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等級
ACS reagent
化驗
97.0-102.0% (ACS specification)
98%
形狀
crystals
反應適用性
reagent type: oxidant
雜質
≤0.005% insolubles
pH值
3.0-5.0 (25 °C, 5%)
負離子痕跡
chloride (Cl-): ≤0.01%
正離子痕跡
Fe: ≤0.001%
SMILES 字串
O.O.O.[PbH2++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI
1S/2ClHO4.3H2O.Pb/c2*2-1(3,4)5;;;;/h2*(H,2,3,4,5);3*1H2;/q;;;;;+2/p-2
InChI 密鑰
KKGGEAQRICYXNM-UHFFFAOYSA-L
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一般說明
Lead(II) perchlorate trihydrate is a perchlorate compound. It leads to protonation of the pyridyl group on interaction with pyridyldithiafulvene ligands.
應用
Lead(II) perchlorate trihydrate may be used in the synthesis of calix[4]arene thioamides and macrocyclic lead(II) complexes.
訊號詞
Danger
危險分類
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Ox. Sol. 2 - Repr. 1A - STOT RE 2
儲存類別代碼
5.1A - Strongly oxidizing hazardous materials
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
Preparation and Crystal Structures of Silver (I), Mercury (II), and Lead (II) Complexes of Oxathia-Tribenzo-Macrocycles.
Bull. Korean Chem. Soc., 34(3), 725-725 (2013)
Pyridyldithiafulvene as N-ligand towards molybdenum carbonyl complexes and evidence of protonation through hydrolysis of lead perchlorate.
Journal of Organometallic Chemistry, 696(7), 1367-1371 (2011)
Lower rim substituted p-tert-butyl calix [4] arene; Part 14. Synthesis, structures and binding studies of calix [4] arene thioamides.
Journal of Inclusion Phenomena and Macrocyclic Chemistry, 68(1-2), 75-83 (2010)
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