2,3-Dihydroxybenzoic acid, 98%
2,3-Dihydroxybenzoic acid, 98%
2,3-Dihydroxybenzoic acid, 98%
Thermo Scientific Chemicals

2,3-Dihydroxybenzoic acid, 98%

CAS: 303-38-8 | C7H6O4 | 154.121 g/mol
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Catalog number A10144.18
also known as A10144-18
Price (USD)
356.65
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396.00
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Quantity:
50 g
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Price (USD)
356.65
Online Exclusive
396.00
Save 39.35 (10%)
Each
Chemical Identifiers
CAS303-38-8
IUPAC Name2,3-dihydroxybenzoic acid
Molecular FormulaC7H6O4
InChI KeyGLDQAMYCGOIJDV-UHFFFAOYSA-N
SMILESOC(=O)C1=CC=CC(O)=C1O
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SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Pale cream to pale brown or pale pink
FormCrystals or powder or crystalline powder
Assay (Aqueous acid-base Titration)≥97.5 to ≤102.5%
Assay (Silylated GC)≥97.5%
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.

Suitable for battery materials development.

Applications
Dihydroxybenzoic acids are used as intermediates for pharmaceuticals and other organic synthesis. Used as matrix for ionization of peptides, proteins and carbohydrates. In industrial field used for resins, polyesters, plasticizers, dyestuffs, preservatives, and rubber chemicals. It is also used as is a selected phenol as MMP (Matrix Metalloproteinase) inhibitor.

Solubility
Soluble in water, methanol and dimethyl sulfoxide.

Notes
Store away from strong oxidizing agents. keep container tightly closed. Store in cool, dry conditions in well sealed containers.
RUO – Research Use Only

General References:

  1. Rubino MT; Maggi D; Laghezza A; Loiodice F; Tortorella P. Identification of novel matrix metalloproteinase inhibitors by screening of phenol fragments library. Arch. Pharm. 2011, 344,(9), 557-63.
  2. James L. Corbin; William A. Bulen. Identification Isolation and identification of 2,3-dihydroxybenzoic acid and .N2,N6-di(2,3-dihydroxybenzoyl)-L-lysine formed by iron-deficient Azotobacter vinelandii. Biochemistry. 1969, 8,(3), 757-762.