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Ammonium (-)-3-Bromo-8-Camphorsulfonate

    • Product Name Ammonium (-)-3-Bromo-8-Camphorsulfonate
    • Alias CBS-A3
    • Einecs 401-080-9
    • 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

    258692

    Chemical Name Ammonium (-)-3-Bromo-8-Camphorsulfonate
    Molecular Formula C10H16BrNO4S
    Molecular Weight 326.21 g/mol
    Cas Number 76956-50-2
    Appearance White to off-white powder
    Solubility Soluble in water
    Storage Temperature Room temperature, dry conditions
    Optical Activity Levorotatory (specific rotation depends on concentration and solvent)
    Iupac Name Ammonium (1R,4R)-3-bromo-1,7,7-trimethylbicyclo[2.2.1]heptane-2-sulfonate
    Purity Typically ≥98%
    Synonyms Camphorsulfonic acid, ammonium salt, bromo derivative
    Hazard Statements May cause irritation to eyes and skin
    Hs Code 292419

    As an accredited Ammonium (-)-3-Bromo-8-Camphorsulfonate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of Ammonium (-)-3-Bromo-8-Camphorsulfonate, securely sealed, labeled with chemical details and safety information.
    Shipping Ammonium (-)-3-Bromo-8-Camphorsulfonate is shipped in secure, clearly labeled containers compliant with chemical transport regulations. The packaging ensures protection from moisture and contamination. All relevant safety documentation accompanies each shipment. The chemical is dispatched via approved carriers, with transit under controlled conditions to preserve product integrity and ensure safe delivery.
    Storage Store Ammonium (-)-3-Bromo-8-Camphorsulfonate in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers and acids. Avoid exposure to moisture. Ensure proper labeling and prevent physical damage to the container. Use appropriate personal protective equipment when handling the chemical.
    Application of Ammonium (-)-3-Bromo-8-Camphorsulfonate

    Applications of Ammonium (-)-3-Bromo-8-Camphorsulfonate in Industrial Manufacturing

    As a specialized manufacturer of fine chemical intermediates, we provide Ammonium (-)-3-Bromo-8-Camphorsulfonate for a range of high-value, regulated industrial sectors. Our material supports downstream clients in pharmaceutical, analytical, and specialty chemical synthesis with high assay and process reliability.

    1. Chiral Resolution Agent for Pharmaceutical API Manufacturing

    Ammonium (-)-3-Bromo-8-Camphorsulfonate serves as a key resolving agent in the production of optically active pharmaceutical intermediates, particularly for chiral amine and alcohol API syntheses. Downstream producers incorporate this salt to achieve high enantiopurity, driven by increasing regulatory pressure on single-enantiomer drug substances. The compound's use supports GMP-compliant separation steps within active ingredient processes.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP <823> for compounding controls
    • 21 CFR Part 210/211 for processing operations
    • European Pharmacopoeia Chiral Drug Regulations

    Typical usage ratio

    • 0.9–1.2 molar equivalents relative to target racemate, with adjustment based on the specific substrate's racemization threshold and solubility requirements.

    Downstream process integration

    • Feeds into resolution and purification stage immediately after racemate synthesis; integrates with crystallization and salt separation units under controlled pH and ionic strength conditions.

    Final product types

    • Enantiopure pharmaceutical intermediates (e.g., chiral amines, alcohols, and acids)
    • APIs requiring strict enantiomeric excess (e.g., antihypertensives, CNS therapeutics)

    2. Ion Chromatography Eluent Additive in Analytical Laboratories

    Major analytical laboratories use this camphorsulfonate derivative as an eluent additive to enhance chiral or trace anion detection sensitivity in ion chromatography applications. It ensures reliable separation for regulated quality control, especially in pharmaceutical batch release and environmental testing.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation
    • FDA 21 CFR Part 11 for analytical data tracking
    • USP <621> Chromatography General Chapter

    Typical usage ratio

    • 5–50 mg/L in eluent solution, set empirically based on required chiral selectivity and analyte affinity during method validation.

    Downstream process integration

    • Added directly into mobile phase reservoirs prior to instrument loading; used in analytical method development and large-scale QC protocols for batch-certified facilities.

    Final product types

    • Validated ion chromatography methods
    • Certified reference results for QC documentation
    • Analytical services reports for regulatory submissions

    3. Intermediate in Agrochemical Active Ingredient Production

    Chemical manufacturers employ this camphorsulfonate salt during chiral modification steps in the synthesis of advanced agrochemical intermediates. It assists in producing optical isomers with improved environmental profiles, addressing both performance and regulatory traceability in crop protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH Regulation (EC) No 1907/2006
    • ISO 9001:2015 for quality management in specialty chemicals

    Typical usage ratio

    • 1.0–1.3 molar equivalents for target racemate, with optimization for yield and chiral purity per batch based on process analytical technology (PAT) feedback.

    Downstream process integration

    • Incorporated during chiral separation/purification phases after core scaffold construction; requires controlled phase transfer and solvent management for residual minimization in compliant facilities.

    Final product types

    • Enantiopure agrochemical intermediates (e.g., stereoselective herbicide bases)
    • Active substances for regulatory submission as low-impact pesticides or seed treatments

    4. Chiral Auxiliaries for Specialty Chemical Synthesis

    Manufacturers of specialty organics utilize this camphorsulfonate compound as a source material for chiral auxiliary synthesis, supporting fine chemical development for electronics, flavors, and specialty coating precursors. Its consistent stereochemical properties increase process reproducibility for value-added downstream derivatives.

    Industry compliance standards

    • ISO 14001 Environmental Management Systems (for specialty chemical sectors)
    • RoHS Directive (EU) 2011/65 restrictions (as applicable)
    • Company-specific supplier qualification guidelines

    Typical usage ratio

    • 0.8–1.5 molar equivalents with respect to the substrate, determined by auxiliary-substrate compatibility for targeted reaction steps and final isomer yield.

    Downstream process integration

    • Fed into intermediate synthetic stage, typically pre-functionalization or selective alkylation, under inert and dry conditions to maintain enantiocontrol.

    Final product types

    • Chiral auxiliaries for use in asymmetric syntheses
    • Electronic functional materials and custom initiators
    • Flavor and fragrance building blocks with defined stereochemistry
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