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Bethanechol (chloride) (Standard)

CAT: 0804-HY-B0406AR-01Size: 25 mgDry Ice: NoHazardous: No
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CAT#:0804-HY-B0406AR-01Size:25 mg
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Description
Bethanechol (chloride) (Standard) is the analytical standard of Bethanechol (chloride) . This product is intended for research and analytical applications. Bethanechol chloride (Carbamyl-β-methylcholine chloride), a parasympathomimetic agent, is a mAChR agonist that exerts its effects via directly stimulating the mAChR (M1, M2, M3, M4, and M5) of the parasympathetic nervous system[1].
CAS Number
590-63-6
Product Name Alternative
Carbamyl-β-methylcholine chloride (Standard)
UNSPSC
12352211
Target
MAChR; Reference Standards
Related Pathways
GPCR/G Protein; Neuronal Signaling; Others
Field of Research
Neurological Disease; Cancer
Smiles
CC(OC(N)=O)C[N+](C)(C)C.[Cl-]
Molecular Formula
C7H17ClN2O2
Molecular Weight
196.68
References & Citations
[1]Inderbir S. Padda, et al. Bethanechol. Treasure Island (FL) : StatPearls Publishing; 2020 Jan-.|[2]M J Fregly, et al. Bethanechol-induced water intake in rats: possible mechanisms of induction. Pharmacol Biochem Behav. 1982 Oct;17 (4) :727-32.|[3]Julia Yuen Hang Liu, et al. Acetylcholine exerts inhibitory and excitatory actions on mouse ileal pacemaker activity: role of muscarinic versus nicotinic receptors. Am J Physiol Gastrointest Liver Physiol. 2020 Jul 1;319 (1) :G97-G107.|[4]Inderbir S. Padda, et al. Bethanechol. Treasure Island (FL) : StatPearls Publishing; 2020 Jan-.|[5]M J Fregly, et al. Bethanechol-induced water intake in rats: possible mechanisms of induction. Pharmacol Biochem Behav. 1982 Oct;17 (4) :727-32.|[6]Julia Yuen Hang Liu, et al. Acetylcholine exerts inhibitory and excitatory actions on mouse ileal pacemaker activity: role of muscarinic versus nicotinic receptors. Am J Physiol Gastrointest Liver Physiol. 2020 Jul 1;319 (1) :G97-G107.
Shipping Conditions
Room temperature
Scientific Category
Reference Standards

Chemical Information

Bethanechol Chloride

Bethanechol chloride is the chloride salt of bethanechol. A slowly hydrolysed muscarinic agonist with no nicotinic effects, it is used to increase smooth muscle tone, as in the gastrointestinal tract following abdominal surgery, treatment of gastro-oesophageal reflux disease, and as an alternative to catheterisation in the treatment of non-obstructive urinary retention. It has a role as a muscarinic agonist. It is a carbamate ester, a chloride salt and a quaternary ammonium salt. It contains a bethanechol.

CAS Number590-63-6
PubChem CID11548
IUPAC Name2-carbamoyloxypropyl(trimethyl)azanium chloride
Molecular FormulaC7H17ClN2O2
Molecular Weight196.67
Topological Polar Surface Area52.3
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Heavy Atom Count12
Formal Charge0
Complexity140
SMILES
CC(C[N+](C)(C)C)OC(=O)N.[Cl-]
InChI
InChI=1S/C7H16N2O2.ClH/c1-6(11-7(8)10)5-9(2,3)4;/h6H,5H2,1-4H3,(H-,8,10);1H
InChIKey
XXRMYXBSBOVVBH-UHFFFAOYSA-N
Chemical Structure
2D Structure
2D structure of Bethanechol Chloride
CAS: 590-63-6
CID: 11548
Formula: C7H17ClN2O2
MW: 196.67
Interactive 3D Structure
Loading 3D structure...
View on PubChemRaw 3D data
Computed Properties
PropertyValue
Molecular Weight196.67
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count3
Rotatable Bond Count4
Exact Mass196.0978555
Monoisotopic Mass196.0978555
Topological Polar Surface Area52.3 Ų
Heavy Atom Count12
Formal Charge0
Complexity140
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count1
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently-Bonded Unit Count2
Compound Is CanonicalizedYes

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