Skip to Content
Merck
CN

23195

Sigma-Aldrich

4-tert-Butylcatechol solution

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

Sign Into View Organizational & Contract Pricing

Select a Size

About This Item

Empirical Formula (Hill Notation):
C10H14O2
CAS Number:
98-29-3
Molecular Weight:
166.22
Beilstein:
2043335
MDL number:
MFCD00002201
UNSPSC Code:
12352100
PubChem Substance ID:
329752395

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Assay

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

form

liquid

impurities

≤15% methanol

loss

≤15% loss on drying, 24 h (vacuum)

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

Looking for similar products? Visit Product Comparison Guide

Signal Word

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
SZBC2470
SZBC2300
SZBC0680
SZBC0130
SZBB2690

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service