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Merck

342483

Sodium phosphate

greener alternative

96%

Sinónimos:

Sodium orthophosphate, Trisodium phosphate

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About This Item

Fórmula lineal:
Na3PO4
Número CAS:
Peso molecular:
163.94
UNSPSC Code:
12352302
NACRES:
NA.23
PubChem Substance ID:
EC Number:
231-509-8
MDL number:
assay:
96%
form:
solid
solubility:
H2O: slightly soluble(lit.)

Nombre del producto

Sodium phosphate, 96%

InChI key

RYFMWSXOAZQYPI-UHFFFAOYSA-K

InChI

1S/3Na.H3O4P/c;;;1-5(2,3)4/h;;;(H3,1,2,3,4)/q3*+1;/p-3

SMILES string

[Na+].[Na+].[Na+].[O-]P([O-])([O-])=O

assay

96%

form

solid

reaction suitability

core: sodium

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

1583 °C (lit.)

solubility

H2O: slightly soluble(lit.)

application(s)

battery precursors
catalysts
material synthesis precursor

greener alternative category

Quality Level

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Application

Sodium phosphate is used as a:
  • component in the preparation of solid crystals of calcium hydroxyapatite substituted by strontium
  • block buffer to study segmental and subcellular distribution of CFTR in the kidney

Other general uses are as pH control agent, water hardness precipitation, laboratory reagent, phosphatizing reagent.

General description

Sodium phosphate is a colorless to white crystalline powder or granules. It is prepared by neutralization of phosphoric acid under controlled conditions with sodium hydroxide or sodium carbonate .
We are committed to bringing you Greener Alternative Products, which belong to one of the four categories of greener alternatives. Sodium phosphate supports cleaner technologies as a versatile buffering and stabilizing agent that helps control pH, mitigate corrosion and side reactions, and extend equipment/component lifetimes—reducing waste, chemical use, and energy demand across processes. Click here for more information.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Huaqing Liu et al.
Journal of neuropathology and experimental neurology, 74(6), 500-511 (2015-05-02)
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
Yue Zhang et al.
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
Junpeng Yan et al.
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
Hsin-Wei Liao et al.
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
Dmitri Kravtsov et al.
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

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