, incorporation ratios, integration points, and end-use formats.

    1. Pharmaceutical Intermediate Synthesis

    Many API production chains, especially for antifungal and antihypertensive drugs, incorporate 1H-imidazole-4-carbaldehyde as a key heterocycle-building intermediate. The compound enters amidation and cyclization routes requiring high purity and traceability for regulatory audit trails. Strict GMP control governs batch release and analytical standards, especially when targeting regulated export markets.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (FDA cGMP for Drugs)
    • EU GMP Directive (Annex 8 and 11)
    • Relevant monographs: Ph. Eur., USP (for related materials)

    Typical usage ratio

    • 0.3–2.7 molar equivalents, depending on synthetic route and impunity profile control; final amount set through route-specific optimization with excess calculated by downstream conversion yield.

    Downstream process integration

    • Introduced during heterocycle ring closure, specifically nucleophilic aromatic substitution and acylation steps in drug intermediate chains.

    Final product types

    • Voriconazole, Losartan, antifungal triazoles, imidazole-based bulk pharmaceutical intermediates

    2. Agrochemical Building Block Manufacturing

    In agrochemical plants, the compound is routinely selected for non-chlorinated ring modification in the preparation of advanced intermediates used in crop protection actives. Precise formulation and documented impurity inventories support regulatory data packages and ensure that downstream synthesis meets the requirements for active substance technical equivalence.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for the Registration of Pesticides
    • ISO 17025 (Analytical Laboratories)
    • REACH Registration (EC 1907/2006) for chemical safety dossiers
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Usually 0.8–1.4 molar equivalents relative to haloalkyl precursors; can adjust addition rate to control substitution selectivity and minimize by-product formation.

    Downstream process integration

    • Introduced in condensation and functionalization of nitrogen-containing base rings during the synthesis of triazole fungicides and novel imidazole herbicidal intermediates.

    Final product types

    • Triazole-based crop protection actives (e.g., prothioconazole intermediates), technical-grade pesticide intermediates

    3. Specialty Resin & Polymer Modifier Production

    Polymer and epoxy systems adopt this compound, particularly as a chain modulator and curing agent for specialty resins. Its aldehyde group participates in epoxy cross-linking while the imidazole ring improves chemical resistance and thermal stability, key for advanced coatings and electronics potting compounds. Compliance with chemical substance regulation ensures downstream polymer safety declarations.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management System for polymers)
    • RoHS Directive (2011/65/EU) for electrical/electronic applications
    • Registration under TSCA for US-bound thermoset intermediates
    • REACH SVHC assessment as required for European supply chains

    Typical usage ratio

    • 0.05–0.2 wt% in resin formulations; proportion set during QC validation to balance cure rate versus final hardness, often tailored for each epoxy grade.

    Downstream process integration

    • Dosed into the pre-polymer mix before resin cross-linking or added as a post-cure chain extender for advanced thermoset matrix design.

    Final product types

    • Electronic encapsulation resins, high-solids coil coatings, chemically stable thermoset composites

    4. Chemical Research and Diagnostic Reagent Synthesis

    Institutes and diagnostic kit manufacturers value this compound for solid-phase synthesis of specialized ligands and reactive probes. The functional aldehyde enables site-specific anchoring or derivatization under research-grade QA/GLP requirements, especially for high-throughput screening and labeled biomolecule development.

    Industry compliance standards

    • OECD GLP Principles for test facility operations
    • ISO 13485:2016 for diagnostic reagent producers
    • Relevant national transport and chemical safety regulations (GHS, CLP)
    • Standard analytical certification under ACS Reagent norms

    Typical usage ratio

    • 1–25 µmol per resin batch or microgram scale, depending upon synthesis loading and ligand density requirements; frequently determined by the target application or probe coupling efficiency

    Downstream process integration

    • Coupled to solid supports via reductive amination or formylation in the initial reagent loading; also used as an intermediate in labeled molecule construction during small-scale synthesis.

    Final product types

    • Chemical biology probes, immobilized affinity ligands, diagnostic kit reagents for biomedical screening
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