产品名称
三氟化硼-1-丁醇 溶液, ~10% in 1-butanol (∼1.3 M), derivatization grade (GC derivatization), LiChropur™
InChI key
WTEOIRVLGSZEPR-UHFFFAOYSA-N
SMILES string
FB(F)F
InChI
1S/BF3/c2-1(3)4
grade
derivatization grade (GC derivatization)
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
Quality Level
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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).
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
存储类别
3 - Flammable liquids
wgk
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
法规信息
监管及禁止进口产品
此项目有
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)
T Mizuno et al.
The Journal of chemical physics, 136(7), 074305-074305 (2012-03-01)
Recoil frame photoelectron angular distributions (RFPADs) of BF(3) molecules are presented over the energy region of the shape resonance in the F 1s continuum. Time-dependent density functional theory calculations are also given to understand the shape resonance dynamics. The RFPADs
The influence of the acidity of ionic liquids on catalysis.
Xinjiang Cui et al.
ChemSusChem, 3(9), 1043-1047 (2010-08-18)
Joanna E Rode et al.
Chirality, 24(1), 5-16 (2011-12-06)
Stabilization energies of the electron donor-acceptor sulfinimine···BF(3) complexes calculated at either the B3LYP/aug-cc-pVTZ or the MP2/aug-cc-pVTZ level do not allow to judge, whether the N- or O-atom in sulfinimine is stronger electron-donor to BF(3) . The problem seems to be
Casey R Wade et al.
Chemical communications (Cambridge, England), 46(34), 6380-6381 (2010-08-07)
The presence of a proximal cationic group in zwitterionic aryltrifluoroborates such as o-(Ph(2)MeP)C(6)H(4)(BF(3)) stabilizes these compounds against hydrolysis.
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