2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate
$360.00
CAS No.: 2016-36-6
Catalog No.: 195061
Purity: 95%
MF: C12H19NO4
MW: 241.287
Storage: 2-8 degree Celsius
SMILES: OCC[N+](C)(C)C.O=C([O-])C1=CC=CC=C1O
Catalog No.: 195061
Purity: 95%
MF: C12H19NO4
MW: 241.287
Storage: 2-8 degree Celsius
SMILES: OCC[N+](C)(C)C.O=C([O-])C1=CC=CC=C1O
2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate; CAS No.: 2016-36-6; 2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate. PROPERTIES: 2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate appears as a white to off-white crystalline powder with a slight acidic odor. Its molecular formula is C10H15NO4, corresponding to a molecular weight of approximately 217.23 g/mol. The compound exhibits a melting point in the range of 150-153 C and demonstrates moderate solubility in water and polar organic solvents such as methanol and dimethylformamide. It is stable under normal laboratory conditions but should be protected from prolonged exposure to moisture and heat. Proper storage involves keeping it in a tightly sealed container at room temperature (15-25 C) in a dry environment. Safety considerations include wearing appropriate protective equipment as the compound may cause skin and eye irritation. Inhalation of dust should be avoided, and in case of accidental exposure, thorough washing with water and medical consultation is advised. APPLICATIONS: 2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate functions as a bioactive compound in pharmaceutical research, particularly valuable in the preparation of antiseptic agents and preservatives where its antimicrobial properties prevent microbial growth in formulations (Journal of Medicinal Chemistry). In materials science, 2-Hydroxy-N,N,N-trimethylethanaminium 2-hydroxybenzoate serves as a building block for creating self-assembled monolayers and surface coatings with antimicrobial properties, leveraging its ability to adsorb onto various substrates and inhibit bacterial adhesion (Langmuir). Additionally, it finds application in the synthesis of certain agrochemicals, though specific applications in this area are limited to non-agricultural research settings (Pest Management Science). The compound is also employed in the preparation of ion-pairing reagents for chromatographic separations, where its charged nature facilitates the selective retention and elution of specific analytes (Journal of Chromatography A).
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