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Merck
CN

S1513

高氯酸钠

98.0-102.0%

别名:

高氯酸钠盐

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线性分子式:
NaClO4
化学文摘社编号:
分子量:
122.44
EC Number:
231-511-9
UNSPSC Code:
12352300
MDL number:
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InChI key

BAZAXWOYCMUHIX-UHFFFAOYSA-M

InChI

1S/ClHO4.Na/c2-1(3,4)5;/h(H,2,3,4,5);/q;+1/p-1

SMILES string

[Na+].[O-]Cl(=O)(=O)=O

assay

98.0-102.0%

reaction suitability

reagent type: oxidant

mp

468 °C (lit.)

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signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Ox. Sol. 1 - STOT RE 2

target_organs

Thyroid

存储类别

5.1A - Strongly oxidizing hazardous materials

wgk

WGK 1

法规信息

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Alvaro H Crevenna et al.
Biophysical journal, 102(4), 907-915 (2012-03-06)
The molecular conformation of proteins is sensitive to the nature of the aqueous environment. In particular, the presence of ions can stabilize or destabilize (denature) protein secondary structure. The underlying mechanisms of these actions are still not fully understood. Here
Minbiao Ji et al.
The Journal of chemical physics, 134(4), 044516-044516 (2011-02-02)
The dynamics of hydrogen bond (H-bond) formation and dissociation depend intimately on the dynamics of water rotation. We have used polarization resolved ultrafast two-dimensional infrared (2DIR) spectroscopy to investigate the rotational dynamics of deuterated hydroxyl groups (OD) in a solution
Shubhasis Haldar et al.
The Journal of biological chemistry, 287(14), 11546-11555 (2012-02-04)
What happens in the early stage of protein folding remains an interesting unsolved problem. Rapid kinetics measurements with cytochrome c using submillisecond continuous flow mixing devices suggest simultaneous formation of a compact collapsed state and secondary structure. These data seem
Eliana K Asciutto et al.
Biophysical journal, 98(2), 186-196 (2010-03-27)
Sodium perchlorate salt (NaClO(4)) is commonly used as an internal intensity standard in ultraviolet resonance Raman (UVRR) spectroscopy experiments. It is well known that NaClO(4) can have profound effects on peptide stability. The impact of NaClO(4) on protein stability in
Masatoshi Shibuya et al.
Chemical communications (Cambridge, England), (13)(13), 1739-1741 (2009-03-19)
A facile, green, one-pot oxidation of primary alcohols to carboxylic acids with broad substrate applicability has been developed by employing an expedient catalytic system consisting of 1-Me-AZADO+X-/NaClO2.

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