CAS 100-69-6

2-Vinylpyridine

Description:

2-Vinylpyridine is an organic compound with the molecular formula C₈H₉N and is classified as a vinyl-substituted pyridine. It features a vinyl group (–CH=CH₂) attached to the second position of the pyridine ring, which is a six-membered aromatic ring containing one nitrogen atom. This compound is a colorless to yellow liquid with a characteristic odor and is soluble in organic solvents such as ethanol and ether, but has limited solubility in water. 2-Vinylpyridine is known for its reactivity, particularly in polymerization reactions, where it can act as a monomer to produce various copolymers. It is used in the synthesis of specialty chemicals, agrochemicals, and as an intermediate in the production of pharmaceuticals. Additionally, it exhibits properties such as being a weak base due to the nitrogen atom in the pyridine ring. Safety precautions should be taken when handling this compound, as it can be irritating to the skin and eyes, and proper ventilation is recommended due to its volatile nature.

Formula: C₇H₇N

InChI: InChI=1S/C7H7N/c1-2-7-5-3-4-6-8-7/h2-6H,1H2

InChI key: InChIKey=KGIGUEBEKRSTEW-UHFFFAOYSA-N

SMILES: C(=C)C1=CC=CC=N1

Synonyms:

• 2-Ethenylpyridine
• 2-Pyridylethylene
• 2-Vinilpiridina
• 2-Vinylpiridine
• 2-Vinylpyridin
• 2-Vinylpyridine Monomer
• Nsc 18255
• Pyridine, 2-ethenyl-
• Pyridine, 2-vinyl-
• ethenyl-Pyridine
• α-Vinylpyridine

2-Vinylpyridine (stabilized with TBC)

CAS: 100-69-6

Formula: C₇H₇N

Purity: >97.0%(GC)

Color and Shape: Colorless to Brown clear liquid

Molecular weight: 105.14

Ref: 3B-V0024

2-Vinylpyridine, 97%, stab. with 0.1% 4-tert-butylcatechol

CAS: 100-69-6

2-Vinylpyridine is a pyridine derivative used in the preparation of poly(2-vinylpyridine) via radical polymerization. 2-Vinylpyridine is used to improve effectiveness of protective polymer coatings on metals. It is a reagent for pyridylethylation for new protection method for active hydrogen compoun

Formula: C₇H₇N

Purity: 0.1%

Color and Shape: Liquid, Clear, colorless or pale yellow to brown

Molecular weight: 105.14

Ref: 02-A14056

2-Vinylpyridine (2-Ethenylpyridine)

CAS: 100-69-6

Compounds containing an unfused pyridine ring in the structure, nesoi

Formula: C₇H₇N

Color and Shape: Light Brown Liquid

Molecular weight: 105.05785

Ref: 45-1A07430

2-Vinylpyridine

CAS: 100-69-6

2-Vinylpyridine

Purity: ≥95%

Molecular weight: 105.14g/mol

Ref: 54-OR3144

2-Vinylpyridine

CAS: 100-69-6

Formula: C₇H₇N

Purity: (GC) ≥ 97.0%

Color and Shape: Clear, colourless to pale yellow or pale brown liquid

Molecular weight: 105.14

Ref: 7W-GK2516

Betahistine EP Impurity A (2-Vinylpyridine)

CAS: 100-69-6

Formula: C₇H₇N

Color and Shape: Pale Brown Liquid

Molecular weight: 105.14

Ref: 4Z-B-361

2-Ethenylpyridine (2-Vinylpyridine)

Controlled Product

CAS: 100-69-6

Formula: C₇H₇N

Color and Shape: Red Brown

Molecular weight: 105.14

Ref: 86-MM0587.01

2-Vinylpyridine (stabilised with tert-Butylcatechol)

CAS: 100-69-6

Formula: C₇H₇N

Purity: 95.0%

Color and Shape: Liquid

Molecular weight: 105.14

Ref: 10-F218994

Betahistine EP Impurity A

CAS: 100-69-6

Formula: C₇H₇N

Molecular weight: 105.14

Ref: ST-EA-CP-B11001

2-Vinylpyridine (stabilized with 0.1% 4-tert-butylcatechol)

CAS: 100-69-6

Stability Light Sensitive, Volatile
Applications 2-Vinylpyridine is a pyridine deriviative used in the preparation of poly(2-vinylpyridine) via radical polymerization. 2-Vinylpyridine is used to improve effectiveness of protective polymer coatings on metals. 2-Vinylpyridine is an impurity of Betahistine (B324000).
Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package
References Shibaev, L.A. et al.: Vysokomolek. Soedin. Ser. A Ser. B, 37, 1874 (1995); Zavrazhina, V.I. et al.: Korr. Mat. Zash., 9, 33 (2004);

Formula: C₇H₇N

Color and Shape: Light Yellow To Light Brown

Molecular weight: 105.14

Ref: TR-V487495

2-Vinylpyridine, stabilized with TBC

CAS: 100-69-6

2-Vinylpyridine is a reactive, organic compound that can form hydrogen bonds with other molecules. It has been used in the synthesis of detergent compositions and as a reactant to produce polymers. 2-Vinylpyridine is also used in the treatment of autoimmune diseases, such as hepatitis C. 2-Vinylpyridine has been shown to bind to proteins by forming hydrogen bonds with amino acid residues that have an amine group or a hydroxyl group. The binding of 2-vinyl pyridine to these sites leads to conformational changes and enzyme inhibition. 2-Vinylpyridine can be synthesized from pyridine and hydrochloric acid in a two step process involving condensation followed by cyclization. 2-Vinylpyridine was first synthesized by Kolbe and Woodward in 1883 using x-ray crystallography, which involved exposing crystals of pyridine to x-rays, thereby providing structural

Formula: C₇H₇N

Purity: Min. 95%

Color and Shape: Clear Liquid

Molecular weight: 105.14 g/mol

Ref: 3D-FV45430