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2-Aminobenzimidazole

    • Product Name 2-Aminobenzimidazole
    • Alias 2-Amino-1H-benzimidazole
    • Einecs 211-769-8
    • 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

    474268

    Iupac Name 2-Amino-1H-benzimidazole
    Molecular Formula C7H7N3
    Molar Mass 133.15 g/mol
    Cas Number 934-32-7
    Appearance Off-white to light brown solid
    Melting Point 270-274°C
    Solubility In Water Slightly soluble
    Pubchem Cid 69890
    Density 1.36 g/cm³
    Smiles c1ccc2nc(N)nc2c1
    Inchi InChI=1S/C7H7N3/c8-7-9-5-3-1-2-4-6(5)10-7/h1-4H,(H3,8,9,10)
    Pka 7.2 (of the amino group)
    Synonyms 2-Amino-1H-benzo[d]imidazole

    As an accredited 2-Aminobenzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Aminobenzimidazole is supplied in a 25-gram amber glass bottle with a tightly sealed screw cap and product labeling.
    Shipping 2-Aminobenzimidazole is shipped in tightly sealed containers, protected from moisture and incompatible substances. It is typically packed according to standard chemical safety regulations, ensuring compliance with transport guidelines. Appropriate hazard labeling and documentation are included. Shipping is performed by certified carriers authorized to handle non-flammable, non-toxic laboratory chemicals.
    Storage 2-Aminobenzimidazole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect it from moisture, heat, and direct sunlight. Always label the container clearly and follow standard laboratory safety procedures when handling or storing this chemical.
    Application of 2-Aminobenzimidazole

    Applications of 2-Aminobenzimidazole in Industrial Manufacturing

    2-Aminobenzimidazole enables advanced performance and functionality in several specialized manufacturing channels. Below we present real downstream sectors making use of this intermediate, with detailed information on regulatory standards, process positioning, and resulting end-products.

    1. Pharmaceutical API Synthesis: Antiviral Drug Intermediates

    In the pharmaceutical sector, downstream producers use 2-aminobenzimidazole as a building block for synthesizing active pharmaceutical ingredients (APIs), particularly in antiviral medication manufacturing. Chemists employ the material during heterocyclic synthesis steps to construct benzimidazole-based pharmaceutical cores, which form the framework of several clinical candidates targeting viral polymerase and protease enzymes. All process steps require rigorous control of material purity and compliance with pharmacopoeial requirements due to direct API contact.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <1092> and <823> Purity & Residual Solvents
    • EU Regulation 2015/831 for intermediates
    • Chinese Pharmacopoeia standards for APIs

    Typical usage ratio

    • 10–25% m/m relative to total heterocycle intermediates; variation based on target molecule synthesis route and desired throughput

    Downstream process integration

    • Charged during early cyclization or condensation stages to assemble benzimidazole frameworks within multi-step batch reactor sequences

    Final product types

    • Avibactam sodium (antibacterial API intermediate)
    • Remdesivir and similar nucleoside antivirals
    • Benzimidazole-based prodrugs for hepatitis treatment
    • Specialty clinical trial intermediates

    2. Polymer Additives: Corrosion Inhibitor Formulations

    Manufacturers of high-performance coatings and resins select 2-aminobenzimidazole as a key additive in formulating corrosion inhibitors for use in water-borne and solvent-borne industrial coatings. Chemists integrate it in blend formulations to provide chelating and passivating activity against ferrous and non-ferrous metals. Blending ratios and dispersion techniques must comply with regional chemical safety regulations and end-user durability specifications.

    Industry compliance standards

    • REACH Annex XVII for chemical additives
    • ISO 12944-6 (Corrosion Protection of Steel by Paint Systems)
    • OSHA GHS labeling for additives in paint systems
    • ASTM D1654 Provisions for Inhibitor Performance Testing

    Typical usage ratio

    • 0.1–2.0% w/w in total paint or resin matrix; adjusted for type of base resin, end-use exposure conditions, and desired lifetime performance

    Downstream process integration

    • Pre-dispersed into resin masterbatch or introduced into final blending step prior to milling and packaging; subject to QC validation before shipping

    Final product types

    • Industrial anti-corrosive primers
    • Heavy-duty marine coatings
    • Engineering-grade polymer resin composites
    • Protective surface coatings for infrastructure

    3. Dye and Pigment Manufacturing: Azo Dye Precursors

    Producers of colorants formulate 2-aminobenzimidazole into coupling components for azo dye synthesis. The chemical undergoes diazotization and subsequent coupling with aromatic amines or phenols, generating vivid shades used in both textile and ink sectors. Compliance with global dye regulations involves strict control of aromatic amine release and final product purity for safe textile and non-textile applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile safety)
    • EU Regulation (EC) No 1907/2006 Annex XVII—Aromatic Amines in Dyes
    • GHS SDS for pigment intermediates
    • ISO 105-X12 (Color Fastness to Rubbing)

    Typical usage ratio

    • 5–15% of total diazo component input; always determined by required molar ratio versus coupling agent and desired color intensity

    Downstream process integration

    • Charged as a diazo precursor fed into batch or continuous aromatic coupling kettles, followed by filtration and spray-drying to isolate the pigment concentrate

    Final product types

    • Disperse dyes for polyester textile printing
    • Acid dyes for nylon and leather
    • Inkjet pigments for industrial digital printing
    • Organic pigment concentrates for plastics coloration

    4. Agrochemical Synthesis: Fungicide Intermediate Manufacturing

    Formulators of modern crop protection chemicals employ 2-aminobenzimidazole for building antifungal active ingredient scaffolds. It enters multi-step synthetic schemes to introduce heterocyclic backbone structures, critical to bioactivity against major crop pathogens. Material inputs and process conditions must align with crop-use residue limits and ensure traceability through the supply chain for regulatory registration.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • EU Regulation (EC) No 1107/2009 (Plant Protection Products)
    • US EPA PRN 98-10 (Inert Ingredients in Pesticides)
    • ISO 9001:2015 (Quality Management Systems for Agrochemicals)

    Typical usage ratio

    • 8–18% w/w of reaction input mass; dosage tuned based on intended target molecule and process yield optimization

    Downstream process integration

    • Introduced during early heterocyclic ring formation, contributing directly to active center construction prior to formulation of technical concentrate

    Final product types

    • Carbendazim and benzimidazole fungicide technical concentrates
    • Broad-spectrum seed treatment active ingredients
    • Suspension and emulsion concentrate crop protection blends
    • Intermediate isolates for registration under agricultural chemical law
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