Skip to Content
MilliporeSigma
All Photos(3)

Documents

L3609

Sigma-Aldrich

2,4-Lutidine

99%

Synonym(s):

2,4-Dimethylpyridine

Sign Into View Organizational & Contract Pricing
All Photos(3)

About This Item

Empirical Formula (Hill Notation):
C7H9N
CAS Number:
108-47-4
Molecular Weight:
107.15
Beilstein/REAXYS Number:
1506
EC Number:
203-586-8
MDL number:
MFCD00006337
UNSPSC Code:
12352100
PubChem Substance ID:
24896348
NACRES:
NA.22

assay

99%

form

liquid

refractive index

n20/D 1.499 (lit.)

bp

159 °C (lit.)

mp

−60 °C (lit.)

density

0.927 g/mL at 25 °C (lit.)

SMILES string

Cc1ccnc(C)c1

InChI

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

InChI key

JYYNAJVZFGKDEQ-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

pictograms

FlameSkull and crossbones
GHS02,GHS06

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

116.6 °F - closed cup

flash_point_c

47 °C - closed cup

ppe

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Umesh Kumar et al.
Inorganic chemistry, 49(1), 62-72 (2009-12-05)
The reactions of Zn(OAc)(2).2H(2)O with various positional isomers of lutidine were explored with a view to understand the factors responsible for the nuclearity/aggregation and acetate coordination modes of the products. The reactions of Zn(OAc)(2).2H(2)O with 3,5-lutidine, 2,3-lutidine, 2,4-lutidine, and 3,4-lutidine
J M Robert et al.
Arzneimittel-Forschung, 47(5), 635-642 (1997-05-01)
Derivatives of N-(4,6-pyridin-2-yl)arylcarboxamides resulting from the integration of the amidic function into 4H-1,2,4-triazole, triazol-3(2H)-one and 1H-tetrazole rings were evaluated as potential anti-inflammatory compounds. The level of activity decreased as compared to carboxamides, nevertheless their precursors and notably the corresponding amidrazones
Roberto Fernández-Maestre et al.
The Analyst, 135(6), 1433-1442 (2010-04-07)
In ion mobility spectrometry (IMS), reduced mobility values (K(0)) are used as a qualitative measure of gas phase ions, and are reported in the literature as absolute values. Unfortunately, these values do not always match with those collected in the
S R Agapova et al.
Molekuliarnaia genetika, mikrobiologiia i virusologiia, (5-6)(5-6), 10-13 (1992-05-01)
Arthrobacter crysallopoietes strain KM-4 degrading 2,6-dimethylpyridine and strain KM-4a degrading both 2,6-dimethylpyridine and pyridine, Arthrobacter sp. KM-4b degrading 2,4-dimethylpyridine were isolated from soil. Arthrobacter crystallopoietes KM-4 and Arthrobacter sp. KM-4b contain 100 Md plasmids pBS320 and pBS323. Arthrobacter crystallopietes KM-4a

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service