CAS 3731-53-1

4-Pyridinemethanamine

Description:

4-Pyridinemethanamine, also known as 4-(Aminomethyl)pyridine, is an organic compound characterized by a pyridine ring substituted with an aminoalkyl group. Its molecular structure features a pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom, and a methanamine group (-CH2NH2) attached to the fourth carbon of the ring. This compound is typically a colorless to pale yellow liquid or solid, depending on its form and purity. It is soluble in water and polar organic solvents, making it versatile for various applications. 4-Pyridinemethanamine is known for its role as a building block in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It can act as a ligand in coordination chemistry and is also utilized in the development of various chemical intermediates. Safety data indicates that it should be handled with care, as it may cause irritation to the skin and eyes. Proper safety protocols should be followed when working with this compound in laboratory settings.

Formula: C₆H₈N₂

InChI: InChI=1/C6H8N2/c7-5-6-1-3-8-4-2-6/h1-4H,5,7H2/p+1

InChI key: InChIKey=TXQWFIVRZNOPCK-UHFFFAOYSA-N

SMILES: C(N)C=1C=CN=CC1

Synonyms:

• (4-Piridilmetil)Amina
• (4-Pyridylmethyl)amin
• (4-Pyridylmethyl)amine
• 1-(4-Pyridyl)methylamine
• 1-(Pyridin-4-yl)methanamine
• 1-Pyridin-4-Ylmethanamine
• 4-(Aminomethyl)-pyridine
• 4-Aminomethylpyridine
• 4-Methylaminopyridine
• 4-Picolinamine
• 4-Picolinylamine
• 4-Pyridinemethanamine
• 4-Pyridinemethaneamine
• 4-Pyridinemethylamine
• 4-Pyridinylmethanamine
• 4-Pyridylmethanamine
• 4-Pyridylmethylamine
• C-(Pyridin-4-yl)methylamine
• N-[(4-Pyridinyl)methyl]amine
• N-methylpyridin-4-amine
• Nsc 59707
• Pyridin-4-Ylmethanaminium
• Pyridin-4-ylmethylamine
• Pyridine, 4- (aminomethyl)-
• a-Amino-g-picoline
• alpha-Amino-gamma-picoline
• p-Picolylamine
• γ-(Aminomethyl)pyridine
• γ-Picolylamine
• γ-Pyridylmethylamine
• 4-Pyridylmethylamine, 95+%
• RARECHEM AL BW 0093
• 4-AMINO METHYLPYRIDINE 98%
• 4-PICOLYLAMIN 98%
• 4-AMINOMETHYL PYRIDINE C-PYRIDIN-4-YL-METHYLAMINE
• OMEGA-AMINO-GAMMA-PICOLINE
• TIMTEC-BB SBB004350
• 4AMPY
• 4-PICOLYLAMINE

4-(Aminomethyl)pyridine, 97+%

CAS: 3731-53-1

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci

Formula: C₆H₈N₂

Purity: 97+%

Color and Shape: Liquid, Clear colorless to yellow to orange

Molecular weight: 108.14

Ref: 02-L06345

4-Pyridinemethaneamine

CAS: 3731-53-1

Formula: C₆H₈N₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 108.1411

Ref: IN-DA003457

4-(Aminomethyl)pyridine

CAS: 3731-53-1

4-(Aminomethyl)pyridine

Formula: C₆H₈N₂

Purity: ≥95%

Color and Shape: colorless to yellow liquid

Molecular weight: 108.14g/mol

Ref: 54-OR23068

4-(Aminomethyl)pyridine (4-Picolylamine)

CAS: 3731-53-1

Formula: C₆H₈N₂

Molecular weight: 108.14

Ref: 7W-GK4428

4-Picolylamine

CAS: 3731-53-1

Formula: C₆H₈N₂

Purity: >98.0%(GC)(T)

Color and Shape: Colorless to Red to Green clear liquid

Molecular weight: 108.14

Ref: 3B-P0779

Amino Impurity of Isoniazid

CAS: 3731-53-1

Formula: C₆H₈N₂

Molecular weight: 108.14

Ref: ST-EA-CP-I10004

1-Pyridin-4-ylmethanamine

CAS: 3731-53-1

Formula: C₆H₈N₂

Purity: 97%

Color and Shape: Liquid, Clear

Molecular weight: 108.144

Ref: 10-F065475

4-(Aminomethyl)pyridine

Controlled Product

CAS: 3731-53-1

Applications 4-(Aminomethyl)pyridine is a compound that has derivatives that act as reversible inhibitors of various copper amine oxidases (CAOs).
References Bertini, V, et al.: J. Med. Chem., 48, 664 (2005);

Formula: C₆H₈N₂

Color and Shape: Neat

Molecular weight: 108.14

Ref: TR-A618090

Pyridin-4-ylmethanamine

CAS: 3731-53-1

Pyridin-4-ylmethanamine is a chemical compound that contains a pyridine ring and an amine (-NH2) group. It is usually used as a building block for the synthesis of other compounds. Pyridin-4-ylmethanamine can be synthesized from picolinic acid, which is obtained through a reaction with sodium hydrochloride in an alkaline solution. This reaction proceeds via two steps: first, the formation of a pyridinecarboxylic acid ester and then the addition of ammonia to form pyridin-4-ylmethanamine. The transfer reactions that occur during this process are highly dependent on temperature and pH. The frequency shift effect can be observed when pyridin-4-ylmethanamine interacts with amines, which changes its absorption spectrum.

Formula: C₆H₈N₂

Purity: Min. 95%

Color and Shape: Colorless Clear Liquid

Molecular weight: 108.14 g/mol

Ref: 3D-FP142396