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204315

Sigma-Aldrich

Selenium dioxide

99.999% trace metals basis

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Synonym(s):
NSC 56753, Selenium oxide
Linear Formula:
SeO2
CAS Number:
7446-08-4
Molecular Weight:
110.96
EC Number:
231-194-7
MDL number:
MFCD00003562
PubChem Substance ID:
24852252
NACRES:
NA.23

vapor pressure

1 mmHg ( 157 °C)

Quality Level

200

Assay

99.999% trace metals basis

form

solid

mp

315 °C (subl.) (lit.)

SMILES string

O=[Se]=O

InChI

1S/O2Se/c1-3-2

InChI key

JPJALAQPGMAKDF-UHFFFAOYSA-N

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Application

Mild oxidizing reagent for allylic olefins and acetylenes. Conversion of 1,3-diketones to 1,2,3-triones.

Signal Word

Danger

Hazard Statements

H301 + H331 - H373 - H410

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - STOT RE 2

Storage Class Code

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

危险化学品

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Tetrahedron Letters, 34, 2979-2979 (1993)
Asian Journal of Chemistry, 19, 4107-4107 (2007)
Zhangrong Lou et al.
Chemical communications (Cambridge, England), 49(24), 2445-2447 (2013-02-19)
Based on a novel strategy for modulating the fluorescence of selenide and selenoxide, we have designed and developed a reversible fluorescent probe for hypochloric acid. And the synthesis, characterization, fluorescence properties, as well as the biological applications in living cells
Zoyne Pedrero et al.
Journal of chromatography. A, 1139(2), 247-253 (2006-12-05)
Selenium speciation in Se-enriched Lens esculenta grown in hydroponic culture containing inorganic selenium as Na(2)SeO(3) and Na(2)SeO(4) was performed. After 16 days of growth, the plants were collected and divided in two parts, roots and stems and then analysed to
Vijay P Singh et al.
Chemistry, an Asian journal, 6(6), 1431-1442 (2011-05-11)
The syntheses of selenenate/seleninate esters and related derivatives by aromatic nucleophilic substitution (S(N)Ar) reactions of 2-bromo-3-nitrobenzylalcohol (13) and 2-bromo-3-nitrobenzaldehyde (17) with Na(2)Se(2)/nBuSeNa are described. The reaction of 13 with Na(2)Se(2) at room temperature afforded 7-nitro-1,2-benzisoselenole(3H) (15) instead of the desired
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