449172
Magnesium chloride
AnhydroBeads™, −10 mesh, 99.99% trace metals basis
Synonym(s):
Magnogene
Sign In to View Organizational & Contract Pricing.
Select a Size
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
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
Looking for similar products? Visit Product Comparison Guide
Related Categories
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)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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)
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)
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service