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2,2'-(1,2-ethanediyldiimino)-4,4'-ditert-butylbisphenol, also known as Bisphenol A diglycidyl ether (BADGE), is a chemical compound with the molecular formula C23H32N2O2. It is a colorless to pale yellow liquid that is soluble in most organic solvents. BADGE is primarily used as a cross-linking agent in the production of epoxy resins, which are widely used in coatings, adhesives, and composite materials. It is also used in the manufacturing of phenolic resins, which are employed in the production of laminates, molding compounds, and other thermosetting plastics. The compound is known for its high reactivity and excellent adhesion properties, making it a valuable component in various industrial applications. However, it is important to note that BADGE is a derivative of bisphenol A (BPA), a chemical that has raised concerns due to its potential health and environmental impacts, leading to its restriction or ban in certain products and regions.

5253-46-3

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5253-46-3 Usage

Common uses

Antioxidant in rubber, plastics, and lubricants; stabilizer in polymer production; monomer in polymer and copolymer synthesis; stabilizer for photocopier toners; additive in liquid crystal polymer production

Function

Inhibits degradation of materials caused by heat, oxygen, and light exposure; extends lifespan and improves performance of materials and products.

Check Digit Verification of cas no

The CAS Registry Mumber 5253-46-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5253-46:
(6*5)+(5*2)+(4*5)+(3*3)+(2*4)+(1*6)=83
83 % 10 = 3
So 5253-46-3 is a valid CAS Registry Number.

5253-46-3Relevant academic research and scientific papers

Facile synthesis of 1,3,6-oxadiazepines from 2,2′-(1,2-ethanediyldiimino)bisphenols

Ochoa, Ma.Eugenia,Rojas-Lima, Susana,H?pfl, Herbert,Rodríguez, Patricia,Castillo, Dolores,Farfán, Norberto,Santillan, Rosa

, p. 55 - 64 (2007/10/03)

A useful sequence of reactions for the syntheses of a variety of heterocyclic systems including an oxadiazepine ring is described. The key step involves the condensation of substituted 2,2′-(1,2-ethanediyldiimino)bisphenols with ethanedial to provide stereoselectively the 6a,7a-trans-6,6a,7a,8,15,16-hexahydro[1,4]benzoxazine[4′,3′:6,7] [1,3,6]oxadiazepino[2,3-c][1,4]-benzoxazine-6,8-diol framework, as established by X-ray diffraction analyses.

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