Skip to Content
Merck

46640

7-Fluorobenzofurazan-4-sulfonic acid ammonium salt

derivatization grade (HPLC), LiChropur™, ≥98.5% (HPLC)

Synonym(s):

4-Fluoro-7-sulfobenzofurazan ammonium salt, 7-Fluorobenz-2,1,3-oxadiazole-4-sulfonic acid ammonium salt, Ammonium 7-fluorobenzofurazan-4-sulfonate, SBD-F

Sign In to View Organizational & Contract Pricing.

Select a Size

All Photos(3)

About This Item

Linear Formula:
C6H3FN2O4S · NH3
CAS Number:
84806-27-9
Molecular Weight:
235.19
UNSPSC Code:
23151817
NACRES:
NA.22
PubChem Substance ID:
329757223
MDL number:
MFCD02682109
Beilstein/REAXYS Number:
5199564

Product Name

7-Fluorobenzofurazan-4-sulfonic acid ammonium salt, derivatization grade (HPLC), LiChropur™, ≥98.5% (HPLC)

InChI

1S/C6H3FN2O4S.H3N/c7-3-1-2-4(14(10,11)12)6-5(3)8-13-9-6;/h1-2H,(H,10,11,12);1H3

SMILES string

N.OS(=O)(=O)c1ccc(F)c2nonc12

InChI key

JXLHNMVSKXFWAO-UHFFFAOYSA-N

grade

derivatization grade (HPLC)

assay

≥98.5% (HPLC)

quality

LiChropur™

technique(s)

HPLC: suitable

fluorescence

λex 385 nm; λem 524 nm in 0.1 M borate pH 9.5 (after derivatization with glutathione)

storage temp.

2-8°C

Quality Level

100

Looking for similar products? Visit Product Comparison Guide

Related Categories

Application

Fluorescent probe for thiols and pre-column labeling of biological thiols for HPLC

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Legal Information

LiChropur is a trademark of Merck KGaA, Darmstadt, Germany

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
BCCH2941

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

B L Ling et al.
Journal of pharmaceutical and biomedical analysis, 10(10-12), 985-988 (1992-10-01)
The present investigation analyses the potentials of capillary chromatography using packed fused silica capillaries filled with 5 microns RP-18 for the fluorescence determination of glutathione in human blood samples. Adaptation of conventional HPLC equipment for miniaturized chromatographic assays proved successful.
N P Dudman et al.
Clinical chemistry, 42(12), 2028-2032 (1996-12-01)
The recognition of homocysteine as a vascular risk factor has led to increased clinical interest in assaying plasma homocysteine concentrations. Our aim was to improve the reliability of a widely used assay based on HPLC of the fluorescent 7-benzo-2-oxa-1, 3-diazole-4-sulfonic
Saori Ichinose et al.
Biomedical chromatography : BMC, 23(9), 935-939 (2009-04-09)
A semi-micro column HPLC-fluorescence method for routine determination of thiol derivatives such as homocysteine (Hcy), cysteine (Cys) and cysteamine (CA) is described. The thiol derivatives labeled with ammonium-7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonate (SBD-F) were isocratically separated within 12 min on a semi-micro ODS column
P E Cornwell et al.
Journal of chromatography, 617(1), 136-139 (1993-07-23)
A modification of a previously published method for analysis of total homocysteine in human serum is presented. The modification was implemented to allow use of a different derivatizing agent (i.e., 7-fluorobenzo-2-oxa-1,3-diazole-4-sulfonamide) which reacts much faster than the original derivatizing reagent
I Daskalakis et al.
Biomedical chromatography : BMC, 10(5), 205-212 (1996-09-01)
A sensitive HPLC-fluorescence method for determining total endogenous plasma homocysteine (Hcy), cysteine (Cys) and cysteinylglycine (Cys-Gly) following derivatization with ammonium 7-fluoro 2,1,3-benzoxadiazole-4-sulphonate (SBD-F) is described. Quantitation utilizes an internal standard, 2-mercaptoethylamine. The derivatization procedure has been optimized for concentration of
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service