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(+/-)-1-Phenylethanol, 97%
CAS: 98-85-1 | C8H10O | 122.167 g/mol
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Catalog number A13837.0E
also known as A13837-0E
Price (USD)
163.65
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Quantity:
2500 g
Price (USD)
163.65
Online Exclusive
182.00Save 18.35 (10%)
Each
Chemical Identifiers
CAS98-85-1
IUPAC Name1-phenylethan-1-ol
Molecular FormulaC8H10O
InChI KeyWAPNOHKVXSQRPX-UHFFFAOYNA-N
SMILESCC(O)C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetFormLiquid
Identification (FTIR)Conforms
Appearance (Color)Clear colorless
Refractive Index1.5250-1.5300 @ 20?C
Assay (GC)≥96.0%
The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynamic kinetic resolution of 1-phenylethanol by transesterification.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynamic kinetic resolution of 1-phenylethanol by transesterification.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, acids.
The Arthrobacter sp. is able to grow with (+ I-,(-)-1-phenylethanol or the racemic mixture as sole source of carbon. Growth is most rapid with the (-)-isomer, doubling time 12 h. Lipases show good activity and, in some cases, improved enantioselectivity when employed in pure ionic liquids for dynamic kinetic resolution of 1-phenylethanol by transesterification.
Solubility
Insoluble in water.
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Store away from strong oxidizing agents, acids.
RUO – Research Use Only
General References:
- Roger E. Cripps,; Peter W. Trudgill,; John G. Whateley. The Metabolism of 1-Phenylethanol and Acetophenone by Nocardia T5 and an Arthrobacter Species. European Journal of Biochemistry. 1978, 86 (1), 175-186.
- Priska Hubera,; Svetoslav Bratovanova,; Stefan Bienz,; Christoph Syldatk,; Markus Pietzsch.Chiral silicon groups as auxiliaries for enantioselective synthesis: access to optically active silanes by biotransformation and the enantiospecific preparation of (R)-(+)-1-phenylethanol . Tetrahedron: Asymmetry. year of publication , 7(1), 69-78.