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111295-09-1

111295-09-1 Structure

111295-09-1 Structure
IdentificationBack Directory
[Name]

2-Oxo-3-hydroxy-LSD (2-Oxo-3-hydroxy-lysergic acid diethylamide)
[CAS]

111295-09-1
[Synonyms]

2-Oxo-3-hydroxy-lysergide
2-Oxo-3-hydroxy-LSD solution
2,3-Dihydro-3-hydroxy-2-oxo Lysergide
N,N-Diethyl-2,3-dihydro-3-hydroxy-2-oxo-lysergaMide
2-Oxo-3-hydroxy-lysergic acid diethylamide solution
2-Oxo-3-hydroxy-LSD (2-Oxo-3-hydroxy-lysergic acid diethylamide)
2,3-Dihydro-3-hydroxy-2-oxo Lysergide (100 μg/mL in Acetonitrile)
(8β)-9,10-Didehydro-N,N-diethyl-2,3-dihydro-3-hydroxy-6-Methyl-2-oxoergoline-8-carboxaMide
Ergoline-8-carboxamide, 9,10-didehydro-N,N-diethyl-2,3-dihydro-3-hydroxy-6-methyl-2-oxo-, (8β)-
(6aR,9R)-N,N-diethyl-5a-hydroxy-7-methyl-5-oxo-6,6a,8,9-tetrahydro-4H-indolo[4,3-fg]quinoline-9-carboxamide
[EINECS(EC#)]

200-835-2
[Molecular Formula]

C20H25N3O3
[MDL Number]

MFCD00798488
[MOL File]

111295-09-1.mol
[Molecular Weight]

355.431
Chemical PropertiesBack Directory
[Fp ]

2℃
[storage temp. ]

-20°C
[solubility ]

soluble in Acetonitrile
[form ]

Pale Yellow to Light Yellow Solution
[Major Application]

forensics and toxicology
[InChI]

1S/C20H25N3O3/c1-4-23(5-2)18(24)12-9-14-13-7-6-8-15-17(13)20(26,19(25)21-15)10-16(14)22(3)11-12/h6-9,12,16,26H,4-5,10-11H2,1-3H3,(H,21,25)/t12-,16-,20?/m1/s1
[InChIKey]

YSZSHHCNLVHCNV-VRORWYBRSA-N
[SMILES]

CCN(CC)C(=O)[C@H]1CN(C)[C@@H]2CC3(O)C(=O)Nc4cccc(C2=C1)c34
Safety DataBack Directory
[Hazard Codes ]

F,Xn
[Risk Statements ]

11-20/21/22-36
[Safety Statements ]

16-36/37
[RIDADR ]

UN 1648 3 / PGII
[WGK Germany ]

2
[Storage Class]

3 - Flammable liquids
[Hazard Classifications]

Acute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Flam. Liq. 2
Hazard InformationBack Directory
[Uses]

2,3-Dihydro-3-hydroxy-2-oxo Lysergide is a major metabolite of Lysergide (L488010). Controlled Substance.
[General Description]

2-Oxo-3-hydroxy-LSD is a major urinary metabolite of lysergic acid diethyl amide, or LSD. This certified solution standard is suitable for use in LC/MS or GC/MS applications for clinical toxicology, forensic analysis, or urine drug testing. Known for its role in 1960′s American counterculture, LSD is one of the most potent psychedelic drugs ever created.
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