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D-090

Supelco

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

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)

concentration

1.0 mg/mL in acetonitrile (as free base)

format

single component solution

storage temp.

−20°C

SMILES string

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

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

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

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

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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_germany

WGK 2

flash_point_f

35.6 °F

flash_point_c

2.0 °C

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Estela M Galván et al.
The Journal of infectious diseases, 189(9), 1556-1564 (2004-04-30)
We examined the ability of blood group A-active glycoconjugates to act as receptors for Escherichia coli heat-labile type I enterotoxin (LT-I) in HT-29 cells. These cells contained ~4 times more specific binding sites for LT-I than for cholera toxin (CT).
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
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)
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
Subhash Basu et al.
Glycoconjugate journal, 20(9), 563-577 (2004-09-30)
Breast cancer is the most common type of cancer, predominantly among women over 20, whereas colo-rectal cancer occurs in both men and women over the age of 50. Chemotherapy of both cancers affect rapidly growing normal as well as cancer
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