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L3609

2,4-Lutidine

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
Assay:
99%
Form:
liquid
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Quality Level

100

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

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Related Categories

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

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

Regulatory Information

危险化学品

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Certificates of Analysis (COA)

Lot/Batch Number
MKCZ8371
MKCK5213
MKBZ0348V
MKBJ1289V
MKBF2883

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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

Global Trade Item Number

SKUGTIN
L3609-100ML04061833951163
L3609-500ML04061833951187
L3609-5ML04061837669545

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