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Tc still has same +7 state after reaction with H2S, so not a reduction
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{{chembox
{{chembox
| Watchedfields = changed
| verifiedrevid = 412782093
| verifiedrevid = 446484697
| ImageFile = Sodium-pertechnetate-2D.png
| ImageFile = Sodium-pertechnetate-2D.png
| ImageAlt = Structural formula of sodium pertechnetate
| ImageSize =
| ImageFile1 = Sodium pertechnetate 3D spacefill.png
| ImageAlt1 = Space-filling models of the component ions of sodium pertechnetate
| IUPACName = Sodium technetate(VII)
| IUPACName = Sodium technetate(VII)
| OtherNames = sodium tetraoxotechnetate (VII)
| OtherNames = sodium tetraoxotechnetate (VII)
| Section1 = {{Chembox Identifiers
|Section1={{Chembox Identifiers
| index1_label={{simpleNuclide|Tc|99}}
| CASNo = 13718-28-0
| CASNo_Ref = {{cascite|correct|CAS}}
|
CASNo_Ref = {{cascite|correct|CAS}}
| ChemSpiderID = 64887107
| PubChem =
| SMILES =
| =
| PubChem = 74086836
}}
| PubChem1 =23689036
| Section2 = {{Chembox Properties
| UNII = A0730CX801
| Formula = NaTcO<sub>4</sub>
| SMILES = [Na+].[O-][Tc](=O)(=O)=O
| MolarMass = 169.89 g/mol
| SMILES1=[O-][99Tc](=O)(=O)=O.[Na+]
| Appearance = White or pale pink solid
| StdInChI=1S/Na.4O.Tc/q+1;;;;-1;
| Density =
| StdInChIKey = MKADDTFVKFMZGF-UHFFFAOYSA-N
| MeltingPt =
}}
| BoilingPt =
|Section2={{Chembox Properties
| Solubility = Soluble
| Formula = NaTcO<sub>4</sub>
}}
| MolarMass = 169.89 g/mol
| Section3 = {{Chembox Hazards
| Appearance = White or pale pink solid
| MainHazards =
| FlashPt =
| =
| MeltingPt = < {{convert|1063|K|C F}}<ref name="german2017"/>
| Autoignition =
| BoilingPt =
}}
| Solubility = Soluble
| Section8 = {{Chembox Related
}}
| OtherAnions = [[Sodium permanganate]]; [[sodium perrhenate]]
|Section3={{Chembox Hazards
| OtherCations = [[Ammonium pertechnetate]]
| OtherFunctn =
| =
| Function =
| =
| AutoignitionPt =
| OtherCpds = [[Technetium heptoxide]]}}
}}
|Section4={{Chembox Structure
|Structure_ref = <ref name="german2017">{{cite journal |last1=German |first1=Konstantin E. |last2=Grigoriev |first2=Mikhail S. |last3=Garashchenko |first3=Bogdan L. |last4=Kopytin |first4=Alexander V. |last5=Tyupina |first5=Ekaterina A. |title=Redetermination of the crystal structure of {{chem|Na|Tc|O|4}} at 100 and 296 K based on single-crystal X-ray data |journal=Acta Crystallographica Section E |date=1 July 2017 |volume=73 |issue=7 |pages=1037–1040 |doi=10.1107/S2056989017008362|pmid=28775877 |pmc=5499285 |s2cid=31507873 }}</ref>
|CrystalStruct = [[Scheelite]]
|SpaceGroup = I4<sub>1</sub>/a
| LattConst_a = {{val|5.3325|(1)||ul=Å}}
| LattConst_c = {{val|11.8503|(3)|u=Å}}
| UnitCellFormulas = 4
}}
}}
|Section8={{Chembox Related
'''Sodium pertechnetate''' is the [[inorganic compound]] with the formula NaTcO<sub>4</sub>. This colourless salt consists of the anion [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup>. The radioactive <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> anion is an important [[radiopharmaceutical]] for [[medical diagnosis|diagnostic]] use. The advantages to <sup>99m</sup>Tc include its short [[half-life]] of 6 hours and the low radiation exposure to the patient, which allow a patient to be injected with activities of more than 30 millicuries.<ref name=schwochau>{{cite journal | author = Schwochau, K. | year = 1994 | title = Technetium Radiopharmaceuticals-Fundamentals, Synthesis, Structure, and Development | journal = [[Angew. Chem. Int. Ed. Engl.]] | volume = 33 | pages = 2258–2267 | doi = 10.1002/anie.199422581 | issue = 22}}</ref> Na[<sup>99m</sup>TcO<sub>4</sub>] is a precursor to a variety of derivatives that are used to image different parts of the body.
| OtherAnions = [[Sodium permanganate]]; [[sodium perrhenate]]
| OtherCations = [[Ammonium pertechnetate]]
| OtherFunction =
| OtherFunction_label =
| OtherCompounds = [[Technetium heptoxide]]}}
}}
'''Sodium pertechnetate''' is the [[inorganic compound]] with the formula NaTcO<sub>4</sub>. This colourless salt contains the [[pertechnetate]] anion, {{chem|Tc|O|4|-}} that has slightly distorted tetrahedron symmetry both at 296 K and at 100 K<ref>{{cite journal |last1=German |first1=K. E. |last2=Grigoriev |first2=M. S. |last3=Garashchenko |first3=B. L. |last4=Kopytin |first4=A. V. |last5=Tyupina |first5=E. A. |date=2017-07-01 |title=Redetermination of the crystal structure of NaTcO4 at 100 and 296 K based on single-crystal X-ray data |url=https://scripts.iucr.org/cgi-bin/paper?wm5391 |journal=Acta Crystallographica Section E: Crystallographic Communications |language=en |volume=73 |issue=7 |pages=1037–1040 |doi=10.1107/S2056989017008362 |issn=2056-9890 |pmc=5499285 |pmid=28775877}}</ref> while the coordination polyhedron of the [https://journals.iucr.org/e/issues/2017/07/00/wm5391/wm5391fig3.html sodium cation] is different from typical for [[scheelite]] structure. The radioactive {{chem|{{simpleNuclide|Tc|99|m}}|O|4|-}} anion is an important [[radiopharmaceutical]] for [[medical diagnosis|diagnostic]] use. The advantages to {{simpleNuclide|Tc|99|m}} include its short [[half-life]] of 6 hours and the low radiation exposure to the patient, which allow a patient to be injected with activities of more than 30 millicuries.<ref name=schwochau>{{cite journal | author = Schwochau, K. | year = 1994 | title = Technetium Radiopharmaceuticals-Fundamentals, Synthesis, Structure, and Development | journal = [[Angew. Chem. Int. Ed. Engl.]] | volume = 33 | pages = 2258–2267 | doi = 10.1002/anie.199422581 | issue = 22}}</ref> {{chem|Na|[|{{simpleNuclide|Tc|99|m}}O|4|]}} is a precursor to a variety of derivatives that are used to image different parts of the body.


