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OLANEXIDINE

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OLANEXIDINE Basic information

Product Name:
OLANEXIDINE
Synonyms:
  • N''-(3,4-dichlorobenzyl)-N'''-octylimidodicarbonimidic diamide
  • 1-[N'-[(3,4-dichlorophenyl)methyl]carbamimidoyl]-2-octylguanidine
  • Olanexidine Impurity 11
  • OLANEXIDINE
  • Imidodicarbonimidic diamide, N-((3,4-dichlorophenyl)methyl)-N'-octyl
  • Olanexidine [inn]
  • N-[(3,4-Dichlorophenyl)methyl]-N'-octylimidodicarbonimidic diamide
  • N1-(3,4-Dichlorobenzyl)-N5-octylbiguanide
CAS:
146510-36-3
MF:
C17H27Cl2N5
MW:
372.34
Mol File:
146510-36-3.mol
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OLANEXIDINE Chemical Properties

Boiling point:
454.7±55.0 °C(Predicted)
Density 
1.22±0.1 g/cm3(Predicted)
pka
11.92±0.10(Predicted)
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OLANEXIDINE Usage And Synthesis

Description

In July 2015, olanexidine gluconate, a biguanide compound with remarkable antibacterial activity, was approved by the Pharmaceuticals and Medical Devices Agency (PMDA) of Japan for skin antisepsis at surgical sites. The drug was developed and marketed by Otsuka Pharmaceutical in Japan and is available as topical solution (1.5%). Olanexidine gluconate exhibited efficacy against a wide range of bacterial strains, especially Grampositive bacteria. In vitro experiments exploring its mechanism of action indicated that olanexidine interacts with bacterial surface molecules (such as lipopolysaccharides and lipoteichoic acid), disrupting the cell membranes of liposomes. These models suggest that the drug permeates the membranes of both Escherichia coli and Staphylococcus aureus and denatures proteins at relatively high concentrations (>160 g/mL).

Definition

ChEBI: Olanexidine is a dichlorobenzene.

Synthesis

The synthesis of olanexidine gluconate is relatively straightforward, involving the linkage of an n-octyl side chain and a dichlorobenzylamine through a bis-guanidyl lynchpin. The synthesis began with the reaction of commercial noctylamine (17) with sodium dicyanamide in the presence of concentrated sulfuric acid in refluxing n-butyl acetate to give rise to 1-cyano-3-octylguanidine (18) in 86% yield . Conditions employed to subsequently secure biguanidine 20 as the HCl salt hemihydrate in 77% yield were nearly identical to those used for the conversion of 17 to 18. Finally, treatment of 20 with sodium hydroxide in the presence of gluconic acid (21) gave rise to olanexidin gluconate (II) in almost quantitative yield.

OLANEXIDINESupplier

Adamas Reagent, Ltd.
Tel
400-6009262 16621234537
Email
chenyj@titansci.com
Beijing HuaMeiHuLiBiological Chemical
Tel
010-56205725
Email
waley188@sohu.com
Tianjin Kailiqi Biotechnology Co., Ltd.
Tel
15076683720
Email
klq@cw-bio.com
Zhengzhou Acme Chemical Co., Ltd.
Tel
0371-037163312495,13303845143 13303845143
Email
3001379618@qq.com
Shandong Chengchuang Blue Sea Pharmaceutical Technology Co., Ltd.
Tel
0531-58897130 15508676053
Email
drug_impurity@sdcclh.com