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Key Documents

142344

Sigma-Aldrich

Butyl phenyl ether

99%

Synonym(s):

1-Phenoxybutane, Butoxybenzene, Butyloxybenzene, Phenyl butyl ether, Phenyl n-butyl ether, n-Butyl phenyl ether

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About This Item

Linear Formula:
C6H5O(CH2)3CH3
CAS Number:
Molecular Weight:
150.22
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.497 (lit.)

bp

210.3 °C (lit.)

mp

−19 °C (lit.)

density

0.935 g/mL at 25 °C (lit.)

SMILES string

CCCCOc1ccccc1

InChI

1S/C10H14O/c1-2-3-9-11-10-7-5-4-6-8-10/h4-8H,2-3,9H2,1H3

InChI key

YFNONBGXNFCTMM-UHFFFAOYSA-N

Application

Butyl phenyl ether was used as model compound to study the transformation of human pharmaceuticals detected in water during chlorine disinfection. It was used in the synthesis of amino acids with aryl-keto function in their side-chains.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

179.6 °F - closed cup

Flash Point(C)

82 °C - closed cup


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Karen E Pinkston et al.
Environmental science & technology, 38(14), 4019-4025 (2004-08-10)
Many of the human pharmaceuticals detected in municipal wastewater effluent, surface water, and groundwater contain functional groups that could undergo transformation reactions during chlorine disinfection. To assess the potential importance of these reactions to the environmental fate of pharmaceuticals, the
M A Bednarek
The journal of peptide research : official journal of the American Peptide Society, 52(3), 195-200 (1998-10-17)
Amino acids with aryl-keto function in their side-chains were obtained in excellent yields in the reaction of omega-carboxyamino acids with liquid HF in the presence of aromatic compounds susceptible to electrophilic substitution, such as anisole, 2-methoxybiphenyl, butyl phenyl ether or

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