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2-Aminoperimidine Hydrobromide

    • Product Name 2-Aminoperimidine Hydrobromide
    • Alias 2-AP HBr
    • Einecs NA
    • 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

    477225

    Productname 2-Aminoperimidine Hydrobromide
    Casnumber 91696-10-9
    Molecularformula C11H10BrN5
    Molecularweight 308.14 g/mol
    Appearance Off-white to light yellow powder
    Meltingpoint 300°C (decomposes)
    Solubility Soluble in water
    Purity Typically ≥98%
    Storageconditions Store at 2-8°C, protected from light and moisture
    Smiles C1=CC=C2C(=C1)C(=NC=N2)N.Br
    Synonyms 2-Aminoperimidine hydrobromide salt
    Iupacname 2-aminoperimidine hydrobromide
    Identificationmethods 1H NMR, MS, IR
    Hazardstatements May cause irritation to skin, eyes, and respiratory tract
    Hscode 2933599590

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

    Packing & Storage
    Packing The 2-Aminoperimidine Hydrobromide, 5g, is packaged in a sealed amber glass bottle with a tamper-evident screw cap.
    Shipping 2-Aminoperimidine Hydrobromide is shipped in tightly sealed containers, protected from light and moisture. It is typically packaged in compliance with chemical safety regulations, labeled appropriately, and cushioned to prevent breakage during transit. Shipping is conducted according to local and international chemical transport guidelines, often via ground or air freight with all necessary documentation.
    Storage 2-Aminoperimidine Hydrobromide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Store at room temperature (15–25°C). Ensure proper labeling and restrict access to authorized personnel. Follow standard chemical storage protocols and consult the safety data sheet for detailed handling instructions.
    Application of 2-Aminoperimidine Hydrobromide

    Applications of 2-Aminoperimidine Hydrobromide in Industrial Manufacturing

    2-Aminoperimidine Hydrobromide supports complex organic syntheses across pharmaceutical, dye, agrochemical, and advanced material pipelines. We supply directly from our ISO-certified facilities, ensuring batch consistency for specialized downstream manufacturing. Below we detail key industrial applications and their unique process integration considerations.

    1. Pharmaceutical Intermediate Synthesis – API Precursor Production

    This compound acts as a key scaffold in synthesizing heterocyclic pharmaceutical actives, especially for anti-neoplastic and anti-viral drug candidates. Process R&D teams typically introduce it in the early or intermediate stages of multi-step reactions, controlling structural isomerism and optimizing yields with tailored stoichiometric ratios. Customers in finished dose production monitor incoming quality for impurity profile and particle size, as these impact downstream API purification and crystallization. Batch documentation and lot traceability remain essential, alongside alignment with stringent GMP norms.

    Industry compliance standards

    • ICH Q7A GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP monograph controls for related impurities (where applicable)
    • FDA/EMA QMS for pharmaceutical raw materials
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.05–0.2 molar equivalents relative to the core API scaffold, adjusted based on target yield and selectivity

    Downstream process integration

    • Charged during heterocyclization or amination steps in reactor systems
    • Quality-controlled prior to reaction to check identity, assay, and residual solvents
    • Integration with multi-stage synthesis flows—frequently followed by filtration, washing, and pH adjustment
    • Material handling in compounding rooms under validated cleanroom environment

    Final product types

    • Anti-cancer drug intermediates (e.g., perimidine-based kinase inhibitors)
    • Antiviral nucleoside analogues
    • Diagnostic reagent building blocks
    • Active pharmaceutical ingredients (second or third generation)

