benzyl triethyl ammonium chloride
benzenemethanaminium, N,N,N-triethyl-, chloride (1:1)
 
Notes:
None found
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      Product(s):
      B0444 Benzyltriethylammonium Chloride >98.0%(T)
       
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benzyl(triethyl)azanium;chloride (Click)
CAS Number: 56-37-1Picture of molecule
Other: 130517-24-7
ECHA EINECS - REACH Pre-Reg: 200-270-1
FDA UNII: 46WDQ3ADML
Beilstein Number: 3574984
MDL: MFCD00011824
Molecular Weight: 227.77734000
Formula: C13 H22 Cl N
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: antistatic agents
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
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US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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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)
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Organoleptic Properties:
  
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Cosmetic Information:
CosIng: cosmetic data
Cosmetic Uses: antistatic agents
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Suppliers:
EMD Millipore
For experimental / research use only.
Benzyl Triethylammonium Chloride
Santa Cruz Biotechnology
For experimental / research use only.
Benzyltriethylammonium Chloride
Sigma-Aldrich: Aldrich
For experimental / research use only.
Benzyltriethylammonium chloride 99%
TCI AMERICA
For experimental / research use only.
Benzyltriethylammonium Chloride >98.0%(T)
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
intravenous-mouse LD50  18 mg/kg
U.S. Army Armament Research & Development Command, Chemical Systems Laboratory, NIOSH Exchange Chemicals. Vol. NX#01867

oral-rat LD50  2219 mg/kg
SKIN AND APPENDAGES (SKIN): HAIR: OTHER BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) GASTROINTESTINAL: CHANGES IN STRUCTURE OR FUNCTION OF SALIVARY GLANDS
Acute Toxicity Data. Journal of the American College of Toxicology, Part B. Vol. 15(Suppl

Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: antistatic agents
Recommendation for benzyl triethyl ammonium chloride usage levels up to:
 not for fragrance use.
 
Recommendation for benzyl triethyl ammonium chloride flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
EPA Substance Registry Services (TSCA): 56-37-1
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 66133
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 1
 benzyl(triethyl)azanium;chloride
Chemidplus: 0000056371
RTECS: BO8275000 for cas# 56-37-1
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References:
 benzyl(triethyl)azanium;chloride
NIST Chemistry WebBook: Search Inchi
Canada Domestic Sub. List: 56-37-1
Pubchem (cid): 66133
Pubchem (sid): 135026087
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Other Information:
(IUPAC): Atomic Weights of the Elements 2009
(IUPAC): Atomic Weights of the Elements 2009 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
HMDB (The Human Metabolome Database): Search
Export Tariff Code: 2923.90.0000
Haz-Map: View
ChemSpider: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
 antistatic agents 
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Occurrence (nature, food, other): note
 not found in nature
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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
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Articles:
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.
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