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546186

Sigma-Aldrich

Coumarin 153

Dye content 99 %

Sinónimos:

2,3,6,7-Tetrahydro-9-(trifluoromethyl)-1H,5H,11H-[1]benzopyrano(6,7,8-ij)quinolizin-11-one, 2,3,6,7-Tetrahydro-9-trifluoromethyl-1H,5H-quinolizino(9,1-gh)coumarin, 8-Trifluoromethyl-2,3,5,6-4H-1,H-11-oxa-3a-aza-benzo[de]anthracen-10-one, Coumarin 540A

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About This Item

Fórmula empírica (notación de Hill):
C16H14F3NO2
Número de CAS:
53518-18-6
Peso molecular:
309.28
Beilstein/REAXYS Number:
3624201
EC Number:
258-600-5
MDL number:
MFCD00041843
UNSPSC Code:
12352103
PubChem Substance ID:
24878878
NACRES:
NA.23

form

solid

composition

Dye content, 99%

mp

164-168 °C (lit.)

λmax

422 nm (lit.)
422 nm

fluorescence

λem 532 nm in ethanol (Lasing peak 550 nm, lasing range 521 - 605 nm (methanol), pump source XeCl (308 nm))

SMILES string

FC(F)(F)C1=CC(=O)Oc2c3CCCN4CCCc(cc12)c34

InChI

1S/C16H14F3NO2/c17-16(18,19)12-8-13(21)22-15-10-4-2-6-20-5-1-3-9(14(10)20)7-11(12)15/h7-8H,1-6H2

InChI key

VSSSHNJONFTXHS-UHFFFAOYSA-N

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Application

Laser dye

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificados de análisis (COA)

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Sigma-Aldrich

410497

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Lien D'Olieslaeger et al.
Journal of colloid and interface science, 504, 527-537 (2017-06-13)
Conjugated polymers are versatile bio-imaging probes as their optical properties can be readily fine-tuned. In this manuscript, fluorescent conjugated polymer nanoparticles are fabricated using three different poly(p-phenylene ethynylene) (PPE) derivatives. The polymers have the same backbone but carry different side
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The equilibrium and dynamic solvation responses of coumarin 153 (C153) in a range of deep eutectic solvents (DESs) based on choline chloride with either urea (molar ratio 1:2, ChCl:U), glycerol (1:2, ChCl:G), ethylene glycol (1:2, ChCl:E), or malonic acid (1:1
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Physical chemistry chemical physics : PCCP, 22(1), 114-128 (2019-12-10)
Ionic liquids (ILs) are highly tailorable solvents with many potential applications. Knowledge about their solvation properties is highly beneficial in the utilization of ILs for specific tasks, though for many ILs this is currently unknown. In this study, we have
Vitaliy Kapishon et al.
Biomacromolecules, 16(7), 2040-2048 (2015-06-13)
Alginate-based amphiphilic graft copolymers were synthesized by single electron transfer living radical polymerization (SET-LRP), forming stable micelles during polymerization induced self-assembly (PISA). First, alginate macroinitiator was prepared by partial depolymerization of native alginate, solubility modification and attachment of initiator. Depolymerized

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