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Assay
93%
form
solid
mp
210-212 °C (lit.)
SMILES string
OC(=O)c1ccc(Cl)cc1O
InChI
1S/C7H5ClO3/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,9H,(H,10,11)
InChI key
LWXFCZXRFBUOOR-UHFFFAOYSA-N
Application
4-Chlorosalicylic acid was used in sensitive spectrofluorometric determination of terbium in mixed rare earths. It was used in preparation of poly(4-chlorosalicylic acid-formaldehyde) via condensation with formaldehyde.
Biochem/physiol Actions
4-Chlorosalicylic acid shows potent antibacterial activity against Escherichia coli.
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
Certificates of Analysis (COA)
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Journal of microbiological methods, 75(1), 117-126 (2008-07-03)
4-Chlorosalicylate (4-CS) can be degraded completely by a bacterial consortium consisting of Pseudomonas reinekei (MT1), Achromobacter spanius (MT3) and Pseudomonas veronii (MT4). The fourth species Wautersiella falsenii (MT2) is thought to act as a 'necrotizer' of the community. Single cell
4-Chlorosalicylic acid-formaldehyde polymer as a polymeric ligand.
Makromol. Chem., 106(1), 223-237 (1982)
Inhibitory effects of 4-chlorosalicylic acid on mushroom tyrosinase and its antimicrobial activities.
Food Chemistry, 107(2), 797-803 (2008)
Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 19(6), 923-925 (2003-07-02)
The quadruple complex formed by terbium with 4-chlorosalicylic acid (CSA), EDTA and cetyltrimethylammonium bromide (CTMAB) has been used for the sensitive spectrofluorometric determination of terbium in mixed rare earths. The effect of the experimental conditions on the fluorescence intensity was
Journal of bacteriology, 185(23), 6790-6800 (2003-11-18)
Pseudomonas sp. strain MT1 is capable of degrading 4- and 5-chlorosalicylates via 4-chlorocatechol, 3-chloromuconate, and maleylacetate by a novel pathway. 3-Chloromuconate is transformed by muconate cycloisomerase of MT1 into protoanemonin, a dominant reaction product, as previously shown for other muconate
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