Neostigmine bromide

Neostigmine bromide Basic information
Product Name:Neostigmine bromide
Synonyms:stigmanolbromide;stigmosanbromide;synstigminbromide;(3-HYDROXYPHENYL)TRIMETHYLAMMONIUM BROMIDE DIMETHYL CARBAMATE;3-[[(DIMETHYLAMINO)CARBONYL]OXY]-N,N,N-TRIMETHYLBENZAMINIUM BROMIDE;3-[[(DIMETHYLAMINO)CARBONYL]OXY]-N,N,N-TRIMETHYLBENZENAMINIUM BROMIDE;(3-DIMETHYLCARBAMOYLOXYPHENYL)TRIMETHYLAMMONIUM BROMIDE;Juvastigmin
CAS:114-80-7
MF:C12H19BrN2O2
MW:303.2
EINECS:204-054-8
Product Categories:CENOLATE;Alkaloids;Ammonium Bromides (Quaternary);Quaternary Ammonium Compounds;Intermediates & Fine Chemicals;Pharmaceuticals;Benzene derivatives;Acetylcholine receptor;1
Mol File:114-80-7.mol
Neostigmine bromide Structure
Neostigmine bromide Chemical Properties
Melting point 175-177 °C(lit.)
density 1.4344 (rough estimate)
refractive index 1.5410 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility H2O: 1 g/mL
form powder
color white
PH5.2~6.2 (100g/l, 25℃)
Water Solubility 1 g/ mL
Merck 14,6464
BCS Class3
EPA Substance Registry SystemBenzenaminium, 3-[[(dimethylamino)carbonyl]oxy]-N,N,N-trimethyl-, bromide (114-80-7)
Safety Information
Hazard Codes T+,T
Risk Statements 26/27/28-36/37/38-42/43-25
Safety Statements 22-26-36/37/39-45-37/39-28A
RIDADR UN 2811 6.1/PG 2
WGK Germany 3
RTECS BR3150000
HazardClass 6.1(a)
PackingGroup II
HS Code 29239000
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
Neostigmine bromide Usage And Synthesis
Chemical PropertiesCrystalline Solid
Usesantiscorbutic, antiviral
UsesCholinergic; miotic; antidote (curare)
UsesA reversible acetylcholinesterase inhibitor
UsesNeostigmine bromide has been used as an acetyl cholinesterase (AChE) inhibitor:
  • to control reaction specificity of acetylcholinesterase in coronal organ of Botryllus schlosseri.
  • to study its effects on abnormal contraction of pyloric circular smooth muscle strips (PCSMS).
  • to study its effects on depolarization of bag cell neurons.

DefinitionChEBI: Neostigmine bromide is the bromide salt of neostigmine. It contains a neostigmine.
General DescriptionNeostigmine bromide, (m-hydroxyphenyl)trimethylammonium bromide dimethylcarbamateor the dimethylcarbamic ester of 3-hydroxyphenyltrimethylammoniumbromide (Prostigmin bromide), is usedas an antidote to nondepolarizing neuromuscular blockingdrugs and in the treatment of myasthenia gravis. It occurs asa bitter, odorless, white, crystalline powder. It is soluble inwater and alcohol. The crystals are much less hygroscopicthan those of neostigmine methylsulfate and thus may beused in tablets. Solutions are stable and may be sterilized byboiling. Aqueous solutions are neutral to litmus.
Biological Activityneostigmine bromide is a reversible inhibitor of acetylcholinesterase.[1]ache (acetylcholinesterase) is a hydrolase that hydrolyzes the neurotransmitter acetylcholine at the neuromuscular junction and cholinergic synaspe. it terminates the signal transductions and plays a role in neuronal apoptosis.neostigmine bromide is a quaternary amine that blocked cholinesterase activity to extend and enhance the muscarinic and nicotinic effects of acetylcholine. it is implicated for the treatment of primary open-angle glaucoma, postoperative urinary retention, paralytic ileus, myasthenia gravis etc. it is also reported to be an adjuvant to local anaesthetics and opioids for post-surgical pain after gynaecological or abdominal surgery. [1]
Biochem/physiol ActionsNeostigmine bromide is a quaternary amine. It is involved in elongating and boosting the muscarinic and nicotinic effects of acetylcholine by inhibiting cholinesterase activity. It is used in anesthesia to reverse the neuromuscular blockade produced by competitive neuromuscular blockers.
Clinical UseUse of physostigmine, as a prototype of an indirect-actingparasympathomimetic drug, facilitated the development ofstigmine, in which a trimethylamine group was placed para toa dimethylcarbamate group in benzene. Better inhibition ofcholinesterase was observed when these groups were placedmeta to each other as in neostigmine, a more active and usefulagent. Although physostigmine contains a methylcarbamatefunctional group, greater chemical stability towardhydrolysis was obtained with the dimethylcarbamyl group inneostigmine.
Safety ProfilePoison by ingestion, subcutaneous, intravenous, and intraperitoneal routes. When heated to decomposition it emits very toxic fumes of Br-, NH3, and NOx. See also CARBAMATES and BROMIDES.
Purification MethodsCrystallise neostigmine bromide from EtOH/diethyl ether. Its solubility in H2O is ~50%. [Beilstein 13 III 939.] (It is cholinergic and highly TOXIC.) The starting material 3-dimethylcarbamoyl-N,N-dimethylaniline [59-99-4] has b 195o/20mm [Beilstein 13 III 936], and its picrate has m 138o (from EtOH).
references[1] el-kosasy am, nebsen m, abd el-rahman mk, salem my, el-bardicy mg. comparative study of 2-hydroxy propyl beta cyclodextrin and calixarene as ionophores in potentiometric ion-selective electrodes for neostigmine bromide. talanta. 2011 aug 15;85(2):913-8.
Neostigmine bromide Preparation Products And Raw materials
Raw materialsMethyl bromide-->Dimethylcarbamoyl chloride
Preparation Products3-AMINOPHENYL N,N-DIMETHYLCARBAMATE, 97
Hydroxyphenyl 3-Dimethylaminoanisole Neostigmine Phenyltrimethylammonium bromide Ammonium hydroxide Dimethyldimethoxysilane 4-Dimethylaminobenzoic acid 4-Dimethylaminobenzaldehyde Dimidium bromide Neostigmine 2-Dimethylaminoethanol Demecarium bromide 1,1-Dimethoxyethane Ethidium bromide Neostigmine Methyl Sulfate Ammonium acetate Ammonium sulfate 4-Dimethylaminopyridine

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