7791-07-3 Usage
Description
Sodium perchlorate monohydrate, with the chemical formula NaClO4·H2O, is a common form of sodium perchlorate that can gradually absorb water from the air to form the monohydrate. It is a white rhombic crystal that is highly soluble in water and alcohol. As a strong oxidizer, it may cause damage to organs through prolonged or repeated exposure. Sodium perchlorate monohydrate is also a chaotropic agent used in standard DNA extraction and hybridization reactions in molecular biology and is widely utilized as a deproteinization agent during nucleic acid synthesis.
Uses
Used in Molecular Biology:
Sodium perchlorate monohydrate is used as a chaotropic agent for DNA extraction and hybridization reactions, facilitating efficient and reliable nucleic acid isolation and analysis.
Used in Nucleic Acid Synthesis:
Sodium perchlorate monohydrate is used as a deproteinization agent during nucleic acid synthesis, helping to remove proteins and other impurities that may interfere with the synthesis process.
Used in Electrochemical Synthesis:
Sodium perchlorate monohydrate is used as a strong oxidizing agent in electrochemical synthesis, enabling the production of various compounds and materials.
Used in Commercial Explosives:
Sodium perchlorate monohydrate can be used as a chemical sensitizing agent for some modern commercial explosives products, enhancing their performance and safety.
References
1.https://pubchem.ncbi.nlm.nih.gov/compound/Sodium_perchlorate_monohydrate#section=Chemical-Vendors
2.https://en.wikipedia.org/wiki/Sodium_perchlorate
3.http://www.arkema.com/export/shared/.content/media/downloads/socialresponsability/safety-summuries/Hydrogen-Peroxides-Sodium-Perchlorate-GPS-2014-12-15-V0.pdf
4.http://www.sciencelab.com/msds.php?msdsId=9927599
Check Digit Verification of cas no
The CAS Registry Mumber 7791-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7791-07:
(6*7)+(5*7)+(4*9)+(3*1)+(2*0)+(1*7)=123
123 % 10 = 3
So 7791-07-3 is a valid CAS Registry Number.
InChI:InChI=1/ClHO4.Na.H2O/c2-1(3,4)5;;/h(H,2,3,4,5);;1H2/q;+1;/p-1
7791-07-3Relevant articles and documents
Kinetics of oxidation of ascorbic acid and 1,4-dihydroxybenzene by semiquinone radical bound to ruthenium(II)
Ghosh, Debjani,Shukla, Atindra D.,Banerjee, Rupendranath,Das, Amitava
, p. 1220 - 1225 (2007/10/03)
In 40% (v/v) MeOH-H2O media, containing [H+] (0.001-0.038 mol dm-3), the semiquinone (sq) radical, bound to Ru(II) in [Ru(bpy)2(sq)]+ 1, oxidises ascorbic acid (H2A) to dehydroascorbic acid (A), and 1,4-dihydroxybenzene (H2Q) to p-benzoquinone (Q); 1 is itself reduced to [Ru(bpy)2(Hcat)]+ 2H. The reactions are centred at sq not Ru(II). The sq/cat couple in 1 is reversible and its E1/2 increases with increasing [H+]; rate of chemical reduction of 1 to 2H increases in parallel. Rate increases also with increasing mole percent of D2O in the solvent suggesting a preliminary protonation equilibrium producing 1H, in which a H+ binds to the π-electron cloud of Ru(II)-bound sq. Under the experimental conditions, the kinetically significant species are 1H, H2Q, H2A and HA-. The kinetic activity of HA- ion is only ≈200 times more than that of H2A. This testifies against a purely outer-sphere mechanism and suggests significant electronic interaction between the redox partners. Increased percentage of MeOH in the solvent decreases λmax for the LMCT band; reaction rate for ascorbic acid decreases in parallel.