| Weight | 116.164 g/mol |
|---|---|
| Formula | C5H12N2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
TETRAMETHYLUREA (632-22-4)
1,1,3,3-tetramethylurea
Score:
#1522 in Physics
,
#4525 in Chemistry
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- Comparison between the use of isopropanol and tetramethylurea for the solubilisation and quantitation of human serum very low density apollpoproteins (Analytical Biochemistry, 1978)
- Influence of Concentration and Temperature on the Dynamics of Water in the Hydrophobic Hydration Shell of Tetramethylurea (Journal of the American Chemical Society, 2010)
- Infrared Spectra of Complexes of Metal Halides with Tetramethylurea and Tetramethylthiourea (Inorganic Chemistry, 1966)
- Solvation Structures of Manganese(II), Iron(II), Cobalt(II), Nickel(II), Copper(II), Zinc(II), Cadmium(II), and Indium(III) Ions in 1,1,3,3-Tetramethylurea As Studied by EXAFS and Electronic Spectroscopy. Variation of Coordination Number (Inorganic Chemistry, 1994)
- Proton Magnetic Resonance CoordinationNumber Study of AlCl3 in Aqueous Mixtures of Acetone, N,NDimethylformamide, Dimethylsulfoxide, Dioxane, Tetrahydrofuran, and Tetramethylurea (Journal of Chemical Physics, 1967)
- Small-angle neutron scattering in aqueous solutions of tetramethylurea (The Journal of Physical Chemistry, 1992)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,1,3,3-tetramethylurea
-
SMILESCN(C)C(=O)N(C)C
-
InChIKeyAVQQQNCBBIEMEU-UHFFFAOYSA-N
- Pubchem - TETRAMETHYLUREA
- Wikipedia - tetramethylurea
Tetramethylurea is a aprotic-polar solvent for organic compounds, especially for aromatic compounds and is used e. g. for Grignard reagents.
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TETRAMETHYLUREA
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