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Key Documents

54680

Sigma-Aldrich

Butyl 4-hydroxybenzoate

≥99.0% (GC)

Synonym(s):

p-Hydroxybenzoic acid n-butyl ester, Butyl paraben

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About This Item

Linear Formula:
HOC6H4CO2(CH2)3CH3
CAS Number:
Molecular Weight:
194.23
Beilstein:
1103741
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

≥99.0% (GC)

bp

156-157 °C/3.5 mmHg (lit.)

mp

67-70 °C (lit.)
68-70 °C

functional group

ester

SMILES string

CCCCOC(=O)c1ccc(O)cc1

InChI

1S/C11H14O3/c1-2-3-8-14-11(13)9-4-6-10(12)7-5-9/h4-7,12H,2-3,8H2,1H3

InChI key

QFOHBWFCKVYLES-UHFFFAOYSA-N

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Application

Butyl 4-hydroxybenzoate can be used to synthesize 4-[(9-oxoxanthen-3-yl)-carbonyloxy]benzoate by reacting with 2-phenoxyterephthaloyl dichloride in hot pyridine.

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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3-(4-Butoxycarbonylphenyloxycarbonyl)-xanthen-9-one.
Centore, R, et al.
Acta Crystallographica Section C, Crystal Structure Communications, 51(6), 1211-1213 (1995)
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Journal of chromatography. A, 1218(38), 6654-6662 (2011-08-25)
The effect of the addition of 25%, 50% and 75% (weight percent, wt%) of larger particles (resp. 3 and 5 μm) to a commercial batch of 1.9 μm particles has been investigated as an academic exercise to study the effects
A Beltran et al.
Analytica chimica acta, 677(1), 72-78 (2010-09-21)
In this paper we describe the synthesis, characterisation and use of two distinct molecularly imprinted polymers (MIPs) prepared using esters of p-hydroxybenzoic acid (parabens) as templates: one MIP was synthesised by precipitation polymerisation using a semi-covalent molecularly imprinting strategy with

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