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Merck
CN

17766

Sigma-Aldrich

DL-α-甘油磷酸盐 镁盐 水合物

~85% (KT)

别名:

rac -甘油-3-磷酸 镁盐, 甘油磷酸镁

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About This Item

经验公式(希尔记法):
C3H7MgO6P · xH2O
CAS号:
分子量:
194.36 (anhydrous basis)
EC 号:
MDL编号:
UNSPSC代码:
12352211
PubChem化学物质编号:
NACRES:
NA.25

生物来源

synthetic

质量水平

方案

~85% (KT)

表单

powder

官能团

hydroxyl

脂质类型

phosphoglycerides

储存温度

room temp

SMILES字符串

O.[Mg++].OCC(O)COP([O-])([O-])=O

InChI

1S/C3H9O6P.Mg.H2O/c4-1-3(5)2-9-10(6,7)8;;/h3-5H,1-2H2,(H2,6,7,8);;1H2/q;+2;/p-2

InChI key

GLZHYLKPDLVZKJ-UHFFFAOYSA-L

相关类别

一般描述

DL-α-甘油磷酸盐是D- 和 L-甘油磷酸盐对映体的外消旋混合物。

应用

DL-α-甘油磷酸镁盐水合物可用于:
  • 氧化酶和脱氢酶测定
  • 作为成骨细胞分化培养基的组分
  • 矿化含碱性磷酸酶的聚乙烯醇(PVA)水凝胶,以用于骨软骨再生


DL-a-甘油磷酸可用于评估无乳噬菌体的溶原-菌株特性

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

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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Inhibition of Escherichia coli respiratory enzymes by short visible femtosecond laser irradiation
Lu CH, et al.
Journal of Physics D: Applied Physics, 47(31), 315402-315402 (2014)
Composites of polyvinyl alcohol (PVA) hydrogel and calcium and magnesium phosphate formed by enzymatic functionalization
Douglas T EL, et al.
Materials Letters, 137, 62-67 (2014)
Luana Lopes Souza et al.
The Journal of endocrinology, 211(1), 65-72 (2011-07-15)
n-3 polyunsaturated fatty acids (n-3 PUFA) from fish oil (FO) exert important lipid-lowering effects, an effect also ascribed to thyroid hormones (TH) and TH receptor β1 (TRβ1)-specific agonists. n-3 PUFA effects are mediated by nuclear receptors, such as peroxisome proliferator-activated
Jiangwei Yao et al.
Biochimica et biophysica acta, 1831(3), 495-502 (2012-09-18)
Membrane phospholipid synthesis is a vital facet of bacterial physiology. Although the spectrum of phospholipid headgroup structures produced by bacteria is large, the key precursor to all of these molecules is phosphatidic acid (PtdOH). Glycerol-3-phosphate derived from the glycolysis via
Heinrich Topp et al.
Pharmacology, 88(3-4), 193-200 (2011-10-12)
The primary aim of the present investigation was to determine and compare the pharmacokinetic (PK) profiles of inorganic phosphate in serum and urine after intravenous administration of sodium glycerophosphate and inorganic sodium phosphate. Additionally, study product safety profiles were evaluated.

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