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Supelco

9-(Hydroxymethyl)-10-carbamoylacridan

analytical standard

Synonym(s):

9-HMCA, 9-OH-CBZ, 9-(Hydroxymethyl)-10(9H)-acridinecarboxamide

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About This Item

Empirical Formula (Hill Notation):
C15H14N2O2
CAS Number:
Molecular Weight:
254.28
Beilstein:
6214413
UNSPSC Code:
41116107
NACRES:
NA.24

grade

analytical standard

Quality Level

Assay

≥98.0% (HPLC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

pharmaceutical

format

neat

storage temp.

2-8°C

SMILES string

NC(N1C2=CC=CC=C2C(CO)C3=C1C=CC=C3)=O

InChI

1S/C15H14N2O2/c16-15(19)17-13-7-3-1-5-10(13)12(9-18)11-6-2-4-8-14(11)17/h1-5,7-8,18H,6,9H2,(H2,16,19)

InChI key

UMRKOEWAECPINL-UHFFFAOYSA-N

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Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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9-Hydroxymethyl-10-carbamoylacridan in human serum is one of the major metabolites of carbamazepine
Seiji ETO, et al.
Biological & Pharmaceutical Bulletin, 18(6), 926-928 (1995)
Carbamazepine and its metabolites in wastewater: Analytical pitfalls and occurrence in Germany and Portugal
Bahlmann A, et al.
Water Research, 57, 104-114 (2014)
N Wad et al.
Therapeutic drug monitoring, 19(3), 314-317 (1997-06-01)
In this article, the authors discuss 9-hydroxymethyl-10-carbamoyl acridan (9-OH-CBZ), another metabolite of carbamazepine (CBZ) found in serum. The retention time of unconjugated 9-OH-CBZ should be known when using a chromatographic method, because it appears in concentrations varying from one eighth
Arnold Bahlmann et al.
Water research, 57, 104-114 (2014-04-08)
The occurrence of carbamazepine (CBZ) and its metabolites in German and Portuguese wastewater was investigated. A total of 46 samples from influent and effluent wastewater were analyzed by liquid-chromatography (LC) tandem mass spectrometry. The five metabolites 10,11-dihydro-10,11-dihydroxy-CBZ (DiOH-CBZ), 10,11-dihydro-10-hydroxy-CBZ (10-OH-CBZ)
The metabolism of carbamazepine in humans: steric course of the enzymic hydrolysis of the 10, 11-epoxide
Bellucci G, et al.
Journal of Medicinal Chemistry, 30(5), 768-773 (1987)

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