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2,4,6-Trihydroxybenzoic acid monohydrate, 90+%, Thermo Scientific Chemicals
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Catalog number B22768.14
also known as B22768-14
Price (USD)/ Each
74.80
-
Quantity:
25 g
Price (USD)/ Each
74.80
2,4,6-Trihydroxybenzoic acid monohydrate, 90+%, Thermo Scientific Chemicals
Catalog numberB22768.14
Price (USD)/ Each
74.80
-
Chemical Identifiers
CAS71989-93-0
IUPAC Name2,4,6-trihydroxybenzoate
Molecular FormulaC7H5O5
InChI KeyIBHWREHFNDMRPR-UHFFFAOYSA-M
SMILESOC1=CC(O)=C(C([O-])=O)C(O)=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)White to pale cream to pale yellow
Assay (Aqueous acid-base Titration)≥90.0 to ≤110.0%
FormPowder
2,4,6-Trihydroxybenzoic acid monohydrate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
2,4,6-Trihydroxybenzoic acid monohydrate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water.
Notes
Store in cool, dry conditions in a sealed container. Incompatible with oxidizing agents.
2,4,6-Trihydroxybenzoic acid monohydrate is an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff fields.
Solubility
Soluble in water.
Notes
Store in cool, dry conditions in a sealed container. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- Russell G. Dushin; Samuel J. Danishefsky. Total syntheses of KS-501, KS-502, and their enantiomers. J. Am. Chem. Soc. 1992, 114 (2), 655-659.
- H. J. Brömme; W. Mörke and E. Peschke. Transformation of barbituric acid into alloxan by hydroxyl radicals: interaction with melatonin and with other hydroxyl radical scavengers. Journal of Pineal Research. 2002, 33 (4), 239-247.