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Memantine

CAS No.
19982-08-2
Chemical Name:
Memantine
Synonyms
C13736;MEMANTINE;AKOS BB-9600;AURORA KA-7643;7-DIMETHYLXANTHINE;TIMTEC-BB SBB002574;Memantine USP/EP/BP;Acid salts MeMantine;Memantine hydrochlor;(51052-62-1) memantine
CBNumber:
CB7436657
Molecular Formula:
C12H21N
Molecular Weight:
179.3
MDL Number:
MFCD02114015
MOL File:
19982-08-2.mol
MSDS File:
SDS
Last updated:2024-11-11 20:33:26

Memantine Properties

Melting point 258 °C
Boiling point 239.8±8.0 °C(Predicted)
Density 1.046
refractive index nD25 1.4941
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform (Slightly), DMSO (Slightly)
form Solid
pka 10.79±0.60(Predicted)
color Colorless Oil to Off-White Waxy
BCS Class 1?
CAS DataBase Reference 19982-08-2(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII W8O17SJF3T
ATC code N06DX01

Pharmacokinetic data

Protein binding 45%
Excreted unchanged in urine 48 (74% plus metabolites)
Volume of distribution 10(L/kg)
Biological half-life 60-100 / 117-156

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazard Codes  Xi
Safety Statements  24/25

Memantine price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M217995 Memantine 19982-08-2 25mg $65 2021-12-16 Buy
TRC M217995 Memantine 19982-08-2 100mg $145 2021-12-16 Buy
TRC M217995 Memantine 19982-08-2 250mg $295 2021-12-16 Buy
Matrix Scientific 126985 3,5-Dimethyladamantan-1-amine >95% 19982-08-2 5g $594 2021-12-16 Buy
American Custom Chemicals Corporation API0003289 MEMANTINE 95.00% 19982-08-2 1G $642.18 2021-12-16 Buy
Product number Packaging Price Buy
M217995 25mg $65 Buy
M217995 100mg $145 Buy
M217995 250mg $295 Buy
126985 5g $594 Buy
API0003289 1G $642.18 Buy

Memantine Chemical Properties,Uses,Production

Description

Memantine is a potent antagonist of the N-methyl-D-aspartate (NMDA) receptor. Experimentally, memantine inhibits and reverses the abnor-mal activity of a protein phosphatase (PP-2A) that leads to tauhyperphosphorylation and to neurofibrillary degeneration inAD. Memantine is effective and well toler-ated in patients with severe AD and wasapproved by the FDA for the treatment of moderate-to-severe AD.

Originator

Akatinol,Merz,W. Germany,1983

Uses

antiulcer

Uses

Recent phase 3 clinical trials have shown that Memantine is an effective way of treatment of both mild and moderate-to-severe Alzheimer''s disease and possibly vascular dementia (multi-infarct dementia). Memantine’s method of action involves an uncompetitive, low-affinity, open-channel blocker; it enters the receptor-associated ion channel preferentially when it is excessively open, and, most importantly, its off-rate is relatively fast so that it does not substantially accumulate in the channel to interfere with normal synaptic transmission.

Definition

ChEBI: A primary aliphatic amine that is the 3,5-dimethyl derivative of 1-aminoadamantane. A low to moderate affinity uncompetitive (open-channel); NMDA receptor antagonist which binds preferentially to the NMDA receptor-operated cation channels.

Application

Memantine has been used in patients with VaD basedon its experimental efficacy in animal models of ischaemiclesions.Memantine acts on potentially contributing factorssuch as neuronal depolarization,mitochondrial dysfunc-tion, magnesium effects on NMDA receptors and chronicglutamatergic overstimulation; it also has shown positiveeffects on long-term potentiation and cognitive tests in stan-dard animal models of impaired synaptic plasticity.

