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HS Code |
399390 |
| Cas Number | 1722-12-5 |
| Iupac Name | 2-chloropyrimidine |
| Molecular Formula | C4H3ClN2 |
| Molecular Weight | 114.54 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.26 g/cm³ |
| Melting Point | -21 °C |
| Boiling Point | 192-194 °C |
| Solubility In Water | Slightly soluble |
| Flash Point | 77 °C |
| Synonyms | Pyrimidine, 2-chloro- |
| Smiles | C1=CN=C(N=C1)Cl |
As an accredited 2-Chloropyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Chloropyrimidine, 99%, 100g: Supplied in a sealed amber glass bottle with a tamper-evident cap and detailed safety labeling. |
| Shipping | 2-Chloropyrimidine is shipped in secure, tightly sealed containers compatible with the chemical's properties, often made of glass or HDPE. Packages are clearly labeled with hazard warnings and comply with international and local regulations for hazardous materials. Shipments are handled by certified carriers specializing in chemical transport, ensuring safe and compliant delivery. |
| Storage | 2-Chloropyrimidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. It should be kept away from moisture and direct sunlight. Use proper chemical safety labeling, and ensure storage in accordance with local regulations for hazardous chemicals. |
Applications of 2-Chloropyrimidine in Industrial Manufacturing2-Chloropyrimidine serves as a fundamental heterocyclic intermediate across varied industrial manufacturing fields. Our direct production supports consistent supply and technical transparency for process integration in pharmaceuticals, agrochemicals, specialty dyes, and advanced material synthesis. 1. Pharmaceutical Active Ingredient SynthesisManufacturers rely on 2-chloropyrimidine for constructing the pyrimidine core in several pharmaceutical actives, notably anti-viral compounds and kinase inhibitors. The material enters as a halogenated building block for nucleophilic aromatic substitution reactions, ensuring high selectivity in downstream syntheses. Used in both batch and flow processes, it serves as a critical intermediate, especially in APIs requiring stringent impurity control and full traceability for regulatory audits. Product lot consistency is key during chloropyrimidine amination and further ring substitution steps before final API crystallization and formulation. Industry compliance standards
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2. Agrochemical Active Ingredient SynthesisLeading agrochemical formulators employ 2-chloropyrimidine for assembling highly specific herbicide and fungicide molecules. Its high reactivity with nucleophilic species enables streamlined construction of active cores for crop protection agents. Manufacturers control trace halide and moisture during integration to avoid catalyst poisoning and undesired side products. Material flow directly feeds alkylation or arylation steps required for active ingredient assembly before formulation into various dosage forms such as granules and emulsifiable concentrates. Industry compliance standards
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3. Dye and Pigment Intermediate for Specialty ColorantsManufacturers in specialty dye and pigment production incorporate 2-chloropyrimidine as a coupling agent to introduce nitrogen-containing heterocycles into chromophore frameworks. Its order and purity must meet analytical specifications for minimal color shifts and stable tinctorial properties. The intermediate is added at the core ring-building stage, allowing downstream azo or anthraquinone dye functionalization. Integrated in both powder and dispersive dye lines, it supports tailored pigment creation for advanced textile and plastics coloration. Industry compliance standards
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4. Organic Electronic and Advanced Material SynthesisAdvanced materials manufacturers employ 2-chloropyrimidine as a versatile precursor for constructing electron-rich or electron-deficient scaffolds in semiconducting polymers and specialty monomers. Material purity directly affects charge transport and dielectric properties in final device applications. The chemical serves in cross-coupling or ring substitution steps during the synthesis of functionalized conjugated systems. Process parameters focus on achieving high conversion and minimal trace impurities to maintain device-grade performance in organic light-emitting diodes (OLEDs), photovoltaics, and specialty sensor coatings. Industry compliance standards
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