Skip to Content
Merck
All Photos(2)

Documents

561452

Sigma-Aldrich

Ethyllithium solution

0.5 M in benzene: cyclohexane

Synonym(s):

Ethyllithium

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
CH3CH2Li
CAS Number:
Molecular Weight:
36.00
Beilstein:
3587196
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Quality Level

concentration

0.5 M in benzene: cyclohexane

density

0.862 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

[Li]CC

InChI

1S/C2H5.Li/c1-2;/h1H2,2H3;

InChI key

BLHLJVCOVBYQQS-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Ethyllithium is a general organolithium reagent used in the nucleophilic addition reaction to synthesize a variety of intermediates.

Packaging

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Signal Word

Danger

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Carc. 1A - Eye Irrit. 2 - Flam. Liq. 2 - Muta. 1B - Repr. 2 - Skin Irrit. 2 - STOT RE 1 - STOT SE 3 - Water-react 2

Target Organs

Blood, Respiratory system

Storage Class Code

4.3 - Hazardous materials which set free flammable gases upon contact with water

WGK

WGK 3

Flash Point(F)

-17.0 °F - closed cup

Flash Point(C)

-27.22 °C - closed cup


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

Conversions of osmabenzyne and isoosmabenzene.
Zhao Q, et al.
Chemistry?A European Journal , 18(37), 11597-11603 (2012)
Interaction of alkyllithium compounds with base. Complex formation between ethyllithium and triethylamine in benzene.
Brown T L, et al.
Journal of the American Chemical Society, 86(11), 2135-2141 (1964)
Highly stereoselective epoxidation of O-protected 3-hydroxy-1-nitroalkenes.
Jain A, et al.
Tetrahedron, 65(40), 8362-8366 (2009)

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