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Sigma-Aldrich

9-Acridinecarboxylic acid hydrate

97%

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About This Item

Empirical Formula (Hill Notation):
C14H9NO2 · xH2O
CAS Number:
332927-03-4
Molecular Weight:
223.23 (anhydrous basis)
Beilstein:
171327
MDL number:
MFCD00149578
UNSPSC Code:
12352100
PubChem Substance ID:
24854802
NACRES:
NA.22

Assay

97%

form

powder

mp

290 °C (dec.) (lit.)

functional group

carboxylic acid

SMILES string

[H]O[H].OC(=O)c1c2ccccc2nc3ccccc13

InChI

1S/C14H9NO2.H2O/c16-14(17)13-9-5-1-3-7-11(9)15-12-8-4-2-6-10(12)13;/h1-8H,(H,16,17);1H2

InChI key

ZQAZWHSZYVXGMP-UHFFFAOYSA-N

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Application

9-Acridinecarboxylic acid hydrate has been used to synthesize a DNA intercalator in order to capture double-stranded DNAs (dsDNAs) duplex from the solution.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBL0788
STBJ4529
STBH2843
STBD5970V
STBB9183V

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Synthesis and chemiluminescent properties of novel biotinylated acridinium esters.
Agiamarnioti k, et al.
Acta Chimica Slovenica, 51(1), 67-76 (2004)
Fabrication of DNA Nanowires by Orthogonal Self-Assembly and DNA Intercalation on a Au Patterned Si/SiO2 Surface.
Kobayashi K, et al.
Langmuir, 24(22), 13203-13211 (2008)
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

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