B99901
4-tert-Butylphenol
99%
Sinónimos:
4-(1,1-Dimethylethyl)phenol, Butylphen, PTBP, p-tert-Butylphenol
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Acerca de este artículo
Fórmula lineal:
(CH3)3CC6H4OH
Número CAS:
Peso molecular:
150.22
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-679-0
Beilstein/REAXYS Number:
1817334
MDL number:
Assay:
99%
Form:
powder
Servicio técnico
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Permítanos ayudarlevapor pressure
1 mmHg ( 70 °C)
Quality Level
assay
99%
form
powder
bp
236-238 °C (lit.)
mp
96-101 °C (lit.)
density
0.908 g/mL at 25 °C (lit.)
SMILES string
CC(C)(C)c1ccc(O)cc1
InChI
1S/C10H14O/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7,11H,1-3H3
InChI key
QHPQWRBYOIRBIT-UHFFFAOYSA-N
Gene Information
mouse ... Esr1(13982)
rat ... Ar(24208)
General description
4-tert-Butylphenol is a phenol derivative. Its contact with skin may lead to leukoderma. It is widely used in the polymer industry. Reaction of 4-tert-Butylphenol with mushroom tyrosinase has been reported to afford 4-t-butyl-o-benzoquinone and kinetics of this enzymatic reaction has been investigated.
Application
4-tert-Butylphenol may be employed as carbon and energy supplement in the culture medium of Sphingobium fuliginis strains.
4-tert-Butylphenol is suitable reagent used in kinetic study of hydroxylation of 4-tert-butylphenol by mushroom tyrosinase. It may be used in the synthesis of calix[7]arene.
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Danger
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Hazard Classifications
Aquatic Chronic 1 - ED ENV 1 - Eye Dam. 1 - Repr. 2 - Skin Irrit. 2
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Calix [7] arene from 4-tert-butylphenol and formaldehyde.
Nakamoto Y and Ishida S-I.
Makromol. Chem., Rapid Commun., 3(10), 705-707 (1982)
K Thörneby-Andersson et al.
Pigment cell research, 13(1), 33-38 (2000-04-13)
Exposure of the skin to certain phenols or catechols such as 4-tert-butylphenol (TBP) and 4-tert-butylcatechol (TBC) may cause leukoderma. These substances are used in the polymer industry and numerous cases have been reported. Several theories of the mechanism for chemical
J R Ros et al.
European journal of biochemistry, 222(2), 449-452 (1994-06-01)
The reaction between 4-tert-butylphenol (BuPhOH) and mushroom tyrosinase was investigated by following 4-tert-butyl-ortho-benzoquinone, whose high stability permits the reaction to be used as a model for the study of the monophenolase activity of tyrosinase. The system evolves to a pseudo-steady