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HS Code |
935538 |
| Product Name | 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide |
| Molecular Formula | C7H8ClNO2 |
| Molecular Weight | 173.6 g/mol |
| Appearance | Solid (expected, usually crystalline) |
| Solubility | Likely soluble in organic solvents |
| Purity | Typically >95% (for research chemicals) |
| Chemical Class | Pyridine N-oxide derivative |
| Smiles | CC1=NC(=C(C=C1OC)Cl)O |
| Inchi | InChI=1S/C7H8ClNO2/c1-5-7(9(10)11)4-6(8)3-12-2/h3-5H,1-2H3 |
| Synonyms | 4-Chloro-3-methoxy-2-methylpyridine 1-oxide |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide, sealed with a tamper-evident screw cap. |
| Shipping | 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide is shipped in tightly sealed containers, compliant with local and international regulations for chemical transport. It must be kept away from moisture, heat, and incompatible substances. Proper hazard labeling and documentation are required. Handle with appropriate safety precautions to ensure safe transit and delivery. |
| Storage | Store 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide in a tightly sealed container in a cool, dry, and well-ventilated area. Keep away from direct sunlight, moisture, heat sources, and incompatible substances such as strong acids and reducing agents. Clearly label the container and ensure it is protected from physical damage. Follow all relevant safety and handling guidelines for storage. |
Applications of 4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide in Industrial Manufacturing4-Chloro-3-Methoxy-2-Methylpyridine N-Oxide serves as a specialized intermediate in various industrial segments. As a manufacturer dedicated to stringent quality and traceability, we supply this material to select sectors where its unique reactivity and compatibility support downstream synthetic and formulation demands. Below we present the principal fields and detailed application settings where this raw material contributes measurable value in regulated and high-purity environments. 1. Pharmaceutical Intermediate SynthesisOur material plays a crucial role in the production of pyridine-based APIs and advanced pharmaceutical intermediates. It offers controlled oxidative potential and a clean impurity profile, allowing for reliable incorporation during multi-step pharmaceutical synthesis projects including heterocyclic building blocks and as precursors in the manufacture of anti-infective and nervous system agents. Consistent batch-to-batch identity and trace element specifications underpin qualification in commercial and clinical trial supply chains. Industry compliance standards
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2. Agrochemical SynthesisThis intermediate is introduced during fine-tuning of pyridine ring systems that serve as core scaffolds in fungicide and herbicide development. Its electron-withdrawing and methoxy substituents enable regioselective transformations essential in building advanced agrochemical actives. All deliveries comply with raw material traceability codes typically required by downstream global agrochemical production partners. Industry compliance standards
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3. Fine Chemical Production for Electronic MaterialsDownstream operations in the electronics industry employ this material for the synthesis of functionalized pyridine derivatives used in photoresist compounds and specialty electronic resins. Its N-oxide structure supports clean electron transfer reactions valuable in the design of intermediates for high-purity semiconductor applications, where strict control of trace metal impurities and reproducibility of material properties is critical in integrated circuit manufacturing. Industry compliance standards
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4. Custom Synthesis for Specialty Dyes and PigmentsThis pyridine N-oxide intermediate is utilized in the preparation of high-performance dyes where electron-rich aromatic rings are required for distinct absorption and stability properties. Custom dye formulators select this material for its capacity to introduce methoxy and chloro substituents into nitrogenous rings during diazotization and oxidative coupling chemistries, producing dyes with improved lightfastness for technical and industrial textiles. Industry compliance standards
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