6030-54-2

Basic information

• Product Name: dimethyl hexane-1,6-diylbiscarbamate
• Synonyms: carbamic acid, N,N'-1,6-hexanediylbis-, dimethyl ester
• CAS NO: 6030-54-2
• Molecular Formula: C₁₀H₂₀N₂O₄
• Molecular Weight: 232.2768
• Mol File: 6030-54-2.mol

Chemical Properties

• Boiling Point: 382.7°C at 760 mmHg
• Flash Point: 185.3°C
• Density: 1.064g/cm³
• Vapor Pressure: 4.63E-06mmHg at 25°C
• Refractive Index: 1.454
• CAS DataBase Reference: dimethyl hexane-1,6-diylbiscarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl hexane-1,6-diylbiscarbamate(6030-54-2)
• EPA Substance Registry System: dimethyl hexane-1,6-diylbiscarbamate(6030-54-2)

Safety Data

• Hazardous Substances Data: 6030-54-2(Hazardous Substances Data)

Usage

Uses

Used in Polyurethane Production:
Dimethyl hexane-1,6-diylbiscarbamate is used as a crosslinking agent for improving the physical and mechanical properties of polyurethane materials, such as durability, strength, and flexibility.
Used in Foam Industry:
Dimethyl hexane-1,6-diylbiscarbamate is used as a chemical component in the production of polyurethane foams, contributing to their enhanced performance characteristics.
Used in Coatings Industry:
Dimethyl hexane-1,6-diylbiscarbamate is used as a key ingredient in the formulation of polyurethane coatings, ensuring their superior durability and strength.
Used in Adhesives Industry:
Dimethyl hexane-1,6-diylbiscarbamate is used as a crucial component in the development of polyurethane adhesives, providing improved bonding strength and flexibility.
It is important to handle dimethyl hexane-1,6-diylbiscarbamate with care and follow proper safety measures due to its potential health hazards and environmental impact.

Upstream product

• 67-56-1 methanol 
• 124-09-4 1,6-Hexanediamine 
• 201230-82-2 carbon monoxide 
• 61578-93-6 N,N'-hexanediyl bis-(thiocarbamic acid (S-phenyl) ester) 
• 3073-59-4 hexamethylene bisacetamide 
• 616-38-6 carbonic acid dimethyl ester 

Downstream Products

• 4991-18-8 N,N'-dinitroso-N,N'-hexanediyl-bis-carbamic acid dimethyl ester 
• 13590-53-9 1-isocyanato-6-methoxycarbonylaminohexane 
• 822-06-0 Hexamethylene diisocyanate 
• 54286-89-4 1,1,6,6-tetramethoxyhexane 

Relevant articles and documents

Iodide-Catalyzed Synthesis of Secondary Thiocarbamates from Isocyanides and Thiosulfonates

A new method for the synthesis of secondary thiocarbamates from readily available isocyanides and thiosulfonates with broad functional group tolerance is reported. The reaction proceeds under mild reaction conditions in isopropanol and is catalyzed by inexpensive sodium iodide.

METHOD FOR PRODUCING CARBAMATE COMPOUND

A task of the present invention is to provide a process for preparation a carbamate compound using a carbonic acid ester and an amide compound in the presence of a basic compound(s), wherein the process is a novel industrial method which is advantageous in that the reaction rate is faster than conventional and the by-produced ester compound can be recovered, and the present invention is directed to a method comprising reacting an amide compound represented by the formula (1) with a carbonic acid ester represented by the formula (2) in the presence of a basic compound(s) to obtain a carbamate compound represented by the formula (3).

First gold(I) complex-catalyzed oxidative carbonylation of amines for the syntheses of carbamates

At 200 °C and 5 MPa of initial total pressure, the oxidative carbonylation of amines for the synthesis of the corresponding carbamates by Au(I) complexes as catalysts was conducted with excellent conversion and selectivity.