3,8-Diamino-6-phenylphenanthridine
| Code | Size | Price |
|---|
| CDX-D0436-G001 | 1 g | £65.00 |
Quantity:
| CDX-D0436-G005 | 5 g | £230.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
+4°C
Documents
Further Information
Alternate Names/Synonyms:
6-Phenylphenathridine-3,8-diamine; 3,8-DAPP; DAPP
Appearance:
Yellow to orange powder.
CAS:
52009-64-0
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H302, H315, H319, H335
InChi:
InChI=1S/C19H15N3/c20-13-6-8-15-16-9-7-14(21)11-18(16)22-19(17(15)10-13)12-4-2-1-3-5-12/h1-11H,20-21H2
InChiKey:
CPNAVTYCORRLMH-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 52009-64-0. Formula: C19H15N3. MW: 285.3. Synthetic. Phenyl-phenanthridine dye with a large pi-conjugated structure and strong luminescence. Used in the synthesis of rigid polyamides and fluorescent probes. DNA intercalator. Used as a chromatographic affinity ligand for the specific separation and purification of supercoiled plasmid DNA (pDNA). It has been investigated for its anti-tumor and anti-viral properties.
MDL:
MFCD00075152
Molecular Formula:
C19H15N3
Molecular Weight:
285.3
Package Type:
Vial
Precautions:
P261, P305, P351, P338
Product Description:
Phenyl-phenanthridine dye with a large pi-conjugated structure and strong luminescence. Used in the synthesis of rigid polyamides and fluorescent probes. DNA intercalator. Used as a chromatographic affinity ligand for the specific separation and purification of supercoiled plasmid DNA (pDNA). It has been investigated for its anti-tumor and anti-viral properties.
Purity:
>98%
Signal word:
Warning
SMILES:
NC1=CC2=C(C(C=CC(N)=C3)=C3N=C2C4=CC=CC=C4)C=C1
Solubility Chemicals:
Soluble in chloroform, dichloromethane or methanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.
References
(1) A.L. Cimecioglu & R.A. Weiss; Macromolecules 28, 6343 (1995) | (2) V.K. Misra & B. Honig; PNAS 92, 4691 (1995) | (3) T. Kubar, et al.; Chem. Eur. J. 12, 280 (2006) | (4) X. Shi & R.B. MacGregor Jr.; J. Phys. Chem. B. 111, 3321 (2007) | (5) S.A. Osadchiia, et al.; Russ. J. Appl. Chem. 84, 1541 (2011) | (6) C. Caramelo-Nunes, et al.; J.Chromatogr. A 1307, 91 (2013) | (7) C. Caramelo-Nunes, et al.; Meth. Mol. Biol. 1286, 47 (2015)
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