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Key Documents

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Safety Information

152706

Sigma-Aldrich

5-Fluorosalicylic acid

97%

Synonym(s):

5-Fluoro-2-hydroxybenzoic acid

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1 G
CN¥252.22
5 G
CN¥959.61

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1 G
CN¥252.22
5 G
CN¥959.61

About This Item

Linear Formula:
FC6H3-2-(OH)CO2H
CAS Number:
345-16-4
Molecular Weight:
156.11
Beilstein:
2209120
EC Number:
206-455-3
MDL number:
MFCD00002456
UNSPSC Code:
12352100
PubChem Substance ID:
24849252
NACRES:
NA.22

CN¥252.22

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Quality Level

100

Assay

97%

form

powder

mp

177-179 °C (lit.)

functional group

carboxylic acid
fluoro

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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Show Differences

1 of 4

This Item
27301247588A79809
5-Fluorosalicylic acid 97%

152706

5-Fluorosalicylic acid

Salicylic acid meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (calc. to the dried substance)

27301

Salicylic acid

Salicylic acid ACS reagent, ≥99.0%

247588

Salicylic acid

5-Aminosalicylic acid 95%

A79809

5-Aminosalicylic acid

assay

97%

assay

99.5-100.5% (calc. to the dried substance)

assay

≥99.0%

assay

95%

Quality Level

100

Quality Level

200

Quality Level

200

Quality Level

200

form

powder

form

-

form

-

form

powder with small lumps

mp

177-179 °C (lit.)

mp

158-161 °C (lit.)

mp

158-161 °C (lit.)

mp

275-280 °C (dec.) (lit.)

Application

5-Fluorosalicylic acid was used as internal standard in the quantification of salicylic acid[1].

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Regulatory Information

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    Certificates of Analysis (COA)

    Lot/Batch Number
    58896EM
    11596DM
    26596PK
    06730MH
    08021TE

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    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
    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
    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
    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
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