CAS 23491-45-4
:Hoechst 33258
Description:
Hoechst 33258 is a fluorescent dye commonly used in molecular biology and biochemistry for staining DNA. It is characterized by its ability to bind specifically to the minor groove of double-stranded DNA, which allows for the visualization of nucleic acids under ultraviolet light. The compound exhibits strong fluorescence upon binding, making it a valuable tool for applications such as flow cytometry, fluorescence microscopy, and cell cycle analysis. Hoechst 33258 is typically used in live and fixed cell assays due to its cell-permeable nature. Its chemical structure includes a bisbenzimidazole moiety, which contributes to its DNA-binding properties. The dye is generally considered to have low toxicity, although appropriate safety precautions should be taken when handling it. Additionally, Hoechst 33258 can be used in combination with other fluorescent markers to facilitate multi-parameter analysis in various experimental setups. Overall, its specificity for DNA and fluorescent properties make it an essential reagent in genetic and cellular research.
Formula:C25H24N6O·3ClH
InChI:InChI=1S/C25H24N6O.3ClH/c1-30-10-12-31(13-11-30)18-5-9-21-23(15-18)29-25(27-21)17-4-8-20-22(14-17)28-24(26-20)16-2-6-19(32)7-3-16;;;/h2-9,14-15,32H,10-13H2,1H3,(H,26,28)(H,27,29);3*1H
InChI key:InChIKey=SMNPLAKEGAEPJD-UHFFFAOYSA-N
SMILES:CN1CCN(C=2C=C3NC(=NC3=CC2)C=4C=C5C(=CC4)N=C(N5)C6=CC=C(O)C=C6)CC1.Cl
Synonyms:- 2-[2-(4-Hydroxyphenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazinyl)benzimidazole trihydrochloride
- 2-[2-(4-Hydroxyphenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)-benzimidazole trihydrochloride
- 2-[2-(4-Hydroxyphenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)benzimidazole trichloride
- 2-[2-(4-Hydroxyphenyl)-6-benzimidazolyl]-6-(1-methyl-4-piperazyl)benzimidazole-3HCl
- 2′-(4-Hydroxyphenyl)-5-(4-methyl-1-piperazinyl)-2,5′-bi-1H-benzimidazole
- 4-[5-[5-(4-Methyl-1-piperazinyl)-2-benzimidazolyl]-2-benzimidazolyl]phenol trihydrochloride
- 4-[6-(4-methylpiperazin-1-yl)-1',3'-dihydro-1H,2'H-2,5'-bibenzimidazol-2'-ylidene]cyclohexa-2,5-dien-1-one trihydrochloride
- Bisbenzimide
- Bisbenzimide (quenchant)
- Bisbenzimide H 33258
- Bisbenzimide trihydrochloride
- H 33258
- Ho 33258
- Hoe 33258
- Hoechst 33258
- NSC 322921
- Phenol, 4-[5-(4-methyl-1-piperazinyl)[2,5′-bi-1H-benzimidazol]-2′-yl]-, trihydrochloride
- Phenol, 4-[6-(4-methyl-1-piperazinyl)[2,6′-bi-1H-benzimidazol]-2′-yl]-, hydrochloride (1:3)
- See more synonyms
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Found 9 products.
Bisbenzimide H 33258 [for Biochemical Research]
CAS:Formula:C25H24N6O·3HClPurity:>98.0%(HPLC)Color and Shape:Light yellow to Brown to Dark green powder to crystalMolecular weight:533.88Bisbenzimide H 33258 (0.2mL×5) (1mg/mL in Water) [for Cell Staining]
CAS:Formula:C25H24N6O·3HClColor and Shape:Light yellow to Yellow clear liquidMolecular weight:533.88Hoechst 33258 trihydrochloride
CAS:Hoechst 33258 trihydrochloridePurity:≥95%Molecular weight:533.9g/molBis-Benzimide H 33258
CAS:<p>Bis-Benzimide H 33258</p>Formula:C25H24N6O·3ClHPurity:By hplc: 99.37% (Typical Value in Batch COA)Color and Shape: yellow solidMolecular weight:533.88g/molHoechst 33258 trihydrochloride
CAS:<p>Hoechst 33258 trihydrochloride (Bisbenzimide) is a benzimidazole anti-filarial agent. Hoechst 33258 is fluorescent when it binds to certain nucleotides in DNA.</p>Formula:C25H24N6O·3HClPurity:95.68% - 99.47%Color and Shape:Yellow-Green PowderMolecular weight:533.9Bisbenzimide H 33258 Fluorochrome trihydrochloride
CAS:Formula:C25H24N6O·3HClPurity:≥ 98.0%Color and Shape:Yellow to dark yellow powderMolecular weight:533.9Hoechst 33258
CAS:<p>Hoechst 33258 is a fluorescent dye that binds to the DNA of cells and can be used as a model system in cell biology. It is also used to detect radiation exposure and has been shown to inhibit the growth of certain bacteria. Hoechst 33258 binds with high affinity to basic proteins, such as histones, which are rich in arginine. This interaction inhibits the ability of DNA polymerase to synthesize DNA and prevents cellular transformation. The drug also inhibits cellular physiology by inhibiting protein synthesis, which may lead to cell death. Hoechst 33258 is not active against most bacteria because it has low affinity for phosphate groups on the bacterial cell wall.</p>Formula:C25H24N6O•(HCl)3Purity:Min. 95%Color and Shape:Yellow PowderMolecular weight:533.88 g/mol






