HOECHST 33258
HOECHST 33258 Basic information
- Product Name:
- HOECHST 33258
- Synonyms:
-
- 2'-(4-HYDROXYPHENYL)-5-(4-METHYL-1-PIPERAZINYL)-2,5'-BI-1H-BENZIMIDAZOLE TRIHYDROCHLORIDE HYDRATE
- BISBENZIMIDE H 33258
- BISBENZIMIDE TRIHYDROCHLORIDE HYDRATE
- CELLSTAIN- HOECHST 33258 SOLUTION
- bisbenzimide trihydrochloride cell*culture tested
- hoechst 33258 (bisbenzimide)
- p-(5-(5-(4-methylpiperazin-1-yl)benzimidazol-2-yl)benzimidazol-2-yl)phenol
- 4-(5-(4-METHYL-1-PIPERAZINYL)(2,5''-BI-1H-BENZIMIDAZOL)2''-YL)PHENOL
- CAS:
- 23491-44-3
- MF:
- C25H24N6O
- MW:
- 424.5
- EINECS:
- 245-689-0
- Mol File:
- 23491-44-3.mol
HOECHST 33258 Chemical Properties
- Melting point:
- 314 °C
- Boiling point:
- 746.9±70.0 °C(Predicted)
- Density
- 1.355±0.06 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- H2O: 10 mg/mL
- form
- powder
- pka
- 9.23±0.15(Predicted)
- color
- Light yellow to yellow
- Stability:
- Stable. Incompatible with strong oxidizing agents. Light sensitive.
- EPA Substance Registry System
- Phenol, 4-[5-(4-methyl-1-piperazinyl)[2,5'-bi-1H-benzimidazol]-2'-yl]- (23491-44-3)
MSDS
- Language:English Provider:ACROS
HOECHST 33258 Usage And Synthesis
Chemical Properties
yellow solid
Uses
Hoechst 33258 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].
Definition
ChEBI: Pibenzimol is a bibenzimidazole and a N-methylpiperazine. It has a role as a fluorochrome and an anthelminthic drug.
References
[1] Wang XJ, et al. Newly synthesized bis-benzimidazole derivatives exerting anti-tumor activity through inductionof apoptosis and autophagy. Bioorg Med Chem Lett. 2012 Oct 1;22(19):6297-300. DOI:10.1016/j.bmcl.2012.06.102
[2] Stoli? I, et al. Synthesis, DNA/RNA affinity and antitumour activity of new aromatic diamidines linked by 3,4-ethylenedioxythiophene. Eur J Med Chem. 2011 Feb;46(2):743-55. DOI:10.1016/j.ejmech.2010.12.010
HOECHST 33258Supplier
- Tel
- 021-65675885 18964387627
- info@efebio.com
- Tel
- 15076683720
- klq@cw-bio.com
- Tel
- 0530-+86-530-529 6766,+86-15666160102 15666160102
- info@chuangli-chem.com
- Tel
- +1-800-259-7612
- info@musechem.com
- Tel
- 025-66061636 18013972705
- qqyang@aikonchem.com