380989
Sodium perrhenate
99.99% trace metals basis
Synonym(s):
Sodium Rhenate(VII), Sodium rhenium oxide, Sodiumoxido(trioxo)rhenium
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About This Item
Linear Formula:
NaReO4
CAS Number:
Molecular Weight:
273.19
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23
Recommended Products
Quality Level
Assay
99.99% trace metals basis
form
powder or crystals
impurities
≤150.0 ppm Trace Metal Analysis
density
5.39 g/mL at 25 °C (lit.)
SMILES string
[Na+].[O-][Re](=O)(=O)=O
InChI
1S/Na.4O.Re/q+1;;;;-1;
InChI key
KMISVFTVBOPTAI-UHFFFAOYSA-N
Related Categories
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Ox. Sol. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
5.1B - Oxidizing hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Technetium-99 (99Tc) is a major contaminant at nuclear power plants and several US Department of Energy sites. Its most common aqueous species, pertechnetate (TcO4-), is very mobile in the environment, and currently there are no effective technologies for its sequestration.
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Advanced healthcare materials, 1(4), 437-442 (2012-11-28)
Configuring RE(2) O(3) nanocrystals with pseudo-2D morphologies confers substantive gains in relaxivities over equivalent spherical counterparts. The most promising arises from Gd(2) O(3) whose ionic transverse and longitudinal relaxivities were as high as r(1) = 12.7 mM(-1) s(-1) and r(2)
Albert Schröckeneder et al.
Inorganic chemistry, 48(24), 11608-11614 (2009-11-27)
Rhenium(V) oxo complexes of the type [ReOX(L)(2)] (1-7; X = Cl, Br) containing beta-ketiminate ligands (L = CH(3)C(O)CH(2)C(NAr)CH(3): Ar = Ph (APOH), 2-MePh (MPOH), 2,6-Me(2)Ph (DPOH), 2,6-(i)Pr(2)Ph (DiPOH)) have been prepared by reaction of [ReOX(3)(OPPh(3))(SMe(2))] (X = Cl, Br) with
Michael J Booth et al.
Science (New York, N.Y.), 336(6083), 934-937 (2012-04-28)
5-Methylcytosine can be converted to 5-hydroxymethylcytosine (5hmC) in mammalian DNA by the ten-eleven translocation (TET) enzymes. We introduce oxidative bisulfite sequencing (oxBS-Seq), the first method for quantitative mapping of 5hmC in genomic DNA at single-nucleotide resolution. Selective chemical oxidation of
Cameron A Lippert et al.
Journal of the American Chemical Society, 132(11), 3879-3892 (2010-03-03)
Five-coordinate oxorhenium(V) anions with redox-active catecholate and amidophenolate ligands are shown to effect clean bimetallic cleavage of O(2) to give dioxorhenium(VII) products. A structural homologue with redox-inert oxalate ligands does not react with O(2). Redox-active ligands lower the kinetic barrier
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