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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.)

functional group

hydroxyl

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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Certificados de análisis (COA)

Lot/Batch Number
BCCK6159
BCCG4429
BCCB2962
BCBW8969
BCBS1726V

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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)
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
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
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