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1,2,4-Triazolylsodium

    • Product Name 1,2,4-Triazolylsodium
    • Alias Sodium 1,2,4-triazolide
    • Einecs 257-582-5
    • 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

    321018

    Cas Number 934-32-7
    Molecular Formula C2H2N3Na
    Molar Mass 91.05 g/mol
    Appearance White to off-white powder
    Solubility In Water Soluble
    Melting Point Decomposes
    Chemical Name 1,2,4-Triazolylsodium
    Ph 1 Solution Neutral to slightly basic
    Storage Conditions Store in a cool, dry place away from moisture
    Synonyms Sodium 1,2,4-triazolate

    As an accredited 1,2,4-Triazolylsodium factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1,2,4-Triazolylsodium is packaged in a 25-gram amber glass bottle with a tight-seal cap and warning labels.
    Shipping 1,2,4-Triazolylsodium should be shipped in tightly sealed containers under an inert atmosphere, such as nitrogen or argon, to prevent moisture absorption and degradation. Package securely to avoid physical damage and label according to hazardous material regulations. Store and transport at cool temperatures, away from incompatible substances and ignition sources.
    Storage 1,2,4-Triazolylsodium should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, due to its sensitivity to moisture and air. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as acids and oxidizers. Store in a designated corrosive/flammable chemicals cabinet if required by local regulations.
    Application of 1,2,4-Triazolylsodium

    Applications of 1,2,4-Triazolylsodium in Industrial Manufacturing

    As a direct manufacturer of 1,2,4-Triazolylsodium, we supply this specialty intermediate to defined sectors where its chemical properties deliver functional advantages. Below, we outline specific industrial application scenarios based on actual downstream usage, covering technical considerations such as compliance adherence, formulation dosing, process step, and the nature of finished products.

    1. Agricultural Fungicide Synthesis

    Leading agrochemical manufacturers use 1,2,4-Triazolylsodium as a key azole ring source in the synthesis of systemic fungicide actives, particularly for triazole-class fungicides that target mildew, rusts, and blight. The compound adds at the hazard-free salt stage, improving solubility for subsequent synthetic transformations in active ingredient production, especially under water-based or mild base conditions. The chemical’s purity and controlled sodium content contribute to batch reproducibility and effectiveness in downstream blending and formulation.

    Industry compliance standards

    • FAO/WHO Specification for Agricultural Pesticides
    • ISO 9001:2015-certified production traceability
    • REACH Annex XVII for triazole derivatives
    • U.S. EPA Active Ingredient Registration (for downstream products)

    Typical usage ratio

    • Employed at 3–8% (w/w) relative to the batch precursor mass; precise dosing depends on targeted synthesis pathway and batch scale optimization, often adjusted to balance yield and purity of the fungicidal end group.

    Downstream process integration

    • Introduced post-ring-opening step, prior to cyclization during triazole core construction
    • Dissolved in water or alcohol as a sodium triazolide generator in intermediate stage reactions
    • Integrated via controlled base-addition under inert atmosphere, monitored by in-line pH sensors for consistent conversion

    Final product types

    • Triazole fungicidal technicals (e.g., tebuconazole, propiconazole intermediates)
    • Wettable powders and suspension concentrate crop protection products
    • Seed-coating formulations for cereals and legumes
    • Premix agricultural sprays containing triazole-based actives

    2. Pharmaceutical Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers sourcing intermediates for certain antifungal and antibacterial APIs select 1,2,4-Triazolylsodium as a versatile nucleophilic agent. It efficiently forms triazole rings under controlled conditions, facilitating stepwise API assembly and reducing impurity formation compared to traditional acid-catalyzed methods. Its traceability and consistent assay enable process chemists to ensure API batch-to-batch reproducibility.

    Industry compliance standards

    • cGMP (ICH Q7) for API manufacturing
    • USP, Ph. Eur., JP reference monograph for triazole-based APIs
    • FDA 21 CFR Part 211 (current Good Manufacturing Practice)
    • EDQM CEP (Certificate of Suitability) route acceptance

    Typical usage ratio

    • Usually added at 1–5 mol% relative to limiting starting material; process R&D may raise or lower within this window to optimize triazole incorporation and minimize unreacted sodium residues.

