质量水平
检测方案
96%
形式
solid
mp
1583 °C (lit.)
溶解性
H2O: slightly soluble(lit.)
SMILES字符串
[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O
InChI
1S/3Na.H3O4P/c;;;1-5(2,3)4/h;;;(H3,1,2,3,4)/q3*+1;/p-3
InChI key
RYFMWSXOAZQYPI-UHFFFAOYSA-K
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一般描述
磷酸钠是一种无色至白色的结晶粉末或颗粒。它是通过在受控条件下用氢氧化钠或碳酸钠中和磷酸而制备的。
应用
磷酸钠可用作:
其他一般用途包括作为pH控制剂、水硬度沉淀、实验室试剂,磷酸化试剂。
- 由锶取代的钙羟磷灰石的固相晶体制备中的组分
- 研究肾脏中CFTR节段和亚细胞分布的封闭缓冲液。
其他一般用途包括作为pH控制剂、水硬度沉淀、实验室试剂,磷酸化试剂。
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Regeneration of sensory neurons after spinal cord injury depends on the function of dividing neuronal-glial antigen 2 (NG2)-expressing cells. We have shown that increases in the number of dividing NG2-positive cells through short-term pharmacologic inhibition of matrix metalloproteinases contributes to
American journal of physiology. Renal physiology, 308(12), F1398-F1408 (2015-04-17)
Extracellular nucleotides acting through P2 receptors facilitate natriuresis. To define how purinergic mechanisms are involved in sodium homeostasis, we used transgenic (TG) mice that globally overexpress human CD39 (hCD39, NTPDase1), an ectonucleotidase that hydrolyzes extracellular ATP/ADP to AMP, resulting in
The Journal of biological chemistry, 290(21), 13279-13292 (2015-04-08)
SAMHD1 is a nuclear deoxyribonucleoside triphosphate triphosphohydrolase that contributes to the control of cellular deoxyribonucleoside triphosphate (dNTP) pool sizes through dNTP hydrolysis and modulates the innate immune response to viruses. CyclinA2-CDK1/2 phosphorylates SAMHD1 at Thr-592, but how this modification controls
The Journal of clinical investigation, 125(12), 4529-4543 (2015-11-17)
Posttranslational modifications to the intracellular domain of the EGFR are known to regulate EGFR functions; however, modifications to the extracellular domain and their effects remain relatively unexplored. Here, we determined that methylation at R198 and R200 of the EGFR extracellular
American journal of physiology. Gastrointestinal and liver physiology, 307(10), G992-G1001 (2014-09-27)
Microvillus inclusion disease (MVID) is an autosomal recessive condition resulting in intractable secretory diarrhea in newborns due to loss-of-function mutations in myosin Vb (Myo5b). Previous work suggested that the apical recycling endosomal (ARE) compartment is the primary location for phosphoinositide-dependent
实验方案
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