775525
Acridine-9-carboxaldehyde
97%
Synonym(s):
Acridine-9-carbaldehyde
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About This Item
Empirical Formula (Hill Notation):
C14H9NO
CAS Number:
Molecular Weight:
207.23
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Form:
solid
InChI
1S/C14H9NO/c16-9-12-10-5-1-3-7-13(10)15-14-8-4-2-6-11(12)14/h1-9H
SMILES string
O=Cc1c2ccccc2nc3ccccc13
InChI key
ISOCABSXIKQOOV-UHFFFAOYSA-N
assay
97%
form
solid
mp
144-149 °C
functional group
aldehyde
storage temp.
2-8°C
Quality Level
Related Categories
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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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
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