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124338

Sigma-Aldrich

Butyrophenone

≥99%

Synonym(s):
NSC 8463, Phenyl propyl ketone, 1-Phenyl-1-butanone, 1-Benzoylpropane
Linear Formula:
C6H5COCH2CH2CH3
CAS Number:
Molecular Weight:
148.20
Beilstein:
508305
EC Number:
MDL number:
PubChem Substance ID:

Quality Level

assay

≥99%

form

liquid

refractive index

n20/D 1.520 (lit.)

bp

228-230 °C (lit.)

mp

11-13 °C (lit.)

density

1.021 g/mL at 25 °C (lit.)

SMILES string

CCCC(=O)c1ccccc1

InChI

1S/C10H12O/c1-2-6-10(11)9-7-4-3-5-8-9/h3-5,7-8H,2,6H2,1H3

InChI key

FFSAXUULYPJSKH-UHFFFAOYSA-N

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Application

Butyrophenone has been used to study the relationship between the electrolyte counter-ion concentration and the critical micelle concentration for several surfactants. It has been used to generate PhCO+ ions by 70 eV electron ionization.

Packaging

25, 100 g in glass bottle

Biochem/physiol Actions

Butyrophenones constitutes neuroleptic drugs and interacts with the opiate receptor by inhibiting the stereospecific binding of 3H-naloxone.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

190.4 °F

Flash Point(C)

88 °C

Personal Protective Equipment

dust mask type N95 (US),Eyeshields,Gloves

Certificate of Analysis

Certificate of Origin

Critical micelle concentration of surfactants in aqueous buffered and unbuffered systems.
Fuguet E, et al.
Analytica Chimica Acta, 548(1), 95-100 (2005)
Hao Chen et al.
Journal of the American Society for Mass Spectrometry, 14(3), 182-188 (2003-03-22)
Phosphonium ions CH(3)P(O)OCH(3)(+) (93 Th) and CH(3)OP(O)OCH(3)(+) (109 Th) react with 1,4-dioxane to form unique cyclic ketalization products, 1,3,2-dioxaphospholanium ions. By contrast, a variety of other types of ions having multiple bonds, including the acylium ions CH(3)CO(+) (43 Th), CH(3)OCO(+)
I Creese et al.
European journal of pharmacology, 36(1), 231-235 (1976-03-01)
Interaction of neuroleptic drugs with the opiate receptors was investigated by inhibition of the stereospecific binding of 3H-naloxone. Benperidol and pimozide, with IC50's of 0.3-0.5 muM, were more potent than the classical opiates meperidine and propoxyphene. A systematic structure-activity relationship
Fabrice Gritti et al.
Journal of chromatography. A, 1410, 118-128 (2015-08-10)
An original method is proposed for the accurate and reproducible measurement of the time-based dispersion properties of short L< 50cm and narrow rc< 50μm tubes at mobile phase flow rates typically used in very high-pressure liquid chromatography (vHPLC). Such tubes
Fabrice Gritti et al.
Journal of chromatography. A, 1420, 54-65 (2015-10-17)
The impact of the column hardware volume (≃ 1.7 μL) on the optimum reduced plate heights of a series of short 2.1 mm × 50 mm columns (hold-up volume ≃ 80-90 μL) packed with 1.8 μm HSS-T3, 1.7 μm BEH-C18

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