==Chemistry==
==Chemistry==
[TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> is the starting material for most of the chemistry of technetium. Pertechnetate salts are usually colorless.<ref>Wells, A. F.; Structural Inorganic Chemistry; Clarendon Press: Oxford, Great Britain; 1984; p. 1050.</ref> [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> is produced by oxidizing technetium with nitric acid or with hydrogen peroxide. The pertechnetate anion is similar to the [[permanganate]] anion but is a weaker [[oxidizing agent]]. It is tetrahedral and diamagnetic. The standard electrode potential for TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup>/TcO<sub>2</sub> is only +0.738 V in acidic solution, as compared to +1.695 V for MnO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup>/MnO<sub>2</sub>.<ref name=schwochau/> Because of its diminished oxidizing power, [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> is stable in alkaline solution. [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> is more similar to ReO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup>. Depending of the reducing agent, [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> can be converted to derivatives containing Tc(VI), Tc(V), and Tc(IV).<ref>''Encyclopedia Britannica: Technetium''</ref> In the absence of strong complexing ligands, TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> is reduced to a +4 oxidation state via the formation of TcO<sub>2</sub> hydrate.<ref name=schwochau />
4 is the starting material for most of the chemistry of technetium. Pertechnetate salts are usually colorless.<ref>Wells, A. F.; Structural Inorganic Chemistry; Clarendon Press: Oxford, Great Britain; 1984; p. 1050.</ref> 4 is produced by oxidizing technetium with nitric acid or with hydrogen peroxide. The pertechnetate anion is similar to the [[permanganate]] anion but is a weaker [[oxidizing agent]]. It is tetrahedral and diamagnetic. The standard electrode potential for 4/2 is only +0.738 V in acidic solution, as compared to +1.695 V for 4/2.<ref name=schwochau/> Because of its diminished oxidizing power, 4 is stable in alkaline solution. 4 is more similar to 4. Depending the reducing agent, 4 can be converted to derivatives containing Tc(VI), Tc(V), and Tc(IV).<ref>'' Britannica: Technetium''</ref> In the absence of strong complexing ligands, 4 is reduced to a +4 oxidation state via the formation of 2 hydrate.<ref name=schwochau />


