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77848

(R)-(+)-1-Phenylethanol

derivatization grade (chiral), LiChropur, ≥99.0%

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:
12352200
NACRES:
NA.05
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2039798

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Product Name

(R)-(+)-1-Phenylethanol, derivatization grade (chiral), LiChropur, ≥99.0%

InChI

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

SMILES string

C[C@@H](O)c1ccccc1

InChI key

WAPNOHKVXSQRPX-SSDOTTSWSA-N

grade

derivatization grade (chiral)

product line

ChiraSelect

assay

≥99.0% (sum of enantiomers, GC)
≥99.0%

form

liquid

optical activity

[α]20/D +45±1°, c = 5% in methanol

optical purity

enantiomeric ratio: ≥99.5:0.5 (GC)

quality

LiChropur

technique(s)

HPLC: suitable

refractive index

n20/D 1.528

bp

88-89 °C/10 mmHg (lit.)

mp

9-11 °C (lit.)

density

1.012 g/mL at 20 °C (lit.)

Quality Level

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General description

(R)-(+)-1-Phenylethanol is a chiral derivatizating agent, which is employed for derivatizing acids for their subsequent analysis using gas chromatography as the analytical technique.

Other Notes

Chiral reagent used for the determination of enantiomeric purity and for resolutions of acids[1]; Asymmetric opening of cyclic anhydrides and of epoxides[2][3][4]
Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Legal Information

ChiraSelect is a trademark of Sigma-Aldrich Co. LLC
LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

pictograms

Exclamation mark

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

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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H. Niwa et al.
Tetrahedron Letters, 29, 5139-5139 (1988)
T. Rosen et al.
Journal of the American Chemical Society, 107, 3731-3731 (1985)
S.V. Ley et al.
Tetrahedron, 46, 4995-4995 (1990)
Y. Takeuchi et al.
Journal of the Chemical Society. Perkin Transactions 1, 2203-2203 (1987)
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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