    2. Organic Dye Synthesis – High-Purity Chromophore Manufacturing

    Downstream pigment and dye manufacturers use 2-Aminoperimidine Hydrobromide as a starting material for polycyclic aromatic chromophores. The amine functionality enables controlled coupling reactions with diazonium salts for the creation of deep-colored, lightfast dye molecules. Strict attention to solvent choice, reaction temperature, and product isolation minimizes unwanted byproducts and enhances product consistency for textile, printing ink, and plastic coloration end uses. Colorists demand reliable batch-to-batch performance, with spectral purity validated by UV-Vis analyses.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (substance registration and SVHC)
    • EN 71-3 Safety of Toys (where pigments are used in children’s products)
    • ISO 9001:2015 for colorant supply chain
    • Oeko-Tex® Standard 100 (for textile applications)

    Typical usage ratio

    • 1.1–1.3 molar equivalents per coupling partner, excess to drive reaction completion and maximize conversion

    Downstream process integration

    • Introduced at primary chromophore assembly step, typically during condensation under inert atmosphere
    • Integrated with reflux and distillation units for solvent recovery
    • Dye purification by repeated recrystallization or column chromatography
    • Final QC by HPLC and UV-Vis spectral testing

    Final product types

    • Textile disperse dyes
    • Printing inks for security features
    • Plastic and polymer masterbatches
    • High-performance liquid chromatography (HPLC) colorant standards

    3. Agrochemical Intermediate – Synthesis of Fungicide and Herbicide Actives

    Major agrochemical manufacturers integrate this material as a nitrogen-based building block in the multi-step synthesis of systemic fungicides and selective herbicides. The compound’s unique core structure supports the generation of heterocyclic motifs with biological activity, contributing to mode-of-action diversity. Careful process control, particularly in regard to reaction pH and oxidant choice, preserves amino group reactivity for subsequent formylation or chlorination steps. Downstream quality criteria emphasize impurity minimization to meet regulatory residue limits.

    Industry compliance standards

    • FAO/WHO Technical Grade Pesticide Specifications
    • Regulation (EC) No 1107/2009 for pesticide registration
    • ISO 9001:2015 for manufacturing traceability
    • OECD Guidelines for the Testing of Chemicals

    Typical usage ratio

    • Varies from 0.1–0.5 molar equivalents based on downstream synthetic strategy for target pesticide class

    Downstream process integration

    • Charged into heterocyclic ring closure reactions under catalytic or basic conditions
    • Raw material is milled to specified particle size for consistent dispersion in solvent systems
    • Monitored for trace metals and halogen content to prevent catalyst poisoning
    • Final crude is isolated and fed into active ingredient formulation units

    Final product types

    • Systemic fungicide AI precursors (e.g., perimidine-type fungicides)
    • Pre-emergent herbicide active intermediates
    • Chemical probes for agrochemical research
    • Agrochemical analytical standards

    4. Specialty Electronic Materials – Synthesis of Functional Organic Compounds

    Advanced electronics and material science sectors use this compound to build tailored nitrogen-rich organic molecules for applications such as thin-film transistors and organic light-emitting diodes (OLEDs). Synthesis protocols involve high-purity solvent systems, rigorous inert atmosphere handling, and stoichiometric control to avoid side-chain oxidation and migration. Material suppliers emphasize metal content and optical purity to ensure downstream film mobility and light emission efficiency. Downstream integration can include solution processing or vacuum deposition, demanding tight control of residual ionic impurities.

    Industry compliance standards

    • IPC-1752A Materials Declaration Management Standard
    • RoHS Directive 2011/65/EU for restricted substances
    • ISO 14001:2015 Environmental Management Systems
    • Customer-specific electronic grade QC protocols

    Typical usage ratio

    • 0.02–0.1 molar equivalents in multistep coupling or cyclization reactions, optimized for film thickness and device design

    Downstream process integration

    • Dosed during solution-phase organic synthesis stages
    • Post-synthesis purification via sublimation or column chromatography to electronic grade
    • Formulation into spin-coating or inkjet printing solutions for device fabrication
    • QC testing for trace alkali metals, ionic contamination, and optical absorption

    Final product types

    • OLED blue and green emitter intermediates
    • Organic semiconductor thin-film transistor precursor compounds
    • Photonic polymer materials
    • Advanced display and touch sensor components
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