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Postion:Product Catalog >Pharmaceutical intermediates>Bulk Drug Intermediates>9-Phenylacridine
9-Phenylacridine
  • 9-Phenylacridine
  • 9-Phenylacridine
  • 9-Phenylacridine
  • 9-Phenylacridine

9-Phenylacridine NEW

Price Get Latest Price
Package 1KG
Min. Order: 0.100000001490116KG
Supply Ability: 1000KGS
Update Time: 2025-11-25

Product Details

Product Name: 9-Phenylacridine CAS No.: 602-56-2
Min. Order: 0.100000001490116KG Purity: 98%
Supply Ability: 1000KGS Release date: 2025/11/25

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9-Phenylacridine Basic information
Product Name:9-Phenylacridine
Synonyms:9-phenyl-acridin;9-Phenylacridin (9-PA);3-propan-2-yloxy-1-cyclohex-2-enone;phenylacridine;9-PHENYLACRIDINE;9-PA;Acridine, 9-phenyl-;9-Phenylacridine>
CAS:602-56-2
MF:C19H13N
MW:255.31
EINECS:210-020-3
Product Categories:Miscellaneous
Mol File:602-56-2.mol
Article illustration

9-Phenylacridine Chemical Properties
Melting point 184°C
Boiling point 388.54°C (rough estimate)
density 0.9418 (rough estimate)
refractive index 1.6500 (estimate)
storage temp. Sealed in dry,Room Temperature
pka5.45±0.10(Predicted)
form powder to crystal
color Light yellow to Amber to Dark green
InChIInChI=1S/C19H13N/c1-2-8-14(9-3-1)19-15-10-4-6-12-17(15)20-18-13-7-5-11-16(18)19/h1-13H
InChIKeyMTRFEWTWIPAXLG-UHFFFAOYSA-N
SMILESC1C2C(=NC3C(C=2C2=CC=CC=C2)=CC=CC=3)C=CC=1
CAS DataBase Reference602-56-2(CAS DataBase Reference)
NIST Chemistry ReferenceAcridine, 9-phenyl-(602-56-2)
EPA Substance Registry SystemAcridine, 9-phenyl- (602-56-2)

Safety Information
Safety Statements 22-24/25
HS Code 2933.99.8210
MSDS Information

9-Phenylacridine Usage And Synthesis
UsesResearch has found that 9-phenylacridine (ACPH) exhibited anticancer activity in cell lines and in vivo animal models. Bioinformatics studies have indicated that it could have topoisomerase I inhibitory activity. It could also act as a PARP 1 inhibitor and was very effective in combination with cisplatin in cell line-based assays. ACPH also satisfied all criteria for a candidate drug from the Lipinski rule and showed good cell uptake. ACPH alone was effective in the A375 melanoma cell line. ACPH could be used as a promising new photosensitizer[1-2]. 9-Phenylacridine is the parent base of chrysaniline or 3,6-diamino-9- phenylacridine, the chief constituent of the dyestuff phosphine. It is commonly used in the electronics industry as a free radical photoinitiator, significantly improving photo speed.
Description9-Phenylacridine has antitumour activity. It can be used as a photosensitiser and can sensitise UVA-induced DNA damage in vitro and in cells. It also enhances cell killing by UVA. In addition. It is also used in photochemical research and as a raw material for organic synthesis.
Biological ActivityHansda et al. suggested that a nontoxic dose of 9-Phenylacridine (ACPH) with UVA light can inhibit the proliferation of A375 cells by inducing DNA damage both in in vitro DNA and in cells through photosensitization. Such treatment enhanced the generation of ROS in cells, leading to lipid peroxidation and depletion of GSH. This led to cell cycle arrest at the G2/M phase to promote apoptosis through the mitochondria-mediated pathway. Although there was a slight increase in the small population of cells undergoing death through autophagy by UVA on ACPH pretreatment, primarily UVA+ACPH resulted in cell death through apoptosis. Thus, using ACPH as a photosensitizer in PDT may be contemplated. Applying ACPH topically to target cells and then illuminating them with UVA can minimize the concern of inducing damage to the surrounding normal cells [1].
References[1] Surajit Hansda, Rita Ghosh, Gargi Ghosh. "9-phenyl acridine photosensitizes A375 cells to UVA radiation." Heliyon (2020): e04733.
[2] Rita Ghosh, Dipanjan Guha, Sudipta Bhowmik. "9-phenyl acridine exhibits antitumour activity by inducing apoptosis in A375 cells." Molecular and Cellular Biochemistry 361 1–2 (2012): 55–66.

9-Phenylacridine Preparation Products And Raw materials
Raw materialsAcridine, 1,2,3,4-tetrahydro-9-phenyl--->9-Phenyl-9,10-dihydroacridine-->Benzonitrile, 2-(phenylamino)--->Methanone, phenyl[2-(phenylamino)phenyl]--->TRIPHENYLMETHYLAMINE-->DIPHENYLAMINE HYDROCHLORIDE-->DIPHENYLIODONIUM TRIFLUOROMETHANESULFONATE-->Acridine-->Phenylboronic acid-->9-Chloroacridine-->DIPHENYLZINC-->Benzonitrile-->Benzoic acid-->Diphenylamine-->2-Cyclohexen-1-one




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