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P42053

Sigma-Aldrich

3-Methylpyridine

99%

Synonym(s):

3-Picoline, 3-Methylpyridine

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About This Item

Empirical Formula (Hill Notation):
C6H7N
CAS Number:
108-99-6
Molecular Weight:
93.13
Beilstein:
1366
EC Number:
203-636-9
MDL number:
MFCD00006402
UNSPSC Code:
12352100
PubChem Substance ID:
24898513
NACRES:
NA.22

vapor density

3.2 (vs air)

vapor pressure

4.4 mmHg ( 20 °C)

Assay

99%

autoignition temp.

~1000 °F

refractive index

n20/D 1.504 (lit.)

bp

144 °C (lit.)

mp

−19 °C (lit.)

density

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

InChI key

ITQTTZVARXURQS-UHFFFAOYSA-N

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General description

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)

Application

  • [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).

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

98.6 °F - closed cup

Flash Point(C)

37 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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2-Amino-3-methylpyridine 95%

Sigma-Aldrich

A75633

2-Amino-3-methylpyridine

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
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
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
Zoran P Visak et al.
The journal of physical chemistry. B, 110(3), 1377-1387 (2006-02-14)
In a previous work (J. Phys. Chem. B 2003, 107, 9837), we reported liquid-liquid-phase splitting at negative pressures in mixtures of H2O + D2O + 3-methylpyridine (3-MP) at the limit of pure H2O as the solvent, thus extending for the
Comparative chronic toxicity of pyridine, alpha-picoline, and beta-picoline to Lemna minor L. and Chlorella vulgaris B.
B B Singh et al.
Bulletin of environmental contamination and toxicology, 75(3), 482-489 (2006-01-03)
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