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Merck
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Key Documents

Altri documenti

G307

Sigma-Aldrich

Galvinoxyl, free radical

Sinonimo/i:

2,6-Di-tert-butyl-α-(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadien-1-ylidene)-p-tolyloxy, free radical

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About This Item

Formula empirica (notazione di Hill):
C29H41O2
Numero CAS:
2370-18-5
Peso molecolare:
421.63
Numero CE:
219-133-2
Numero MDL:
MFCD00001616
Codice UNSPSC:
12352000
ID PubChem:
24895112
NACRES:
NA.22

Punto di fusione

158-159 °C (lit.)

Temperatura di conservazione

2-8°C

Stringa SMILE

CC(C)(C)c1cc(\C=C2\C=C(C(=O)C(=C2)C(C)(C)C)C(C)(C)C)cc(c1[O])C(C)(C)C

InChI

1S/C29H41O2/c1-26(2,3)20-14-18(15-21(24(20)30)27(4,5)6)13-19-16-22(28(7,8)9)25(31)23(17-19)29(10,11)12/h13-17H,1-12H3
GNZDAXRYGVFYPU-UHFFFAOYSA-N

Applicazioni

Free radical and free-radical scavenger.

Codice della classe di stoccaggio

11 - Combustible Solids

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

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2,2-Diphenyl-1-picrylhydrazyl

Sigma-Aldrich

D9132

2,2-Diphenyl-1-picrylhydrazyl

4-Hydroxy-TEMPO 95%

Sigma-Aldrich

176141

4-Hydroxy-TEMPO

1,1-Diphenyl-2-picrylhydrazine 97%

Sigma-Aldrich

281689

1,1-Diphenyl-2-picrylhydrazine

1,1-Diphenylethylene 97%

Sigma-Aldrich

D206806

1,1-Diphenylethylene

TEMPO purified by sublimation, 99%

Sigma-Aldrich

426369

TEMPO

Shuichi Shimakawa et al.
Lipids, 38(3), 225-231 (2003-06-06)
Nitroxyl radicals are known to act as radical scavenging antioxidants. In the present study, a lipophilic nitroxyl radical, cyclohexane-1-spiro-2'-(4'-oxyimidazolidine-1'-oxyl)-5'-spiro-1"-cyclohexane (nitroxyl radical I) was synthesized and its antioxidant capacity was assessed in comparison with a hydrophilic nitroxyl radical, 4-hydroxy-2,2,6,6-tetra-methylpiperidine-N-oxyl (Tempol). Both
Lloyd L Lumata et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 227, 14-19 (2012-12-19)
The goal of this work was to test feasibility of using galvinoxyl (2,6-di-tert-butyl-α-(3,5-di-tert-butyl-4-oxo-2,5-cyclohexadien-1-ylidene)-p-tolyloxy) as a polarizing agent for dissolution dynamic nuclear polarization (DNP) NMR spectroscopy. We have found that galvinoxyl is reasonably soluble in ethyl acetate, chloroform, or acetone and
Donald B McPhail et al.
Journal of agricultural and food chemistry, 51(6), 1684-1690 (2003-03-06)
There is current interest in the use of naturally occurring flavonoids as antioxidants for the preservation of foods and the prevention of diseases such as atherosclerosis and cancers. To establish the molecular characteristics required for maximum antioxidant activity, electron spin
Jens Z Pedersen et al.
The Journal of pharmacy and pharmacology, 59(12), 1721-1728 (2007-12-07)
Polyphenolic coumarins are known to act as antioxidants in biological systems, but it is difficult to distinguish their antioxidant activity from the many other effects they produce in cells. We have determined the radical scavenging capacity of 22 structurally related
Abolfazl Barzegar et al.
PloS one, 6(10), e26012-e26012 (2011-10-22)
Curcumin has many pharmaceutical applications, many of which arise from its potent antioxidant properties. The present research examined the antioxidant activities of curcumin in polar solvents by a comparative study using ESR, reduction of ferric iron in aqueous medium and
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