23195
4-tert-Butylcatechol solution
≥98% (calc. to the dried substance, GC), liquid
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About This Item
Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
Molecular Weight:
166.22
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
2043335
MDL number:
Assay:
≥98% (calc. to the dried substance, GC)
Form:
liquid
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
assay
≥98% (calc. to the dried substance, GC)
form
liquid
impurities
≤15% methanol
loss
≤15% loss on drying, 24 h (vacuum)
signalword
Danger
Hazard Classifications
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
target_organs
Eyes,Central nervous system
wgk
WGK 3
ppe
Faceshields, Gloves, Goggles
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Contact sensitivity to para-tertiary-butylcatechol in an artificial limb.
A W Macfarlane et al.
Contact dermatitis, 22(1), 56-57 (1990-01-01)
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
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
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
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
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