449172
氯化镁
AnhydroBeads™, −10 mesh, 99.99% trace metals basis
别名:
氯化镁
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关于此项目
线性分子式:
MgCl2
化学文摘社编号:
分子量:
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
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
SMILES string
Cl[Mg]Cl
InChI
1S/2ClH.Mg/h2*1H;/q;;+2/p-2
InChI key
TWRXJAOTZQYOKJ-UHFFFAOYSA-L
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General description
氯化镁可作为起始原料用于制备多硫化镁液流电池中的电解质溶液。
Legal Information
AnhydroBeads is a trademark of Sigma-Aldrich Co. LLC
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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
实验方案
Accurately measure the moisture content in Magnesium Chloride (MgCl2) through Karl Fischer titration, using both Volumetric and Coulometric methods.
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 449172-10G | 04061832316994 |
| 449172-50G | 04061838139917 |
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