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190284

Sigma-Aldrich

3-Phenoxybenzyl alcohol

98%

Sinónimos:

(3-Phenoxyphenyl)methanol, 1-Hydroxymethyl-3-phenoxybenzene, 3-(Hydroxymethyl)diphenyl ether, 3-Phenoxybenzenemethanol, m-Phenoxybenzyl alcohol

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About This Item

Fórmula lineal:
C6H5OC6H4CH2OH
Número de CAS:
13826-35-2
Peso molecular:
200.23
Beilstein/REAXYS Number:
475312
EC Number:
237-525-1
MDL number:
MFCD00004636
UNSPSC Code:
12352100
PubChem Substance ID:
24851426
NACRES:
NA.22

vapor pressure

0.1 mmHg ( 37.7 °C)

assay

98%

refractive index

n20/D 1.591 (lit.)

bp

135-140 °C/0.1 mmHg (lit.)

density

1.149 g/mL at 25 °C (lit.)

SMILES string

OCc1cccc(Oc2ccccc2)c1

InChI

1S/C13H12O2/c14-10-11-5-4-8-13(9-11)15-12-6-2-1-3-7-12/h1-9,14H,10H2

InChI key

KGANAERDZBAECK-UHFFFAOYSA-N

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Application

3-Phenoxybenzyl alcohol has been used in the synthesis of 3-phenoxylbenzyl β-D-glucuronide.

pictograms

Exclamation mark
GHS07

signalword

Warning

hcodes

H302

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

588.2 °F

flash_point_c

309 °C

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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Development of a class selective immunoassay for the type II pyrethroid insecticides.
Mak SK, et al.
Analytica Chimica Acta, 534(1), 109-120 (2005)
N Kaushik et al.
Journal of environmental science and health. Part. B, Pesticides, food contaminants, and agricultural wastes, 36(3), 289-300 (2001-06-20)
The metabolism of fluvalinate in chickpea plants in the field under sub-tropical climatic conditions has been investigated. Ten days after spraying with fluvalinate, leaves were collected and extracted in acetone. The extract was fractionated and the metabolites were identified by
G E Bast et al.
Archives of toxicology, 71(3), 179-186 (1997-01-01)
Isolated rabbit ears were single-pass perfused with a protein-free medium. Permethrin (0.05-23.5%, w/w) was applied in four distinct ointments. Permethrin, 3-phenoxybenzyl alcohol, 3-phenoxybenzaldehyde, and 3-phenoxybenzoic acid were analysed by HPLC. Permethrin was not detected in the effluent. The permeation coefficient
G E Bast et al.
Skin pharmacology and applied skin physiology, 11(4-5), 250-257 (1999-01-14)
The formation of 3-phenoxybenzoic acid from 3-phenoxybenzyl alcohol was determined in (a) rabbit ears, single-pass perfused with a protein-free buffer, pH 7.4; (b) the microsomal fraction and its supernatant from homogenized rabbit skin; and (c) purified alcohol dehydrogenase from horse
Brian Laffin et al.
Toxicology, 267(1-3), 39-44 (2009-10-27)
Synthetic pyrethroids are one of the most frequently and widely used class of insecticides, primarily because they have a higher insect to mammalian toxicity ratio than organochlorines or organophosphates. The basic structure of pyrethroids can be characterized as an acid
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