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Structure of 93-05-0
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The reaction of chlorine and N,N-diethyl-p-phenylenediamine for sensitive square-wave voltammetric detection of chlorine has been studied.N,N-Diethyl-p-phenylenediamine has been employed as a reference probe to investigate rapid chlorination rate constants by a stopped-flow spectrophotometric competition kinetics method.
N1,N1-Diethylbenzene-1,4-diamine serves as a versatile bifunctional building block in synthetic organic chemistry, enabling the construction of heterocyclic scaffolds and conjugated systems. Its electron-rich aromatic core and amine functionality offer robust reactivity in coupling reactions, condensation processes, and polymer synthesis. The diethyl substitution enhances solubility and reduces basicity compared to unsubstituted analogs, improving handling and purification. This compound functions reliably in multi-step syntheses requiring stable, bench-accessible diamines with predictable reactivity profiles.
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GHS Pictogram :
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GHS No : GHS05,GHS06
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Signal Word : Danger
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UN#: 2922
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Class : 8 (6.1)
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Packing Group : Ⅱ
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Hazard Statements : H301-H314
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Precautionary Statements : P260-P264-P270-P280-P301+P330+P331-P304+P340-P330-P363-P405-P501
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Lot numbers can be found on the outside label of a product: