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B87806

Sigma-Aldrich

4-Butoxyphenol

98%

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About This Item

Linear Formula:
CH3(CH2)3OC6H4OH
CAS Number:
122-94-1
Molecular Weight:
166.22
EC Number:
204-583-4
MDL number:
MFCD00002336
UNSPSC Code:
12352100
PubChem Substance ID:
24892093
NACRES:
NA.22

Assay

98%

form

solid

impurities

2% hydroquinone

mp

65-66 °C (lit.)

SMILES string

CCCCOc1ccc(O)cc1

InChI

1S/C10H14O2/c1-2-3-8-12-10-6-4-9(11)5-7-10/h4-7,11H,2-3,8H2,1H3

InChI key

MBGGFXOXUIDRJD-UHFFFAOYSA-N

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificates of Analysis (COA)

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Frédéric L P Gabriel et al.
Applied and environmental microbiology, 73(10), 3320-3326 (2007-03-21)
Recently we showed that degradation of several nonylphenol isomers with alpha-quaternary carbon atoms is initiated by ipso-hydroxylation in Sphingobium xenophagum Bayram (F. L. P. Gabriel, A. Heidlberger, D. Rentsch, W. Giger, K. Guenther, and H.-P. E. Kohler, J. Biol. Chem.
A Davydov et al.
Biochemical and biophysical research communications, 258(2), 322-325 (1999-05-18)
The regeneration of the tyrosyl radical in chemically reduced native or p-butoxyphenol-treated radical free forms of mouse ribonucleotide reductase R2 protein has been studied. Chemical reduction has been achieved by treatment with light-activated flavin compounds: deazaflavin, flavin mononucleotide, or deazaflavin

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