GF39171517
Terbium
foil, 50x50mm, thickness 0.1mm, as rolled, 99%
Synonym(s):
Terbium, TB000210
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About This Item
Empirical Formula (Hill Notation):
Tb
CAS Number:
Molecular Weight:
158.93
MDL number:
UNSPSC Code:
12141614
PubChem Substance ID:
NACRES:
NA.23
Assay
99%
form
foil
manufacturer/tradename
Goodfellow 391-715-17
resistivity
116 μΩ-cm, 20°C
size × thickness
50x50 mm × 0.1 mm
bp
3230 °C (lit.)
mp
1356 °C (lit.)
density
8.234 g/mL at 25 °C (lit.)
SMILES string
[Tb]
InChI
1S/Tb
InChI key
GZCRRIHWUXGPOV-UHFFFAOYSA-N
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Kamal P Mani et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 148, 412-419 (2015-04-29)
Terbium molybdate nanophosphors were synthesized through a facile sol-gel route. The structure of the phosphors was characterized by X-ray diffraction, Raman spectra and Fourier transform infrared spectroscopy analysis. The X-ray diffraction studies revealed that the structure of the nanophosphor gradually
Lei Rao et al.
International journal of food microbiology, 205, 73-80 (2015-04-19)
The objective of this study was to investigate the inactivation of the Bacillus subtilis spores by high pressure CO2 combined with high temperature (HPCD+HT) and to analyze the clumping effect of the spores on their HPCD+HT resistance. The spores of
Dinari A Harris et al.
Current protocols in nucleic acid chemistry, Chapter 6, Unit 6-Unit 6 (2008-04-23)
The function of an RNA molecule is determined by its overall secondary and tertiary structure. The tertiary structure is facilitated and stabilized by the interaction with metal ions. The current chapter offers a detailed protocol on the use of the
Zhi Shi et al.
Cancer research, 75(1), 147-158 (2014-11-02)
Cables1 is a candidate tumor suppressor that negatively regulates cell growth by inhibiting cyclin-dependent kinases. Cables1 expression is lost frequently in human cancer but little is known about its regulation. Here, we report that Cables1 levels are controlled by a
Xavier Sainsily et al.
Biochemical pharmacology, 92(2), 280-288 (2014-09-02)
The vasoactive urotensin-II (UII), a cyclic undecapeptide widely distributed in cardiovascular, renal and endocrine systems, specifically binds the UII receptor (UT receptor), a G protein-coupled receptor (GPCR). The involvement of this receptor in numerous pathophysiological conditions including atherosclerosis, heart failure
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