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Usage

Uses

Used in Adhesives Industry:
N,N'-BIS(4-METHOXYBENZYLIDENE)-ALPHA,ALPHA'-BI-P-TOLUIDINE is used as a photoinitiator for the production of adhesives. It enables rapid curing of adhesives under UV light, improving the manufacturing process and ensuring strong bonding between materials.
Used in Coatings Industry:
In the coatings industry, N,N'-BIS(4-METHOXYBENZYLIDENE)-ALPHA,ALPHA'-BI-P-TOLUIDINE is utilized as a photoinitiator to facilitate the polymerization of coating materials. This results in the formation of durable and high-quality coatings with improved adhesion, scratch resistance, and weather resistance properties.
Used in Printing Inks Industry:
N,N'-BIS(4-METHOXYBENZYLIDENE)-ALPHA,ALPHA'-BI-P-TOLUIDINE is used as a photoinitiator in the manufacturing of printing inks. Its ability to initiate polymerization under UV light allows for quick drying and curing of inks, ensuring sharp and vibrant print quality.
It is crucial to handle and store N,N'-BIS(4-METHOXYBENZYLIDENE)-ALPHA,ALPHA'-BI-P-TOLUIDINE with care, as it may pose health and environmental risks if not managed properly. Proper safety measures should be taken to minimize any potential hazards associated with its use.

Upstream product

• 621-95-4 4,4'-diaminodihydrostilbene 
• 123-11-5 4-methoxy-benzaldehyde 
• 736-30-1 1,2-bis(4-nitrophenyl)ethane 

Relevant academic research and scientific papers

Synthesis and Fungicidal Activity of Novel 4,4′-Bis(2″ -aryl-5″-methyl/unsubstituted-4″-oxo-thiazolidin-3″-yl) Bibenzyl

Reduction followed by nitration of benzil I yielded 4,4′- dinitrobibenzyl (III) which by reduction furnished quantitatively and analytically pure 4,4′-diaminobibenzyl (IV) which on condensation with different carbonyl compounds gave 4,4′-bis (benzylideneamino) bibenzyls (Va-f). Compounds (Va-f) on cycloaddition with mercaptoacetic acid/2-mercaptopropionic acid yielded the corresponding 4-oxothiazolidin-3-yl bibenzyls (Vla-I). The compounds VIg-I have two chiral centers in each thiazolidinone moiety so two diastereomers are possible, but on crystallization and repeated chromatography, one diastereomer was obtained. The absolute configuration of the diastereomer was tentatively assigned on the basis of 1H NMR spectra. 1H NMR spectra of the product showed a distinct doublet at δ 1.22 for C5-CH3 of thiazolidinone ring (22, 23) and a distinct quartet at δ4.20 for the C5-H proton. Similarly, the C2 proton showed an independent singlet at δ 5.95, so the diastereomers obtained were assigned trans configuration. Compounds Va-f and Vla-I were evaluated in vitro for their fungitoxicities against Fusarium oxysporium and Penicillium citrinum. All the compounds were found to be antifungal active. Some of the compounds displayed activities comparable with that of the commercial fungicide Dithane M-45. Structure-activity relationships for the screened compounds are discussed.