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Merck
CN

23195

Sigma-Aldrich

4-叔丁基儿茶酚 溶液

≥98% (calc. to the dried substance, GC), liquid

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关于此项目

经验公式(希尔记法):
C10H14O2
化学文摘社编号:
分子量:
166.22
Beilstein:
2043335
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
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方案

≥98% (calc. to the dried substance, GC)

表单

liquid

杂质

≤15% methanol

缺失

≤15% loss on drying, 24 h (vacuum)

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. 3 Dermal - Acute Tox. 4 Oral - Aquatic Chronic 2 - Carc. 1B - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B - Skin Sens. 1 - STOT SE 1

靶器官

Eyes,Central nervous system

WGK

WGK 3

个人防护装备

Faceshields, Gloves, Goggles

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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
María José Peñalver et al.
Biochimica et biophysica acta, 1597(1), 140-148 (2002-05-16)
The stoichiometry of oxygen consumption during tyrosinase-catalyzed oxidation of an o-diphenol (4-tert-butylcatechol, TBC) and a monophenol (4-tert-butylphenol, TBP) has been determined. At high [substrate]/[enzyme] ratios, in the case of o-diphenols, the stoichiometry of the enzyme-catalyzed reaction was always 1 O(2)/2
Contact sensitivity to para-tertiary-butylcatechol in an artificial limb.
A W Macfarlane et al.
Contact dermatitis, 22(1), 56-57 (1990-01-01)

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