Basic information Safety Supplier Related

HOECHST 33258

Basic information Safety Supplier Related

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
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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)
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Safety Information

Hazard Codes 
Xn
Risk Statements 
22-36/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
SM1140500
3-8-10

MSDS

  • Language:English Provider:ACROS
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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

Shanghai EFE Biological Technology Co., Ltd.
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021-65675885 18964387627
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Tianjin Kailiqi Biotechnology Co., Ltd.
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15076683720
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klq@cw-bio.com
Heze Development Zone chuangli Chemical Co., Ltd.
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0530-+86-530-529 6766,+86-15666160102 15666160102
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Musechem
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+1-800-259-7612
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Aikon International Limited
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025-66061636 18013972705
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qqyang@aikonchem.com