152706
5-Fluorosalicylic acid
97%
Synonym(s):
5-Fluoro-2-hydroxybenzoic acid
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All Photos(2)
About This Item
Linear Formula:
FC6H3-2-(OH)CO2H
CAS Number:
Molecular Weight:
156.11
Beilstein:
2209120
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
97%
form
powder
mp
177-179 °C (lit.)
SMILES string
OC(=O)c1cc(F)ccc1O
InChI
1S/C7H5FO3/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,9H,(H,10,11)
InChI key
JWPRICQKUNODPZ-UHFFFAOYSA-N
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Application
5-Fluorosalicylic acid was used as internal standard in the quantification of salicylic acid.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Terézia Szabó-Plánka et al.
Journal of inorganic biochemistry, 105(1), 75-83 (2010-12-08)
The complexation of 3-, 4-, and 6-fluorosalicylic acids (HL) with copper(II) was investigated in aqueous solution by pH-potentiometry combined with UV-visible spectrophotometry, and in 50 v/v % water-methanol mixture by the two-dimensional ESR simulation method. Both methods showed the formation
Terézia Szabó-Plánka et al.
Journal of inorganic biochemistry, 102(1), 101-109 (2007-08-28)
The copper(II)-5-fluorosalicylic acid system was investigated in water and 50 v/v% water-methanol mixture by pH potentiometry combined with UV-vis spectrophotometry, and by the two-dimensional ESR simulation method, respectively. The data revealed that the stable paramagnetic mono- and bis(salicylato) copper(II) complexes
Wilfried Rozhon et al.
Analytical and bioanalytical chemistry, 382(7), 1620-1627 (2005-07-06)
Salicylic acid (SA) is an important signaling compound in plants and is involved in various defense responses. Here we report a new method for quantification of free and total soluble SA in Arabidopsis thaliana with 5-fluorosalicylic acid (5-FSA) as internal
Daiki Asakawa et al.
Journal of the American Society for Mass Spectrometry, 22(7), 1224-1233 (2011-09-29)
The use of 5-formylsalicylic acid (5-FSA) and 5-nitrosalicylic acid (5-NSA) as novel matrices for in-source decay (ISD) of peptides in matrix-assisted laser desorption/ionization (MALDI) is described. The use of 5-FSA and 5-NSA generated a- and x-series ions accompanied by oxidized
T K Christopoulos et al.
Analytical chemistry, 64(4), 342-346 (1992-02-15)
We report an ultrasensitive, enzymatically amplified, time-resolved fluorescence immunoassay with a terbium chelate as the detectable moiety. In this immunoassay, the primary label is the enzyme alkaline phosphatase (ALP). ALP cleaves phosphate out of a fluorogenic substrate, 5-fluorosalicyl phosphate, to
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