Reaction of cyanuric chloride and its derivatives with polyamide fibers in non-aqueous medium was written by Hanna, H. L.;Abd El-Thalouth, I.;Hebeish, A.. And the article was included in Angewandte Makromolekulare Chemie in 1978.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine The following contents are mentioned in the article:
Cyanuric chloride [108-77-0] did not react with polyamide fibers in non-aqueous medium but became phys. adhered to the fiber. Increasing the concentration of cyanuric chloride caused a substantial increase in the amount of extra N content of the fiber. Greater adsorption occurred in xylene than in tetrachloroethylene but a 1:3 mixture of tetrachloroethylene and xylene gave the best results. Chem. reaction was achieved by use of 2-anilino-4,6-dichloro-1,3,5-triazine [2272-40-4] and disperse dyes containing chlorotriazine rings. This study involved multiple reactions and reactants, such as 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine).
4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine (cas: 2272-40-4) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.Safety of 4,6-Dichloro-N-phenyl-1,3,5-triazin-2-amine
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics