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HS Code |
786973 |
| Chemical Name | 2-Nitrophenyl Selenocyanate |
| Cas Number | 27140-12-3 |
| Molecular Formula | C7H4N2O2Se |
| Molar Mass | 241.09 g/mol |
| Appearance | Yellow to orange solid |
| Melting Point | 94-98°C |
| Solubility | Slightly soluble in common organic solvents |
| Purity | Typically ≥98% |
| Storage Temperature | Store below 30°C, protected from light and moisture |
| Synonyms | o-Nitrophenyl selenocyanate |
| Smiles | C1=CC=C(C(=C1)[N+](=O)[O-])[Se]C#N |
| Inchi | InChI=1S/C7H4N2O2Se/c8-5-13-6-3-1-2-4-7(6)9(10)11/h1-4H |
As an accredited 2-Nitrophenyl Selenocyanate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, sealed cap, hazard labels, product name and CAS displayed, contains 5 grams of 2-nitrophenyl selenocyanate. |
| Shipping | 2-Nitrophenyl Selenocyanate is shipped in tightly sealed containers, protected from light and moisture. Transport requires compliant hazardous materials packaging and labeling. The substance should be stored at room temperature, away from incompatible materials. Shipping follows relevant international and local regulations for handling toxic and potentially harmful chemicals. |
| Storage | 2-Nitrophenyl Selenocyanate should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight. Keep it away from sources of ignition, moisture, and incompatible materials like strong oxidizers. Proper labeling and secondary containment are advised to prevent accidental exposure. Handle under a fume hood and use appropriate personal protective equipment. |
Applications of 2-Nitrophenyl Selenocyanate in Industrial Manufacturing2-Nitrophenyl Selenocyanate serves as a specialized reagent and intermediate in several advanced chemical manufacturing processes. Our direct supply supports high-purity needs for pharmaceutical, agrochemical, and specialized materials producers. Below, we outline representative downstream applications in real industrial sectors, focusing on application-specific compliance, technical formulation, and end-use integration. 1. Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers use this compound in constructing organoselenium-containing APIs, especially in the synthesis of novel anti-tumor, anti-inflammatory, and anti-infective agents. Its role as a selenium donor facilitates the preparation of selenoethers, selenoamides, and functionalized small molecules. Process engineers select batch or continuous synthesis routes depending on the target molecule and scale, applying strict in-process controls to ensure purity and minimize residual selenium. Handling protocols and dosing are adapted to comply with cGMP and pharmacopoeial monographs for each finished drug. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingProducers of crop-protection chemicals employ this reagent for the selenocyanation of aromatic and heterocyclic cores in the research and development of selective fungicides and insecticides. The compound's reactivity under controlled conditions supports targeted modification of precursor molecules, allowing for tunable performance characteristics and environmental behavior. In all applications, manufacturers comply with international pesticide ingredient guidelines and restrict batch impurity profiles according to downstream registration requirements. Industry compliance standards
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3. Custom Organic Material ProductionSpecialty material manufacturers incorporate this chemical as a selective selenium donating agent to modify organic electronic and optical materials. Precisely controlled addition enables the creation of conjugated polymers and low-molecular-weight compounds exhibiting enhanced conductivity, photostability, or charge transport. Process developers employ this step to structure-morphology relationships relevant for advanced device prototyping, adhering to strict in-house and market standards. Industry compliance standards
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4. Analytical Reagent FormulationLaboratory and specialty reagent producers formulate analytical kits using this compound for selenium determination, aryl-selenocyanate derivatization strategies, and mechanistic studies in academic and industrial research. Its selective reactivity allows researchers to derivatize specific functional groups, facilitating high-sensitivity quantitation and mechanistic tracking by chromatographic or spectroscopic methods. Quality-control teams rigorously test each batch to ensure low residual impurities and conformity to research-grade specifications. Industry compliance standards
Typical usage ratio
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