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Key Documents

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:
Molecular Weight:
200.23
Beilstein:
475312
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

vapor pressure

0.1 mmHg ( 37.7 °C)

Quality Level

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

Signal Word

Warning

Hazard Statements

Precautionary Statements

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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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
Sh T Iskandarova
Gigiena i sanitariia, (6)(6), 6-8 (1995-11-01)
The threshold level of 3-phenoxybenzyl alcohol (3-PBA) in ambient air was set up at 0.48 mg/m3. Inhalation of 3-PBA in concentrations of 4.86 and 0.518 mg/m3 caused changes in the central nervous system, metabolic processes, liver function, reduced the nonspecific
Hee-Joo Kim et al.
Journal of agricultural and food chemistry, 55(10), 3750-3757 (2007-04-26)
Pyrethroids are widely used in agriculture as insecticides. This study describes a sensitive enzyme-linked immunosorbent assay for the detection of the glucuronide conjugate of 3-phenoxybenzyl alcohol, a putative pyrethroid metabolite that may be used as a biomarker of exposure to
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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