Octenidine Free Base

  • CAT Number: I033802
  • CAS Number: 71251-02-0
  • Molecular Formula: C36H62N4
  • Molecular Weight: 550.92
  • Purity: 98%
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Octenidine Free Base (Cat.No:I033802) is a broad-spectrum antimicrobial agent used in various medical and personal care products. It exhibits strong activity against bacteria, fungi, and some viruses. Octenidine Free Base is commonly employed in wound care, oral hygiene products, and disinfectants. Its effectiveness, low toxicity, and long-lasting antimicrobial action make it a valuable component in infection control.

Catalog Number I033802
CAS Number 71251-02-0
Molecular Formula

C36H62N4

Purity 98
Solubility To be determined
Storage Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
IUPAC Name 1-Octanamine, N,N'-(1,10-decanediyldi-1(4H)-pyridinyl-4-ylidene)bis-
InChI InChI=1S/C36H62N4/c1-3-5-7-9-15-19-27-37-35-23-31-39(32-24-35)29-21-17-13-11-12-14-18-22-30-40-33-25-36(26-34-40)38-28-20-16-10-8-6-4-2/h23-26,31-34H,3-22,27-30H2,1-2H3
InChIKey ZVXNYZWXUADSRV-UHFFFAOYSA-N
SMILES CCCCCCCC/N=C1C=CN(CCCCCCCCCCN(C=C/2)C=CC2=N/CCCCCCCC)C=C/1
Reference

1: Assadian O. Octenidine dihydrochloride: chemical characteristics and antimicrobial properties. J Wound Care. 2016 Mar;25(3 Suppl):S3-6. doi: 10.12968/jowc.2016.25.Sup3.S3. PMID: 26949863.
2: Hübner NO, Siebert J, Kramer A. Octenidine dihydrochloride, a modern antiseptic for skin, mucous membranes and wounds. Skin Pharmacol Physiol. 2010;23(5):244-58. doi: 10.1159/000314699. Epub 2010 May 18. PMID: 20484966.
3: Lopez KM, Hobden JA, Warner IM. Octenidine/carbenicillin GUMBOS as potential treatment for oropharyngeal gonorrhoea. J Antimicrob Chemother. 2020 Dec 1;75(12):3576-3581. doi: 10.1093/jac/dkaa346. PMID: 32830243.
4: Clanner-Engelshofen BM, French LE, Reinholz M. Octenidine disinfection during the SARS-CoV-2 pandemia. Eur J Dermatol. 2020 Oct 1;30(5):613-614. doi: 10.1684/ejd.2020.3856. PMID: 32972908; PMCID: PMC8120489.
5: Yakuschenko IK, Pozdeeva NN, Mumyatova VA, Terentiev AA, Gadomsky SY. Iso- octenidine: Promising Octenidine Analogue with Improved Solubility. Curr Org Synth. 2020 Dec 30. doi: 10.2174/1570179417666201231104453. Epub ahead of print. PMID: 33390116.
6: Shepherd MJ, Moore G, Wand ME, Sutton JM, Bock LJ. Pseudomonas aeruginosa adapts to octenidine in the laboratory and a simulated clinical setting, leading to increased tolerance to chlorhexidine and other biocides. J Hosp Infect. 2018 Nov;100(3):e23-e29. doi: 10.1016/j.jhin.2018.03.037. Epub 2018 Mar 31. PMID: 29614247.
7: Szostak K, Czogalla A, Przybyło M, Langner M. New lipid formulation of octenidine dihydrochloride. J Liposome Res. 2018 Jun;28(2):106-111. doi: 10.1080/08982104.2016.1275678. Epub 2017 Jan 18. PMID: 28006995.
8: Melhorn S, Staubach P. Octenidindihydrochlorid : Das Antiseptikum, das nicht jede Grundlage mag [Octenidine dihydrochloride : The antiseptic that does not like every base formulation]. Hautarzt. 2018 May;69(5):427-429. German. doi: 10.1007/s00105-018-4139-0. PMID: 29532135.
9: Htun HL, Hon PY, Holden MTG, Ang B, Chow A. Chlorhexidine and octenidine use, carriage of qac genes, and reduced antiseptic susceptibility in methicillin- resistant Staphylococcus aureus isolates from a healthcare network. Clin Microbiol Infect. 2019 Sep;25(9):1154.e1-1154.e7. doi: 10.1016/j.cmi.2018.12.036. Epub 2019 Jan 6. PMID: 30625411.
10: Daeschlein G. Antimicrobial and antiseptic strategies in wound management. Int Wound J. 2013 Dec;10 Suppl 1(Suppl 1):9-14. doi: 10.1111/iwj.12175. PMID: 24251838; PMCID: PMC7950476.

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