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483052

Sigma-Aldrich

Silver tetrafluoroborate

≥99.99% trace metals basis

Synonym(s):

Silver borofluoride

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About This Item

Linear Formula:
AgBF4
CAS Number:
14104-20-2
Molecular Weight:
194.67
EC Number:
237-956-5
MDL number:
MFCD00003408
UNSPSC Code:
12352302
PubChem Substance ID:
24871863
NACRES:
NA.23

Quality Level

100

assay

≥99.99% trace metals basis

form

powder

reaction suitability

reagent type: catalyst
core: silver

impurities

≤100.0 ppm Trace Metal Analysis

mp

70-73 °C (lit.)

SMILES string

[Ag+].F[B-](F)(F)F

InChI

1S/Ag.BF4/c;2-1(3,4)5/q+1;-1

InChI key

CCAVYRRHZLAMDJ-UHFFFAOYSA-N

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Related Categories

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS6012
MKCK5846
MKCJ6333
MKCG3413
MKCD3255

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Omar Green et al.
Journal of the American Chemical Society, 126(19), 5952-5953 (2004-05-13)
Incorporation of silver tetrafluoroborate (AgBF4) into poly(vinyl phenyl ketone) (PVPK) renders the photoluminescent polymer responsive to ethylene. Polymer films prepared with a 2:1 ratio of Ag+ ions to polymer acetophenone groups responded with a quench of photoluminescence. Conditioned films showed
Min Li et al.
Talanta, 78(4-5), 1364-1370 (2009-04-14)
The extraction/enrichment of omega-3 polyunsaturated fatty acid methyl esters (PUFAMEs) by hydrophobic ionic liquids (ILs) containing silver salts as the extraction phase has been extended to include equilibrium studies. The extraction time, organic solvents, IL structures, and AgBF4 concentrations all
M Yoshida et al.
Chemical & pharmaceutical bulletin, 38(1), 273-275 (1990-01-01)
Silver tetrafluoroborate (AgBF4) in trifluoroacetic acid (TFA) has been found to cleave the S-trimethylacetamidomethyl (Tacm) group or the S-acetamidomethyl (Acm) group without affecting other functional groups in the peptide chain. Newly isolated porcine brain natriuretic peptide-32 (pBNP-32) was synthesized using
Zbigniew J Kamiński et al.
Journal of the American Chemical Society, 127(48), 16912-16920 (2005-12-01)
A new generation of triazine-based coupling reagents (TBCRs), designed according to the concept of "superactive esters", was obtained by treatment of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium (DMTMM) chloride with lithium or silver tetrafluoroborate. The structure of 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium tetrafluoroborate was confirmed by X-ray diffraction. Activation
Matthew C Achilonu et al.
Organic letters, 10(17), 3865-3868 (2008-08-06)
A novel and efficient method for the oxidative condensation of tetra-O-methyl-3-oxocatechin 4 with tetra-O-methylcatechin is described. Treatment of a solution of 3 (2 equiv) and 4 (1 equiv) with silver tetrafluoroborate readily affords the phenolic per-O-methyl ethers of 3-oxocatechin(4-8)-catechin 18
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