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Merck
CN

63042

Magnesium ion solution for ISE

0.1 M Mg, analytical standard (for ion-selective electrodes)

Synonym(s):

Magnesium chloride solution

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About This Item

Linear Formula:
MgCl2
CAS Number:
Molecular Weight:
95.21
NACRES:
NB.61
PubChem Substance ID:
UNSPSC Code:
26111700
MDL number:
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InChI

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

InChI key

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

grade

analytical standard (for ion-selective electrodes)

shelf life

limited shelf life, expiry date on the label

concentration

0.1 M Mg

General description

Magnesium chloride is an organic salt commonly used a coagulant during wastewater treatment,and for removal of industrial dye wastes and other colouring matters via chemical precipitation method.1It also acts as a source of magnesium ions during PCR (Polymerase Chain Reaction).
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Preparation Note

prepared with MgCl2.6H2O and H2O

Storage Class

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


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Removal of dyes and industrial dye wastes by magnesium chloride.
Tan, Boon Hai, Tjoon Tow Teng, and AK Mohd Omar
Water Research, 34 (2), 597-601 (2000)
Stephen Q Wong et al.
Oncotarget, 6(2), 1115-1127 (2014-12-30)
Melanoma is often caused by mutations due to exposure to ultraviolet radiation. This study reports a recurrent somatic C > T change causing a P131L mutation in the RQCD1 (Required for Cell Differentiation1 Homolog) gene identified through whole exome sequencing
Hideyuki Arita et al.
Brain tumor pathology, 32(1), 22-30 (2014-04-22)
Assessment of the mutational status of the isocitrate dehydrogenase 1/2 (IDH1/2) gene has become an integral part of the standard diagnostic procedure and, therefore, needs to be accurate. This may, however, be compromised by various factors including the method of
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.
Susanne Hellmuth et al.
The EMBO journal, 33(10), 1134-1147 (2014-05-02)
The universal triggering event of eukaryotic chromosome segregation is cleavage of centromeric cohesin by separase. Prior to anaphase, most separase is kept inactive by association with securin. Protein phosphatase 2A (PP2A) constitutes another binding partner of human separase, but the

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