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Rivastigmine tartrate

CAS No.
129101-54-8
Chemical Name:
Rivastigmine tartrate
Synonyms
CS-118;ENA-713;SDZ-ENA 713;Rivastigmine tartrate;Rivastigimine tartrate;RivastigMine L-Tartrate;RivastigMine Bitartrate;S-Rivastigmine tartrate;rivastigMine ditartrate;Rivastigmine-d6 tartarate
CBNumber:
CB9500851
Molecular Formula:
C18H28N2O8
Molecular Weight:
400.42
MDL Number:
MFCD03700731
MOL File:
129101-54-8.mol
MSDS File:
SDS
Last updated:2023-10-25 17:20:02

Rivastigmine tartrate Properties

Melting point 123-1250C
alpha D20 +4.7° (c = 5 in ethanol)
storage temp. 2-8°C
solubility H2O: soluble15mg/mL, clear
form powder
color white to beige
InChI InChI=1/C14H22N2O2.C4H6O6/c1-6-16(5)14(17)18-13-9-7-8-12(10-13)11(2)15(3)4;5-1(3(7)8)2(6)4(9)10/h7-11H,6H2,1-5H3;1-2,5-6H,(H,7,8)(H,9,10)/t11-;1-,2-/s3
InChIKey GWHQHAUAXRMMOT-AAUFCPPMNA-N
SMILES C1(=CC=CC([C@H](C)N(C)C)=C1)OC(=O)N(C)CC.[C@H](O)(C(=O)O)[C@@H](O)C(=O)O |&1:5,18,23,r|
CAS DataBase Reference 129101-54-8(CAS DataBase Reference)
FDA UNII 9IY2357JPE
NCI Drug Dictionary rivastigmine tartrate

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS06,GHS09
Signal word  Danger
Hazard statements  H300-H411
Precautionary statements  P264-P270-P273-P301+P310-P391-P405
RIDADR  UN 2811 6.1 / PGII
WGK Germany  3
RTECS  FA9550000
HazardClass  6.1
PackingGroup  III
HS Code  29242990
NFPA 704
0
4 0

Rivastigmine tartrate price More Price(52)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML0881 Rivastigmine tartrate ≥98% (HPLC) 129101-54-8 50mg $147 2024-03-01 Buy
Sigma-Aldrich 1604858 Rivastigmine tartrate United States Pharmacopeia (USP) Reference Standard 129101-54-8 200mg $472 2024-03-01 Buy
TCI Chemical R0093 Rivastigmine L-Tartrate >98.0%(HPLC)(T) 129101-54-8 1g $186 2024-03-01 Buy
TCI Chemical R0093 Rivastigmine L-Tartrate >98.0%(HPLC)(T) 129101-54-8 5g $644 2024-03-01 Buy
Cayman Chemical 14270 Rivastigmine (tartrate) ≥95% 129101-54-8 100mg $117 2024-03-01 Buy
Product number Packaging Price Buy
SML0881 50mg $147 Buy
1604858 200mg $472 Buy
R0093 1g $186 Buy
R0093 5g $644 Buy
14270 100mg $117 Buy

Rivastigmine tartrate Chemical Properties,Uses,Production

Pharmacological effects

Rivastigmine tartrate is rivastigmine Alzheimer's disease drugs, rivastigmine is physostigmine derivative by Novartis for the first time successfully developed the trade name Exelon (exelon), a molecule with there carbamate structure, is a kind of amino acid of selective cerebral cholinesterase inhibitor, can also inhibit the acetylcholinesterase and butyrylcholinesterase, cholinergic neurons by delaying the release of acetylcholine degradation and energy promoting cholinergic nerve conduction, can improve cognitive function disorders mediated by cholinergic, thereby improving the cognitive function of Alzheimer's disease patients. Rivastigmine plasma protein binding is weak, easily through the blood-brain barrier, which has a high degree of brain selectivity. It not only selectively acts on the most easily affected cerebral cortex and hippocampus, but also preferentially inhibits the dominant subtype of AChE in the brain, resulting in a reduction in the efficacy of peripheral cholinergic side effects. Rivastigmine in vivo half-life is short and long duration of action. Unlike tacrine, this product in the hippocampus and cortex of G1 enzyme inhibitory effect is stronger. Clinic for the treatment of mild to moderate Alzheimer-type dementia, or Alzheimer's disease can be suspected Alzheimer's disease clinically.

