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483052

Sigma-Aldrich

Silver tetrafluoroborate

≥99.99% trace metals basis

Sinônimo(s):

Silver borofluoride

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About This Item

Fórmula linear:
AgBF4
Número CAS:
14104-20-2
Peso molecular:
194.67
Número CE:
237-956-5
Número MDL:
MFCD00003408
Código UNSPSC:
12352302
ID de substância PubChem:
24871863
NACRES:
NA.23
Ensaio:
≥99.99% trace metals basis
Formulário:
powder

Nível de qualidade

100

Ensaio

≥99.99% trace metals basis

Formulário

powder

adequação da reação

reagent type: catalyst
core: silver

Impurezas

≤100.0 ppm Trace Metal Analysis

pf

70-73 °C (lit.)

cadeia de caracteres SMILES

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

InChI

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

chave InChI

CCAVYRRHZLAMDJ-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Corrosion
GHS05

Palavra indicadora

Danger

Frases de perigo

H314

Classificações de perigo

Eye Dam. 1 - Skin Corr. 1B

Código de classe de armazenamento

8A - Combustible corrosive hazardous materials

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

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

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Certificados de análise (COA)

Lot/Batch Number
MKCK5846
MKCJ6333
MKCG3413
MKCD3255
MKBZ5501V

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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
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
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
M Yoshida et al.
Chemical & pharmaceutical bulletin, 38(6), 1551-1557 (1990-06-01)
Silver tetrafluoroborate (AgBF4) in trifluoroacetic acid (TFA) has been found to cleave the S-trimethyl-acetamidomethyl (Tacm) group or the S-acetamidomethyl (Acm) group without affecting other functional groups in a peptide chain. A newly isolated porcine brain natriuretic peptide-32 (pBNP-32) was synthesized
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
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