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Merck

449172

Magnesium chloride

AnhydroBeads, −10 mesh, 99.99% trace metals basis

Synonym(s):

Magnogene

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About This Item

Linear Formula:
MgCl2
CAS Number:
Molecular Weight:
95.21
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
232-094-6
MDL number:
assay:
99.99% trace metals basis
grade:
synthesis grade

Product Name

Magnesium chloride, AnhydroBeads, −10 mesh, 99.99% trace metals basis

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

InChI

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

SMILES string

Cl[Mg]Cl

grade

synthesis grade

product line

AnhydroBeads

assay

99.99% trace metals basis

reaction suitability

core: magnesium

impurities

≤150.0 ppm Trace Metal Analysis

particle size

−10 mesh

mp

714 °C (lit.)

density

2.32 g/mL at 25 °C (lit.)

application(s)

electroplating
material synthesis precursor

Quality Level

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General description

Magnesium chloride can be used as a starting material to prepare electrolyte solutions for Mg-polysulfide flow batteries.

Legal Information

AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC

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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Stability and Disproportionation of Magnesium Polysulfides and the Effects on the Mg-Polysulfide Flow Battery
Peng He, et al.
Journal of the Electrochemical Society, 168, 110516-110516 (2021)
Role of chloride for a simple, non-grignard Mg electrolyte in ether-based solvents
Niya Sa, et al
ACS Applied Materials & Interfaces, 8, 16002-16008 (2016)
Manal A Farg et al.
Human molecular genetics, 23(13), 3579-3595 (2014-02-20)
Intronic expansion of a hexanucleotide GGGGCC repeat in the chromosome 9 open reading frame 72 (C9ORF72) gene is the major cause of familial amyotrophic lateral sclerosis (ALS) and frontotemporal dementia. However, the cellular function of the C9ORF72 protein remains unknown.
Benjamin Dombert et al.
PloS one, 9(10), e110846-e110846 (2014-10-23)
Spinal muscular atrophy (SMA) is caused by deficiency of the ubiquitously expressed survival motoneuron (SMN) protein. SMN is crucial component of a complex for the assembly of spliceosomal small nuclear ribonucleoprotein (snRNP) particles. Other cellular functions of SMN are less
Fernando Cartón-García et al.
Scientific reports, 5, 12312-12312 (2015-07-24)
Inherited MYO5B mutations have recently been associated with microvillus inclusion disease (MVID), an autosomal recessive syndrome characterized by intractable, life-threatening, watery diarrhea appearing shortly after birth. Characterization of the molecular mechanisms underlying this disease and development of novel therapeutic approaches

Protocols

Accurately measure the moisture content in Magnesium Chloride (MgCl2) through Karl Fischer titration, using both Volumetric and Coulometric methods.

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