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5-Chloro-1,3-Dimethylpyrazole

    • Product Name 5-Chloro-1,3-Dimethylpyrazole
    • Alias 5-chloro-1,3-dimethyl-1H-pyrazole
    • Einecs 694-006-2
    • 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

    749542

    Chemicalname 5-Chloro-1,3-Dimethylpyrazole
    Casnumber 6249-72-9
    Molecularformula C5H7ClN2
    Molecularweight 130.58
    Appearance White to off-white solid
    Meltingpoint 77-80°C
    Purity Typically >97%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles CC1=NN(C)C(Cl)=C1
    Inchikey LVBGSBPVQXLPAP-UHFFFAOYSA-N

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

    Packing & Storage
    Packing The packaging is a sealed amber glass bottle containing 25 grams of 5-Chloro-1,3-Dimethylpyrazole, labeled with safety and chemical information.
    Shipping 5-Chloro-1,3-Dimethylpyrazole is typically shipped in sealed, chemical-resistant containers to prevent leakage or contamination. It should be transported in accordance with local, national, and international regulations for hazardous chemicals, with appropriate documentation, labeling, and safety data sheets included. Store and ship away from incompatible substances and extremes of temperature.
    Storage Store **5-Chloro-1,3-Dimethylpyrazole** in a tightly sealed container, away from light, heat, and sources of ignition. Keep in a cool, dry, and well-ventilated area. Avoid contact with incompatible substances such as strong oxidizers. Label the container properly and ensure it is stored in accordance with safety and chemical hygiene regulations. Use secondary containment to prevent spills or leaks.
    Application of 5-Chloro-1,3-Dimethylpyrazole

    Applications of 5-Chloro-1,3-Dimethylpyrazole in Industrial Manufacturing

    As a direct manufacturer, we supply 5-Chloro-1,3-Dimethylpyrazole into advanced chemical production sectors where consistent reactivity and specification control determine downstream performance. The following industrial application paths reflect real markets served by this intermediate, each requiring distinct formulation expertise and industry compliance.

    1. Agrochemical Synthesis: Herbicide and Fungicide Intermediate

    Downstream crop protection product manufacturers incorporate this raw material as a core building block in the synthesis of specific triazole and pyrazole-based herbicides and fungicides. Our clients implement batch and continuous processes, using this intermediate in selective mono- or multi-step reactions, often by nucleophilic substitution or condensation methods. Usage rates depend on proprietary formulation yields and impurity tolerances, typically set by global agricultural standards. End manufacture relies on direct synthesis within integrated pesticide API process lines. Product purity, residual solvent management, and particle sizing all impact the final stability, shelf-life, and regulatory acceptability of the finished crop control agent.

    Industry compliance standards

    • FAO/WHO Joint Meeting on Pesticide Specifications (JMPS)
    • EU Regulation (EC) No 1107/2009
    • US EPA 40 CFR Part 180 (Pesticide Tolerances)
    • OECD Principles of Good Laboratory Practice (GLP)

    Typical usage ratio

    • Intermediate loading: 0.7–1.2 mol per mol final active ingredient
    • Process adjusted based on downstream impurity profile and target yield
    • Reaction solvent ratios: 8–12% by volume depending on synthesis method
    • Pilot to commercial scale runs often require in-process adjustments within a 5–15% range

    Downstream process integration

    • Introduced at key condensation or substitution step during API pre-synthesis
    • Directly charged into jacketed reactors under nitrogen atmosphere
    • In-line yield control via HPLC to optimize final actives content
    • Feeds slurry or solution into granulation or spray-drying downstream units

    Final product types

    • Triazole-based fungicide technical concentrates
    • Selective herbicide actives for cereals and orchards
    • Emulsifiable concentrate (EC) pesticide formulations
    • Water-dispersible granules (WG) for direct field application

    2. Pharmaceutical Intermediates: Specialty API Synthesis

    Our material serves as a registered intermediate in the multi-step synthesis of select active pharmaceutical ingredients by licensed GMP API producers. Here, each batch follows validated protocols to limit cross-contaminants and meets strict traceability and documentation requirements. Manufacturers demand batch-specific CoA and supply chain transparency since the pyrazole moiety transfers to regulated API structures via controlled C-N or C-C coupling reactions. Process chemists optimize ratios to control impurity generation and maximize coupling efficiency, aligning practices with both regional and global cGMP standards. The compound enters early-to-mid stage synthesis depending on the target molecule, impacting final product purity and API crystallization stages.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia Monograph (where applicable)
    • US FDA 21 CFR Parts 210/211 (cGMP requirements)
    • China Pharmacopoeia (for domestic Chinese API plants)

