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Merck

M2545

Magnesium acetate tetrahydrate

BioXtra, ≥99%

Synonym(s):

Acetic acid magnesium salt

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About This Item

Linear Formula:
(CH3COO)2Mg · 4H2O
CAS Number:
16674-78-5
Molecular Weight:
214.45
NACRES:
NA.25
PubChem Substance ID:
24896744
eCl@ss:
39021909
UNSPSC Code:
12161700
EC Number:
205-554-9
MDL number:
MFCD00149214
Beilstein/REAXYS Number:
3730605

Key Documents

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Product Name

Magnesium acetate tetrahydrate, BioXtra, ≥99%

InChI

1S/2C2H4O2.Mg.4H2O/c2*1-2(3)4;;;;;/h2*1H3,(H,3,4);;4*1H2/q;;+2;;;;/p-2

SMILES string

O.O.O.O.CC(=O)O[Mg]OC(C)=O

InChI key

XKPKPGCRSHFTKM-UHFFFAOYSA-L

product line

BioXtra

assay

≥99%

form

solid

impurities

≤0.0005% Phosphorus (P)
≤0.005% Insoluble matter

mp

72-75 °C (lit.)

solubility

H2O: 1 M, clear, colorless

anion traces

chloride (Cl-): ≤0.001%
sulfate (SO42-): ≤0.005%

cation traces

Al: ≤0.002%
Ba: ≤0.001%
Ca: ≤0.002%
Cu: ≤0.0005%
Fe: ≤0.0005%
K: ≤0.005%
Mn: ≤0.005%
NH4+: ≤0.05%
Na: ≤0.005%
Pb: ≤0.001%
Sr: ≤0.005%
Zn: ≤0.001%

Quality Level

200

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Application


  • Synthesis and application of SiO2-MgO coated MWCNTs: Magnesium acetate tetrahydrate was utilized in the synthesis of SiO2-MgO coatings on multi-walled carbon nanotubes (MWCNTs). This method showcases the versatility of magnesium acetate as a precursor in creating advanced materials for potential applications in molecular biology and biochemical research, enhancing the performance of functional materials in various scientific assays (Nemeth et al., 2019).

Storage Class

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000515202
0000515202
0000473347
0000452506
0000452506

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Christiane Iserman et al.
Cell, 181(4), 818-831 (2020-05-04)
Cells sense elevated temperatures and mount an adaptive heat shock response that involves changes in gene expression, but the underlying mechanisms, particularly on the level of translation, remain unknown. Here we report that, in budding yeast, the essential translation initiation
Yoshihito Kitaoku et al.
Planta, 242(4), 895-907 (2015-05-23)
We first solved the crystal structure of class III catalytic domain of a chitinase from fern (PrChiA-cat), and found a structural difference between PrChiA-cat and hevamine. PrChiA-cat was found to have reduced affinities to chitin oligosaccharides and allosamidin. Plant class
Tanja Rozman Peterka et al.
Journal of pharmaceutical and biomedical analysis, 110, 67-75 (2015-03-26)
Tacrolimus is macrolide drug that is widely used as a potent immunosuppressant. In the present work compatibility testing was conducted on physical mixtures of tacrolimus with excipients and on compatibility mixtures prepared by the simulation of manufacturing process used for
Catarina M S S Neves et al.
Physical chemistry chemical physics : PCCP, 17(47), 32044-32052 (2015-11-18)
Due to scarce available experimental data, as well as due to the absence of predictive models, the influence of salts on the solubility of ionic liquids (ILs) in water is still poorly understood. To this end, this work addresses the
Andrey G Malyutin et al.
ACS applied materials & interfaces, 7(22), 12089-12098 (2015-05-20)
Here we explore the formation of virus-like nanoparticles (VNPs) utilizing 22-24 nm iron oxide nanoparticles (NPs) as cores and proteins derived from viral capsids of brome mosaic virus (BMV) or hepatitis B virus (HBV) as shells. To accomplish that, hydrophobic

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