4013-43-8

Basic information

• Product Name: 1,2-Ethenediamine
• Synonyms: ethylene-1,2-diamine;1,2-ethylendiamine;1,2-ETHENEDIAMINE;1,2-Ethylenediamine;1,2-Ethenediamine,(1E)
• CAS NO: 4013-43-8
• Molecular Formula: C2H6N2
• Molecular Weight: 58.08
• Mol File: 4013-43-8.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 115.6±23.0 °C(Predicted)
• Density: 0.929±0.06 g/cm3(Predicted)
• CAS DataBase Reference: 1,2-Ethenediamine (CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Ethenediamine (4013-43-8)
• EPA Substance Registry System: 1,2-Ethenediamine (4013-43-8)

Safety Data

• Hazardous Substances Data: 4013-43-8(Hazardous Substances Data)

Usage

Physical state

Colorless liquid

Appearance

Colorless organic compound

Reactivity

Highly reactive

Versatility

Highly versatile

Functional groups

Two amine groups

Uses

a. Production of polymers
b. Pharmaceuticals
c. Agrochemicals
d. Synthesis of chelating agents
e. Corrosion inhibitors
f. Textile chemicals
g. Epoxy curing agents
h. Fuel additives
i. Chemical reagents

Safety precautions

Corrosive and toxic if not properly handled

Handling

Requires caution and proper safety measures

Upstream product

• 51-06-9 4-amino-N-(2-diethylaminoethyl)benzamide 
• 614-39-1 procainamide hydrochloride 

Downstream Products

• 66639-12-1 2-{2-[4-(4,5-dihydro-1H-imidazol-2-yl)-phenyl]-benzothiophen-5-yl}-4,5-dihydro-1H-imidazole 
• 328546-65-2 9-nitro-1,2,3,4-tetrahydro-5H-1,4-benzodiazepin-5-one 
• 1148011-01-1 2-[(8Z,11R)-11-hydroxyheptadec-8-enyl]-1H-imidazole 
• 109273-24-7 2,3-diaminopropionic acid t-butyl ester 
• 41555-92-4 N-<(2-aminoethyl)aminomethyl>triethoxysilane 
• 93394-59-3 3,3'-ethylenebis<6,9-dioxo-8-phenyl-3-azabicyclo<3.3.1>nonane> 

Relevant articles and documents

Oxidation of procainamide by diperiodatocuprate(III) complex in aqueous alkaline medium: a comparative kinetic study

A comparative study of uncatalysed and ruthenium(III) catalyzed oxidation of procainamide(PAH) was carried out spectrophotometrically using diperiodatocuprate(III) in aqueous alkali. Stoichiometry observed was 1:2 (PAH: DPC). The reaction was of first order in both catalyzed and uncatalyzed cases, with respect to [DPC] & [Ru(III)], less than unit order in [PAH] and [alkali]. Negative fraction in [periodate]. Other kinetic parameters viz., ionic strength, dielectric constant, temperature effect and intervention of free radical were also studied. The main oxidation products were characterized by different techniques. The activation parameters with respect to slow step of the mechanism, also the thermodynamic quantities were determined.