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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

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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
Assay:
≥98.5% (HPLC)

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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

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Related Categories

Application

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

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Other Notes

Discover LiChropur reagents ideal for HPLC or LC-MS analysis

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)

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Certificates of Analysis (COA)

Lot/Batch Number
BCCH2941

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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
Total plasma homocysteine analysis by HPLC with SBD-F precolumn derivatization.
I Fermo et al.
Methods in molecular biology (Clifton, N.J.), 159, 237-244 (2000-10-29)
J Tanaka et al.
Journal of biochemistry, 127(4), 597-601 (2000-03-31)
Pseudomonas sp. 109 produces a unique lipase (LipL) which efficiently catalyzes intramolecular transesterification of omega-hydroxyesters to form macrocyclic lactones. The production of the enzymatically active LipL requires a specific molecular chaperon (LimL protein) together with a low-M(r) lipase-activation-factor (LAF) of
K Noguchi et al.
Journal of pharmaceutical and biomedical analysis, 10(7), 515-520 (1992-07-01)
A HPLC method is developed for the determination of glutathione isopropyl ester, a drug for the treatment of cerebral vascular disease, in rat, dog and human blood. The blood is deproteinized with sulphosalicylic acid and the clear supernatant treated with
Fluorometric assay of thiols with fluorobenzoxadiazoles.
K Imai et al.
Methods in enzymology, 143, 67-75 (1987-01-01)
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