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Merck

M0250

Sigma-Aldrich

Cloruro de magnesio hexahydrate

ReagentPlus®, ≥99.0%

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About This Item

Fórmula lineal:
MgCl2 · 6H2O
Número de CAS:
Peso molecular:
203.30
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.21

Quality Level

product line

ReagentPlus®

assay

≥99.0%

form

solid

SMILES string

O.O.O.O.O.O.Cl[Mg]Cl

InChI

1S/2ClH.Mg.6H2O/h2*1H;;6*1H2/q;;+2;;;;;;/p-2

InChI key

DHRRIBDTHFBPNG-UHFFFAOYSA-L

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General description

Magnesium chloride hexahydrate is a hydrated form of magnesium chloride. It is used as a catalyst in organic synthesis. In molecular biology, it is used as a source of magnesium ions.

Application

Magnesium chloride hexahydrate can be used as:      
  • A catalyst to synthesize dihydropyrimidine derivatives by Biginelli condensation of aldehydes, 1,3?dicarbonyl compounds, and urea.      
  • A precursor salt to prepare Mg-Fe bi-metal oxide catalyst by treating with iron(II) sulfate heptahydrate. Mg-Fe bi-metal oxide is applicable as a renewable solid base catalyst to synthesize 2-aminothiophenes via Gewald′s reaction.

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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Analytica chimica acta, 837, 70-82 (2014-07-09)
This article describes a liquid chromatographic/tandem mass spectrometric method, based on the use of precursor ion scan as the acquisition mode, specifically developed to detect indole-derived cannabinoids (phenylacetylindoles, naphthoylindoles and benzoylindoles) in biological fluids (saliva, urine and blood). The method
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Nature biotechnology, 38(3), 297-302 (2020-02-26)
The scarcity of donor organs may be addressed in the future by using pigs to grow humanized organs with lower potential for immunological rejection after transplantation in humans. Previous studies have demonstrated that interspecies complementation of rodent blastocysts lacking a
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International journal of pharmaceutics, 471(1-2), 258-263 (2014-05-20)
Telmisartan (TEL) belongs to BCS class II (low solubility/high permeability) and exhibits the pH-dependent drug release. Since 3-aminopropyl functionalized magnesium phyllosilicate (aminoclay) can intercalate or adsorb the negatively charged molecules via the electrostatic interaction, TEL-aminoclay complex was synthesized to improve
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Tegafur (FT), a prodrug of 5-fluorouracil, is a chiral molecule, a racemate of R- and S-isomers, and CYP2A6 plays an important role in the enantioselective metabolism of FT in human liver microsomes (R-FT > S-FT). This study examined the enantioselective

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