42088-91-5

Basic information

• Product Name: 1-PYRIDIN-2-YL-ETHYLAMINE
• Synonyms: 1-PYRIDIN-2-YL-ETHYLAMINE;1-(2-Pyridyl)ethylamine;2-(1-Aminoethyl)pyridine;1-Pyridin-2-yl-ethylamine oxalate;1-(2-Pyridyl)ethaneamine;1-(2-Pyridinyl)ethylamine;1-Pyridine-2-yl-ethylamine;2-Pyridinemethanamine, .alpha.-methyl-
• CAS NO: 42088-91-5
• Molecular Formula: C₇H₁₀N₂
• Molecular Weight: 122.17
• Product Categories: pharmacetical
• Mol File: 42088-91-5.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 194.5 °C at 760 mmHg
• Flash Point: 78℃
• Appearance: /
• Density: 1.002 g/mL at 25 °C
• Vapor Pressure: 0.44mmHg at 25°C
• Refractive Index: n20/D1.528
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• PKA: 9.05±0.39(Predicted)
• Sensitive: Air Sensitive
• CAS DataBase Reference: 1-PYRIDIN-2-YL-ETHYLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-PYRIDIN-2-YL-ETHYLAMINE(42088-91-5)
• EPA Substance Registry System: 1-PYRIDIN-2-YL-ETHYLAMINE(42088-91-5)

Safety Data

• Hazard Codes: T,Xi
• Statements: 25-37/38-41
• Safety Statements: 26-36/37/39-45
• RIDADR: UN2735
• WGK Germany: nwg
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 42088-91-5(Hazardous Substances Data)

Usage

General Description

1-Pyridin-2-yl-ethylamine, also known as beta-phenylethylamine, is a chemical compound with the molecular formula C8H11N. It is a derivative of phenethylamine and is commonly used as a precursor in the synthesis of various pharmaceuticals and biologically active compounds. 1-Pyridin-2-yl-ethylamine has been studied for its potential therapeutic effects on the central nervous system, as it has been shown to modulate neurotransmitter levels in the brain. It is also known for its psychoactive properties and is classified as a stimulant drug. Additionally, it is used in the production of agricultural chemicals, dyes, and pigments. Overall, 1-Pyridin-2-yl-ethylamine is a versatile chemical with a range of applications in both the pharmaceutical and industrial fields.

InChI:InChI=1/C7H10N2/c1-6(8)7-4-2-3-5-9-7/h2-6H,8H2,1H3/p+1/t6-/m1/s1

Upstream product

• 1122-62-9 2-acetylpyridine 
• 87227-77-8 bishydrochloride salt of cis-1,4-diamino-but-2-ene 
• 110-60-1 1,4-diaminobutane 

Downstream Products

• 1013624-57-1 C₁₄H₁₄N₂O₂ 
• 115519-41-0 5-[4-(1,1-dimethylethyl)phenoxy]-2,2-dimethyl-N-[1-(2-pyridinyl)ethyl]pentanamide 
• 115519-43-2 5-(4-hexylphenoxy)-2,2-dimethyl-N-[1-(2-pyridinyl)ethyl]pentanamide 
• 115519-39-6 2,2-dimethyl-5-(4-methylphenoxy)-N-[1-(2-pyridinyl)ethyl]pentanamide 
• 408368-54-7 N-{4-[2-(2-aminoanilino)-2-oxoethyl]phenyl}-4'-(trifluoromethyl)-1,1'-biphenyl-2-carboxamide 
• 515160-13-1 (C₄H₂NC(C₆H₅))3C₄H₂NC(C₆H₄NHC(O)C₅H₃NC(O)NHCH(CH₃)C₅H₄N)Zn 
• 1300737-69-2 7-(3,5-dimethyl-4-isoxazolyl)-6-(methyloxy)-4-{[(1R)-1-(2-pyridinyl)ethyl]amino}-3-quinolinecarboxamide 

Relevant articles and documents

Biocatalytic transamination with near-stoichiometric inexpensive amine donors mediated by bifunctional mono- and di-amine transaminases

The discovery and characterisation of enzymes with both monoamine and diamine transaminase activity is reported, allowing conversion of a wide range of target ketone substrates with just a small excess of amine donor. The diamine co-substrates (putrescine, cadaverine or spermidine) are bio-derived and the enzyme system results in very little waste, making it a greener strategy for the production of valuable amine fine chemicals and pharmaceuticals.

Voltammetric, potentiometric and spectrophotometric studies of some hydrazones and their metal complexes in ethanolic-aqueous buffered solutions

The electrochemical behavior of some hydrazones derived from 6-chloro-2-hydrazinopyridine in the Britton-Robinson universal buffer of pH 2-11 containing 35% ethanol was investigated at the mercury electrode using dc-polarography, controlled-potential coulometry, and cyclic voltammetry techniques. The examined hydrazones were reduced in solutions of pH 2 single bond. The mechanistic pathway of the electrode reaction of the studied compounds was elucidated and discussed. The pK a values of the examined hydrazones and the stoichiometry of their complexes in solution with some transition metal ions were determined spectrophotometrically. The dissociation constants and the thermodynamic parameters of the investigated hydrazones, and the stability constants of their metal complexes in solution were determined potentiometrically. Springer-Verlag 2006.