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Merck
CN

15716

Boron trifluoride-methanol solution

~10% (~1.3 M), derivatization grade (GC derivatization), LiChropur

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About This Item

Linear Formula:
BF3 · MeOH
CAS Number:
Molecular Weight:
99.85
UNSPSC Code:
12352104
NACRES:
NA.05
PubChem Substance ID:
EC Number:
206-766-4
Beilstein/REAXYS Number:
3611499
MDL number:
Concentration:
~10% (~1.3 M)
Form:
liquid
Grade:
derivatization grade (GC derivatization)
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grade

derivatization grade (GC derivatization)

Quality Level

product line

LiChropur

form

liquid

quality

LiChropur

reaction suitability

reagent type: derivatization reagent
reaction type: Esterifications

concentration

~10% (~1.3 M)

technique(s)

gas chromatography (GC): suitable

density

0.86 g/mL at 20 °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 (BF3) is a Lewis acid; it is a very useful reagent for forming esters from acids. Boron trifluoride is commercially available as a 14% solution in methanol for forming esters derivatives. It catalysed reactions carried out in a water bath are very rapid and can be completed in a few minutes. Boron-trifluoride-catalysed transesterification of vegetable oils is one of the most popular methods. For transesterification of vegetable oils, BF3 is used in methanol (15 to 20% w/v).

Application

Boron trifluoride-methanol solution may be used for catalysing a method, used for the synthesis of bishydroperoxides and their derivatives, based on a reaction of ketals with a solution of hydrogen peroxide in anhydrous ether. It may also be used for the rapid preparation of fatty acid esters for gas chromatographic analysis, as it converts fatty acids to their respective methyl esters in about 2 minutes.
Learn more in the Product Information
Suitable for derivatization of hydroxy fatty acids.

Other Notes

Reagent for esterifying fatty acid for gas chromatographic analysis.
Reagent for methyl ester, O-acetyl.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany


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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

Regulatory Information

危险化学品

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Biodiesel: A Realistic Fuel Alternative for Diesel Engines.
Demirbas A.
Technology & Engineering, 123-124 (2007)
Christian F Ruiz et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 34(8), 10574-10589 (2020-06-23)
Cancer cells require extensive metabolic reprograming in order to provide the bioenergetics and macromolecular precursors needed to sustain a malignant phenotype. Mutant KRAS is a driver oncogene that is well-known for its ability to regulate the ERK and PI3K signaling
A new method for the synthesis of bishydroperoxides based on a reaction of ketals with hydrogen peroxide catalyzed by boron trifluoride complexes.
Alexander TO
Tetrahedron Letters, 44 (39), 7359-7363 (2003)



Global Trade Item Number

SKUGTIN
15716-10X1ML04061837683121
15716-1L04061838743220
15716-100ML04061838743206
15716-250ML04061837810619
15716-10ML04061838743213
15716-1ML04061837683138