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Merck
CN

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

Key Documents

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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

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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 Hanada et al.
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Sphingolipid metabolism and metabolites are important in various cellular events in eukaryotes. However, little is known about their function in plasmodial parasites. Here we demonstrate that neutral sphingomyelinase (SMase) involved in the sphingomyelin (SM) catabolism is retained by the intraerythrocytic
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We have previously shown that multidrug-resistant cancer cells display elevated levels of glucosylceramide (Lavie, Y., Cao, H., Bursten, S. L., Giuliano, A. E., and Cabot, M. C. (1996) J. Biol. Chem. 271, 19530-19536). In this study we used the multidrug-resistant
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