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HS Code |
982195 |
| Name | 2,4-Dichloropyrimidine |
| Cas Number | 3934-20-1 |
| Molecular Formula | C4H2Cl2N2 |
| Molecular Weight | 148.98 |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 55-58°C |
| Boiling Point | 233°C at 760 mmHg |
| Density | 1.43 g/cm3 |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Store in a cool, dry, well-ventilated place, away from light |
| Refractive Index | 1.597 |
| Smiles | C1=CN=C(N=C1Cl)Cl |
As an accredited 2,4-Dichloropyrimidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,4-Dichloropyrimidine is packaged in a 250-gram sealed amber glass bottle with a tamper-evident cap and safety labeling. |
| Shipping | 2,4-Dichloropyrimidine is shipped in tightly sealed containers, typically made of glass or high-density polyethylene, to prevent moisture and contamination. It is classified as hazardous, so shipping complies with relevant regulations, including labeling and documentation. Packages are cushioned and securely packed to minimize breakage or leaks during transportation. |
| Storage | 2,4-Dichloropyrimidine 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. Protect it from moisture and direct sunlight. Clearly label the storage area and ensure access is restricted to trained personnel. Store at recommended temperatures indicated by the supplier or Material Safety Data Sheet (MSDS). |
Applications of 2,4-Dichloropyrimidine in Industrial Manufacturing2,4-Dichloropyrimidine is a key intermediate in multiple chemical manufacturing sectors, delivering essential reactivity for downstream synthesis. We provide direct supply to industrial clients operating under regulated conditions, ensuring purity and process reliability in diverse high-value segments. 1. Pharmaceutical API Synthesis: Oncology and Antiviral IntermediatesThis compound is widely used as a core heterocycle in the synthesis of targeted anti-cancer and antiviral active pharmaceutical ingredients. Pharmaceutical manufacturers introduce it into pyrimidine coupling steps, enabling the construction of kinase inhibitors, nucleoside analogs, and specialty antivirals. The molecule’s dichloro activation allows efficient nucleophilic aromatic substitution, supporting production of intermediates for final API crystallization and purification processes. Industry compliance standards
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2. Crop Protection Actives: Herbicide and Fungicide SynthesisAgrochemical active ingredient producers employ 2,4-dichloropyrimidine for constructing pyrimidine-based herbicides and fungicides. Its reactivity allows efficient functionalization in high-throughput synthesis of novel actives, where site-selective substitution forms key intermediates during multi-step production flows. The compound’s stability enables storage and micro-plant blending, minimizing batch-to-batch deviations in plant protection product manufacturing. Industry compliance standards
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3. Electronic Chemicals: Semiconductor Photoresist and Display Materials2,4-Dichloropyrimidine serves as a synthetic unit in the preparation of advanced organic compounds used in semiconductor photoresists and active-matrix display formulations. Electronic materials manufacturers incorporate it at the molecular design phase to adjust electronic properties. Its dichloro substitution patterns support controlled organic thin-film transistor (OTFT) construction, enabling high-mobility organic semiconductors for flexible devices, OLED displays, and precision photoresist developers. Industry compliance standards
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4. Chemical Intermediates for Dyes and PigmentsSpecialty dye and pigment manufacturers rely on 2,4-dichloropyrimidine for constructing advanced colorants, especially in the synthesis of azo and anthraquinone derivatives. The dichloro structure acts as a robust precursor for functional group modification, supporting the development of water-soluble dyes and lightfast pigments. Manufacturers use controlled substitution reactions to introduce sulfonate, alkylamino, or other groups, tuning absorption profiles for textile, plastic, and ink applications. Industry compliance standards
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