Skip to Content
Merck
All Photos(2)

Documents

241814

Sigma-Aldrich

Lithium tri-tert-butoxyaluminum hydride solution

1.0 M in THF

Synonym(s):

LTTBA, Lithium hydrotri-tert-butoxyaluminate, Tri-tert-butoxyaluminumlithium hydride

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
LiAlH[OC(CH3)3]3
CAS Number:
17476-04-9
Molecular Weight:
254.27
Beilstein:
5796791
MDL number:
MFCD00011532
UNSPSC Code:
12352000
PubChem Substance ID:
24854332
NACRES:
NA.22

form

liquid

reaction suitability

reagent type: reductant

concentration

1.0 M in THF

density

0.904 g/mL at 25 °C

SMILES string

[Li+].CC(C)(C)O[AlH-](OC(C)(C)C)OC(C)(C)C

InChI

1S/3C4H9O.Al.Li.H/c3*1-4(2,3)5;;;/h3*1-3H3;;;/q3*-1;+2;+1;

InChI key

BYBIDFZFKATBFH-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Lithium tri-tert-butoxyaluminum hydride is a mild reducing agent mainly used for the selective reduction of ketones.

Application

  • Reducing agent

Signal Word

Danger

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B - STOT SE 3 - Water-react 1

Target Organs

Respiratory system

Supplementary Hazards

EUH014,EUH019

Storage Class Code

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

WGK

WGK 1

Flash Point(F)

1.4 °F - closed cup

Flash Point(C)

-17 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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

Customers Also Viewed

Slide 1 of 1

1 of 1

Lithium tert-butoxide 97%

Sigma-Aldrich

400173

Lithium tert-butoxide

The use of 4, 4-disubstituted nopinones for natural-product synthesis. Synthesis of elemanoid sesquiterpenes.
Kato M, et al.
The Journal of Organic Chemistry, 56(25), 7071-7076 (1991)
Synthesis of an Anti???Amino Epoxide by One?Carbon Homologation of an ??Amino Ester:(2S, 3S)?1, 2?Epoxy?3?(Boc?Amino)?4?Phenylbutane.
Wang D & Nugent WA
Organic Syntheses, 58-67 (2007)
Stereoselectivity of lithium tri-tert-butoxyaluminum hydride.
Ashby EC, et al.
The Journal of Organic Chemistry, 36(1), 197-199 (1971)
Synthesis of an enantiomerically pure intermediate containing the CD substructure of taxol.
Isaacs RC, et al.
The Journal of Organic Chemistry, 58(15), 3938-3941 (1993)
M Gobbini et al.
Bioorganic & medicinal chemistry, 6(10), 1889-1894 (1998-12-05)
The four stereoisomers of the 2-hydroxy derivatives of digitoxigenin and 3-epidigitoxigenin have been synthesized, their structures established by NMR, and their binding affinity for the digitalis receptor on Na+, K(+)-ATPase evaluated. These derivatives showed lower affinities than the parent compounds.

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