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| | 1,3-Dimethyl-2-imidazolidinone Basic information |
| Product Name: | 1,3-Dimethyl-2-imidazolidinone | | Synonyms: | DIMETHYLETHYLENE UREA;1,3-DiMethyl-2-iMidazolidinone, 98% 1KG;Tetrahydro-2H-imidazol-2-one, 1,3-Dimethyl-2-oxoimidazolidine;1,3-DIMETHYL-2-IMIDAZOLIDINONE FOR SYNTH;DiMethyl-2-iMidazolidin;1,3-DiMethyl-2-iMidazolidinone >=99.0% (GC);1,3-DiMethyl-2-iMidazolidinone absolute, over Molecular sieve (H2O <=0.04%), >=99.5% (GC);1,3-DiMethyl-2-iMidazolidinone reagent grade | | CAS: | 80-73-9 | | MF: | C5H10N2O | | MW: | 114.15 | | EINECS: | 201-304-8 | | Product Categories: | Heterocyclic Compounds;Imidazol&Benzimidazole;Building Blocks;Chemical Synthesis;Heterocyclic Building Blocks;Imidazolines/Imidazolidines;bc0001;80-73-9 | | Mol File: | 80-73-9.mol |  |
| | 1,3-Dimethyl-2-imidazolidinone Chemical Properties |
| Melting point | 8.2 °C | | Boiling point | 224-226 °C (lit.) | | density | 1.056 g/mL at 25 °C (lit.) | | vapor pressure | <1 hPa (20 °C) | | refractive index | n20/D 1.472(lit.) | | Fp | 220 °F | | storage temp. | Store at +5°C to +30°C. | | solubility | toluene: soluble(lit.) | | form | Liquid | | pka | -0.65±0.20(Predicted) | | color | Clear | | explosive limit | 1.3-8.4%(V) | | Water Solubility | freely soluble | | Sensitive | Hygroscopic | | Merck | 14,3249 | | BRN | 108808 | | InChIKey | CYSGHNMQYZDMIA-UHFFFAOYSA-N | | LogP | -0.3 at 25℃ | | CAS DataBase Reference | 80-73-9(CAS DataBase Reference) | | NIST Chemistry Reference | 1,3-Dimethyl-2-imidazolidinone(80-73-9) | | EPA Substance Registry System | N,N'-Dimethylimidazolidinone (80-73-9) |
| Hazard Codes | Xn,Xi | | Risk Statements | 21/22-38-41-36/38-62-22 | | Safety Statements | 26-36-36/37/39-36/37 | | RIDADR | UN 2810 6.1/PG 3 | | WGK Germany | 3 | | RTECS | NJ0660000 | | F | 3 | | Autoignition Temperature | 305 °C | | Hazard Note | Harmful/Irritant | | TSCA | Yes | | HazardClass | 6.1 | | PackingGroup | Ⅲ | | HS Code | 29332990 | | Toxicity | LD50 orally in Rabbit: 1261 mg/kg LD50 dermal Rabbit 986 mg/kg |
| | 1,3-Dimethyl-2-imidazolidinone Usage And Synthesis |
| Description | DMI, a high purity aprotic solvent, is composed of nitrogen containing five membered ring compound and widely recognized as an epoch making solvent. It is a colorless, transparent, high polar solvent with high thermal and chemical stability and non-corrosiveness. The material has a high boiling point of 222° C, a high flash point of 120° C (open method) / 95° C (close method), and a low melting point of 7.5° C. | | Chemical Properties | Almost colorless, clear liquid | | Uses | 1,3-Dimethyl-2-imidazolidinone may be used:
- As substitute solvent for hexamethylphosphoric triamide (HMPA) in the synthesis of 1,2-bis(trimethylsilyl)benzene.
- As solvent during the α-regioselective prenylation of imine.
- As component of mobile phase for the size-exclusion chromatographic analysis of cellulose.
| | Uses | 1,3-Dimethyl-2-imidazolidinone is used as a high-boiling polar aprotic solvent. It is used as a substitute solvent for toxic hexamethylphosphoramide. It finds application in detergents, dyestuffs, electronic materials and in the manufacture of polymers. It is involved in the preparation of 1,2-bis(trimethylsilyl)benzene. Further, it is utilized as a solvent during alfa-regioselective prenylation of imines. In addition to this, it constitutes the mobile phase during size-exclusion chromatographic analysis of cellulose. | | Uses | DMI can be used in a variety of applications including detergents, dyestuffs, electronic materials and in the manufacture of polymers. Its versatility can be attributed to it. Of particular note are its excellent solubility for inorganic and organic compounds and high dielectric constant and solvation effect. | | Definition | ChEBI: 1,3-Dimethyl-2-imidazolidinon is an imidazolidinone. | | General Description | 1,3-Dimethyl-2-imidazolidinone (DMI) is an imidazolidine derivative. It is reported to act as a promoter by minimizing the formation of dialkylation byproducts and accelerating the rate of monoalkylation of γ-butyrolactone. Conversion of CO2 to form lower alcohols by homogeneous catalytic hydrogenation using DMI as solvent has been investigated. | | Flammability and Explosibility | Non flammable |
| | 1,3-Dimethyl-2-imidazolidinone Preparation Products And Raw materials |
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