124338
Butyrophenone
≥99%
Synonym(s):
1-Benzoylpropane, 1-Phenyl-1-butanone, NSC 8463, Phenyl propyl ketone
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About This Item
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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.)
functional group
ketone
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.
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
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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(+)
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Analytica Chimica Acta, 548(1), 95-100 (2005)
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
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