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Merck

T24503

Sigma-Aldrich

Tetramethylurea

99%

Sinónimos:

1,1,3,3-Tetramethylurea, TMU

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About This Item

Fórmula lineal:
(CH3)2NCON(CH3)2
Número de CAS:
Peso molecular:
116.16
Beilstein/REAXYS Number:
773898
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

refractive index

n20/D 1.451 (lit.)

bp

177 °C (lit.)
62-63 °C/12 mmHg (lit.)

mp

−1 °C (lit.)

density

0.968 g/mL at 20 °C (lit.)

SMILES string

CN(C)C(=O)N(C)C

InChI

1S/C5H12N2O/c1-6(2)5(8)7(3)4/h1-4H3

InChI key

AVQQQNCBBIEMEU-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Application

  • Role of Tetramethylurea in Synthesizing Mesoporous Alumina: Tetramethylurea was used to synthesize mesoporous alumina via a hydrothermal method, affecting pore structure and thermal stability (Ghosh et al., 2014).

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Repr. 1B - Skin Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

167.0 °F - closed cup

flash_point_c

75 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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Y L A Rezus et al.
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We have used femtosecond midinfrared spectroscopy to study the orientational mobility of water molecules in the hydration shells of hydrophobic groups. Our results show that hydrophobic groups are surrounded by a number of water molecules that display much slower orientational
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Journal of the American Chemical Society, 132(44), 15671-15678 (2010-10-19)
We study the influence of the amphipilic compound tetramethylurea (TMU) on the dynamical properties of water, using dielectric relaxation spectroscopy in the regime between 0.2 GHz and 2 THz. This technique is capable of resolving different water species, their relative
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We have developed what we call the 1-propanol(1P) probing methodology. By using it, we determined the relative hydrophobicity/hydrophilicity indices of 2-butoxyethanol, a typical hydrophobe; urea, a typical hydrophile; and trimethylamine-N-oxide, an amphiphile. By comparing these indices with those for other
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