    Typical usage ratio

    • Process-dependent: 1.0–1.3 molar equivalent per target intermediate
    • Solvent carrier ratio: 10–15% to optimize selectivity in high-throughput reactors
    • Usage tuning based on target API impurity profile limits & in-process analytics
    • Excess controlled within 3–7% to minimize cost of purification

    Downstream process integration

    • Handled within isolated reaction vessels for pre-pharma synthesis steps
    • Fed into N-acylation, alkylation, or heterocycle-building process stages
    • Monitored by real-time FTIR or HPLC for reaction endpoint determination
    • Feeds directly into crystallization or liquid–liquid extraction modules

    Final product types

    • Anti-inflammatory API intermediates
    • Novel CNS small molecules (with pyrazole pharmacophore)
    • Oncology API scaffold compounds
    • Specialty clinical trial material for NCE evaluation

    3. Fine Chemical Synthesis: Catalyst and Ligand Precursor

    Manufacturers of advanced catalysts rely on this raw material as a precursor for constructing custom pyrazole ligands and heterocyclic ligand families. In industrial-scale ligand synthesis, the compound participates in controlled mono- or poly-functionalization steps under anhydrous conditions. This enables precise tailoring of chelating sites and donor atoms that suit downstream transition metal catalyst manufacture. Compliance focuses on raw material traceability, batch reproducibility, and ligand purity—critical for catalyst consistency. High-purity grades undergo additional QC checks to meet customer process qualification for specialty chemical synthesis lines.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH (EC 1907/2006) registration for imported ligands
    • In-house analytical validation (GC, NMR, elemental analysis)
    • Material Safety Data Sheet (MSDS) verification during handling

    Typical usage ratio

    • Dosage: 0.9–1.1 equivalents per metal center, adjusted for ligand design
    • 10–20% batch excess in R&D lots for structural elaboration
    • Plant-scale: matched to catalyst designer’s stoichiometry requirements
    • Final ratio optimized for downstream single-pot synthesis steps

    Downstream process integration

    • Injected during ligand skeleton assembly (usually condensation or cyclization)
    • Precursor for further halogenation or alkylation before metal complexation
    • Integrated into catalyst precursor mixing tanks with stringent temperature and moisture control
    • Feeds into metal–ligand complexation modules for final catalyst building

    Final product types

    • Homogeneous and heterogeneous metal catalysts
    • Engineered coordination complexes for olefin polymerization
    • Custom ligand packages sold for pharmaceutical and materials R&D
    • Initiators for controlled free-radical and ring-opening polymerizations

    4. Polymer Additive Synthesis: UV Stabilizer Precursor

    The chemical enters high-value polymer additive production as a core intermediate in the manufacture of specialized UV absorbers and light stabilizers used in plastics and coatings. Downstream processors use this compound during the assembly of pyrazole derivative stabilizer molecules that inhibit photodegradation and yellowing in polymers exposed to sunlight. Usage ratios align with desired additive concentration in masterbatch or direct compounding feeds. The compound usually undergoes alkylation or functionalization before final additive formation, and is introduced under closed, dry conditions to ensure active site preservation. QC checks on residual chlorine and purity directly impact additive performance in automotive, construction, and packaging plastics.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for additive safety
    • US FDA 21 CFR Parts 177, 178 (for indirect food contact plastics)
    • ISO 9001:2015 for additive production traceability
    • ASTM D5208: Practice for Fluorescent UV-Condensation Exposure of Plastics

    Typical usage ratio

    • Starter intermediate: 1.0 equivalent per stabilizer target molecule
    • Final additive target: 0.2–2.0% w/w depending on polymer and UV exposure level
    • Compound input adjusted for loss during intermediary synthesis and side reaction control
    • Batch processes may employ 10–15% excess to drive complete conversion

    Downstream process integration

    • Mainly charged in early-stage condensation or functionalization reactors
    • Wet or melt phase handling to ensure full incorporation into UV stabilizer core
    • Feeds into downstream granulation or liquid additive blending lines
    • Direct input into masterbatch compounding for plastics extrusion and film manufacture

    Final product types

    • UV stabilizer masterbatches for polyethylene and polypropylene
    • Light stabilizer concentrates for PVC and engineering polymers
    • Anti-yellowing additives for automotive and building materials
    • Coating additives for weather-resistant films and plastics
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