54699-28-4 Usage
Uses
Used in Coatings Industry:
2,2'-Methylenebisoxybis(2-methylbutane) is used as a solvent in the coatings industry for its ability to dissolve various types of resins and pigments, improving the flow and leveling properties of the coating.
Used in Inks Industry:
In the inks industry, 2,2'-Methylenebisoxybis(2-methylbutane) is used as a solvent to enhance the solubility of ink components, ensuring smooth flow and even distribution of the ink on various surfaces.
Used in Adhesives Industry:
2,2'-Methylenebisoxybis(2-methylbutane) is used as a solvent in adhesives to improve the adhesive's viscosity and bonding properties, making it suitable for various substrates.
Used in Consumer Products:
Although not a primary component, 2,2'-Methylenebisoxybis(2-methylbutane) can be found in some consumer products, where it serves as a solvent for specific ingredients.
Safety Precautions:
It is important to handle 2,2'-Methylenebisoxybis(2-methylbutane) with care, as it can be harmful if swallowed or inhaled, and it can cause skin and eye irritation. Proper safety precautions, such as wearing protective gear and working in well-ventilated areas, should be taken when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 54699-28-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,6,9 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54699-28:
(7*5)+(6*4)+(5*6)+(4*9)+(3*9)+(2*2)+(1*8)=164
164 % 10 = 4
So 54699-28-4 is a valid CAS Registry Number.
54699-28-4Relevant academic research and scientific papers
Free-radical transformations of di-tert-alkoxymethanes in the absence of solvent and in chloroform
Rol'nik, L. Z.,Kalashnikov, S. M.,Pastushenko, E. V.,Zlotskii, S. S.,Rakhmankulov, D. L.
, p. 614 - 618 (2007/10/02)
In chloroform in the presence of tert-butyl peroxide di-tert-alkoxymethanes from the corresponding tert-alkyl formates, tert-alkyl chlorides, and alkanes; here the chloroform is converted into methylene chloride and 1,1,2,2-tetrachloroethane.The relationships between the accumulation rate of the reaction products and the concentration of acetal, chloroform, and initiator were determined.An unbranched radical-chain mechanism was established for the fragmentation of the acetals with quadratic termination at the tert-alkyl and dichloromethyl radicals.
