P24055
1-Phenyl-1,2-ethanediol
97%
Synonym(s):
(±)-1-Phenyl-1,2-ethanediol, (±)-Phenylethylene glycol
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About This Item
Linear Formula:
C6H5CH(OH)CH2OH
CAS Number:
Molecular Weight:
138.16
EC Number:
202-258-1
Beilstein/REAXYS Number:
1306723
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Assay:
97%
Form:
solid
Product Name
1-Phenyl-1,2-ethanediol, 97%
SMILES string
OCC(O)c1ccccc1
InChI key
PWMWNFMRSKOCEY-UHFFFAOYSA-N
InChI
1S/C8H10O2/c9-6-8(10)7-4-2-1-3-5-7/h1-5,8-10H,6H2
assay
97%
form
solid
bp
272-274 °C/760 mmHg (lit.)
mp
66-68 °C (lit.)
Quality Level
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Related Categories
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Ashwini C Mathpati et al.
Journal of biotechnology, 262, 1-10 (2017-09-30)
Kinetic resolution of rac-1,2-diols using the biocatalyst Burkholderia cepacia lipase (BCL) immobilized on a biodegradable binary blend support of hydroxypropyl methyl cellulose(HPMC)/polyvinyl alcohol (PVA) has been investigated. The immobilization technique improved enzyme activity significantly and it has excellent recyclability with
Li Cao et al.
Biotechnology and bioengineering, 94(3), 522-529 (2006-02-25)
Soluble epoxide hydrolase (EH) from the potato Solanum tuberosum and an evolved EH of the bacterium Agrobacterium radiobacter AD1, EchA-I219F, were purified for the enantioconvergent hydrolysis of racemic styrene oxide into the single product (R)-1-phenyl-1,2-ethanediol, which is an important intermediate
Cesar Mateo et al.
Analytical biochemistry, 314(1), 135-141 (2003-03-14)
In this paper we report the development of a novel and simple spectrophotometric assay which allows one to achieve the continuous, rapid, sensitive, and accurate determination of an epoxide hydrolase activity. This assay is based on the elaboration of a
O Spiegelstein et al.
Pharmaceutical research, 17(2), 216-221 (2000-04-06)
The purpose of this study was to evaluate the in vitro inhibitory potency of various amide analogues and derivatives of valproic acid toward human microsomal epoxide hydrolase (mEH). mEH inhibition was evaluated in human liver microsomes with 25 microM (S)-(+)-styrene
Yanbin Liu et al.
Journal of industrial microbiology & biotechnology, 33(4), 274-282 (2005-12-02)
A microorganism with the ability to catalyze the resolution of racemic phenyloxirane was isolated and identified as Aspergillus niger SQ-6. Chiral capillary electrophoresis was successfully applied to separate both phenyloxirane and phenylethanediol. The epoxide hydrolase (EH) involved in this resolution
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