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Merck
CN

E8512

Sigma-Aldrich

Ethylmorphine

Synonym(s):

Morphine 3-ethyl ether

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About This Item

Empirical Formula (Hill Notation):
C19H23NO3
CAS Number:
76-58-4
Molecular Weight:
313.39
EC Number:
200-970-7
MDL number:
MFCD00083327
UNSPSC Code:
12352200
PubChem Substance ID:
24894676
NACRES:
NA.77

Key Documents

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drug control

USDEA Schedule II; Home Office Schedule 2; stupéfiant (France); kontrollierte Droge in Deutschland; regulated under CDSA - not available from Sigma-Aldrich Canada; estupefaciente (Spain); Decreto Lei 15/93: Tabela IA (Portugal); Kábítószer / Narcotic Drug (Hungary), 78/2022. (XII. 28.) BM rendelet

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
veterinary

storage temp.

2-8°C

SMILES string

CCOc1ccc2C[C@@H]3C4C=C[C@H](O)[C@@H]5Oc1c2[C@]45CCN3C

InChI

1S/C19H23NO3/c1-3-22-15-7-4-11-10-13-12-5-6-14(21)18-19(12,8-9-20(13)2)16(11)17(15)23-18/h4-7,12-14,18,21H,3,8-10H2,1-2H3/t12-,13+,14-,18-,19-/m0/s1

InChI key

OGDVEMNWJVYAJL-LEPYJNQMSA-N

Biochem/physiol Actions

Narcotic analgesic; antitussive

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302,H336

Precautionary Statements

P301 + P312 + P330

Hazard Classifications

Acute Tox. 4 Oral - STOT SE 3

Target Organs

Central nervous system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
049K4008
107K4116
077K4072
037K4074
037K4011

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Aliaa Nabil ElMeshad et al.
AAPS PharmSciTech, 21(7), 244-244 (2020-08-29)
Ethylmorphine hydrochloride (EtM) is a derivative of morphine used as analgesic to treat severe pain in case of cancer and bone injury. This study aimed to formulate and evaluate core in cup tablets containing 2 doses of EtM, the cup
Virginia Tzankova et al.
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie, 92, 569-579 (2017-06-04)
The toxic liver impairment caused by free radical injury or excessive reactive oxigen species (ROS) formation could be effectivelly attenuated by natural antioxidants. The present study aimed to explore and compare the hepatoprotective and antioxidant effects of free and encapsulated
W A Daniel et al.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology, 15(1), 103-110 (2004-12-02)
The aim of the present study was to investigate the influence of classic and atypical neuroleptics on the activity of rat CYP2D measured as a rate of ethylmorphine O-deethylation. The reaction was studied in control liver microsomes in the presence
Elisabeth Leere Oiestad et al.
Journal of analytical toxicology, 35(5), 280-293 (2011-05-31)
An ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS-MS) method for screening of drugs in whole blood has been developed and validated. Samples were prepared by supported liquid-liquid extraction on ChemElute(®) columns with ethyl acetate/heptane (4:1). LC separation was achieved with an
G Virkel et al.
Journal of veterinary pharmacology and therapeutics, 33(3), 295-303 (2010-06-19)
The intestinal mucosa plays a capital role in dictating the bioavailability of a large array of orally ingested drugs and toxicants. The activity and the expression of several xenobiotic metabolizing enzymes were measured in subcellular fractions from the duodenal mucosa
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