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03-5000

Sigma-Aldrich

Butyl 4-hydroxybenzoate

SAJ first grade, ≥99.0%

Synonym(s):

p-Hydroxybenzoic acid n-butyl ester, Butyl paraben

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About This Item

Linear Formula:
HOC6H4CO2(CH2)3CH3
CAS Number:
94-26-8
Molecular Weight:
194.23
Beilstein/REAXYS Number:
1103741
EC Number:
202-318-7
MDL number:
MFCD00016478
UNSPSC Code:
12352108
PubChem Substance ID:
329747726

grade

SAJ first grade

assay

≥99.0%

availability

available only in Japan

bp

156-157 °C/3.5 mmHg (lit.)

mp

67-70 °C (lit.)

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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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H315,H318

Hazard Classifications

Eye Dam. 1 - Skin Irrit. 2

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

ppe

Eyeshields, Gloves, type N95 (US)

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Reproductive toxicology (Elmsford, N.Y.), 28(1), 26-31 (2009-06-06)
Parabens, a class of preservatives routinely added to cosmetics, pharmaceuticals, and foods, have estrogenic properties. Given that intrauterine implantation of fertilized ova in inseminated females can be disrupted by minute levels of exogenous estrogens, we assessed the impact of parabens
Anuschka Liekens et al.
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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