S1513
Sodium perchlorate
98.0-102.0%
Synonym(s):
Hyperchloric acid sodium salt
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Assay
98.0-102.0%
reaction suitability
reagent type: oxidant
mp
468 °C (lit.)
SMILES string
[Na+].[O-]Cl(=O)(=O)=O
InChI
1S/ClHO4.Na/c2-1(3,4)5;/h(H,2,3,4,5);/q;+1/p-1
InChI key
BAZAXWOYCMUHIX-UHFFFAOYSA-M
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Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Ox. Sol. 1 - STOT RE 2
Target Organs
Thyroid
Storage Class Code
5.1A - Strongly oxidizing hazardous materials
WGK
WGK 1
Regulatory Information
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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
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
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
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
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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