6281-19-2

Basic information

• Product Name: 1,3,5-tridodecyl-1,3,5-triazinane
• CAS NO: 6281-19-2
• Molecular Formula: C₃₉H₈₁N₃
• Molecular Weight: 592.0805
• Mol File: 6281-19-2.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 629.4°C at 760 mmHg
• Flash Point: 279.6°C
• Density: 0.861g/cm³
• Vapor Pressure: 9.46E-16mmHg at 25°C
• Refractive Index: 1.469
• CAS DataBase Reference: 1,3,5-tridodecyl-1,3,5-triazinane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tridodecyl-1,3,5-triazinane(6281-19-2)
• EPA Substance Registry System: 1,3,5-tridodecyl-1,3,5-triazinane(6281-19-2)

Safety Data

• Hazardous Substances Data: 6281-19-2(Hazardous Substances Data)

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

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

Relevant articles and documents

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

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.

The aminomethylation of isobutyraldehyde with free primary amines in homogenous and heterogenous media. II. Mannich bases

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