N1,N1,N1,N6,N6,N6-Hexamethylhexane-1,6-diaminium chloride dihydrate

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Reagent Code: #53823
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CAS Number 16986-49-5

science Other reagents with same CAS 16986-49-5

blur_circular Chemical Specifications

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Weight 309.3166 g/mol
Formula C₁₂H₃₄Cl₂N₂O₂
inventory_2 Storage & Handling
Storage room temperature

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N1,N1,N1,N6,N6,N6-Hexamethylhexane-1,6-diaminium chloride dihydrate (hexamethonium chloride dihydrate) is a bis-quaternary ammonium salt. It is primarily used in pharmacological and biomedical research as a ganglionic blocking agent, antagonizing nicotinic acetylcholine receptors at autonomic ganglia to inhibit sympathetic and parasympathetic neurotransmission. This property makes it valuable for studying autonomic nervous system functions and as a tool in experimental hypertension models. In synthetic chemistry, it serves as a phase-transfer catalyst to enhance reactions between immiscible phases. Its cationic nature also enables applications as a surfactant, antimicrobial agent, and in formulation of ionic liquids or electrolytes.

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inventory 5g
10-20 days ฿1,593.00

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N1,N1,N1,N6,N6,N6-Hexamethylhexane-1,6-diaminium chloride dihydrate
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N1,N1,N1,N6,N6,N6-Hexamethylhexane-1,6-diaminium chloride dihydrate (hexamethonium chloride dihydrate) is a bis-quaternary ammonium salt. It is primarily used in pharmacological and biomedical research as a ganglionic blocking agent, antagonizing nicotinic acetylcholine receptors at autonomic ganglia to inhibit sympathetic and parasympathetic neurotransmission. This property makes it valuable for studying autonomic nervous system functions and as a tool in experimental hypertension models. In synthetic c

N1,N1,N1,N6,N6,N6-Hexamethylhexane-1,6-diaminium chloride dihydrate (hexamethonium chloride dihydrate) is a bis-quaternary ammonium salt. It is primarily used in pharmacological and biomedical research as a ganglionic blocking agent, antagonizing nicotinic acetylcholine receptors at autonomic ganglia to inhibit sympathetic and parasympathetic neurotransmission. This property makes it valuable for studying autonomic nervous system functions and as a tool in experimental hypertension models. In synthetic chemistry, it serves as a phase-transfer catalyst to enhance reactions between immiscible phases. Its cationic nature also enables applications as a surfactant, antimicrobial agent, and in formulation of ionic liquids or electrolytes.

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