148-85-6 Usage
Uses
Used in Polymer Production Industry:
ABBC is used as an initiator for free radical polymerization for the production of acrylic resins and polystyrene. Its thermal decomposition at temperatures above 80°C releases nitrogen gas, which initiates the polymerization process, making it a valuable component in the synthesis of various polymer materials.
Used in UV-curable Coatings and Inks Industry:
ABBC also functions as a photoinitiator in the manufacturing of UV-curable coatings and inks. Its ability to initiate polymerization upon exposure to UV light makes it an essential component in the production of these materials, which are widely used in various applications, including automotive, packaging, and printing industries.
However, it is important to handle ABBC with caution, as it may cause skin, eye, and respiratory irritation, and may also trigger allergic reactions in some individuals.
Check Digit Verification of cas no
The CAS Registry Mumber 148-85-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,4 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 148-85:
(5*1)+(4*4)+(3*8)+(2*8)+(1*5)=66
66 % 10 = 6
So 148-85-6 is a valid CAS Registry Number.
148-85-6Relevant academic research and scientific papers
Self-assembled multilayers of CdSe nanocrystals and carboxylate-handled phenylene-based molecules: Optical, electrochemical and photoconductive properties
Vercelli, Barbara,Zotti, Gianni,Berlin, Anna,Pasini, Mariacecilia,Natali, Marco
supporting information; experimental part, p. 8645 - 8652 (2012/01/15)
A series of linear phenylene-based molecules, bearing carboxylic acid or carboxylate functionalities at both ends, were reacted with (hexadecylamine/ stearate)-capped CdSe nanocrystals (7.5 nm diameter) dispersed in CHCl 3 to form multilayers on ITO-glass surfaces via layer-by-layer (LBL) alternation. The new multilayered materials were investigated by UV-Vis spectroscopy, cyclic voltammetry, photoelectrochemistry and photoconductivity. The conjugated linkers, with reversible reduction potentials in the range -1.7 to -2.8 V vs. Ag/Ag+, ease charge transport between dots (LUMO at -1.4 V). Photoconduction is dominated by interdot distance and linker characteristics rather than by LUMO energy levels. The logarithm of photoconductivity and linker length are linearly related, as in conduction of molecular wires, and the tunnelling attenuation factor β value is 2.4 nm-1. Comparison of n-type aromatics and p-type oligothiophenes is discussed.
