Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
BF3 · MeOH
CAS Number:
Molecular Weight:
99.85
UNSPSC Code:
12352104
NACRES:
NA.23
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
3611499
Concentration:
12-16% (titration by NaOH), 14% in methanol
Form:
liquid
form
liquid
Quality Level
reaction suitability
reagent type: catalyst
core: boron
concentration
12-16% (titration by NaOH), 14% in methanol
density
0.859 g/mL at 25 °C
storage temp.
2-8°C
SMILES string
CO.FB(F)F
InChI
1S/CH4O.BF3/c1-2;2-1(3)4/h2H,1H3;
InChI key
JBXYCUKPDAAYAS-UHFFFAOYSA-N
General description
Boron trifluoride-methanol (BF-M) is an esterification reagent. BF-M is a powerful acidic catalyst for the esterification of the fatty acids. It easily cleaves acetylated dyes resulting in free amino groups. BF-M catalyzed trans esterification of vegetable oils forms biodiesel.
Application
Used in the deactylation of acetanilides.It is also used to study the synthesis of amino group containing cyanine dyes of different types and to prepare fatty acid methyl esters.
Packaging
Bottle with screw-cap closure.
Still not finding the right product?
Explore all of our products under Boron trifluoride-methanol solution
signalword
Danger
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1A - STOT RE 2 Inhalation - STOT SE 1
target_organs
Eyes,Central nervous system, Kidney
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
49.5 °F
flash_point_c
9.7 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Related Content
Product Information Sheet
Donghee Kim et al.
The British journal of nutrition, 121(2), 137-145 (2018-12-07)
Conversion of α-linolenic acid (ALA) into the longer chain n-3 PUFA has been suggested to be affected by the dietary intake of linoleic acid (LA), but the mechanism is not well known. Therefore, the purpose of this study was to
Deacylation of N-Acetylated Amines with Alcohol and Boron Trifluoride.
Acta Chemica Scandinavica, 8, 529-530 (1954)
Martin Trépanier et al.
Applied and environmental microbiology, 71(9), 5341-5347 (2005-09-10)
Lipids are the major form of carbon storage in arbuscular-mycorrhizal fungi. We studied fatty acid synthesis by Glomus intraradices and Gigaspora rosea. [(14)C]Acetate and [(14)C]sucrose were incorporated into a synthetic culture medium to test fatty acid synthetic ability in germinating



