449172
Chlorure de magnésium
AnhydroBeads™, −10 mesh, 99.99% trace metals basis
Synonyme(s) :
Magnogène
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A propos de cet article
Formule linéaire :
MgCl2
Numéro CAS:
Poids moléculaire :
95.21
MDL number:
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
12352302
EC Number:
232-094-6
Assay:
99.99% trace metals basis
Grade:
synthesis grade
Service technique
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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
SMILES string
Cl[Mg]Cl
InChI
1S/2ClH.Mg/h2*1H;/q;;+2/p-2
InChI key
TWRXJAOTZQYOKJ-UHFFFAOYSA-L
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
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Classe de stockage
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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Protocoles
Accurately measure the moisture content in Magnesium Chloride (MgCl2) through Karl Fischer titration, using both Volumetric and Coulometric methods.
Kadri Õunap et al.
PloS one, 10(7), e0133841-e0133841 (2015-07-28)
The human WBSCR22 protein is a 18S rRNA methyltransferase involved in pre-rRNA processing and ribosome 40S subunit biogenesis. Recent studies have shown that the protein function in ribosome synthesis is independent of its enzymatic activity. In this work, we have
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.
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
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 449172-10G | 04061832316994 |
| 449172-50G | 04061838139917 |