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Merck
CN

33125-U

Supelco

BF3 - Butanol solution

10 % (w/w)

Synonym(s):

Boron trifluoride

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About This Item

CAS Number:
7637-07-2
MDL number:
MFCD00011316
UNSPSC Code:
23151816
PubChem Substance ID:
329754459

Key Documents

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grade

derivatization grade ((GC derivatization))

reaction suitability

reagent type: derivatization reagent
reaction type: Acylations
reagent type: derivatization reagent
reaction type: Esterifications

packaging

pkg of 1 × 100 mL (33125-U)

concentration

10 % (w/w)

SMILES string

FB(F)F

InChI

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

InChI key

WTEOIRVLGSZEPR-UHFFFAOYSA-N

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General description

Boron trifluoride is a colourless gas which readily reacts with water to form hydrates. It has been widely used as catalyst for polymerizations, alkylations and condensation reactions. It is used as gas flux for internal soldering or brazing. It also finds application in being used as extinguisher for magnesium fires. Furthermore esterification by BF3-butanol helps in obtaining volatile derivatives of aliphatic acids such as hydroxyacids.

Application

It was used in extraction and derivatization of γ−hydroxybutyrate from human plasma or urine during a study to determine 1,4-butanediol and γ-hydroxybutyrate using capillary gas chromatography.

Other Notes

Reagent for butyl esters and trifluoroacetyl.

Signal Word

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 Code

3 - Flammable liquids

WGK

WGK 1

Flash Point(F)

99.0 °F - closed cup

Flash Point(C)

37.2 °C - closed cup

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
LC21144V
LC08711

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J L Iverson et al.
Journal - Association of Official Analytical Chemists, 60(2), 284-288 (1977-03-01)
Butter oil is extracted from butter with hexane, using a rolling boil technique. The resulting 10% butter oil in hexane is converted to butyl esters, using butanol in place of methanol as specified in the official final action method, 28.063-28.067.
M.A. Lambert and C.W. Moss
Journal of Chromatography A, 74, 335-335 (1972)
Compressed Gas Association
Handbook of Compressed Gases, 271-271 (2012)
Ramanathan Rajaganesh et al.
Carbohydrate research, 345(12), 1649-1657 (2010-06-29)
BF(3).Et(2)O-catalysed O-glycosylation of 1,2,3-tri-O-acetyl-4,6-O-butylidene- and ethylidene-beta-d-glucopyranose with different aliphatic and aromatic alcohols proceeds for the most part with complete retention of anomeric configuration. Antioxidant activity of O-glycosides shows significant inhibition (IC(50) approximately 77%). 1,3-Dipolar cycloaddition of terminal alkyne derivatives of
Joseph J Topczewski et al.
The Journal of organic chemistry, 74(18), 6965-6972 (2009-08-25)
The first total synthesis of (+)-schweinfurthin B, a potent and differentially active cytotoxic agent, has been accomplished. Completion of the synthesis required just 16 steps in the longest linear sequence from commercially available vanillin. Key synthetic transformations included a Shi
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