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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:
1126-79-0
Molecular Weight:
150.22
EC Number:
214-426-1
MDL number:
MFCD00009438
UNSPSC Code:
12352100
PubChem Substance ID:
24848519
NACRES:
NA.22

Quality Level

100

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

Related Categories

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
GHS07

signalword

Warning

hcodes

H319

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

179.6 °F - closed cup

flash_point_c

82 °C - closed cup

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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

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