Bisbenzimide

Bisbenzimide
Names
	IUPAC name 2′-(4-Ethoxyphenyl)-6-(4-methyl-1-piperazinyl)-1H,3′H-2,5′-bibenzimidazole
	Other names Hoechst 33342; Hoe 33342
Identifiers
CAS Number	23491-52-3 ; 23491-45-4 (trihydrochloride);
3D model (JSmol)	Interactive image;
ChemSpider	1420;
ECHA InfoCard	100.041.523
PubChem CID	1464;
UNII	99KZS6CNZX ; MHT095273M (trihydrochloride) ;
CompTox Dashboard (EPA)	DTXSID80178059 ;
	InChI InChI=1S/C27H28N6O/c1-3-34-21-8-4-18(5-9-21)26-28-22-10-6-19(16-24(22)30-26)27-29-23-11-7-20(17-25(23)31-27)33-14-12-32(2)13-15-33/h4-11,16-17H,3,12-15H2,1-2H3,(H,28,30)(H,29,31) Key: PRDFBSVERLRRMY-UHFFFAOYSA-N; InChI=1/C27H28N6O/c1-3-34-21-8-4-18(5-9-21)26-28-22-10-6-19(16-24(22)30-26)27-29-23-11-7-20(17-25(23)31-27)33-14-12-32(2)13-15-33/h4-11,16-17H,3,12-15H2,1-2H3,(H,28,30)(H,29,31) Key: PRDFBSVERLRRMY-UHFFFAOYAR;
	SMILES CCOc1ccc(cc1)c2[nH]c3cc(ccc3n2)c4[nH]c5cc(ccc5n4)N6CCN(CC6)C;
Properties
Chemical formula	C27H28N6O
Molar mass	452.562 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Bisbenzimide (Hoechst 33342) is an organic compound used as a fluorescent stain for DNA in molecular biology applications.^[1] Several related chemical compounds are used for similar purposes and are collectively called Hoechst stains.

Application

Bisbenzimide tends to bind to adenine–thymine-rich regions of DNA and can decrease its density. Bisbenzimide mixed with DNA samples can then be used to separate DNA according to their AT percentage using a cesium chloride (CsCl) gradient centrifugation.

References

^ "bisBenzimide H 33342 trihydrochloride". Sigma-Aldrich.

External links

Fluorescence Spectra: http://www.fluorophores.tugraz.at/substance/463

[1] "bisBenzimide H 33342 trihydrochloride". Sigma-Aldrich.

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