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About This Item
Linear Formula:
TlNO3
CAS Number:
Molecular Weight:
266.39
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
assay
99.999% trace metals basis
form
solid
reaction suitability
core: thallium
mp
206 °C (lit.)
SMILES string
[Tl+].[O-][N+]([O-])=O
InChI
1S/NO3.Tl/c2-1(3)4;/q-1;+1
InChI key
FYWSTUCDSVYLPV-UHFFFAOYSA-N
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Application
- 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).
signalword
Danger
Hazard Classifications
Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - Ox. Sol. 3 - STOT RE 2
Storage Class
5.1B - Oxidizing hazardous materials
wgk_germany
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
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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
Tl+ increases the permeability of the inner membranes of rat liver mitochondria for monovalent cations.
S M Korotkov et al.
Doklady. Biochemistry and biophysics, 378, 145-149 (2001-11-20)
I A Skul'skiĭ et al.
Zhurnal evoliutsionnoi biokhimii i fiziologii, 24(6), 817-821 (1988-11-01)
Studies have been made of the effect of inhibitors of energy metabolism on maintenance of Na and K concentrations, as well as on accumulation of Rb (as an analogue of K) in single neurones of the mollusc P. corneus. Concentrations
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
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