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204609

Sigma-Aldrich

Thallium(I)-nitrat

99.999% trace metals basis

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About This Item

Lineare Formel:
TlNO3
CAS-Nummer:
10102-45-1
Molekulargewicht:
266.39
EG-Nummer:
233-273-1
MDL-Nummer:
MFCD00011280
UNSPSC-Code:
12352302
PubChem Substanz-ID:
24852281
NACRES:
NA.23

Qualitätsniveau

200

Assay

99.999% trace metals basis

Form

solid

Eignung der Reaktion

core: thallium

mp (Schmelzpunkt)

206 °C (lit.)

SMILES String

[Tl+].[O-][N+]([O-])=O

InChI

1S/NO3.Tl/c2-1(3)4;/q-1;+1

InChIKey

FYWSTUCDSVYLPV-UHFFFAOYSA-N

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Anwendung

  • Thallium(I) nitrate: Primarily used in the synthesis of other thallium compounds due to its reactivity and solubility. It finds applications in the production of special glasses where thallium improves the refractive index and density of the glass. Caution is advised in its use due to its high toxicity and potential environmental impact (Sigma-Aldrich, CAS 10102-45-1).

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Ox. Sol. 3 - STOT RE 2

Lagerklassenschlüssel

5.1B - Oxidizing hazardous materials

WGK

WGK 3

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Analysenzertifikate (COA)

Lot/Batch Number
BCCM3336
BCCK6263
BCCG6317
BCCF4399
BCCB4868

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Vânia M T Carneiro et al.
The Journal of organic chemistry, 75(9), 2877-2882 (2010-04-10)
A diastereoselective route to (+)-bakkenolide A is presented from the readily available optically active Wieland-Miescher ketone. This novel synthesis of this sesquiterpene lactone features the following as key stereoselective transformations: (i) the ring contraction reaction of a octalone mediated by
Cecilia Eliana Hanzel et al.
Toxicology and applied pharmacology, 236(1), 59-70 (2009-04-18)
Thallium (Tl) is a highly toxic metal though yet its mechanisms are poorly understood. Previously, we demonstrated that rat pheochromocytoma (PC12) cells exposure to thallous (Tl(I)) or thallic (Tl(III)) cations leads to mitochondrial damage and reduced cell viability. In the
P Thanigaimalai et al.
Bioorganic & medicinal chemistry, 18(12), 4441-4445 (2010-05-18)
The oxidative cyclization of 2'-hydroxy-6'-cyclohexylmethoxychalcones 5 using thallium (III) nitrate (TTN) in alcoholic solvents produced isoflavones 2 and (or) aurones 3 depending on the electronic nature of p-substituents on ring B. Chalcones with strong electron donating substituents (OH, OCH(3)) were
A Salinas-Castillo et al.
Analytical and bioanalytical chemistry, 376(7), 1111-1114 (2003-06-28)
The applicability of heavy atom-induced room-temperature phosphorescence to pharmaceutical samples is demonstrated in this work. Thus a new, simple, rapid, and selective phosphorimetric method for dipyridamole determination is proposed. The phosphorescence signals are a consequence of intermolecular protection when analytes
Sergey M Korotkov
Journal of bioenergetics and biomembranes, 41(3), 277-287 (2009-07-25)
It is known that permeability of the inner mitochondrial membrane is low to most univalent cations (K(+), Na(+), H(+)) but high to Tl(+). Swelling, state 4, state 3, and 2,4-dinitrophenol (DNP)-stimulated respiration as well as the membrane potential (DeltaPsi(mito)) of
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