Skip to Content
Merck
All Photos(1)

Documents

236608

Sigma-Aldrich

Tri-tert-butyl borate

98%

Synonym(s):

Boron tert-butoxide, Tri-tert-butoxyborane

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
[(CH3)3CO]3B
CAS Number:
Molecular Weight:
230.15
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.389 (lit.)

bp

101 °C/74 mmHg (lit.)

mp

18-19 °C (lit.)

density

0.811 g/mL at 25 °C (lit.)

SMILES string

CC(C)(C)OB(OC(C)(C)C)OC(C)(C)C

InChI

1S/C12H27BO3/c1-10(2,3)14-13(15-11(4,5)6)16-12(7,8)9/h1-9H3

InChI key

ZMCWFMOZBTXGKI-UHFFFAOYSA-N

General description

Tri-tert-butyl borate is an organoborate commonly used to prepare other borate esters. It is also used as a substrate in Rh-catalyzed carbonylation reactions.

Application

Tri-tert-butyl borate can be used as:
  • An additive in the synthesis of chiral α-hydroxy esters by reacting dimethylzinc with α-ketoesters using (−)-2-exo-morpholinoisobornane-10-thiol.
  • A starting material in the synthesis of boronate of (+)-pinane-2,3-diol.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

84.2 °F - closed cup

Flash Point(C)

29 °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

Asymmetric addition of dimethylzinc to α-ketoesters catalyzed by (−)-MITH
Wu H, et al.
The Journal of Organic Chemistry, 73(16), 6445-6447 (2008)
Tri?tert ?butylborate
e-EROS Encyclopedia of Reagents for Organic Synthesis (2012)
Tri?tert ?butylborate
e-EROS Encyclopedia of Reagents for Organic Synthesis. (2012)
Chiral carbanions, part 4: Borylation of (trimethylsilyl) methyl N, N-dialkylcarbamates-Diastereoselectivity and structural studies
Simov BP, et al.
Synthesis, 2004(16), 2704-2710 (2004)

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