MedKoo Cat#: 558490 | Name: Perylene Red
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Description:

WARNING: This product is for research use only, not for human or veterinary use.

Perylene Red is a fluorescent dye molecule.

Chemical Structure

Perylene Red
CAS#123174-58-3

Theoretical Analysis

MedKoo Cat#: 558490

Name: Perylene Red

CAS#: 123174-58-3

Chemical Formula: C72H58N2O8

Exact Mass: 1078.4193

Molecular Weight: 1079.26

Elemental Analysis: C, 80.13; H, 5.42; N, 2.60; O, 11.86

Price and Availability

Size Price Availability Quantity
1g USD 550.00 2 Weeks
2g USD 950.00 2 Weeks
5g USD 2,050.00 2 Weeks
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Related CAS #
No Data
Synonym
Perylene Red; Lumogen Red 300; KF-856; KF856; KF 856; N,N'-Bis(2,6-diisopropylphenyl)-1,6,7,12-tetraphenoxy-3,4,9,10-perylenetetracarboxylic Diimide;
IUPAC/Chemical Name
2,9-bis(2,6-diisopropylphenyl)-5,6,12,13-tetraphenoxyanthra[2,1,9-def:6,5,10-d'e'f']diisoquinoline-1,3,8,10(2H,9H)-tetraone
InChi Key
ZZSIDSMUTXFKNS-UHFFFAOYSA-N
InChi Code
InChI=1S/C72H58N2O8/c1-39(2)47-31-21-32-48(40(3)4)67(47)73-69(75)51-35-55(79-43-23-13-9-14-24-43)61-63-57(81-45-27-17-11-18-28-45)37-53-60-54(72(78)74(71(53)77)68-49(41(5)6)33-22-34-50(68)42(7)8)38-58(82-46-29-19-12-20-30-46)64(66(60)63)62-56(80-44-25-15-10-16-26-44)36-52(70(73)76)59(51)65(61)62/h9-42H,1-8H3
SMILES Code
O=C1N(C2=C(C(C)C)C=CC=C2C(C)C)C(C3=CC(OC4=CC=CC=C4)=C(C5=C(OC6=CC=CC=C6)C=C7C(N(C8=C(C(C)C)C=CC=C8C(C)C)C(C9=CC(OC%10=CC=CC=C%10)=C%11C5=C97)=O)=O)C%12=C%11C(OC%13=CC=CC=C%13)=CC1=C3%12)=O
Appearance
Solid powder
Purity
>95% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info
Product Data
Certificate of Analysis
Safety Data Sheet (SDS)
Biological target:
Perylene Red is a fluorescent dye molecule.
In vitro activity:
TBD
In vivo activity:
TBD

