Direkt zum Inhalt
Merck
Alle Fotos(1)

Key Documents

View All Documentation

775525

Sigma-Aldrich

Acridine-9-carboxaldehyde

97%

Synonym(e):

Acridine-9-carbaldehyde

Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)

About This Item

Empirische Formel (Hill-System):
C14H9NO
CAS-Nummer:
885-23-4
Molekulargewicht:
207.23
MDL-Nummer:
MFCD00616515
UNSPSC-Code:
12352100
PubChem Substanz-ID:
329767767
NACRES:
NA.22

Assay

97%

Form

solid

mp (Schmelzpunkt)

144-149 °C

Funktionelle Gruppe

aldehyde

Lagertemp.

2-8°C

SMILES String

O=Cc1c2ccccc2nc3ccccc13

InChI

1S/C14H9NO/c16-9-12-10-5-1-3-7-13(10)15-14-8-4-2-6-11(12)14/h1-9H

InChIKey

ISOCABSXIKQOOV-UHFFFAOYSA-N

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H302,H319

Gefahreneinstufungen

Acute Tox. 4 Oral - Eye Irrit. 2

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
MKBP6466V

Die passende Version wird nicht angezeigt?

Wenn Sie eine bestimmte Version benötigen, können Sie anhand der Lot- oder Chargennummer nach einem spezifischen Zertifikat suchen.

Suche nach COA

Besitzen Sie dieses Produkt bereits?

In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.

Die Dokumentenbibliothek aufrufen

Kunden haben sich ebenfalls angesehen

Slide 1 of 1

1 of 1

9-Anthracencarboxaldehyd 97%

Sigma-Aldrich

278688

9-Anthracencarboxaldehyd

S M Furst et al.
International journal of immunopharmacology, 17(5), 445-452 (1995-05-01)
Carbamazepine, a widely used anticonvulsant, is associated with a wide range of adverse reactions including agranulocytosis, aplastic anemia and drug-induced lupus. It has also been reported to alter immune function in a variety of ways. We had previously demonstrated that
Olivier Mathieu et al.
Xenobiotica; the fate of foreign compounds in biological systems, 41(2), 91-100 (2010-11-23)
Carbamazepine (CBZ) is a useful anticonvulsive drug associated with rare severe adverse drug reactions. The physio-pathological mechanisms of these reactions are unknown although evidence of immunological activation has been reported. The ability of 9-acridinecarboxaldehyde, a CBZ metabolite, to interact with
Olivier Mathieu et al.
Pharmacological reports : PR, 63(1), 86-94 (2011-03-29)
Carbamazepine is a widely used anticonvulsive agent. Its metabolic pathway leads not only to the major active metabolite, carbamazepine-10,11-epoxide, but also to minor terminal metabolites such as iminostilbene and acridine. Carbamazepine is usually well-tolerated, but it may lead to rare
Wolf-Ulrich Palm
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 17(7), 964-974 (2018-06-20)
Dark and photolysis reactions in solution were investigated for 9-acridinecarboxaldehyde (ACL). ACL reacts in the dark at T = 20 °C and pH = 7.0 in an air saturated solution to the main product 9-acridinecarboxylic acid (ACA) and to the
Mei Lu et al.
Journal of the American Society for Mass Spectrometry, 26(10), 1676-1685 (2015-08-06)
Electrochemistry (EC) combined with mass spectrometry (MS) is a powerful tool for elucidation of electrochemical reaction mechanisms. However, direct online analysis of electrochemical reaction in aqueous phase was rarely explored. This paper presents the online investigation of several electrochemical reactions

Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..

Setzen Sie sich mit dem technischen Dienst in Verbindung.