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Merck
CN

07366

(R)-(+)-1-Phenylethanol

≥98.5% (sum of enantiomers, GC)

Synonym(s):

(+)-Methyl phenyl carbinol, (R)-(+)-α-Methylbenzyl alcohol

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About This Item

Empirical Formula (Hill Notation):
C8H10O
CAS Number:
Molecular Weight:
122.16
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2039798
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Product Name

(R)-(+)-1-Phenylethanol, ≥98.5% (sum of enantiomers, GC)

InChI key

WAPNOHKVXSQRPX-SSDOTTSWSA-N

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

assay

≥98.5% (sum of enantiomers, GC)

form

liquid

optical activity

[α]/D +45±2°, c = 5% in methanol

optical purity

enantiomeric ratio: ≥97:3 (GC)

refractive index

n20/D 1.527

bp

88-89 °C/10 mmHg (lit.)

mp

9-11 °C (lit.)

density

1.012 g/mL at 20 °C (lit.)

functional group

hydroxyl
phenyl

Quality Level

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pictograms

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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

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


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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

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