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62760

Sigma-Aldrich

2,6-Lutidine

purum, ≥96.0% (GC)

Synonym(s):

2,6-Dimethylpyridine

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About This Item

Empirical Formula (Hill Notation):
C7H9N
CAS Number:
Molecular Weight:
107.15
Beilstein:
105690
EC Number:
MDL number:
UNSPSC Code:
12352000

grade

purum

Assay

≥96.0% (GC)

refractive index

n20/D 1.497 (lit.)
n20/D 1.498

bp

143-145 °C (lit.)

mp

−6 °C (lit.)

density

0.92 g/mL at 25 °C (lit.)

SMILES string

Cc1cccc(C)n1

InChI

1S/C7H9N/c1-6-4-3-5-7(2)8-6/h3-5H,1-2H3

InChI key

OISVCGZHLKNMSJ-UHFFFAOYSA-N

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Pictograms

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Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

91.4 °F

Flash Point(C)

33 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Wensheng Yu et al.
Organic letters, 6(19), 3217-3219 (2004-09-10)
[reaction: see text] Oxidative cleavage of olefins by OsO(4)-NaIO(4) sometimes suffers from low yields due to the formation of side products. It is found that the addition of 2,6-lutidine can suppress the side reactions and dramatically improve the yield of
Qingnan Liu et al.
The journal of physical chemistry. A, 113(16), 4387-4396 (2009-03-24)
Collision rates and energy transfer distributions are reported for HOD with highly vibrationally excited 2-methylpyridine (2-picoline, E = 38 310 cm(-1)) and 2,6-dimethylpyridine (2,6-lutidine, E = 38 700 cm(-1)). High resolution transient IR absorption is used measured to complete product
Cyrille Costentin et al.
Journal of the American Chemical Society, 132(29), 10142-10147 (2010-07-06)
The effect of base pairing by cytosine on the electrochemical oxidation of guanine is examined by means of cyclic voltammetry on carefully purified reactants in a solvent, CHCl(3), which strongly favors the formation of an H-bonded pair. The thermodynamics and
Jun Gao et al.
Journal of hazardous materials, 130(1-2), 141-147 (2005-10-26)
The homogeneous catalytic N-oxidation of two picolines and two lutidines by hydrogen peroxide has been studied calorimetrically using a heat flow and power compensation SIMULAR reaction calorimeter. The objective of this work was to extend a previously developed kinetic model
Elena Arceo et al.
Nature chemistry, 5(9), 750-756 (2013-08-24)
Asymmetric catalytic variants of sunlight-driven photochemical processes hold extraordinary potential for the sustainable preparation of chiral molecules. However, the involvement of short-lived electronically excited states inherent to any photochemical reaction makes it challenging for a chiral catalyst to dictate the

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