吡啶-2-甲酸鋅
化合物
吡啶-2-甲酸鋅是一種有機酸鹽,化學式為Zn(C6H4O2N)2,或簡寫為ZnPic。[1]它可由吡啶-2-甲酸和硫酸鋅反應製得,所用的吡啶-2-甲酸可由2-甲基吡啶的氧化反應得到。[2][3]
吡啶-2-甲酸鋅 | |
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識別 | |
CAS號 | 17949-65-4 ![]() |
PubChem | 9904746 |
ChemSpider | 8080400 |
SMILES |
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危險性 | |
GHS危險性符號![]() ![]() | |
GHS提示詞 | 警告 |
H-術語 | H302, H315, H319, H335, H400, H410 |
P-術語 | P261, P264, P270, P271, P273, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313 |
若非註明,所有數據均出自標準狀態(25 ℃,100 kPa)下。 |
參考文獻
- ^ Paavo Lumme, Georg Lundgren, Wanda Mark, "The crystal structure of zinc picolinate tetrahydrate (頁面存檔備份,存於網際網路檔案館), Acta Chemica Scandinavica, vol. 23, pp. 3011-3022, 1969
- ^ 丁彩峰, 朱小剛, 劉 芳,等. 2-吡啶甲酸鋅的合成方法:, CN 101597257 A[P]. 2009.
- ^ 張愛娟. 吡啶羧酸金屬絡活物的合成和應用[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" (頁面存檔備份,存於網際網路檔案館) 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" (頁面存檔備份,存於網際網路檔案館), Agents and Actions, vol. 21, iss. 1-2, pp. 223-228, June 1987.