Skip to Content
Merck
All Photos(2)

Key Documents

212806

Sigma-Aldrich

Diethylaluminum chloride solution

1.0 M in hexanes

Synonym(s):

Chlorodiethylaluminum, Dichlorotetraethyldialuminium, Diethylaluminum monochloride

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(C2H5)2AlCl
CAS Number:
Molecular Weight:
120.56
Beilstein:
4123259
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

form

liquid

Quality Level

concentration

1.0 M in hexanes

density

0.711 g/mL at 25 °C

SMILES string

CC[Al](Cl)CC

InChI

1S/2C2H5.Al.ClH/c2*1-2;;/h2*1H2,2H3;;1H/q;;+1;/p-1

InChI key

YNLAOSYQHBDIKW-UHFFFAOYSA-M

Looking for similar products? Visit Product Comparison Guide

Application

Diethylaluminum chloride solution can be used:
  • As a Lewis acid for the synthesis of Lewis acid-base bifunctional asymmetric catalysts for cyanosilylation of aldehydes and in Strecker reaction.
  • For the synthesis of precursors for lanthanide/aluminum catalysts for diene polymerization.
  • As a co-initiator in the cationic polymerization of isobutylene.

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 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Skin Corr. 1B - STOT SE 3 - Water-react 1

Target Organs

Central nervous system

Storage Class Code

4.2 - Pyrophoric and self-heating hazardous materials

WGK

WGK 3

Flash Point(F)

-7.6 °F

Flash Point(C)

-22 °C

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Lanthanide carboxylate precursors for diene polymerization catalysis: Syntheses, structures, and reactivity with Et2AlCl.
Evans WJ, et al.
Organometallics, 20(26), 5751-5758 (2001)
Synthesis of new graft copolymers by combining the DPE technique and cationic polymerization.
Wieland PC, et al.
Macromolecular Rapid Communications, 23(14), 809-813 (2002)
A Catalytic asymmetric Strecker-Type Reaction Promoted by Lewis Acid-Lewis Base Bifunctional Catalvst.
Takamura M, et al.
Chemical & Pharmaceutical Bulletin, 48(10), 1586-1592 (2000)
Highly enantioselective cyanosilylation of aldehydes catalyzed by a Lewis acid-Lewis base bifunctional catalyst.
Hamashima Y, et al
Tetrahedron, 57(5), 805-814 (2001)

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