Chemodex

Hoechst 33342 Solution

CHF 135.00
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CDX-B0447-L0055 mlCHF 135.00
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Product Details
Synonyms 2'-(4-Ethoxyphenyl)-5-(4-methyl-1-piperazinyl)-2,5'-bi-1H-benzimidazole trihydrochloride; BisBenzimide H 33342; HOE 33342
Product Type Chemical
Properties
Formula

C27H28N6O . 3HCl . xH2O

MW 561.93
CAS 23491-52-3
RTECS DT4200000
Source/Host Chemicals Synthetic
Purity Chemicals ≥98% (HPLC)
Appearance Liquid.
Solubility Soluble in water.
Concentration 1mg/ml in water
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 PRDFBSVERLRRMY-UHFFFAOYSA-N
Smiles CN(CC1)CCN1C2=CC=C(NC(C3=CC(NC(C4=CC=C(OCC)C=C4)=N5)=C5C=C3)=N6)C6=C2
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage +4°C
Handling Advice Protect from light and moisture.
Use/Stability Stable for at least 2 years after receipt when stored at +4°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description

The Hoechst stains are a family of fluorescent stains for labeling DNA in fluorescence microscopy. The blue fluorescent Hoechst dye is a cell permeable nucleic acid stain that has multiple applications, including sensitive detection of DNA in the presence of RNA in agarose gels, automated DNA determination, sensitive determination of cell number and chromosome sorting. Useful vital stain for the flow cytometric recognition of DNA damage and other viability measurements by monitoring the emission spectral shifts of the dyes. Because this fluorescent stain labels DNA, it can also be used to visualize nuclei and mitochondria. Hoechst 33342 is a cell-permeable, benzimidazole dye that stains DNA by binding to the minor groove of adenine and thymine-rich sequences. It emits blue fluorescence (excitation 350 nm/emission maximum 461 nm) when bound to double stranded DNA and is useful as a marker of nuclei for cell cycle studies and to distinguish nuclear morphology in apoptotic cells.

Product References

(1) D.J. Pierce et al.: Exp. Hematol. 35(9), 1437 (2007) | (2) M.E. Lalande et al.: Proc. Natl. Acad. Sci. USA 78, 363 (1981) | (3) M.J. Lydon et al.: J. Cell. Physiol. 102, 175 (1980)

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