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trimethyl isocyanurate

CAS No.
827-16-7
Chemical Name:
trimethyl isocyanurate
Synonyms
trimethyl isocyanurate;1,3,5-Trimethylisocyanuric acid;Trimethyl-1,3,5-triazinane-2,4,6-trione;1,3,5-Trimethylhexahydro-1,3,5-triazine-2,4,6-trione;1,3,5-Trimethyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-trimethyl-
CBNumber:
CB01374465
Molecular Formula:
C6H9N3O3
Molecular Weight:
171.15
MDL Number:
MOL File:
827-16-7.mol
MSDS File:
SDS
Last updated:2022-12-21 16:56:50

trimethyl isocyanurate Properties

Melting point 176.5°C
Boiling point 301.12°C (rough estimate)
Density 1.3994 (rough estimate)
refractive index 1.5800 (estimate)
storage temp. Sealed in dry,Room Temperature
pka -2.13±0.20(Predicted)
FDA UNII MWL7B55ECL
EPA Substance Registry System Trimethyl isocyanurate (827-16-7)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338

trimethyl isocyanurate price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC B536770 Trimethyl-1,3,5-triazinane-2,4,6-trione 827-16-7 2.5mg $150 2021-12-16 Buy
Product number Packaging Price Buy
B536770 2.5mg $150 Buy

trimethyl isocyanurate Chemical Properties,Uses,Production

Uses

The crystal structure of Trimethyl-1,3,5-triazinane-2,4,6-trione has been reported previously to have low accurancy and without H-atom position, this compound in its molecular complex with 1,3,5-trinitrobenzene has been used in the construction of suprmolecular networks stabilized by hydrogen bonds.

Synthesis Reference(s)

Journal of the American Chemical Society, 78, p. 4358, 1956 DOI: 10.1021/ja01598a043

General Description

Monoclinic prisms (from water or alcohol).

Reactivity Profile

Isocyanates and thioisocyanates, such as trimethyl isocyanurate, are incompatible with many classes of compounds, reacting exothermically to release toxic gases. Reactions with amines, aldehydes, alcohols, alkali metals, ketones, mercaptans, strong oxidizers, hydrides, phenols, and peroxides can cause vigorous releases of heat. Acids and bases initiate polymerization reactions in these materials. Some isocyanates react with water to form amines and liberate carbon dioxide. Polyurethanes are formed by the condensation reaction of diisocyanates with, for example, ethyl glycol.

Fire Hazard

Flash point data for trimethyl isocyanurate are not available. trimethyl isocyanurate is probably combustible.

67-56-1
598-55-0
827-16-7
115-10-6
6642-30-4
616-38-6
Synthesis of trimethyl isocyanurate from Methanol and Methyl carbamate

trimethyl isocyanurate Preparation Products And Raw materials

Raw materials

Preparation Products

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trimethyl isocyanurate 1,3,5-Trimethyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione 1,3,5-Trimethylhexahydro-1,3,5-triazine-2,4,6-trione 1,3,5-Trimethylisocyanuric acid 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione,1,3,5-trimethyl- Trimethyl-1,3,5-triazinane-2,4,6-trione 827-16-7