All Photos(2)
About This Item
Linear Formula:
CH3CH(C6H5)CH2CHO
CAS Number:
Molecular Weight:
148.20
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.5179 (lit.)
bp
93-94 °C/16 mmHg (lit.)
density
0.997 g/mL at 25 °C (lit.)
SMILES string
[H]C(=O)CC(C)c1ccccc1
InChI
1S/C10H12O/c1-9(7-8-11)10-5-3-2-4-6-10/h2-6,8-9H,7H2,1H3
InChI key
MYHGOWDLVRDUFA-UHFFFAOYSA-N
Application
3-Phenylbutyraldehyde was used as a reactant to study the kinetics of the reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G.
Storage Class Code
10 - Combustible liquids
WGK
WGK 2
Flash Point(F)
206.6 °F - closed cup
Flash Point(C)
97.00 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Holger Bühler et al.
Chembiochem : a European journal of chemical biology, 6(4), 711-717 (2005-04-07)
The influence of Trp128-substituted mutants of the hydroxynitrile lyase from Manihot esculenta (MeHNL) on the stereoselectivity of MeHNL-catalyzed HCN additions to aldehydes with stereogenic centers, which yield the corresponding cyanohydrins, is described. In rac-2-phenylpropionaldehyde (rac-1) reactions, wild-type (wtMeHNL) and all
G M Raner et al.
Journal of inorganic biochemistry, 81(3), 153-160 (2000-10-29)
The reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G results in the covalent modification of the heme cofactor of this monooxygenase. Analysis of the resulting heme by electronic absorption spectrophotometry indicates that the reaction in the BM3
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