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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 | 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. |
Applications of 1,2,4-Triazolylsodium in Industrial ManufacturingAs 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 SynthesisLeading 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
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2. Pharmaceutical Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical 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
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3. Corrosion Inhibitor Additives for Industrial Water TreatmentIn 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
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4. Polymer Stabilizer and UV Absorber IntermediatesProducers 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
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5. Analytical Reagent and Chromogenic Substrate ManufacturingIn 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
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