Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | 2ClO4.Mg |
| Molecular Weight | 223.206 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[Mg++].[O-]Cl(=O)(=O)=O.[O-]Cl(=O)(=O)=O
InChI
InChIKey=MPCRDALPQLDDFX-UHFFFAOYSA-L
InChI=1S/2ClHO4.Mg/c2*2-1(3,4)5;/h2*(H,2,3,4,5);/q;;+2/p-2
| Molecular Formula | Mg |
| Molecular Weight | 24.305 |
| Charge | 2 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
| Molecular Formula | ClO4 |
| Molecular Weight | 99.451 |
| Charge | -1 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Magnesium perchlorate is a strong oxidizing agent. Magnesium perchlorate has been found to be an efficient catalyst for the synthesis of imines and phenylhydrazones by the reaction of carbonyl compounds with amines and phenylhydrazine in high yields at room temperatures and in short times. Magnesium perchlorate has being shown to be a radiosensitizer in in vitro radiolysis of nucleotides.
Approval Year
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
Sources: https://www.ncbi.nlm.nih.gov/pubmed/2168728 |
Primary | Unknown Approved UseUnknown |
PubMed
| Title | Date | PubMed |
|---|---|---|
| Synthesis and herbicidal activity evaluation of novel α-amino phosphonate derivatives containing a uracil moiety. | 2016-02-15 |
|
| Synthesis and Biological Activity Evaluation of Novel α-Amino Phosphonate Derivatives Containing a Pyrimidinyl Moiety as Potential Herbicidal Agents. | 2015-08-19 |
|
| Carbon monoxide as a metabolic energy source for extremely halophilic microbes: implications for microbial activity in Mars regolith. | 2015-04-07 |
|
| Revision of the Mg(ClO4)2·4H2O crystal structure. | 2012-02 |
|
| Magnesium perchlorate anhydrate, Mg(ClO4)2, from laboratory X-ray powder data. | 2011-06 |
|
| An extremely efficient three-component reaction of aldehydes/ketones, amines, and phosphites (Kabachnik-Fields reaction) for the synthesis of alpha-aminophosphonates catalyzed by magnesium perchlorate. | 2007-02-16 |
|
| Phase inversion cellulose acetate membranes for suppression of protein interferences in anodic stripping voltammetry 2(1). Improvement of the membrane preparation procedure. | 1996-08 |
|
| Flavin-photosensitized monomerization of dimethylthymine cyclobutane dimer in the presence of magnesium perchlorate. | 1993-11 |
Patents
| Substance Class |
Chemical
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Mon Mar 31 18:51:56 GMT 2025
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| Record UNII |
7N77Z541YF
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m7012
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MAGNESIUM PERCHLORATE
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PARENT -> SALT/SOLVATE |