    Downstream process integration

    • Charged after raw material purification in high-purity, closed-system reactors
    • Reaction under nitrogen or argon at 50–80°C, monitored by in-process HPLC/MS for complete conversion
    • Integrated typically just prior to triazole ring closure or acylation coupling step

    Final product types

    • Pharmaceutical grade antifungal APIs (e.g., fluconazole, itraconazole intermediates)
    • Precursor blocks for beta-lactamase inhibitors
    • Clinical trial material batches using triazole substructures
    • Regulatory-submitted intermediate bulks for further synthesis

    3. Corrosion Inhibitor Additives for Industrial Water Treatment

    In the water treatment industry, 1,2,4-Triazolylsodium enters as a corrosion inhibitor precursor, reacting with metal ions to form protective complexes in closed-circuit cooling water, boiler water, and process water systems. Operators select it for its rapid dissolution, controlled sodium input, and strong adsorption onto ferrous and copper surfaces, thus reducing pitting and scaling under alkaline and mildly acidic conditions.

    Industry compliance standards

    • ASTM D1384 standard practice for corrosion inhibitors
    • NSF/ANSI 60 certification for drinking water system additives (final blend registrations)
    • ISO 14001:2015 for environmental management in production
    • RoHS Directive 2011/65/EU (where applicable to plant output)

    Typical usage ratio

    • Commonly dosed at 0.05–0.5% (w/w) in industrial water treatment concentrate formulations; optimal intake dictated by system volume, water hardness, and ion content.

    Downstream process integration

    • Premixed as a solid or added as a solution directly into blending tanks for multifunctional water treatment additive formulations
    • Dosed at the concentrate preparation phase, prior to liquid packaging or solid granule extrusion
    • Included in QC-monitored batches, supported by ICP analysis for sodium and triazole content

    Final product types

    • Multi-component water treatment blends for industrial cooling towers
    • Pressurized system boiler water corrosion inhibitors
    • Closed loop heating system additive packs
    • Scale and pitting prevention premixes for process plants

    4. Polymer Stabilizer and UV Absorber Intermediates

    Producers of specialty plastics and coatings utilize 1,2,4-Triazolylsodium in the synthesis of polymer stabilizer intermediates and UV absorbers. The compound reacts selectively with aromatic and alkyl halides, enabling production of triazole-based chromophores that extend polymer service life, especially in outdoor exposure. Its high purity supports consistent coloring, transparency, and mechanical properties in final polymer masterbatches and coatings.

    Industry compliance standards

    • EU Regulation (EC) No 1907/2006 (REACH) for polymer additives
    • GB/T 33372 for plastic additives (China)
    • ISO 9001:2015 for production batch QA/QC
    • Applicable FDA 21 CFR Sections for food-contact plastics (when used in downstream compliant masterbatches)

    Typical usage ratio

    • Incorporated at 0.1–2% (w/w) in additive intermediate synthesis, with adjustments for polymer type, UV intensity targets, and required shelf life.

    Downstream process integration

    • Blended with aromatic halides in initial triazole-coupling phase via batch or continuous flow reactors
    • Finished stabilizer intermediates granulated or dissolved before masterbatch compounding
    • Trace impurities removed by liquid-liquid extraction or crystallization prior to final product integration

    Final product types

    • Light-stabilized HDPE, PP, and PVC masterbatches for cable, pipe, and packaging applications
    • UV-absorbing transparent coatings for automotive and architectural uses
    • Plastic stabilizer concentrate granules for industrial and consumer markets
    • Polymer additive dispersions for paint and adhesive formulations

    5. Analytical Reagent and Chromogenic Substrate Manufacturing

    In the analytical chemicals sector, laboratory and industrial reagent producers incorporate 1,2,4-Triazolylsodium in the synthesis of chromogenic triazole derivatives for metal ion detection and enzymatic assays. The compound, supplied with certified assay and trace metal levels, functions as a controlled triazolide generator in colorimetric substrate preparation, thus ensuring reliable color development and test sensitivity across diagnostic reagent lots.

    Industry compliance standards

    • ISO 17025-accredited analytical reagent specification
    • ASTM D3697 for analysis of metal ions in water using organic reagents
    • European Pharmacopoeia general reagents (Ph. Eur. 4.1.1)
    • Analytical Reagent Grade (AR) certification for product release

    Typical usage ratio

    • Formulated at 0.2–1.2% (w/w) in liquid or solid reagent mixes; usage refined based on target analyte concentration detection sensitivity and required visual endpoint range.

    Downstream process integration

    • Added during synthesis of chromogenic triazole derivatives by direct nucleophilic substitution
    • Incorporated under strictly controlled pH and temperature settings to minimize side reactions
    • Final mixtures undergo filtration and, where needed, lyophilization for dry-format kits

    Final product types

    • Chromogenic reagent powder and liquid kits for Cu, Fe, Ni analysis
    • Enzyme assay chromophores for clinical and research labs
    • Water test strips for on-site ion detection
    • Standardized analytical reagents for spectrophotometric and visual endpoint testing
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