Manufacturing Process

A mixture of 24 g of 1,3-dimethyladamantane and 80 ml of bromine was refluxed for 6 hours. The reaction product mixture was cooled, taken up in about 200 ml of chloroform, and poured onto ice. The excess bromine was removed by adding sodium hydrosulfite. The chloroform layer was separated from the aqueous layer, dried, concentrated in vacuo, and distilled at reduced pressure to yield 30.5 g of product having a boiling point of about 118°C at 5- 6 mm; nD25 = 1.5169-1.5182. The product was identified by nuclear magnetic resonance (NMR) and elemental analyses as 1-bromo-3,5- dimethyladamantane.
A mixture of 20 g of 1-bromo-3,5-dimethyladamantane, 75 ml of acetonitrile, and 150 ml of concentrated sulfuric acid was allowed to react overnight at ambient room temperature. The red reaction product mixture was poured over crushed ice, and the white solid which precipitated was taken up in benzene and the benzene solution dried over sodium hydroxide pellets. The benzene solution was filtered from the drying agent and evaporated to dryness in vacuo to yield 18.2 g of product having a melting point of about 97°C and identified by infrared spectrum as 1-scetamido-3,5-dimethyladamantane.
A mixture of 18 g of 1-acetamido-3,5-dimethyladamantane, 38 g of sodium hydroxide, and 300 ml of diethylene glycol was refluxed for a period of 6 hours. The reaction product mixture was cooled and poured onto about 2,000 ml of crushed ice. The basic solution thus obtained was extracted five times with 250 ml portions of benzene and the aqueous layer was discarded. The combined benzene extracts were dried over sodium hydroxide and the dried benzene solution concentrated in vacuo to give a crude oil weighing 14 g and having nD25 = 1.4941, A 4 g sample of the crude oil was dissolved in ether and the solution saturated with anhydrous hydrogen chloride. The solid which precipitated was filtered off and recrystallized from a mixture of alcohol and ether to yield product weighing 3.5 g and melting at 258°C.
It was identified by analysis as 1-amino-3,5-dimethyladamantane hydrochloride.

Therapeutic Function

Spasmolytic

Biological Activity

An antagonist at the NMDA receptor, binding to the ion channel site. Used in the treatment of Parkinsonism.

Clinical Use

NMDA-receptor antagonist:
Treatment of moderate to severe dementia in Alzheimer’s disease

Drug interactions

Potentially hazardous interactions with other drugs
Anaesthetics: increased risk of CNS toxicity with ketamine – avoid.
Analgesics: increased risk of CNS toxicity with dextromethorphan – avoid.
Dopaminergics: possibly enhances effects of dopaminergics and selegiline; increased risk of CNS toxicity with amantadine – avoid.

Metabolism

Memantine undergoes partial hepatic metabolism to form mainly three polar metabolites which possess minimal NMDA receptor antagonistic activity: the N-glucuronide conjugate, 6-hydroxy memantine, and 1-nitrosodeaminated memantine. Renal clearance involves active tubular secretion moderated by pH dependent tubular reabsorption.

Memantine Preparation Products And Raw materials

Global( 200)Suppliers
Supplier Tel Email Country ProdList Advantage
Capot Chemical Co.,Ltd.
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career henan chemical co
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SHANDONG ZHI SHANG CHEMICAL CO.LTD
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BOC Sciences
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Chongqing Chemdad Co., Ltd
+86-023-6139-8061 +86-86-13650506873 sales@chemdad.com China 39894 58
Alchem Pharmtech,Inc.
8485655694 sales@alchempharmtech.com United States 63687 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49374 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32079 58

View Lastest Price from Memantine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Memantine pictures 2024-11-14 Memantine
19982-08-2
US $50.00-114.00 / mg ≥98% 10g TargetMol Chemicals Inc.
Memantine pictures 2024-09-25 Memantine
19982-08-2
US $0.00-0.00 / g 1g 98% 20kg Wuhan Senwayer Century Chemical Co.,Ltd
Memantine USP/EP/BP pictures 2021-07-27 Memantine USP/EP/BP
19982-08-2
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited
  • Memantine pictures
  • Memantine
    19982-08-2
  • US $50.00-114.00 / mg
  • ≥98%
  • TargetMol Chemicals Inc.
  • Memantine pictures
  • Memantine
    19982-08-2
  • US $0.00-0.00 / g
  • 98%
  • Wuhan Senwayer Century Chemical Co.,Ltd

Memantine Spectrum

AKOS BB-9600 MEMANTINE AURORA KA-7643 TIMTEC-BB SBB002574 3,5-dimethyladamantan-1-amine HCl 1-Amino-3,5-dimethyladamantane 3,5-Dimethyl-1-aminoadamantane 1,3-Dimethylaminoadamantane 3,5-DIMETHYL-1-AMINOADAMANTANE(MEMANTINE) 3,5-Dimethyltricyclo(3.3.1.1(3,7))decan-1-amine Tricyclo[3.3.1.13,7]decan-1-aMine,3,5-diMethyl- memantine(3,5-dimethyl-1-adamantanamine) MEMENTINE HYDROCHHLORIDE 1-Adamantanamine, 3,5-dimethyl- 3,5-Dimethyltricyclo(3.3.1.1(sup 3,7))decan-1-amine Tricyclo(3.3.1.1(sup 3,7))decan-1-amine, 3,5-dimethyl- Acid salts MeMantine 1,3-dimethyl-2-adamantanamine (51052-62-1) memantine Memantine USP/EP/BP Memantine hydrochlor 3,5-dimethyl adamantine 3,5-dimethyl adamantine 7-DIMETHYLXANTHINE C13736 Memantine (amantadine) (1r,3R,5S,7r)-3,5-dimethyladamantan-1-amine 19982-08-2 GASTERIL Elisa Kit-Mouse Elisa Kit