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Merck
CN

T8266

Thallium(I) acetate

≥99%

Synonym(s):

Acetic acid thallium(I) salt

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About This Item

Linear Formula:
CH3COOTl
CAS Number:
Molecular Weight:
263.43
UNSPSC Code:
12352103
NACRES:
NA.23
PubChem Substance ID:
EC Number:
209-257-5
Beilstein/REAXYS Number:
3693914
MDL number:
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Product Name

Thallium(I) acetate, ≥99%

form

powder

InChI key

HQOJMTATBXYHNR-UHFFFAOYSA-M

InChI

1S/C2H4O2.Tl/c1-2(3)4;/h1H3,(H,3,4);/q;+1/p-1

SMILES string

CC(=O)O[Tl]

assay

≥99%

reaction suitability

core: thallium
reagent type: catalyst

Quality Level

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Application

Thallium(I) acetate can be used as:
  • A thallium precursor in sol-gel methods to synthesize Tl-2212 (Tl₂Ba₂CaCu₂O₈₋δ) superconducting films.
  • A catalyst in organic synthesis, facilitating reactions such as the conversion of alkenes to alkynes under controlled conditions. This application is supported by its role in specialized catalytic cycles.
  • A precursor in material science for synthesizing thallium-containing compounds, including optical glasses and high-density solutions for ore separation processes.

General description

Thallium(I) acetate (TlOAc) is a white crystalline compound with moderate water solubility, commonly used in specialized chemical synthesis and material science. Its unique Lewis acid-base properties (boron as Lewis acid, amine as Lewis base) and reactivity make it valuable in catalysis and energy applications. Due to its hazardous nature, it requires careful handling.

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Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

铊类化学品
危险化学品
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Properties and Structures of Thallium (I) Derivatives of Aromatic Diols.
El-Hadad AA, et al.
Inorganic Chemistry, 34(1), 120-123 (1995)
V Eybl et al.
Ceskoslovenska farmacie, 41(7-8), 243-245 (1992-10-01)
Experiments carried out on male mice (ICR) demonstrated a protective effect of premedication with the preparation Sho-Saiko-To (TJ 9, Tsumura and Comp.) against the hepatotoxic effects of CCl4 and T1-acetate, which were manifested by increased peroxidation of lipids and increased
H Wiegand et al.
Archives of toxicology, 58(4), 265-270 (1986-04-01)
Endplate potentials (EPP's) and miniature endplate potentials (MEPP's) were recorded from neuromuscular junctions of the mouse phrenic nerve-diaphragm preparation, blocked by high Mg++ (12 X 10(-3) mol/l)-Ringer. Superfusion of the preparations with Mg++-Ringer solutions containing thallium acetate (5 X 10(-4)
J G Tully et al.
Sexually transmitted diseases, 10(4 Suppl), 256-260 (1983-10-01)
Specimens from the cervix or posterior vaginal fornix of 50 women attending a venereal disease clinic and from the urethra of 50 men with nongonococcal urethritis were cultured for Mycoplasma hominis. Recovery of the organism in two conventional mycoplasma culture
Summertime.
Robin Ferner
BMJ (Clinical research ed.), 344, e4245-e4245 (2012-06-22)

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