78717-59-6

Basic information

• Product Name: 4,6-dichloro-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,5-triazin-2-amine
• Synonyms: 1,3,5-Triazin-2-amine, 4,6-dichloro-N-(2,2,6,6-tetramethyl-4-piperidinyl)-
• CAS NO: 78717-59-6
• Molecular Formula: C₁₂H₁₉Cl₂N₅
• Molecular Weight: 304.2188
• Mol File: 78717-59-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 439.2°C at 760 mmHg
• Flash Point: 219.4°C
• Density: 1.227g/cm³
• Vapor Pressure: 6.52E-08mmHg at 25°C
• Refractive Index: 1.544
• CAS DataBase Reference: 4,6-dichloro-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,5-triazin-2-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 4,6-dichloro-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,5-triazin-2-amine(78717-59-6)
• EPA Substance Registry System: 4,6-dichloro-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,5-triazin-2-amine(78717-59-6)

Safety Data

• Hazardous Substances Data: 78717-59-6(Hazardous Substances Data)

Upstream product

• 36768-62-4 4-AMINO-2,2,6,6-TETRAMETHYLPIPERIDINE 
• 108-77-0 1,3,5-trichloro-2,4,6-triazine 
• 202590-19-0 C₉H₂₀N₂ 

Downstream Products

• 1216935-74-8 C₁₈H₂₄ClFN₆ 

Relevant articles and documents

Triazine quaternary ammonium salt halamine antibacterial agent and preparation method thereof, and salt-free antibacterial finishing method

The invention provides a triazine quaternary ammonium salt halamine antibacterial agent. The triazine quaternary ammonium salt halamine antibacterial agent is a compound with a structure as shown in a formula (I) in the specification. The preparation method comprises the following steps: (1) dropwise adding an organic solution of 2,2,6,6-tetramethyl-4-piperidylamine into an aqueous or organic solution of cyanuric chloride or cyanuric fluoride, and carrying out a reaction for 1 to 4 h; (2) pouring an aqueous solution of chlorinated N-(2-ethylamino)-pyridine into the reaction solution, carrying out a reaction for 2 to 6 h, dropwise adding an acid-binding agent in the whole process of the reaction, and allowing the pH value of the reaction solution to be 5.0 to 8.0; (3) after the reaction is completed, carrying out filtering, purifying and drying so as to obtain a triazine quaternary ammonium salt halamine antibacterial precursor; and (4) placing the triazine quaternary ammonium salt halamine antibacterial precursor into a halogenated solution, carrying out standing at room temperature for 0.5 to 1.5 h, and after completion of standing, carrying out filtering and drying so as to obtain a quaternary ammonium salt halamine antibacterial agent product. The triazine quaternary ammonium salt halamine antibacterial agent provided by the invention is a salt-free reaction-type halamine antibacterial agent with excellent antibacterial properties and good precursor water-solubility.

Polytriazine derivatives containing polyalkylpiperidinyloxy or polyalkylpiperidinylamino groups

Compounds of the formula (I) STR1 wherein n is a number from 1 to 20; the radicals R1 are independently of one another hydrogen, C1 -C8 alkyl, --O, --OH, --CH2 CN, C1 -C18 alkoxy, C5 -C12 cycloalkoxy, C3 -C6 alkenyl, C7 -C9 phenylalkyl which is unsubstituted or substituted on the phenyl by 1, 2 or 3 C1 -C4 alkyl; or C1 -C8 acyl; R2 has one of the meanings given for R1 ; X is C2 -C10 alkylene; and Y is --O-- or >NH; with the proviso that in the individual recurrent units of the formula (I), each of the radicals R1, R2, X and Y has the same or different definitions; are very effective as light stabilizers, heat stabilizers and oxidation stabilizers for organic materials, in particular synthetic polymers.