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Boron trifluoride - 1-butanol solution

~10% in 1-butanol (∼1.3 M), derivatization grade (GC derivatization), LiChropur

Synonym(s):

BF3 - Butanol solution

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$35.30
100 ML
$312.00

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10 ML
$35.30
100 ML
$312.00

About This Item

CAS Number:
MDL number:
UNSPSC Code:
12352200
PubChem Substance ID:
NACRES:
NA.05

$35.30


10 left in stockDetails

Request a Bulk Order

grade

derivatization grade (GC derivatization)

Quality Level

form

solution

quality

LiChropur
for esterification of fatty acids for GC purposes

reaction suitability

reagent type: derivatization reagent
reaction type: Alkylations

concentration

~10% in 1-butanol (∼1.3 M)

technique(s)

gas chromatography (GC): suitable

density

0.87 g/mL at 20 °C

storage temp.

2-8°C

SMILES string

FB(F)F

InChI

1S/BF3/c2-1(3)4

InChI key

WTEOIRVLGSZEPR-UHFFFAOYSA-N

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Application

Learn more in the Product Information
Boron trifluoride-1-butanol solution may be used as a derivatization agent in the separation and identification of water‐soluble low‐molecular‐weight carboxylic acids using capillary electrophoresis (CE) and gas chromatography coupled with mass spectrometry (GC-MS).[1]
Reagent for the esterification of carboxylic acids for GC analysis

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 3 - Skin Corr. 1A - STOT SE 3

target_organs

Central nervous system, Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 1

flash_point_f

95.0 °F - closed cup

flash_point_c

35 °C - closed cup

ppe

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


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Capillary electrophoresis determinative and GC-MS confirmatory method for water-soluble organic acids in airborne particulate matter and vehicle emission.
Dabek-Zlotorzynska E, et al.
Journal of Separation Science, 28(13), 1520-1528 (2005)
Karsten Müller et al.
Journal of chromatography. A, 1260, 9-15 (2012-09-11)
A method for the ultra trace analysis of 21 fluorobenzoic acids (FBAs) via GC-MS based on solid-phase extraction (SPE) and derivatization with BF3·MeOH is described. All fluorobenzoic acids were enriched and determined simultaneously. Solid-phase extraction on hydrophilic-lipophilic-balanced reversed-phase cartridges containing
Brieuc Guillerm et al.
Macromolecular rapid communications, 33(19), 1600-1612 (2012-07-05)
Polyoxazolines (POx) are increasingly being studied as polymeric building blocks due to the possibility of affording tunable properties. Additionally, as the biocompatibility and stealth behavior of POx are similar to that of poly(ethylene glycol) (PEG), it has become challenging to
G K Surya Prakash et al.
Organic letters, 13(15), 4128-4131 (2011-07-14)
The one-pot synthesis of 1,1,1-trifluoro- and 1,1-difluoro-2,2-diarylethanes from arenes and fluorinated hemiacetals in the BF(3)-H(2)O system is described. The reaction is simple, clean, and convenient, eliminating the use of organic solvents and other expensive acid systems. BF(3)-H(2)O is economic, is
Gewu Lu et al.
ACS nano, 2(11), 2342-2348 (2009-02-12)
Polythiophene (Pth) films with aligned nanotubule arrays were adhered strongly on various smooth surfaces such as glass, mica, and GaAs after drying from their wet states under ambient condition. The normal and shear dry adhesion forces of the films on

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