Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

207934

Sigma-Aldrich

Tetrafluoroboric acid solution

48 wt. % in H2O

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

About This Item

Linear Formula:
HBF4
CAS Number:
16872-11-0
Molecular Weight:
87.81
MDL number:
MFCD00011345
UNSPSC Code:
12352106
PubChem Substance ID:
329752030
NACRES:
NA.21

vapor density

3 (vs air)

Quality Level

200

vapor pressure

5 mmHg ( 20 °C)

form

liquid

concentration

46.0-52.0% in NaOH (titration)
48 wt. % in H2O

density

1.4 g/mL at 25 °C

SMILES string

F.FB(F)F

InChI

1S/BF3.FH/c2-1(3)4;/h;1H

InChI key

LEMQFBIYMVUIIG-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

Tetrafluoroboric acid is used as a catalyst for the protection and deprotection reactions of various carbohydrates. It participates in the synthesis of 4-sulfonic acid phenyl diazonium tetrafluoroborate, which was required for the preparation of sulfonated graphene (SG).

Application

Tetrafluoroboric acid solution may be used as a catalyst for the hydration of aromatic haloalkynes to α-halomethyl ketones in the absence of metal catalysts. It may also be used the epoxidized soybean oil (ESBO) ring opening step of fatty acids preparation.

Pictograms

Corrosion
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8B - Non-combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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

Tetrafluoroboric acid, an efficient catalyst in carbohydrate protection and deprotection reactions.
Albert R, et al.
Carbohydrate Research, 137, 282-290 (1985)
Polyols and polyurethanes prepared from epoxidized soybean oil ring-opened by polyhydroxy fatty acids with varying OH numbers.
Chen R, et al.
Journal of Applied Polymer Science, 132(1) (2015)
Arnis Abolins et al.
Materials (Basel, Switzerland), 14(4) (2021-03-07)
A second-generation bio-based feedstock-tall oil fatty acids-was epoxidised via two pathways. Oxirane rings were introduced into the fatty acid carbon backbone using a heterogeneous epoxidation catalyst-ion exchange resin Amberlite IR-120 H or enzyme catalyst Candida antarctica lipase B under the
Dong-Su Kim et al.
Organic letters, 12(5), 1092-1095 (2010-02-13)
A novel series of alkyne-containing potassium organotrifluoroborates were prepared in good yields from the corresponding haloaryltrifluoroborates and various alkynes via Sonogashira coupling reaction. Also, the Suzuki-Miyaura cross-coupling reaction of alkynylaryltrifluoroborates with aryl and alkenyl bromides was achieved in the presence
M P Dariel et al.
Dental materials : official publication of the Academy of Dental Materials, 11(3), 208-217 (1995-05-01)
The purpose of this study was to develop a new technology for preparing mercury-free metallic dental restorative materials. The novel approach relies on the cold welding of surface treated silver particles. At ambient temperature, intermetallic compound formation takes place spontaneously
View All Related Papers

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