ZnAF-1F Solution

CHF 482.00
In stock
CDX-Z0509-M0011 mgCHF 482.00
 
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Product Details
Synonyms 5-{2-[Bis(2-pyridylmethyl)amino]ethylamino}-2′,7′-difluorofluorescein
Product Type Chemical
Properties
Formula C34H26F2N4O5
MW 608.59
CAS 443302-08-7
Source/Host Chemicals Synthetic.
Purity Chemicals ≥90% (HPCE)
Appearance Liquid.
Solubility Soluble in DMSO.
Concentration 5mM in DMSO (1mg in 0.33ml DMSO)
Identity Determined by 1H-NMR.
Declaration Manufactured by Chemodex.
Other Product Data

Click here for Original Manufacturer Product Datasheet
Our product description may differ slightly from the original manufacturers product datasheet.

InChi Key VRUAOMSCYBFMTB-UHFFFAOYSA-N
Smiles OC1=CC2=C(C=C1F)C1(OC(=O)C3=C1C=CC(NCCN(CC1=CC=CC=N1)CC1=NC=CC=C1)=C3)C1=CC(F)=C(O)C=C1O2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Keep cool and dry.
Protect from light.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Inquire
Product Specification Sheet
Datasheet Download PDF
ZnAF-1F and ZnAF-2F do not fluoresce in the presence of other biologically important cations such as Ca2+ and Mg2+, and are insensitive to change of pH. The complexes with Zn2+ of previously developed ZnAFs, ZnAF-1, and ZnAF-2 decrease in fluorescence intensity below pH 7.0 owing to protonation of the phenolic hydroxyl group of fluorescein, whose pKa value is 6.2. On the other hand, the Zn2+ complexes of ZnAF-1F and ZnAF-2F emit stable fluorescence under neutral and slightly acidic conditions because the pKa values are shifted to 4.9 by substitution of electron-withdrawing fluorine at the ortho position of the phenolic hydroxyl group. Spectral data: λex 492nm; λem 517nm in PBS.
Product References
(1) T. Hirano et al. JACS 124, 6555 (2002)
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