114254-48-7 Usage
Uses
Used in Laboratory Research:
N1,N1-Bis(4-amino-phenyl)benzene-1,4-diamine trihydrochloride is used as a reagent for the determination of hydrogen peroxide and glucose, playing a crucial role in the accurate measurement of these substances in various experiments.
Used in Analytical Chemistry:
In the field of analytical chemistry, N1,N1-Bis(4-amino-phenyl)benzene-1,4-diamine trihydrochloride is utilized for the spectrophotometric determination of cerium and uranium. Its reducing capabilities are essential for the colorimetric assays that facilitate the detection and quantification of these elements.
Used in Chemical Analysis:
N1,N1-Bis(4-amino-phenyl)benzene-1,4-diamine trihydrochloride contributes to the field of chemical analysis by enabling the precise identification and measurement of specific compounds, thereby supporting the advancement of scientific research and understanding of chemical reactions and processes.
Check Digit Verification of cas no
The CAS Registry Mumber 114254-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,2,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114254-48:
(8*1)+(7*1)+(6*4)+(5*2)+(4*5)+(3*4)+(2*4)+(1*8)=97
97 % 10 = 7
So 114254-48-7 is a valid CAS Registry Number.
114254-48-7Relevant academic research and scientific papers
Zhu, Weihong,Xu, Yisheng,Zhang, Yan,Shen, Jianping,Tian, He
, p. 1362 - 1367 (2005)
A series of star-shaped naphthalimide derivatives (TPA-NP) were synthesized with a triphenylamine (TPA) core and chromophores at the rim. Their steady-state absorption, fluorescence, and transient fluorescence spectra were investigated, indicative of severely fluorescent quenching with regard to the corresponding 1,8-naphthalimide (NP) parent chromophores. Excitation into either the triphenylamine or naphthalimide absorption bands results in the occurrence of singlet energy transfer and photoinduced electron transfer (PIET) effectively. Single photon-counting experiments show a fast charge separation and a thermally activated back reaction. As a consequence, the fluorescent lifetime of the naphthalimide moiety in the system of TPA-NP is reduced by more than an order of magnitude, which mainly arises from the intramolecular PIET process of TPA and naphthalimide. The kinetics and PIET mechanism involving TPA-NP were elucidated.
