ABD-F
| Code | Size | Price |
|---|
| CDX-F0016-M010 | 10 mg | £157.00 |
Quantity:
Prices exclude any Taxes / VAT
Overview
Regulatory Status: RUO
Shipping:
Ambient
Storage:
-20 °C
Documents
Further Information
Alternate Names/Synonyms:
4-Fluoro-7-sulfobenzofurazan
Appearance:
White to yellow powder.
CAS:
91366-65-3
EClass:
32160000
Form (Short):
solid
GHS Symbol:
GHS07
Handling Advice:
Protect from light and moisture.
Hazards:
H315, H319, H335
InChi:
InChI=1S/C6H4FN3O3S/c7-3-1-2-4(14(8,11)12)6-5(3)9-13-10-6/h1-2H,(H2,8,11,12)
InChiKey:
XROXHZMRDABMHS-UHFFFAOYSA-N
Long Description:
Chemical. CAS: 91366-65-3. Formula: C6H4FN3O3S. MW: 217.18. Synthetic. Highly reactive fluorogenic reagent for the labeling of thiols for HPLC. ABD-F is nonfluorescent until reacted with thiols and therefore can be used to quantitate thiols in solution, as well as thiols separated by HPLC or TLC. ABD-F also reportedly reacts slowly with the hydroxy group of some tyrosine residues as well as amino groups in some proteins, forming products that are nonfluorescent but can be detected by absorbance at 385 nm.
MDL:
MFCD00036687
Molecular Formula:
C6H4FN3O3S
Molecular Weight:
217.18
Package Type:
Vial
Precautions:
P261, P305, P351, P338
Product Description:
Highly reactive fluorogenic reagent for the labeling of thiols for HPLC. ABD-F is nonfluorescent until reacted with thiols and therefore can be used to quantitate thiols in solution, as well as thiols separated by HPLC or TLC. ABD-F also reportedly reacts slowly with the hydroxy group of some tyrosine residues as well as amino groups in some proteins, forming products that are nonfluorescent but can be detected by absorbance at 385 nm.
Purity:
>98% (HPLC)
Signal Word:
Warning
SMILES:
NS(=O)(=O)C1=CC=C(F)C2=NON=C12
Solubility Chemicals:
Soluble in 1M ammonium hydroxide (50 mg/ml).
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) R. Karlsson, et al.; Anal. Biochem. 349(1), 136 (2006) | (2) R. B. Thompson et al.; J. Neurosc. Meth. 118(1), 63 (2002) | (3) T. Toyooka, K. Imai et al.; Anal. Chem. 56, 2461 (1984)