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323527

Sigma-Aldrich

Selenium tetrachloride

Synonyme(s) :

Selenium (Ⅳ) chloride

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About This Item

Formule linéaire :
SeCl4
Numéro CAS:
10026-03-6
Poids moléculaire :
220.77
Numéro CE :
233-053-5
Numéro MDL:
MFCD00011225
Code UNSPSC :
12352302
ID de substance PubChem :
24859372
Nomenclature NACRES :
NA.23

Forme

powder or crystals

Concentration

35.0-36.5% Se (after reduction with sulphite, gravimetric)

Densité

2.6 g/mL at 25 °C (lit.)

Chaîne SMILES 

Cl[Se](Cl)(Cl)Cl

InChI

1S/Cl4Se/c1-5(2,3)4

Clé InChI

LNBXMNQCXXEHFT-UHFFFAOYSA-N

Pictogrammes

Skull and crossbonesHealth hazardEnvironment
GHS06,GHS08,GHS09

Mention d'avertissement

Danger

Mentions de danger

H301 + H331,H373,H410

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

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

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H Matsumura et al.
Proceedings of the National Academy of Sciences of the United States of America, 88(20), 9046-9050 (1991-10-15)
Prostaglandin (PG) D2 has been postulated to be an endogenous sleep-promoting factor in rats, and SeCl4 and Na2SeO3 recently have been shown to inhibit the PGD synthase (prostaglandin-H2 D-isomerase, EC 5.3.99.2) activity of rat brain. The effect of these selenium
Brenda Lee et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 22(13), 5679-5686 (2002-07-05)
It has been proposed that prostaglandin (PG) D(2) induces physiological sleep in mammals by acting on sleep centers located in the anterior hypothalamus. In fetal sheep, definitive rapid-eye-movement and non-rapid-eye-movement sleep states appear at approximately 125 d gestation (term is
F Islam et al.
Archives of biochemistry and biophysics, 289(1), 161-166 (1991-08-15)
Various inorganic selenocompounds dose-dependently inhibited the rat brain prostaglandin (PG) D synthase, both in the purified enzyme preparation and in the crude brain supernatant. All of the quadrivalent selenium compounds tested had a very limited range of IC50 values in
R Takahata et al.
Brain research, 623(1), 65-71 (1993-09-24)
Prostaglandin (PG) D2 has been postulated to be an endogenous sleep-promoting factor. Biosynthesis of PGD2 is catalyzed by PGD synthase (prostaglandin-H2 D-isomerase, EC 5.3.99.2), the activity of which is inhibited by inorganic selenium compounds such as SeCl4 and Na2SeO3. We
Sun-Chol Yu et al.
Organic & biomolecular chemistry, 8(4), 828-834 (2010-02-06)
Low molecular weight seleno-organic compounds exhibit glutathione peroxidase (GPx)-like activity; the well-known compound ebselen is being used in clinical trials as a stroke medication. Here, we describe the facile one-step synthesis of novel 5-selenized salicylic acid derivatives using selenium tetrachloride.
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