Skip to Content
MilliporeSigma
All Photos(1)

Documents

77848

Supelco

(R)-(+)-1-Phenylethanol

for chiral derivatization, LiChropur™, ≥99.0%

Synonym(s):

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

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

About This Item

Empirical Formula (Hill Notation):
C8H10O
CAS Number:
1517-69-7
Molecular Weight:
122.16
Beilstein/REAXYS Number:
2039798
MDL number:
MFCD00064263
UNSPSC Code:
12000000
PubChem Substance ID:
329767971
NACRES:
NA.05

grade

for chiral derivatization

Quality Level

100

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.)

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

Looking for similar products? Visit Product Comparison Guide

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; Asymmetric opening of cyclic anhydrides and of epoxides

Recommended products

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
GHS07

signalword

Warning

Hazard Classifications

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

wgk_germany

WGK 3

flash_point_f

185.0 °F

flash_point_c

85 °C

ppe

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

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCBX0029
BCBJ8366V
BCBH2166V
BCBF8473V
1290950

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Customers Also Viewed

Slide 1 of 2

1 of 2

(R)-(+)-α-Methylbenzylamine for chiral derivatization, LiChropur™, ≥99.0%

Supelco

77879

(R)-(+)-α-Methylbenzylamine

D-(−)-Tartaric acid ReagentPlus®, 99%

Sigma-Aldrich

T206

D-(−)-Tartaric acid

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