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Structure of 18364-71-1
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4-((Dimethylamino)methyl)benzoic acid features a para-substituted benzene ring bearing a carboxylic acid and a dimethylaminomethyl group, combining strong electron-donating character with enhanced solubility. This dual functionality enables efficient coupling in peptide synthesis and facilitates conjugation strategies requiring both nucleophilic and electrophilic handles. The molecule exhibits robust stability under standard bench conditions and integrates seamlessly into bioconjugation workflows.
4-((Dimethylamino)methyl)benzoic acid serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient access to bioactive heterocycles via standard functional group transformations. The ortho-directed amidation and carboxylic acid reactivity facilitate conjugation with amines, peptides, and nucleophiles under mild conditions. Bench-stable and amenable to purification by recrystallization or chromatography, it functions effectively in solid-phase and solution-phase workflows.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H318
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P363-P405-P501
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Lot numbers can be found on the outside label of a product: