吡啶-2-甲酸锌
化合物
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 
|
| PubChem | 9904746 |
| ChemSpider | 8080400 |
| SMILES |
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| 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。 | |
参考文献 编辑
- ^ 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
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.
- ^ 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.