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Sodium Cyanate

    • Product Name Sodium Cyanate
    • Alias sodium-cyanate
    • Einecs 209-730-1
    • 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

    422902

    Chemical Name Sodium Cyanate
    Chemical Formula NaOCN
    Molar Mass 65.01 g/mol
    Appearance White crystalline solid
    Melting Point 550 °C
    Solubility In Water Very soluble
    Cas Number 917-61-3
    Density 2.02 g/cm³
    Odor Odorless
    Ph Aqueous Solution Approximately 10 (alkaline)
    Boiling Point Decomposes before boiling
    Synonyms Cyanic acid sodium salt

    As an accredited Sodium Cyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sodium Cyanate, 500g, packaged in a tightly sealed, corrosion-resistant HDPE bottle with clear hazard labeling and tamper-evident cap.
    Shipping Sodium cyanate should be shipped in tightly sealed containers, clearly labeled, and protected from moisture and incompatible substances. It must be handled as a hazardous material, following regulatory requirements. Store and transport in a cool, dry, and well-ventilated area, avoiding exposure to acids or reducing agents to prevent hazardous reactions.
    Storage Sodium cyanate should be stored in a tightly sealed container in a cool, dry, well-ventilated area, away from heat, moisture, and incompatible substances such as acids and oxidizers. It should be kept away from food and drink, and storage areas must be labeled clearly. Protective equipment is recommended when handling, as sodium cyanate is toxic and may release hazardous fumes.
    Application of Sodium Cyanate

    Applications of Sodium Cyanate in Industrial Manufacturing

    Sodium cyanate serves critical roles in multiple industrial processes due to its unique chemical properties. Our manufacturing expertise ensures consistent quality, enabling reliable integration into downstream operations across various sectors. Below, we cover key industrial applications, with detailed insights into compliance, usage ratios, workflow integration, and end product outputs as observed in current large-scale production environments.

    1. Heat Treatment of Steel (Case Hardening and Nitriding)

    Sodium cyanate is a principal nitrogen donor in heat treatment baths for ferritic nitrocarburizing operations, significantly improving steel surface hardness, wear resistance, and fatigue strength. It decomposes at elevated temperatures to yield active nitrogen and carbon, diffusing into the surface of steel components. This compound is most widely adopted in salt bath nitrocarburizing, such as the Tufftride and Tenifer processes. The chemical ensures precise control of case depth and uniformity, vital for gear, shaft, and automotive part performance.

    Industry compliance standards

    • ISO 15787:2022 (Steels — Heat treatment — Nitrocarburizing)
    • SAE AMS 2759/12 (Heat treatment of steel parts, nitriding and nitrocarburizing)
    • REACH (Regulation EC No 1907/2006) compliance for use and disposal
    • OSHA 1910.1200 (Hazard Communication Standard)

    Typical usage ratio

    • 15–40% by weight in salt bath formulations, often blended with sodium carbonate and potassium carbonate.
    • Exact ratio depends on steel alloy, bath temperature (up to 580°C), and targeted case depth.

    Downstream process integration

    • Direct addition to heated salt bath following pre-melt of base carbonate mixture.
    • Active control of bath chemistry through titration and replenishment during batch runs.
    • Post-treatment via quenching and optional oxidation.

    Final product types

    • Nitrocarburized engine pistons and piston rings
    • Gears, camshafts, crankshafts
    • Bearing surfaces and hydraulic parts
    • Tool steels for dies and punches

    2. Production of Pharmaceutical Intermediates (Carbamate and Urea Derivatives)

    This material functions as a high-reactivity carbamoylating agent in the synthesis of key intermediates for pharmaceutical active ingredients. It reacts with primary amines, hydrazines, or hydroxyl compounds to form N-carbamoyl or O-carbamoyl derivatives under controlled stoichiometry. These intermediates become precursors for analgesics, non-steroidal anti-inflammatory agents, and other specialty drugs. Our production history supports precise grade control and documentation for regulated customers.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)
    • USP and EP monograph testing for intermediates
    • REACH registration for chemical handling in synthetic use

    Typical usage ratio

    • Molar ratio calculated based on substrate, typically 1.05–1.10:1 (cyanate:amine) to ensure full conversion with minimized side product formation.
    • Process parameters—solvent volume, temperature, and base—tailored to individual synthesis.

    Downstream process integration

    • Charged to reactor after amine or alcohol feed under inert atmosphere.
    • Monitored addition to control exotherm and by-product formation.
    • Post-reaction workup via extraction and crystallization of the intermediate.

    Final product types

    • Carbamate intermediates for antiepileptic and anxiolytic agents
    • Urea and semicarbazide pharmaceutical raw materials
    • Pesticide precursors used in crop protection formulations
    • Active pharmaceutical ingredient sidechains

    3. Gold and Silver Mining (Ore Processing and Recovery)

    Within precious metals hydrometallurgy, sodium cyanate is added to leaching circuits to enhance gold and silver extraction from refractory ores, either by oxidizing sulfur species or by in situ generation of cyanide ions under alkaline conditions. It serves as a cyanide substitute or reagent booster, lowering consumption of sodium cyanide and improving yield from sulfide and carbonaceous ores. Operators choose the dosage based on ore composition and desired metal recovery profile.

