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T49409

2,4,6-Tri-tert-butylphenol

98%

Synonym(s):

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

Linear Formula:
[(CH3)3C]3C6H2OH
CAS Number:
732-26-3
Molecular Weight:
262.43
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24900239
EC Number:
211-989-5
Beilstein/REAXYS Number:
1913256
MDL number:
MFCD00008821
Assay:
98%
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Quality Level

100

assay

98%

bp

277 °C (lit.)

mp

125-130 °C (lit.)

SMILES string

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

InChI key

PFEFOYRSMXVNEL-UHFFFAOYSA-N

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signalword

Danger

target_organs

Liver

Storage Class

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

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Hazard Classifications

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

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB3381
SDBB0624
STBL2785
STBK7177
STBK8743

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David E Lansky et al.
Inorganic chemistry, 45(13), 5119-5125 (2006-06-20)
High-valent metal-oxo complexes are postulated as key intermediates for a wide range of enzymatic and synthetic processes. To gain an understanding of these processes, the reactivity of an isolated, well-characterized Mn(V)-oxo complex, (TBP8Cz)MnVO (1), (TBP8Cz = octakis(para-tert-butylphenyl)corrolazinato(3-)) has been examined.
K Matsumoto et al.
The Journal of toxicological sciences, 16(4), 167-179 (1991-11-01)
In order to study the chronic toxicity of 2, 4, 6-tri-tert-butylphenol (TTBP), groups of 40 Slc: Wistar rats of either sex were fed diet containing 0, 30, 100, 300 or 1000 ppm of TTBP for up to 24 months. Hematological
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
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Global Trade Item Number

SKUGTIN
T49409-100G04061837346835