==Pharmaceutical use==
==Pharmaceutical use==
The half-life of <sup>99m</sup>Tc is long enough that labelling synthesis of the [[radiopharmaceutical]] and scintigraphic measurements can be performed without significant loss of radioactivity.<ref name=schwochau/> The energy emitted from <sup>99m</sup>Tc is 140 keV, which allows for the study of deep body organs. Radiopharmaceuticals have no intended pharmacologic effect and are used in very low concentrations. Radiopharmaceuticals containing <sup>99m</sup>Tc are currently being applied in the determining morphology of organs, testing of organ function, and scintigraphic and emission tomographic imaging. The gamma radiation emitted by the radionuclide allows organs to be imaged ''in vivo'' tomographically. Currently, over 80% of radiopharmaceuticals used clinically are labelled with <sup>99m</sup>Tc. A majority of radiopharmaceuticals labelled with <sup>99m</sup>Tc are synthesized by the reduction of the pertechnetate ion in the presence of ligands chosen to confer organ specificity of the drug. The resulting <sup>99m</sup>Tc compound is then injected into the body and a "gamma camera" is focused on sections or planes in order to image the spacial distribution of the <sup>99m</sup>Tc.
The half-life of Tc is long enough that labelling synthesis of the [[radiopharmaceutical]] and scintigraphic measurements can be performed without significant loss of radioactivity.<ref name=schwochau/> The energy emitted from Tc is 140 keV, which allows for the study of deep body organs. Radiopharmaceuticals have no intended pharmacologic effect and are used in very low concentrations. Radiopharmaceuticals containing Tc are currently being applied in the determining morphology of organs, testing of organ function, and scintigraphic and emission tomographic imaging. The gamma radiation emitted by the radionuclide allows organs to be imaged ''in vivo'' tomographically. Currently, over 80% of radiopharmaceuticals used clinically are labelled with Tc. A majority of radiopharmaceuticals labelled with Tc are synthesized by the reduction of the pertechnetate ion in the presence of ligands chosen to confer organ specificity of the drug. The resulting Tc compound is then injected into the body and a "gamma camera" is focused on sections or planes in order to image the distribution of the Tc.


===Specific imaging applications===
===Specific imaging applications===
<sup>99m</sup>Tc is used primarily in the study of the thyroid gland - its morphology, vascularity, and function. [TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> and [[iodide]], due to their comparable charge/radius ratio, are similarly incorporated into the thyroid gland. The pertechnetate ion is not incorporated into the [[thyroglobulin]]. It is also used in the study of blood perfusion, regional accumulation, and cerebral lesions in the brain, as it accumulates primarily in the [[choroid plexus]].
Tc is used primarily in the study of the thyroid gland - its morphology, vascularity, and function. 4 and [[iodide]], due to their comparable charge/radius ratio, are similarly incorporated into the thyroid gland. The pertechnetate ion is not incorporated into the [[thyroglobulin]]. It is also used in the study of blood perfusion, regional accumulation, and cerebral lesions in the brain, as it accumulates primarily in the [[choroid plexus]].


