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400386

Sigma-Aldrich

Alane N,N-dimethylethylamine complex solution

0.5 M in toluene

Synonym(s):

(Ethyldimethylamine)trihydroaluminum, Dimethylethylamine alane

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About This Item

Linear Formula:
C2H5N(CH3)2 · AlH3
CAS Number:
124330-23-0
Molecular Weight:
103.14
MDL number:
MFCD00191709
UNSPSC Code:
12352116
PubChem Substance ID:
24864913
NACRES:
NA.22

form

liquid

Quality Level

100

reaction suitability

reagent type: reductant

concentration

0.5 M in toluene

density

0.837 g/mL at 25 °C

functional group

amine

SMILES string

[AlH3].CCN(C)C

InChI

1S/C4H11N.Al.3H/c1-4-5(2)3;;;;/h4H2,1-3H3;;;;

InChI key

CXNFERZVFRNSPE-UHFFFAOYSA-N

Related Categories

Application

Alane N,N-dimethylethylamine complex solution can be used as a selective reducing agent for the reduction of brominated γ-lactams to synthesize dihydroflustramine C and flustramine E alkaloids.
Reactant for:
  • Preparation of aluminum nanoparticles
  • Fluorination reactions
  • Aluminum metal-organic chemical vapor deposition for the growth of aluminum films
  • Ligand-exchange reactions
  • Hydroalumination of nitriles and isonitriles

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system

Storage Class

4.2 - Pyrophoric and self-heating hazardous materials

wgk_germany

WGK 3

flash_point_f

-4.0 °F

flash_point_c

-20 °C

ppe

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

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Certificates of Analysis (COA)

Lot/Batch Number
SHBN1279
SHBL2185
SHBJ9637
SHBH1160V
SHBF3985V

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Hossein Robatjazi et al.
Science advances, 5(2), eaav5340-eaav5340 (2019-02-21)
Metal-organic frameworks (MOFs) and metal nanoparticles are two classes of materials that have received considerable recent attention, each for controlling chemical reactivities, albeit in very different ways. Here, we report the growth of MOF shell layers surrounding aluminum nanocrystals (Al
First total syntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Flustra foliacea.
Morales-Rios MS, et al.
Tetrahedron, 58(8), 1479-1484 (2002)

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