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4-Fluoro-N-methylaniline, 97%, Thermo Scientific Chemicals
| Catalog Number | Quantity |
|---|---|
| ALFH55105.06 | 5 g |
Catalog number ALFH55105.06
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Quantity:
5 g
Specifications
Chemical Name or Material4-Fluoro-N-methylaniline
CAS459-59-6
Health Hazard 1H227-H302+H312+H332-H315-H319-H335
Health Hazard 2GHS H Statement
H318-H302-H317-H335-H227-H315
Causes serious eye damage.
Harmful if swallowed.
May cause an allergic skin reaction.
May cause respiratory irritation.
Combustible liquid.
Causes skin irritation.
H318-H302-H317-H335-H227-H315
Causes serious eye damage.
Harmful if swallowed.
May cause an allergic skin reaction.
May cause respiratory irritation.
Combustible liquid.
Causes skin irritation.
Health Hazard 3P210-P235-P261-P264b-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P362-P370+P378q-P501c
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4-Fluoro-N-methylaniline is used as a model compound to study the biotransformation of secondary aromatic amines.
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-Fluoro-N-methylaniline is used as a model compound to study the biotransformation of secondary aromatic amines.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents , acids, acid chloride, acid anhydride and chloroformates.
4-Fluoro-N-methylaniline is used as a model compound to study the biotransformation of secondary aromatic amines.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents , acids, acid chloride, acid anhydride and chloroformates.
RUO – Research Use Only
General References:
- James P. Driscoll.; Ignacio Aliagas.; Jennifer J. Harris, Jason S. Halladay.; Sheerin Khatib-Shahidi.; Alan Deese.; Nathaniel Segraves.; S. Cyrus Khojasteh-Bakht. Formation of a Quinoneimine Intermediate of 4-Fluoro-N-methylaniline by FMO1: Carbon Oxidation Plus Defluorination. Chem. Res. Toxico. 2011, 23 (5), 861-863.
- M G Boersma.; N H Cnubben.; W J van Berkel.; M Blom.; J Vervoor.; I M Rietjens. Role of cytochromes P-450 and flavin-containing monooxygenase in the biotransformation of 4-fluoro-N-methylaniline. DMD. 1993, 21 (2), 218-230.