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Merck
CN

03-4881

Sigma-Aldrich

4-叔丁基儿茶酚

SAJ first grade, ≥98.0%

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About This Item

线性分子式:
(CH3)3CC6H3-1,2-(OH)2
CAS号:
分子量:
166.22
Beilstein:
2043335
EC 号:
MDL编号:
UNSPSC代码:
12352104
PubChem化学物质编号:

等级

SAJ first grade

方案

≥98.0%

存货情况

available only in Japan

沸点

285 °C (lit.)

mp

52-55 °C (lit.)

SMILES字符串

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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Danger

危险分类

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

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

235.4 °F - closed cup

闪点(°C)

113 °C - closed cup

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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An unusual delayed patch test reaction to para-tertiary-butylcatechol.
R C Yu et al.
Contact dermatitis, 22(2), 110-111 (1990-02-01)
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
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
T Kawashima et al.
The Journal of investigative dermatology, 82(1), 53-56 (1984-01-01)
4-Tertiary butyl catechol (TBC) causes depigmentation in humans and animals and stimulates formation of pheomelanosomes. In this study, we investigated the effects of noncytotoxic doses of TBC on glutathione S-transferase (GST) activity in the skin of Uscd strain mice and
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

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