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IMPM-005-06

Supelco

10-Oxomorphine solution

100 μg/mL in methanol, ampule of 1 mL, certified reference material, Cerilliant®

Sinônimo(s):

10-Ketomorphine

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About This Item

Fórmula empírica (Notação de Hill):
C17H17NO4
Número CAS:
68254-48-8
Peso molecular:
299.32
Número CE:
200-659-6
Número MDL:
MFCD09841138
Código UNSPSC:
41116107
ID de substância PubChem:
329815688
NACRES:
NA.24

grau

certified reference material

Formulário

liquid

Características

Snap-N-Spike®/Snap-N-Shoot®

embalagem

ampule of 1 mL

fabricante/nome comercial

Cerilliant®

concentração

100 μg/mL in methanol

técnica(s)

gas chromatography (GC): suitable
liquid chromatography (LC): suitable

aplicação(ões)

forensics and toxicology

Formato

single component solution

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CN1CC[C@]23[C@H]4Oc5c(O)ccc(C(=O)[C@@H]1[C@@H]2C=C[C@@H]4O)c35

InChI

1S/C17H17NO4/c1-18-7-6-17-9-3-5-11(20)16(17)22-15-10(19)4-2-8(12(15)17)14(21)13(9)18/h2-5,9,11,13,16,19-20H,6-7H2,1H3/t9-,11-,13-,16-,17-/m0/s1

chave InChI

HNJBQZPKNKFLFM-CBEJNMEVSA-N

Descrição geral

A certified solution standard of the decomposition product measured in manufactured morphine sulfate drug products or APIs using LC or LC/MS.

Informações legais

CERILLIANT is a registered trademark of Merck KGaA, Darmstadt, Germany
Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

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Palavra indicadora

Danger

Classificações de perigo

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

Órgãos-alvo

Eyes

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

49.5 °F - closed cup

Ponto de fulgor (°C)

9.7 °C - closed cup

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Certificados de análise (COA)

Lot/Batch Number

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B Proksa
Die Pharmazie, 39(10), 687-688 (1984-10-01)
10-Oxomorphine, a decomposition product of morphine, was synthesized from 6-O-acetylcodeine, which was oxidized with chromic acid to 6-O-acetyl-10-hydroxycodeine. This substance was then oxidized with manganese dioxide to 6-O-acetyl-10-oxocodeine, which on hydrolysis and O-demethylation gave 10-oxomorphine. UV-, fluorimetric spectrometry, TLC and
Seán S Kelly et al.
Journal of pharmaceutical sciences, 92(3), 485-493 (2003-02-15)
Stability testing of morphine sulfate formulated with nonpareil sugar seeds (consisting of sucrose and starch) and fumaric acid revealed the formation of the three impurities 5-(hydroxymethyl)-2-furfural, 10-hydroxymorphine and 10-oxomorphine. 5-(Hydroxymethyl)-2-furfural was isolated via semipreparative HPLC utilizing volatile mobile phase constituents

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