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Memantine

Product Name
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
Formula Weight
179.3
MOL File
19982-08-2.mol
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Memantine Property

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)
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Safety

Hazard Codes 
Xi
Safety Statements 
24/25
Hazardous Substances Data
19982-08-2(Hazardous Substances Data)
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P270Do not eat, drink or smoke when using this product.

P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.

P330Rinse mouth.

P501Dispose of contents/container to..…

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N-Bromosuccinimide Price

TRC
Product number
M217995
Product name
Memantine
Packaging
25mg
Price
$65
Updated
2021/12/16
TRC
Product number
M217995
Product name
Memantine
Packaging
100mg
Price
$145
Updated
2021/12/16
TRC
Product number
M217995
Product name
Memantine
Packaging
250mg
Price
$295
Updated
2021/12/16
Matrix Scientific
Product number
126985
Product name
3,5-Dimethyladamantan-1-amine
Purity
>95%
Packaging
5g
Price
$594
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
API0003289
Product name
MEMANTINE
Purity
95.00%
Packaging
1G
Price
$642.18
Updated
2021/12/16
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Memantine Chemical Properties,Usage,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

Raw materials

Preparation Products

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Memantine Suppliers

Wuhan Yingnuo Pharmaceutical Technology Co., Ltd.
Tel
+86-027-59232304 15387063101
Email
2881924050@qq.com
Country
China
ProdList
9956
Advantage
58
Xianning Shen Lan Biomedical Research and Development Co., Ltd.
Tel
18171815831
Email
1341138380@qq.com
Country
China
ProdList
3401
Advantage
58
J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
Country
China
ProdList
94657
Advantage
76
3B Pharmachem (Wuhan) International Co.,Ltd.
Tel
821-50328103-801 18930552037
Fax
86-21-50328109
Email
3bsc@sina.com
Country
China
ProdList
15839
Advantage
69
Beijing HwrkChemical Technology Co., Ltd
Tel
010-89508211 18501085097
Fax
010-89508210
Email
sales.bj@hwrkchemical.com
Country
China
ProdList
8418
Advantage
55
Capot Chemical Co., Ltd
Tel
+86 (0) 571 85 58 67 18
Fax
0086-571-85864795
Email
sales@capotchem.com
Country
China
ProdList
18207
Advantage
66
JinYan Chemicals(ShangHai) Co.,Ltd.
Tel
13817811078
Fax
86-021-50426522,50426273
Email
sales@jingyan-chemical.com
Country
China
ProdList
9976
Advantage
60
LGM Pharma
Tel
1-(800)-881-8210
Fax
615-250-9817
Email
inquiries@lgmpharma.com
Country
United States
ProdList
2123
Advantage
70
Nanjing Chemlin Chemical Co., Ltd
Tel
025-83697070
Fax
+86-25-83453306
Email
info@chemlin.com.cn
Country
China
ProdList
19179
Advantage
64
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
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View Lastest Price from Memantine manufacturers

Wuhan Senwayer Century Chemical Co.,Ltd
Product
Memantine 19982-08-2
Price
US $0.00-0.00/g
Min. Order
1g
Purity
98%
Supply Ability
20kg
Release date
2023-02-10
Dideu Industries Group Limited
Product
Memantine 19982-08-2
Price
US $1.10/g
Min. Order
1g
Purity
99.9%
Supply Ability
100 Tons min
Release date
2021-07-26
Career Henan Chemical Co
Product
Memantine 19982-08-2
Price
US $1.00/kg
Min. Order
1g
Purity
99%
Supply Ability
100KG
Release date
2018-12-21

19982-08-2, MemantineRelated Search:


  • 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-
  • C13736
  • 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
  • Memantine (amantadine)
  • (1r,3R,5S,7r)-3,5-dimethyladamantan-1-amine
  • 19982-08-2
  • GASTERIL
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