Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

197335

Sigma-Aldrich

Triisopropyl borate

≥98%

Synonym(s):

Boric acid triisopropyl ester, Boron isopropoxide, Triisopropoxyborane

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
[(CH3)2CHO]3B
CAS Number:
5419-55-6
Molecular Weight:
188.07
Beilstein:
1701469
EC Number:
226-529-9
MDL number:
MFCD00008872
UNSPSC Code:
12352103
PubChem Substance ID:
24851823
NACRES:
NA.22

vapor pressure

76 mmHg ( 75 °C)

Quality Level

200

Assay

≥98%

form

liquid

impurities

1% isopropanol

refractive index

n20/D 1.376 (lit.)

bp

139-141 °C (lit.)

density

0.815 g/mL at 25 °C (lit.)

SMILES string

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

InChI

1S/C9H21BO3/c1-7(2)11-10(12-8(3)4)13-9(5)6/h7-9H,1-6H3

InChI key

NHDIQVFFNDKAQU-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Trialkyl borate with good thermal properties.

Application

Reagent used to ortho-borylate 1-substituted naphthalenes for Pd-catalyzed coupling with aryl halides.

Flash Point(F)

62.6 °F - closed cup

Flash Point(C)

17 °C - closed cup

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
SHBP4362
SHBN4807
SHBL4792
SHBB8729V
SHBB8728V

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Synthesis, 3478-3478 (2006)
Tetrahedron, 60, 4887-4893 (2004)
Yersica Rios Yepes et al.
Dalton transactions (Cambridge, England : 2003), 49(4), 1124-1134 (2020-01-03)
A set of alkyl aluminum complexes supported by non-symmetric ferrocenyl amidine ligands were used as catalysts for the preparation of cyclic carbonates from epoxides and carbon dioxide using Bu4NI as a co-catalyst. A modified method for the synthesis of aminoferrocene
Yongtai Zheng et al.
Nature communications, 8(1), 100-100 (2017-07-26)
Photochromic molecules have shown much promise as molecular components of stimuli-responsive materials, but despite recent achievements in various photoresponsive materials, quantitative conversion in photochemical reactions in solids is hampered by the lack of intrinsic structural flexibility available to release stress

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