benzyl triethyl ammonium chloride

benzenemethanaminium, N,N,N-triethyl-, chloride (1:1)

CAS: 56-37-1 C13 H22 Cl N MW: 227.77734000

Identification

Namebenzyl triethyl ammonium chloride
CAS Number56-37-1
EINECS200-270-1
FDA UNII46WDQ3ADML
Molecular FormulaC13 H22 Cl N
Molecular Weight227.77734000
MDL NumberMFCD00011824
Beilstein3574984

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Flash Point 32.00 °F. TCC ( 0.00 °C. ) (est)
Soluble in water, 2.238e+005 mg/L @ 25 °C (est)

Cosmetic Information

CosIngcosmetic data
Cosmetic Usesantistatic agents

No sensory data available

Safety Information

Preferred SDSView
Oral/Parenteral Toxicityintravenous-mouse LD50 18 mg/kg
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements', 'U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01867']

Safety in Use

Categoryantistatic agents
Recommendation for benzyl triethyl ammonium chloride usage levels up tonot for fragrance use.
Recommendation for benzyl triethyl ammonium chloride flavor usage levels up tonot for flavor use.

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Potential Uses

antistatic agents

Natural Occurrence

not found in nature

Synonyms

ammonium, benzyltriethyl-, chloride benzenemethanaminium, N,N,N-triethyl-, chloride benzenemethanaminium, N,N,N-triethyl-, chloride (1:1) benzyl triethylammonium chloride N- benzyl-N,N-diethylethanaminium chloride benzyl-triethyl ammonium chloride benzyl(triethyl)azanium;chloride benzyltriethyl ammonium chloride benzyltriethylammonium chloride benzyltriethylammoniumchloride BTEAC N,N- diethyl-N-(phenylmethyl)ethanaminium chloride TEBAC N,N,N- triethyl-N-benzylammonium chloride N,N,N- triethylbenzenemethanaminium chloride triethylbenzylammonium chloride PubMed: Method transfer from high-pressure liquid chromatography to ultra-high-pressure liquid chromatography. I. A thermodynamic perspective. PubMed: Fluoroponytailed crown ethers and quaternary ammonium salts as solid-liquid phase transfer catalysts in organic synthesis. PubMed: (5R)-5-[(1R)-2,2-Dichloro-1-methyl-cyclo-prop-yl]-2-methyl-cyclo-hex-2-en-1-one. PubMed: Synthesis and exploration of QSAR model of 2-methyl-3-[2-(2-methylprop-1-en-1-yl)-1H-benzimidazol-1-yl]pyrimido[1,2-a]benzimidazol-4(3H)-one as potential antibacterial agents. PubMed: Bis(benzyl-triethyl-ammonium) hexa-chloridostannate(IV). PubMed: Adsorptive removal of cationic surfactants from aqueous solutions onto high-area activated carbon cloth monitored by in situ UV spectroscopy. PubMed: Characterisation of a proposed internet synthesis of N,N-dimethyltryptamine using liquid chromatography/electrospray ionisation tandem mass spectrometry. PubMed: Sensitive HPLC-ESI-MS method for the determination of tiotropium in human plasma. PubMed: Ethoxylation of p-chloronitrobenzene using phase-transfer catalysts by ultrasound irradiation: a kinetic study. PubMed: Activation of pentafluorophenylsilanes by weak Lewis bases in reaction with iminium cations. PubMed: Sorption of nitroaromatic compounds to synthesized organoclays. PubMed: Heterocyclizations with tosylmethyl isocyanide derivatives. A new approach to substituted azolopyrimidines. PubMed: Spiro-annulation of barbituric acid derivatives and its analogs by ring-closing metathesis reaction. PubMed: Ultrasound effect on Suzuki reactions. 1. Synthesis of unsymmetrical biaryls. PubMed: Heteroconjugation-based capillary electrophoretic separation of phenolic compounds in acetonitrile and propylene carbonate. PubMed: Phase-transfer catalysis and ultrasonic waves II: saponification of vegetable oil. PubMed: Extractive spectrophotometric determination of trace amounts of iron(III) with benzyltriethylammonium chloride. PubMed: Catalytic hydration of terminal alkenes to primary alcohols. PubMed: Comparison of polymerization of ancrod and thrombin fibrin monomers.