Phenanthridine

Base Information Edit

Chemical Name:Phenanthridine
CAS No.:229-87-8
Molecular Formula:C13H9N
Molecular Weight:179.221
Hs Code.:29333990
European Community (EC) Number:205-934-4
NSC Number:73482
UN Number:2811
UNII:62QGS7CPS6
DSSTox Substance ID:DTXSID3074288
Nikkaji Number:J45.283A
Wikipedia:Phenanthridine
Wikidata:Q400082
Metabolomics Workbench ID:55358
ChEMBL ID:CHEMBL504941
Mol file:229-87-8.mol

Synonyms:PHENANTHRIDINE;229-87-8;Benzo[c]quinoline;6-Phenanthridine;3,4-Benzoquinoline;9-Azaphenanthrene;3,4-Benzoisoquinoline;5-Azaphenanthrene;Benzo(c)quinoline;CCRIS 1234;EINECS 205-934-4;NSC 73482;UNII-62QGS7CPS6;BRN 0120204;62QGS7CPS6;MLS000736807;CHEBI:36421;NSC73482;NSC-73482;5-20-08-00223 (Beilstein Handbook Reference);MFCD00004989;Phenanthridine, 98%;SCHEMBL8666;MLS001180225;CHEMBL504941;SCHEMBL9374538;DTXSID3074288;HMS2782F15;HMS2799K17;AKOS024015156;GS-5414;NCGC00246947-01;SMR000447031;SMR000475748;LS-102704;CS-0204779;FT-0631882;P1047;Phenanthridine, >=99%, purified by sublimation;A816460;AC-907/25014315;Q400082;J-014930;Phenanthridine, BioReagent, suitable for fluorescence, >=98.0% (GC)

Suppliers and Price of Phenanthridine

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Phenanthridine
1g
$ 110.00

TCI Chemical
Phenanthridine >98.0%(GC)
10g
$ 156.00

Sigma-Aldrich
Phenanthridine ≥99%, purified by sublimation
1g
$ 90.20

Sigma-Aldrich
Phenanthridine BioReagent, suitable for fluorescence, ≥98.0% (GC)
1g
$ 85.90

Sigma-Aldrich
Phenanthridine 98%
5g
$ 138.00

Crysdot
Phenanthridine 95+%
100g
$ 692.00

Chem-Impex
Phenanthridine,≥98%(GC) ≥98%(GC)
10G
$ 176.80

American Custom Chemicals Corporation
PHENANTHRIDINE 98.00%
1G
$ 123.90

American Custom Chemicals Corporation
PHENANTHRIDINE 98.00%
100G
$ 2887.50

Alichem
Phenanthridine
100g
$ 733.52

Total 35 raw suppliers

Chemical Property of Phenanthridine Edit

Chemical Property:

Appearance/Colour:white to beige powder
Vapor Pressure:0.000166mmHg at 25°C
Melting Point:104-107 °C(lit.)
Refractive Index:1.726
Boiling Point:350.436 °C at 760 mmHg
PKA:5.58(at 20℃)
Flash Point:155.851 °C
PSA：12.89000
Density:1.188 g/cm³
LogP:3.38800
Solubility.:phosphate buffer: soluble
Water Solubility.:0.3g/L(20 oC)
XLogP3:3.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:179.073499291
Heavy Atom Count:14
Complexity:201
Transport DOT Label:Poison

Purity/Quality:

97% ^*data from raw suppliers

Phenanthridine ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn
Statements: 22-37/38-41
Safety Statements: 26-39

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Polycyclic Aromatic Hydrocarbons
Canonical SMILES:C1=CC=C2C(=C1)C=NC3=CC=CC=C23
Uses Phenanthridine is an isomeric compound of acridine. It is a nitrogen heterocycle that is the basis of DNA-binding fluorescent dyes through intercalation. Ethidium bromide and propidium iodide are the examples of such intercalating dyes. It is used as a dye in biological and chemical sensors. It is also used in the study of ecotoxicity and rotational spectroscopic investigations and radio astronomical searches.

Technology Process of Phenanthridine

There total 319 articles about Phenanthridine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 97.0%

: 80554-69-4
1-(6H-Phenanthridin-5-yl)-4-phenyl-butan-1-one

: 229-87-8
phenanthridine

: 1821-12-1
4-Phenylbutyric acid

Guidance literature:: With ammonium cerium(IV) nitrate; In water; acetonitrile; for 0.25h; Product distribution; deprotection;
DOI:10.1246/cl.1981.1551