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Merck

P42053

Sigma-Aldrich

3-Methylpyridin

99%

Synonym(e):

3-Picolin, 3-Methyl-pyridin

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About This Item

Empirische Formel (Hill-System):
C6H7N
CAS-Nummer:
Molekulargewicht:
93.13
Beilstein:
1366
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

3.2 (vs air)

Dampfdruck

4.4 mmHg ( 20 °C)

Assay

99%

Selbstzündungstemp.

~1000 °F

Brechungsindex

n20/D 1.504 (lit.)

bp

144 °C (lit.)

mp (Schmelzpunkt)

−19 °C (lit.)

Dichte

0.957 g/mL at 25 °C (lit.)

SMILES String

Cc1cccnc1

InChI

1S/C6H7N/c1-6-3-2-4-7-5-6/h2-5H,1H3

InChIKey

ITQTTZVARXURQS-UHFFFAOYSA-N

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Verwandte Kategorien

Allgemeine Beschreibung

3-methylpyridine acts as a nucleophile in cross-coupling reactions, enabling the formation of aryl-pyridine bonds and facilitating the synthesis of pyridine derivatives. It is used as a precursor in the synthesis of niacin (vitamin B3)

Anwendung

  • [The effect of new quaternary ammonium compounds on bacteria and fungi. 5: Synthesis of 3-methyl-n-alkylthiomethylpyridinium-, 1-methyl-3-n-alkylthiomethylimidazolium- and 1-ethyl-3-n-alkylthioimidazolinium chloride].: This research focuses on the synthesis of various quaternary ammonium compounds, including derivatives of 3-Methylpyridine, and evaluates their antimicrobial properties against bacteria and fungi (Pernak et al., 1983).
  • Stereochemistry of cobalt porphyrins. I. The structure and characterization of 2,3,7,8,12,13,17,18-octaethylporphinatobis(3-methylpyridine)cobalt(II).: This paper discusses the synthesis, structural analysis, and stereochemical properties of cobalt porphyrins complexed with 3-Methylpyridine, highlighting their potential applications in catalysis and materials science (Little and Ibers, 1974).

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1B

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 1

Flammpunkt (°F)

98.6 °F - closed cup

Flammpunkt (°C)

37 °C - closed cup

Persönliche Schutzausrüstung

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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A New Synthesis of 3-Ethylpyridine
Herzenberg et al.
Industrial & Engineering Chemistry Research, 6, 195-197 (1967)
3-Methylpyridine: Synthesis and Applications
Yin et al.
Chemistry - An Asian Journal, 202400467-202400467 (2024)
Hidemi Arai et al.
Physical chemistry chemical physics : PCCP, 14(5), 1576-1580 (2011-12-23)
O 1s X-ray emission and X-ray absorption spectroscopy is applied to probe hydrogen bonding of water (D(2)O) in 3-methylpyridine. Owing to element selectivity of X-ray spectroscopies the electronic structure of water in the binary mixture was observed selectively. Based on
H Lee et al.
Mutagenesis, 10(3), 179-183 (1995-05-01)
The three IQ (2-amino-3-methylimidazo[4,5-f]quinoline) compounds IQ, MeIQx (2-amino-3,4-dimethyl[4,5-f]quinoxaline) and MeIQ (2-amino-3,4-dimethylimidazo[4,5-f]quinoline) have been found in boiled pork juice. To determine which Maillard reaction products are important in the formation of IQ-type mutagens in boiled pork juice, six Maillard reaction products
Necmi Dege et al.
Acta crystallographica. Section C, Crystal structure communications, 62(Pt 9), m401-m403 (2006-09-07)
In the crystal structure of the title compound {systematic name: bis[6-methyl-1,2,3-oxathiazin-4(3H)-one 2,2-dioxide(1-)-kappa2N3,O4]bis(3-methylpyridine)copper(II)}, [Cu(C4H4NO4S)2(C6H7N)2], the CuII centre resides on a centre of symmetry and has an octahedral geometry that is distorted both by the presence of four-membered chelate rings and because

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