ChemicalBook--->CAS DataBase List--->23554-99-6

23554-99-6

23554-99-6 Structure

23554-99-6 Structure
IdentificationBack Directory
[Name]

HOE-32020
[CAS]

23554-99-6
[Synonyms]

HOE32020
HOE-32020
HOE 32020
2,5'-Bi-1H-benzimidazole, 2'-(4-chlorophenyl)-5-(4-methyl-1-piperazinyl)- (9CI)
[Molecular Formula]

C25H23ClN6
[MDL Number]

MFCD25976773
[MOL File]

23554-99-6.mol
[Molecular Weight]

442.94
Chemical PropertiesBack Directory
[Boiling point ]

715.6±70.0 °C(Predicted)
[density ]

1.356±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Store in freezer, under -20°C
[solubility ]

25℃: DMSO or water Protect from light
[form ]

Powder
[pka]

10.68±0.10(Predicted)
[color ]

Light green to green
[Appearance]

Solid Powder
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Piperazine-->Imidazole-->Chlorobenzene
Hazard InformationBack Directory
[Description]

HOE 32020 is one of Hoechst stains which are Bis-benzimides used as blue fluorescent dyes to stain DNA.

[Uses]

HOE 32020 is a marker dye in Hoechst series. Hoechst is A live nuclear marker dye. Hoechst binds to the grooves in the DNA double strand, which tends to be A/ T-rich DNA strand. Although it binds to all nucleic acids, the A/ T-rich double strand DNA significantly enhances fluorescence intensity Therefore,Hoechst dye can be used for living cell labeling. The fluorescence intensity of Hoechst dye increases with the increase of pH of solution[1].
[References]

[1] Latt SA, Stetten G, Juergens LA, Recent developments in the detection of deoxyribonucleic acid synthesis by 33258 Hoechst fluorescence. The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 23 (7): 493-505. DOI:10.1177/23.7.1095650
[2] a b c "Hoechst Stains". Invitrogren (Molecular Probes).
[3] Portugal J, Waring MJ. Assignment of DNA binding sites for 4',6-diamidine-2-phenylindole and bisbenzimide (Hoechst 33258). A comparative footprinting study. Biochimica et Biophysica Acta 949 (2): 158-68. DOI:10.1016/0167-4781(88)90079-6
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