MedKoo Cat#: 592206 | Name: Metamfepramone HCl
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Metamfepramone is a stimulant structurally related to cathinone, primarily acts as a norepinephrine-dopamine reuptake inhibitor (NDRI), enhancing synaptic neurotransmitter levels. Its psychostimulant effects are comparable to amphetamines but with a shorter duration of action. Studies indicate that metamfepramone increases locomotor activity and exhibits anorectic properties in animal models, suggesting potential for appetite suppression. Its affinity for monoamine transporters, particularly dopamine and norepinephrine, is responsible for its central nervous system stimulation

Chemical Structure

Metamfepramone HCl
CAS#10105-90-5 (HCl)

Theoretical Analysis

MedKoo Cat#: 592206

Name: Metamfepramone HCl

CAS#: 10105-90-5 (HCl)

Chemical Formula: C11H16ClNO

Exact Mass: 177.1154

Molecular Weight: 213.71

Elemental Analysis: 61.82; H, 7.55; Cl, 16.59; N, 6.55; O, 7.49

Price and Availability

Size Price Availability Quantity
10mg USD 350.00 2 weeks
50mg USD 950.00 2 weeks
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Related CAS #
15351-09-4 (free base) 10105-90-5 (HCl) 35026-79-0 (S-isomer HCl) 35026-80-3 (R-isomer HCl) 65528-82-7 (R-isomer free base)
Synonym
Metamfepramone hydrochloride; NSC 234706; NSC-234706; NSC234706; N,N-DMC; N,N-Dimethylcathinone HCl; N,N-DMC;
IUPAC/Chemical Name
1-Propanone, 2-(dimethylamino)-1-phenyl- hydrochloride
InChi Key
APOWZIQNQJSLKG-UHFFFAOYSA-N
InChi Code
InChI=1S/C11H15NO.ClH/c1-9(12(2)3)11(13)10-7-5-4-6-8-10;/h4-9H,1-3H3;1H
SMILES Code
CC(N(C)C)C(C1=CC=CC=C1)=O.[H]Cl
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info
Product Data
Biological target:
Metamfepramone is a sympathomimetic agent metamfepramone.
In vitro activity:
TBD
In vivo activity:
TBD
Solvent mg/mL mM comments
Solubility
DMF 1.0 4.68
DMSO 2.0 9.36
Ethanol 2.0 9.36
Methanol 1.0 4.68
PBS (pH 7.2) 10.0 46.79
Note: There can be variations in solubility for the same chemical from different vendors or different batches from the same vendor. The following factors can affect the solubility of the same chemical: solvent used for crystallization, residual solvent content, polymorphism, salt versus free form, degree of hydration, solvent temperature. Please use the solubility data as a reference only. Warming and sonication will facilitate dissolving. Still have questions? Please contact our Technical Support scientists.

Preparing Stock Solutions

The following data is based on the product molecular weight 213.71 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
1: Thevis M, Sigmund G, Thomas A, Gougoulidis V, Rodchenkov G, Schänzer W. Doping control analysis of metamfepramone and two major metabolites using liquid chromatography-tandem mass spectrometry. Eur J Mass Spectrom (Chichester). 2009;15(4):507-15. doi: 10.1255/ejms.1010. PubMed PMID: 19661559. 2: Rispoli V, Rotiroti D, Carelli V, Liberatore F, Scipione L, Marra R, Giorgioni G, Di Stefano A. Choline pivaloyl esters improve in rats cognitive and memory performances impaired by scopolamine treatment or lesions of the nucleus basalis of Meynert. Neurosci Lett. 2004 Feb 19;356(3):199-202. PubMed PMID: 15036629. 3: Pokrajac M, Miljković B, Misailović B. Mass spectrometric investigation of 2-aminopropiophenones and some of their metabolites. Rapid Commun Mass Spectrom. 1991 Feb;5(2):59-61. PubMed PMID: 1804406. 4: Markantonis SL, Kyroudis A, Beckett AH. The in vitro reduction of dimethylpropion. Biochem Med Metab Biol. 1989 Aug;42(1):1-8. PubMed PMID: 2775559. 5: Markantonis SL, Kyroudis A, Beckett AH. Evaluation of the percutaneous absorption and metabolism of some aminopropiophenones. J Pharm Pharmacol. 1986 Jul;38(7):515-9. PubMed PMID: 2875152. 6: Markantonis SL, Kyroudis A, Beckett AH. The stereoselective metabolism of dimethylpropion and monomethylpropion. Biochem Pharmacol. 1986 Feb 1;35(3):529-32. PubMed PMID: 3947386. 7: Soholing WE. [Therapy of the orthostatic syndrome. Studies using dimepropion-HCI]. Fortschr Med. 1982 Feb 18;100(7):289-93. German. PubMed PMID: 7042502.