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Merck

M8266

Sigma-Aldrich

氯化镁

anhydrous, ≥98%

别名:

氯化镁

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About This Item

线性分子式:
MgCl2
CAS号:
分子量:
95.21
EC號碼:
MDL號碼:
分類程式碼代碼:
12352302
PubChem物質ID:
NACRES:
NA.23
化驗:
≥98%
等級:
anhydrous
形狀:
powder

等級

anhydrous

品質等級

化驗

≥98%

形狀

powder

雜質

≤0.5% Insolubles

bp

1412 °C/1 atm (lit.)

mp

714 °C (lit.)

密度

2.32 g/mL at 25 °C (lit.)

應用

cell analysis

SMILES 字串

Cl[Mg]Cl

InChI

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

InChI 密鑰

TWRXJAOTZQYOKJ-UHFFFAOYSA-L

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一般說明

氯化镁是一种白色结晶固体,溶于水和乙醇。 由Mg2+离子占据的八面体孔层交替紧密堆积而成立方结构。它广泛应用于太阳能电池和电池领域。

應用

氯化镁可用于:
  • 制造钝化ZnO纳米粒子,以作为PbS量子点太阳能电池的电子传输层。这将减少电池缺陷并大幅提高效率。
  • 制备杂环Mg/Li可充电电池的双盐电解质,以增强离子导电性。
  • 作为掺杂剂制备Mg掺杂TiO2电子传输层,用于低温制备平面异质结钙钛矿太阳能电池。镁掺杂有助于大幅提高太阳能电池的能量转换效率。

注意

灰/黑斑外观不影响使用。

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 1

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The effect of temperature and humidity on electrospinning.
J. Mater. Sci., 44(5), 1357-1362 (2009)
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.
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

TE Buffer; Elution Buffer; 10x Ligation Buffer; 0.5 M PIPES Buffer; Inoue Transformation Buffer

Summary application report for analysis of moisture in Magnesium chloride

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