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Structure of 51114-94-4
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This triphenylphosphonium derivative delivers a targeted carboxyethyl group for mitochondrial delivery, combining lipophilic stability with enhanced aqueous solubility. The bromide counterion ensures high reactivity in conjugation workflows. Designed for bioconjugation and redox-active probe synthesis, it enables efficient cellular targeting through established phosphonium transport mechanisms.
(2-Carboxyethyl)triphenylphosphonium bromide serves as a versatile phosphonium salt for the synthesis of Wittig-type reagents and functionalized alkenes. Its carboxylic acid group enables conjugation to biomolecules or incorporation into polymer backbones, while the triphenylphosphonium moiety facilitates efficient ylide formation under mild conditions. The compound exhibits good bench stability and is compatible with standard organic reaction protocols, offering reliable access to α,β-unsaturated systems in medicinal chemistry and materials science applications.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: