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190284

Sigma-Aldrich

3-Phenoxybenzyl alcohol

98%

Synonym(s):

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

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About This Item

Linear Formula:
C6H5OC6H4CH2OH
CAS Number:
13826-35-2
Molecular Weight:
200.23
Beilstein:
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)

Quality Level

100

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.)

functional group

hydroxyl
phenoxy

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

Signal Word

Warning

Hazard Statements

H302

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

588.2 °F

Flash Point(C)

309 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCK6159
BCCG4429
BCCB2962
BCBW8969
BCBS1726V

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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
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
Development of a class selective immunoassay for the type II pyrethroid insecticides.
Mak SK, et al.
Analytica Chimica Acta, 534(1), 109-120 (2005)
[Gas chromatographic determination of butyl alcohols in the atmospheric air].
V A Ushakova et al.
Gigiena i sanitariia, (2)(2), 68-69 (1990-02-01)
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