2092-58-2

Basic information

• Product Name: 1,3-bis(2,4,4-trimethylpentan-2-yl)urea
• CAS NO: 2092-58-2
• Molecular Formula: C₁₇H₃₆N₂O
• Molecular Weight: 284.4805
• Mol File: 2092-58-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 389.9°C at 760 mmHg
• Flash Point: 105.8°C
• Density: 0.877g/cm³
• Vapor Pressure: 2.76E-06mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: 1,3-bis(2,4,4-trimethylpentan-2-yl)urea(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-bis(2,4,4-trimethylpentan-2-yl)urea(2092-58-2)
• EPA Substance Registry System: 1,3-bis(2,4,4-trimethylpentan-2-yl)urea(2092-58-2)

Safety Data

• Hazardous Substances Data: 2092-58-2(Hazardous Substances Data)

Usage

Composition

Two molecules of 2,4,4-trimethylpentan-2-yl urea linked by a nitrogen atom

Chemical classification

Urea derivative

Fuel additive application

Improves performance and efficiency of diesel engines

Emission reduction

Reduces emissions of nitrogen oxides and particulate matter

Potential applications

Organic chemistry synthesis of various compounds

Unique properties

Utilized due to its specific molecular structure and properties

Upstream product

• 107-45-9 tert-Octylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 100-51-6 benzyl alcohol 
• 64-17-5 ethanol 

Downstream Products

• 6045-01-8 N-phenyl-N'-(1,1,3,3-tetramethyl-butyl)-urea 
• 101452-64-6 N-cyclohexyl-N'-(1,1,3,3-tetramethyl-butyl)-urea 
• 1611-57-0 1,1,3,3-tetramethylbutyl isocyanate 

Relevant articles and documents

Isocyanates - Part 3. Synthesis of carbamates by DMAP-catalyzed reaction of amines with di-tert-butyldicarbonate and alcohols

Carbamates are prepared by DMAP-catalyzed reaction of amines with di-tert-butyldicarbonate and subsequent trapping of the intermediate isocyanates with alcohols.