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alpha-Phthalimidopropiophenone

alpha-Phthalimidopropiophenone Structure
  • ₹0
  • Product name: alpha-Phthalimidopropiophenone
  • CAS: 19437-20-8
  • MF: C17H13NO3
  • MW: 279.29
  • EINECS:
  • MDL Number:MFCD00060520
  • Synonyms:2-(1-Methyl-2-oxo-2-phenylethyl)-1H-isoindole-1,3(2H)-dione;A-PHTHALIMIDOPROPIOPHENONE;ALPHA-PHTHALIMIDOPROPIOPHENONE;a-Phtalimidopropiophnone;-Phthalimidopropiophenone;2-PhthaliMido-1-phenylpropan-1-one;2-(1-oxo-1-phenylpropan-2-yl)isoindole-1,3-dione;1H-Isoindole-1,3(2H)-dione, 2-(1-methyl-2-oxo-2-phenylethyl)-
Manufacturer Product number Product description Packaging Price Updated Buy

Properties

Melting point :87-88°C
Boiling point :447.2±28.0 °C(Predicted)
Density :1.304±0.06 g/cm3(Predicted)
solubility :DMF: 30 mg/ml; DMF:PBS (pH 7.2) (1:1): 0.5 mg/ml; DMSO: 20 mg/ml; Ethanol: 10 mg/ml
form :A crystalline solid
pka :-2.45±0.20(Predicted)
CAS DataBase Reference :19437-20-8(CAS DataBase Reference)
NIST Chemistry Reference :«ALPHA»-phthalimidopropiophenone(19437-20-8)

Safety Information

Symbol(GHS): GHS hazard pictogramsGHS hazard pictograms
Signal word: Warning
Hazard statements:
Code Hazard statements Hazard class Category Signal word Pictogram P-Codes
H302 Harmful if swallowed Acute toxicity,oral Category 4 Warning GHS hazard pictograms P264, P270, P301+P312, P330, P501
H410 Very toxic to aquatic life with long lasting effects Hazardous to the aquatic environment, long-term hazard Category 1 Warning GHS hazard pictograms P273, P391, P501
Precautionary statements:
P264 Wash hands thoroughly after handling.
P264 Wash skin thouroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P273 Avoid release to the environment.
P301+P312 IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330 Rinse mouth.
P391 Collect spillage. Hazardous to the aquatic environment
P501 Dispose of contents/container to..…

Description

α-Phthalimidopropiophenone is a cathinone analog that has been identified in capsules being distributed by the illicit drug market. The substitution of the phthalimido moiety for the typical α-amino group may increase the stability of this cathinone in storage. Alternatively, similar nitrogen-protected propiophenones have been shown to be metabolized in vivo to produce cathinone, suggesting that this compound may act as a prodrug. The physiological and toxicological properties of this compound are not known. This product is intended for forensic and research applications.

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