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D199

Supelco

Dimethcathinone hydrochloride

Synonym(e):

(±)-2-Dimethylamino-1-phenyl-1-propanone hydrochloride

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About This Item

Empirische Formel (Hill-System):
C11H15NO · HCl
CAS-Nummer:
15351-09-4
Molekulargewicht:
213.70
EG-Nummer:
239-384-1
MDL-Nummer:
MFCD00467677
UNSPSC-Code:
41116107
PubChem Substanz-ID:
329798721

Arzneimittelkontrolle

USDEA Schedule I; Home Office Schedule 1; regulated under CDSA - not available from Sigma-Aldrich Canada

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

Löslichkeit

H2O: soluble

Format

neat

SMILES String

Cl.CC(N(C)C)C(=O)c1ccccc1

InChI

1S/C11H15NO.ClH/c1-9(12(2)3)11(13)10-7-5-4-6-8-10;/h4-9H,1-3H3;1H

InChIKey

APOWZIQNQJSLKG-UHFFFAOYSA-N

Anwendung

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Biochem./physiol. Wirkung

Sympathomimetic CNS stimulant; exhibits amphetamine-like effects.

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

Gefahreneinstufungen

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Die Dokumentenbibliothek aufrufen

S L Markantonis et al.
The Journal of pharmacy and pharmacology, 38(7), 515-519 (1986-07-01)
The absorption of diethylpropion (DEP I), dimethylpropion (DMP I) and some of their basic metabolites into and passage through the skin was investigated and a comparison of their metabolism following oral and percutaneous administration made. High percentages (60-80%) of DEP
S L Markantonis et al.
Biochemical medicine and metabolic biology, 42(1), 1-8 (1989-08-01)
A study of the in vitro metabolism of dimethylpropion using different tissue homogenates of certain animals showed that: 1. Only the two major metabolites of dimethylpropion, i.e., methylpseudoephedrine and monomethylpropion were formed. 2. Species variation was observed with regard to
M Pokrajac et al.
Rapid communications in mass spectrometry : RCM, 5(2), 59-61 (1991-02-01)
Complex metabolic mixtures of 2-aminopropiophenones, obtained both after in vitro and human in vivo metabolism of these compounds, have been investigated using both mass spectrometry and gas chromatography/mass spectrometry. The mass spectrometric fragmentation schemes of the compounds have been proposed
W E Soholing
Fortschritte der Medizin, 100(7), 289-293 (1982-02-18)
We treated 30 patients between 22 to 30 years of age, who showed static labile circulatory disturbances of blood pressure. We carried out a double blind study following a two week schedule using for treatment an "indirect" sympathomimeticum Dimepropion-HCI. Control
The stereoselective metabolism of dimethylpropion and monomethylpropion.
S L Markantonis et al.
Biochemical pharmacology, 35(3), 529-532 (1986-02-01)
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