L3609
2,4-Lutidine
99%
Synonym(s):
2,4-Dimethylpyridine
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Empirical Formula (Hill Notation):
C7H9N
CAS Number:
Molecular Weight:
107.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
203-586-8
Beilstein/REAXYS Number:
1506
MDL number:
Assay:
99%
Form:
liquid
Quality Level
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
Still not finding the right product?
Explore all of our products under 2,4-Lutidine
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
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| L3609-100ML | 04061833951163 |
| L3609-500ML | 04061833951187 |
| L3609-5ML | 04061837669545 |