Basic information
- CAS
306-53-6- Standard SMILES
CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC.[Br-].[Br-]- InChIKey
UPCIBFUJJLCOQG-UHFFFAOYSA-L- Molecular formula
- C13H33Br2N3
- Average molar mass
- 391.23 g/mol
- Monoisotopic mass
- 389.10412
Overview
RN given refers to parent cpd; structure in Merck
Names & identifiers
- Preferred name
- Azamethonium Bromide
- IUPAC
- ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium dibromide
- English name
- azamethonium bromide
- Molecular formula
- C13H33Br2N3
- Molecular weight
- 391.22922
Names & synonyms
Azamethonium bromidePentamethazine306-53-6AzametonPendiomidPendiomidePentaminePentaminumPentamonPentomidGanlionPrapar
Show more names
AzamethoniumC-9295CIBA-9295306-53-6---azamethonium bromide2,2'-(Methylimino)bis(N-ethyl-N,N-dimethylethanaminium) dibromide
Pendiomide bromidePendiomide dibromideBromuro de azametonioPraparat 9295Bromure d'azamethoniumPentamethazene dibromideAzametonio bromuropentamethazene
Database identifiers
- CAS
306-53-6- PubChem CID
- 9382
- DTXSID
DTXSID90877364- ChEMBL
CHEMBL125869- UNII
- 4K6NEI0MSR
- EC Number
- 206-186-1
Properties
Computed structural properties
- Topological polar surface area
- 3.2 Ų
- Hydrogen bond donors
- 0
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 8
- Heavy atoms
- 18
- Formal charge
- 0
- Complexity
- 168
Physicochemical properties
- Melting point
- 212 · 212-215°
- FDA UNII
- 4 K6NEI0MSR · 4K6NEI0MSR
- Toxicity
- 50 in · LD50 in mice (mg/kg): 2500 orally; 60 i.v. (Uranov); LD50 in rabbits (mg/kg): 3000 orally; 160 s.c.; 75 i.v. (Bein, Meier, 1951)
Safety & regulation
Safety information is for reference only and does not replace the supplier’s Safety Data Sheet (SDS), applicable regulations, or professional assessment.
Safety data
- Toxicity
- LD50 in mice (mg/kg): 2500 orally; 60 i.v. (Uranov); LD50 in rabbits (mg/kg): 3000 orally; 160 s.c.; 75 i.v. (Bein, Meier, 1951)
Chemistry & industry
Pharmacology
MeSH Pharmacological Classification
Agents having as their major action the interruption of neural transmission at nicotinic receptors on postganglionic autonomic neurons. Because their actions are so broad, including blocking of sympathetic and parasympathetic systems, their therapeutic use has been largely supplanted by more specific drugs. They may still be used in the control of blood pressure in patients with acute dissecting aortic aneurysm and for the induction of hypotension in surgery.
Suppliers3 total
陕西缔都医药化工有限公司029-029-81120477 17792793610 · [email protected]
河南天孚化工有限公司+86-0371-55170693 +86-19937530512 · [email protected]
BOC Sciences+1-631-485-4226 · [email protected]
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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