    Industry compliance standards

    • International Cyanide Management Code (ICMC)
    • EPA 40 CFR Part 440 (Ore Mining and Dressing Point Source Category)
    • AU/NZS 4801:2001 (Occupational Health and Safety Management Systems)
    • Local environmental discharge permits

    Typical usage ratio

    • 0.2–1.5 kg per tonne of ore, adjusted according to ore mineralization and pre-existing cyanide residue levels.
    • Operators optimize addition to balance cost, yield, and environmental emissions.

    Downstream process integration

    • Pulsed or continuous dosing to grinding or leaching tanks.
    • Process monitoring for cyanate and cyanide concentrations on-line.
    • Used in pre-leach conditioning or main leach step.

    Final product types

    • Dore bullion bars of gold and silver
    • High-purity gold/silver powders for electronic, jewelry, and investment sectors
    • Metallic precipitates for further refining
    • Residue products for tailings management

    4. Dye and Pigment Production (Isocyanate Chemistry)

    Sodium cyanate enters specialty chemical synthesis for diazotization and isocyanate-based pigment manufacture, especially in production of azo dyes and triphenylmethane colorants. Its strong carbamoylating nature supports controlled insertion of functional groups into aromatic rings, enabling complex chromophore architectures and reactive dye intermediates. Manufacturers precisely meter cyanate addition to achieve targeted shade, intensity, and lightfastness in textile and ink industries.

    Industry compliance standards

    • OEKO-TEX Standard 100 textile restrictions
    • EN 71-3 (Safety of Toys – Migration of certain elements)
    • REACH Annex XVII Substances of Very High Concern (SVHC)
    • ISO 9001:2015 for chemical quality assurance

    Typical usage ratio

    • Variable from 1–8% by molar ratio in dye intermediate synthesis steps.
    • Process chemists adjust based on precursor molecular weight and desired chromophore substitution level.

    Downstream process integration

    • Introduced mid-stream after initial diazotization, often in stirred reactors under temperature control.
    • Real-time color strength and purity analysis guides incremental dosing.
    • Purification via crystallization, filtration, and drying.

    Final product types

    • Reactive azo dyes for cotton, wool, and silk
    • Triphenylmethane pigments for plastic and ink applications
    • Specialty pigments for coatings, plastics, and digital printing
    • Reactive dye intermediates for export formulation

    5. Organic Synthesis of Heterocyclic Compounds

    Sodium cyanate provides a critical building block for synthesizing heterocyclic compounds such as s-triazines, oxadiazoles, and hydantoins. These structures serve as performance enhancers, crosslinkers, stabilizers, and UV absorbers for plastics and rubbers. Its reliable reactivity with ylidene-carbonyl compounds, aldehydes, and hydrazones supports process yields and product consistency, making it a preferred choice in advanced material and specialty chemical synthesis workflows.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System (for specialty chemical manufacturing)
    • GHS (Globally Harmonized System of Classification and Labelling of Chemicals)
    • REACH registration for specialty molecule synthesis
    • SDS (Safety Data Sheet) requirements under GHS for workplace safety

    Typical usage ratio

    • Stoichiometric quantities based on target heterocycle, typically 1:1 or slightly excess (1.05–1.2 equivalents) to ensure full conversion.
    • Fine-tuning during scale-up based on batch size and impurity profile.

    Downstream process integration

    • Added to main reaction vessel after base or catalytic initiator.
    • Strict pH and temperature monitoring supports reproducible yields and minimized decomposition.
    • Downstream purification includes column chromatography and distillation.

    Final product types

    • UV absorbers for polycarbonate and polyester plastics
    • Stabilizers for polyolefin and PVC resins
    • Pharmaceutical and agrochemical heterocycles
    • Crosslinkers in specialty polymers and adhesives

    6. Modification of Natural and Synthetic Polymers

    The use of sodium cyanate extends to the controlled modification of cellulosic materials, polyvinyl alcohol, and polyacrylamide, introducing urea or carbamoyl functionalities for improved solubility, film strength, or dye affinity. The agent can be applied for cold- or hot-stage reaction with fiber or film substrates, followed by downstream neutralization and washing steps. These modifications advance performance in filtration media, adhesives, paper, and nonwoven textiles.

    Industry compliance standards

    • ISO 1833 (Textiles — Quantitative chemical analysis)
    • FDA 21 CFR 177.1200 (Cellophane for food contact, if intended for such use)
    • OEKO-TEX Standard 100 for dyeable textiles
    • REACH Annex XIV/Annex XVII obligations

    Typical usage ratio

    • Between 1–10% by weight of polymer for surface treatment or reaction, optimized for specific property modification.
    • Dosage depends on required carbamoylation degree and molecular weight of polymer substrate.

    Downstream process integration

    • Dissolved in aqueous media for dipping or spraying on polymeric substrate.
    • Thermal activation or pH adjustment triggers carbamoyl group formation.
    • Subsequent neutralization and drying in continuous or batch format.

    Final product types

    • Cationically-modified cellulose for paper and filter media
    • Hydrophilic nonwovens with enhanced binding sites
    • Textiles with specialty dye uptake properties
    • Crosslinked adhesives and specialty coatings
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