24-1050
Ácido perclórico
SAJ first grade, 60.0-62.0%
Sinônimo(s):
PCA
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About This Item
Fórmula linear:
HClO4
Número CAS:
Peso molecular:
100.46
Número MDL:
Código UNSPSC:
12352106
ID de substância PubChem:
concentração:
60.0-62.0%
grau:
SAJ first grade
Produtos recomendados
grau
SAJ first grade
Formulário
liquid
adequação da reação
reagent type: oxidant
disponibilidade
available only in Japan
concentração
60.0-62.0%
densidade
154 g/cm3
cadeia de caracteres SMILES
OCl(=O)(=O)=O
InChI
1S/ClHO4/c2-1(3,4)5/h(H,2,3,4,5)
chave InChI
VLTRZXGMWDSKGL-UHFFFAOYSA-N
Procurando produtos similares? Visita Guia de comparação de produtos
Palavra indicadora
Danger
Frases de perigo
Declarações de precaução
Classificações de perigo
Acute Tox. 4 Oral - Eye Dam. 1 - Met. Corr. 1 - Ox. Liq. 1 - Skin Corr. 1A - STOT RE 2
Órgãos-alvo
Thyroid
Código de classe de armazenamento
5.1A - Strongly oxidizing hazardous materials
Classe de risco de água (WGK)
WGK 1
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
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Journal of the American Chemical Society, 135(10), 4018-4026 (2013-02-28)
Catalytic four-electron reduction of O2 by ferrocene (Fc) and 1,1'-dimethylferrocene (Me2Fc) occurs efficiently with a dinuclear copper(II) complex [Cu(II)2(XYLO)(OH)](2+) (1), where XYLO is a m-xylene-linked bis[(2-(2-pyridyl)ethyl)amine] dinucleating ligand with copper-bridging phenolate moiety], in the presence of perchloric acid (HClO4) in
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Journal of the American Chemical Society, 135(7), 2825-2834 (2013-02-12)
Selective two-electron plus two-proton (2e(-)/2H(+)) reduction of O(2) to hydrogen peroxide by ferrocene (Fc) or 1,1'-dimethylferrocene (Me(2)Fc) in the presence of perchloric acid is catalyzed efficiently by a mononuclear copper(II) complex, [Cu(II)(tepa)](2+) (1; tepa = tris[2-(2-pyridyl)ethyl]amine) in acetone. The E(1/2)
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The journal of pain : official journal of the American Pain Society, 15(12), 1248-1256 (2014-09-23)
Most clinically used opioids are mu-opioid receptor agonists. Therefore, genetic variation of the OPRM1 gene that encodes the mu-opioid receptor is of great interest for understanding pain management. A polymorphism 118A>G (rs1799971) within the OPRM1 gene results in a missense
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British journal of cancer, 103(2), 178-185 (2010-06-17)
The multidrug resistance (MDR) proteins are present in a majority of human tumours. Their activity is important to understand the chemotherapeutic failure. A search for MDR-reversing compounds was conducted among various Betti-base derivatives of tylosin. Here, we evaluate the in
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