Alzheimerdisease

Alzheimer's disease (Alzheimerdisease, AD) is a kind of onset hidden attack the development of dementia, clinical with memory disorders, aphasia, apraxia, agnosia, executive function and cognitive impairment features. At the same time, that is accompanied by the psychological and behavioral abnormalities and obvious function of social life decline. AD duration course is 3 to 7 years, after the onset of a small number of patients can survive for more than 10 years or longer. In 1906, German neurologist Alzheimer first reported one case of 51-year-old female patient, brain autopsy found that age spots, he added that the disease has been reported neurofibrillary changes. Kraepelin (1913) would be named the disease of Alzheimer's disease. Thought that the disease is only found in pre-elderly, it is also known as Alzheimer's (preseniledementia). Later found brain senile dementia (seniledementia) and even the health of the elderly also have the same AD pathology, only a difference in degree. In the 1970s, the US National Institute of Gerontology Research Institute (NIA), the National neurology, language barriers and Stroke Research Institute (NINCDS) and the National Institute of Mental Health (NIMH) unified on senile dementia and AD mutual understanding of the relationship, in addition to age sooner than thought, both clinical symptoms and pathological brain changes were not significantly different, the Department of the same disease. Although the incidence of pre-elderly has been proposed, said AD2 type, is equivalent to the previous Alzheimer's disease, old age of  AD1 type, the equivalent to senile dementia, but in the new diagnostic classification of literature in general, the onset before the age of 65 said early-onset AD, after 65 years, the onset of said late onset AD; in families predisposed called familial AD (FAD), said that no family predisposed sporadic AD.

Pharmacokinetics

Absorption: Rivastigmine completely absorbed quickly. About 1 hour to reach the peak plasma concentration. Because interacts with the target enzyme, biological drugs increase using more than the increased dose is expected values of about 1.5 times. The absolute bioavailability of taking 3 mg is about 36%. Rivastigmine with food can be allowed to absorb Tmax an extra 90 minutes to reduce the Cmax, AUC increased nearly 30%.
Distribution: the binding capacity of Rivastigmine with plasma protein is weak (approximately 40%). It easily passes the blood-brain barrier, surface volume of distribution is 1.8~2.7L/kg.
Metabolism: Rivastigmine mainly goes through cholinesterase mediated hydrolysis and rapid, extensive metabolism (plasma half-life of about 1 hour). In vitro experiment results show that this metabolite only a weak cholinesterase inhibition (<10%). In vitro and animal experimental results show that the majority of the cytochrome P450 isoenzymes are rarely involved in rivastigmine hydrogen tartrate metabolism. In vivo experiments also confirmed the bitartrate.
Excretion: In urine, it is not found rivastigmine hydrogen tartrate prototype drug. The main metabolites excreted through the kidneys. 14C isotope labeled rivastigmine hydrogen tartrate administered within 24 hours, most rapidly excreted by the kidneys (> 90%) and only <1% of the drug excreted in the faeces. Alzheimer's disease patients have no body weight Rivastigmine or a metabolite accumulation.
Elderly subjects: Despite the elderly Rivastigmine biological utilization degree is higher than that of healthy young volunteers, but after 50 to 92 years in patients with Alzheimer test results showed that the bioavailability does not change with increasing age.
Reference: Yuanyong Gui, Tang Yong editor psychiatric outpatient and emergency manual Nanjing: Jiangsu Science and Technology Publishing House .2006.

Indications

Used to treat the symptoms of mild to moderate Alzheimer's disease dementia symptoms.