Preparing Stock Solutions

The following data is based on the product molecular weight 1,079.26 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
TBD
In vitro protocol:
TBD
In vivo protocol:
TBD
1: Mertens S, Siegmund B, Vandewal K. Ultra-precise photothermal measurements reveal near unity photoluminescence quantum yields of molecular emitters in solution. Mater Horiz. 2023 Feb 6;10(2):594-600. doi: 10.1039/d2mh00936f. PMID: 36504131. 2: Rehhagen C, Rather SR, Schwarz KN, Scholes GD, Lochbrunner S. The effect of intermolecular electronic coupling on the exciton dynamics in perylene red nanoparticles. Phys Chem Chem Phys. 2022 Apr 13;24(15):8695-8704. doi: 10.1039/d1cp05375b. PMID: 35373223. 3: Kaysir MR, Fleming S, Argyros A. Gain investigation of Perylene-Red-doped PMMA for stimulated luminescent solar concentrators. Appl Opt. 2018 Apr 1;57(10):2459-2466. doi: 10.1364/AO.57.002459. PMID: 29714228. 4: Avellanal-Zaballa E, Durán-Sampedro G, Prieto-Castañeda A, Agarrabeitia AR, García-Moreno I, López-Arbeloa I, Bañuelos J, Ortiz MJ. Rational molecular design enhancing the photonic performance of red-emitting perylene bisimide dyes. Phys Chem Chem Phys. 2017 May 24;19(20):13210-13218. doi: 10.1039/c7cp01626c. PMID: 28492633. 5: Kaysir MR, Fleming S, MacQueen RW, Schmidt TW, Argyros A. Optical gain characterization of Perylene Red-doped PMMA for different pump configurations. Appl Opt. 2016 Jan 1;55(1):178-83. doi: 10.1364/AO.55.000178. PMID: 26835639. 6: Williams RM, Vân Anh N, van Stokkum IH. Triplet formation by charge recombination in thin film blends of perylene red and pyrene: developing a target model for the photophysics of organic photovoltaic materials. J Phys Chem B. 2013 Sep 26;117(38):11239-48. doi: 10.1021/jp402086p. Epub 2013 Jul 9. PMID: 23745814. 7: Green AP, Buckley AR. Application of gauge R&R to the rigorous measurement of quantum yield in fluorescent organic solid state systems. Rev Sci Instrum. 2012 Jul;83(7):073108. doi: 10.1063/1.4737631. PMID: 22852672. 8: Fennel F, Lochbrunner S. Long distance energy transfer in a polymer matrix doped with a perylene dye. Phys Chem Chem Phys. 2011 Feb 28;13(8):3527-33. doi: 10.1039/c0cp01211d. Epub 2011 Jan 6. PMID: 21212888. 9: Ortiz MJ, Garcia-Moreno I, Agarrabeitia AR, Duran-Sampedro G, Costela A, Sastre R, López Arbeloa F, Bañuelos Prieto J, López Arbeloa I. Red-edge- wavelength finely-tunable laser action from new BODIPY dyes. Phys Chem Chem Phys. 2010 Jul 28;12(28):7804-11. doi: 10.1039/b925561c. Epub 2010 May 25. PMID: 20502810. 10: García-Moreno I, Costela A, Pintado-Sierra M, Martín V, Sastre R. Enhanced laser action of Perylene-Red doped polymeric materials. Opt Express. 2009 Jul 20;17(15):12777-84. doi: 10.1364/oe.17.012777. PMID: 19654683. 11: Ahn TS, Al-Kaysi RO, Müller AM, Wentz KM, Bardeen CJ. Self-absorption correction for solid-state photoluminescence quantum yields obtained from integrating sphere measurements. Rev Sci Instrum. 2007 Aug;78(8):086105. doi: 10.1063/1.2768926. PMID: 17764365. 12: Al-Kaysi RO, Sang Ahn T, Müller AM, Bardeen CJ. The photophysical properties of chromophores at high (100 mM and above) concentrations in polymers and as neat solids. Phys Chem Chem Phys. 2006 Aug 7;8(29):3453-9. doi: 10.1039/b605925b. Epub 2006 Jun 19. PMID: 16855725. 13: Tanaka N, Barashkov N, Heath J, Sisk WN. Photodegradation of polymer- dispersed perylene di-imide dyes. Appl Opt. 2006 Jun 1;45(16):3846-51. doi: 10.1364/ao.45.003846. PMID: 16724148. 14: Schlosser M, Lochbrunner S. Exciton migration by ultrafast Förster transfer in highly doped matrixes. J Phys Chem B. 2006 Mar 30;110(12):6001-9. doi: 10.1021/jp0557565. PMID: 16553409. 15: Dubois A, Canva M, Brun A, Chaput F, Boilot JP. Photostability of dye molecules trapped in solid matrices. Appl Opt. 1996 Jun 20;35(18):3193-9. doi: 10.1364/AO.35.003193. PMID: 21102699. 16: Rahn MD, King TA. Comparison of laser performance of dye molecules in sol- gel, polycom, ormosil, and poly(methyl methacrylate) host media. Appl Opt. 1995 Dec 20;34(36):8260-71. doi: 10.1364/AO.34.008260. PMID: 21068943.