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Merck

M8266

Magnesium chloride

≥98%

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:
≥98%
Grade:
anhydrous
Form:
powder
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grade

anhydrous

Quality Level

assay

≥98%

form

powder

reaction suitability

core: magnesium

impurities

≤0.5% Insolubles

bp

1412 °C/1 atm (lit.)

mp

714 °C (lit.)

density

2.32 g/mL at 25 °C (lit.)

SMILES string

Cl[Mg]Cl

InChI

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

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

General description

Magnesium chloride is a white crystalline solid which is soluble in water and alcohol. It has cubic close packing structure with alternate layers of octahedral holes occupied by Mg2+ ions. It is widely used in the field of solar cells and batteries.

Application

Magnesium chloride can be used:
  • To fabricate passivated ZnO nanoparticles as electron transport layer for PbS quantum dot solar cells. This will reduce the cell defects and significantly improves efficiency.
  • To prepare dual salt electrolyte for hydrid Mg/Li rechargeable batteries to enhance ionic conductivity.
  • As a dopant to prepare Mg doped TiO2 electron transport layer for low-temperature processed planar heterojunction perovskite solar cells. Mg doping significantly helps to enhance the power conversion efficiency of solar cells.

Disclaimer

The appearance of gray/black specks should not affect use.


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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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The effect of temperature and humidity on electrospinning.
J. Mater. Sci., 44(5), 1357-1362 (2009)
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