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T49409

Sigma-Aldrich

2,4,6-Tri-tert-butylphenol

98%

Sinonimo/i:

2,4,6-Tri-t-butylphenol, 2,4,6-Tri-tert-butyl-1-hydroxybenzene, 2,4,6-Tris(1,1-dimethylethyl)phenol, 2,4,6-Tris(tert-butyl)phenol, 2,4,6-Tritert-butylphenol

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About This Item

Formula condensata:
[(CH3)3C]3C6H2OH
Numero CAS:
732-26-3
Peso molecolare:
262.43
Beilstein:
1913256
Numero CE:
211-989-5
Numero MDL:
MFCD00008821
Codice UNSPSC:
12352100
ID PubChem:
24900239
NACRES:
NA.22

Livello qualitativo

100

Saggio

98%

P. ebollizione

277 °C (lit.)

Punto di fusione

125-130 °C (lit.)

Stringa SMILE

CC(C)(C)c1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C

InChI

1S/C18H30O/c1-16(2,3)12-10-13(17(4,5)6)15(19)14(11-12)18(7,8)9/h10-11,19H,1-9H3
PFEFOYRSMXVNEL-UHFFFAOYSA-N

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Avvertenze

Danger

Indicazioni di pericolo

H302,H317,H360D,H373,H410

Classi di pericolo

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Repr. 1B - Skin Sens. 1B - STOT RE 2

Organi bersaglio

Liver

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

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Certificati d'analisi (COA)

Lot/Batch Number
STBK7177
STBK5463
STBK2520
STBJ9419
STBJ7684

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1,3,5-Tri-tert-butylbenzene 97%

Sigma-Aldrich

223778

1,3,5-Tri-tert-butylbenzene

3-tert-Butylphenol 99%

Sigma-Aldrich

124281

3-tert-Butylphenol

2,5-Di-tert-butylhydroquinone 99%

Sigma-Aldrich

112976

2,5-Di-tert-butylhydroquinone

2,6-Di-tert-butyl-1,4-benzoquinone 98%

Sigma-Aldrich

153931

2,6-Di-tert-butyl-1,4-benzoquinone

O Takahashi et al.
Xenobiotica; the fate of foreign compounds in biological systems, 13(5), 319-326 (1983-05-01)
Single oral doses of the haemorrhagic antioxidant 2,4,6-tri-t-butylphenol (260 mg/kg) were well absorbed in the rat. Peak blood levels of this compound were reached in 15-60 min. The blood elimination half-lives were 18.2 min for the alpha-phase and 11.8 h
S Nemoto et al.
Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan, 42(6), 359-366 (2002-03-06)
An analytical method has been developed for the determination of 2,4,6-tri-tert-butylphenol (TTBP) in foods. TTBP was determined by GC/MS (SIM) after extraction from food samples using a steam distillation technique. The developed method was able to determine simultaneously 2,4-di-tert-butylphenol (2,4-DTBP)
Christian R Goldsmith et al.
Journal of the American Chemical Society, 124(1), 83-96 (2002-01-05)
Lipoxygenases are mononuclear non-heme iron enzymes that regio- and stereospecifcally convert 1,4-pentadiene subunit-containing fatty acids into alkyl peroxides. The rate-determining step is generally accepted to be hydrogen atom abstraction from the pentadiene subunit of the substrate by an active ferric
Yoshinori Kadoma et al.
Chemosphere, 74(5), 626-632 (2008-12-17)
To clarify the mechanism of phenol toxicity, the radical-scavenging activity of 2- or 2,6-di-tert-butyl- and 2-methoxy-substituted phenols was investigated by combining two distinct approaches: first, the induction period method for methacrylate polymerization initiated by benzoyl peroxide or 2,2'-azobisisobutyronitrile; and secondly
A L Wilcox et al.
Chemical research in toxicology, 6(4), 413-416 (1993-07-01)
13-Hydroperoxyoctadeca-9,11,15-trienoic acid was reacted with a catalytic amount of 5,10,15,20-tetraphenyl-21H,23H-porphyrin iron(III) chloride in dichloromethane containing 2,4,6-tri-tert-butylphenol. The principal products were identified as 13-oxooctadeca-9,11,15-trienoic acid, 13-oxotrideca-9,11-dienoic acid, and a series of isomeric epoxyaryl ethers [9-(2,4,6-tri-tert-butylphenoxy)-12,13-epoxyoctadec-10-enoic acids and 11-(2,4,6-tri-tert-butylphenoxy)-12,13-epoxyoctadec-9-enoic acids]. The epoxyaryl
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