6281-19-2

Usage

Chemical class

Triazinanes

Nitrogen-containing

Heterocyclic compound

Side chains

Three dodecyl side chains attached to nitrogen atoms

Common uses

Corrosion inhibitor, stabilizer in industrial applications

Function

Forms a protective layer on metal surfaces to prevent corrosion and degradation

Thermal stability

Excellent

Oxidative stability

Excellent

Applications

Lubricants, fuels, and polymers

Protection

Against degradation under harsh environmental conditions

Upstream product

• 50-00-0 formaldehyd 
• 124-22-1 n-Dodecylamine 

Downstream Products

• 906666-50-0 Ti(N-2,6-C₆H₃(i)Pr₂)(1,3,5-tris(n-dodecyl)triazacyclohexane)Cl₂ 
• 7505-51-3 1,3-didodecylthiourea 

Relevant academic research and scientific papers

Catalyst ligand for directly synthesizing lubricating oil base oil from alpha-olefin, and coordination compound thereof, and preparation methods and applications of catalyst ligand and coordination compound

The present invention belongs to the field of lubricating oil preparation, and provides a preparation method and applications of a catalyst ligand for directly synthesizing lubricating oil base oil from alpha-olefin. According to the present invention, th

Oligomerization catalyst

An oligomerization catalyst for olefins is obtainable from a) a chromium compound CrX3 and the at least equimolar amount, based on the chromium compound CrX3, of a ligand L or from an existing chromium complex CrX3L, in which the groups X are, independently of one another, abstractable counterions and L is a 1,3,5-triazacyclohexane of the formula I ?where the groups R1 to R9 are, independently of one another: hydrogen or organosilicon or substituted or unsubstituted carboorganic groups having from 1 to 30 carbon atoms, where two geminal or vicinal radicals R1 to R9 may also be joined to form a five—or six-membered ring, andb) at least one activating additive and also a process for preparing oligomers of olefins using these catalysts, the oligomers thus obtainable, and the oxo alcohols obtainable from these oligomers.

OLIGOMERISATION CATALYST

An oligomerization catalyst for olefins is obtainable froma) a chromium compound CrX3 and the at least equimolar amount, based on the chromium compound CrX3, of a ligand L or from an existing chromium complex CrX3L, in which the groups X are, independently of one another, abstractable counterions and L is a 1,3,5-triazacyclohexane of the formula Iwhere the groups Rto Rare, independently of one another: hydrogen or organosilicon or substituted or unsubstituted carboorganic groups having from 1 to 30 carbon atoms, where two geminal or vicinal radicals Rto Rmay also be joined to form a five-or six-membered ring, andb) at least one activating additiveand also a process for preparing oligomers of olefins using these catalysts, the oligomers thus obtainable, and the oxo alcohols obtainable from these oligomers.

Preparation of N,O-Aminals as Synthetic Equivalents of H2C=NAr and (H2C=NHAr)+ ions: Neutral- and Acid-promoted Transformations

A general method for the synthesis of N, O-aminals derived from primary aromatic amines is described.The reactivity of these compounds under neutral and acidic conditions has been studied and the title compounds can be envisaged as general purpose H2C=NAr or (H2C=NAr)+ equivalents.N,O-Aminals have been converted into perhydrotriazines by moderate heating and into bis(4-aminoaryl)methane derivatives or N-benzylarylamines, respectively, when heated in acidid media with pH control.Reduction od N,O-acetals with sodium cyanoborohydride has revealed that the C-O bond is broken exclusively in acidic media.