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211176

Sigma-Aldrich

Selenous acid

98%

Synonym(s):

Selenious acid

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About This Item

Linear Formula:
H2SeO3
CAS Number:
7783-00-8
Molecular Weight:
128.97
EC Number:
231-974-7
MDL number:
MFCD00011331
UNSPSC Code:
12352301
PubChem Substance ID:
24852658
NACRES:
NA.22

Quality Level

200

assay

98%

form

solid

mp

70 °C (dec.) (lit.)

density

3.004 g/mL at 25 °C (lit.)

SMILES string

O[Se](O)=O

InChI

1S/H2O3Se/c1-4(2)3/h(H2,1,2,3)

InChI key

MCAHWIHFGHIESP-UHFFFAOYSA-N

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Application

Selenous acid can be used as a reagent to synthesize:
  • α-Ketoacectals by reacting with acetophenones and triethylorthoformate in the presence of boron trifluoride etherate as a catalyst.
  • 4-Formyl-7-methylcoumarin using 4,7-dimethylcoumarin in the presence of xylene as a solvent.
  • Selenium substituted quinoxaline derivatives from 2,3-dichloro quionoxaline.

signalword

Danger

Hazard Classifications

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

Storage Class

6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
STBK8898
STBK2145
STBJ7660
STBJ2502
STBH3328

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D Seidel et al.
Journal of clinical chemistry and clinical biochemistry. Zeitschrift fur klinische Chemie und klinische Biochemie, 16(7), 407-411 (1978-07-01)
A simple one-vial-method was developed for the quantitative determination of sphingomyelinase activity in human leukocytes and urine, using [14C-methyl] sphingomyelin. The measured activities of healthy control persons show a higher scatter in (n=50) urine (1.2 +/- 0.5 nmol/h . ml
One-pot synthesis of alpha-ketoacetals from aryl methyl ketones in the presence of selenous acid catalyzed by boron trifluoride etherate
Kharkongor I, et al.
Tetrahedron Letters, 56, 4359-4362 (2015)
Thomas G Back et al.
Journal of the American Chemical Society, 124(41), 12104-12105 (2002-10-10)
1,2-Oxaselenolane Se-oxide is a novel cyclic seleninate ester that functions as a remarkably efficient glutathione peroxidase mimetic by catalyzing the reduction of tert-butyl hydroperoxide to tert-butyl alcohol in the presence of benzyl thiol. The seleninate ester can be conveniently generated
Y Kayanoki et al.
Journal of biochemistry, 119(4), 817-822 (1996-04-01)
Selenium-dependent glutathione peroxidase (GPx) plays a protective role in oxidative stress-induced apoptosis. In this study, we demonstrated that MDBK cells, a bovine renal epithelial cell line, exhibited internucleosomal DNA fragmentation characteristic of apoptotic cell death under selenium-deficient conditions with lower
Yuki Ohta et al.
Toxicology and applied pharmacology, 226(2), 169-177 (2007-11-09)
All nutritional selenium sources are transformed into the assumed common intermediate selenide for the syntheses of selenoproteins for utilization and/or of selenosugar for excretion. Methylselenol [monomethylselenide, MMSe] is the assumed intermediate leading to other methylated metabolites, dimethylselenide (DMSe) and trimethylselenonium
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