102308-48-5

Basic information

• Product Name: DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE
• Synonyms: TIMTEC-BB SBB010376;N,N-DIMETHYL-2-PIPERIDIN-4-YLETHANAMINE;CHEMBRDG-BB 4111084;DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE;N,N-DIMETHYL-N-[2-(4-PIPERIDYL)ETHYL]AMINE;UKRORGSYN-BB BBV-182959;N,N-dimethyl-2-piperidin-4-ylethanamine(SALTDATA: 2HCl);N,N-dimethyl-4-Piperidineethanamine
• CAS NO: 102308-48-5
• Molecular Formula: C₉H₂₀N₂
• Molecular Weight: 156.27
• EINECS: 200-258-5
• Mol File: 102308-48-5.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 201.2°C at 760 mmHg
• Flash Point: 60.5°C
• Appearance: /
• Density: 0.866g/cm³
• Vapor Pressure: 0.311mmHg at 25°C
• Refractive Index: 1.452
• Storage Temp.: Keep in dark place,Inert atmosphere,Room temperature
• CAS DataBase Reference: DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE(CAS DataBase Reference)
• NIST Chemistry Reference: DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE(102308-48-5)
• EPA Substance Registry System: DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE(102308-48-5)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 102308-48-5(Hazardous Substances Data)

Usage

General Description

DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE is a chemical compound that belongs to the class of organic compounds known as amines. DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE is characterized by the presence of two methyl groups attached to a nitrogen atom, in addition to a 2-piperidin-4-yl-ethyl group. Amines, including DIMETHYL-(2-PIPERIDIN-4-YL-ETHYL)-AMINE, are widely used in pharmaceuticals, as they can act as precursors to both bioactive bases and nucleophiles, which enable them to interact with different biological systems and properties. The detailed properties such as melting point, boiling point, density, and solubility of this compound would vary based on its purity, concentration, and other factors. The chemical safety, toxicity or potential health effects, if any, of Dimethyl-(2-piperidin-4-yl-ethyl)-amine are not readily available and thus would need to be evaluated by relevant health organizations.

InChI:InChI=1/C9H20N2/c1-11(2)8-5-9-3-6-10-7-4-9/h9-10H,3-8H2,1-2H3

Upstream product

• 622-26-4 4-(2-Hydroxyethyl)piperidine 
• 98-88-4 benzoyl chloride 
• 100-43-6 4-vinylpyridine 
• 38223-06-2 4-<2-(dimethylamino)ethyl>pyridine 

Downstream Products

• 1192684-39-1 2-[3-(3-chlorophenyl)-7-{4-[2-(dimethylamino)ethyl]-1-piperidinyl}-1-oxopyrrolo[1,2-a]pyrazin-2(1H)-yl]-N-(1-methylethyl)acetamide 
• 63916-14-3 4-[2-(dimethyl-propyl-ammonio)-ethyl]-1-methyl-1-propyl-piperidinium; diiodide 
• 63887-38-7 1-ethyl-4-[2-(ethyl-dimethyl-ammonio)-ethyl]-1-methyl-piperidinium; diiodide 
• 63887-35-4 1,1-dimethyl-4-(2-trimethylammonio-ethyl)-piperidinium; diiodo 

Relevant articles and documents

Benzenesulphonamide derivatives, method for production and use thereof for treatment of pain

The present invention concerns novel benzenesulphonamide compounds, defined by formula I and the description, their method of preparation and their use in therapy.

Synthesis and structure-activity relationship of some 5- [[[(dialkylamino)alkyl]-1-piperidinyl]acetyl]-10,11-dihydro-5H- benzo[b,e][1,4]diazepin-11-ones as M2-selective antimuscarinics

A series of 5-[[[(dialkylamino)alkyl]-1-piperidinyl]acetyl]-10,11-dihydro- 5H-dibenzo[b,e][1,4]-diazepin-11-ones were prepared as potential M2- selective ligands. The compounds were evaluated for their affinity and selectivity for the muscarinic cholinergic receptor. The best M2-selective antimuscarinic agent studied is 5-[[4-[4-(diethylamino)butyl]-1- piperidinyl]acetyl]-10,11-dihydro-5H-dibenzo[b,e][1,4]diazepin-11-one, which is approximately 10 times more potent at M2 receptors than previously known compounds such as 11-[[4-[4-(diethylamino)butyl]-1-piperidinyl]acetyl]-5,11- dihydro-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one (AQ-RA 741).