Skip to Content
MilliporeSigma
All Photos(2)

Documents

650412

Sigma-Aldrich

Borane tetrahydrofuran complex solution

1.0 M in THF, contains 0.005 M N-Isopropyl-N-methyl-tert-butylamine as stabilizer

Synonym(s):

Borane-THF (1:1), Borane-THF complex (1:1)

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BH3OC4H8
CAS Number:
Molecular Weight:
85.94
Beilstein/REAXYS Number:
3668402
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:

contains

0.005 M N-Isopropyl-N-methyl-tert-butylamine as stabilizer

Quality Level

reaction suitability

reagent type: reductant

concentration

1.0 M in THF

density

0.880 g/mL at 25 °C

storage temp.

2-8°C

SMILES string

B.C1CCOC1

InChI

1S/C4H8O.BH3/c1-2-4-5-3-1;/h1-4H2;1H3

InChI key

RMCYTHFAWCWRFA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

This useful reagent for reductions and other transformations is now safer in transport utilizing this new stabilizer
Used to reduce nylon surface amide groups to secondary amines.

Packaging

The 25 mL Sure/Seal bottle is recommended as a single-use bottle. Repeated punctures will likely result in decreased performance of product.

Legal Information

Sure/Seal is a trademark of Sigma-Aldrich Co. LLC

Related product

Product No.
Description
Pricing

signalword

Danger

Hazard Classifications

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

target_organs

Central nervous system, Respiratory system

supp_hazards

wgk_germany

WGK 3

flash_point_f

closed cup

flash_point_c

closed cup

ppe

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


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

Hisanori Ueki et al.
The Journal of organic chemistry, 71(9), 3506-3511 (2006-04-22)
This paper presents a highly stereoselective synthesis of trifluoro- or difluoromethylated olefins via an S(N)2' type fluorination or reductions of gem-difluorinated vinyloxiranes. Their fluorination with HF-Py furnished trifluoromethylated allylic alcohols with exclusive E selectivity. On the other hand, their reduction
Polymer, 47, 4916-4916 (2006)
Jung Seok Lee et al.
Macromolecular bioscience, 15(9), 1314-1322 (2015-06-04)
We designed poly(β-amino esters) (PBAEs) bearing both UV light- and pH-sensitive groups and used PBAEs to prepare nanoparticles (NPs) that can be utilized for on-demand burst release of guest molecules in response to multiple triggers. Due to the presence of

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