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D199

Supelco

Dimethcathinone hydrochloride

Sinônimo(s):

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

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About This Item

Fórmula empírica (Notação de Hill):
C11H15NO · HCl
Número CAS:
15351-09-4
Peso molecular:
213.70
Número CE:
239-384-1
Número MDL:
MFCD00467677
Código UNSPSC:
41116107
ID de substância PubChem:
329798721

controle de medicamentos

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

técnica(s)

HPLC: suitable
gas chromatography (GC): suitable

solubilidade

H2O: soluble

Formato

neat

cadeia de caracteres SMILES

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

chave InChI

APOWZIQNQJSLKG-UHFFFAOYSA-N

Aplicação

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

Ações bioquímicas/fisiológicas

Sympathomimetic CNS stimulant; exhibits amphetamine-like effects.

Pictogramas

Exclamation mark
GHS07

Palavra indicadora

Warning

Frases de perigo

H302 + H312 + H332

Classificações de perigo

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

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Gloves

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Certificados de análise (COA)

Lot/Batch Number
079H0989

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The stereoselective metabolism of dimethylpropion and monomethylpropion.
S L Markantonis et al.
Biochemical pharmacology, 35(3), 529-532 (1986-02-01)
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
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