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(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID

Product Name
(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID
CAS No.
87219-22-5
Chemical Name
(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID
Synonyms
109340;2-(2-Oxoimidazolidin-1-yl);2-Oxo-1-imidazolidineacetic acid;2-Oxoimidazolidine-1-acetic Acid;1-Imidazolidineacetic acid, 2-oxo-;(2-oxo-imidazolidin-l-yl)-acetic acid;2-(2-oxoiMidazolidin-1-yl)acetic acid
CBNumber
CB41008973
Molecular Formula
C5H8N2O3
Formula Weight
144.13
MOL File
87219-22-5.mol
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(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID Property

Boiling point:
487.1±24.0 °C(Predicted)
Density 
1.379
storage temp. 
Sealed in dry,Room Temperature
pka
4.41±0.10(Predicted)
Appearance
White to off-white Solid
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

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N-Bromosuccinimide Price

TRC
Product number
O991215
Product name
2-(2-Oxoimidazolidin-1-yl)aceticacid
Packaging
50mg
Price
$65
Updated
2021/12/16
AK Scientific
Product number
Z5232
Product name
2-(2-Oxoimidazolidin-1-yl)aceticacid
Packaging
250mg
Price
$232
Updated
2021/12/16
Matrix Scientific
Product number
095804
Product name
2-(2-Oxoimidazolidin-1-yl)acetic acid
Purity
95+%
Packaging
250mg
Price
$394
Updated
2021/12/16
AK Scientific
Product number
Z5232
Product name
2-(2-Oxoimidazolidin-1-yl)aceticacid
Packaging
1g
Price
$492
Updated
2021/12/16
Matrix Scientific
Product number
095804
Product name
2-(2-Oxoimidazolidin-1-yl)acetic acid
Purity
95+%
Packaging
1g
Price
$874
Updated
2021/12/16
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(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID Chemical Properties,Usage,Production

Synthesis

3699-54-5

87219-22-5

General procedure for the synthesis of (2-ketoimidazolyl)-acetic acid from 1-(2-hydroxyethyl)-2-imidazolidinone: 15% aqueous sodium bicarbonate (21 ml) was added to a solution of 1-(2-hydroxyethyl)-2-imidazolidinone (1.00 g, 7.68 mmol) in acetone (70 ml) to form a white slurry, which was subsequently cooled to 0°C (Refs. JOC 2003, 68, 4999-5001). Sodium bromide (0.16 g, 1.54 mmol) and TEMPO (0.024 g, 0.15 mmol) were added sequentially and the mixture was stirred for 10 min. Subsequently, trichloroisocyanuric acid (3.57 g, 15.4 mmol) was added in five equal portions, each five minutes apart. The light yellow slurry was warmed to 25°C and stirring was continued for 12 hours to obtain a yellow solution. Isopropanol (9 ml) was added and stirred for 45 minutes to form a white slurry which was filtered through diatomaceous earth. The filter cake was washed with an appropriate amount of solvent. The filtrate was concentrated under reduced pressure, neutralized with saturated aqueous sodium bicarbonate and extracted with ethyl acetate (50 ml). The aqueous phase was adjusted to pH ≈ 2 with 4N HCl and then extracted continuously with a 5% methanol/dichloromethane solvent mixture (~120 ml) for 16 hours. The organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give (2-oxoimidazolidin-1-yl)acetic acid (0.530 g, 48% yield) as a white solid.

References

[1] Patent: WO2006/138350, 2006, A2. Location in patent: Page/Page column 87-88

(2-OXO-IMIDAZOLIDIN-1-YL)-ACETIC ACID Preparation Products And Raw materials

Raw materials

Preparation Products

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