4015-16-1

Basic information

• Product Name: 1,3,5-tripropyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione
• Synonyms: 1,3,5-tripropyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione;Einecs 223-668-7
• CAS NO: 4015-16-1
• Molecular Formula: C₁₂H₂₁N₃O₃
• Molecular Weight: 255.31344
• EINECS: 223-668-7
• Mol File: 4015-16-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 361.5°Cat760mmHg
• Flash Point: 147.4°C
• Appearance: /
• Density: 1.103g/cm³
• Vapor Pressure: 2.06E-05mmHg at 25°C
• Refractive Index: 1.489
• CAS DataBase Reference: 1,3,5-tripropyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-tripropyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(4015-16-1)
• EPA Substance Registry System: 1,3,5-tripropyl-1,3,5-triazine-2,4,6(1H,3H,5H)-trione(4015-16-1)

Safety Data

• Hazardous Substances Data: 4015-16-1(Hazardous Substances Data)

Usage

Chemical class

Belongs to the triazine class of compounds

Structure

Consists of a triazine ring with three propyl groups attached and three carbonyl groups at the 2, 4, and 6 positions

Applications

a. Stabilizer in swimming pool chlorine products
b. Production of various plastics and resins

Safety precautions

a. Toxic if ingested or inhaled
b. Can cause irritation to the skin and eyes
c. Handle and use with caution

InChI:InChI=1/C12H21N3O3/c1-4-7-13-10(16)14(8-5-2)12(18)15(9-6-3)11(13)17/h4-9H2,1-3H3

Upstream product

• 110-78-1 Propyl isocyanate 
• 622-58-2 p-Tolylisocyanate 
• 119543-22-5 1,3,5-Tripropyl-[1,3,5]triazinane-2,4,6-triylidenetriamine 

Relevant articles and documents

Cyclotrimerisation of isocyanates catalysed by low-coordinate Mn(ii) and Fe(ii) m-terphenyl complexes

Two- and three-coordinate m-terphenyl complexes of manganese and iron are efficient catalysts for the selective cyclotrimerisation of primary aliphatic isocyanates affording isocyanurates in short reaction times and under mild conditions.

Synthesis of isomelamines and isocyanurates and their biological evaluation

The reaction of cyanogen bromide (1) with primary amines (2a-p), including arylmethylamines (21-p), gave the corresponding cyanamides (3a- p). Trimerization of 3a-p gave 1,3,5-trisubstituted 2,4,6-triiminohexahydro- 1,3,5-triazines (isomelamines) (4a-p), which were treated with hydrochloric acid to give the corresponding 1,3,5-trisubstituted 2,4,6-trioxohexahydro- 1,3,5-triazines (isocyanurates) (5a-c, f) and 1,3,5-trisubstituted 2-imino- 4,6-dioxohexahydro-1,3,5- triazines (5b'-e'). Biological evaluation of 4a- p, 5a-c, f, and 5b'-e' was carried out, and some of these compounds showed bronchodilator and positive inotropic activities.