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1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trioctyl- is a complex organic compound with the chemical formula C24H41N3O6. It is a derivative of the triazine ring system, which consists of a six-membered ring containing three nitrogen atoms. In this specific compound, the triazine ring is fully saturated with three carbonyl groups (C=O) at the 2, 4, and 6 positions, and three octyl chains (C8H17) are attached to the nitrogen atoms at the 1, 3, and 5 positions. 1,3,5-Triazine-2,4,6(1H,3H,5H)-trione, 1,3,5-trioctyl- is known for its surfactant properties and is used in various industrial applications, such as in the production of detergents, emulsifiers, and foaming agents. Its amphiphilic nature, with both hydrophilic (polar) and hydrophobic (non-polar) regions, allows it to interact with both water and oil, making it effective in stabilizing emulsions and dispersions.

1908-35-6

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1908-35-6 Usage

Chemical Structure

A triazine ring with three carbonyl (C=O) groups attached at the 2, 4, and 6 positions

Functionality

Stabilizer and antioxidant

Application

Production of polymers and plastics

Specific Use

Heat and light stabilizer for polyolefins (e.g., polypropylene and polyethylene)

Mechanism

Inhibits degradation of polymers caused by heat, oxygen, and UV radiation

Purpose

Maintains physical and mechanical properties of the final plastic product

Check Digit Verification of cas no

The CAS Registry Mumber 1908-35-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,0 and 8 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1908-35:
(6*1)+(5*9)+(4*0)+(3*8)+(2*3)+(1*5)=86
86 % 10 = 6
So 1908-35-6 is a valid CAS Registry Number.

1908-35-6Downstream Products

1908-35-6Relevant academic research and scientific papers

Application of the study of reactivity of alkaline salts of isocyanuric acid to the synthesis of mono and trisubstituted isocyanurates

Chiron-Charrier,Caubere

, p. 2659 - 2672 (1993)

Reactivity of alkaline salts of isocyanuric acid has been studied. It has been established that the nucleophilic substitution is not selective because of the protonic exchanges between salts and substituted derivatives. The synthesis of mono or trisubstituted derivative is due to secondary reactions and to solvent effects. With this study, it has been possible to settle a method to prepare mono and trisubstituted derivatives of isocyanuric acid.

Investigations providing a plausible mechanism in the hexamethyldisilazane- catalyzed trimerization of alkyl isocyanates

Roman, Mihaela,Andrioletti, Bruno,Lemaire, Marc,Bernard, Jean-Marie,Schwartz, Johannes,Barbeau, Philippe

scheme or table, p. 1506 - 1510 (2011/03/22)

Using HMDS as catalyst for the trimerization of isocyanates presents many advantages as the expected isocyanurate is not contaminated by the catalyst or other side-products resulting from its degradation. In addition, HMDS presents a low toxicity, and is compatible with industrial applications. This article describes the hexamethyldisilazane (HMDS)-catalyzed trimerization of octylisocyanate. Experimental investigations and mechanistic considerations indicate that the true catalyst of the trimerization is trimethylsilyloctylamine, which results from the preliminary condensation of HMDS with octylisocyanate.

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