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Merck

19671

Sigma-Aldrich

4-tert-Butylcatechol

≥99.0%

Sinónimos:

4-(1,1-Dimethylethyl)benzene-1,2-diol, 4-tert-Butylcatechin, 4-tert-Butylpyrocatechol, 4-TBC, p-tert-Butylcatechol

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About This Item

Fórmula lineal:
(CH3)3CC6H3-1,2-(OH)2
Número de CAS:
Peso molecular:
166.22
Beilstein/REAXYS Number:
2043335
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99.0%

form

powder

bp

285 °C (lit.)

mp

52-55 °C (lit.)
56-58 °C

solubility

methanol: soluble 1 g/10 mL, clear, colorless

SMILES string

CC(C)(C)c1ccc(O)c(O)c1

InChI

1S/C10H14O2/c1-10(2,3)7-4-5-8(11)9(12)6-7/h4-6,11-12H,1-3H3

InChI key

XESZUVZBAMCAEJ-UHFFFAOYSA-N

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General description

4-tert-Butylcatechol,in the presence of O2 catalyzed by tyrosinase, yields 4-tert-butyl-o-benzoquinone. Electrochemical oxidation of 4-tert-Butylcatechol in the presence of 4-hydroxycoumarin as nucleophile has been studied using cyclic voltammetry and controlled-potential coulometry. It undergoes electrochemical trimerization via anodic oxidation and mechanism of trimerization has been studied using cyclic voltammetry and controlled-potential coulometry.

Application

  • Antioxidant source for radical reactions: Research identified 4-tert-Butylcatechol as a viable source of hydrogen atoms in radical reactions, specifically in deiodination processes, expanding its utility in synthetic organic chemistry (Povie et al., 2016).

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1 - Skin Corr. 1B - Skin Sens. 1

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Los clientes también vieron

Electrochemical study of 3, 4-dihydroxybenzoic acid and 4-tert-butylcatechol in the presence of 4-hydroxycoumarin application to the electro-organic synthesis of coumestan derivatives.
Golabi SM and Nematollahi D.
Journal of Electroanalytical Chemistry, 430(1), 141-146 (1997)
Mechanistic study of electrochemical oxidation of 4-tert-butylcatechol: A facile electrochemical method for the synthesis of new trimer of 4-tert-butylcatechol.
Nematollahi D, et al.
Electrochimica Acta, 49(15), 2495-2502 (2004)
Y Furukawa et al.
Biochemical pharmacology, 40(10), 2337-2342 (1990-11-15)
A series of 4-alkylcatechols and 1,2-diacetoxy-4-alkylbenzenes (from methyl to butyl) were chemically synthesized for in vitro evaluation as stimulators of nerve growth factor (NGF) synthesis. All compounds were proven to be potent in stimulating NGF synthesis in L-M cells (a
K Yonemoto et al.
Biochemical pharmacology, 32(8), 1379-1382 (1983-04-15)
Topical application of 4-tertiary butyl catechol (TBC) causes vitiligo in the skin of man and animals, and previous electron microscopic studies showed pheomelanin formation in the affected areas. In the present study, we investigated changes of enzyme activities, eumelanin content
Occupational vitiligo and contact sensitivity to para-tertiary butyl catechol.
D J Gawkrodger et al.
Contact dermatitis, 25(3), 200-201 (1991-09-01)

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