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7-Amino-4-nitro-2,1,3-benzoxadiazole

Product Code:
 
CDX-A0176
Product Group:
 
Dyes, Stains, and Probes
Supplier:
 
Chemodex
Regulatory Status:
 
RUO
Shipping:
 
Ambient
Storage:
 
+4°C
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Chemical Structure
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Chemical Structure

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CDX-A0176-M100100 mg£139.00
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CDX-A0176-M500500 mg£529.00
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This product comes from: Switzerland.
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Further Information

Alternate Names/Synonyms:
7-Amino-NBD; 7-Amino-4-nitro-2,1,3-benzoxadiazole; 7-Nitro-4-aminobenzofurazan; ABF
Appearance:
White powder.
CAS:
10199-91-4
EClass:
32160000
Form (Short):
liquid
GHS Symbol:
GHS07
Handling Advice:
Keep cool and dry.Protect from light and moisture.
Hazards:
H315, H319
InChi:
InChI=1S/C6H4N4O3/c7-3-1-2-4(10(11)12)6-5(3)8-13-9-6/h1-2H,7H2
InChiKey:
YXKOGLINWAPXPE-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 10199-91-4. Formula: C6H4N4O3. MW: 180.12. Synthetic. Fluorogenic amine. Building block and reagent for synthesis of fluorescent probes. Used for the preparation of fluorogenic substrates, chemosensors and probes, in which NBD-amine is the high fluoresence component after release. Shows constant fluorescence intensity from pH2-9. Spectral data: Ex=472nm, Em=555nm (TRIS buffer, pH7.8)
MDL:
MFCD00168449
Molecular Formula:
C6H4N4O3
Molecular Weight:
180.12
Package Type:
Vial
Precautions:
P280, P302+P352, P305+P351+P338
Product Description:
Fluorogenic amine. Building block and reagent for synthesis of fluorescent probes. Used for the preparation of fluorogenic substrates, chemosensors and probes, in which NBD-amine is the high fluoresence component after release. Shows constant fluorescence intensity from pH2-9. Spectral data: Ex=472nm, Em=555nm (TRIS buffer, pH7.8)
Purity:
>99% (HPLC)
Signal word:
Warning
SMILES:
NC1=CC=C(C2=NON=C12)[N+]([O-])=O
Solubility Chemicals:
Soluble in methanol.
Source / Host:
Synthetic.
Transportation:
Non-hazardous
UNSPSC Category:
Fluorescent Reagents
UNSPSC Number:
41105331
Use & Stability:
Stable for at least 2 years after receipt when stored at -20°C.

References

(1) E. Sato, et al.; Chem. Pharm. Bull. 32, 336 (1984) | (2) S. Uchiyama, et al.; J. Chem. Soc. Perkin Trans. 2, 2165 (1998) | (3) H. Ikeda, et al.; Org. Biomol. Chem. 3, 4262 (2005) | (4) W. Jiang, et al.; Angew. Chem. Int. Ed. 46, 8445 (2007) | (5) B. Heyne, et al.; Org. Biomol. Chem. 6, 354 (2008) | (6) G. Zhou, et al.; Tetrahedron 69, 867 (2013)