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Merck
CN

03-4881

4-tert-Butylcatechol

SAJ first grade, ≥98.0%

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About This Item

Linear Formula:
(CH3)3CC6H3-1,2-(OH)2
CAS Number:
98-29-3
Molecular Weight:
166.22
EC Number:
202-653-9
UNSPSC Code:
12352104
PubChem Substance ID:
329747724
Beilstein/REAXYS Number:
2043335
MDL number:
MFCD00002201

Key Documents

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InChI key

XESZUVZBAMCAEJ-UHFFFAOYSA-N

InChI

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

SMILES string

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

grade

SAJ first grade

assay

≥98.0%

availability

available only in Japan

bp

285 °C (lit.)

mp

52-55 °C (lit.)

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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

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
U0564
U1473
U1380
U0253
U1175

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J N Rodríguez-López et al.
Biochimica et biophysica acta, 1548(2), 238-256 (2001-08-22)
Using gas chromatography-mass spectrometry, the direct enzymatic release of o-diphenol (4-tert-butylcatechol) during the action of tyrosinase on a monophenol (4-tert-butylphenol) has been demonstrated for the first time in the literature. The findings confirm the previously proposed mechanism to explain the
Sirley V Pereira et al.
The Analyst, 136(22), 4745-4751 (2011-10-11)
In this article we report the development of an integrated microfluidic system coupled to a screen-printed carbon electrode (SPCE) applied to the quantitative determination of IgG specific antibodies present in serum samples of patients that suffer from Chagas disease. This
An unusual delayed patch test reaction to para-tertiary-butylcatechol.
R C Yu et al.
Contact dermatitis, 22(2), 110-111 (1990-02-01)
T Kawashima et al.
Biochemical pharmacology, 34(19), 3517-3521 (1985-10-01)
Intermediates of pheomelanin in tissue cultured B16 melanoma cells were analyzed by high performance liquid chromatography, and reduced glutathione (GSH), L-dopa, 2-[(L)-S-cysteinyl]-L-dopa (2-SCD) and 5-[(L)-S-cysteinyl]-L-dopa (5-SCD) were quantified. The effects of 4-tertiary butylcatechol (TBC), an antioxidant which causes skin depigmentation
Martín A Fernández-Baldo et al.
Talanta, 79(3), 681-686 (2009-07-07)
Botrytis cinerea is a plant-pathogenic fungus that produces the disease known as grey mould in a wide variety of agriculturally important hosts in many countries. This paper describes the development of an immunosensor coupled to carbon-based screen-printed electrodes (SPCE) modified
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