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Principaux documents

M1651

Sigma-Aldrich

Sodium molybdate dihydrate

≥99.5%, suitable for plant cell culture

Synonyme(s) :

Molybdic acid sodium salt dihydrate

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About This Item

Formule linéaire :
Na2MoO4 · 2H2O
Numéro CAS:
Poids moléculaire :
241.95
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352207
ID de substance PubChem :
Nomenclature NACRES :
NA.71

Niveau de qualité

Pureté

≥99.5%

Pertinence de la réaction

core: molybdenum

Technique(s)

cell culture | plant: suitable

Pf

100 °C (dec.) (lit.)

Chaîne SMILES 

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

InChI

1S/Mo.2Na.2H2O.4O/h;;;2*1H2;;;;/q;2*+1;;;;;2*-1

Clé InChI

FDEIWTXVNPKYDL-UHFFFAOYSA-N

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Application

<ul>
<li><strong>Synthesis and characterization of Anderson-Evans type polyoxometalates, antibacterial properties:</strong> This study focuses on the synthesis and characterization of Anderson-Evans type polyoxometalates, utilizing Sodium molybdate dihydrate, exploring its potential in enhancing antibacterial properties (Avci Özbek H, 2023).</li>
<li><strong>Molybdenum Exposure in Drinking Water Vs Feed Impacts Apparent Absorption of Copper Differently in Beef Cattle Consuming a High-Forage Diet:</strong> This research examines how Sodium molybdate dihydrate, when introduced through water compared to feed, affects the absorption of copper in beef cattle, highlighting its role in agricultural nutrient management (Thorndyke MP et al., 2021).</li>
<li><strong>Molybdate Attenuates Lipid Accumulation in the Livers of Mice Fed a Diet Deficient in Methionine and Choline:</strong> This study demonstrates the effectiveness of Sodium molybdate dihydrate in reducing lipid accumulation in the livers of mice, offering insights into its potential therapeutic applications in liver health (Lee S et al., 2018).</li>
</ul>

Code de la classe de stockage

13 - Non Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 1

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

Eyeshields, Gloves, type N95 (US)


Certificats d'analyse (COA)

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Consulter la Bibliothèque de documents

Saraswathi Panneerselvam et al.
Chemico-biological interactions, 145(2), 159-163 (2003-04-11)
Diabetes mellitus is a disease, which virtually affects all the systems in the body including the immune system. Bacterial infections are important causes of increased morbidity and mortality in diabetic patients. In the present study, we assessed the effect of
S W Ball et al.
Canadian journal of physiology and pharmacology, 80(3), 205-209 (2002-05-07)
A focus of current diabetes research is the development of insulinomimetic compounds for oral treatment of diabetes and its associated cardiac complications. Screening compounds for their potential insulinomimetic effects usually involves the use of radioactive isotopes. The focus of this
Vaddypally Shivaiah et al.
Inorganic chemistry, 44(24), 8846-8854 (2005-11-22)
Two Anderson-type heteropolyanion-supported copper phenanthroline complexes, [Al(OH)6Mo6O18[Cu(phen)(H2O)2]2]1+ (1c) and [Al(OH)6Mo6O18[Cu(phen)(H2O)Cl]2]1- (1a) complement their charges in one of the title compounds [Al(OH)6Mo6O18[Cu(phen)(H2O)2]2][Al(OH)6Mo6O18[Cu(phen)(H2O)Cl]2].5H2O [1c][1a].5 H2O 1. Similar charge complementarity exists in the chromium analogue, [Cr(OH)6Mo6O18[Cu(phen)(H2O)2]2][Cr(OH)6Mo6O18[Cu(phen)(H2O)Cl]2].5 H2O [2c][2a].5 H2O 2. The chloride coordination
Ana Acacia de Sá Pinheiro et al.
Experimental parasitology, 115(4), 352-358 (2006-11-23)
In this work, an ecto-phosphatase activity of Entamoeba histolytica was characterized using intact cells. This activity presented the following biochemical characteristics: (i) it hydrolyzes p-NPP with V(max) of 8.00+/-0.22 nmol p-NP x h(-1) x 10(-5) cells and K(m) of 2.68+/-0.25
Bo-Geon Yun et al.
Biochemistry, 43(25), 8217-8229 (2004-06-24)
Hsp90 functions to facilitate the folding of newly synthesized and denatured proteins. Hsp90 function is modulated through its interactions with cochaperones and the binding and hydrolysis of ATP. Recently, novobiocin has been shown to bind to a second nucleotide binding

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