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About This Item
Linear Formula:
NOBF4
CAS Number:
Molecular Weight:
116.81
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352101
EC Number:
238-679-2
MDL number:
Assay:
95%
InChI key
KGCNVGDHOSFKFT-UHFFFAOYSA-N
InChI
1S/BF4.NO/c2-1(3,4)5;1-2/q-1;+1
SMILES string
N#[O+].F[B-](F)(F)F
assay
95%
reaction suitability
reagent type: oxidant
storage temp.
2-8°C
Quality Level
Related Categories
Application
Nitrosyl tetrafluoroborate is an efficient nitrosating and diazotizing agent. It reacts with alcohols and secondary amines to yield alkyl nitrites and nitrosamines, respectively. It reacts with primary amines to yield diazonium tetrafluoroborates. NOBF4 is also a mild oxidant and commonly used for single electron transfer oxidation.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
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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Angang Dong et al.
Journal of the American Chemical Society, 133(4), 998-1006 (2010-12-24)
The ability to engineer surface properties of nanocrystals (NCs) is important for various applications, as many of the physical and chemical properties of nanoscale materials are strongly affected by the surface chemistry. Here, we report a facile ligand-exchange approach, which
Azodesilylierung?eine neue aprotische Diazotierungstechnik.
Weiss
Chemische Berichte, 117(5), 1965-1972 (1984)
New synthetic reagents and reactions.
Olah, George A
Aldrichimica Acta, 12,
number=(3), 43-49 (1979)
S Mohr et al.
The Journal of biological chemistry, 274(14), 9427-9430 (1999-03-27)
S-Nitrosylation of protein thiol groups by nitric oxide (NO) is a widely recognized protein modification. In this study we show that nitrosonium tetrafluoroborate (BF4NO), a NO+ donor, modified the thiol groups of glyceraldehyde-3-phosphate dehydrogenase (GAPDH) by S-nitrosylation and caused enzyme
Electronically regulated thermally and light-gated electron transfer from anions to naphthalenediimides.
Guha, Samit et al.
Journal of the American Chemical Society, 133(39), 15256-15259 (2011)
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