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546127

Sigma-Aldrich

Coumarin 30

Dye content 99 %

Synonym(s):

3-(2-N-Methylbenzimidazolyl)-7-N,N-diethylaminocoumarin, Coumarin 515

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About This Item

Empirical Formula (Hill Notation):
C21H21N3O2
CAS Number:
41044-12-6
Molecular Weight:
347.41
EC Number:
255-186-8
MDL number:
MFCD00051349
UNSPSC Code:
12352103
PubChem Substance ID:
57651480
NACRES:
NA.23

form

solid

Quality Level

200

composition

Dye content, 99%

mp

225-229 °C (lit.)

λmax

413 nm

fluorescence

λem 478 nm in ethanol (Lasing peak 510 nm, lasing range 492 - 550 nm (ethylene glycol), pump source Ar (458 nm))

SMILES string

CCN(CC)c1ccc2C=C(C(=O)Oc2c1)c3nc4ccccc4n3C

InChI

1S/C21H21N3O2/c1-4-24(5-2)15-11-10-14-12-16(21(25)26-19(14)13-15)20-22-17-8-6-7-9-18(17)23(20)3/h6-13H,4-5H2,1-3H3

InChI key

KZFUMWVJJNDGAU-UHFFFAOYSA-N

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General description

Coumarin 30 (C30) is a laser dye that has a fluorescence yield that tends to unity, which can be potentially used in optical communications and sensors. It is highly stable on the spin coating and shows high quantum efficiency upon low concentration doping.

Application

C30 can form a thin film on p-silicon (p-Si) semiconductor, which can be used to fabricate the aluminum/C30/p-Si based diodes. It can be used as a donor with fluorescein as an acceptor to study the time resolved fluorescence resonance energy transfer (FRET).
Laser dye

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
BCCL6330
BCCH9525
BCCH3986
BCCF0917
BCCC5045

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Effect of coumarin on blue light-emitting diodes based on carbazol polymers.
Gautier-Thianche E, et al.
Journal of Applied Physics, 83(8), 4236-4241 (1998)
The nature of photoinduced intermolecular charger transfer in fluorescence resonance energy transfer.
Zong H, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 209(8), 228-233 (2019)
Electrical and photoelectrical characterization of an organic-inorganic heterojunction based on quinoline yellow dye.
Ugur A, et al.
Materials Science in Semiconductor Processing, 39(8), 569-574 (2015)
Fabrication and electrical properties of an organic-inorganic device based on Coumarin 30 dye.
Tombak A, et al.
Materials Science in Semiconductor Processing, 24(8), 187-192 (2014)
Tobias Abel et al.
Chemistry Central journal, 6(1), 124-124 (2012-10-30)
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