L3609

2,4-Lutidine

Name: 2,4-Lutidine
Brand: ALDRICH

99%

Synonym(s):

2,4-Dimethylpyridine

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About This Item

Empirical Formula (Hill Notation):

C₇H₉N

CAS Number:

108-47-4

Molecular Weight:

107.15

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24896348

EC Number:

203-586-8

Beilstein/REAXYS Number:

1506

MDL number:

MFCD00006337

Key Documents

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Product Name

2,4-Lutidine, 99%

InChI

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

InChI key

JYYNAJVZFGKDEQ-UHFFFAOYSA-N

SMILES string

Cc1ccnc(C)c1

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.)

Quality Level

100

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Show Differences

1 of 4

This Item	L3501	L4001	L3900
Sigma-Aldrich L3609 2,4-Lutidine	Sigma-Aldrich L3501 2,3-Lutidine	Sigma-Aldrich L4001 3,4-Lutidine	Sigma-Aldrich L3900 2,6-Lutidine
assay 99%	assay 99%	assay 98%	assay 98%
Quality Level 100	Quality Level 100	Quality Level 100	Quality Level 200
refractive index n20/D 1.499 (lit.)	refractive index n20/D 1.508 (lit.)	refractive index n20/D 1.511 (lit.)	refractive index n20/D 1.497 (lit.)
density 0.927 g/mL at 25 °C (lit.)	density 0.945 g/mL at 25 °C (lit.)	density 0.954 g/mL at 25 °C (lit.)	density 0.92 g/mL at 25 °C ((lit.)), 0.92 g/mL at 25 °C (lit.)
bp 159 °C (lit.)	bp 162-163 °C (lit.)	bp 163-164 °C (lit.)	bp 143-145 °C ((lit.)), 143-145 °C (lit.)
form liquid	form -	form liquid	form liquid

pictograms

GHS02,GHS06

signalword

Danger

hcodes

H226,H301 + H311 + H331,H315,H319,H335

pcodes

P210 - P280 - P301 + P310 - P303 + P361 + P353 - P304 + P340 + P311 - P305 + P351 + P338

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

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

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Chemical standards in ion mobility spectrometry.

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

Factors dictating the nuclearity/aggregation and acetate coordination modes of lutidine-coordinated zinc(II) acetate complexes.

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

Synthesis and anti-inflammatory activity of polyazaheterocyclic derivatives of 6-amino-2,4-lutidine and their precursors.

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

[Plasmids for biodegradation of 2,6-dimethylpyridine, 2,4-dimethylpyridine, and pyridine in strains of Arthrobacter].

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

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