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3-Bromobenzylguanidinium Sulfate

    • Product Name 3-Bromobenzylguanidinium Sulfate
    • Alias NSC 25808
    • Einecs 697-416-4
    • 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

    181473

    Chemical Name 3-Bromobenzylguanidinium Sulfate
    Molecular Formula C8H12BrN4O4S
    Molecular Weight 355.18 g/mol
    Appearance white to off-white solid
    Solubility soluble in water
    Melting Point decomposes above 250°C
    Cas Number 1191-58-8
    Pubchem Cid 85636
    Storage Conditions store at room temperature, tightly closed
    Synonyms 3-Bromobenzylguanidine sulfate
    Ph Of 1 Percent Solution 5.0-7.0
    Odor odorless
    Stability stable under recommended conditions

    As an accredited 3-Bromobenzylguanidinium Sulfate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 3-Bromobenzylguanidinium Sulfate is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 3-Bromobenzylguanidinium Sulfate should be shipped in tightly sealed containers, protected from moisture and physical damage. It is recommended to use secondary containment and appropriate labeling, comply with local and international regulations, and transport via a recognized courier specializing in chemicals. Proper documentation should accompany the shipment to ensure safe and legal handling throughout transit.
    Storage 3-Bromobenzylguanidinium sulfate should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers. Store at room temperature or as specified by the manufacturer. Use appropriate safety precautions to avoid ingestion, inhalation, or skin contact with the compound.
    Application of 3-Bromobenzylguanidinium Sulfate

    Applications of 3-Bromobenzylguanidinium Sulfate in Industrial Manufacturing

    3-Bromobenzylguanidinium Sulfate supports precision synthesis in pharmaceutical, agrochemical, specialty chemical, dye, and electronic material sectors. Manufactured to order, this raw material enables producers to meet demanding downstream process requirements.

    1. Pharmaceutical Intermediate Synthesis

    This compound acts as an advanced intermediate in targeted synthesis routes for selective kinase inhibitors and anti-infective agents. Downstream R&D uses it for substitution and coupling steps in active pharmaceutical ingredient (API) production, particularly in benzimidazole and guanidine-functionalized scaffolds. Accurate control of reactivity is essential during scale-up, so direct input into closed multi-step batch reactors maintains traceability and batch integrity. Final API quality depends on impurity profile stability, process lock-in, and compliance with global pharmacopoeial requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • US FDA 21 CFR Part 211
    • EU EMA Guidelines on GMP for Pharmaceutical Production
    • JP Pharmaceutical Excipients Standards (JPE)

    Typical usage ratio

    • Typically 0.15 to 0.40 molar equivalent relative to substrate, adjusted according to desired substitution or protection level in target molecule synthesis.

    Downstream process integration

    • Integrated during staged addition to intermediate feed tanks before controlled heating and solvent exchange steps.
    • Used during final crystallization by precise dosing under inert atmosphere to regulate side product formation.

    Final product types

    • Active pharmaceutical ingredients (APIs) for targeted therapy
    • Small molecule kinase inhibitors
    • Antimicrobial intermediates
    • Research-grade chemical probes

    2. Agricultural Fungicidal Compound Manufacturing

    Fungicide producers use this raw material as a functionalized guanidine source to synthesize aromatic guanidine-based crop protection agents. It is typically introduced at the nucleophilic addition stage, yielding robust and stable functional groups suitable for broad-spectrum fungicide development. This enables precise targeting of plant pathogenic fungi, especially in high-value fruit and vegetable crop segments. Quality monitoring throughout compounding and granulation phases is crucial to ensure field performance consistency.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • EU Regulation (EC) No 1107/2009 on Plant Protection Products
    • US EPA Pesticide Registration Requirements, 40 CFR Part 158
    • ISO 9001:2015 for Agricultural Input Manufacturing

    Typical usage ratio

    • Ranges from 8% to 20% by weight in technical concentrates, with the percentage determined by target actives and formulation technology (wettable powder or emulsifiable concentrate).

    Downstream process integration

    • Dosed during initial batch blending to maximize reaction yield and ensure uniform product dispersion.
    • Monitored by in-line NMR inspection at critical process points for residue minimization.

    Final product types

    • Crop protection fungicides
    • Seed treatment agents
    • Specialized bioactive granules
    • Pre-mixed wettable powders

    3. Specialty Dye and Pigment Synthesis

    Colorant manufacturers incorporate this molecule as a guanidine donor or functional protective group in multi-step syntheses for cationic dyes and pigment dispersants. Its controlled release properties offer selectivity when reacting with aromatic and heterocyclic partners, supporting manufacture of stable dye intermediates and highly soluble pigment salts. Attention to impurity carry-over is critical during large-scale processing to meet downstream color fastness and solubility requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 (textile ecological safety)
    • REACH Regulation (EC) No 1907/2006
    • ISO 787-24:2019 (General Methods of Test for Pigments and Extenders)
    • CFR Title 21 Part 74 (Color Additives Permitted for Use in Food, Drugs, and Cosmetics, for applicable sectors)

    Typical usage ratio

    • 0.5% to 2.5% by molarity, relative to precursor aromatic ring system, adjusted to meet desired chromatic intensity and solubility properties.

    Downstream process integration

    • Batch-fed during diazotization and condensation steps, enabling tight reaction time control and minimizing side color formation.
    • Dosed together with surfactant dispersants in pigment salt formulation stages.

    Final product types

    • Cationic textile dyes
    • Inkjet printing pigments
    • Aqueous pigment dispersions
    • Heat-resistant colorants for polymer composites

    4. Organic Electronics and Sensor Material Fabrication

    R&D and pilot-scale fabrication lines for organic electronics use this compound as a molecular modifier for surface-binding and conductivity control in printed electronics, sensor coatings, and ion-selective membranes. Controlled application is essential during thin-film deposition, either via solution casting or vapor-assisted processes, where the material improves ionic transport or modulates electron affinity in host polymer matrices. Robust QC steps focus on ensuring batch purity to achieve reliable device calibration and electrical performance.

    Industry compliance standards

    • IEC 62341 for Organic Light Emitting Diode (OLED) Devices
    • ISO/TS 80004-8:2020 Nanotechnologies — Sensors
    • RoHS Directive 2011/65/EU for Electronic Equipment
    • IPC J-STD-033 for Handling, Packaging, and Moisture Protection of Electronic Compounds

    Typical usage ratio

    • 0.01% to 1.0% by weight in formulation mixes for sensor films, with loading based on thickness, substrate compatibility, and function (conductive vs ion-exchange properties).

    Downstream process integration

    • Dispensed in solution during functional layer printing or spin-coating onto substrate films.
    • Post-deposition curing at controlled temperature to stabilize the guanidinium-functional surface.

    Final product types

    • Printed circuit sensor arrays
    • Ionic conductor layers in flexible electronics
    • Membrane materials for integrated microfluidic devices
    • Electrochemical diagnostic strip coatings
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