124338
Butyrophenone
≥99%
別名:
1-Benzoylpropane, 1-Phenyl-1-butanone, NSC 8463, Phenyl propyl ketone
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この商品について
化学式:
C6H5COCH2CH2CH3
CAS番号:
分子量:
148.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-799-7
Beilstein/REAXYS Number:
508305
MDL number:
Assay:
≥99%
Form:
liquid
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.)
functional group
ketone, phenyl
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
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.
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保管分類
10 - Combustible liquids
wgk
WGK 3
flash_point_f
190.4 °F
flash_point_c
88 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Group 4: Flammable liquids + Type 3 petroleums + Hazardous rank III + Water insoluble liquid
fsl
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(+)
Critical micelle concentration of surfactants in aqueous buffered and unbuffered systems.
Fuguet E, et al.
Analytica Chimica Acta, 548(1), 95-100 (2005)
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