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CAS RN: 29270-56-2 | Product Number: A5593
NBD-F (=4-Fluoro-7-nitro-2,1,3-benzoxadiazole) [for HPLC Labeling]
Purity: >99.0%(HPLC)
Synonyms:
- 4-Fluoro-7-nitrobenzofurazan
- 4-Fluoro-7-nitro-2,1,3-benzoxadiazole
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days |
---|---|---|---|
100MG |
$174.00
|
≥100 | 20 |
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* The storage conditions are subject to change without notice.
Product Number | A5593 |
Purity / Analysis Method | >99.0%(HPLC) |
Molecular Formula / Molecular Weight | C__6H__2FN__3O__3 = 183.10 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Frozen (<0°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Heat Sensitive |
Packaging and Container | 100MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 29270-56-2 |
Reaxys Registry Number | 1077571 |
PubChem Substance ID | 87563200 |
SDBS (AIST Spectral DB) | 50330 |
MDL Number | MFCD00010196 |
Specifications
Appearance | White to Yellow to Green powder to crystal |
Purity(HPLC) | min. 99.0 area% |
Effect test of HPLC derivatization | Effective as labeling agent for L-Isoleucine |
Properties (reference)
Melting Point | 55 °C |
Solubility (soluble in) | Chloroform |
GHS
Pictogram | |
Signal Word | Warning |
Hazard Statements | H315 : Causes skin irritation. H319 : Causes serious eye irritation. |
Precautionary Statements | P264 : Wash skin thoroughly after handling. P280 : Wear protective gloves/ eye protection/ face protection. P302 + P352 : IF ON SKIN: Wash with plenty of water. P337 + P313 : If eye irritation persists: Get medical advice/ attention. P305 + P351 + P338 : IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. P362 + P364 : Take off contaminated clothing and wash it before reuse. P332 + P313 : If skin irritation occurs: Get medical advice/ attention. |
Related Laws:
Transport Information:
H.S.code* | 2934.99-000 |
Application
HPLC Labeling Reagent for Amines and Thiols
The compound 1 which is an HPLC fluorescence labeling reagent having a 2,1,3-benzoxadiazole skeleton, can easily react with amino or mercapto groups to form the corresponding derivatives. 1 itself does not fluoresce, and its ethanol solution is relatively stable for a week in a refrigerator. The derivatives can reach the detector without any decomposition under reversed phase HPLC. An excellent chromatogram can be obtained by fluorescence detection at the excitation and emission wavelengths of 470 nm and 530 nm, respectively. Since their excitation and fluorescence wavelengths are at longer wavelengths, detection has less interference by contaminants. Thus, further highly sensitive detection can be done by using laser induced fluorescence detector. When the reagent is hydrolyzed (NBD-OH), its fluorescence can be erased under an acidic condition. Therefore, this hydrolyzed reagent can be used as a post column reaction reagent5,7).
Application example:
[Amino acids] 2,3)
To 10 µL of 50 µM amino acid standard solution, add 10 µL of 0.1 M boric acid buffer solution (pH 8.0) and 20 µL of 50 mM labeling reagent 1 in ethanol solution, and incubate the mixture at 60 °C for 1 min. Immediately cool it with ice bath, and add 460 µL of 5 mM HCl to the reactant solution. Use 10 µL of the solution as an HPLC sample.
[Amino acids] 2,3)
To 10 µL of 50 µM amino acid standard solution, add 10 µL of 0.1 M boric acid buffer solution (pH 8.0) and 20 µL of 50 mM labeling reagent 1 in ethanol solution, and incubate the mixture at 60 °C for 1 min. Immediately cool it with ice bath, and add 460 µL of 5 mM HCl to the reactant solution. Use 10 µL of the solution as an HPLC sample.
TCI Products Pamphlet
HPLC Labeling Reagents ( PDF 10MB )
HPLC Labeling Reagents ( PDF 10MB )
References
- 1)K. Imai, Y. Watanabe, Anal. Chim. Acta 1981, 130, 377.
- 2)Y. Watanabe, K. Imai, Anal. Biochem. 1981, 116, 471.
- 3)Y. Watanabe, K. Imai, J. Chromatogr. 1982, 239, 723.
- 4)T. Toyo’oka, Y. Watanabe, K. Imai, Anal. Chim. Acta 1983, 149, 305.
- 5)Y. Watanabe, K. Imai, Anal. Chem. 1983, 55, 1786.
- 6)Y. Watanabe, K. Imai, J. Chromatogr. 1984, 309, 279.
- 7)H. Miyano, T. Toyo’oka, K. Imai, Anal. Chim. Acta 1985, 170, 81.
- 8)H. Kotaniguchi, M. Kawakatsu, T. Toyo’oka, K. Imai, J. Chromatogr. 1987, 420, 141.
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