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Structure of 171670-23-8
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Methyl 6-(aminomethyl)picolinate hydrochloride features a pyridine ring bearing both methyl ester and aminomethyl substituents, delivering a bifunctional handle for conjugation. The protonated amine enhances solubility in aqueous media while maintaining stability under standard bench conditions. This salt form facilitates efficient incorporation into peptide and small-molecule scaffolds via amide coupling or alkylation.
Methyl 6-(aminomethyl)picolinate hydrochloride serves as a versatile building block for medicinal chemistry, enabling efficient access to bioactive heterocycles. The amine functionality facilitates conjugation and derivatization, while the methyl ester supports selective transformations. Its bench-stable hydrochloride salt enhances handling and solubility in aqueous-organic media, making it well-suited for multi-step synthesis and process development workflows.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: