吡啶-2-甲酸锌

吡啶-2-甲酸锌是一种有机酸盐，化学式为Zn(C₆H₄O₂N)₂，或简写为ZnPic。^[1]它可由吡啶-2-甲酸和硫酸锌反应制得，所用的吡啶-2-甲酸可由2-甲基吡啶的氧化反应得到。^[2][3]

吡啶-2-甲酸锌
识别
CAS号	17949-65-4  Y
PubChem	9904746
ChemSpider	8080400
SMILES	C1=CC=NC(=C1)C(=O)[O-].C1=CC=NC(=C1)C(=O)[O-].[Zn+2]
危险性
GHS危险性符号
GHS提示词	警告
H-术语	H302, H315, H319, H335, H400, H410
P-术语	P261, P264, P270, P271, P273, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313
若非注明，所有数据均出自标准状态（25 ℃，100 kPa）下。

它可用作膳食补锌剂。^[4][5][6]

参考文献

1. Paavo Lumme, Georg Lundgren, Wanda Mark, "The crystal structure of zinc picolinate tetrahydrate （页面存档备份，存于互联网档案馆）, Acta Chemica Scandinavica, vol. 23, pp. 3011-3022, 1969
2. 丁彩峰, 朱小刚, 刘 芳,等. 2-吡啶甲酸锌的合成方法:, CN 101597257 A[P]. 2009.
3. 张爱娟. 吡啶羧酸金属络活物的合成和应用[J]. 乙醛醋酸化工, 2005(12):34-36.
4. Carol Walsh, Harold Sandstead, Ananda S Prasad, Paul M Newberne,Pamela J, Fraker, "Zinc: health effects and research priorities for the 1990s" （页面存档备份，存于互联网档案馆） Environmental Health Perspectives, vol. 102 (supplement 2), pp. 5-46, June,1994.
5. Fumitaka Sakai, Shinya Yoshida, Sohei Endo & Hiroshi Tomita, "Double-blind, Placebo-controlled Trial of Zinc Picolinate for Taste Disorders", Acta Oto-Laryngologica, vol. 122, iss. 4, pp. 129-133, 2002.
6. S A Barrie, J V Wright, J E Pizzorno, E Kutter, P C Barron, "Comparative absorption of zinc picolinate, zinc citrate and zinc gluconate in humans" （页面存档备份，存于互联网档案馆）, Agents and Actions, vol. 21, iss. 1-2, pp. 223-228, June 1987.