25455
4-Chloro-7-nitrobenzofurazan
BioReagent, suitable for fluorescence, ≥97.0% (HPLC)
Synonyme(s) :
4-Chloro-7-nitro-1,2,3-benzoxadiazole, NBD-chloride
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A propos de cet article
Formule empirique (notation de Hill) :
C6H2ClN3O3
Numéro CAS:
Poids moléculaire :
199.55
UNSPSC Code:
12352100
NACRES:
NA.32
PubChem Substance ID:
EC Number:
233-496-4
Beilstein/REAXYS Number:
614212
MDL number:
Assay:
≥97.0% (HPLC)
Service technique
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BioReagent
Quality Segment
assay
≥97.0% (HPLC)
mp
97-100 °C, 97-99 °C (lit.)
fluorescence
λex 336 nm in methanol, λex 420 nm; λem ~540 nm in ethanol (after derivatization with glycine)
suitability
suitable for fluorescence
SMILES string
[O-][N+](=O)c1ccc(Cl)c2nonc12
InChI
1S/C6H2ClN3O3/c7-3-1-2-4(10(11)12)6-5(3)8-13-9-6/h1-2H
InChI key
IGHBXJSNZCFXNK-UHFFFAOYSA-N
Application
4-Chloro-7-nitrobenzofurazan (NBD-chloride) is a fluorescence assay reagent used to label free sulfhydryls and N-terminals within proteins. NBD-chloride is used as an enzyme inhibitor and as a trapping agent for cysteine sulfenic acid.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Classe de stockage
11 - Combustible Solids
wgk
WGK 3
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Leslie B Poole et al.
Methods in enzymology, 348, 122-136 (2002-03-12)
C165S AhpC in its sulfenate (Cys-SO-) and presumed thiolate (Cys-S-) forms at pH 7 (pKa for sulfenic acid about pH 6.1) exhibit low extinction absorbance bands around 367 and 324 nm, respectively. Sulfenic acid content of the protein can be
Rob van Zwieten et al.
Biochimica et biophysica acta, 1821(12), 1493-1500 (2012-09-11)
Maintenance of the asymmetric distribution of phospholipids across the plasma membrane is a prerequisite for the survival of erythrocytes. Various stimuli have been shown to induce scrambling of phospholipids and thereby exposure of phosphatidylserine (PS). In two types of patients
Rolffy Ortiz-Andrade et al.
Journal of ethnopharmacology, 143(2), 455-462 (2012-07-24)
Justicia spicigera is a plant species used for the Teenak (Huesteca Potosina) and Mayan (Yucatan peninsula) indigenous for the empirical treatment of diabetes, infections and as stimulant. To evaluate the cytotoxicity, antioxidant and antidiabetic properties of J. spicigera. The effects
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 25455-5G | 04061825998763 |
| 25455-1G | 04061825998749 |
| 25455-25G | 04061825998756 |