Skip to Content
Merck
CN

795526

2,8-Diethyl-1,3,5,7-tetramethyl-9-phenylbipyrromethene difluoroborate

99% (HPLC)

Synonym(s):

BODIPY dye, Boron dipyrromethene fluorophore

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C23H27BF2N2
CAS Number:
Molecular Weight:
380.28
PubChem Substance ID:
UNSPSC Code:
12352103
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

2,8-Diethyl-1,3,5,7-tetramethyl-9-phenylbipyrromethene difluoroborate, 99% (HPLC)

InChI

1S/C23H27BF2N2/c1-7-19-14(3)22-21(18-12-10-9-11-13-18)23-15(4)20(8-2)17(6)28(23)24(25,26)27(22)16(19)5/h9-13H,7-8H2,1-6H3

InChI key

CPRBYGLKLOXFPA-UHFFFAOYSA-N

SMILES string

CC(C(CC)=C1C)=C(N1B2(F)F)C(C3=CC=CC=C3)=C4[N]2=C(C)C(CC)=C4C

assay

99% (HPLC)

form

powder

mp

183-188 °C

fluorescence

λex 520; λem 532 in methanol

Application

BODIPY laser dyes are used to generate fluorescent conjugates of proteins, nucleotides, oligonucleotides and dextrans, and to prepare fluorescent enzyme substrates, fatty acids, phospholipids, lipopolysaccharides, receptor ligands and polystyrene microspheres.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yong Qian et al.
Nature communications, 2, 495-495 (2011-10-13)
Aqueous sulphides, including hydrogen sulphide, have important roles in biological signalling and metabolic processes. Here we develop a selective sulphide-trapping strategy involving sulphide addition to an aldehyde; the resulting hemithioacetal undergoes a Michael addition with an adjacent unsaturated acrylate ester
T Govender et al.
Bioresource technology, 114, 507-511 (2012-04-03)
In order to develop feasible production processes for microalgal biodiesel, the isolation of high neutral lipid producing microalgae is crucial. Since the established Nile Red (NR) method for detection of intracellular lipids has been successful only for some microalgae, a
Siang Hui Lim et al.
Journal of medicinal chemistry, 53(7), 2865-2874 (2010-03-05)
To understand the effects of substitution patterns on photosensitizing the ability of boron dipyrromethene (BODIPY), two structural variations that either investigate the effectiveness of various iodinated derivatives to maximize the "heavy atom effect" or focus on the effect of extended
Isaac A Klein et al.
Science (New York, N.Y.), 368(6497), 1386-1392 (2020-06-20)
The nucleus contains diverse phase-separated condensates that compartmentalize and concentrate biomolecules with distinct physicochemical properties. Here, we investigated whether condensates concentrate small-molecule cancer therapeutics such that their pharmacodynamic properties are altered. We found that antineoplastic drugs become concentrated in specific

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service