1-Aminoimidazolidine-2,4-dione
1-Aminoimidazolidine-2,4-dione
CAS: 6301-02-6
Molecular Formula: C3H5N3O2
1-Aminoimidazolidine-2,4-dione - Names and Identifiers
| Name | 1-Aminoimidazolidine-2,4-dione |
| Synonyms | NSC 44144 1-Aminohydantoin 1-AMINOHYDANTOIN 1-Aminoimidazolidine-2,4-dione 1-AMINO-IMIDAZOLIDINE-2,4-DIONE 2,4-Imidazolidinedione, 1-amino- |
| CAS | 6301-02-6 |
| EINECS | 228-593-3 |
| InChI | InChI=1/C3H5N3O2/c4-6-1-2(7)5-3(6)8/h1,4H2,(H,5,7,8) |
1-Aminoimidazolidine-2,4-dione - Physico-chemical Properties
| Molecular Formula | C3H5N3O2 |
| Molar Mass | 115.09 |
| Density | 1.506±0.06 g/cm3(Predicted) |
| Melting Point | 195-196 °C |
| Solubility | Acetonitrile (Slightly), DMSO (Slightly), Methanol (Slightly) |
| Appearance | Solid |
| Color | White to Off-White |
| pKa | 7.88±0.10(Predicted) |
| Storage Condition | Hygroscopic, -20°C Freezer, Under inert atmosphere |
| Refractive Index | 1.556 |
| Use | Herbicide intermediates for pharmaceuticals or pesticides |
1-Aminoimidazolidine-2,4-dione - Introduction
1-Aminoimidazolidine-2,4-dione(1-Aminoimidazolidine-2,4-dione) is an organic compound with the chemical formula Cover Hover N₂ O₂. It is a white crystal that is soluble in water and acidic solutions.
1-Aminoimidazolidine-2,4-dione has a variety of uses. First of all, it is an important synthetic intermediate, which is widely used in drug synthesis and organic synthesis. Secondly, it can be used as a formulation component of medicaments, such as for the treatment of epilepsy and painful neuropathies. In addition, it can also be used as a thickener and moisturizer in cosmetics and skin care products.
There are several methods for preparing 1-Aminoimidazolidine-2,4-dione. One commonly used method is by reacting 1-iminodimethylurea with formaldehyde. The specific synthesis step is to react 1-iminodimethylurea with formaldehyde in a warm reaction system under alkaline conditions to produce 1-Aminoimidazolidine-2,4-dione. The method is simple and the reaction efficiency is high.
Regarding safety information, 1-Aminoimidazolidine-2,4-dione has low toxicity under normal use conditions. However, it is still necessary to pay attention to the following safety measures: avoid direct contact with skin and eyes, avoid inhaling dust or gas, and maintain good ventilation conditions. During operation, appropriate personal protective equipment such as gloves, goggles and protective clothing should be worn. If you come into contact with a substance, rinse immediately with plenty of water and seek medical help. During storage, 1-Aminoimidazolidine-2,4-dione should be kept in a dry, cool place, away from fire and oxidizing agents.
1-Aminoimidazolidine-2,4-dione has a variety of uses. First of all, it is an important synthetic intermediate, which is widely used in drug synthesis and organic synthesis. Secondly, it can be used as a formulation component of medicaments, such as for the treatment of epilepsy and painful neuropathies. In addition, it can also be used as a thickener and moisturizer in cosmetics and skin care products.
There are several methods for preparing 1-Aminoimidazolidine-2,4-dione. One commonly used method is by reacting 1-iminodimethylurea with formaldehyde. The specific synthesis step is to react 1-iminodimethylurea with formaldehyde in a warm reaction system under alkaline conditions to produce 1-Aminoimidazolidine-2,4-dione. The method is simple and the reaction efficiency is high.
Regarding safety information, 1-Aminoimidazolidine-2,4-dione has low toxicity under normal use conditions. However, it is still necessary to pay attention to the following safety measures: avoid direct contact with skin and eyes, avoid inhaling dust or gas, and maintain good ventilation conditions. During operation, appropriate personal protective equipment such as gloves, goggles and protective clothing should be worn. If you come into contact with a substance, rinse immediately with plenty of water and seek medical help. During storage, 1-Aminoimidazolidine-2,4-dione should be kept in a dry, cool place, away from fire and oxidizing agents.
Last Update：2024-04-09 20:02:46
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