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Merck
CN

252662

Triethylaluminum solution

1.0 M in hexanes

Synonym(s):

Aluminumtriethanide

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About This Item

Linear Formula:
Al(C2H5)3
CAS Number:
97-93-8
Molecular Weight:
114.16
UNSPSC Code:
12352103
NACRES:
NA.22
PubChem Substance ID:
24855229
MDL number:
MFCD00009015
Beilstein/REAXYS Number:
3587229

Key Documents

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InChI

1S/3C2H5.Al/c3*1-2;/h3*1H2,2H3;

SMILES string

CC[Al](CC)CC

InChI key

VOITXYVAKOUIBA-UHFFFAOYSA-N

form

liquid

concentration

1.0 M in hexanes

density

0.692 g/mL at 25 °C

Quality Level

100

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Application

Triethylaluminum solution can be used:
  • As a reagent in Alumino-Mannich reaction, where it reacts with iminium ion substrates for which the corresponding Petasis borono-Mannich reaction is unsuccessful.
  • In the synthesis of macrocyclic binuclear aluminum complexes with efficient activities toward ring-opening polymerization of ε-caprolactone.
  • To promote Claisen rearrangement of allyl vinyl ether derivatives along with the transfer of ethyl group to aldehydic carbon.
  • As a reagent for copper-catalyzed asymmetric conjugate addition of alkenyl- and alkylalanes to α,β-unsaturated lactams.
  • As a precursor to synthesize diethylaluminium cyanide, which is used as hydrocyanating reagent.

signalword

Danger

target_organs

Respiratory system

supp_hazards

EUH014

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk

WGK 3

flash_point_f

-0.4 °F - closed cup

flash_point_c

-18 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Hazard Classifications

Aquatic Chronic 2 - Asp. Tox. 1 - Eye Dam. 1 - Flam. Liq. 2 - Pyr. Liq. 1 - Repr. 2 - Self-heat. 2 - Skin Corr. 1A - STOT SE 3 - Water-react. 1

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
SHBT1155
SHBT0964
SHBT0568
SHBR2066
SHBQ7133

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Binuclear aluminum complexes with amine?imine type ligands derived from 1, 3-benzenedialdehyde: synthesis, structures and their catalytic properties in ring-opening polymerization.
Wu C, et al.
Journal of Coordination Chemistry, 69(6), 1066-1075 (2016)
Hydrocyanation. IV. New hydrocyanation methods using hydrogen cyanide and an alkylaluminum, and an alkylaluminum cyanide.
Nagata W, et al.
Journal of the American Chemical Society, 94(13), 4635-4643 (1972)
Copper-Catalyzed Asymmetric Conjugate Addition of Alkenyl-and Alkylalanes to ?, ?-Unsaturated Lactams.
Cottet P, et al.
Organic Letters, 15(4), 828-831 (2013)
Aliphatic Claisen rearrangement promoted by organoaluminium reagents.
Takai K, et al.
Bulletin of the Chemical Society of Japan, 57(2), 446-451 (1984)
An Alumino?Mannich Reaction of Organoaluminum Reagents, Silylated Amines, and Aldehydes.
Tarasewicz A, et al.
Chemistry?A European Journal , 24(23), 6071-6074 (2018)

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