(R)-(+)-1-Phenylethanol

(R)-(+)-1-Phenylethanol
  • CAS No.:1517-69-7
Other grades of this product :
(R)-(+)-1-Phenylethanol Basic information
Product Name:(R)-(+)-1-Phenylethanol
Synonyms:(R)-(+)-PHENYLETHANOL;(R)-(+)-SEC-PHENETHYL ALCOHOL;(R)-(+)-SEC-PHENYLETHYL ALCOHOL;(R)-(+)-1-METHYLBENZYL ALCOHOL;(R)-(+)-1-PHENYLETHYL ALCOHOL;(R)-(+)-1-PHENYLETHANOL;(R)-1-PHENYLETHANOL;(R)(+)-ALPHA-PHENETHYL ALCOHOL
CAS:1517-69-7
MF:C8H10O
MW:122.16
EINECS:604-814-2
Product Categories:chiral;Building Blocks for Liquid Crystals;Chiral Building Blocks;Chiral Compounds (Building Blocks for Liquid Crystals);Functional Materials;Simple Alcohols (Chiral);Alcohols, Hydroxy Esters and Derivatives;Chiral Compounds;Synthetic Organic Chemistry;Alcohols;Chiral Building Blocks;Organic Building Blocks
Mol File:1517-69-7.mol
(R)-(+)-1-Phenylethanol Chemical Properties
Melting point 9-11 °C (lit.)
Boiling point 88-89 °C/10 mmHg (lit.)
alpha 42.5 º (NEAT)
density 1.012 g/mL at 20 °C (lit.)
refractive index n20/D 1.528
Fp 85 °C
storage temp. Sealed in dry,Room Temperature
solubility 20g/l
pka14.43±0.20(Predicted)
form clear liquid
color Colorless to Light yellow
PH7 (H2O)
optical activity[α]22/D +44.0°, c = 5%
Water Solubility 20 G/L (20 ºC)
BRN 2039798
Stability:Stable. Flammable. Incompatible with strong acids, strong oxidizing agents.
InChIKeyWAPNOHKVXSQRPX-SSDOTTSWSA-N
CAS DataBase Reference1517-69-7(CAS DataBase Reference)
NIST Chemistry ReferenceBenzenemethanol, «alpha»-methyl-, (R)-(1517-69-7)
Safety Information
Hazard Codes Xn
Risk Statements 22-38-41-36/37/38
Safety Statements 26-39-37/39
RIDADR UN 2937 6.1/PG 3
WGK Germany 3
HazardClass 6.1
PackingGroup III
HS Code 29062990
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
ALFA English
(R)-(+)-1-Phenylethanol Usage And Synthesis
Chemical PropertiesColorless to light yellow liqui
Uses(R)-(+)-1-Phenylethanol is used in the synthesis of optically active products. It is also useful in the determination of enantiomeric purity and for resolutions of acids.
General Description(R)-1-Phenylethanol can be prepared from ethylbenzene via enantioselective hydroxylation of ethylbenzene catalyzed by peroxygenase enzyme.

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