328010-96-4 Usage
Type of compound
Trisubstituted amine
Structural feature
Three 4-N,N-dimethylamino-phenyl groups attached to a central 2-phenyl-ethane backbone
Common uses
Fluorescent dye, reagent in chemical and biological research
Applications in biology
Fluorescent labeling of cellular structures and intracellular processes
Utilization in molecular probes
Detection of biomolecules such as proteins and nucleic acids
Chemical properties
The presence of the amine group (-NH2) and the dimethylamino groups (-N(CH3)2) contribute to its reactivity and solubility in organic solvents
Physical properties
The compound is likely to be a solid at room temperature, given its molecular size and complexity
Optical properties
Exhibits fluorescence, which is useful for its applications in biological research and molecular probes
Stability
The compound is likely to be stable under normal laboratory conditions, but may be sensitive to light, heat, or strong acids and bases
Solubility
Soluble in organic solvents such as ethanol, methanol, and dimethyl sulfoxide (DMSO) due to the presence of the amine and dimethylamino groups
Safety precautions
As with any chemical compound, it is important to handle 1,1,1-Tris-(4-N,N-dimethylamino-phenyl)-2-phenyl-ethane with care, using appropriate personal protective equipment (PPE) and following proper laboratory safety protocols.
Check Digit Verification of cas no
The CAS Registry Mumber 328010-96-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,0,1 and 0 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 328010-96:
(8*3)+(7*2)+(6*8)+(5*0)+(4*1)+(3*0)+(2*9)+(1*6)=114
114 % 10 = 4
So 328010-96-4 is a valid CAS Registry Number.
328010-96-4Relevant articles and documents
Photochemistry and photophysics of triarylmethane dye leuconitriles
Jarikov,Neckers
, p. 659 - 671 (2007/10/03)
The photochemical reactions of crystal violet leuconitrile (CVCN) were investigated by the means of product analysis and trapping experiments, laser flash and steady-state photolysis, and steady-state fluorescence. The influence of oxygen on the reaction was examined in detail. The photochemistry of malachite green leuconitrile (MGCN), basic fuchsin leuconitrile (BFCN), and crystal violet leucomethyl (CVMe) and leucobenzyl (CVBn), as well as triphenylacetonitrile, was studied. The results suggest ionization occurs from S1, while the di-π-methane reaction is the photochemical route from T1.
