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289027

Sigma-Aldrich

3-Phenylbutyraldehyde

97%

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About This Item

Linear Formula:
CH3CH(C6H5)CH2CHO
CAS Number:
16251-77-7
Molecular Weight:
148.20
EC Number:
240-362-9
MDL number:
MFCD00010698
UNSPSC Code:
12352100
PubChem Substance ID:
24857379
NACRES:
NA.22

Quality Level

100

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.)

functional group

aldehyde
phenyl

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCJ4799
MKCG4143
MKBT3570V
MKBG2419V
24596TJ

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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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