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Merck

04304

Supelco

9-(Hydroxymethyl)-10-carbamoylacridan

analytical standard

Synonim(y):

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

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About This Item

Wzór empiryczny (zapis Hilla):
C15H14N2O2
Numer CAS:
Masa cząsteczkowa:
254.28
Beilstein:
6214413
Kod UNSPSC:
41116107
NACRES:
NA.24

klasa czystości

analytical standard

Poziom jakości

Próba

≥98.0% (HPLC)

okres trwałości

limited shelf life, expiry date on the label

metody

HPLC: suitable
gas chromatography (GC): suitable

Zastosowanie

pharmaceutical

format

neat

temp. przechowywania

2-8°C

ciąg SMILES

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)

Klucz InChI

UMRKOEWAECPINL-UHFFFAOYSA-N

Polecane produkty

Find a digital Reference Material for this product available on our online platform ChemisTwin® for NMR. You can use this digital equivalent on ChemisTwin® for your sample identity confirmation and compound quantification (with digital external standard). An NMR spectrum of this substance can be viewed and an online comparison against your sample can be performed with a few mouseclicks. Learn more here and start your free trial.
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Kod klasy składowania

13 - Non Combustible Solids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

Not applicable

Temperatura zapłonu (°C)

Not applicable


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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

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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