Zinc picolinate (or ZnPic) is the zinccoordination complex derived from picolinic acid and zinc(II). It has the formula Zn(NC5H4CO2)2(H2O)2. The complex adopts an octahedral molecular geometry, containing two bidentate picolinate ligands (conjugate base of picolinic acid) and two aquo ligands. Additionally, two water of crystallization are present, thus the compound crystallizes with the formula Zn(NC5H4CO2)2(H2O)2·2H2O. It is a colorless solid.
Related compounds
Other zinc(II) complexes of picolinic acid have been described. Isostructural with the zinc complex are M(NC5H4CO2)2(H2O)2·2H2O (M = Co and Ni).
Dietary supplement
Zinc picolinate has been used as a dietary zinc supplement.
References
↑Lumme, Paavo; Lundgren, Georg; Mark, Wanda; Lundström, Hans; Borch, Gunner; Craig, J. Cymerman (1969). "The Crystal Structure of Zinc Picolinate Tetrahydrate, Zn(C6H4O2N)2(H2O)4". Acta Chemica Scandinavica. 23: 3011–3022. doi:10.3891/acta.chem.scand.23-3011.
↑Vargová, Zuzana; Zeleòák, Vladimı́r; Cı́Saøová, Ivana; Györyová, Katarı́na (2004). "Correlation of Thermal and Spectral Properties of Zinc(II) Complexes of Pyridinecarboxylic Acids with Their Crystal Sructures". Thermochimica Acta. 423 (1–2): 149–157. doi:10.1016/j.tca.2004.03.016.
↑Tella, Adedibu C.; Oladipo, Adetola C.; Adeyemi, Olalere G.; Oluwafemi, Oluwatobi S.; Oguntoye, Stephen O.; Alimi, Lukman O.; Ajayi, Joseph T.; Degni, Sylvestre K. (2017). "Solid State Synthesis, Spectroscopic and X-Ray Studies of Metal Complexes of 2-Picolinic Acid and Vapochromic Behavior of [Co(Pic)2(H2O)2]·2H2O". Solid State Sciences. 68: 1–9. doi:10.1016/j.solidstatesciences.2017.03.017.
↑Sakai F, Yoshida S, Endo S, Tomita H (2002). "Double-Blind, Placebo-Controlled Trial of Zinc Picolinate for Taste Disorders". Acta Oto-Laryngologica. Supplementum. 122 (546): 129–33. doi:10.1080/00016480260046517. PMID12132610. S2CID23717414.
↑Barrie SA, Wright JV, Pizzorno JE, Kutter E, Barron PC (June 1987). "Comparative Absorption of Zinc Picolinate, Zinc Citrate and Zinc Gluconate in Humans". Agents and Actions. 21 (1–2): 223–8. doi:10.1007/BF01974946. PMID3630857. S2CID23567370.