INTRODUCTION
Octenidine dihydrochloride is a cationic surfactant, with a gemini-surfactant structure. Since 1987, it has been used primarily in Europe as an antiseptic prior to medical procedures, including on neonates. It is safe to handle and chemically stable.
Manufacture
This quaternary compound salt is derived from octenidine and hydrochloric acid.
| Synonym | N-octyl-1-[10-(4-octyliminopyridin-1-yl)decyl]pyridin-4-imine;dihydrochloride |
| CAS no. | 70775-75-6 |
| EINECS no. | 274-861-8 |
| Molecular formula | C36H64Cl2N4 |
| Molecular weight | 623.83 |
| Structure |  |
APPLICATIONS
| Octenidine dihydrochloride finds extensive application in medical, industrial, and even food and cosmetic realms |
|---|
| Widely recognized for its exceptional antiseptic, antibacterial, and antifungal properties, It is used for the treatment of wound infections and for disinfecting the skin and mucous membrane. |
| Also, it exhibits anti-inflammatory and analgesic properties, providing relief from inflammation and pain. |
| Octenidine dihydrochloride has been subject to extensive in vitro studies. Its efficacy in treating bacterial and fungal infections has been explored, showcasing its effectiveness against both gram-positive and gram-negative bacteria. |
| Researchers have evaluated its potential as a combatant against viruses, revealing its favorable outcomes in combating select viral strains. |
SPECIFICATIONS
| Test | Unit | Specification |
|---|---|---|
| Description | – | A white to off white powder |
| Solubility | – | Freely soluble in Methanol and Dichloromethane, slightly soluble in N,N‐dimethyl formamide |
| Identification | ||
| a. By IR spectrum | – | a. The IR spectrum of sample should be concordant with that of working standard of Octenidine Dihydrochloride |
| b. Chloride | – | b. It gives reaction for chloride |
| Assay by HPLC | % | Between 98.0 to 101.0 on anhydrous basis |
| Related substances by HPLC | ||
| a. 4-Octyl amino pyridine | % | NMT 0.15 |
| b. Single unknown impurity | % | NMT 0.10 |
| c. Total impurities | % | NMT 0.5 |
| Heavy metals | ppm | NMT 10.0 |
| Sulphated ash | % | NMT 0.5 |
| Water content | % | NMT 2.0 |
| Residual solvents | ||
| Methanol | ppm | NMT 3000 |
| N,N-Dimethyl formamide | ppm | NMT 880 |
| Acetone | ppm | NMT 5000 |
PACKING
25 kg Fiber drum.
STORAGE
Keep containers tightly closed in a dry, cool and well-ventilated place. Store at room temperature.
CERTIFICATION
WHO-GMP and DMF
No matter the quantity you need, our exceptional quality and service will make ExSyn your supplier of choice! If you need any additional information or SDS, please contact us.
(S)-Oxetan-2-yl-methanamine is a chiral oxetane-containing primary amine. The compound features a strained four-membered oxetane ring and an aminomethyl substituent, making it a valuable building block in modern medicinal chemistry. Due to its unique physicochemical properties, including increased polarity and metabolic stability compared with conventional alkyl groups, it is widely employed as an advanced pharmaceutical intermediate in drug discovery and development programs.
Guanidine carbonate is a white, crystalline, water-soluble compound with an alkaline and ionic nature. Composed of guanidinium cations and carbonate anions, it offers chemical stability, buffering capacity, and good formulation compatibility. In textile applications, it is used in formulations and fabric treatments for its thickening, softening, lubricating, anti-static, and flame-retardant properties, contributing to improved fabric finish and performance.
Tin(II) sulfide (SnS) has emerged as a safe and sustainable semiconductor owing to its non-toxicity, low cost, and natural abundance. It has attracted significant interest for solar energy conversion in thin-film photovoltaic devices because of its suitable band gap, which is approximately 1.3 eV in the orthorhombic phase and 1.5-1.7 eV in the cubic phase. In addition to photovoltaic applications, SnS is used in solid-state lubricants, near-infrared detectors, Lithium-ion batteries, and various sensing devices.
Nikethamide is a synthetic organic compound derived from nicotinic acid (vitamin B₃). It consists of a pyridine ring linked to a diethyl amide functional group and belongs to the class of pyridine amide derivatives.
(2-Methoxy-1-methyl-2-oxoethyl)triphenylphosphonium bromide is a stabilized phosphonium salt widely used as an intermediate in organic synthesis. Due to presence of an ester group, the compound generates a stabilized ylide that is particularly useful for synthesizing α, β-unsaturated esters, valuable intermediates in pharmaceuticals, agrochemicals, fragrances, and fine chemicals.
p-tert-Butylphenol (PTBP), is an aromatic organic compound consists of a phenol ring substituted with a tert-butyl group at the para (4-) position, giving it improved thermal stability and hydrophobic properties compared to phenol. PTBP features significant hydrogen bonding capabilities, which enhance its solubility in organic solvents. PTBP is used primarily as an intermediate in the manufacturing of polycarbonate plastics, phenolic resins, and epoxy resins.
Yttrium oxide (Y2O3), also known as yttria, is an air-stable, odorless white powder. It is a highly stable, chemically inert ceramic with a very high melting point. It is insoluble in water but readily dissolves in most strong acids. Increasing the specific surface area and porosity of Y2O3 can further improve its relevant physical and chemical properties.
Ethyl 7,7,7-trifluoro-3-hydroxy-3-methylheptanoate is a fluorinated aliphatic hydroxy ester. The presence of the trifluoromethyl group imparts enhanced metabolic stability, lipophilicity, and unique physicochemical properties compared with non-fluorinated analogues. This compound is primarily used as a synthetic intermediate in pharmaceutical and agrochemical research.
2-Chloro-1,1,1-trimethoxyethane is an organochlorine orthoester compound commonly used as a versatile synthetic intermediate in organic and pharmaceutical chemistry. It is a colorless to pale yellow liquid with good reactivity toward nucleophilic substitution and cyclization reactions, making it valuable in the preparation of heterocyclic and bioactive molecules.