60717-08-0

Upstream product

• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 112-92-5 1-octadecanol 

Downstream Products

• 119147-48-7 N-Benzyloxycarbonyl-O--L-serin 
• 119147-50-1 N^α-Benzyloxycarbonyl-N^ε-<4,6-bis(octadecyloxy)-1,3,5-triazin-2-yl>-L-lysin 
• 119147-46-5 O-<4,6-Bis(octadecyloxy)-1,3,5-triazin-2-yl>-N-trityl-L-serin-methylester 

Relevant academic research and scientific papers

Synthesis and Aggregation Behaviour of Chiral Cysteine Amphiphiles with s-Triazine as Connecting Unit

Several homologous liposome building blocks 3 with L-cysteine as chiral hydrophilic head group are synthesized. s-Triazine serves as connecting unit between cysteine and the lipophilic alkyl chains.The phase transition temperatures of the lipids are determined by DSC or fluorescence anisotropy.It can be shown, that the relationship between nature and length of the chains and the phase transition temperature corresponds to that of phospholipids.Encapsulation experiments with ionic water-soluble dyes give some hints that the vesicles prepared in phosphate buffer (pH = 7.0) interact with cationic but not with anionic hydrophilic substances.

Novel monochloro-s-triazine derivatives

Novel monochloro-s-triazine derivatives of the formula: STR1 wherein R1 and R2 are independently alkyl or substituted alkyl of 6 to 20 carbon atoms, alkenyl having 6 to 20 carbon atoms, cycloalkyl having 6 carbon atoms, or furfuryl, and which derivatives provide antioxidants and UV stabilizers for polymers such as polyolefins are prepared by reacting an alcohol with cyanuric chloride in the presence of an acid acceptor having a pKb ≤3, in an organic solvent which is inert to the reaction components.