17784-47-3

Basic information

• Product Name: ACRIDINE HYDROCHLORIDE
• Synonyms: acridine,monohydrochloride;ACRIDINE HYDROCHLORIDE;ACRIDINIUM CHLORIDE;Acridine HydrochlorideHydrate ;ACRIDINE HYDROCHLORIDE, FOR FLUOR-ESCENC E;AcridiniumchlorideHCl;ACRIDINE HYDROCHLORIDE HYDRATE, 98+;Acridine hydrochloride,97%
• CAS NO: 17784-47-3
• Molecular Formula: C₁₃H₁₀N*Cl
• Molecular Weight: 215.68
• EINECS: 241-762-6
• Product Categories: Alphabetical;Fluorescent Stains;Nucleic Acid Stains
• Mol File: 17784-47-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 250-255 °C (dec.)
• Boiling Point: 346.7°Cat760mmHg
• Flash Point: 153.8°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.000113mmHg at 25°C
• Storage Temp.: Inert atmosphere,Room Temperature
• Merck: 14,122
• CAS DataBase Reference: ACRIDINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: ACRIDINE HYDROCHLORIDE(17784-47-3)
• EPA Substance Registry System: ACRIDINE HYDROCHLORIDE(17784-47-3)

Safety Data

• Hazard Codes: Xi,Xn
• Statements: 36/37/38-22
• Safety Statements: 26-36-22
• WGK Germany: 3
• RTECS: AR9322000
• Hazardous Substances Data: 17784-47-3(Hazardous Substances Data)

Usage

Uses

Acridine Hydrochloride is a fluorescent compound. It is used in the synthetic preparation of fluorescent probes.

InChI:InChI=1/C13H9N.ClH/c1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)14-12;/h1-9H;1H

Upstream product

• 260-94-6 acridine 

Downstream Products

• 934472-79-4 9-(4-amino-2,5-dimethoxyphenyl)acridine 
• 35586-87-9 9-(3,4-diaminophenyl)acridine 
• 109277-15-8 9-(N-benzyl-4-methanesulphonamidophenyl)acridine 
• 109277-10-3 9-(N-methyl-4-methanesulphonamidophenyl)acridine 
• 109277-09-0 9-(4-methanesulphonamidophenyl)acridine 

Relevant articles and documents

Carbon nanotube-acridine nanohybrids: Spectroscopic characterization of photoinduced electron transfer

Single-walled carbon nanotubes (NT) were covalently functionalized with either 9-phenyl acridine (PhA) or 10-methyl-9-phenyl acridinium (PhMeA +). Absorption and fluorescence properties of acridine derivatives tethered to the nanotubes were studied in homogeneous dispersions. Exciplex emission was observed for NT functionalized with 9-phenylacridine. This phenomenon was attributed to an " intramolecular" interaction between excited phenyl acridine and carbon nanotubes. Interestingly, reverse photoinduced electron transfer from the nanotube to 10-methyl-9-phenylacridinium was detected for the NTPhMeA+ nanohybrid. This electron transfer led to a strong quenching of the acridinium fluorescence and to the formation of a metastable acridine radical. Evidence for the formation of this radical was obtained by ESR studies.