Sodium pertechnetate cannot pass through the [[blood-brain barrier]]. In addition to the salivary and thyroid glands, <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> localizes in the stomach. <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> is renally eliminated for the first three days after being injected. After a scanning is performed, it is recommended that a patient drink large amounts of water in order to expedite elimination of the radionuclide.<ref>{{cite journal | author = Shukla, S. K., Manni, G. B., and Cipriani, C. | year = 1977 | title = The Behaviour of the Pertechnetate Ion in Humans | journal = [[Journal of Chromatography]] | volume = 143 | issue = 5 | pages = 522–526 | pmid = 893641 | doi = 10.1016/S0378-4347(00)81799-5}}</ref> Other methods of <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> administration include intraperitoneal, intramuscular, subcutaneous, as well as orally. The behavior of the <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> ion is essentially the same, with small differences due to the difference in rate of absorption, regardless of the method of administration.<ref>{{Cite journal | last1 = Razzak | first1 = M. A. | last2 = Naguib | first2 = M. | last3 = El-Garhy | first3 = M. | year = 1967 | title = Fate of Sodium Pertechnetate-Technetium-99m | url = | journal = Journal of Nuclear Medicine | volume = 8 | issue = 1| pages = 50–59 | pmid = 6019138 }}</ref>
Sodium pertechnetate cannot pass through the [[ barrier]]. In addition to the salivary and thyroid glands, 4 localizes in the stomach. 4 is renally eliminated for the first three days after being injected. After a scanning is performed, it is recommended that a patient drink large amounts of water in order to expedite elimination of the radionuclide.<ref>{{cite journal | author = Shukla, S. K., Manni, G. B., and Cipriani, C. | year = 1977 | title = The Behaviour of the Pertechnetate Ion in Humans | journal = [[Journal of Chromatography]] | volume = 143 | issue = 5 | pages = 522–526 | pmid = 893641 | doi = 10.1016/S0378-4347(00)81799-5}}</ref> Other methods of 4 administration include intraperitoneal, intramuscular, subcutaneous, as well as orally. The behavior of the 4 ion is essentially the same, with small differences due to the difference in rate of absorption, regardless of the method of administration.<ref>{{ journal | last1 = Razzak | first1 = M. A. | last2 = Naguib | first2 = M. | last3 = El-Garhy | first3 = M. | year = 1967 | title = Fate of Sodium Pertechnetate-Technetium-99m | journal = Journal of Nuclear Medicine | volume = 8 | issue = 1| pages = 50–59 | pmid = 6019138 }}</ref>

Other examples of organ-specific radiopharmaceuticals include:

==Preparation of <sup>99m</sup>TcO<sub>4</sub><sup>−</sup>==
<sup>99m</sup>Tc is conveniently available in high radionuclidic purity from [[molybdenum]]-99, which decays with 87% probability to <sup>99m</sup>Tc. The subsequent decay of <sup>99m</sup>Tc leads to either <sup>99</sup>Tc or <sup>99</sup>Rb. <sup>99</sup>Mo can be produced in a nuclear reactor via [[irradiation]] of either molybdenum-98 or naturally occurring molybdenum with thermal neutrons, but this is not the method currently in use today. Currently, <sup>99</sup>Mo is recovered as a product of the nuclear fission reaction of <sup>235</sup>U,<ref>{{cite journal | author = Beasley, T. M., Palmer, H. E., and Nelp, W. B. | year = 1966 | title = Distriubtion and Excretion of Technetium in Humans | journal = [[Health Physics]] | volume = 12 | issue = 10 | pages = 1425–1435 | url = http://www.health-physics.com/pt/re/healthphys/abstract.00004032-196610000-00004.htm | doi = 10.1097/00004032-196610000-00004 | pmid=5972440}}</ref> separated from other fission products via a multistep process and loaded onto a column of alumina that forms the core of a <sup>99</sup>Mo/<sup>99m</sup>Tc radioisotope "generator".

As the <sup>99</sup>Mo continuously decays to <sup>99m</sup>Tc, the <sup>99m</sup>Tc can be removed periodically (usually daily) by flushing a saline solution (0.15 M NaCl in water) through the alumina column: the more highly charged <sup>99</sup>MoO<sub>4</sub><sup>2−</sup> is retained on the column, where it continues to undergo radioactive decay, while the medically useful radioisotope <sup>99m</sup>TcO<sub>4</sub><sup>−</sup> is eluted in the saline. The eluate from the column must be sterile and pyrogen free, so that the Tc drug can be used directly, usually within 12 hours of elution.<ref name=schwochau/> In a few cases, sublimation or solvent extraction may be used.

==Synthesis of <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> radiopharmaceuticals==
<sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> is advantageous for the synthesis of a variety of radiopharmaceuticals because Tc can adopt a number of oxidation states.<ref name=schwochau/> The oxidation state and coligands dictate the specificity of the radiopharmaceutical. The starting material Na<sup>99m</sup>TcO<sub>4</sub>, made available after elution from the generator column, as mentioned above, can be reduced in the presence of complexing ligands. Many different reducing agents can be used, but transition metal reductants are avoided because they compete with <sup>99m</sup>Tc for ligands. Oxalates, formates, hydroxylamine, and hydrazine are also avoided because they form complexes with the technetium. Electrochemical reduction is impractical.

Ideally, the synthesis of the desired radiopharmaceutical from <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup>, a reducing agent, and desired ligands should occur in one container after elution, and the reaction must be performed in a solvent that can be injected intravenously, such as a saline solution. Kits are available that contain the reducing agent, usually tin(II) and ligands. These kits are sterile, pyrogen-free, easily purchased, and can be stored for long periods of time. The reaction with <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> takes place directly after elution from the generator column and shortly before its intended use. A high organ specificity is important because the injected activity should accumulate in the organ under investigation, as there should be a high activity ratio of the target organ to nontarget organs. If there is a high activity in organs adjacent to the one under investigation, the image of the target organ can be obscured. Also, high organ specificity allows for the reduction of the injected activity, and thus the exposure to radiation, in the patient. The radiopharmaceutical must be kinetically inert, in that it must not change chemically ''in vivo'' en route to the target organ.

===Examples===
*A complex that can penetrate the blood-brain barrier is generated by reduction of <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> with tin(II) in the presence of the ligand "''d,l''-[[HMPAO]]" to form TcO-''d,l''-HMPAO (HM-PAO is hexamethylpropyleneamino [[oxime]]).
*A complex that for imaging the lungs, "[[Tc-MAA]]," is generated by reduction of <sup>99m</sup>TcO<sub>4</sub><sup>−</sup> with SnCl<sub>2</sub> in the presence of human serum albumin.
*[<sup>99m</sup>Tc(OH<sub>2</sub>)<sub>3</sub>(CO)<sub>3</sub>]<sup>+</sup>, which is both water and air stable, is generated by reduction of <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> with carbon monoxide. This compound is a precursor to complexes that can be used in cancer diagnosis and therapy involving DNA-DNA pretargeting.<ref>{{cite journal | author = R. Alberto, R. Schibli, A. Egli, A. P. Schubiger, U. Abram and T. A. Kaden | title = A Novel Organometallic Aqua Complex of Technetium for the Labeling of Biomolecules: Synthesis of [<sup>99m</sup>Tc(OH<sub>2</sub>)<sub>3</sub>(CO)<sub>3</sub>]<sup>+</sup> from [<sup>99m</sup>TcO<sub>4</sub>]<sup><nowiki>&minus;</nowiki></sup> in Aqueous Solution and Its Reaction with a Bifunctional Ligand | year = 1998 | journal = [[J. Am. Chem. Soc.]] | volume = 120 | issue = 31 | pages = 7987–7988 | doi = 10.1021/ja980745t}}</ref>


==Other reactions involving the pertechnetate ion==
==Other reactions involving the pertechnetate ion==
*Radiolysis of TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> in nitrate solutions proceeds through the reduction to TcO<sub>4</sub><sup>2<nowiki>&minus;</nowiki></sup> which induces complex disproportionation processes:
*Radiolysis of 4 in nitrate solutions proceeds through the reduction to 42 which induces complex disproportionation processes:
:<math chem>\begin{array}{l}
:: TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> + e<sup><nowiki>&minus;</nowiki></sup> → TcO<sub>4</sub><sup>2<nowiki>&minus;</nowiki></sup>
\ce{{TcO4^-} + {e^-} -> TcO4^2-} \\
:: 2 TcO<sub>4</sub><sup>2<nowiki>&minus;</nowiki></sup> → TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> + Tc(V)
\ce{2TcO4^{2-} -> {TcO4^-} + Tc^V} \\
::2 Tc(V) → TcO<sub>4</sub><sup>2<nowiki>&minus;</nowiki></sup> + Tc(IV)
\ce{2Tc^V -> {TcO4^{2-}} + Tc^{IV}} \\
::Tc(V) + TcO<sub>4</sub><sup>2<nowiki>&minus;</nowiki></sup> → Tc(IV) + TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup>
\ce{{Tc^V} + TcO4^{2-} -> {Tc^{IV}} + TcO4-}
*Pertechnetate can be reduced by [[Hydrogen sulfide|H<sub>2</sub>S]] to give Tc<sub>2</sub>S<sub>7</sub>.<sup>10</sup>
\end{array}</math>
*Pertechnetate is also be reduced to Tc(IV/V) compounds in alkaline solutions in nuclear waste tanks without adding catalytic metals, reducing agents, or external radiation. Reactions of mono- and disaccharides with <sup>99m</sup>TcO<sub>4</sub><sup><nowiki>&minus;</nowiki></sup> yield Tc(IV) compounds that are water soluble.<ref>{{cite journal | author = D. E. Berning, N. C. Schroeder and R. M. Chamberlin | title = The autoreduction of pertechnetate in aqueous, alkaline solutions | year = 2005 | journal = [[Journal of Radioanalytical and Nuclear Chemistry]] | volume = 263 | issue = 3| pages = 613–618 | doi = 10.1007/s10967-005-0632-x}}</ref>
*Pertechnetate can react with {{chem|link=Hydrogen sulfide|H|2|S}} to give {{chem|Tc|2|S|7}}.<ref>{{cite book|last1=Emeléus|first1=H. J.|url=https://books.google.com/books?id=-SnCsg5jM_kC&pg=PA26|title=Advances in Inorganic Chemistry and Radiochemistry, Volume 11|last2=Sharpe|first2=A. G.|date=1968|publisher=Academic Press|isbn=978-0-08-057860-6|pages=26}}</ref>
*Pertechnetate can also be reduced to Tc(IV/V) compounds in alkaline solutions in nuclear waste tanks without adding catalytic metals, reducing agents, or external radiation. Reactions of mono- and disaccharides with {{chem|{{simpleNuclide|Tc|99|m}}|O|4|-}} yield Tc(IV) compounds that are water-soluble.<ref>{{cite journal | author = D. E. Berning, N. C. Schroeder and R. M. Chamberlin | title = The autoreduction of pertechnetate in aqueous, alkaline solutions | year = 2005 | journal = [[Journal of Radioanalytical and Nuclear Chemistry]] | volume = 263 | issue = 3| pages = 613–618 | doi = 10.1007/s10967-005-0632-x| s2cid = 95071892 | url = https://zenodo.org/record/1232814 }}</ref>


==References==
==References==
{{reflist}}
{{reflist}}
<!-- Dead note "7": Lukens, W. W., Bucher, J. J., Edelstein, N. M., and Shuh, D. K. (2001) Radiolysis of <sup>99m</sup>TcO<sub>4</sub><sup>-</sup> in Alkaline, Nitrate Solutions: Reduction by NO<sub>3</sub><sup>2-</sup>. ''J. Phys. Chem. A,'' ''105'', 9611-9615. -->
<!-- Dead note "7": Lukens, W. W., Bucher, J. J., Edelstein, N. M., and Shuh, D. K. (2001) Radiolysis of 4- in Alkaline, Nitrate Solutions: Reduction by NO<sub>3</sub><sup></sup>. ''J. Phys. Chem. A,'' ''105'', 9611-9615. -->


{{Technetium compounds}}
{{Sodium compounds}}
{{Sodium compounds}}
{{Thyroid therapy}}
{{Thyroid therapy}}
{{Thyroid hormone receptor modulators}}


[[Category:Pertechnetates]]
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