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2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine

    • Product Name 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine
    • Alias DEAI
    • Einecs EINECS 412-070-7
    • 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

    525343

    Chemical Name 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine
    Cas Number 111983-38-5
    Molecular Formula C7H13N3
    Molecular Weight 139.20
    Appearance Colorless to pale yellow liquid
    Purity Typically >97%
    Solubility Soluble in water and organic solvents
    Density Approx. 1.02 g/cm³ (estimated)
    Functional Groups Pyrazole ring, amine group
    Smiles CC1=CC(=NN1)CCN
    Iupac Name 2-(3,5-dimethyl-1H-pyrazol-1-yl)ethan-1-amine
    Storage Temperature 2-8°C (Refrigerated, recommended)

    As an accredited 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine packaged in a sealed amber glass bottle with safety labeling and hazard information.
    Shipping **Shipping Description:** 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine should be shipped in tightly sealed containers, protected from moisture and light. The packaging must meet applicable regulations for chemicals, ensuring safety during transit. Handle as a potentially hazardous chemical—use appropriate labeling, documentation, and temperature control if required. Consult SDS and local regulations before shipping.
    Storage Store 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine in a tightly sealed container in a cool, dry, and well-ventilated area away from heat sources and incompatible substances like oxidizers and acids. Avoid moisture and direct sunlight. Use appropriate personal protective equipment (PPE) when handling. Label storage clearly and keep the chemical away from food and drink. Follow all local safety regulations.
    Application of 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine

    Applications of 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine in Industrial Manufacturing

    2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine is an advanced specialty chemical widely adopted as an intermediate or performance enhancer in several precise downstream manufacturing fields. The following sections detail its principal industrial applications, with specific usage practices grounded in real-world factory operations.

    1. Triazole-Type Plant Growth Regulator Synthesis

    This compound serves as a core building block in the industrial synthesis of next-generation triazole-based plant growth regulators. Process engineers introduce it during the fine chemical stage, where its structure enables the formulation of molecules such as uniconazole and paclobutrazol, essential for crop yield optimization in commercial agriculture.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Growth Regulators
    • ISO 25119 Crop Protection Standards
    • REACH Registration (EU Regulation EC No 1907/2006)
    • China National GB/T Standards for Agricultural Chemicals (GB 20665, GB/T 20713)

    Typical usage ratio

    • Reaction charge between 0.15–0.25 molar equivalents per triazole target molecule; optimized per batch scale and catalyst system

    Downstream process integration

    • Added after initial condensation, serving as a nucleophile in heterocycle assembly during the third or fourth reaction step in plant regulator API synthesis
    • Isolated intermediate subjected to further derivatization and purification before formulation

    Final product types

    • Bulk uniconazole and paclobutrazol technical powders
    • Emulsifiable concentrates and aqueous solutions for agricultural spraying
    • Water-dispersible granules for crop application

    2. Industrial Corrosion Inhibitor Formulations

    The molecule acts as a performance modifier for iron and steel corrosion inhibitor blends deployed in cooling water treatment and oilfield systems. It is incorporated during formulation for its ability to chelate metal ions and form protective surface films, which extends system service life under demanding operational cycles.

    Industry compliance standards

    • ASTM D1384 and D665 Metal Corrosion Evaluation
    • ISO 8044 Corrosion Terminology
    • API Recommended Practice 5L2 for Pipeline Corrosion Inhibitors
    • GB/T 50050 Water Treatment Engineering Code

    Typical usage ratio

    • Dosage in final blend: 0.2%–1.0% w/w, adjusted for water quality, temperature, and system metal content

    Downstream process integration

    • Blended as a tertiary active during batch blending of multi-component aqueous inhibitor concentrates
    • Dosed into recirculating systems via automated metering for continuous protection

    Final product types

    • Closed-loop cooling water corrosion inhibitors
    • Oil and gas pipeline corrosion inhibitor packages
    • Industrial water treatment chemical drums

    3. High-Purity Specialty Ligand Manufacturing for Catalysts

    Our facility utilizes 2-(3,5-Dimethyl-Pyrazol-1-Yl)-Ethylamine as a precursor in the large-scale custom synthesis of ligand building blocks for homogeneous and polymerization catalysts. Its pyrazole structure provides electronic and steric tuning abilities in ligand design, impacting catalytic selectivity in major downstream polymer and fine chemical processes.

    Industry compliance standards

    • IUPAC Recommendations for Ligand Design and Characterization
    • ISO 9001 Certified Quality Management Systems (for specialty chemicals)
    • SHE Audit Requirements for Catalysis Raw Materials (as per Dow, BASF)

    Typical usage ratio

    • Initiation charge: 1.0 equivalent relative to metal source, or 1.1–1.5 equivalents in bidentate ligand systems

    Downstream process integration

    • Fed into ligand synthesis reactors under controlled temperature, forming metal complexes in subsequent coordination steps
    • Final purification via column chromatography or crystallization before QA release

    Final product types

    • NN- or NNN-type ligand libraries for organometallic catalysts
    • Batch-specific ligand formulations for polymerization catalyst kits
    • Catalyst precursor packages for pilot and full-scale production

    4. Pharmaceutical Intermediate for Pyrazole Derivative APIs

    This product functions as a key intermediate in the multi-step synthesis routes of pharmaceutical active ingredients featuring pyrazole motifs, such as certain CNS therapeutic APIs and kinase inhibitor scaffolds. It delivers precise reactivity needed in core ring assembly and tailored side-chain extension during chemical drug API manufacture.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) and United States Pharmacopeia (USP) for relevant APIs
    • GMP-compliant documentation and batch traceability

    Typical usage ratio

    • 0.9–1.2 equivalents within API synthetic step, precise adjustment per impurity profile and scale-up batch

    Downstream process integration

    • Loaded during core pyrazole ring formation, followed by protection/deprotection and functional group elaboration in later stages
    • Intermediate isolated by distillation, chromatography, and analytical QC before use in final coupling steps

    Final product types

    • API-grade pyrazole-containing pharmaceuticals (e.g., antipyretic/analgesic drugs, kinase inhibitors, CNS agents)
    • Regulatory-submitted API intermediates for CDMO partners
    • Custom pyrazole derivatives for drug discovery pipelines

    5. Fine Chemical Intermediate in Dye and Pigment Synthesis

    Downstream dye producers apply this intermediate for high-value pyrazole azo dye production, especially for textile and leather coloration. Its structure introduces unique chromophore characteristics, enabling precise hue control and improved color fastness on synthetic and natural fiber substrates.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile colorants
    • REACH Annex XVII Restrictions on Azo Dyes
    • ZDHC Manufacturing Restricted Substances List (MRSL) compliance

    Typical usage ratio

    • 0.10–0.30 mol ratio to diazonium salts in coupling step, determined by targeted chromophore intensity and product cost constraints

    Downstream process integration

    • Undergoes diazo coupling under acid or alkaline conditions as part of pigment assembly
    • Followed by milling, spray-drying, or granulation based on targeted particle size distribution

    Final product types

    • Disperse and reactive azo dyes for synthetic fibers
    • Pigmented granular and powder dyes for fabrics, leather, and paper
    • Printing ink or colorant concentrates
    Free Quote

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