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Red Sun’s 2,3,5-Trichloropyridine (CAS No. 16063-70-0, Molecular Formula: C₅H₂Cl₃N) is a high-purity chemical intermediate widely recognized in the fields of pharmaceutical synthesis, agrochemical production, and life sciences research. As a crucial building block in the fine chemical industry, it delivers reliable quality and consistency, enabling manufacturers to develop advanced formulations and downstream compounds. Unlike herbicides applied directly in agricultural settings, 2,3,5-Trichloropyridine functions as a key precursor, ensuring precision and efficiency in multi-step synthesis pathways.
Typical applications include:
Herbicide synthesis: Essential for producing active ingredients such as oxyfluorfen, known for its broad-spectrum weed control in crops.
Agrochemical intermediates: Supports the synthesis of advanced compounds like 2,3-difluoro-5-chloropyridine, commonly used in the preparation of quizalofop-based herbicides.
Pharmaceutical and biochemical research: Serves as a core raw material in developing novel organic molecules for life science studies, ensuring high stability and reproducibility in experimental processes.
With Red Sun’s expertise in fine chemical manufacturing, 2,3,5-Trichloropyridine is produced under strict quality control, meeting the demands of global markets for high-performance intermediates in agriculture, healthcare, and biotechnology.
2,3,5-Trichloropyridine reacts with alkali metal hydroxides to produce 3,5-dichloro-2-pyridinol. This intermediate is then used to synthesize the herbicide oxyfluorfen for broad-spectrum weed control in agriculture.
The compound undergoes fluorination to form 2,3-difluoro-5-chloropyridine. This substance is a key raw material for manufacturing quizalofop-based herbicides applied in crop protection.
It is used in microemulsion electrokinetic chromatography to study separation and migration behaviors. Researchers rely on this compound for consistent performance in life science experiments.
As a chemical building block, it supports the synthesis of pyridine derivatives including 2-chloropyridine and 2-aminopyridine, enabling further production in industrial chemical processes.
Red Sun supplies 2,3,5-Trichloropyridine with purity above 98%. This meets both research and industrial production requirements. Consistent quality ensures predictable performance in chemical synthesis.
The product supports multiple reaction pathways such as Suzuki coupling and fluorination. These reactions enable the production of a wide range of agrochemical intermediates for downstream applications.
The synthesis process follows green chemistry principles. It reduces emissions and minimizes waste, supporting safer handling and lower environmental impact during production.
Red Sun leverages its pyridine-based supply chain to secure raw materials and core technologies. This integration ensures steady product availability and reliable delivery to global markets.
Intermediate Production
Red Sun produces 2,3,5-Trichloropyridine as a key intermediate for herbicide synthesis, including oxyfluorfen and quizalofop derivatives.
Research Support
The compound is supplied for laboratory use in pharmaceuticals, agrochemicals, and life science studies.
Industrial Integration
Facilities link raw material supply and downstream processing, ensuring stable production capacity.
Quality Management
Operations follow standardized testing and monitoring to maintain consistent product specifications.
Environmental Practices
Manufacturing applies green chemistry principles to reduce emissions and waste.
The product carries the Xi hazard symbol and is classified under risk codes 52/53-36/37/38. It is labeled as an irritant under hazard notes.
Follow safety codes 61-37/39-26. Use protective gloves, goggles, and clothing. Avoid direct skin and eye contact.
Classified under UN2811 with packing group PG3. Transport according to international hazardous material standards.
Registered under WGK Germany class 2. Handle and dispose of materials following environmental regulations.
Listed under RTECS number UU0525000. Refer to toxicology references for exposure limits and medical guidance.