Side effects

The most commonly reported adverse drug reactions were gastrointestinal reactions,, including nausea (38%), vomiting (23%), especially in the dosage of the more obvious. In clinical trials,it found that women were more prone to gastrointestinal reactions and weight loss.
The following table lists the adverse reactions of this product, including clinical trials and post-marketing reports of all cumulative.
Adverse reactions    Frequency of occurrence
Cardiac                       abnormalities   
Arrhythmia                  Very rare
Angina                         rare
Vascular                        abnormalities   
hypertension              Very rare
Gastrointestinal          system disorder   
nausea                       Very common
Vomit                           Very common
Loss of appetite           Very common
diarrhea                      Very common
Abdominal pain and indigestion    common
Gastric and duodenal ulcers    rare
Gastrointestinal bleeding            Very rare
Mild pancreatitis                 Very rare
Skin and subcutaneous tissue abnormalities   
Increased sweating              common
rash                                   rare
General                            exception   
Fatigue and weakness    common
Unwell                              common
Accidental fall                  Occasionally
survey   
Weight loss                       common
Above Pictured: The common adverse reactions of Rivastigmine in various body systems table.
The frequency of adverse reactions were follows conversion: very common (>=1/10), common (>=1/100, <1/10), occasionally (>=1/1 000, <1/100), rare (>=1/10000, <1/1 000), very rare (<1/10000), including case reports.
In addition, the following side effects in patients taking Exelon in patients with the occurrence rate of at least a given placebo 2%, increased sweating, general malaise, weight loss, tremor. Female patients with nausea, vomiting, loss of appetite and weight loss are more sensitive. Exelon does not cause changes in any laboratory examinations, including liver function, or electrocardiogram, and there is no need special care.
There is a case of patients taking this product, while the joint use of several other drugs, the emergence of Stevense-Johnson syndrome.
In the initial phase of treatment, the incidence of adverse reactions is higher than the maintenance phase. In case of severe intolerable (such as severe nausea, vomiting, etc.), you should consider taking 3 times a day.

Pregnant and lactating women

Pregnancy: Animal experiments show that rivastigmine has no teratogenic effects. Because the lack of experimental data security using this service when people pregnancy, so pregnant women using this service should be weighed the pros and cons.
Lactation: whether the product is secreted from human milk, which is unclear. However, in animals rivastigmine tartrate can be secreted from the milk. Patients using this service should stop breastfeeding. Accordingly, patients with ongoing breast feeding should not be using this service.

Pediatric

Children are not recommended to take this product.

Elderly patients

Although the elderly’s rivastigmine bitartrate bioavailability is higher than that of young healthy volunteers, but after 50 to 92 years in patients with Alzheimer test results show that rivastigmine tartrate bioavailability does not change with increasing age.

Drug Interactions

(1) Rivastigmine is mainly through hydrolysis cholinesterase metabolism, cytochrome P450 isozymes are rarely involved in its metabolism. Therefore, the product and by other drugs metabolized by these enzymes does not exist pharmacokinetic interactions.
(2) study in healthy volunteers found the product (a single dose of 3mg) with digoxin, warfarin, diazepam or fluoxetine, have no pharmacokinetic interactions. Warfarin induced by prothrombin time extension are not affected by this product. After combination of digoxin and the product found no adverse impact on cardiac conduction.
(3) In clinical studies of patients with Alzheimer's disease (AD), the goods and some commonly used prescription drugs combined, such as antacids, antiemetics, hypoglycemic agents, β-blockers, calcium channel blockers agents, inotropic agents, anti-angina drugs, non-steroidal anti-inflammatory drugs, estrogens, analgesics, tranquilizers, antihistamines, etc., and risk of clinically relevant adverse reaction does not increase
(4) In view of the pharmacokinetic effect of this product, this product should not be used in combination with other cholinergic drugs, it may interfere with the activity of anticholinergic drugs.
(5) There is no experience of this product with anti Parkinson drugs, anti anxiety drugs (except for stability), antipsychotic drugs, antiepileptic drugs, antidepressant drugs.
(6) rivastigmine tartrate as a cholinesterase inhibitor, during anesthesia, it can be used to enhance succinylcholine-type muscle relaxant effect.

