21036-96-4

Basic information

• Product Name: 1,3-dipropylimidazolidine-2,4,5-trione
• Synonyms: 1,3-dipropylimidazolidine-2,4,5-trione
• CAS NO: 21036-96-4
• Molecular Formula: C9H14N2O3
• Molecular Weight: 198.22
• Mol File: 21036-96-4.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 322.8°C at 760 mmHg
• Flash Point: 142.4°C
• Appearance: /
• Density: 1.176g/cm³
• Vapor Pressure: 0.000272mmHg at 25°C
• Refractive Index: 1.496
• CAS DataBase Reference: 1,3-dipropylimidazolidine-2,4,5-trione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dipropylimidazolidine-2,4,5-trione(21036-96-4)
• EPA Substance Registry System: 1,3-dipropylimidazolidine-2,4,5-trione(21036-96-4)

Safety Data

• Hazardous Substances Data: 21036-96-4(Hazardous Substances Data)

Usage

Derivative of

Imidazolidine-2,4,5-trione (barbituric acid)

Physical state

White solid

Solubility

Soluble in water and organic solvents

Usage

Intermediate in the synthesis of pharmaceuticals and organic compounds

Therapeutic properties

Potential anticonvulsant and sedative effects

Safety

Handle with care due to potential hazardous health effects if not used properly

InChI:InChI=1/C9H14N2O3/c1-3-5-10-7(12)8(13)11(6-4-2)9(10)14/h3-6H2,1-2H3

Upstream product

• 79-37-8 oxalyl dichloride 
• 623-95-0 1,3-dipropylurea 

Relevant articles and documents

Dithiolene Metal Complex Colorless IR Absorbers

The invention relates to the use of compounds of formulae (1) and/or (11) as colorless 1R absorbers wherein M is Ni, Pd, Pt, Au, Ir, Fe, Zn, W, Cu, Mo, In, Mn, Co, Mg, V, Cr or Ti, X1, X2 and X3 are each independently of the others sulfur or oxygen, R1, R2, R3, R4, R5 and R6 are each independently of the others hydrogen, NR7R8, unsubstituted or substituted C1-C18alkyl, C1-C18 alkyl wherein the alkylene chain is interrupted with oxygen, unsubstituted or substituted C1-C18alkenyl, unsubstituted or substituted aryl, unsubstituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, R7 and R8, each independently of the other, being unsubstituted or substituted C1-C18alkyl, unsubstituted or substituted aryl, un substituted or substituted arylalkyl or unsubstituted or substituted heteroarylalkyl, a further IR absorber optionally being added to the compounds of formulae (I) and (II). The invention relates also to novel dithiolene compounds of formulae (I) and (II) wherein X1 is oxygen and X2 and X3 are oxygen or sulfur. The invention relates furthermore to novel dithiolene compounds of formulae (I) and (II) wherein R1 to R6 are NR7R8.