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1,3-Dimethylpyrazole-5-Carboxylic Acid

    • Product Name 1,3-Dimethylpyrazole-5-Carboxylic Acid
    • Alias 1,3-DMP-5-COOH
    • Einecs 680-885-4
    • 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

    112355

    Chemical Name 1,3-Dimethylpyrazole-5-Carboxylic Acid
    Molecular Formula C6H8N2O2
    Molecular Weight 140.14 g/mol
    Cas Number 7251-97-8
    Appearance White to off-white solid
    Melting Point 175-180°C
    Solubility Soluble in water and polar organic solvents
    Purity Typically ≥98%
    Smiles CC1=NN(C(=C1)C(=O)O)C
    Inchi InChI=1S/C6H8N2O2/c1-4-5(6(9)10)8(2)7-3-4/h3H,1-2H3,(H,9,10)
    Storage Conditions Store at room temperature, keep container tightly closed

    As an accredited 1,3-Dimethylpyrazole-5-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging consists of a 25-gram amber glass bottle sealed with a screw cap, labeled with the chemical name and hazard information.
    Shipping 1,3-Dimethylpyrazole-5-carboxylic acid is typically shipped in sealed containers, protected from moisture and light. Containers should be clearly labeled and handled according to standard chemical safety protocols. During transport, ensure stability and avoid extreme temperatures. Comply with local and international regulations for shipping chemicals, including necessary documentation.
    Storage 1,3-Dimethylpyrazole-5-carboxylic acid should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect the chemical from moisture and direct sunlight. Follow standard safety precautions, including labeling and using secondary containment to prevent accidental spills or exposure. Store at room temperature unless otherwise specified.
    Application of 1,3-Dimethylpyrazole-5-Carboxylic Acid

    Applications of 1,3-Dimethylpyrazole-5-Carboxylic Acid in Industrial Manufacturing

    1,3-Dimethylpyrazole-5-Carboxylic Acid supports advanced synthesis and formulation in modern chemical manufacturing. As the original producer, we supply this intermediate for tightly regulated, high-value industrial sectors. The following scenarios detail real downstream uses, each with specific compliance regimes, technical processing data, and finished product categories.

    1. Agrochemical Synthesis: Selective Herbicide Intermediate

    This molecule frequently enters the synthesis pathway for selective herbicides, especially triazole-type and pyrazole-derived active ingredients. Downstream formulators rely on its reactivity for building heterocyclic rings essential to modern crop protection compounds. The material must comply with strict agricultural regulatory frameworks, with technical control over active content and impurity profiles.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 (EU Plant Protection Products)
    • US EPA 40 CFR Part 158 (Pesticide Data Requirements)
    • ISO 17025 lab accreditation for QC testing
    • Chinese GB 2763 residue limits for agrochemical formulations

    Typical usage ratio

    • 5–15% w/w in technical intermediate synthesis batches
    • Precise ratio depends on targeted structure activity relationship and impurity threshold

    Downstream process integration

    • Charged during cyclization and condensation stages
    • Serves as a key N-heterocycle precursor prior to esterification or amide formation
    • Removal of process byproducts under controlled temperatures and vacuum
    • Monitored via HPLC and GC for purity >99.5%

    Final product types

    • Active ingredients for broadleaf weed control
    • Formulated liquid and SC (suspension concentrate) herbicides
    • Co-formulants for controlled-release crop solutions
    • Low-toxicity herbicidal blends for specialty crops

    2. Pharmaceutical Active Pharmaceutical Ingredient (API) Intermediate

    Major pharmaceutical manufacturers use this compound as a building block for the synthesis of specific antidiabetic, antiviral, and anti-inflammatory APIs containing pyrazole frameworks. Access to high-purity material supports validated cGMP synthesis. It enables efficient ring closures and functional group modifications during multi-step production.

    Industry compliance standards

    • cGMP as per ICH Q7 guidelines
    • USP (United States Pharmacopeia) general chapter 232/233 for elemental impurities
    • EDQM CEP (Certificate of Suitability) for EU market entry
    • FDA DMF registration for import into the US

    Typical usage ratio

    • 3–10 mol% relative to final API batch size
    • Ratio determined by step yield, risk of overreaction, and downstream conversion factor

    Downstream process integration

    • Enters amidation or acylation step following initial pyrazole scaffold formation
    • Solubilized under inert atmosphere using polar aprotic solvents
    • Removal of residual acids by preparative column chromatography
    • Strict control of residual solvent and heavy metal traces in intermediate

    Final product types

    • Type II diabetes therapeutics (e.g., DPP-4 inhibitors with pyrazole moieties)
    • Novel antiviral drug candidates with fused heterocyclic cores
    • Non-steroidal anti-inflammatory drugs (NSAIDs) using pyrazole linkers
    • Clinical trial standard reference APIs

    3. Specialty Polymer Modification: Polymer Chain Extenders

    Advanced polyurethanes and engineered resins utilize this carboxylic acid as a functional chain modifier. It participates in controlled polymerization to introduce specific functional groups, improving mechanical and thermal properties for specialty end uses. Downstream manufacturing integrates this material at critical feed points to achieve homogeneity and precise molecular weight distribution.

    Industry compliance standards

    • REACH Registration, Evaluation, Authorization, and Restriction of Chemicals (Annex XVII restrictions on additives)
    • EN ISO 9001:2015 for process and QC management
    • ASTM D2578 (polymer surface energy testing)
    • RoHS Directive (if used in E&E resins)

    Typical usage ratio

    • 0.2–2.0% by polymer mass for chain extension or end-group functionality
    • Ratio adjusted based on final desired soft/hard segment characteristics and cure speed

    Downstream process integration

    • Added to pre-polymer reactor during end-capping and extension phases
    • Participates in melt mixing under nitrogen at 80–120°C
    • Monitored by GPC for molecular weight changes and FTIR for functional group incorporation
    • Process includes vacuum degassing to remove unreacted acid and volatiles

    Final product types

    • Elastomeric polyurethane belts and gaskets
    • Coatings for automotive and aerospace applications
    • Reactive hot-melt adhesives
    • Flame-retardant engineering plastics

    4. Fine Chemical Synthesis: Heterocyclic Building Block for Electronic Chemicals

    Manufacturers of electronic grade chemicals use this raw material to produce intermediates tailored for photoresists and specialty electronic substrates. The functionalized pyrazole ring enables unique optoelectronic properties after targeted derivatization. Downstream processes demand microtraced impurity limits to prevent contamination in high-value electronic applications.

    Industry compliance standards

    • SEMI C92 (High-purity chemical requirements—electronics manufacturing)
    • ISO 14644 (Cleanroom process standards for microelectronics)
    • IEC 62474 (Material declaration for electronic components—hazardous substance tracking)
    • Japanese Industrial Standards (JIS K 5600-1-7 for chemical analysis of coatings and resists)

    Typical usage ratio

    • 0.01–0.5% in electronic photoresist precursor synthesis
    • Usage tailored to targeted electronic function, impurity risk, and end-use device specification

    Downstream process integration

    • Dosed to coupling reaction vessels via automated microfeeders for reproducible batch results
    • Strictly filtered through submicron filters to ensure particulate-free solutions
    • Further purified by continuous crystallization and zone refining steps
    • Purity validated by ICP-MS and trace anion/cation analysis

    Final product types

    • Photoresist chemicals for semiconductor lithography
    • Anti-static coatings for display screens
    • Functional monomers for OLED and sensor substrates
    • Chemical-mechanical planarization (CMP) polishing components
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