Contraindications

It is known for rivastigmine tartrate, other carbamate derivatives or other components of the formulation in patients allergic to this ban. Severe liver failure patients with severe Rivastigmine efficacy and safety have not been studied.

Precautions

1. As inhibitors of acetylcholinesterase, rivastigmine tartrate can improve succinylcholine-type muscle relaxant effect. Therefore, before anesthesia should have the right to stop taking this interim period. The goods and other cholinergic or anti-cholinergic agents in combination, should be particularly cautious (see Drug Interactions).
2. Due to their pharmacological effects, cholinesterase inhibitors on heart rate may produce vagal nervous effects. Like with other cholinergic drugs, when administered to sick sinus syndrome or other heart block in patients using this service, you must be more cautious (see Adverse reactions).
3. cholinergic nerve excitability can cause gastric acid secretion. Although no evidence of corresponding symptoms worsen during the clinical trials, there is a high risk of gastric ulcer patients, such as those with a history of ulcer disease, or accept non-steroidal anti-inflammatory drugs in patients with concomitant therapy should be used with caution.
4. Like other cholinesterase inhibitors, patients with a history of asthma or other obstructive pulmonary disease should be used with caution to rivastigmine bitartrate.

Chemical Properties

White to Off-White Powder

Uses

Nootropic & Alzheimer’s treatment

Uses

Rivastigmine Tartrate, a cholinesterase inhibitor with IC50 of 5.5 μM, ues as a parasympathomimetic or cholinergic agent for the treatment of mild to moderate Alzheimer disease.

Uses

A brain selective acetylcholinesterase inhibitor. Nootropic.

Definition

ChEBI: A tartrate salt obtained by reaction of rivastigmine with one equivalent of (R,R)-tartaric acid. A reversible cholinesterase inhibitor.

General Description

Pharmaceutical secondary standards for application in quality control provide pharma laboratories and manufacturers with a convenient and cost-effective alternative to the preparation of in-house working standards

Biochem/physiol Actions

Rivastigmine is an orally available, brain penetrant, reversible cholinesterase inhibitor that enhances cognitive function in patients with Alzheimer′s and Parkinson′s diseases. Rivastigmine inhibits both butyrylcholinesterase and acetylcholinesterase.

