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Home > Encyclopedia > 1,1-Dimethyl-4-phenylpiperazinium iodide

1,1-Dimethyl-4-phenylpiperazinium iodide

1,1-Dimethyl-4-phenylpiperazinium iodide structure

1,1-Dimethyl-4-phenylpiperazinium iodide 

structure
  • CAS No:

    54-77-3

  • Formula:

    C12H19N2.I

  • Chemical Name:

    1,1-Dimethyl-4-phenylpiperazinium iodide

  • Synonyms:

    Piperazinium,1,1-dimethyl-4-phenyl-,iodide (1:1);Piperazinium,1,1-dimethyl-4-phenyl-,iodide;1,1-Dimethyl-4-phenylpiperazinium iodide;DMPP iodide;N,N-Dimethyl-N′-phenylpiperazinium iodide;Dimethylphenylpiperazinium iodide;DMPP;1,1-Dimethyl-4-phenylpiperazine iodide;DMPP (nicotinic agonist)

  • Categories:

    Biochemical Engineering  >  Amino Acids and Proteins

Description

white fine crystalline powder


1,1-dimethyl-4-phenylpiperazinium iodide is a N-arylpiperazine, a quaternary ammonium salt, a piperazinium salt and an organic iodide salt. It has a role as a nicotinic acetylcholine receptor agonist.|A selective nicotinic cholinergic agonist used as a research tool. DMPP activates nicotinic receptors in autonomic ganglia but has little effect at the neuromuscular junction.

1,1-Dimethyl-4-phenylpiperazinium iodide Basic Attributes

318.197

318.059296

424-640-9

X95H7DRX99

89754

2933599090

Characteristics

3.24000

-1.38920

white powder

1.3965 (estimate)

234-238 °C(lit.)

-20ºC

Safety Information

NONH for all modes of transport

3

R36/37/38

S26-S36

TM3385000

Xi: Irritant;

P261-P305 + P351 + P338

H315-H319-H335

|Warning|H315 (97.44%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 39 companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

Drugs that bind to and activate nicotinic cholinergic receptors (RECEPTORS, NICOTINIC). Nicotinic agonists act at postganglionic nicotinic receptors, at neuroeffector junctions in the peripheral nervous system, and at nicotinic receptors in the central nervous system. Agents that function as neuromuscular depolarizing blocking agents are included here because they activate nicotinic receptors, although they are used clinically to block nicotinic transmission. (See all compounds classified as Nicotinic Agonists.)|Agents that mimic neural transmission by stimulation of the nicotinic receptors on postganglionic autonomic neurons. Drugs that indirectly augment ganglionic transmission by increasing the release or slowing the breakdown of acetylcholine or by non-nicotinic effects on postganglionic neurons are not included here nor are the nonspecific cholinergic agonists. (See all compounds classified as Ganglionic Stimulants.)

1,1 Dimethyl 4 phenylpiperazine Iodide

Computed Properties

Molecular Weight:318.20
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:318.05930
Monoisotopic Mass:318.05930
Topological Polar Surface Area:3.2
Heavy Atom Count:15
Complexity:173
Covalently-Bonded Unit Count:2
Compound Is Canonicalized:Yes

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