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Merck
CN

D-090

3-Desmethylprodine hydrochloride solution

1.0 mg/mL in acetonitrile (as free base), ampule of 1 mL, certified reference material, Cerilliant®

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About This Item

Empirical Formula (Hill Notation):
C15H21NO2 · HCl
CAS Number:
4968-48-3
Molecular Weight:
283.79
UNSPSC Code:
41116107

Key Documents

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InChI

1S/C15H21NO2.ClH/c1-3-14(17)18-15(9-11-16(2)12-10-15)13-7-5-4-6-8-13;/h4-8H,3,9-12H2,1-2H3;1H

InChI key

WQANBUZBKNCRKH-UHFFFAOYSA-N

SMILES string

CN1CCC(OC(CC)=O)(C2=CC=CC=C2)CC1.Cl

grade

certified reference material

feature

(Snap-N-Spike®)

packaging

ampule of 1 mL

manufacturer/tradename

Cerilliant®

drug control

Narcotic Licence Schedule A (Switzerland); estupefaciente (Spain); Decreto Lei 15/93: Tabela IA (Portugal), kontrollierte Droge in Deutschland

concentration

1.0 mg/mL in acetonitrile (as free base)

format

single component solution

storage temp.

−20°C

General description

A certified Snap-N-Spike® Solution suitable for LC/MS or GC/MS methods and applications in clinical toxicology, forensic analysis, urine drug testing, or pain prescription monitoring. MPPP or 3-Desmethylprodine is an opioid analgesic developed in the 1940s for use as a pharmaceutical but abused illegally today as a recreational drug. This designer drug is an analog of meperidine (Demerol®) but is listed by US DEA as a Schedule I drug since it has no medicinal use.

Legal Information

German
Dieses Produkt fällt unter das Betäubungsmittelgesetz (BtMG). Für eine Bestellung dieses Produktes ist eine Erlaubnis nach § 3 BtMG zwingend erforderlich, es sei denn, es greift eine Ausnahme von der Erlaubnispflicht nach § 4 oder § 26 BtMG.

English
This product is subject to the German Narcotics Act. A permit under Section 3 of the German Narcotics Act is mandatory for ordering this product unless an exemption from the permit requirement under Section 4 or Section 26 of the German Narcotics Act applies.
CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Demerol is a registered trademark of Sanofi-Aventis
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Danger

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 2

Storage Class

3 - Flammable liquids

wgk

WGK 2

flash_point_f

35.6 °F

flash_point_c

2.0 °C

Regulatory Information

监管及禁止进口产品
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Certificates of Analysis (COA)

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K Sandvig et al.
Molecular biology of the cell, 7(9), 1391-1404 (1996-09-01)
The human epidermoid carcinoma cell line A431 becomes highly sensitive to Shiga toxin upon treatment with butyric acid. This strong sensitization (> 1000-fold) is accompanied by an increase in the fraction of cell-associated toxin transported to the Golgi apparatus and
Gas-liquid chromatographic-mass spectrometric determination of 1-methyl-4-phenyl-4-propionoxypiperidine using a stable isotope-labeled analogue as an internal standard.
S P Jindal et al.
Journal of chromatography, 408, 356-359 (1987-11-06)
Rong Qi et al.
Molecular pharmaceutics, 7(1), 267-279 (2009-12-23)
The GM1/caveolin-1 lipid raft mediated endocytosis mechanism was explored for generation 5 and 7 poly(amidoamine) dendrimer polyplexes employing the Cos-7, 293A, C6, HeLa, KB, and HepG2 cell lines. Expression levels of GM1 and caveolin-1 were measured using dot blot and
J N Johannessen et al.
Drug and alcohol dependence, 13(4), 367-374 (1984-07-01)
The intravenous use of an illicit synthetic drug preparation has caused permanent parkinsonism in a number of addicts. Chemical analysis has revealed the ingredients to be two related compounds 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) and 1-methyl-4-phenyl-4-propionoxypiperidine (MPPP). The opiate properties of these two
Masood A Khan et al.
Immunology, 125(1), 80-90 (2008-03-19)
The stimulation of programmed cell death can either enhance or inhibit antigen presentation by classic major histocompatibility complex molecules. In the current study, we report that the induction of apoptosis by topoisomerase I inhibition or elevation of intracellular ceramide levels
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