EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes
 

acetyl choline chloride
acetylcholine hydrochloride

Supplier Sponsors

Name:acetyloxyethyl(trimethyl)azanium;chloride
CAS Number: 60-31-1Picture of molecule3D/inchi
Other(deleted CASRN):1784-29-8
ECHA EINECS - REACH Pre-Reg:200-468-8
FDA UNII: AF73293C2R
Nikkaji Web:J231.275A
Beilstein Number:3571875
MDL:MFCD00011698
Molecular Weight:181.66192000
Formula:C7 H16 Cl N O2
BioActivity Summary:listing
NMR Predictor:Predict (works with chrome, Edge or firefox)
Category:pharmaceuticals / chemical synthisis
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
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Google Patents:Search
US Patents:Search
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Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Melting Point: 150.00 °C. @ 760.00 mm Hg
Flash Point: 32.00 °F. TCC ( 0.00 °C. ) (est)
logP (o/w): -3.904 (est)
Soluble in:
 water, 1e+006 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
Acetylcholine Chloride >98%
Odor: characteristic
Use: Acetylcholine is an organic molecule that acts as a neurotransmitter in many organisms, including humans.
Penta International
ACETYL CHOLINE CHLORIDE
Santa Cruz Biotechnology
For experimental / research use only.
Acetylcholine chloride ≥99%
Sigma-Aldrich: Sigma
For experimental / research use only.
Acetylcholine chloride ≥99% (TLC)
TCI AMERICA
For experimental / research use only.
Acetylcholine Chloride >98.0%(T)
 
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:
parenteral-frog LDLo 200 mg/kg
CARDIAC: OTHER CHANGES BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX) BEHAVIORAL: STIFFNESS
Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 166, Pg. 437, 1932.

unreported-frog LDLo 500 mg/kg
PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE BEHAVIORAL: ALTERED SLEEP TIME (INCLUDING CHANGE IN RIGHTING REFLEX)
Naunyn-Schmiedeberg's Archiv fuer Experimentelle Pathologie und Pharmakologie. Vol. 164, Pg. 346, 1932.

intravenous-guinea pig LD50 7700 ug/kg
Archives Internationales de Pharmacodynamie et de Therapie. Vol. 170, Pg. 461, 1967.

intraperitoneal-mouse LD50 15300 ug/kg
LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: CONVULSIONS OR EFFECT ON SEIZURE THRESHOLD
Farmakologiya i Toksikologiya Vol. 20(4), Pg. 32, 1957.

intravenous-mouse LD50 10 mg/kg
PERIPHERAL NERVE AND SENSATION: SPASTIC PARALYSIS WITH OR WITHOUT SENSORY CHANGE
Journal of Pharmacology and Experimental Therapeutics. Vol. 119, Pg. 541, 1957.

oral-mouse LD50 3000 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 337, 1936.

intravenous-rat LD50 22 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 337, 1936.

oral-rat LD50 2500 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 337, 1936.

Dermal Toxicity:
subcutaneous-mouse LD50 170 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 337, 1936.

subcutaneous-rat LD50 250 mg/kg
Journal of Pharmacology and Experimental Therapeutics. Vol. 58, Pg. 337, 1936.

Inhalation Toxicity:
Not determined
 
Safety in Use Information:
Category:
pharmaceuticals / chemical synthisis
Recommendation for acetyl choline chloride usage levels up to:
 not for fragrance use.
 
Recommendation for acetyl choline chloride flavor usage levels up to:
 not for flavor use.
 
Safety References:
EPI System: View
ClinicalTrials.gov:search
Daily Med:search
AIDS Citations:Search
Cancer Citations:Search
Toxicology Citations:Search
EPA Substance Registry Services (TSCA):60-31-1
EPA ACToR:Toxicology Data
EPA Substance Registry Services (SRS):Registry
Laboratory Chemical Safety Summary :6060
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:2
acetyloxyethyl(trimethyl)azanium;chloride
Chemidplus:0000060311
RTECS:FZ9800000 for cas# 60-31-1
 
References:
 acetyloxyethyl(trimethyl)azanium;chloride
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):6060
Pubchem (sid):134972929
 
Other Information:
(IUPAC):Atomic Weights of the Elements 2011 (pdf)
Videos:The Periodic Table of Videos
tgsc:Atomic Weights use for this web site
(IUPAC):Periodic Table of the Elements
CHEBI:View
CHEMBL:View
HMDB (The Human Metabolome Database):Search
Export Tariff Code:2915.39.3500
ChemSpider:View
Wikipedia:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 not found in nature
 
Synonyms:
 acecholin
 acecoline
2-acetoxy-N,N,N-trimethylethanaminium chloride
2-acetoxy-N,N,N-trimethylethanium chloride
2-acetoxyethyltrimethylammonium chloride
 acetyl choline chloride USP
 acetylcholine chloride
 acetylcholine hydrochloride
 acetylcholinechloride
 acetylcholinium chloride
2-acetyloxy-N,N,N-trimethylethanaminium chloride
2-acetyloxy-N,N,N-trimethylethanium chloride
2-(acetyloxy)-N,N,N-trimethylethanaminium chloride
[2-(acetyloxy)ethyl]trimethylazanium chloride
2-acetyloxyethyl-trimethyl-azanium
2-acetyloxyethyl(trimethyl)azanium;chloride
 ethanaminium, 2-(acetyloxy)-N,N,N-trimethyl-, chloride (1:1)
(2-hydroxyethyl)trimethylammonium chloride acetate
2-(trimethylamino)ethyl acetate, chloride
 
 
Notes:
a neurotransmitter. acetylcholine in vertebrates is the major transmitter at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system. it is generally not used as an administered drug because it is broken down very rapidly by cholinesterases, but it is useful in some ophthalmological applications.
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