449172
氯化镁
AnhydroBeads™, −10 mesh, 99.99% trace metals basis
别名:
氯化镁
登录 查看组织和合同定价。
选择尺寸
变更视图
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
Quality Level
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
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
Still not finding the right product?
Explore all of our products under 氯化镁
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)
实验方案
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 449172-10G | 04061832316994 |
| 449172-50G | 04061838139917 |