ChemicalBook--->CAS DataBase List--->6281-42-1

6281-42-1

6281-42-1 Structure

6281-42-1 Structure
IdentificationMore
[Name]

1-(2-Aminoethyl)imidazolidin-2-one
[CAS]

6281-42-1
[Synonyms]

1-(2-AMINOETHYL)-2-IMIDAZOLIDINONE
1-(2-AMINOETHYL)-2-IMIDAZOLIDONE
1-(2-AMINOETHYL)IMIDAZOLIDIN-2-ONE
1-(BETA-AMINOETHYL)-2-IMIDAZOLIDONE
BUTTPARK 52\06-90
CHEMBRDG-BB 4005390
1-(2-aminoethyl)-2-imidazolidinon
1-(2-aminoethyl)-2-imidazolone
2-Imidazolidinone, 1-(2-aminoethyl)-
1-(2-aminoethyl)imidazolidin-2-one(50% solution in i.p.a.)
1-(2-Aminoethyl)-imidazolidinone
1-(2-aminoethyl)imidazolidin-2-one(50% solution in Isopropyl alcohol)
1-(2-Aminoethyl)imidazolidin-2-one ,96%
[EINECS(EC#)]

228-491-9
[Molecular Formula]

C5H11N3O
[MDL Number]

MFCD00086348
[Molecular Weight]

129.16
[MOL File]

6281-42-1.mol
Chemical PropertiesBack Directory
[Boiling point ]

138-140/0.11mm
[density ]

1.137±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

viscous oil
[pka]

14.42±0.20(Predicted)
[color ]

Orange
[Detection Methods]

HPLC,NMR
[InChI]

InChI=1S/C5H11N3O/c6-1-3-8-4-2-7-5(8)9/h1-4,6H2,(H,7,9)
[InChIKey]

PODSUMUEKRUDEI-UHFFFAOYSA-N
[SMILES]

C1(=O)N(CCN)CCN1
[CAS DataBase Reference]

6281-42-1(CAS DataBase Reference)
[EPA Substance Registry System]

2-Imidazolidinone, 1-(2-aminoethyl)- (6281-42-1)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R34:Causes burns.
[Safety Statements ]

S22:Do not breathe dust .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
[RIDADR ]

3259
[Hazard Note ]

Irritant
[TSCA ]

TSCA listed
[HazardClass ]

8
[HS Code ]

29332900
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Urea-->Diethylenetriamine-->2-Imidazolidinethione, 1-(2-aminoethyl)--->2-Imidazolidinone, 1,1'-(1,2-ethanediyl)bis--->1,3-Diethylurea-->1-(2-Chloroethyl)imidazolidin-2-one-->2,3,5,6-tetrahydro-1H-iMidazo[1,2-a]iMidazole-->1-(2-Hydroxyethyl)-2-imidazolidinone-->Ethylenediamine-->Carbon dioxide-->Dimethyl carbonate-->2-Imidazolidone
Hazard InformationBack Directory
[Chemical Properties]

Colorless to off-white liquid
[Uses]

1-(2-Aminoethyl)-2-imidazolidone is a useful research chemical compound used in the preparation of alkyl and aryl azides by chemoselective diazotization of primary amines with in situ-generated fluorosulfonyl azide and their use in the preparation of a combinatorial library of 1,2,3-triazole.
[Flammability and Explosibility]

Notclassified
[Synthesis]

Diethylenetriamine

111-40-0

Urea

57-13-6

1-(2-Aminoethyl)imidazolidin-2-one

6281-42-1

693 kg (6.728 kmol) of diethylenetriamine (DETA) was added to a 1 m3 stirred reactor equipped with a double jacket, a liquid feed device, a nitrogen inerting system, a reaction vessel, and a scrubber tower for recovery of ammonia and ammonia solution. The reaction system was warmed up to 130°C while nitrogen was introduced to remove oxygen from the DETA. When the temperature reached 130 °C, slow addition of a 40% aqueous urea solution totaling 671.4 kg (4.476 kmol) was initiated, resulting in a molar ratio of DETA to urea of 1.5:1. The addition of the urea solution continued for a period of 4 h in batches. The ammonia released immediately at the beginning of the reaction was recovered through a scrubbing tower, and the scrubbing solution and the aqueous ammonia solution were collected in a special container. After the addition was completed, the reaction mixture was kept at 130°C for 1.5 hours to ensure complete water removal. Subsequently, the reaction temperature was gradually increased: first to 140 °C in 45 min and held for 45 min, then to 150 °C and held for 45 min, and finally at 160 °C for 5 h. The reaction temperature was then increased to 140 °C in 45 min and held for 45 min. At the end of the reaction, the system was cooled to 125 °C and the excess DETA was removed by distillation under a reduced pressure of 10 to 1.5 mbar and a mild nitrogen stream, a process that did not take more than 5 hours. After restoring the system to atmospheric pressure, it was cooled to 60 °C and the product was removed from the reactor. The resulting product contained 95-96% of 1-(2-aminoethyl)-2-imidazolidinone (UDETA) and 1-2.5% of tetraethyleneurea (TETU).

[References]

[1] Patent: US2013/23667, 2013, A1. Location in patent: Paragraph 0044; 0045; 0046; 0047
[2] Patent: US2613212, 1950,
[3] Patent: US6630599, 2003, B1. Location in patent: Page/Page column 10
Spectrum DetailBack Directory
[Spectrum Detail]

1-(2-Aminoethyl)imidazolidin-2-one(6281-42-1)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Acros Organics]

1-(2-Aminoethyl)imidazolidin-2-one(50% solution in I.P.A.), 55%(6281-42-1)
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