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MilliporeSigma

S0882

Sigma-Aldrich

Sodium selenate

≥95% (elemental analysis)

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1 UNIT
€682.00
1 UNIT
€1,990.00

€682.00


Estimated to ship onJanuary 30, 2025Details


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1 UNIT
€682.00
1 UNIT
€1,990.00

About This Item

Linear Formula:
Na2SeO4
CAS Number:
Molecular Weight:
188.94
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.55

Assay:
≥95% (elemental analysis)
form:
powder or crystals

€682.00


Estimated to ship onJanuary 30, 2025Details


Request a Bulk Order

Quality Level

Assay

≥95% (elemental analysis)

form

powder or crystals

pH

5.5-7.5 (25 °C, 18.9 g/L)

SMILES string

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

InChI

1S/2Na.H2O4Se/c;;1-5(2,3)4/h;;(H2,1,2,3,4)/q2*+1;/p-2

InChI key

MHQOTKLEMKRJIR-UHFFFAOYSA-L

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Show Differences

1 of 4

This Item
1.506051.519081.50828
separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

separation technique

reversed phase

particle size

5 μm

particle size

5 μm

particle size

5 μm

particle size

5 μm

matrix active group

C18 bonding phase

matrix active group

C18 bonding phase

matrix active group

C18 bonding phase

matrix active group

C18 bonding phase

pore size

100 Å pore size

pore size

100 Å pore size

pore size

100 Å pore size

pore size

100 Å pore size

agency

suitable for USP L1

agency

suitable for USP L1

agency

suitable for USP L1

agency

suitable for USP L1

Application


  • Selenium nanoparticles alleviate ischemia reperfusion injury-induced acute kidney injury by modulating GPx-1/NLRP3/Caspase-1 pathway.: This study demonstrates that selenium nanoparticles, including sodium selenate, mitigate acute kidney injury caused by ischemia reperfusion. The nanoparticles modulate key pathways, offering potential therapeutic applications in renal injury treatment (Wang et al., 2022).

  • Phosphoproteomic profiling of selenate-treated Alzheimer′s disease model cells.: This research provides a detailed phosphoproteomic profile of Alzheimer′s disease model cells treated with sodium selenate, uncovering its effects on protein phosphorylation and implications for neuroprotection (Chen et al., 2014).

Signal Word

Danger

Hazard Classifications

Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - STOT RE 2

Storage Class Code

6.1B - Non-combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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M Djanaguiraman et al.
Plant physiology and biochemistry : PPB, 48(12), 999-1007 (2010-10-19)
Oxidative stress is commonly induced when plants are grown under high temperature (HT) stress conditions. Selenium often acts as an antioxidant in plants; however, its role under HT-induced oxidative stress is not definite. We hypothesize that selenium application can partly
Maria Łabanowska et al.
Journal of plant physiology, 169(3), 275-284 (2011-12-14)
Biochemical analyses of antioxidant content were compared with measurements of fluorescence and electron paramagnetic resonance (EPR) to examine the alteration of radicals in wheat seedlings exposed to 2 days of selenium stress. Two genotypes of Polish and one of Finnish
Beatrice Pezzarossa et al.
Journal of the science of food and agriculture, 92(4), 781-786 (2011-09-29)
We investigated the effects of the foliar and fruit application of sodium selenate on selenium (Se) accumulation, fruit growth and ripening in peach and pear. Trials were conducted in two growing seasons. In 2008 selenate was applied at a rate
W C Stewart et al.
Journal of animal science, 90(2), 577-584 (2011-10-04)
Adequate Se transfer from ewes to lambs is important to prevent Se-deficiency diseases. To evaluate how different chemical forms of Se administered at comparative dosages to mature ewes affect Se status of their lambs, 240 ewes were divided into 8
Nigel C Jones et al.
Neurobiology of disease, 45(3), 897-901 (2011-12-21)
Tau hyperphosphorylation has been implicated in the pathogenesis of a variety of forms of human epilepsy. Here we investigated whether treatment with sodium selenate, a drug which reduces pathological hyperphosphorylated tau by enhancement of PP2A activity, would inhibit seizures in

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