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2-Phenylbenzylamine Hydrochloride

    • Product Name 2-Phenylbenzylamine Hydrochloride
    • Alias 2-PBA HCl
    • Einecs 629-729-6
    • 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

    930167

    Chemical Name 2-Phenylbenzylamine Hydrochloride
    Cas Number 21782-62-9
    Molecular Formula C13H14N·HCl
    Molecular Weight 219.72 g/mol
    Appearance White to off-white crystalline powder
    Purity Typically ≥98%
    Melting Point 186-190°C
    Solubility Soluble in water, methanol
    Storage Condition Store at 2-8°C, tightly closed
    Smiles c1ccccc1c2ccccc2CN.Cl
    Inchi InChI=1S/C13H13N.ClH/c14-10-12-8-4-7-11-6-2-1-3-5-11;1-2/h1-8H,9-10,14H2;1H

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

    Packing & Storage
    Packing Sealed 100g amber glass bottle, white powder labeled "2-Phenylbenzylamine Hydrochloride," with hazard symbols, batch number, and expiry date.
    Shipping 2-Phenylbenzylamine Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is packaged according to regulatory guidelines, labeled appropriately, and transported under controlled conditions. Proper documentation and safety data sheets accompany the shipment to ensure safe handling during transit and upon delivery to the recipient.
    Storage **2-Phenylbenzylamine Hydrochloride** should be stored in a tightly sealed container, protected from moisture and light. Keep it in a cool, dry, and well-ventilated area, ideally at room temperature (15–25°C). Avoid exposure to incompatible substances such as strong oxidizers. Ensure storage area is clearly labeled, secure, and accessible only to trained personnel. Dispose of according to local regulations.
    Application of 2-Phenylbenzylamine Hydrochloride

    Applications of 2-Phenylbenzylamine Hydrochloride in Industrial Manufacturing

    2-Phenylbenzylamine Hydrochloride plays a vital role as a controlled intermediate in the production processes of several industrial sectors. Our direct manufacturing expertise ensures strict alignment with regulatory demands and precise process integration in each application area. Below, we outline the principal downstream segments where this specialty amine salt proves essential, highlighting distinctive compliance standards, recommended concentration strategies, integration points, and end-product outcomes for each sector.

    1. Pharmaceutical Intermediate Synthesis

    This compound serves as a protected amine intermediate during the multistep synthesis of certain pharmaceutical active ingredients, especially within small-molecule innovative drug development pipelines and custom API manufacturing. It provides reactivity suitable for C-N bond formation, reductive aminations, or N-alkylation routes during the construction of target benzylic and phenethylamine motifs. Process specialists choose this intermediate when downstream purification and crystallization steps demand specific hydrochloride salt formation and defined amine reactivity.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • EU GMP EudraLex Volume 4
    • 21 CFR Parts 210/211 (FDA cGMPs)
    • Relevant USP/EP/JP monographs (when applicable for intermediates)

    Typical usage ratio

    • Usually dosed at 1.0–1.5 equivalents relative to the target substrate in stepwise amine introduction stages; precise amounts depend on desired conversion rate and reaction selectivity.

    Downstream process integration

    • Introduced after initial core scaffold formation; participates in condensation, alkylation, or coupling reactions under controlled pH, with subsequent salt formation and isolation prior to API assembly.

    Final product types

    • Active pharmaceutical ingredient (API) intermediates
    • Custom pharmaceutical building blocks for NCE (new chemical entity) research
    • Finished APIs and advanced intermediates for CNS or cardiovascular agents

    2. Agrochemical Active Ingredient Manufacturing

    Downstream agrochemical producers employ this compound as a nitrogen donor for assembling selective benzylamine-based herbicides and pesticide active ingredients. Its hydrochloride salt enhances stagewise process control for diverse alkylation and condensation reactions, especially when tailored to minimize by-product formation and improve overall yield in high-purity actives manufacturing. Application engineers validate addition levels to reduce contaminant carryover when formulating custom crop protection products.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 9001:2015 Quality Management System
    • REACH Registration and Evaluation (for European market entry)
    • China GB/T Standards for Pesticide Raw Materials

    Typical usage ratio

    • 0.8–1.2 equivalents based on the target coupling agent; the range is fine-tuned according to the reactivity of the co-reactant and the final desired activity profile.

    Downstream process integration

    • Added at the heterocycle formation or N-alkylation step, following initial precursor condensation and prior to target benzylamine finalization; subsequent work-up includes washing and crystallization specific to agrochemical actives requirements.

    Final product types

    • Selective herbicide intermediates (e.g., phenylbenzylamines used for specific crop applications)
    • Active ingredients for foliage-applied insecticides
    • Bespoke fungicide precursor compounds

    3. Specialty Dye and Pigment Synthesis

    Manufacturers of high-performance colorants and pigments in the textile, plastics, and coatings sectors incorporate this amine salt as a controlled nucleophile for C-N and diazo coupling reactions. Its use is preferred where product brightness, color uniformity, and salt purity directly affect final product stability or compliance with migration limits. Multi-stage batch operators regulate addition according to reaction tracking and downstream solvent exchange demands.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for textile dyes)
    • EN 71-3:2019 (Toy Safety requirements—restricted substances in pigments)
    • ISO 9001:2015 for pigment process QA
    • EU REACH Annex XVII for restricted aromatic amines

    Typical usage ratio

    • 0.5–1.1 molar equivalents relative to diazo component in azo dye synthesis; adjusted lower or higher depending on intended chromophore intensity and functional group excess.

    Downstream process integration

    • Fed into the amination or diazotization reactor during controlled temperature runs, prior to neutralization and filtration for pigment refinement; colorant specialists select precise addition points for reproducible shade and lightfastness.

    Final product types

    • High-purity azo and anthraquinone dyes
    • Engineered pigments for plastics and masterbatch
    • Special effect textile colorants for athletic fabrics

    4. Fine Chemical and Performance Additive Manufacturing

    This raw material acts as an adaptable intermediate in the synthesis of bespoke fine chemicals, including chemical reagents and performance additives for lubricants, polymer stabilizers, and corrosion inhibition systems. Application chemists select hydrochloride amine intermediates when reaction switching, product isolation, and shelf-life performance require precise salt forms for downstream incorporation. Batch recipe managers apply analytical controls to adjust for molecular weight and solvent compatibility in each case.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production
    • GHS/CLP labeling (EU Regulation (EC) No 1272/2008)
    • REACH (EU) and TSCA (US) chemical substance compliance (where applicable)
    • Automotive OEM materials specifications (for finished additives)

    Typical usage ratio

    • 0.9–1.3 equivalents per batch, subject to final product molecular design and required performance; formulation chemists may further modulate to limit residual salt in performance additive streams.

    Downstream process integration

    • Added in main condensation or ring-closure steps, or as a precursor for further functionalization; typically followed by solvent extraction, drying, and downstream compounding into master formulations.

    Final product types

    • Chemical intermediates for laboratory and analysis reagents
    • Stabilizers and antioxidant additive bases for lubricants
    • Corrosion inhibitor components for coatings and paints
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