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Dansyl-X, acid

Compared to Dansyl chloride, Dansyl-X acid gives better yield for labeling peptides and nucleotides. Dansyl dyes have environmentally sensitive fluorescence quantum yields and emission maxima along with large Stokes shifts. This environment-sensitive fluorescence property has made Dansyl dyes an important tool for biophysical studies. They are particularly useful for preparing fluorescent drug or ligand analogs that are expected to bind to hydrophobic sites in proteins or membranes or other biological receptors. Dansyl protein conjugates have fluorescence lifetimes of 10-20 nanoseconds.

Calculators

Common stock solution preparation

Table 1. Volume of DMSO needed to reconstitute specific mass of Dansyl-X, acid to given concentration. Note that volume is only for preparing stock solution. Refer to sample experimental protocol for appropriate experimental/physiological buffers.

0.1 mg0.5 mg1 mg5 mg10 mg
1 mM274.379 µL1.372 mL2.744 mL13.719 mL27.438 mL
5 mM54.876 µL274.379 µL548.757 µL2.744 mL5.488 mL
10 mM27.438 µL137.189 µL274.379 µL1.372 mL2.744 mL

Molarity calculator

Enter any two values (mass, volume, concentration) to calculate the third.

Mass (Calculate)Molecular weightVolume (Calculate)Concentration (Calculate)Moles
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Spectrum

Product family

NameExcitation (nm)Emission (nm)Extinction coefficient (cm -1 M -1)
Dansyl-X, SE3355183300
NBD-X acid *CAS 88235-25-0*46753922000

References

View all 33 references: Citation Explorer
Phenylisothiocyanate and dansyl chloride precolumn derivatizations for the high-performance liquid chromatography analysis of the antitumoral agent ES-285 in dog plasma
Authors: Maraschiello C, Mir and a E, Millan E, Floriano P, Vilageliu J.
Journal: J Chromatogr B Analyt Technol Biomed Life Sci (2003): 1
Dansyl chloride derivatization of methamphetamine: a method with advantages for screening and analysis of methamphetamine in urine
Authors: Yamada H, Yamahara A, Yasuda S, Abe M, Oguri K, Fukushima S, Ikeda-Wada S.
Journal: J Anal Toxicol (2002): 17
Determination of the xenoestrogens 4-nonylphenol and bisphenol A by high-performance liquid chromatography and fluorescence detection after derivatisation with dansyl chloride
Authors: Naassner M, Mergler M, Wolf K, Schuphan I.
Journal: J Chromatogr A (2002): 133
Automated pre-column derivatization of amines in biological samples with dansyl chloride and with or without post-column chemiluminescence formation by using TCPO-H2O2
Authors: Molins-Legua C, Campins-Falco P, Sevillano-Cabeza A.
Journal: Analyst (1998): 2871
A new screening method for amphetamine and methamphetamine using dansyl chloride derivatization and cartridge fluorescence
Authors: Yamada H, Ikeda-Wada S, Oguri K.
Journal: Biol Pharm Bull (1998): 778
Page updated on April 6, 2022

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Physical properties

Molecular weight

364.46

Solvent

DMSO

Spectral properties

Correction Factor (280 nm)

0.387

Extinction coefficient (cm -1 M -1)

3300

Excitation (nm)

335

Emission (nm)

518

Storage, safety and handling

H-phraseH303, H313, H333
Hazard symbolXN
Intended useResearch Use Only (RUO)
R-phraseR20, R21, R22

Storage

Freeze (< -15 °C); Minimize light exposure
UNSPSC12171501
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