storage

Store at RT

Rivastigmine tartrate Preparation Products And Raw materials

Raw materials

Preparation Products

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View Lastest Price from Rivastigmine tartrate manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Rivastigmine tartrate pictures 2024-03-12 Rivastigmine tartrate
129101-54-8
US $0.00-0.00 / KG 1KG 98% HPLC 1000kg shandong perfect biotechnology co.ltd
Rivastigmine tartrate pictures 2023-10-09 Rivastigmine tartrate
129101-54-8
US $0.00 / kg 1kg 0.99 20tons Hebei Yanxi Chemical Co., Ltd.
Rivastigmine tartrate pictures 2023-08-10 Rivastigmine tartrate
129101-54-8
US $200.00 / kg 1kg 99% 1000tons Henan Bao Enluo International TradeCo.,LTD
Rivastigimine tartrate 3-[(S)-1-(Dimethylamino)ethyl]phenyl N-Ethyl-N-methylcarbamate L-Tartrate N-Ethyl-N-methylcarbamic Acid 3-[(S)-1-(Dimethylamino)ethyl]phenyl Ester L-Tartrate (S)-3-(1-(diMethylaMino)ethyl)phenyl ethyl(Methyl)carbaMate (2R,3R)-2,3-dihydroxysuccinate (S)-EthylMethylcarbaMic Acid 3-[1-(DiMethylaMino)ethyl]phenyl Ester [R-(R*,R*)]-2,3-Dihydroxybutanedioate N-Ethyl-N-MethylcarbaMic Acid 3-[(1S)-1-(DiMethylaMino)ethyl]phenyl Ester (2R,3R)-2,3-Dihydroxybutanedioate RivastigMine Bitartrate RivastigMine L-Tartrate G830 RivastigMine tartrate RivastigMine-d6 tartarate (raceMic) RivastigMine-d6 Hydrogen Tartrate N-Ethyl-N-methyl-carbamic acid 3-[(1S)-1-(dimethylamino)ethyl]phenyl ester tartrate Rivastigmine for system suitability S-Rivastigmine tartrate N-ethyl-N-methyl-carbamic acid 3-[(1S)-1-(dimethylamino)ethyl]phenyl ester, (2R,3R)-2,3-dihydroxybutanedioate (1:1) Rivastigmine tartrate (S)-N-Ethyl-3-[(1-dimethylamino)ethyl]-N-methylphenylcarbamate hydrogen tartrate RIVASTIGMINE TARTRATE SALT Rivastigmine tartrate; SDZ-ENA 713 SDZ-ENA 713 Ethylmethyl-carbamic Acid 3-[(1S)-1-(Dimethylamino)ethyl]phenyl Ester, Bitartrate RIVASTIGIMINETARTRATE(FORR&DONLY) (S)-N-Ethyl-3-[(1-dimethylamino)ethyl]-N-methylphenylcarbamate hydrogen tartrate Rivastigmine tartrate ENA-713 Methylethylcarbamic acid 3-[(S)-1-(dimethylamino)ethyl]phenyl·(2R,3R)-2,3-dihydroxybutanedioic acid Carbamic acid, ethylmethyl-, 3-((1S)-1-(dimethylamino)ethyl)phenyl ester, (2R,3R)-2,3-dihydroxybutanedioate (1:1) Rivastigmine-d6 tartarate Rivastigmine Tartrate (200 mg) rivastigMine ditartrate Carbamic acid, ethylmethyl-, 3-(1-(dimethylamino)ethyl)phenyl ester, (S)-, (R-(R*,R*))-2,3-dihydroxybutanedioate (1:1) (S)-N-Ethyl-3-[(1-dimethylamino)ethyl]-N-methylphenylcarbamate tartrate Rivastigmine tartrate, 98%, acetylcholinesterase and butyrylcholinesterase inhibitor Rivastigmine hydrogen tartrate CRS Rivastigmine L-Tartrate > Carbamic acid, N-ethyl-N-methyl-, 3-[(1S)-1-(dimethylamino)ethyl]phenyl ester, (2R,3R)-2,3-dihydroxybutanedioate (1:1) 3-[(S)-1-(Dimethylamino)ethyl]phenyl N-Ethyl-N-methylcarbamate L-Tartrate N-Ethyl-N-methylcarbamic Acid 3-[(S)-1-(Dimethylamino)ethyl]phenyl Ester L-Tartrate Rivastigmine tartrate USP/EP/BP Rivastigmine intermediate,Rivastigmine tartrate Rivastigmine Tartrate (ENA713 Rivastigmine TartrateQ: What is Rivastigmine Tartrate Q: What is the CAS Number of Rivastigmine Tartrate Q: What is the storage condition of Rivastigmine Tartrate Q: What are the applications of Rivastigmine Tartrate Rivastigmine Tartrate (1604858) CS-118 Rivastigmine Hydrogen Tartrate(Exelon) Carbalatin heavy tartrate Rivastigmine tartrate (lisdexamfetamine tartrate) Rivastigmine L-Tartrate, ≥ 98.0% 129101-54-8 C14H22N2O2C4H6O6 C14H16D6N2O2C4H6O6 Isotopically Labeled Pharmaceutical Reference Standard Intermediates & Fine Chemicals Neurochemicals Pharmaceuticals Rivastigmine Amines Aromatics Chiral Reagents