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*For research and further manufacturing use only, not for direct human use.
Structure of 575-89-3
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This chlorinated phenoxyacetic acid features a trichlorophenyl ring system that confers enhanced lipophilicity and metabolic stability. The carboxylic acid group enables direct conjugation or salt formation, facilitating integration into agrochemical formulations. Designed for robust environmental persistence and plant growth regulation, it serves as a key intermediate in herbicide synthesis under standard bench conditions.
2-(2,4,6-Trichlorophenoxy)acetic acid serves as a well-established auxin-type herbicide scaffold, enabling efficient synthesis of phenoxyalkanoic acid derivatives via standard esterification and amidation protocols. Its trichlorophenoxy group provides enhanced lipophilicity and metabolic stability, facilitating use in agrochemical development. The compound exhibits bench-stable handling, tolerates diverse functional groups, and functions reliably in coupling reactions for targeted pesticide and crop protection research.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H319
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Precautionary Statements : P264-P270-P280-P301+P310-P305+P351+P338-P330-P337+P313-P501
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Lot numbers can be found on the outside label of a product: