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Pertechnetate
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<h2 id="chemistry">Chemistry</h2> <p>TcO−4 is the starting material for most of the chemistry of technetium. Pertechnetate salts are usually colorless.<a class="footnote-ref" id="fnref:5" href="#fn:5"><sup>5</sup></a> TcO−4 is produced by oxidizing technetium with nitric acid or with hydrogen peroxide. The pertechnetate anion is similar to the <a href="/facts/Permanganate/nJa04jVh">permanganate</a> anion but is a weaker <a href="/facts/Oxidizing_agent/1FQzB8pQ">oxidizing agent</a>. It is tetrahedral and diamagnetic. The standard electrode potential for TcO−4/TcO2 is only +0.738 V in acidic solution, as compared to +1.695 V for MnO−4/MnO2.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> Because of its diminished oxidizing power, TcO−4 is stable in alkaline solution. TcO−4 is more similar to <a href="/facts/Perrhenate/uKvDsaoY">ReO−4</a>. Depending on the reducing agent, TcO−4 can be converted to derivatives containing Tc(VI), Tc(V), and Tc(IV).<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> In the absence of strong complexing ligands, TcO−4 is reduced to a +4 oxidation state via the formation of TcO2 hydrate.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a> </p><p>Some metals like actinides,<a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a> barium, scandium, yttrium <a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a> or zirconium <a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a> may form complex salts with pertechnetate thus strongly effecting its liquid-liquid extraction behavior.<a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a> </p> <h2 id="preparation-of-99mtco4">Preparation of 99mTcO4−</h2> <p class="note">Main article: <a href="/facts/Technetium-99m_generator/Ys7Kjnmk">technetium-99m generator</a></p> <p>99mTc is conveniently available in high radionuclidic purity from <a href="/facts/Molybdenum/RX6vp2bF">molybdenum</a>-99, which decays with 87% probability to 99mTc. The subsequent decay of 99mTc leads to either 99Tc or 99Ru. 99Mo can be produced in a nuclear reactor via <a href="/facts/Irradiation/fHW0QNAa">irradiation</a> of either molybdenum-98 or naturally occurring molybdenum with thermal neutrons, but this is not the method currently in use today. Currently, 99Mo is recovered as a product of the nuclear fission reaction of <a href="/facts/Uranium-235/pe0RznDM">235U</a>,<a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> separated from other fission products via a multistep process and loaded onto a column of alumina that forms the core of a 99Mo/99mTc radioisotope generator. </p><p>As the 99Mo continuously decays to 99mTc, the 99mTc 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 99MoO2−4 is retained on the column, where it continues to undergo radioactive decay, while the medically useful radioisotope 99mTcO−4 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.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> In a few cases, sublimation or solvent extraction may be used. </p> <h3>Examples</h3> <ul><li>A complex that can penetrate the blood–brain barrier is generated by reduction of 99mTcO−4 with tin(II) in the presence of the ligand hexamethylpropylene amine oxime (HMPAO) to form <a href="/facts/Technetium_(99mTc)_exametazime/J4tW12pN">TcO-<i>D,L</i>-HMPAO</a>.</li> <li>A complex that for imaging the lungs, <a href="/facts/Tc-MAA/0v3xhNxF">Tc-MAA</a>, is generated by reduction of 99mTcO−4 with <a href="/facts/Tin(II)_chloride/4TdjMLEk">SnCl2</a> in the presence of human serum albumin.</li> <li>[99mTc(OH2)3(CO)3]+, which is both water and air stable, is generated by reduction of 99mTcO−4 with carbon monoxide. This compound is a precursor to complexes that can be used in cancer diagnosis and therapy involving DNA-DNA pretargeting.<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a></li></ul> <h2 id="compounds">Compounds</h2> <table><tbody><tr><th>Formula</th><th>name</th><th>crystal structure</th><th>cell dimensions (Å)</th><th>unit cell volume (Å3)</th><th>remarks</th><th>references</th></tr><tr><td>LiTcO4</td><td>lithium pertechnetate</td><td></td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a></td></tr><tr><td>LiTcO4·2H2O</td><td>lithium pertechnetate dihydrate</td><td></td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a></td></tr><tr><td>LiTcO4·3H2O</td><td>lithium pertechnetate trihydrate</td><td></td><td></td><td><i>P</i>t3/<i>mc</i></td><td></td><td><a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a></td></tr><tr><td>NaTcO4</td><td><a href="/facts/Sodium_pertechnetate/9bdHcur9">sodium pertechnetate</a></td><td>tetragonal</td><td>a = 5.342, c = 1.874</td><td>338.91</td><td>absorbs water from atmosphere</td><td><a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a></td></tr><tr><td>NaTcO4·H2O</td><td>sodium pertechnetate monohydrate</td><td></td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a></td></tr><tr><td>NaTcO4·2H2O</td><td>sodium pertechnetate dihydrate</td><td></td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a></td></tr><tr><td>NaTcO4·4H2O</td><td>sodium pertechnetate tetrahydrate</td><td></td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a></td></tr><tr><td>KTcO4</td><td>potassium pertechnetate</td><td>tetragonal</td><td>a = 5.647, c = 12.91</td><td>411.73</td><td>used to prepare radiopharmaceuticals</td><td><a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a></td></tr><tr><td>RbTcO4</td><td>rubidium pertechnetate</td><td>tetragonal</td><td>a = 5.762, c =13.543</td><td>449.65</td><td></td><td><a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a></td></tr><tr><td>α-CsTcO4</td><td>α-caesium pertechnetate</td><td>tetragonal</td><td>a = 5.898, c = 14.38</td><td></td><td>volatile at temperatures >470K</td><td><a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a></td></tr><tr><td>β-CsTcO4</td><td>β-caesium pertechnetate</td><td>orthorhombic</td><td>a = 5.737, b = 5.92, c = 14.341</td><td>486.38</td><td></td><td><a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a></td></tr><tr><td>TlTcO4</td><td>thallium pertechnetate</td><td>orthorhombic</td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:27" href="#fn:27"><sup>27</sup></a></td></tr><tr><td>TlTcO4</td><td>thallium pertechnetate</td><td>tetragonal</td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:28" href="#fn:28"><sup>28</sup></a></td></tr><tr><td>NH4TcO4</td><td><a href="/facts/Ammonium_pertechnetate/Ivm8RmMI">ammonium pertechnetate</a></td><td>tetragonal</td><td></td><td></td><td>technetium may be supplied in this form</td><td><a class="footnote-ref" id="fnref:29" href="#fn:29"><sup>29</sup></a></td></tr><tr><td>AgTcO4</td><td>silver pertechnetate</td><td>tetragonal</td><td></td><td></td><td></td><td><a class="footnote-ref" id="fnref:30" href="#fn:30"><sup>30</sup></a></td></tr></tbody></table> <h2 id="reactions">Reactions</h2> <ul><li>Radiolysis of TcO−4 in nitrate solutions proceeds through the reduction to TcO2−4 which induces complex disproportionation processes:</li></ul> TcO 4 − + e − ⟶ TcO 4 2 − 2 TcO 4 2 − ⟶ TcO 4 − + Tc V 2 Tc V ⟶ TcO 4 2 − + Tc IV Tc V + TcO 4 2 − ⟶ Tc IV + TcO 4 − {\displaystyle {\begin{array}{l}{\ce {{TcO4^{-}}+{e^{-}}->TcO4^{2}-}}\\{\ce {2TcO4^{2-}->{TcO4^{-}}+Tc^{V}}}\\{\ce {2Tc^{V}->{TcO4^{2-}}+Tc^{IV}}}\\{\ce {{Tc^{V}}+TcO4^{2-}->{Tc^{IV}}+TcO4-}}\end{array}}} <ul><li>Pertechnetate can be reduced by <a href="/facts/Hydrogen_sulfide/UbCqjMMk">H2S</a> to give Tc2S7.<a class="footnote-ref" id="fnref:31" href="#fn:31"><sup>31</sup></a></li> <li>Pertechnetate is also 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 99mTcO−4 yield Tc(IV) compounds that are water-soluble.<a class="footnote-ref" id="fnref:32" href="#fn:32"><sup>32</sup></a></li></ul> <h2 id="uses">Uses</h2> <h3>Pharmaceutical use</h3> <p>The half-life of 99mTc is long enough that labelling synthesis of the <a href="/facts/Radiopharmaceutical/x3g6zbB6">radiopharmaceutical</a> and scintigraphic measurements can be performed without significant loss of radioactivity.<a class="footnote-ref" id="fnref:33" href="#fn:33"><sup>33</sup></a> The energy emitted from 99mTc 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 99mTc 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 <i>in vivo</i> tomographically. Currently, over 80% of radiopharmaceuticals used clinically are labelled with 99mTc. A majority of radiopharmaceuticals labelled with 99mTc are synthesized by the reduction of the pertechnetate ion in the presence of ligands chosen to confer organ specificity of the drug. The resulting 99mTc compound is then injected into the body and a "gamma camera" is focused on sections or planes in order to image the spatial distribution of the 99mTc. </p> <h4>Specific imaging applications</h4> <p>99mTc is used primarily in the study of the thyroid gland - its morphology, vascularity, and function. TcO−4 and <a href="/facts/Iodide/JyVRGWMX">iodide</a>, due to their comparable charge/radius ratio, are similarly incorporated into the thyroid gland. The pertechnetate ion is not incorporated into the <a href="/facts/Thyroglobulin/whhQ9Dyb">thyroglobulin</a>. It is also used in the study of blood perfusion, regional accumulation, and cerebral lesions in the brain, as it accumulates primarily in the <a href="/facts/Choroid_plexus/glqWkmkG">choroid plexus</a>. </p><p>Pertechnetate salts, such as sodium pertechnetate, cannot pass through the <a href="/facts/Blood%25E2%2580%2593brain_barrier/xYzvVwdu">blood–brain barrier</a>. In addition to the salivary and thyroid glands, 99mTcO−4 localizes in the stomach. 99mTcO−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.<a class="footnote-ref" id="fnref:34" href="#fn:34"><sup>34</sup></a> Other methods of 99mTcO−4 administration include intraperitoneal, intramuscular, subcutaneous, as well as orally. The behavior of the 99mTcO−4 ion is essentially the same, with small differences due to the difference in rate of absorption, regardless of the method of administration.<a class="footnote-ref" id="fnref:35" href="#fn:35"><sup>35</sup></a> </p> <h3>Synthesis of 99mTcO4− radiopharmaceuticals</h3> <p>99mTcO−4 is advantageous for the synthesis of a variety of radiopharmaceuticals because Tc can adopt a number of oxidation states.<a class="footnote-ref" id="fnref:36" href="#fn:36"><sup>36</sup></a> The oxidation state and coligands dictate the specificity of the radiopharmaceutical. The starting material Na[99mTcO4], 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 99mTc for ligands. <a href="/facts/Oxalate/u0Gdem0A">Oxalates</a>, <a href="/facts/Formate/Py3GhI7L">formates</a>, <a href="/facts/Hydroxylamine/BXzuazgo">hydroxylamine</a>, and <a href="/facts/Hydrazine/G7P5ITzU">hydrazine</a> are also avoided because they form complexes with the technetium. Electrochemical reduction is impractical. </p><p>Ideally, the synthesis of the desired radiopharmaceutical from 99mTcO−4, 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 99mTcO−4 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 <i>in vivo</i> en route to the target organ. </p> <h3>As a 99mTc carrier</h3> <p>A <a href="/facts/Technetium-99m_generator/Ys7Kjnmk">technetium-99m generator</a> provides the pertechnetate containing the short-lived isotope <a href="/facts/Technetium-99m/HgIqtvrv">99mTc</a> for medical uses. This compound is generated directly from <a href="/facts/Molybdate/YPvSY2jM">molybdate</a> held on alumina within the generator (see this topic for detail). </p> <h4>In nuclear medicine</h4> <p>Pertechnetate has a wide variety of uses in diagnostic <a href="/facts/Nuclear_medicine/L9Dzjd90">nuclear medicine</a>. Since technetate(VII) can substitute for <a href="/facts/Iodine/JlfMecMf">iodine</a> in the Na/I symporter (NIS) channel in follicular cells of the <a href="/facts/Thyroid/bjovTJVu">thyroid</a> gland, inhibiting uptake of iodine into the follicular cells, 99mTc-pertechnetate can be used as an alternative to 123I in imaging of the thyroid, although it specifically measures uptake and not organification.<a class="footnote-ref" id="fnref:37" href="#fn:37"><sup>37</sup></a> It has also been used historically to evaluate for <a href="/facts/Testicular_torsion/y74oJWyP">testicular torsion</a>, although <a href="/facts/Ultrasound/31Pa5IH9">ultrasound</a> is more commonly used in current practice, as it does not deliver a radiation dose to the <a href="/facts/Testes/Doy40hoq">testes</a>. It is also used in labeling of autologus <a href="/facts/Red_blood_cell/Kggpq8Jh">red blood cells</a> for <a href="/facts/Radionuclide_angiography/ye8JCW1y">MUGA</a> scans to evaluate left ventricular cardiac function, localization of gastrointestinal bleeding prior to embolization or surgical management, and in damaged red blood cells to detect ectopic <a href="/facts/Spleen/6NKn9d8s">splenic</a> tissue. </p><p>It is actively accumulated and secreted by the mucoid cells of the gastric mucosa,<a class="footnote-ref" id="fnref:38" href="#fn:38"><sup>38</sup></a> and therefore, technetate(VII) radiolabeled with technetium-99m is injected into the body when looking for ectopic gastric tissue as is found in a <a href="/facts/Meckel%2527s_diverticulum/pvHLIf1E">Meckel's diverticulum</a> with Meckel's scans.<a class="footnote-ref" id="fnref:39" href="#fn:39"><sup>39</sup></a> </p> <h3>Non-radioactive uses</h3> <p>All technetium salts are mildly radioactive, but some of them have explored use of the element for its chemical properties. In these uses, its radioactivity is incidental, and generally the least radioactive (longest-lived) isotopes of Tc are used. In particular, <a href="/facts/Tc-99/0w2EE0G2">99Tc</a> (half-life 211,000 years) is used in corrosion research, because it is the decay product of the easily obtained commercial 99mTc isotope.<a class="footnote-ref" id="fnref:40" href="#fn:40"><sup>40</sup></a> Solutions of technetate(VII) react with the surface of <a href="/facts/Iron/QK1JYy8E">iron</a> to form technetium dioxide, in this way it is able to act as an anodic <a href="/facts/Corrosion_inhibitor/3PIHf1A8">corrosion inhibitor</a>.<a class="footnote-ref" id="fnref:41" href="#fn:41"><sup>41</sup></a> </p> <h2 id="see-also">See also</h2> <ul><li><a href="/facts/Permanganate/nJa04jVh">Permanganate</a></li> <li><a href="/facts/Perrhenate/uKvDsaoY">Perrhenate</a></li> <li><a href="/facts/Sodium_pertechnetate/9bdHcur9">Sodium pertechnetate</a></li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>"pertechnetate". Merriam-Webster.com Dictionary. Merriam-Webster. <a href="https://www.merriam-webster.com/dictionary/pertechnetate" target="_blank">https://www.merriam-webster.com/dictionary/pertechnetate</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>Ustynyuk, Yuri A.; Gloriozov, Igor P.; Zhokhova, Nelly I.; German, Konstantin E.; Kalmykov, Stepan N. (November 2021). "Hydration of the pertechnetate anion. DFT study". Journal of Molecular Liquids. 342: 117404. doi:10.1016/j.molliq.2021.117404. ISSN 0167-7322. <a href="https://doi.org/10.1016/j.molliq.2021.117404" target="_blank">https://doi.org/10.1016/j.molliq.2021.117404</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>Weaver, Jamie; Soderquist, Chuck Z.; Washton, Nancy M.; Lipton, Andrew S.; Gassman, Paul L.; Lukens, Wayne W.; Kruger, Albert A.; Wall, Nathalie A.; McCloy, John S. (21 February 2017). "Chemical Trends in Solid Alkali Pertechnetates". Inorganic Chemistry. 56 (5): 2533–2544. doi:10.1021/acs.inorgchem.6b02694. PMID 28221786. <a href="https://doi.org/10.1021%2Facs.inorgchem.6b02694" target="_blank">https://doi.org/10.1021%2Facs.inorgchem.6b02694</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> <li id="fn:4"><p>Weaver, Jamie; Soderquist, Chuck Z.; Washton, Nancy M.; Lipton, Andrew S.; Gassman, Paul L.; Lukens, Wayne W.; Kruger, Albert A.; Wall, Nathalie A.; McCloy, John S. (21 February 2017). "Chemical Trends in Solid Alkali Pertechnetates". Inorganic Chemistry. 56 (5): 2533–2544. doi:10.1021/acs.inorgchem.6b02694. PMID 28221786. <a href="https://doi.org/10.1021%2Facs.inorgchem.6b02694" target="_blank">https://doi.org/10.1021%2Facs.inorgchem.6b02694</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li> <li id="fn:5"><p>Wells, A. F.; Structural Inorganic Chemistry; Clarendon Press: Oxford, Great Britain; 1984; p. 1050. <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li> <li id="fn:6"><p>Schwochau, K. (1994). "Technetium Radiopharmaceuticals-Fundamentals, Synthesis, Structure, and Development". Angew. Chem. Int. Ed. Engl. 33 (22): 2258–2267. doi:10.1002/anie.199422581. <a href="/wiki/Angew._Chem._Int._Ed._Engl." target="_blank">/wiki/Angew._Chem._Int._Ed._Engl.</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li> <li id="fn:7"><p>Encyclopædia Britannica: Technetium <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li> <li id="fn:8"><p>Schwochau, K. (1994). "Technetium Radiopharmaceuticals-Fundamentals, Synthesis, Structure, and Development". Angew. Chem. Int. Ed. Engl. 33 (22): 2258–2267. doi:10.1002/anie.199422581. <a href="/wiki/Angew._Chem._Int._Ed._Engl." target="_blank">/wiki/Angew._Chem._Int._Ed._Engl.</a> <a href="#fnref:8" class="footnote-back-ref">↩</a></p></li> <li id="fn:9"><p>Fedosseev, A. M.; Budantseva, N. A.; Grigoriev, M. S.; Guerman, K. E.; Krupa, J.-C. (2003-03-01). "Synthesis and properties of neptunium(VI,V) and plutonium(VI) pertechnetates". Radiochimica Acta. 91 (3): 147–152. doi:10.1524/ract.91.3.147.19976. ISSN 2193-3405. <a href="https://www.degruyter.com/document/doi/10.1524/ract.91.3.147.19976/html" target="_blank">https://www.degruyter.com/document/doi/10.1524/ract.91.3.147.19976/html</a> <a href="#fnref:9" class="footnote-back-ref">↩</a></p></li> <li id="fn:10"><p>Strub, Erik; Grödler, Dennis; Zaratti, Daniele; Yong, Clarence; Dünnebier, Lisa; Bazhenova, Sonja; Roca Jungfer, Maximilian; Breugst, Martin; Zegke, Markus (2024-05-08). "Pertechnetates – A Structural Study Across the Periodic Table". Chemistry – A European Journal. 30 (26). doi:10.1002/chem.202400131. ISSN 0947-6539. <a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202400131" target="_blank">https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202400131</a> <a href="#fnref:10" class="footnote-back-ref">↩</a></p></li> <li id="fn:11"><p>Shohel, Mohammad; Bustos, Jenna; Roseborough, Alexander; Nyman, May (2023-12-28). "Pertechnetate/perrhenate‐capped Zr/Hf‐Dihydroxide Dimers: Elucidating Zr−TcO 4 Co‐Mobility in the Nuclear Fuel Cycle". Chemistry – A European Journal. doi:10.1002/chem.202303218. ISSN 0947-6539. <a href="https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202303218" target="_blank">https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202303218</a> <a href="#fnref:11" class="footnote-back-ref">↩</a></p></li> <li id="fn:12"><p>Shohel, Mohammad; Bustos, Jenna; Roseborough, Alexander; Nyman, May (2024-02-16). 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