Skip to Content
MilliporeSigma
All Photos(1)

Documents

685828

Sigma-Aldrich

(R)-1-Phenylethanol

97%

Synonym(s):

(+)-α-Methylbenzyl alcohol, (+)-α-Phenethyl alcohol, (+)-α-Phenylethanol, (+)-1-Phenylethanol, (+)-1-Phenylethyl alcohol, (+)-sec-Phenethyl alcohol

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
C6H5CH(OH)CH3
CAS Number:
1517-69-7
Molecular Weight:
122.16
MDL number:
MFCD00064263
UNSPSC Code:
12352002
PubChem Substance ID:
329761001
NACRES:
NA.22

assay

97%

form

liquid

optical activity

[α]22/D +44.0°, c = 5%

refractive index

n20/D 1.528

density

0.9986 g/mL at 25 °C

SMILES string

C[C@@H](O)c1ccccc1

InChI

1S/C8H10O/c1-7(9)8-5-3-2-4-6-8/h2-7,9H,1H3/t7-/m1/s1

InChI key

WAPNOHKVXSQRPX-SSDOTTSWSA-N

Related Categories

General description

(R)-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk_germany

WGK 3

flash_point_f

185.0 °F - closed cup

flash_point_c

85 °C - closed cup

ppe

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Peroxygenase-Catalyzed Oxyfunctionalization Reactions Promoted by the Complete Oxidation of Methanol.
Ni Y, et al.
Angewandte Chemie (International Edition in English), 55(2), 798-801 (2016)
Sachiko Sugimoto et al.
Phytochemistry, 108, 189-195 (2014-12-03)
Three aromatic glycosides (1-3), two sulfur and nitrogen-containing compound glucosides (4, 5), and one flavonoid glycoside (6) were isolated from the leaves of Ixora undulata. Their structures were established by extensive 1D, 2D NMR, and HRESIMS experiments, and structure 4

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service