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541281

Sigma-Aldrich

Methaneseleninic acid

95%

Synonym(s):

Methylseleninic acid

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About This Item

Linear Formula:
CH3SeO2H
CAS Number:
Molecular Weight:
127.00
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

95%

mp

128-132 °C (lit.)

SMILES string

C[Se](O)=O

InChI

1S/CH4O2Se/c1-4(2)3/h1H3,(H,2,3)

InChI key

UEQANLFPOFICBH-UHFFFAOYSA-N

General description

Methaneseleninic acid is an oxidizing agent useful in organic synthesis. It is formed as major product during the oxidations of γ-glutamyl-Se-methylselenocysteine and Se-methylselenocysteine.

Application

Methaneseleninic acid may be employed as a ligand in the preparation of lanthanide complexes. It may also be used in the synthesis of a 12-membered macrocycle [(p-MeO-C6H4)2Te(μ-O)-(μ-MeSeO2)(μ4-Cl)]2 by reacting with bis(p-methoxyphenyl)tellurium dichloride.

Signal Word

Danger

Hazard Classifications

Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - STOT RE 2

Storage Class Code

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic 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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M Kotrebai et al.
Journal of chromatography. A, 866(1), 51-63 (2000-02-19)
Increasing speciation demands in clinical chemistry, toxicology and nutrition have made the determination of the total elements in a sample inadequate; the amount of an element and the chemical forms in which it is present need to be known. Inductively
Novel europium and gadolinium complexes with methaneseleninate as ligand: Synthesis, characterization and spectroscopic study.
Souza AP, et al.
Inorganic Chemistry Communications, 15, 97-101 (2012)
Shutao Yin et al.
Apoptosis : an international journal on programmed cell death, 17(4), 388-399 (2011-12-20)
ABT-737, a novel small molecule inhibitor of Bcl-2 family proteins, holds great promise to complement current cancer therapies. However many types of solid cancer cells are resistant to ABT-737. One practical approach to improve its therapeutic efficacy is to combine
Haitao Zhang et al.
The Prostate, 70(12), 1265-1273 (2010-07-14)
Previous studies have demonstrated that physiological concentrations of methylseleninic acid (MSA) inhibits the growth of prostate cancer cells. The growth inhibitory effect could be attributed to cell cycle block and apoptosis induction. The current study was designed to investigate the
12-Membered Macrocycles Containing Ditelluroxane and Selenotelluroxane Units.
Srungavruksham NK and Baskar V.
European Journal of Inorganic Chemistry, 2012(1), 136-142 (2012)

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