4-Nitrobenzenediazonium tetrafluoroborate, 97%
4-Nitrobenzenediazonium tetrafluoroborate, 97%
4-Nitrobenzenediazonium tetrafluoroborate, 97%
4-Nitrobenzenediazonium tetrafluoroborate, 97%
Thermo Scientific Chemicals

4-Nitrobenzenediazonium tetrafluoroborate, 97%

CAS: 456-27-9 | C6H4BF4N3O2 | 236.92 g/mol
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Catalog NumberQuantity
ALFH55315.031 g
Catalog number ALFH55315.03
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1 g
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Specifications
Chemical Name or Material4-Nitrobenzenediazonium tetrafluoroborate
CAS456-27-9
Health Hazard 1H302+H312+H332-H314-H335
Health Hazard 2GHS H Statement
H314-H318-H302-H312-H332
Causes severe skin burns and eye damage.
Causes serious eye damage.
Harmful if swallowed.
Harmful in contact with skin.
Harmful if inhaled.
Health Hazard 3P260-P264b-P270-P271-P280-P303+P361+P353-P304+P340-P305+P351+P338-P310-P330-P331-P363-P501c
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4-Nitrobenzenediazonium tetrafluoroborate is widely used as a standard reagent in organic synthesis. It is used as a dye for enterochromaffin cells. It is used for the spectrophotometric determination of common aromatic diisocyanates [toluene-2,4-diyl diisocyanate and 4,4'-methylenebis(phenyl isocyanate)] and gallic acid. It is also used for tissue staining and determination of trace phenols.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
4-Nitrobenzenediazonium tetrafluoroborate is widely used as a standard reagent in organic synthesis. It is used as a dye for enterochromaffin cells. It is used for the spectrophotometric determination of common aromatic diisocyanates [toluene-2,4-diyl diisocyanate and 4,4′-methylenebis(phenyl isocyanate)] and gallic acid. It is also used for tissue staining and determination of trace phenols.

Solubility
Soluble in acetonitrile and dimethyl sulfoxide.

Notes
Moisture sensitive. Store in a cool place. Keep the container tightly closed. Incompatible with strong bases, strong oxidizing agents and moisture.
RUO – Research Use Only

General References:

  1. Brisset, F.; Vieillard, J.; Berton, B.; Grognet, S. M.; Poc, C. D.; Derf, F. L. Surface functionalization of cyclic olefin copolymer with aryldiazonium salts: A covalent grafting method. Appl. Surf. Sci. 2015, 329, 337-346.
  2. Mooste, M.; Kibena, E.; Kozlova, J.; Marandi, M.; Matisen, L.; Niilisk, A.; Sammelselg, V.; Tammeveski, K. Electrografting and morphological studies of chemical vapour deposition grown graphene sheets modified by electroreduction of aryldiazonium salts. Electrochim. Acta 2015, 161, 195-204.